Variant report

Variant rs57987646
Chromosome Location chr4:125354669-125354670
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:125350600-125358800 Weak transcription Fetal Intestine Small intestine
2 chr4:125350800-125357000 Weak transcription Pancreas Pancrea
3 chr4:125350800-125357200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr4:125350800-125359000 Weak transcription Right Atrium heart
5 chr4:125352400-125356000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr4:125352600-125354800 Enhancers A549 lung
7 chr4:125353800-125357000 Weak transcription Fetal Adrenal Gland Adrenal Gland
8 chr4:125353800-125358800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr4:125354200-125354800 Enhancers Fetal Heart heart
10 chr4:125354400-125354800 Enhancers HUVEC blood vessel
11 chr4:125354400-125355000 Enhancers Gastric stomach
12 chr4:125354400-125356200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr4:125354400-125358800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr4:125354400-125359000 Weak transcription Stomach Mucosa stomach
15 chr4:125354600-125356200 Weak transcription Fetal Lung lung
16 chr4:125354600-125358800 Weak transcription Muscle Satellite Cultured Cells --
17 chr4:125354600-125358800 Weak transcription Rectal Mucosa Donor 31 rectum
18 chr4:125354600-125358800 Weak transcription NHEK skin

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