Variant report

Variant rs6684389
Chromosome Location chr1:94247031-94247032
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 chr1:94236200-94247400 Weak transcription Fetal Intestine Small intestine
3 chr1:94241000-94247400 Enhancers HMEC breast
4 chr1:94241000-94249000 Enhancers Hela-S3 cervix
5 chr1:94241200-94248400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:94243000-94247800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:94243600-94248400 Enhancers Placenta Placenta
8 chr1:94244000-94248000 Enhancers Placenta Amnion Placenta Amnion
9 chr1:94245600-94253000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr1:94245800-94247800 Weak transcription HepG2 liver
11 chr1:94245800-94248400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:94245800-94249000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:94246200-94247400 Enhancers NHEK skin
14 chr1:94246600-94255400 Weak transcription ES-I3 Cell Line embryonic stem cell
15 chr1:94246800-94266600 Weak transcription A549 lung

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