Variant report

Variant rs569320902
Chromosome Location chr13:111221220-111221221
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:111214800-111226400 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr13:111215600-111222600 Weak transcription Ovary ovary
3 chr13:111216000-111227800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr13:111216000-111227800 Weak transcription Gastric stomach
5 chr13:111216200-111221600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr13:111216200-111223200 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr13:111216200-111226400 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr13:111216600-111223000 Weak transcription Fetal Intestine Small intestine
9 chr13:111217200-111227600 Weak transcription Spleen Spleen
10 chr13:111217200-111227800 Weak transcription Pancreas Pancrea
11 chr13:111217400-111227400 Weak transcription H9 Cell Line embryonic stem cell
12 chr13:111217600-111223400 Weak transcription Duodenum Mucosa Duodenum
13 chr13:111217600-111224400 Weak transcription ES-I3 Cell Line embryonic stem cell
14 chr13:111217800-111221600 Weak transcription Rectal Mucosa Donor 31 rectum
15 chr13:111218800-111227800 Weak transcription HUES48 Cell Line embryonic stem cell
16 chr13:111220000-111222800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr13:111220400-111223200 Weak transcription Fetal Intestine Large intestine
18 chr13:111221000-111221600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
19 chr13:111221000-111221600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
20 chr13:111221200-111221600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell

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