Variant report

Variant rs4908958
Chromosome Location chr3:17728043-17728044
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17707000-17734800 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr3:17709200-17732000 Weak transcription Psoas Muscle Psoas
3 chr3:17711400-17755000 Weak transcription Primary B cells from peripheral blood blood
4 chr3:17712600-17732600 Weak transcription Primary hematopoietic stem cells blood
5 chr3:17720000-17747400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr3:17720200-17734200 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr3:17720600-17734400 Weak transcription Dnd41 blood
8 chr3:17723400-17735200 Weak transcription Gastric stomach
9 chr3:17723600-17728200 Weak transcription Aorta Aorta
10 chr3:17723600-17734400 Weak transcription Primary B cells from cord blood blood
11 chr3:17723600-17736000 Weak transcription Pancreas Pancrea
12 chr3:17723600-17736800 Weak transcription Ovary ovary
13 chr3:17724600-17734800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr3:17725600-17729000 Weak transcription Small Intestine intestine
15 chr3:17725800-17734400 Weak transcription A549 lung
16 chr3:17726600-17734200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
17 chr3:17726800-17742200 Weak transcription Stomach Mucosa stomach
18 chr3:17727600-17728200 Enhancers Brain Substantia Nigra brain
19 chr3:17727600-17728400 Enhancers Brain Anterior Caudate brain

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