Variant report

Variant rs17339378
Chromosome Location chr8:53732113-53732114
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:53728200-53738600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr8:53729000-53739200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:53730800-53732200 Enhancers H9 Cell Line embryonic stem cell
4 chr8:53730800-53732200 Enhancers HUES6 Cell Line embryonic stem cell
5 chr8:53730800-53732200 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr8:53731000-53732200 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr8:53731200-53732200 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr8:53731400-53732200 Enhancers H1 Cell Line embryonic stem cell
9 chr8:53731600-53734000 Enhancers Hela-S3 cervix
10 chr8:53731600-53737000 Weak transcription ES-WA7 Cell Line embryonic stem cell
11 chr8:53731800-53740200 Enhancers HMEC breast
12 chr8:53732000-53733200 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr8:53732000-53733200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr8:53732000-53733800 Enhancers NHEK skin
15 chr8:53732000-53734000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr8:53732000-53734600 Enhancers Liver Liver
17 chr8:53732000-53737200 Weak transcription ES-I3 Cell Line embryonic stem cell
18 chr8:53732000-53738600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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