Variant report

Variant rs61807786
Chromosome Location chr1:172124828-172124829
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172114400-172137000 Weak transcription Brain Angular Gyrus brain
2 chr1:172115000-172133800 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr1:172115600-172132600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:172119000-172125000 Weak transcription Placenta Amnion Placenta Amnion
5 chr1:172122200-172125400 Enhancers NHEK skin
6 chr1:172122400-172125000 Weak transcription Fetal Lung lung
7 chr1:172123400-172125200 Enhancers Primary T helper memory cells from peripheral blood 2 blood
8 chr1:172123400-172125200 Enhancers NH-A brain
9 chr1:172123400-172149200 Weak transcription Brain Anterior Caudate brain
10 chr1:172123800-172125000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:172123800-172125200 Enhancers Muscle Satellite Cultured Cells --
12 chr1:172123800-172125400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr1:172123800-172125600 Enhancers NHLF lung
14 chr1:172124000-172125000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr1:172124000-172125000 Weak transcription Fetal Kidney kidney
16 chr1:172124000-172125400 Enhancers NHDF-Ad bronchial
17 chr1:172124200-172125000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
18 chr1:172124200-172125400 Enhancers Osteobl bone
19 chr1:172124800-172125200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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