| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102110197-102110471 | Common:1; Rare:105 | ||||
| chr11:102112113-102112116 | |||||
| chr11:102317241-102317546 | Rare:60 | ||||
| chr11:102347105-102347449 | Common:4; Rare:100 | ||||
| chr11:102448853-102449145 | Rare:64 | ||||
| chr11:102452605-102452899 | Common:1; Rare:96 | ||||
| chr11:103092052-103092262 | Common:1; Rare:69 | ||||
| chr11:106077326-106077730 | Common:2; Rare:125 | ||||
| chr11:107457744-107457965 | Common:3; Rare:73 | ||||
| chr11:107858862-107859213 | Common:1; Rare:76 | ||||
| chr11:108008810-108009180 | Common:1; Rare:94 | ||||
| chr11:108009264-108009361 | Rare:47 | ||||
| chr11:108121360-108121672 | Common:5; Rare:109; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222591-108223146 | Common:1; Rare:177; Clinvar:9; Clinvar (benign):1 | ||||
| chr11:108223365-108223447 | Rare:18 |