Variant report

Variant rs16937529
Chromosome Location chr8:49417380-49417381
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49413600-49418800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:49414200-49420000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr8:49414400-49419800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr8:49414600-49418600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr8:49414600-49418600 Weak transcription Fetal Muscle Leg muscle
6 chr8:49414600-49427000 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr8:49415400-49422000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr8:49415600-49420400 Weak transcription NHDF-Ad bronchial
9 chr8:49415800-49425200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr8:49416600-49417400 Enhancers Fetal Muscle Trunk muscle
11 chr8:49416600-49417400 Enhancers Pancreas Pancrea
12 chr8:49416800-49417400 Enhancers Fetal Intestine Small intestine
13 chr8:49416800-49417400 Enhancers Stomach Mucosa stomach
14 chr8:49417000-49417400 Enhancers NHEK skin
15 chr8:49417200-49417400 Enhancers Colonic Mucosa Colon
16 chr8:49417200-49417600 Enhancers Hela-S3 cervix
17 chr8:49417200-49417800 Enhancers Esophagus oesophagus

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