The 2.0 version of rSNPBase

Variant report

Variant rs73740587
Chromosome Location chr6:28187719-28187720
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:28186600-28192400 Weak transcription Spleen Spleen
2 chr6:28187000-28188000 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr6:28187000-28188000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr6:28187000-28188200 Weak transcription NH-A brain
5 chr6:28187000-28188600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr6:28187000-28192400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr6:28187000-28192400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr6:28187200-28188200 Enhancers Placenta Placenta
9 chr6:28187200-28189800 Weak transcription NHEK skin
10 chr6:28187200-28190800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr6:28187200-28192000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr6:28187200-28192000 Weak transcription HMEC breast
13 chr6:28187200-28192200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr6:28187400-28188000 Enhancers HepG2 liver
15 chr6:28187400-28192000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr6:28187400-28192000 Weak transcription Hela-S3 cervix
17 chr6:28187600-28187800 Enhancers K562 blood

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Last update: Aug 31, 2015