Variant report

Variant rs16936986
Chromosome Location chr8:49334320-49334321
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49330600-49334400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr8:49331000-49334600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr8:49331000-49334600 Enhancers NHDF-Ad bronchial
4 chr8:49331200-49334400 Enhancers Fetal Lung lung
5 chr8:49331200-49334800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr8:49331600-49334400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr8:49332200-49335000 Weak transcription Fetal Stomach stomach
8 chr8:49332400-49340200 Weak transcription Fetal Intestine Small intestine
9 chr8:49332800-49334400 Enhancers Fetal Brain Male brain
10 chr8:49332800-49334600 Enhancers NHLF lung
11 chr8:49332800-49338600 Weak transcription Spleen Spleen
12 chr8:49333000-49334400 Enhancers HSMM muscle
13 chr8:49333000-49335200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr8:49333200-49334400 Enhancers Fetal Brain Female brain
15 chr8:49333400-49339800 Weak transcription Pancreas Pancrea
16 chr8:49333600-49334600 Enhancers Muscle Satellite Cultured Cells --
17 chr8:49333800-49341400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr8:49334000-49335200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr8:49334000-49339800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
20 chr8:49334200-49335200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
21 chr8:49334200-49339800 Weak transcription Right Atrium heart

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