The 2.0 version of rSNPBase

Variant report

Variant rs11803914
Chromosome Location chr1:197665078-197665079
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:197653000-197665200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr1:197653000-197665400 Weak transcription Osteobl bone
3 chr1:197657000-197677000 Weak transcription Ovary ovary
4 chr1:197658000-197665200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr1:197658200-197668200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
6 chr1:197659400-197665200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:197659400-197665800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr1:197659400-197674800 Weak transcription Primary T regulatory cells fromperipheralblood blood
9 chr1:197659600-197665200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:197659600-197665600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr1:197659600-197665600 Weak transcription K562 blood
12 chr1:197659600-197667000 Weak transcription Primary B cells from cord blood blood
13 chr1:197659800-197674400 Weak transcription Primary hematopoietic stem cells short term culture blood
14 chr1:197664400-197665600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
15 chr1:197664400-197666000 Weak transcription Primary T helper cells fromperipheralblood blood
16 chr1:197665000-197666400 Enhancers NHEK skin

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Last update: Aug 31, 2015