Variant report

Variant rs16853028
Chromosome Location chr2:167999594-167999595
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:167992200-167999800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr2:167993800-167999800 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr2:167995000-167999600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr2:167996200-168001400 Enhancers Fetal Heart heart
5 chr2:167996200-168001400 Enhancers Skeletal Muscle Female skeletal muscle
6 chr2:167997200-167999600 Weak transcription Psoas Muscle Psoas
7 chr2:167997400-167999600 Weak transcription NHLF lung
8 chr2:167997400-168001000 Enhancers Skeletal Muscle Male skeletal muscle
9 chr2:167997600-168000800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr2:167998200-167999800 Weak transcription Muscle Satellite Cultured Cells --
11 chr2:167998200-167999800 Weak transcription HSMM muscle
12 chr2:167998200-168000000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr2:167999200-168001400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr2:167999400-168000000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr2:167999400-168002200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

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