Variant report

Variant rs13023666
Chromosome Location chr2:20332049-20332050
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:20326400-20334800 Weak transcription Esophagus oesophagus
2 chr2:20326400-20336800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr2:20328000-20332200 Enhancers Fetal Intestine Large intestine
4 chr2:20329800-20333600 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr2:20330400-20332800 Weak transcription Fetal Kidney kidney
6 chr2:20331000-20334000 Weak transcription Stomach Mucosa stomach
7 chr2:20331000-20335000 Weak transcription Liver Liver
8 chr2:20331000-20335600 Weak transcription NHEK skin
9 chr2:20331200-20333000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr2:20331200-20334800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr2:20331200-20335000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr2:20331200-20335400 Weak transcription Rectal Mucosa Donor 31 rectum
13 chr2:20331200-20335800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:20331400-20335600 Weak transcription Fetal Lung lung
15 chr2:20331600-20334000 Weak transcription HMEC breast
16 chr2:20331600-20337000 Weak transcription Colonic Mucosa Colon
17 chr2:20331800-20335600 Weak transcription Rectal Mucosa Donor 29 rectum
18 chr2:20331800-20338600 Weak transcription Small Intestine intestine
19 chr2:20332000-20335600 Weak transcription Fetal Intestine Small intestine

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