ID: 132089736 | Neanderthal introgressed variant-containing enhancer experimental_110728 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95739270..95739439) | | |
ID: 132089735 | Neanderthal introgressed variant-containing enhancer experimental_110694 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95573600..95573769) | | |
ID: 132089734 | Neanderthal introgressed variant-containing enhancer experimental_110687 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95547373..95547542) | | |
ID: 130002135 | ATAC-STARR-seq lymphoblastoid silent region 20074 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95762616..95762665) | | |
ID: 130002134 | ATAC-STARR-seq lymphoblastoid active region 28641 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95724485..95724584) | | |
ID: 129662482 | ReSE screen-validated silencer GRCh37_chr9:98472872-98473055 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95710590..95710773) | | |
ID: 127815371 | H3K4me1 hESC enhancer GRCh37_chr9:98534876-98535833 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95772503..95773551) | | |
ID: 127815370 | H3K4me1 hESC enhancer GRCh37_chr9:98499629-98500151 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95737347..95737869) | | |
ID: 127815369 | H3K4me1 hESC enhancer GRCh37_chr9:98499106-98499628 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95736824..95737346) | | |
ID: 127815368 | H3K4me1 hESC enhancer GRCh37_chr9:98432177-98433092 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95669895..95670810) | | |
ID: 127815367 | H3K4me1 hESC enhancer GRCh37_chr9:98431260-98432176 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95668978..95669894) | | |
ID: 127815366 | H3K4me1 hESC enhancer GRCh37_chr9:98363413-98363912 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95601131..95601630) | | |
ID: 127815365 | H3K4me1 hESC enhancer GRCh37_chr9:98362911-98363412 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95600629..95601130) | | |
ID: 127815364 | H3K4me1 hESC enhancer GRCh37_chr9:98327201-98327700 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95564919..95565418) | | |
ID: 127815363 | H3K4me1 hESC enhancer GRCh37_chr9:98326699-98327200 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95564417..95564918) | | |
ID: 127815362 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:98315131-98316095 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95552849..95553813) | | |
ID: 127815361 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:98314166-98315130 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95551884..95552848) | | |
ID: 124310601 | Sharpr-MPRA regulatory region 8876 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95666527..95666821) | | |
ID: 117134610 | proteasome subunit alpha 7 pseudogene 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95652887..95653171) | PSMA7P | |
ID: 113839574 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:98389397-98390596 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95626583..95628314) | | |