Variant report

Variant rs927580
Chromosome Location chr9:102062259-102062260
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:102058800-102063600 Weak transcription K562 blood
2 chr9:102059200-102062400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr9:102059200-102068600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr9:102059400-102062800 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr9:102060000-102062400 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr9:102060400-102062400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr9:102060600-102063000 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr9:102061000-102062400 Enhancers ES-WA7 Cell Line embryonic stem cell
9 chr9:102061200-102062400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr9:102061200-102062400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:102061200-102062400 Enhancers NHLF lung
12 chr9:102061600-102063600 Weak transcription Placenta Placenta
13 chr9:102061600-102063800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr9:102061800-102062400 Enhancers Fetal Brain Male brain
15 chr9:102061800-102062800 Weak transcription iPS-20b Cell Line embryonic stem cell
16 chr9:102061800-102066200 Weak transcription H9 Cell Line embryonic stem cell
17 chr9:102061800-102069400 Weak transcription HUES64 Cell Line embryonic stem cell
18 chr9:102062000-102063200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
19 chr9:102062200-102066400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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