Variant report

Variant rs628800
Chromosome Location chr11:64769247-64769248
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:64764800-64769600 Weak transcription Left Ventricle heart
2 chr11:64764800-64774000 Weak transcription NHDF-Ad bronchial
3 chr11:64764800-64774000 Weak transcription NHLF lung
4 chr11:64764800-64781200 Weak transcription Right Atrium heart
5 chr11:64765000-64769400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr11:64765000-64770400 Weak transcription Fetal Stomach stomach
7 chr11:64765000-64774000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr11:64765000-64780600 Weak transcription H9 Cell Line embryonic stem cell
9 chr11:64766800-64770200 Weak transcription Placenta Placenta
10 chr11:64767400-64774000 Weak transcription A549 lung
11 chr11:64767400-64780400 Weak transcription Pancreas Pancrea
12 chr11:64768800-64769800 Enhancers K562 blood
13 chr11:64769000-64769600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr11:64769000-64770800 Enhancers HepG2 liver
15 chr11:64769200-64769800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr11:64769200-64769800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr11:64769200-64770000 Enhancers Right Ventricle heart
18 chr11:64769200-64770200 Enhancers Spleen Spleen
19 chr11:64769200-64771200 Enhancers Fetal Muscle Leg muscle
20 chr11:64769200-64771400 Enhancers Fetal Muscle Trunk muscle

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