Variant report

Variant rs2596566
Chromosome Location chr6:31350822-31350823
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31345000-31361600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:31345600-31353200 Weak transcription Right Atrium heart
3 chr6:31345800-31367400 Weak transcription Gastric stomach
4 chr6:31348000-31354200 Weak transcription Lung lung
5 chr6:31348400-31354000 Weak transcription Adipose Nuclei Adipose
6 chr6:31348800-31364400 Weak transcription Primary T cells from cord blood blood
7 chr6:31350200-31354200 Strong transcription Breast Myoepithelial Primary Cells Breast
8 chr6:31350200-31367400 Weak transcription Aorta Aorta
9 chr6:31350600-31361600 Weak transcription Ovary ovary
10 chr6:31350800-31351000 Enhancers H1 Cell Line embryonic stem cell
11 chr6:31350800-31351000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr6:31350800-31351000 Enhancers HMEC breast
13 chr6:31350800-31351400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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