Variant report

Variant	rs111978
Chromosome Location	chr7:18311577-18311578
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	chr7:18311330..18313091-chr7:18314736..18317305,2	K562	blood:
2	chr7:18310468..18313091-chr7:18314736..18317253,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10265242	0.85[EUR][1000 genomes]
rs10281630	0.86[EUR][1000 genomes]
rs109251	0.85[ASN][1000 genomes]
rs11769668	0.89[ASN][1000 genomes]
rs1178313	0.82[ASN][1000 genomes]
rs1178331	0.83[EUR][1000 genomes]
rs122617	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13227027	0.85[ASN][1000 genomes]
rs13232015	0.85[ASN][1000 genomes]
rs1431334	0.81[ASN][1000 genomes]
rs17418362	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2005774	0.80[ASN][1000 genomes]
rs302140	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs302141	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs302147	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs302148	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs302153	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs302155	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs302162	0.89[ASN][1000 genomes]
rs302164	0.89[ASN][1000 genomes]
rs302165	0.88[ASN][1000 genomes]
rs302168	0.87[ASN][1000 genomes]
rs302173	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302174	0.82[ASN][1000 genomes]
rs302176	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34060940	0.91[ASN][1000 genomes]
rs35307869	0.82[EUR][1000 genomes]
rs35676223	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs366909	0.83[EUR][1000 genomes]
rs436270	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55744175	0.84[ASN][1000 genomes]
rs56398383	0.85[ASN][1000 genomes]
rs583769	0.87[ASN][1000 genomes]
rs623532	0.83[ASN][1000 genomes]
rs624811	0.89[ASN][1000 genomes]
rs647270	0.81[ASN][1000 genomes]
rs679492	0.81[ASN][1000 genomes]
rs680882	0.88[ASN][1000 genomes]
rs758089	0.80[ASN][1000 genomes]
rs917329	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer 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	20 gene(s)	inside rSNPs	diseases
3	nsv1026629	chr7:17862477-18362404	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1025023	chr7:17865796-18357630	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv1030201	chr7:17898410-18491985	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
6	nsv606357	chr7:17938491-18375245	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
7	nsv606358	chr7:18084843-18416097	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
8	nsv887810	chr7:18193589-18391557	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv830914	chr7:18196730-18376047	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1029901	chr7:18205779-18387956	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv830916	chr7:18254299-18433349	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv887811	chr7:18295790-18346230	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18311400-18315000	Weak transcription	Aorta	Aorta

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