Variant report

Variant rs4722671
Chromosome Location chr7:27230988-27230989
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27226400-27232400 Weak transcription NHDF-Ad bronchial
2 chr7:27226800-27236000 Weak transcription A549 lung
3 chr7:27227200-27233800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr7:27228400-27232000 Bivalent Enhancer Placenta Placenta
5 chr7:27228800-27231600 Weak transcription Pancreas Pancrea
6 chr7:27229400-27231200 Enhancers HSMMtube muscle
7 chr7:27229400-27231600 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
8 chr7:27229800-27233200 Active TSS HSMM muscle
9 chr7:27230400-27231000 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
10 chr7:27230400-27231000 Active TSS Colon Smooth Muscle Colon
11 chr7:27230600-27231600 Flanking Active TSS Rectal Mucosa Donor 31 rectum
12 chr7:27230600-27231800 Flanking Bivalent TSS/Enh Rectal Mucosa Donor 29 rectum
13 chr7:27230600-27232200 Flanking Bivalent TSS/Enh Fetal Muscle Leg muscle
14 chr7:27230800-27231000 Flanking Bivalent TSS/Enh Rectal Smooth Muscle rectum
15 chr7:27230800-27231200 Active TSS Colonic Mucosa Colon
16 chr7:27230800-27231200 Flanking Bivalent TSS/Enh Skeletal Muscle Male skeletal muscle
17 chr7:27230800-27231400 Bivalent Enhancer Primary T helper naive cells fromperipheralblood blood
18 chr7:27230800-27231800 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
19 chr7:27230800-27231800 Flanking Active TSS Osteobl bone
20 chr7:27230800-27233200 Flanking Active TSS Muscle Satellite Cultured Cells --

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