| ID: 129999004 | ATAC-STARR-seq lymphoblastoid active region 26403 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101244865..101245104) | | |
| ID: 129999003 | ATAC-STARR-seq lymphoblastoid active region 26402 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101244725..101244774) | | |
| ID: 129999002 | ATAC-STARR-seq lymphoblastoid active region 26401 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101217758..101217877) | | |
| ID: 129999001 | ATAC-STARR-seq lymphoblastoid silent region 18481 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101217378..101217657) | | |
| ID: 129662063 | ReSE screen-validated silencer GRCh37_chr7:100870334-100870510 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101227053..101227229) | | |
| ID: 127457204 | H3K4me1 hESC enhancer GRCh37_chr7:100883201-100883744 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101239920..101240463) | | |
| ID: 127457203 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100874831-100875752 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101231550..101232471) | | |
| ID: 127457202 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100861252-100861793 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101217971..101218512) | | |
| ID: 127457201 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100859968-100860490 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101216687..101217237) | | |
| ID: 127457200 | H3K4me1 hESC enhancer GRCh37_chr7:100846277-100847083 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101202996..101203802) | | |
| ID: 127457199 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100845469-100846276 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101202188..101202995) | | |
| ID: 652624 | ribosomal protein SA pseudogene 46 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101203600..101204571, complement) | RPSA_14_827 | |
| ID: 646409 | diacylglycerol O-acyltransferase 2 like 7, pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101201813..101203275, complement) | DGAT2L7 | |
| ID: 51024 | fission, mitochondrial 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101239472..101245081, complement) | CGI-135, TTC11 | 609003 |
| ID: 24146 | claudin 15 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101232094..101238820, complement) | | 615778 |
| ID: 10467 | zinc finger HIT-type containing 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101218165..101224190) | CG1I, ZNFN4A1, p18(Hamlet) | 618617 |
| ID: 8985 | procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101205984..101217581, complement) | BCARD, LH3 | 603066 |