Variant report

Variant rs17767339
Chromosome Location chr19:20156140-20156141
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:20150400-20162600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr19:20151000-20156200 Weak transcription HUES64 Cell Line embryonic stem cell
3 chr19:20151000-20162400 Weak transcription Primary T helper naive cells from peripheral blood blood
4 chr19:20155000-20156200 Enhancers Fetal Muscle Leg muscle
5 chr19:20155000-20156200 Enhancers Left Ventricle heart
6 chr19:20155000-20156400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr19:20155000-20156400 Enhancers Skeletal Muscle Female skeletal muscle
8 chr19:20155200-20156400 Enhancers Fetal Lung lung
9 chr19:20155400-20156200 Enhancers Right Atrium heart
10 chr19:20155400-20156400 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr19:20155600-20156400 Enhancers Right Ventricle heart
12 chr19:20155600-20157000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr19:20155600-20157200 Enhancers Fetal Heart heart
14 chr19:20156000-20156400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr19:20156000-20156400 Enhancers NHEK skin
16 chr19:20156000-20157400 Enhancers iPS-15b Cell Line embryonic stem cell
17 chr19:20156000-20157400 Enhancers iPS-20b Cell Line embryonic stem cell

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