The 2.0 version of rSNPBase

Variant report

Variant rs10914098
Chromosome Location chr1:180743894-180743895
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr1:180743400-180744000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
12 chr1:180743400-180746200 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr1:180743400-180757200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:180743400-180763000 Weak transcription HSMM muscle

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Last update: Aug 31, 2015