Variant report

Variant rs9390075
Chromosome Location chr6:143598107-143598108
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143570800-143609200 Weak transcription Fetal Intestine Large intestine
2 chr6:143583400-143606000 Weak transcription Fetal Intestine Small intestine
3 chr6:143583800-143615400 Weak transcription K562 blood
4 chr6:143589000-143607400 Weak transcription Aorta Aorta
5 chr6:143591400-143605200 Weak transcription Liver Liver
6 chr6:143592200-143605600 Weak transcription Adipose Nuclei Adipose
7 chr6:143593200-143606800 Weak transcription NHEK skin
8 chr6:143593400-143607000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:143595400-143605400 Weak transcription HepG2 liver
10 chr6:143595600-143602800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr6:143597400-143598200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr6:143597400-143598400 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr6:143597600-143598200 Enhancers Primary monocytes fromperipheralblood blood
14 chr6:143597600-143598200 Enhancers Primary B cells from peripheral blood blood
15 chr6:143597600-143598200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr6:143598000-143598200 Flanking Active TSS GM12878-XiMat blood

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