Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:101129784-101130116 | Rare:60 | ||||
chr11:101914850-101915393 | Common:8; Rare:162 | ||||
chr11:102047322-102047489 | Common:1; Rare:55 | ||||
chr11:102110048-102110460 | Common:1; Rare:143 | ||||
chr11:102317241-102317571 | Rare:65 | ||||
chr11:102325236-102325563 | Common:1; Rare:86 | ||||
chr11:102347150-102347298 | Common:2; Rare:57 | ||||
chr11:102452526-102452943 | Common:2; Rare:137 | ||||
chr11:103109215-103109508 | Common:1; Rare:78; Clinvar (benign):1 | ||||
chr11:104163870-104164392 | Common:4; Rare:157 | ||||
chr11:106077307-106077740 | Common:2; Rare:140 | ||||
chr11:107565718-107565793 | Rare:22 | ||||
chr11:108008958-108009034 | Common:1; Rare:22 | ||||
chr11:108009142-108009168 | Rare:7 | ||||
chr11:108009291-108009384 | Rare:43 |