Variant report

Variant rs34032561
Chromosome Location chr1:173093402-173093403
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173091400-173096400 Weak transcription Small Intestine intestine
2 chr1:173092400-173093800 Enhancers Fetal Brain Female brain
3 chr1:173092600-173093800 Enhancers Fetal Intestine Small intestine
4 chr1:173092600-173093800 Enhancers Stomach Mucosa stomach
5 chr1:173092800-173094600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:173092800-173096400 Enhancers Liver Liver
7 chr1:173092800-173097800 Weak transcription Pancreas Pancrea
8 chr1:173093000-173095200 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr1:173093000-173095600 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr1:173093000-173096400 Enhancers HepG2 liver
11 chr1:173093000-173096600 Weak transcription A549 lung
12 chr1:173093000-173097400 Weak transcription Duodenum Mucosa Duodenum
13 chr1:173093000-173097400 Weak transcription Rectal Mucosa Donor 31 rectum
14 chr1:173093000-173097800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:173093000-173097800 Weak transcription HMEC breast
16 chr1:173093000-173101600 Weak transcription Placenta Amnion Placenta Amnion
17 chr1:173093000-173106600 Weak transcription HSMMtube muscle
18 chr1:173093200-173096200 Weak transcription Fetal Intestine Large intestine
19 chr1:173093200-173097600 Weak transcription NHEK skin
20 chr1:173093200-173097800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
21 chr1:173093400-173097800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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