Variant report

Variant	rs11972032
Chromosome Location	chr7:14043029-14043030
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:14041454..14043443-chr7:14049924..14051909,2	K562	blood:
2	chr7:14041943..14044192-chr7:14049527..14051909,2	K562	blood:
3	chr7:14039554..14043175-chr7:14045654..14048765,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL4A-9	chr7:14042922-14043734	NONHSAT119261

Variant related genes	Relation type
ENSG00000252374	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10251025	0.91[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10262618	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10263141	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11772292	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11973792	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2190065	0.88[AMR][1000 genomes]
rs2190066	0.85[AMR][1000 genomes]
rs28633703	0.90[AMR][1000 genomes]
rs3888604	0.85[AMR][1000 genomes]
rs4308625	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57156278	0.91[EUR][1000 genomes]
rs58361379	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs58447577	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62452790	0.85[AMR][1000 genomes]
rs6954954	0.83[AMR][1000 genomes]
rs6969768	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6970150	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7785120	0.81[EUR][1000 genomes]
rs917136	0.89[AMR][1000 genomes]
rs9639172	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv887698	chr7:13841798-14056075	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1030645	chr7:14015533-14078153	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv538739	chr7:14015533-14078153	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14041600-14044800	Active TSS	K562	blood
2	chr7:14043000-14043200	Flanking Active TSS	Placenta	Placenta

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