The 2.0 version of rSNPBase

Variant report

Variant rs10914100
Chromosome Location chr1:180747033-180747034
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180713000-180814200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr1:180715400-180747600 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr1:180722600-180751000 Weak transcription Left Ventricle heart
4 chr1:180738000-180751200 Weak transcription Brain Anterior Caudate brain
5 chr1:180740200-180751000 Weak transcription Fetal Brain Female brain
6 chr1:180740200-180753000 Weak transcription Small Intestine intestine
7 chr1:180740200-180761000 Weak transcription Psoas Muscle Psoas
8 chr1:180740800-180775600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr1:180741000-180757200 Weak transcription Primary B cells from cord blood blood
10 chr1:180741600-180784000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr1:180743400-180757200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr1:180743400-180763000 Weak transcription HSMM muscle
13 chr1:180744000-180757200 Weak transcription Primary T cells from cord blood blood
14 chr1:180744400-180751000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
15 chr1:180746600-180748400 Enhancers Liver Liver
16 chr1:180746600-180751400 Weak transcription Fetal Brain Male brain
17 chr1:180747000-180756800 Weak transcription Pancreatic Islets Pancreatic Islet

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Last update: Aug 31, 2015