Variant report

Variant rs57046573
Chromosome Location chr4:3454327-3454328
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3452400-3457000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:3453000-3454400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr4:3453000-3454400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr4:3453000-3454400 Enhancers Liver Liver
5 chr4:3453200-3454400 Enhancers Muscle Satellite Cultured Cells --
6 chr4:3453200-3454400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
7 chr4:3453200-3454400 Enhancers Fetal Stomach stomach
8 chr4:3453200-3454600 Enhancers Stomach Mucosa stomach
9 chr4:3453400-3454400 Enhancers NHDF-Ad bronchial
10 chr4:3453600-3454400 Enhancers HMEC breast
11 chr4:3453600-3454400 Enhancers HSMM muscle
12 chr4:3453600-3454800 Enhancers Fetal Intestine Small intestine
13 chr4:3453800-3454400 Flanking Active TSS HepG2 liver
14 chr4:3453800-3454600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr4:3453800-3454800 Enhancers Fetal Intestine Large intestine
16 chr4:3454000-3454400 Weak transcription Pancreas Pancrea
17 chr4:3454200-3454400 Enhancers Esophagus oesophagus

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