Variant report

Variant	rs9541006
Chromosome Location	chr13:67689805-67689806
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:67685964..67690654-chr13:67706296..67711657,6	K562	blood:
2	chr13:67681587..67685897-chr13:67688405..67692463,6	K562	blood:
3	chr13:67686001..67691093-chr13:67707345..67712221,5	K562	blood:
4	chr13:67674917..67677595-chr13:67687583..67689856,3	K562	blood:

Extended variants
information (count: 111 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs1028899	1.00[ASN][1000 genomes]
rs10492596	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10492597	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10507741	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];1.00[ASN][1000 genomes]
rs11148737	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs11148738	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12184632	0.87[EUR][1000 genomes]
rs12184736	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12372837	0.85[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1323923	1.00[CHB][hapmap]
rs1408171	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs149448	0.88[EUR][1000 genomes]
rs17195259	0.88[EUR][1000 genomes]
rs17195266	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17517286	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.95[ASN][1000 genomes]
rs17517438	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.95[ASN][1000 genomes]
rs17587572	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17588668	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];1.00[ASN][1000 genomes]
rs17589427	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.95[ASN][1000 genomes]
rs17791056	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1927811	1.00[ASN][1000 genomes]
rs1927812	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs260131	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs260140	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs260160	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs260162	0.88[EUR][1000 genomes]
rs260164	0.88[EUR][1000 genomes]
rs260165	0.88[EUR][1000 genomes]
rs2875517	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs56226179	0.87[EUR][1000 genomes]
rs56309321	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56915128	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61191692	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61959247	0.88[EUR][1000 genomes]
rs61959248	0.88[EUR][1000 genomes]
rs61959249	0.88[EUR][1000 genomes]
rs61959360	0.84[AMR][1000 genomes]
rs61959362	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61959363	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61959367	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61959407	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61961771	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61961774	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7330064	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7987478	1.00[CHB][hapmap]
rs7992494	1.00[ASN][1000 genomes]
rs7999949	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8001394	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9317633	1.00[CHB][hapmap]
rs9317637	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9317642	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9529163	0.85[CEU][hapmap]
rs9529166	0.85[EUR][1000 genomes]
rs9529167	0.85[EUR][1000 genomes]
rs9529169	0.85[EUR][1000 genomes]
rs9529174	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9529180	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9529182	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9529183	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9529185	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9529186	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9529187	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9529188	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9529189	1.00[ASN][1000 genomes]
rs9529190	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9540950	1.00[CHB][hapmap]
rs9540967	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs9540968	0.84[EUR][1000 genomes]
rs9540969	0.85[EUR][1000 genomes]
rs9540971	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs9540980	0.88[EUR][1000 genomes]
rs9540982	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9540983	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9540984	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9540987	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9540988	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9540989	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9540993	0.85[CEU][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9540994	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9540995	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9540996	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9540997	0.87[EUR][1000 genomes]
rs9540998	0.87[EUR][1000 genomes]
rs9540999	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9541000	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9541001	0.83[AMR][1000 genomes]
rs9541002	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9541003	0.87[EUR][1000 genomes]
rs9541004	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9541007	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9541008	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9541012	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9541013	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.95[ASN][1000 genomes]
rs9541015	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9571705	1.00[CHB][hapmap]
rs9571714	1.00[ASN][1000 genomes]
rs972419	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530605	chr13:67126136-67697306	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv900414	chr13:67515590-67701341	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1045093	chr13:67517932-67693875	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv541821	chr13:67517932-67693875	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv430581	chr13:67572850-67762288	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv430582	chr13:67589898-67762299	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv1037217	chr13:67589937-67728156	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv1039600	chr13:67593961-67726047	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv541823	chr13:67593961-67726047	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv1040715	chr13:67668189-67699198	ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv832641	chr13:67671691-67708713	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1053514	chr13:67687520-67775011	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9541006	PCDH9	cis	Nerve Tibial	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67683600-67692000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr13:67688000-67691600	Enhancers	Brain Angular Gyrus	brain
3	chr13:67688000-67693400	Enhancers	Brain Substantia Nigra	brain
4	chr13:67688200-67690000	Enhancers	A549	lung
5	chr13:67688400-67695000	Weak transcription	K562	blood
6	chr13:67688800-67693400	Enhancers	Brain Hippocampus Middle	brain
7	chr13:67689400-67690000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr13:67689600-67690600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:67689600-67690600	Weak transcription	Brain Anterior Caudate	brain
10	chr13:67689600-67690600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr13:67689600-67690800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr13:67689600-67701400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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