Variant report

Variant	rs13357191
Chromosome Location	chr5:119839603-119839604
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:119834205..119836736-chr5:119837818..119840539,3	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10035683	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10052263	0.83[AFR][1000 genomes]
rs10052315	1.00[ASN][1000 genomes]
rs10052334	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10060164	0.83[AFR][1000 genomes]
rs10064623	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10065330	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10213989	0.82[AFR][1000 genomes]
rs10214171	1.00[ASN][1000 genomes]
rs10477605	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10478471	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10478472	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10478473	0.83[AFR][1000 genomes]
rs10478474	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11949016	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11957506	1.00[ASN][1000 genomes]
rs11958925	1.00[ASN][1000 genomes]
rs11960555	1.00[ASN][1000 genomes]
rs12109423	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13356306	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13356782	1.00[ASN][1000 genomes]
rs13359288	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13359350	1.00[ASN][1000 genomes]
rs13360299	1.00[ASN][1000 genomes]
rs13361121	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13362523	1.00[ASN][1000 genomes]
rs1454982	0.82[AFR][1000 genomes]
rs2604164	1.00[ASN][1000 genomes]
rs300956	0.83[AFR][1000 genomes]
rs4476747	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4895159	1.00[ASN][1000 genomes]
rs4895160	1.00[ASN][1000 genomes]
rs4895257	1.00[ASN][1000 genomes]
rs4895258	1.00[ASN][1000 genomes]
rs4895259	1.00[ASN][1000 genomes]
rs6595236	1.00[ASN][1000 genomes]
rs6595239	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6871554	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6892665	0.80[AFR][1000 genomes]
rs73264200	1.00[ASN][1000 genomes]
rs73266107	1.00[ASN][1000 genomes]
rs7448156	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7706025	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7710004	0.83[AFR][1000 genomes]
rs7710626	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7710848	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7710928	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7712847	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7728098	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7733397	1.00[ASN][1000 genomes]
rs7733602	0.82[AFR][1000 genomes]
rs9327144	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9327145	0.82[AFR][1000 genomes]
rs9327146	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830463	chr5:119806643-119968825	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv462427	chr5:119838923-119928674	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv599601	chr5:119838923-119928674	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119812200-119840000	Weak transcription	Fetal Lung	lung
2	chr5:119816600-119843000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr5:119818200-119845600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:119834400-119843600	Weak transcription	HSMMtube	muscle
5	chr5:119835800-119843000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr5:119836400-119852400	Weak transcription	HSMM	muscle
7	chr5:119838800-119842600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:119838800-119843600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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