Variant report

Variant rs227199
Chromosome Location chr1:210265384-210265385
allele C/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 chr1:210250800-210278800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:210257800-210275000 Weak transcription H9 Cell Line embryonic stem cell
4 chr1:210260600-210285200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:210262000-210279600 Weak transcription NH-A brain
6 chr1:210263200-210269800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:210263600-210267000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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