Variant report

Variant rs17755520
Chromosome Location chr6:140313294-140313295
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:140305600-140317200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr6:140311600-140313800 Weak transcription Placenta Placenta
3 chr6:140312200-140317400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr6:140312400-140313800 Weak transcription Fetal Intestine Small intestine
5 chr6:140312400-140313800 Weak transcription Skeletal Muscle Male skeletal muscle
6 chr6:140312600-140313800 Weak transcription Fetal Intestine Large intestine
7 chr6:140312600-140322200 Weak transcription NHDF-Ad bronchial
8 chr6:140312800-140313400 Weak transcription Left Ventricle heart
9 chr6:140312800-140313800 Weak transcription Aorta Aorta
10 chr6:140312800-140313800 Weak transcription Placenta Amnion Placenta Amnion
11 chr6:140312800-140313800 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr6:140312800-140317200 Weak transcription Osteobl bone
13 chr6:140312800-140317400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr6:140312800-140322200 Weak transcription NHLF lung
15 chr6:140312800-140322600 Weak transcription Ovary ovary
16 chr6:140313200-140314000 Weak transcription Fetal Heart heart

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