Variant report

Variant rs9804097
Chromosome Location chr1:85502337-85502338
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85485400-85513000 Weak transcription Pancreas Pancrea
2 chr1:85485800-85505200 Weak transcription Duodenum Mucosa Duodenum
3 chr1:85486000-85513000 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr1:85495000-85512800 Weak transcription HMEC breast
5 chr1:85496800-85512400 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr1:85498600-85506000 Weak transcription Aorta Aorta
7 chr1:85499600-85506000 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:85501200-85507800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:85501800-85504600 Strong transcription Fetal Intestine Small intestine
10 chr1:85502000-85505200 Strong transcription Fetal Intestine Large intestine

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