Variant report

Variant rs62294129
Chromosome Location chr4:784176-784177
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 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 chr4:781000-786000 Weak transcription Pancreas Pancrea
5 chr4:781200-784600 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr4:781800-785600 Weak transcription Primary T helper 17 cells PMA-I stimulated --
7 chr4:782000-786000 Weak transcription GM12878-XiMat blood
8 chr4:782400-784200 Enhancers Rectal Mucosa Donor 31 rectum
9 chr4:782600-784600 Bivalent Enhancer Duodenum Mucosa Duodenum
10 chr4:782600-786600 Bivalent Enhancer Fetal Muscle Leg muscle
11 chr4:782800-784800 Enhancers Liver Liver
12 chr4:783000-786600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr4:783200-784600 Bivalent Enhancer Fetal Intestine Small intestine
14 chr4:783800-784600 Bivalent Enhancer Colonic Mucosa Colon
15 chr4:783800-784600 Bivalent Enhancer Fetal Intestine Large intestine
16 chr4:783800-785800 Weak transcription Gastric stomach
17 chr4:784000-784200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr4:784000-784200 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
19 chr4:784000-784200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr4:784000-789800 Bivalent Enhancer Placenta Placenta

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