Variant report

Variant rs4547819
Chromosome Location chr4:76977768-76977769
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:76975400-76979200 Weak transcription HMEC breast
2 chr4:76975800-76977800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr4:76976000-76978000 Enhancers HUES64 Cell Line embryonic stem cell
4 chr4:76976000-76979800 Weak transcription Fetal Intestine Small intestine
5 chr4:76976000-76980800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr4:76976200-76978000 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr4:76976200-76979800 Weak transcription Fetal Intestine Large intestine
8 chr4:76976200-76980000 Weak transcription Primary monocytes fromperipheralblood blood
9 chr4:76976400-76977800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr4:76976400-76978000 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr4:76976400-76980200 Weak transcription Rectal Mucosa Donor 31 rectum
12 chr4:76976600-76979400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr4:76976600-76979400 Weak transcription Stomach Mucosa stomach
14 chr4:76976600-76980600 Weak transcription Primary B cells from cord blood blood
15 chr4:76977000-76977800 Enhancers H9 Cell Line embryonic stem cell
16 chr4:76977000-76979400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr4:76977200-76979400 Weak transcription NHEK skin
18 chr4:76977200-76980000 Weak transcription K562 blood
19 chr4:76977400-76977800 Enhancers GM12878-XiMat blood
20 chr4:76977400-76978000 Enhancers HUES48 Cell Line embryonic stem cell
21 chr4:76977400-76981600 Weak transcription Primary B cells from peripheral blood blood
22 chr4:76977600-76977800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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