Variant report

Variant	rs72743821
Chromosome Location	chr9:101372492-101372493
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs59069726	0.88[EUR][1000 genomes]
rs59673494	0.81[EUR][1000 genomes]
rs6478791	0.88[EUR][1000 genomes]
rs6478792	0.88[EUR][1000 genomes]
rs7033772	0.82[EUR][1000 genomes]
rs72743826	0.88[EUR][1000 genomes]
rs72743828	0.88[EUR][1000 genomes]
rs72743831	0.88[EUR][1000 genomes]
rs7849195	0.88[EUR][1000 genomes]
rs7860838	0.88[EUR][1000 genomes]
rs7873740	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv614936	chr9:101182698-101680380	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv893614	chr9:101340316-101671634	Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv893615	chr9:101356515-101678036	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv466441	chr9:101362833-101419832	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv614952	chr9:101362833-101419832	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv893616	chr9:101371017-101472921	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101365400-101386800	Weak transcription	Brain Angular Gyrus	brain
2	chr9:101370600-101372600	Weak transcription	NH-A	brain
3	chr9:101370800-101373600	Enhancers	HUVEC	blood vessel
4	chr9:101371400-101375400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:101371800-101373200	Enhancers	Fetal Lung	lung
6	chr9:101372000-101372800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:101372000-101373600	Enhancers	Fetal Intestine Large	intestine
8	chr9:101372200-101372600	Enhancers	Lung	lung
9	chr9:101372200-101372800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr9:101372200-101373000	Enhancers	Brain Cingulate Gyrus	brain
11	chr9:101372200-101374200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:101372400-101372800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:101372400-101373000	Enhancers	Fetal Stomach	stomach
14	chr9:101372400-101375200	Enhancers	Fetal Intestine Small	intestine
15	chr9:101372400-101376000	Enhancers	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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