Variant report

Variant rs11164989
Chromosome Location chr1:94248230-94248231
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94220000-94254200 Weak transcription Aorta Aorta
2 chr1:94241000-94249000 Enhancers Hela-S3 cervix
3 chr1:94241200-94248400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:94243600-94248400 Enhancers Placenta Placenta
5 chr1:94245600-94253000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr1:94245800-94248400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:94245800-94249000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:94246600-94255400 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr1:94246800-94266600 Weak transcription A549 lung
10 chr1:94247400-94249200 Weak transcription HMEC breast
11 chr1:94247400-94249200 Weak transcription NHEK skin
12 chr1:94247600-94251000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr1:94247800-94248400 Enhancers HepG2 liver
14 chr1:94247800-94251400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr1:94248200-94248400 Enhancers HUVEC blood vessel

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