Variant report

Variant rs12998100
Chromosome Location chr2:33091601-33091602
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33088000-33092000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
2 chr2:33088400-33092000 Enhancers NH-A brain
3 chr2:33088600-33092000 Enhancers HSMMtube muscle
4 chr2:33089200-33091800 Enhancers HSMM muscle
5 chr2:33091200-33092000 Enhancers Osteobl bone
6 chr2:33091200-33092200 Enhancers NHEK skin
7 chr2:33091200-33101200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:33091600-33091800 Bivalent Enhancer Primary T cells from cord blood blood
9 chr2:33091600-33091800 Bivalent Enhancer NHLF lung
10 chr2:33091600-33092000 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
11 chr2:33091600-33092200 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
12 chr2:33091600-33092200 ZNF genes & repeats ES-WA7 Cell Line embryonic stem cell
13 chr2:33091600-33092200 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
14 chr2:33091600-33092200 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells blood
15 chr2:33091600-33092200 Flanking Active TSS Pancreatic Islets Pancreatic Islet
16 chr2:33091600-33092200 Active TSS GM12878-XiMat blood
17 chr2:33091600-33092200 ZNF genes & repeats HUVEC blood vessel
18 chr2:33091600-33092200 Flanking Bivalent TSS/Enh K562 blood

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