Variant report

Variant rs60165186
Chromosome Location chr1:172074655-172074656
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172040600-172076600 Weak transcription Brain Angular Gyrus brain
2 chr1:172046600-172076800 Weak transcription Fetal Brain Female brain
3 chr1:172048000-172083800 Weak transcription Aorta Aorta
4 chr1:172049400-172110800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:172052400-172091600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:172062400-172109200 Weak transcription Brain Cingulate Gyrus brain
7 chr1:172069200-172076400 Weak transcription Fetal Adrenal Gland Adrenal Gland
8 chr1:172069200-172102000 Weak transcription Brain Hippocampus Middle brain
9 chr1:172074200-172074800 Enhancers Liver Liver
10 chr1:172074200-172075000 Enhancers HUVEC blood vessel
11 chr1:172074400-172074800 Enhancers Muscle Satellite Cultured Cells --
12 chr1:172074400-172074800 Enhancers A549 lung
13 chr1:172074400-172078400 Weak transcription Fetal Kidney kidney
14 chr1:172074600-172076600 Weak transcription Fetal Lung lung
15 chr1:172074600-172076600 Weak transcription Fetal Stomach stomach
16 chr1:172074600-172076600 Weak transcription NHDF-Ad bronchial
17 chr1:172074600-172077800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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