Variant report

Variant rs55721111
Chromosome Location chr7:27233666-27233667
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27226800-27236000 Weak transcription A549 lung
2 chr7:27227200-27233800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
3 chr7:27231400-27236400 Active TSS Colon Smooth Muscle Colon
4 chr7:27231600-27234000 Bivalent Enhancer Primary T helper naive cells from peripheral blood blood
5 chr7:27231800-27233800 Bivalent/Poised TSS Rectal Mucosa Donor 29 rectum
6 chr7:27232800-27233800 Flanking Bivalent TSS/Enh Skeletal Muscle Male skeletal muscle
7 chr7:27232800-27234000 Flanking Active TSS Osteobl bone
8 chr7:27233000-27238200 Weak transcription Pancreas Pancrea
9 chr7:27233200-27233800 Bivalent/Poised TSS Fetal Intestine Small intestine
10 chr7:27233200-27238000 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
11 chr7:27233400-27233800 Bivalent Enhancer H1 Cell Line embryonic stem cell
12 chr7:27233400-27233800 Flanking Active TSS Rectal Mucosa Donor 31 rectum
13 chr7:27233400-27233800 Flanking Active TSS Rectal Smooth Muscle rectum
14 chr7:27233600-27233800 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
15 chr7:27233600-27233800 Enhancers Hela-S3 cervix
16 chr7:27233600-27233800 Enhancers HSMM muscle
17 chr7:27233600-27234400 Active TSS Placenta Placenta
18 chr7:27233600-27234800 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin

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