Variant report

Variant rs11634180
Chromosome Location chr15:51895757-51895758
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr15:51890000-51902000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr15:51891800-51903800 Weak transcription Primary hematopoietic stem cells blood
4 chr15:51892600-51913000 Weak transcription Rectal Mucosa Donor 31 rectum
5 chr15:51893000-51911000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr15:51893800-51904000 Weak transcription Fetal Stomach stomach
7 chr15:51894000-51906000 Weak transcription Dnd41 blood
8 chr15:51894600-51895800 Active TSS ES-I3 Cell Line embryonic stem cell
9 chr15:51894600-51895800 Active TSS A549 lung
10 chr15:51894800-51895800 Active TSS ES-WA7 Cell Line embryonic stem cell
11 chr15:51894800-51896200 Active TSS iPS-15b Cell Line embryonic stem cell
12 chr15:51894800-51901600 Weak transcription Primary monocytes fromperipheralblood blood
13 chr15:51895000-51896000 Active TSS K562 blood
14 chr15:51895000-51911600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr15:51895200-51913000 Weak transcription HMEC breast
16 chr15:51895400-51898000 Weak transcription Monocytes-CD14+_RO01746 blood

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