Variant report

Variant rs7884321
Chromosome Location chrX:109494748-109494749
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:109486000-109501400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chrX:109487600-109494800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chrX:109488600-109495200 Weak transcription Primary T cells from cord blood blood
4 chrX:109489200-109496200 Weak transcription H9 Cell Line embryonic stem cell
5 chrX:109490000-109496200 Weak transcription ES-WA7 Cell Line embryonic stem cell
6 chrX:109490000-109499800 Weak transcription HUES64 Cell Line embryonic stem cell
7 chrX:109490400-109497200 Weak transcription HUES6 Cell Line embryonic stem cell
8 chrX:109490400-109502200 Weak transcription Primary T regulatory cells fromperipheralblood blood
9 chrX:109490600-109498600 Weak transcription HUES48 Cell Line embryonic stem cell
10 chrX:109490600-109499000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
11 chrX:109490800-109498600 Weak transcription Primary T helper cells PMA-I stimulated --
12 chrX:109490800-109501200 Weak transcription Primary T helper cells fromperipheralblood blood
13 chrX:109492400-109498400 Weak transcription iPS-18 Cell Line embryonic stem cell
14 chrX:109492600-109497400 Weak transcription iPS-15b Cell Line embryonic stem cell
15 chrX:109492800-109496200 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chrX:109493400-109495200 Enhancers K562 blood
17 chrX:109494000-109495000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chrX:109494200-109495000 Bivalent Enhancer Fetal Lung lung
19 chrX:109494200-109495200 Enhancers NHEK skin
20 chrX:109494600-109494800 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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