Variant report

Variant rs1196618
Chromosome Location chr11:64767951-64767952
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:64764200-64768400 Enhancers Dnd41 blood
2 chr11:64764800-64769200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr11:64764800-64769200 Weak transcription Right Ventricle heart
4 chr11:64764800-64769600 Weak transcription Left Ventricle heart
5 chr11:64764800-64774000 Weak transcription NHDF-Ad bronchial
6 chr11:64764800-64774000 Weak transcription NHLF lung
7 chr11:64764800-64781200 Weak transcription Right Atrium heart
8 chr11:64765000-64769000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr11:64765000-64769400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr11:64765000-64770400 Weak transcription Fetal Stomach stomach
11 chr11:64765000-64774000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr11:64765000-64780600 Weak transcription H9 Cell Line embryonic stem cell
13 chr11:64766600-64769200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr11:64766800-64769200 Weak transcription Fetal Muscle Trunk muscle
15 chr11:64766800-64769200 Weak transcription Fetal Muscle Leg muscle
16 chr11:64766800-64770200 Weak transcription Placenta Placenta
17 chr11:64767200-64768200 Weak transcription K562 blood
18 chr11:64767400-64769200 Weak transcription Spleen Spleen
19 chr11:64767400-64774000 Weak transcription A549 lung
20 chr11:64767400-64780400 Weak transcription Pancreas Pancrea
21 chr11:64767800-64769000 Weak transcription HepG2 liver

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