Variant report

Variant rs11070861
Chromosome Location chr15:51894270-51894271
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:51889400-51909400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr15:51890000-51894800 Weak transcription Gastric stomach
3 chr15:51890000-51902000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr15:51891400-51895200 Enhancers HMEC breast
5 chr15:51891800-51903800 Weak transcription Primary hematopoietic stem cells blood
6 chr15:51892600-51894600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr15:51892600-51913000 Weak transcription Rectal Mucosa Donor 31 rectum
8 chr15:51893000-51894600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr15:51893000-51894600 Weak transcription A549 lung
10 chr15:51893000-51911000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr15:51893200-51894400 Enhancers Monocytes-CD14+_RO01746 blood
12 chr15:51893200-51894600 Weak transcription NHEK skin
13 chr15:51893200-51894800 Enhancers Primary monocytes fromperipheralblood blood
14 chr15:51893600-51895000 Flanking Active TSS K562 blood
15 chr15:51893800-51904000 Weak transcription Fetal Stomach stomach
16 chr15:51894000-51906000 Weak transcription Dnd41 blood
17 chr15:51894200-51895000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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