Variant report

Variant rs10890460
Chromosome Location chr1:47574363-47574364
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47572200-47574400 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr1:47572200-47574800 Enhancers HMEC breast
3 chr1:47573200-47574800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:47573200-47578000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:47573600-47574400 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr1:47573600-47574400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr1:47573600-47574600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:47573600-47575600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr1:47573600-47575600 Enhancers Hela-S3 cervix
10 chr1:47573600-47575600 Enhancers NHEK skin
11 chr1:47573600-47577200 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr1:47573600-47578600 Weak transcription iPS-20b Cell Line embryonic stem cell
13 chr1:47573800-47574600 Enhancers HUVEC blood vessel
14 chr1:47574000-47574400 Enhancers HSMM muscle
15 chr1:47574200-47574400 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr1:47574200-47578400 Weak transcription HUES48 Cell Line embryonic stem cell

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