The 2.0 version of rSNPBase

Variant report

Variant rs6667089
Chromosome Location chr1:223685954-223685955
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:223683200-223686800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr1:223683400-223686800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
3 chr1:223683800-223686400 Weak transcription Primary T cells from cord blood blood
4 chr1:223684800-223689000 Weak transcription Right Atrium heart
5 chr1:223685000-223686200 Enhancers Placenta Placenta
6 chr1:223685200-223686000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:223685200-223689000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:223685800-223689000 Weak transcription HMEC breast
9 chr1:223685800-223690400 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
10 chr1:223685800-223690600 Enhancers Primary T cells fromperipheralblood blood

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Last update: Aug 31, 2015