Variant report

Variant rs76295932
Chromosome Location chr1:154882647-154882648
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:154879200-154893200 Weak transcription Stomach Smooth Muscle stomach
2 chr1:154879800-154894800 Weak transcription Aorta Aorta
3 chr1:154880400-154894400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
4 chr1:154881000-154883800 Weak transcription Right Ventricle heart
5 chr1:154881400-154894800 Weak transcription Brain Inferior Temporal Lobe brain
6 chr1:154881600-154895800 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr1:154881800-154883200 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr1:154882200-154891200 Weak transcription Fetal Stomach stomach
9 chr1:154882400-154883600 Enhancers Spleen Spleen
10 chr1:154882400-154897800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr1:154882600-154882800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr1:154882600-154882800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
13 chr1:154882600-154885000 Enhancers Esophagus oesophagus
14 chr1:154882600-154889200 Weak transcription Fetal Intestine Small intestine

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