Variant report

Variant rs74079818
Chromosome Location chr1:59309362-59309363
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59294000-59311000 Weak transcription Gastric stomach
2 chr1:59300600-59314800 Weak transcription Aorta Aorta
3 chr1:59306600-59314000 Weak transcription Osteobl bone
4 chr1:59306800-59313200 Weak transcription NHEK skin
5 chr1:59306800-59314000 Weak transcription Muscle Satellite Cultured Cells --
6 chr1:59307000-59309800 Weak transcription HMEC breast
7 chr1:59307000-59312800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:59307200-59309600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr1:59307200-59311600 Weak transcription Lung lung
10 chr1:59307400-59313200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:59308000-59312800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr1:59308000-59313400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr1:59308200-59309800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:59308200-59310000 Weak transcription A549 lung
15 chr1:59308200-59312800 Weak transcription NHDF-Ad bronchial
16 chr1:59308200-59314200 Weak transcription Small Intestine intestine
17 chr1:59308800-59310400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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