| ID: 130066951 | ATAC-STARR-seq lymphoblastoid silent region 13454 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19122297..19122736) | | |
| ID: 130066950 | ATAC-STARR-seq lymphoblastoid silent region 13452 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19109713..19109762) | | |
| ID: 130066949 | ATAC-STARR-seq lymphoblastoid silent region 13451 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19036019..19036188) | | |
| ID: 127895273 | H3K27ac hESC enhancer GRCh37_chr22:19109284-19109785 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19121771..19122272) | | |
| ID: 127895272 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:19101726-19102620 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19114213..19115107) | | |
| ID: 127895271 | H3K4me1 hESC enhancer GRCh37_chr22:19097874-19098375 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19110361..19110862) | | |
| ID: 127895270 | H3K4me1 hESC enhancer GRCh37_chr22:19097371-19097873 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19109858..19110360) | | |
| ID: 127895269 | H3K4me1 hESC enhancer GRCh37_chr22:19093647-19094147 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19106134..19106634) | | |
| ID: 127895268 | H3K4me1 hESC enhancer GRCh37_chr22:19074057-19074556 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19086544..19087043) | | |
| ID: 127895267 | H3K4me1 hESC enhancer GRCh37_chr22:19073555-19074056 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19086042..19086543) | | |
| ID: 127895266 | H3K4me1 hESC enhancer GRCh37_chr22:19024185-19024805 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19036672..19037292) | | |
| ID: 124905078 | uncharacterized LOC124905078 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19094687..19100184, complement) | | |
| ID: 117134596 | family with sequence similarity 246 member C (gene/pseudogene) [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19029524..19030221) | | |
| ID: 100996435 | CA15 pseudogene 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19031528..19034922, complement) | | |
| ID: 100129262 | ribosomal protein L28 pseudogene 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19055841..19056187) | | |
| ID: 26220 | DiGeorge syndrome critical region gene 5 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18970468..19031242) | DGCR10, DGCR9, DGS-A, DGS-B, LINC00037, NCRNA00037, POM121L5P, RIP | 618040 |
| ID: 25786 | DiGeorge syndrome critical region gene 11 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19046162..19048375, complement) | DGS-D | |
| ID: 23752 | testis specific serine kinase 1A (pseudogene) [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19124874..19125887) | SPOGA1, STK22A, TSSK1P, TSSK1b, TSSK7P, TSSK1A | |
| ID: 9993 | DiGeorge syndrome critical region gene 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19036286..19122412, complement) | DGS-C, IDD, LAN, SEZ-12 | 600594 |