Variant report

Variant rs10912534
Chromosome Location chr1:173095989-173095990
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173091400-173096400 Weak transcription Small Intestine intestine
2 chr1:173092800-173096400 Enhancers Liver Liver
3 chr1:173092800-173097800 Weak transcription Pancreas Pancrea
4 chr1:173093000-173096400 Enhancers HepG2 liver
5 chr1:173093000-173096600 Weak transcription A549 lung
6 chr1:173093000-173097400 Weak transcription Duodenum Mucosa Duodenum
7 chr1:173093000-173097400 Weak transcription Rectal Mucosa Donor 31 rectum
8 chr1:173093000-173097800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr1:173093000-173097800 Weak transcription HMEC breast
10 chr1:173093000-173101600 Weak transcription Placenta Amnion Placenta Amnion
11 chr1:173093000-173106600 Weak transcription HSMMtube muscle
12 chr1:173093200-173096200 Weak transcription Fetal Intestine Large intestine
13 chr1:173093200-173097600 Weak transcription NHEK skin
14 chr1:173093200-173097800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr1:173093400-173097800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr1:173093800-173096400 Weak transcription Fetal Intestine Small intestine
17 chr1:173093800-173096400 Weak transcription Stomach Mucosa stomach
18 chr1:173095600-173096000 Enhancers HUES6 Cell Line embryonic stem cell
19 chr1:173095800-173101600 Weak transcription iPS-18 Cell Line embryonic stem cell

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