Variant report

Variant rs59569849
Chromosome Location chr17:59561636-59561637
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:59543200-59564800 Genic enhancers NHLF lung
2 chr17:59545600-59563000 Weak transcription Lung lung
3 chr17:59548200-59563400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr17:59553000-59563800 Weak transcription Fetal Intestine Large intestine
5 chr17:59554400-59564000 Genic enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr17:59555000-59563200 Strong transcription Fetal Muscle Leg muscle
7 chr17:59555800-59563200 Genic enhancers Fetal Lung lung
8 chr17:59557800-59562400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr17:59558200-59563400 Weak transcription Fetal Intestine Small intestine
10 chr17:59559000-59563400 Weak transcription Placenta Placenta
11 chr17:59560000-59563800 Weak transcription H9 Cell Line embryonic stem cell
12 chr17:59560400-59562600 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr17:59560600-59562600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr17:59560600-59563000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr17:59560800-59561800 Enhancers Fetal Brain Male brain
16 chr17:59561400-59561800 Strong transcription Fetal Muscle Trunk muscle
17 chr17:59561600-59563000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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