Variant report

Variant rs61826950
Chromosome Location chr1:174628947-174628948
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174607600-174637000 Weak transcription Primary B cells from peripheral blood blood
2 chr1:174607600-174677800 Weak transcription Primary B cells from cord blood blood
3 chr1:174612400-174638200 Weak transcription Aorta Aorta
4 chr1:174613600-174637000 Weak transcription Primary T cells from cord blood blood
5 chr1:174625400-174636600 Weak transcription Primary T cells fromperipheralblood blood
6 chr1:174625800-174634800 Weak transcription GM12878-XiMat blood
7 chr1:174626200-174629400 Weak transcription Fetal Brain Male brain
8 chr1:174627600-174630800 Weak transcription Primary T helper 17 cells PMA-I stimulated --
9 chr1:174627800-174635200 Weak transcription Rectal Mucosa Donor 31 rectum
10 chr1:174628200-174629600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr1:174628200-174633800 Weak transcription Sigmoid Colon Sigmoid Colon
12 chr1:174628400-174629600 Enhancers NHEK skin
13 chr1:174628400-174630000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:174628400-174630200 Enhancers HMEC breast
15 chr1:174628600-174629600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr1:174628600-174629800 Enhancers Fetal Heart heart
17 chr1:174628600-174630000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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