Variant report

Variant rs4926826
Chromosome Location chr1:47575446-47575447
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47573200-47578000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr1:47573600-47575600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:47573600-47575600 Enhancers Hela-S3 cervix
4 chr1:47573600-47575600 Enhancers NHEK skin
5 chr1:47573600-47577200 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr1:47573600-47578600 Weak transcription iPS-20b Cell Line embryonic stem cell
7 chr1:47574200-47578400 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr1:47574400-47577200 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr1:47574400-47578600 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr1:47574400-47578600 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr1:47574600-47576000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:47574800-47586400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:47575200-47576000 Enhancers HMEC breast

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