Variant report

Variant rs11119404
Chromosome Location chr1:210262467-210262468
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210248600-210273200 Weak transcription Fetal Brain Female brain
2 chr1:210250400-210263000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:210250800-210278800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr1:210257800-210275000 Weak transcription H9 Cell Line embryonic stem cell
5 chr1:210260200-210263600 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:210260600-210285200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr1:210262000-210279600 Weak transcription NH-A brain

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