| ID: 130000040 | ATAC-STARR-seq lymphoblastoid silent region 19028 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23559376..23559435) | | |
| ID: 130000039 | ATAC-STARR-seq lymphoblastoid silent region 19027 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23558976..23559065) | | |
| ID: 130000038 | ATAC-STARR-seq lymphoblastoid active region 27121 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23552769..23552938) | | |
| ID: 130000037 | ATAC-STARR-seq lymphoblastoid active region 27120 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23529990..23530059) | | |
| ID: 130000036 | ATAC-STARR-seq lymphoblastoid silent region 19026 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23529240..23529489) | | |
| ID: 130000035 | ATAC-STARR-seq lymphoblastoid silent region 19025 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23528830..23529189) | | |
| ID: 130000034 | ATAC-STARR-seq lymphoblastoid active region 27119 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23528650..23528699) | | |
| ID: 127458954 | H3K4me1 hESC enhancer GRCh37_chr8:23407857-23408358 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23550344..23550845) | | |
| ID: 127458953 | H3K4me1 hESC enhancer GRCh37_chr8:23399784-23400565 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23542271..23543052) | | |
| ID: 127458952 | H3K4me1 hESC enhancer GRCh37_chr8:23339113-23340081 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23481600..23482568) | | |
| ID: 121009645 | ENTPD4 divergent transcript [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23457771..23494895) | | |
| ID: 116186924 | CRISPRi-validated cis-regulatory element chr8.847 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23508623..23509479) | | |
| ID: 106481194 | RNA, U4 small nuclear 71, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23600026..23600138, complement) | | |
| ID: 105379327 | uncharacterized LOC105379327 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23491477..23494202, complement) | | |
| ID: 646721 | SINHCAF pseudogene 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23634875..23635649, complement) | FAM60DP | |
| ID: 646708 | DnaJ heat shock protein family (Hsp40) member C5 pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23480987..23483716, complement) | | |
| ID: 51312 | solute carrier family 25 member 37 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23528956..23575463) | HT015, MFRN, MFRN1, MSC, MSCP, PRO1278, PRO1584, PRO2217 | 610387 |