Variant report

Variant rs4435674
Chromosome Location chr3:17794200-17794201
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:26 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17789400-17794800 Weak transcription HSMMtube muscle
2 chr3:17789600-17795000 Weak transcription Muscle Satellite Cultured Cells --
3 chr3:17790600-17795200 Enhancers Primary neutrophils fromperipheralblood blood
4 chr3:17791200-17800800 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr3:17791400-17796800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr3:17791600-17794200 Weak transcription K562 blood
7 chr3:17791600-17794600 Weak transcription Stomach Mucosa stomach
8 chr3:17791600-17794800 Weak transcription HepG2 liver
9 chr3:17791600-17796800 Weak transcription HMEC breast
10 chr3:17791600-17796800 Weak transcription NHEK skin
11 chr3:17791800-17794200 Weak transcription Liver Liver
12 chr3:17791800-17797200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
13 chr3:17791800-17797200 Weak transcription Primary T regulatory cells fromperipheralblood blood
14 chr3:17792200-17797000 Weak transcription GM12878-XiMat blood
15 chr3:17792200-17797200 Weak transcription Dnd41 blood
16 chr3:17793400-17795600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr3:17793600-17795800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr3:17793800-17795400 Enhancers Adipose Nuclei Adipose
19 chr3:17794000-17795400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
20 chr3:17794000-17795400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
21 chr3:17794000-17795400 Enhancers NHDF-Ad bronchial
22 chr3:17794000-17795600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
23 chr3:17794000-17795600 Enhancers Fetal Muscle Leg muscle
24 chr3:17794000-17795600 Enhancers Pancreas Pancrea
25 chr3:17794200-17795600 Enhancers Liver Liver
26 chr3:17794200-17795600 Enhancers K562 blood

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