Variant report

Variant rs2485729
Chromosome Location chrX:138982219-138982220
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:138941800-138988200 Weak transcription Primary T cells fromperipheralblood blood
2 chrX:138973000-138984400 Weak transcription ES-WA7 Cell Line embryonic stem cell
3 chrX:138979400-138988000 Weak transcription Primary T cells from cord blood blood
4 chrX:138979800-138985200 Weak transcription Fetal Intestine Small intestine
5 chrX:138980800-138989400 Weak transcription Liver Liver
6 chrX:138981200-138983800 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chrX:138981600-138991600 Weak transcription Primary B cells from cord blood blood
8 chrX:138982200-138990000 Weak transcription Fetal Stomach stomach

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