Variant report

Variant rs10771272
Chromosome Location chr12:26400587-26400588
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:26394000-26404600 Weak transcription Pancreas Pancrea
2 chr12:26396000-26401000 Enhancers Stomach Mucosa stomach
3 chr12:26397000-26401000 Enhancers HMEC breast
4 chr12:26397800-26401200 Enhancers Rectal Mucosa Donor 31 rectum
5 chr12:26399000-26400600 Enhancers Gastric stomach
6 chr12:26399200-26400800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr12:26399200-26400800 Weak transcription Small Intestine intestine
8 chr12:26399800-26400800 Weak transcription Fetal Intestine Small intestine
9 chr12:26399800-26402200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr12:26400200-26401000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr12:26400400-26401000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr12:26400400-26402200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr12:26400400-26402400 Weak transcription NHEK skin

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