The 2.0 version of rSNPBase

Variant report

Variant esv2376444
Chromosome Location chr1:174689445-174689446
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174678200-174708600 Weak transcription Primary T cells from cord blood blood
2 chr1:174678600-174706400 Weak transcription Primary Natural Killer cells fromperipheralblood blood
3 chr1:174682200-174704800 Weak transcription Primary B cells from peripheral blood blood
4 chr1:174684200-174689600 Weak transcription HepG2 liver
5 chr1:174685000-174689800 Weak transcription Fetal Heart heart
6 chr1:174687800-174705200 Weak transcription Primary B cells from cord blood blood
7 chr1:174689000-174695400 Weak transcription Fetal Intestine Large intestine
8 chr1:174689000-174695800 Weak transcription Fetal Intestine Small intestine
9 chr1:174689200-174689800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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Last update: Aug 31, 2015