Variant report

Variant	rs73654039
Chromosome Location	chr9:94480583-94480584
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94474813..94478609-chr9:94479157..94482495,5	K562	blood:
2	chr9:94479518..94481920-chr9:94486342..94488730,2	K562	blood:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs73654028	0.94[AFR][1000 genomes]
rs73654029	0.94[AFR][1000 genomes]
rs73654031	0.94[AFR][1000 genomes]
rs73654047	1.00[AFR][1000 genomes]
rs7861983	0.94[AFR][1000 genomes]
rs7872427	0.94[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045332	chr9:94352661-94656016	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv531631	chr9:94373847-94633213	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94458000-94489800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:94473800-94483400	Weak transcription	K562	blood
3	chr9:94474200-94480600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:94474200-94486000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:94476400-94485400	Weak transcription	Fetal Lung	lung
6	chr9:94477000-94483400	Weak transcription	Colon Smooth Muscle	Colon
7	chr9:94477000-94487000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr9:94477200-94483000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr9:94477200-94483400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr9:94477200-94484600	Weak transcription	Ovary	ovary
11	chr9:94477200-94489800	Weak transcription	Right Atrium	heart
12	chr9:94477200-94496800	Weak transcription	NHLF	lung
13	chr9:94477200-94533000	Weak transcription	Fetal Kidney	kidney
14	chr9:94477800-94483200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:94477800-94483800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr9:94478800-94484400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:94478800-94484600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr9:94479400-94484400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr9:94480000-94480800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr9:94480200-94482000	Strong transcription	Fetal Stomach	stomach
21	chr9:94480400-94480600	ZNF genes & repeats	Gastric	stomach

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