Variant report

Variant rs411665
Chromosome Location chr1:174625701-174625702
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174607600-174628600 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
2 chr1:174607600-174637000 Weak transcription Primary B cells from peripheral blood blood
3 chr1:174607600-174677800 Weak transcription Primary B cells from cord blood blood
4 chr1:174612400-174638200 Weak transcription Aorta Aorta
5 chr1:174613600-174637000 Weak transcription Primary T cells from cord blood blood
6 chr1:174617800-174625800 Weak transcription HepG2 liver
7 chr1:174622200-174626000 Weak transcription Fetal Intestine Small intestine
8 chr1:174622800-174625800 Weak transcription Fetal Intestine Large intestine
9 chr1:174623200-174628600 Weak transcription Fetal Heart heart
10 chr1:174623400-174626000 Weak transcription Left Ventricle heart
11 chr1:174625200-174626200 Enhancers Fetal Brain Male brain
12 chr1:174625400-174636600 Weak transcription Primary T cells fromperipheralblood blood
13 chr1:174625600-174626200 Enhancers Liver Liver
14 chr1:174625600-174626600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood

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