Variant report

Variant rs6699123
Chromosome Location chr1:66997508-66997509
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:66988400-66998200 Weak transcription Osteobl bone
2 chr1:66991800-66998600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr1:66993600-66997600 Weak transcription Fetal Heart heart
4 chr1:66993600-66998200 Weak transcription NHEK skin
5 chr1:66993800-66998000 Weak transcription Muscle Satellite Cultured Cells --
6 chr1:66994000-66998000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:66996200-66998000 Weak transcription H1 Cell Line embryonic stem cell
8 chr1:66996200-66998200 Weak transcription H9 Cell Line embryonic stem cell
9 chr1:66996600-66997800 Enhancers Primary B cells from cord blood blood
10 chr1:66996800-66998000 Weak transcription Primary hematopoietic stem cells blood
11 chr1:66997000-66997600 Enhancers NHLF lung
12 chr1:66997000-66998000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr1:66997200-66997600 Bivalent/Poised TSS ES-WA7 Cell Line embryonic stem cell
14 chr1:66997200-66997600 Enhancers Fetal Kidney kidney
15 chr1:66997200-66998200 Active TSS IMR90 fetal lung fibroblasts Cell Line lung
16 chr1:66997200-66998200 Enhancers HUVEC blood vessel
17 chr1:66997400-66997600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
18 chr1:66997400-66997600 Enhancers Pancreatic Islets Pancreatic Islet
19 chr1:66997400-66998200 Enhancers NHDF-Ad bronchial
20 chr1:66997400-66998400 Weak transcription Breast Myoepithelial Primary Cells Breast
21 chr1:66997400-66998400 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
22 chr1:66997400-66998400 Enhancers Brain Substantia Nigra brain
23 chr1:66997400-66998400 Weak transcription Left Ventricle heart

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