Variant report

Variant rs2164660
Chromosome Location chr5:59011507-59011508
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:59006000-59012600 Weak transcription Right Ventricle heart
2 chr5:59008600-59012800 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
3 chr5:59009400-59018600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr5:59009600-59019800 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr5:59009800-59013600 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr5:59009800-59013800 Weak transcription Colon Smooth Muscle Colon
7 chr5:59009800-59023400 Weak transcription Fetal Lung lung
8 chr5:59010000-59013200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr5:59010000-59014400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr5:59010400-59012400 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr5:59010600-59011600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr5:59011000-59012200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr5:59011000-59012400 Weak transcription Fetal Stomach stomach
14 chr5:59011200-59012400 Genic enhancers Gastric stomach
15 chr5:59011200-59012800 Strong transcription Hela-S3 cervix
16 chr5:59011200-59013000 Weak transcription Fetal Muscle Leg muscle
17 chr5:59011200-59020400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
18 chr5:59011200-59020600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
19 chr5:59011400-59014000 Strong transcription A549 lung

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