Variant report

Variant rs17658820
Chromosome Location chr5:17429605-17429606
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:17426600-17435200 Weak transcription Primary B cells from cord blood blood
2 chr5:17427000-17431400 Weak transcription Monocytes-CD14+_RO01746 blood
3 chr5:17428000-17431400 Weak transcription GM12878-XiMat blood
4 chr5:17428600-17430000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr5:17428800-17430000 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr5:17428800-17430000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr5:17428800-17430200 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr5:17428800-17430200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr5:17428800-17430400 Weak transcription H1 Cell Line embryonic stem cell
10 chr5:17428800-17430400 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr5:17428800-17433000 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr5:17429400-17430200 Enhancers NHEK skin
13 chr5:17429400-17430400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr5:17429400-17430400 Enhancers HMEC breast
15 chr5:17429600-17430200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr5:17429600-17430200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr5:17429600-17431000 Weak transcription Primary neutrophils fromperipheralblood blood

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