Variant report

Variant rs57414836
Chromosome Location chr7:17067496-17067497
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17050600-17071800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
2 chr7:17063000-17074800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:17063400-17068200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
4 chr7:17064200-17069200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
5 chr7:17066000-17070800 Enhancers Primary T helper 17 cells PMA-I stimulated --
6 chr7:17066200-17068000 Enhancers Liver Liver
7 chr7:17066800-17070600 Enhancers Primary monocytes fromperipheralblood blood
8 chr7:17067000-17067600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
9 chr7:17067200-17067600 Enhancers HMEC breast
10 chr7:17067200-17068000 Enhancers Placenta Placenta
11 chr7:17067200-17068400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr7:17067400-17068200 ZNF genes & repeats Adipose Nuclei Adipose
13 chr7:17067400-17068800 Enhancers Primary T regulatory cells fromperipheralblood blood

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