Variant report

Variant rs519221
Chromosome Location chr11:59624536-59624537
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59614600-59624800 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr11:59618000-59624800 Weak transcription Pancreas Pancrea
3 chr11:59622200-59624600 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr11:59622200-59625000 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr11:59622400-59624600 Enhancers Hela-S3 cervix
6 chr11:59622400-59624800 Enhancers K562 blood
7 chr11:59623600-59626000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr11:59623800-59626200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:59624000-59626000 Enhancers HMEC breast
10 chr11:59624000-59626200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr11:59624000-59626400 Enhancers NHEK skin
12 chr11:59624200-59624800 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr11:59624200-59625400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr11:59624200-59625600 Enhancers HUES6 Cell Line embryonic stem cell
15 chr11:59624400-59624800 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr11:59624400-59625000 Weak transcription Primary neutrophils fromperipheralblood blood
17 chr11:59624400-59626000 Enhancers HUVEC blood vessel

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