Variant report

Variant rs114034507
Chromosome Location chr6:31213318-31213319
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31202600-31213600 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr6:31211400-31213600 Weak transcription Primary T regulatory cells fromperipheralblood blood
3 chr6:31211600-31213400 Weak transcription Primary hematopoietic stem cells blood
4 chr6:31211600-31213400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr6:31211600-31213600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr6:31211600-31213600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:31212000-31213400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:31213000-31214400 Enhancers NHEK skin
9 chr6:31213200-31213400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
10 chr6:31213200-31213400 Enhancers Primary T helper cells PMA-I stimulated --
11 chr6:31213200-31213400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr6:31213200-31213800 Enhancers Hela-S3 cervix
13 chr6:31213200-31214000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr6:31213200-31214600 Enhancers HMEC breast

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