Variant report

Variant rs73319573
Chromosome Location chr7:41094502-41094503
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41086000-41094800 Weak transcription HSMM muscle
2 chr7:41088400-41099000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr7:41088600-41095000 Weak transcription HSMMtube muscle
4 chr7:41090200-41097000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:41091400-41097800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr7:41092200-41094600 Weak transcription Fetal Brain Male brain
7 chr7:41092200-41095600 Weak transcription Ovary ovary
8 chr7:41092200-41098800 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr7:41093200-41095000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr7:41093200-41095000 Enhancers Muscle Satellite Cultured Cells --
11 chr7:41094000-41095200 Strong transcription Aorta Aorta
12 chr7:41094000-41095400 Enhancers Liver Liver
13 chr7:41094000-41096000 Enhancers Fetal Muscle Leg muscle
14 chr7:41094200-41094600 Enhancers HUES48 Cell Line embryonic stem cell
15 chr7:41094200-41094600 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr7:41094200-41094800 Enhancers ES-I3 Cell Line embryonic stem cell
17 chr7:41094200-41094800 Enhancers H1 Cell Line embryonic stem cell
18 chr7:41094200-41094800 Enhancers iPS-18 Cell Line embryonic stem cell
19 chr7:41094200-41095600 Enhancers Fetal Stomach stomach

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