Variant report

Variant rs79433188
Chromosome Location chr6:31211200-31211201
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr6:31210600-31211400 Enhancers Primary T regulatory cells fromperipheralblood blood
3 chr6:31210800-31211400 Enhancers Primary T helper naive cells from peripheral blood blood
4 chr6:31210800-31211600 Enhancers Primary T helper cells PMA-I stimulated --
5 chr6:31210800-31211600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr6:31211000-31211600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr6:31211000-31211600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
8 chr6:31211000-31211600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr6:31211000-31211600 Enhancers NHEK skin
10 chr6:31211200-31211400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr6:31211200-31211400 Enhancers Hela-S3 cervix
12 chr6:31211200-31211400 Enhancers HMEC breast
13 chr6:31211200-31211400 Bivalent Enhancer NHDF-Ad bronchial
14 chr6:31211200-31211600 Enhancers Primary hematopoietic stem cells blood
15 chr6:31211200-31211600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr6:31211200-31211600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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