Variant report

Variant rs73687908
Chromosome Location chr7:41175030-41175031
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41129200-41175200 Weak transcription Aorta Aorta
2 chr7:41168200-41175600 Enhancers Fetal Brain Male brain
3 chr7:41169000-41175400 Enhancers Fetal Brain Female brain
4 chr7:41169800-41175200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr7:41170600-41175200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr7:41171400-41175400 Enhancers Primary neutrophils fromperipheralblood blood
7 chr7:41173400-41175200 Enhancers Placenta Amnion Placenta Amnion
8 chr7:41173400-41175400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr7:41173400-41175800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr7:41173600-41175200 Enhancers Muscle Satellite Cultured Cells --
11 chr7:41173600-41175600 Enhancers HMEC breast
12 chr7:41174000-41175200 Weak transcription Esophagus oesophagus
13 chr7:41174000-41177200 Weak transcription Right Atrium heart
14 chr7:41174200-41175200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr7:41174400-41177200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr7:41174400-41187800 Weak transcription NHLF lung
17 chr7:41174800-41175400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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