Variant report

Variant rs333454
Chromosome Location chr1:174623077-174623078
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr1:174621600-174623400 Enhancers Left Ventricle heart
8 chr1:174621600-174625200 Enhancers Fetal Lung lung
9 chr1:174621800-174623200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr1:174621800-174623200 Enhancers Fetal Heart heart
11 chr1:174622200-174623200 Weak transcription Fetal Brain Male brain
12 chr1:174622200-174623400 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr1:174622200-174626000 Weak transcription Fetal Intestine Small intestine
14 chr1:174622600-174623200 Enhancers HUES6 Cell Line embryonic stem cell
15 chr1:174622800-174625800 Weak transcription Fetal Intestine Large intestine

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