Variant report

Variant rs17328709
Chromosome Location chrX:138930940-138930941
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:138914400-138931800 Weak transcription Primary T cells from cord blood blood
2 chrX:138914600-138934400 Weak transcription Primary hematopoietic stem cells blood
3 chrX:138924600-138934600 Weak transcription Fetal Intestine Small intestine
4 chrX:138926600-138933200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chrX:138927000-138933400 Weak transcription H1 Cell Line embryonic stem cell
6 chrX:138927200-138931800 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chrX:138927400-138932600 Weak transcription ES-WA7 Cell Line embryonic stem cell
8 chrX:138927400-138933000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chrX:138927400-138933000 Weak transcription Aorta Aorta
10 chrX:138927400-138960200 Weak transcription Liver Liver
11 chrX:138927600-138932400 Weak transcription HUES6 Cell Line embryonic stem cell
12 chrX:138927600-138935000 Weak transcription GM12878-XiMat blood
13 chrX:138928000-138931200 Weak transcription Primary B cells from peripheral blood blood
14 chrX:138928000-138932400 Weak transcription HUES64 Cell Line embryonic stem cell
15 chrX:138928200-138932400 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chrX:138929200-138931800 Weak transcription HUES48 Cell Line embryonic stem cell
17 chrX:138929600-138934600 Weak transcription Primary B cells from cord blood blood
18 chrX:138930200-138933200 Weak transcription H9 Cell Line embryonic stem cell

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