ID: 130006752 | ATAC-STARR-seq lymphoblastoid silent region 3902 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111871217..111871526) | | |
ID: 130006751 | ATAC-STARR-seq lymphoblastoid active region 5521 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111829702..111829841) | | |
ID: 130006750 | ATAC-STARR-seq lymphoblastoid active region 5520 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111829264..111829383) | | |
ID: 130006749 | ATAC-STARR-seq lymphoblastoid silent region 3901 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111797209..111797288) | | |
ID: 130006748 | ATAC-STARR-seq lymphoblastoid silent region 3900 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111777386..111777545) | | |
ID: 130006747 | ATAC-STARR-seq lymphoblastoid active region 5519 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111766405..111766454) | | |
ID: 127822502 | H3K27ac hESC enhancer GRCh37_chr11:111749557-111750176 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111878833..111879452) | | |
ID: 127822501 | H3K4me1 hESC enhancer GRCh37_chr11:111709725-111710226 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111839002..111839503) | | |
ID: 127822500 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:111636139-111637042 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111765415..111766384) | | |
ID: 127822499 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:111605768-111606404 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111735044..111735680) | | |
ID: 127822498 | H3K4me1 hESC enhancer GRCh37_chr11:111603371-111604187 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111732647..111733463) | | |
ID: 127822497 | H3K4me1 hESC enhancer GRCh37_chr11:111594031-111594566 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111723307..111723842) | | |
ID: 127822496 | H3K4me1 hESC enhancer GRCh37_chr11:111563346-111563859 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111692622..111693135) | | |
ID: 126861338 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr11:111685391-111686590 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111814667..111815866) | | |
ID: 124902756 | uncharacterized LOC124902756 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111794308..111802685) | | |
ID: 100101932 | G protein subunit gamma 5 pseudogene 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111864193..111864698) | | |
ID: 644338 | ribosomal protein L37a pseudogene 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111889136..111889822, complement) | RPL37A_3_1174 | |
ID: 91893 | ferredoxin-fold anticodon binding domain containing 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111874056..111879165, complement) | hCG_2033039 | |
ID: 79796 | ALG9 alpha-1,2-mannosyltransferase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111768025..111871581, complement) | CDG1L, DIBD1, GIKANIS, LOH11CR1J | 606941 |
ID: 64776 | cilia and flagella associated protein 68 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111879541..111885975) | C11orf1 | |