Variant report

Variant rs7613953
Chromosome Location chr3:17743150-17743151
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17711400-17755000 Weak transcription Primary B cells from peripheral blood blood
2 chr3:17720000-17747400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr3:17731600-17755600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr3:17732200-17749400 Weak transcription NHEK skin
5 chr3:17732600-17755400 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr3:17733200-17755600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr3:17733400-17747000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr3:17734800-17753200 Weak transcription Primary hematopoietic stem cells blood
9 chr3:17735200-17747600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr3:17735200-17755600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr3:17735200-17755800 Weak transcription Lung lung
12 chr3:17735400-17750800 Weak transcription Monocytes-CD14+_RO01746 blood
13 chr3:17735400-17754200 Weak transcription Primary B cells from cord blood blood
14 chr3:17735400-17755400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
15 chr3:17735400-17755600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr3:17735400-17755800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
17 chr3:17736000-17745000 Weak transcription HepG2 liver
18 chr3:17736000-17747600 Weak transcription Dnd41 blood
19 chr3:17743000-17743200 ZNF genes & repeats Fetal Intestine Small intestine

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