Variant report

Variant rs10173973
Chromosome Location chr2:36891804-36891805
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:36880000-36895000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr2:36887400-36894800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr2:36890000-36892000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr2:36890400-36892800 Enhancers NHLF lung
5 chr2:36890600-36892000 Enhancers HSMM muscle
6 chr2:36890600-36892400 Enhancers NHDF-Ad bronchial
7 chr2:36890800-36892800 Enhancers Fetal Stomach stomach
8 chr2:36891000-36893000 Enhancers Fetal Lung lung
9 chr2:36891200-36893200 Weak transcription Aorta Aorta
10 chr2:36891400-36892000 Enhancers A549 lung
11 chr2:36891400-36894800 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr2:36891400-36894800 Weak transcription iPS-20b Cell Line embryonic stem cell
13 chr2:36891400-36895000 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr2:36891400-36897800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr2:36891400-36897800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr2:36891600-36892000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr2:36891600-36897600 Weak transcription Osteobl bone
18 chr2:36891800-36892000 Bivalent Enhancer Liver Liver
19 chr2:36891800-36892000 Enhancers Fetal Kidney kidney
20 chr2:36891800-36894800 Weak transcription HUVEC blood vessel

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