Variant report

Variant rs72633041
Chromosome Location chr8:39961967-39961968
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:39951000-39968000 Weak transcription Rectal Smooth Muscle rectum
2 chr8:39956000-39963800 Weak transcription Colon Smooth Muscle Colon
3 chr8:39957000-39962200 Enhancers Placenta Amnion Placenta Amnion
4 chr8:39958000-39970800 Weak transcription Rectal Mucosa Donor 31 rectum
5 chr8:39959600-39964000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr8:39959600-39965800 Weak transcription HUVEC blood vessel
7 chr8:39959600-39976400 Weak transcription Pancreas Pancrea
8 chr8:39960800-39962000 Enhancers HepG2 liver
9 chr8:39960800-39962400 Enhancers Stomach Mucosa stomach
10 chr8:39961000-39962000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr8:39961000-39962600 Enhancers Fetal Intestine Small intestine
12 chr8:39961000-39963000 Enhancers Fetal Intestine Large intestine
13 chr8:39961000-39964000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr8:39961200-39963200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr8:39961600-39962000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
16 chr8:39961600-39962200 Flanking Active TSS A549 lung
17 chr8:39961600-39962200 Enhancers Hela-S3 cervix
18 chr8:39961800-39970400 Weak transcription Placenta Placenta

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