Variant report

Variant rs72609882
Chromosome Location chr8:130529437-130529438
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr8:130528400-130529600 Enhancers HUES48 Cell Line embryonic stem cell
4 chr8:130528400-130530000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr8:130528600-130529600 Enhancers Fetal Heart heart
6 chr8:130528600-130530000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr8:130528800-130530000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr8:130528800-130532600 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr8:130529000-130531000 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr8:130529000-130532800 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr8:130529200-130529600 ZNF genes & repeats Dnd41 blood
12 chr8:130529200-130530800 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
13 chr8:130529200-130538400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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