Variant report

Variant rs2146564
Chromosome Location chr1:174685352-174685353
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174678200-174689000 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr1:174678200-174689200 Weak transcription Primary mononuclear cells fromperipheralblood Blood
3 chr1:174678200-174708600 Weak transcription Primary T cells from cord blood blood
4 chr1:174678600-174706400 Weak transcription Primary Natural Killer cells fromperipheralblood blood
5 chr1:174679200-174687000 Weak transcription Primary B cells from cord blood blood
6 chr1:174681000-174685400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:174681000-174686200 Weak transcription Lung lung
8 chr1:174681200-174688600 Weak transcription Fetal Intestine Large intestine
9 chr1:174682200-174704800 Weak transcription Primary B cells from peripheral blood blood
10 chr1:174682800-174688600 Weak transcription Fetal Intestine Small intestine
11 chr1:174683600-174688000 Weak transcription Liver Liver
12 chr1:174684200-174689600 Weak transcription HepG2 liver
13 chr1:174685000-174689800 Weak transcription Fetal Heart heart
14 chr1:174685200-174687000 Weak transcription Breast Myoepithelial Primary Cells Breast

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