Variant report

Variant rs9584567
Chromosome Location chr13:98049318-98049319
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:97995400-98050200 Weak transcription Small Intestine intestine
2 chr13:98028000-98056400 Weak transcription Psoas Muscle Psoas
3 chr13:98038600-98049400 Weak transcription Rectal Smooth Muscle rectum
4 chr13:98039600-98054400 Weak transcription Primary T cells from cord blood blood
5 chr13:98040000-98049800 Weak transcription Lung lung
6 chr13:98040200-98049400 Weak transcription Stomach Smooth Muscle stomach
7 chr13:98041400-98050200 Weak transcription Fetal Stomach stomach
8 chr13:98041800-98050800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr13:98042000-98052800 Weak transcription Fetal Muscle Leg muscle
10 chr13:98044600-98049400 Weak transcription Fetal Muscle Trunk muscle
11 chr13:98044600-98059400 Weak transcription Left Ventricle heart
12 chr13:98045400-98059400 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr13:98046600-98049400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr13:98048200-98050200 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr13:98048400-98052200 Weak transcription NHLF lung
16 chr13:98049000-98050200 Enhancers Fetal Lung lung
17 chr13:98049200-98049800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
18 chr13:98049200-98049800 Enhancers Colon Smooth Muscle Colon

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