Variant report

Variant rs10262723
Chromosome Location chr7:111918525-111918526
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:111893200-111926000 Weak transcription Primary T cells from cord blood blood
2 chr7:111896800-111922200 Weak transcription Pancreas Pancrea
3 chr7:111903400-111949200 Weak transcription Fetal Intestine Small intestine
4 chr7:111903800-111926000 Weak transcription Psoas Muscle Psoas
5 chr7:111905400-111926000 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr7:111907200-111922400 Weak transcription Primary hematopoietic stem cells blood
7 chr7:111907400-111928400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:111913200-111965200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr7:111913400-111926000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr7:111913400-111938400 Weak transcription Primary hematopoietic stem cells short term culture blood
11 chr7:111913600-111929800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr7:111913600-111949600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr7:111915400-111919600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
14 chr7:111918000-111963000 Weak transcription Aorta Aorta

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