ID: 129993527 | ATAC-STARR-seq lymphoblastoid active region 22267 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186201897..186201946) | | |
ID: 129993526 | ATAC-STARR-seq lymphoblastoid silent region 15858 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186191364..186191893) | | |
ID: 127402088 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:187185702-187186473 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186264548..186265319) | | |
ID: 127402087 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr4:187170964-187171708 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186249810..186250554) | | |
ID: 127402086 | H3K27ac hESC enhancer GRCh37_chr4:187164982-187165509 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186243828..186244355) | | |
ID: 127402085 | NANOG-H3K27ac hESC enhancer GRCh37_chr4:187164453-187164981 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186243299..186243827) | | |
ID: 127402084 | NANOG-H3K27ac hESC enhancer GRCh37_chr4:187162259-187162864 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186241105..186241710) | | |
ID: 127402083 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:187147168-187147838 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186226014..186226684) | | |
ID: 126807251 | MED14-independent group 3 enhancer GRCh37_chr4:187091342-187092541 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186170109..186171387) | | |
ID: 124900873 | uncharacterized LOC124900873 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186238405..186240494) | | |
ID: 100873907 | LTO1 pseudogene 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186170863..186171257, complement) | ORAOV1P1 | |
ID: 651430 | uncharacterized LOC651430 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186189032..186191490, complement) | | |
ID: 285441 | F11 antisense RNA 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186286098..186501058, complement) | | |
ID: 285440 | cytochrome P450 family 4 subfamily V member 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186191567..186213463) | BCD, CYP4AH1 | 608614 |
ID: 25854 | family with sequence similarity 149 member A [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186104704..186175337) | MST119, MSTP119 | |
ID: 3818 | kallikrein B1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186210853..186258471) | KLK3, PKK, PKKD, PPK | 229000 |
ID: 2160 | coagulation factor XI [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186266189..186289681) | FXI, PTA | 264900 |