Variant report

Variant rs557483792
Chromosome Location chr1:92969594-92969595
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92952800-92991400 Weak transcription Pancreas Pancrea
2 chr1:92961600-92969800 Weak transcription Primary T helper naive cells from peripheral blood blood
3 chr1:92967400-92969800 Enhancers Dnd41 blood
4 chr1:92967600-92969600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr1:92967800-92970000 Enhancers HMEC breast
6 chr1:92967800-92978400 Weak transcription Fetal Intestine Small intestine
7 chr1:92967800-92986000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:92968000-92970000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:92968200-92975200 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr1:92968200-92977400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:92968200-93042800 Weak transcription HSMM muscle
12 chr1:92968400-92997600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr1:92968600-92971800 Enhancers Fetal Thymus thymus
14 chr1:92969000-92969800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr1:92969000-92969800 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr1:92969000-92970200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr1:92969000-92971400 Enhancers Thymus Thymus
18 chr1:92969200-92970800 Enhancers GM12878-XiMat blood
19 chr1:92969200-92970800 Flanking Active TSS HepG2 liver
20 chr1:92969400-92969600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
21 chr1:92969400-92969800 Enhancers NH-A brain
22 chr1:92969400-92969800 Flanking Active TSS Osteobl bone
23 chr1:92969400-92970000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
24 chr1:92969400-92979800 Weak transcription HSMMtube muscle

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