Variant report

Variant rs12088650
Chromosome Location chr1:174627698-174627699
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr1:174623200-174628600 Weak transcription Fetal Heart heart
7 chr1:174625400-174636600 Weak transcription Primary T cells fromperipheralblood blood
8 chr1:174625800-174634800 Weak transcription GM12878-XiMat blood
9 chr1:174626000-174628400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:174626200-174629400 Weak transcription Fetal Brain Male brain
11 chr1:174626400-174628600 Weak transcription HepG2 liver
12 chr1:174627600-174630800 Weak transcription Primary T helper 17 cells PMA-I stimulated --

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