Variant report

Variant rs2970054
Chromosome Location chr17:50223260-50223261
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:50221000-50223400 Enhancers ES-I3 Cell Line embryonic stem cell
2 chr17:50221000-50228200 Enhancers NHEK skin
3 chr17:50221600-50224400 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr17:50222000-50228000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr17:50222200-50223400 Enhancers ES-WA7 Cell Line embryonic stem cell
6 chr17:50222200-50223400 Enhancers HUES64 Cell Line embryonic stem cell
7 chr17:50222200-50223400 Enhancers Hela-S3 cervix
8 chr17:50222200-50227800 Enhancers HMEC breast
9 chr17:50222400-50228000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr17:50222600-50223600 Enhancers NH-A brain
11 chr17:50222600-50227600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr17:50223000-50223800 Enhancers Primary T helper 17 cells PMA-I stimulated --
13 chr17:50223000-50225200 Weak transcription HUES6 Cell Line embryonic stem cell

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