Variant report

Variant rs12678378
Chromosome Location chr8:53730643-53730644
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:53725400-53730800 Enhancers Primary monocytes fromperipheralblood blood
2 chr8:53727600-53731200 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr8:53728200-53730800 Weak transcription HUES48 Cell Line embryonic stem cell
4 chr8:53728200-53730800 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr8:53728200-53731000 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr8:53728200-53731200 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr8:53728200-53731400 Weak transcription H1 Cell Line embryonic stem cell
8 chr8:53728200-53738600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr8:53728400-53730800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr8:53728400-53731000 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr8:53729000-53731200 Enhancers HMEC breast
12 chr8:53729000-53739200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr8:53729600-53731600 Weak transcription Hela-S3 cervix
14 chr8:53729800-53732000 Weak transcription Liver Liver
15 chr8:53730200-53731000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr8:53730200-53731000 Enhancers NHEK skin
17 chr8:53730400-53731000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr8:53730600-53731200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
19 chr8:53730600-53732000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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