Variant report

Variant rs7010651
Chromosome Location chr8:126417768-126417769
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:126404400-126424400 Weak transcription Spleen Spleen
2 chr8:126414000-126422800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr8:126417000-126417800 Enhancers HUES6 Cell Line embryonic stem cell
4 chr8:126417000-126418000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr8:126417000-126418200 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr8:126417000-126418200 Enhancers HepG2 liver
7 chr8:126417000-126418200 Enhancers HUVEC blood vessel
8 chr8:126417200-126417800 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr8:126417200-126417800 Enhancers H1 Cell Line embryonic stem cell
10 chr8:126417200-126417800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr8:126417200-126417800 Enhancers Fetal Muscle Trunk muscle
12 chr8:126417200-126417800 Enhancers NH-A brain
13 chr8:126417400-126417800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr8:126417400-126417800 Enhancers HUES64 Cell Line embryonic stem cell
15 chr8:126417400-126417800 Enhancers Ovary ovary
16 chr8:126417600-126418000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
17 chr8:126417600-126418000 Enhancers A549 lung
18 chr8:126417600-126423000 Weak transcription Lung lung

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