Variant report

Variant rs571211798
Chromosome Location chr1:94247954-94247955
allele -/GGG
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 chr1:94244000-94248000 Enhancers Placenta Amnion Placenta Amnion
6 chr1:94245600-94253000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:94245800-94248400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:94245800-94249000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:94246600-94255400 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr1:94246800-94266600 Weak transcription A549 lung
11 chr1:94247400-94249200 Weak transcription HMEC breast
12 chr1:94247400-94249200 Weak transcription NHEK skin
13 chr1:94247600-94251000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
14 chr1:94247800-94248400 Enhancers HepG2 liver
15 chr1:94247800-94251400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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