Variant report

Variant rs5023958
Chromosome Location chr5:177513215-177513216
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177509200-177513400 Weak transcription Esophagus oesophagus
2 chr5:177512600-177514400 Enhancers Stomach Mucosa stomach
3 chr5:177512800-177514200 Weak transcription Hela-S3 cervix
4 chr5:177513200-177513400 Active TSS ES-I3 Cell Line embryonic stem cell
5 chr5:177513200-177513400 Enhancers H1 Cell Line embryonic stem cell
6 chr5:177513200-177513400 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin01 Skin
7 chr5:177513200-177513400 Bivalent Enhancer NHEK skin
8 chr5:177513200-177513600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr5:177513200-177513600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr5:177513200-177513600 Active TSS iPS-15b Cell Line embryonic stem cell
11 chr5:177513200-177513600 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
12 chr5:177513200-177513600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
13 chr5:177513200-177513600 Flanking Bivalent TSS/Enh Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr5:177513200-177513600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
15 chr5:177513200-177513600 Flanking Active TSS Placenta Placenta
16 chr5:177513200-177513600 Enhancers HMEC breast
17 chr5:177513200-177513800 Active TSS ES-WA7 Cell Line embryonic stem cell
18 chr5:177513200-177513800 Active TSS H9 Cell Line embryonic stem cell
19 chr5:177513200-177513800 Active TSS HUES6 Cell Line embryonic stem cell
20 chr5:177513200-177513800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
21 chr5:177513200-177513800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin

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