Variant report

Variant rs13205655
Chromosome Location chr6:143602840-143602841
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143570800-143609200 Weak transcription Fetal Intestine Large intestine
2 chr6:143583400-143606000 Weak transcription Fetal Intestine Small intestine
3 chr6:143583800-143615400 Weak transcription K562 blood
4 chr6:143589000-143607400 Weak transcription Aorta Aorta
5 chr6:143591400-143605200 Weak transcription Liver Liver
6 chr6:143592200-143605600 Weak transcription Adipose Nuclei Adipose
7 chr6:143593200-143606800 Weak transcription NHEK skin
8 chr6:143593400-143607000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:143595400-143605400 Weak transcription HepG2 liver
10 chr6:143598600-143620200 Weak transcription Brain Angular Gyrus brain
11 chr6:143600600-143609200 Weak transcription Brain Anterior Caudate brain
12 chr6:143602200-143603200 Enhancers Fetal Heart heart
13 chr6:143602800-143603200 Enhancers HMEC breast
14 chr6:143602800-143603600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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