Variant report

Variant rs17650275
Chromosome Location chr5:154465058-154465059
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:154461000-154466600 Weak transcription Fetal Heart heart
2 chr5:154462200-154474400 Weak transcription Right Ventricle heart
3 chr5:154462400-154466600 Weak transcription HSMMtube muscle
4 chr5:154462800-154468000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr5:154464000-154467400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr5:154464000-154467400 Enhancers HMEC breast
7 chr5:154464000-154468200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr5:154464000-154472000 Enhancers Placenta Placenta
9 chr5:154464200-154469200 Weak transcription HUVEC blood vessel
10 chr5:154464200-154472800 Enhancers Placenta Amnion Placenta Amnion
11 chr5:154464400-154467400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr5:154464600-154468800 Enhancers Fetal Stomach stomach
13 chr5:154464800-154465200 Flanking Active TSS NHEK skin
14 chr5:154464800-154465600 Enhancers Esophagus oesophagus
15 chr5:154464800-154468400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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