Variant report

Variant rs17043467
Chromosome Location chr3:17393455-17393456
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17339400-17442200 Weak transcription Fetal Intestine Small intestine
2 chr3:17344400-17439000 Weak transcription Aorta Aorta
3 chr3:17356200-17412800 Weak transcription Left Ventricle heart
4 chr3:17365600-17413000 Weak transcription Primary hematopoietic stem cells blood
5 chr3:17370000-17406200 Weak transcription Primary B cells from peripheral blood blood
6 chr3:17370800-17411000 Weak transcription Monocytes-CD14+_RO01746 blood
7 chr3:17372400-17410600 Weak transcription Primary monocytes fromperipheralblood blood
8 chr3:17378200-17393600 Weak transcription Dnd41 blood
9 chr3:17379800-17414400 Weak transcription HSMM muscle
10 chr3:17388400-17394200 Weak transcription Primary Natural Killer cells fromperipheralblood blood
11 chr3:17390200-17412600 Weak transcription Primary T helper cells fromperipheralblood blood
12 chr3:17390800-17411600 Weak transcription GM12878-XiMat blood
13 chr3:17391000-17411000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr3:17391800-17398200 Weak transcription ES-I3 Cell Line embryonic stem cell
15 chr3:17393000-17394200 Weak transcription Primary B cells from cord blood blood

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