Variant report

Variant rs6762367
Chromosome Location chr3:101276655-101276656
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:101273000-101277600 Weak transcription H1 Cell Line embryonic stem cell
2 chr3:101274600-101280400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr3:101276000-101280000 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr3:101276400-101276800 Active TSS Fetal Adrenal Gland Adrenal Gland
5 chr3:101276600-101276800 Flanking Active TSS Foreskin Melanocyte Primary Cells skin03 Skin
6 chr3:101276600-101276800 Flanking Active TSS K562 blood
7 chr3:101276600-101277000 Enhancers HepG2 liver
8 chr3:101276600-101280400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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