Variant report

Variant rs536127570
Chromosome Location chr4:1399450-1399451
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1396200-1400800 Enhancers Pancreas Pancrea
2 chr4:1396800-1402600 Bivalent Enhancer Fetal Brain Male brain
3 chr4:1397000-1399600 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
4 chr4:1397200-1401000 Bivalent Enhancer Brain Hippocampus Middle brain
5 chr4:1397600-1401000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
6 chr4:1397600-1401200 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr4:1397600-1402400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
8 chr4:1398000-1400600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
9 chr4:1398000-1401600 Bivalent Enhancer Duodenum Smooth Muscle Duodenum
10 chr4:1398600-1402600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
11 chr4:1398800-1399600 Bivalent Enhancer Brain Germinal Matrix brain
12 chr4:1398800-1401000 Bivalent Enhancer Spleen Spleen
13 chr4:1398800-1402400 Bivalent Enhancer Right Ventricle heart
14 chr4:1399000-1399600 Bivalent Enhancer H1 Cell Line embryonic stem cell
15 chr4:1399000-1402200 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
16 chr4:1399200-1399800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
17 chr4:1399200-1399800 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
18 chr4:1399400-1399600 Bivalent Enhancer Fetal Intestine Small intestine
19 chr4:1399400-1400400 Bivalent Enhancer Esophagus oesophagus

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