Variant report

Variant rs552370324
Chromosome Location chr6:106825192-106825193
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:106819400-106844400 Weak transcription Fetal Intestine Large intestine
2 chr6:106822200-106829800 Weak transcription Fetal Intestine Small intestine
3 chr6:106823000-106826600 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr6:106824000-106825400 Enhancers Colon Smooth Muscle Colon
5 chr6:106824200-106826400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr6:106824400-106825200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr6:106824400-106826400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:106824600-106826000 Weak transcription Pancreas Pancrea
9 chr6:106824600-106826000 Enhancers HUVEC blood vessel
10 chr6:106824600-106829600 Weak transcription Esophagus oesophagus
11 chr6:106824800-106825200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr6:106824800-106825200 Flanking Active TSS HMEC breast
13 chr6:106824800-106825200 Bivalent Enhancer Osteobl bone
14 chr6:106824800-106825400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr6:106824800-106826000 Enhancers NH-A brain
16 chr6:106824800-106826200 Enhancers Hela-S3 cervix
17 chr6:106824800-106828200 Weak transcription Rectal Smooth Muscle rectum
18 chr6:106825000-106825200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
19 chr6:106825000-106825200 Flanking Active TSS Muscle Satellite Cultured Cells --
20 chr6:106825000-106825400 Flanking Active TSS NHEK skin
21 chr6:106825000-106826000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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