Variant report

Variant rs11774794
Chromosome Location chr8:130530327-130530328
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130526800-130531800 Strong transcription K562 blood
2 chr8:130527400-130530600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr8:130528800-130532600 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr8:130529000-130531000 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr8:130529000-130532800 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr8:130529200-130530800 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
7 chr8:130529200-130538400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr8:130530000-130530400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr8:130530000-130530600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr8:130530000-130530600 Genic enhancers Dnd41 blood
11 chr8:130530000-130530800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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