The 2.0 version of rSNPBase

Variant report

Variant rs2668644
Chromosome Location chr17:44331572-44331573
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:44321200-44337200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr17:44323000-44341400 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
3 chr17:44323200-44337000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr17:44323200-44337200 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr17:44324800-44337200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr17:44325400-44337200 Weak transcription Right Atrium heart
7 chr17:44326800-44336600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr17:44326800-44337200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr17:44331200-44331600 Enhancers Primary T helper naive cells from peripheral blood blood
10 chr17:44331200-44331600 Active TSS K562 blood
11 chr17:44331400-44331600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr17:44331400-44331600 Genic enhancers Colon Smooth Muscle Colon
13 chr17:44331400-44331600 Active TSS A549 lung

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Last update: Aug 31, 2015