Variant report

Variant rs11753940
Chromosome Location chr6:64442472-64442473
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:64423600-64444400 Weak transcription Primary T regulatory cells fromperipheralblood blood
2 chr6:64424200-64450400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr6:64436400-64444600 Weak transcription HepG2 liver
4 chr6:64436800-64445400 Weak transcription Primary T cells from cord blood blood
5 chr6:64437400-64459600 Weak transcription Aorta Aorta
6 chr6:64437800-64445000 Weak transcription Primary hematopoietic stem cells blood
7 chr6:64441200-64443200 Enhancers Muscle Satellite Cultured Cells --
8 chr6:64441200-64443200 Enhancers HUVEC blood vessel
9 chr6:64441400-64443600 Enhancers Hela-S3 cervix
10 chr6:64441600-64442800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr6:64441600-64442800 Enhancers Osteobl bone
12 chr6:64441600-64443200 Enhancers HMEC breast
13 chr6:64441600-64443800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr6:64441800-64442800 Enhancers NH-A brain
15 chr6:64441800-64442800 Enhancers NHLF lung
16 chr6:64441800-64443200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr6:64441800-64443400 Enhancers NHDF-Ad bronchial
18 chr6:64442000-64443000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr6:64442000-64451800 Weak transcription Fetal Intestine Small intestine
20 chr6:64442000-64451800 Weak transcription Small Intestine intestine
21 chr6:64442200-64444600 Weak transcription NHEK skin
22 chr6:64442400-64445400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
23 chr6:64442400-64450200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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