Variant report

Variant rs573819357
Chromosome Location chr4:782509-782510
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:778600-784800 Bivalent Enhancer Fetal Thymus thymus
2 chr4:780400-784800 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr4:780800-788800 Weak transcription Right Atrium heart
4 chr4:781000-782800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
5 chr4:781000-786000 Weak transcription Pancreas Pancrea
6 chr4:781200-782600 Weak transcription Left Ventricle heart
7 chr4:781200-782800 Weak transcription Right Ventricle heart
8 chr4:781200-784600 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr4:781400-783600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
10 chr4:781400-783600 Enhancers Spleen Spleen
11 chr4:781800-785600 Weak transcription Primary T helper 17 cells PMA-I stimulated --
12 chr4:782000-782600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
13 chr4:782000-786000 Weak transcription GM12878-XiMat blood
14 chr4:782200-783000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
15 chr4:782400-782600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
16 chr4:782400-782600 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
17 chr4:782400-782600 Bivalent Enhancer Placenta Placenta
18 chr4:782400-782800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
19 chr4:782400-782800 Flanking Active TSS Liver Liver
20 chr4:782400-783000 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
21 chr4:782400-783200 Flanking Bivalent TSS/Enh HepG2 liver
22 chr4:782400-783600 Enhancers Esophagus oesophagus
23 chr4:782400-783600 Bivalent Enhancer Fetal Intestine Large intestine
24 chr4:782400-783800 Enhancers Gastric stomach
25 chr4:782400-784200 Enhancers Rectal Mucosa Donor 31 rectum

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