Variant report

Variant rs9641372
Chromosome Location chr7:106691486-106691487
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:106686800-106707200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:106687800-106697400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr7:106688200-106697200 Weak transcription Brain Germinal Matrix brain
4 chr7:106689000-106694400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr7:106689200-106692600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr7:106689400-106692200 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr7:106689400-106692400 Weak transcription Fetal Brain Male brain
8 chr7:106690000-106691800 Genic enhancers K562 blood
9 chr7:106690400-106692400 Enhancers Duodenum Smooth Muscle Duodenum
10 chr7:106690600-106691600 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr7:106690800-106705800 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr7:106691000-106691600 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr7:106691000-106692000 Enhancers HUVEC blood vessel
14 chr7:106691000-106692200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr7:106691200-106691800 Enhancers Fetal Stomach stomach
16 chr7:106691400-106691600 Enhancers Fetal Brain Female brain
17 chr7:106691400-106692200 Weak transcription NHLF lung
18 chr7:106691400-106692600 Enhancers Rectal Smooth Muscle rectum

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