Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:102736844-102736928 | Common:1; Rare:36 | ||||
chr2:105037833-105038110 | Common:3; Rare:97 | ||||
chr2:105337448-105337658 | Common:2; Rare:86 | ||||
chr2:106065554-106065754 | Common:3; Rare:54 | ||||
chr2:106194243-106194568 | Common:6; Rare:138 | ||||
chr2:108377844-108377993 | Common:1; Rare:33 | ||||
chr2:108534199-108534483 | Common:7; Rare:117 | ||||
chr2:108719414-108719577 | Common:2; Rare:67; Clinvar (benign):2 | ||||
chr2:109613841-109613996 | Common:1; Rare:58 | ||||
chr2:110204956-110205109 | Rare:67; Clinvar:1 | ||||
chr2:111884151-111884234 | Rare:24 | ||||
chr2:112275404-112275642 | Common:1; Rare:78 | ||||
chr2:112542126-112542493 | Common:1; Rare:113 | ||||
chr2:112584358-112584633 | Common:1; Rare:72 | ||||
chr2:112645701-112645947 | Common:1; Rare:91 |