Variant report

Variant rs57326886
Chromosome Location chr8:39957828-39957829
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:39951000-39958600 Weak transcription H9 Cell Line embryonic stem cell
2 chr8:39951000-39968000 Weak transcription Rectal Smooth Muscle rectum
3 chr8:39954800-39958000 Enhancers Rectal Mucosa Donor 31 rectum
4 chr8:39955400-39959600 Enhancers Stomach Mucosa stomach
5 chr8:39956000-39958600 Weak transcription HUVEC blood vessel
6 chr8:39956000-39963800 Weak transcription Colon Smooth Muscle Colon
7 chr8:39956200-39958000 Enhancers Fetal Intestine Small intestine
8 chr8:39956400-39958000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr8:39956800-39958000 Enhancers Fetal Intestine Large intestine
10 chr8:39957000-39958000 Flanking Active TSS A549 lung
11 chr8:39957000-39962200 Enhancers Placenta Amnion Placenta Amnion
12 chr8:39957200-39959600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr8:39957600-39959000 Enhancers Hela-S3 cervix
14 chr8:39957600-39959400 Weak transcription Placenta Placenta
15 chr8:39957600-39961200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr8:39957800-39958200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr8:39957800-39960200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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