Variant report

Variant rs12589872
Chromosome Location chr14:68818292-68818293
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:68808600-68819200 Weak transcription Primary hematopoietic stem cells blood
2 chr14:68811000-68829800 Weak transcription Primary T helper naive cells from peripheral blood blood
3 chr14:68812400-68818600 Enhancers Fetal Stomach stomach
4 chr14:68813600-68825600 Weak transcription Primary B cells from cord blood blood
5 chr14:68814200-68820400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr14:68815800-68818400 Enhancers Fetal Intestine Small intestine
7 chr14:68816400-68826000 Weak transcription Fetal Muscle Trunk muscle
8 chr14:68816400-68826200 Weak transcription Pancreas Pancrea
9 chr14:68816600-68825600 Weak transcription Fetal Thymus thymus
10 chr14:68816600-68826600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr14:68816800-68825000 Weak transcription Aorta Aorta
12 chr14:68817000-68818400 Weak transcription Sigmoid Colon Sigmoid Colon
13 chr14:68817400-68824400 Weak transcription Primary T helper naive cells fromperipheralblood blood
14 chr14:68817400-68825000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
15 chr14:68817400-68826200 Weak transcription Skeletal Muscle Female skeletal muscle
16 chr14:68817600-68818600 Enhancers Fetal Lung lung
17 chr14:68817800-68819400 Weak transcription Fetal Muscle Leg muscle
18 chr14:68818200-68818400 Enhancers Fetal Kidney kidney
19 chr14:68818200-68818800 Enhancers Primary B cells from peripheral blood blood

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