Variant report

Variant rs7556849
Chromosome Location chr2:167999082-167999083
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr2:167995000-167999400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr2:167995000-167999600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr2:167996200-168001400 Enhancers Fetal Heart heart
6 chr2:167996200-168001400 Enhancers Skeletal Muscle Female skeletal muscle
7 chr2:167997000-167999200 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr2:167997200-167999400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr2:167997200-167999600 Weak transcription Psoas Muscle Psoas
10 chr2:167997400-167999600 Weak transcription NHLF lung
11 chr2:167997400-168001000 Enhancers Skeletal Muscle Male skeletal muscle
12 chr2:167997600-168000800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr2:167998200-167999800 Weak transcription Muscle Satellite Cultured Cells --
14 chr2:167998200-167999800 Weak transcription HSMM muscle
15 chr2:167998200-168000000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr2:167998400-167999200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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