Variant report

Variant rs10162660
Chromosome Location chr15:34808134-34808135
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:34806200-34808200 Bivalent/Poised TSS Rectal Mucosa Donor 29 rectum
2 chr15:34807200-34808200 Bivalent Enhancer Primary T helper memory cells from peripheral blood 1 blood
3 chr15:34807400-34808200 Enhancers Primary T helper memory cells from peripheral blood 2 blood
4 chr15:34807400-34808400 Flanking Active TSS GM12878-XiMat blood
5 chr15:34807600-34808400 Bivalent Enhancer NHEK skin
6 chr15:34807600-34808600 Weak transcription Gastric stomach
7 chr15:34807600-34813200 Weak transcription Spleen Spleen
8 chr15:34807600-34820200 Weak transcription Pancreas Pancrea
9 chr15:34807800-34808200 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
10 chr15:34807800-34808200 Enhancers Adipose Nuclei Adipose
11 chr15:34807800-34808400 Enhancers K562 blood
12 chr15:34808000-34808200 Flanking Bivalent TSS/Enh Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr15:34808000-34808200 Bivalent/Poised TSS Stomach Smooth Muscle stomach
14 chr15:34808000-34808400 Enhancers Ovary ovary
15 chr15:34808000-34808400 Flanking Bivalent TSS/Enh HepG2 liver
16 chr15:34808000-34809200 Weak transcription Primary T helper 17 cells PMA-I stimulated --

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