Variant report

Variant rs6532158
Chromosome Location chr4:76977964-76977965
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:76975400-76979200 Weak transcription HMEC breast
2 chr4:76976000-76978000 Enhancers HUES64 Cell Line embryonic stem cell
3 chr4:76976000-76979800 Weak transcription Fetal Intestine Small intestine
4 chr4:76976000-76980800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr4:76976200-76978000 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr4:76976200-76979800 Weak transcription Fetal Intestine Large intestine
7 chr4:76976200-76980000 Weak transcription Primary monocytes fromperipheralblood blood
8 chr4:76976400-76978000 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr4:76976400-76980200 Weak transcription Rectal Mucosa Donor 31 rectum
10 chr4:76976600-76979400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:76976600-76979400 Weak transcription Stomach Mucosa stomach
12 chr4:76976600-76980600 Weak transcription Primary B cells from cord blood blood
13 chr4:76977000-76979400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr4:76977200-76979400 Weak transcription NHEK skin
15 chr4:76977200-76980000 Weak transcription K562 blood
16 chr4:76977400-76978000 Enhancers HUES48 Cell Line embryonic stem cell
17 chr4:76977400-76981600 Weak transcription Primary B cells from peripheral blood blood
18 chr4:76977800-76978800 Weak transcription GM12878-XiMat blood

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