Variant report

Variant	rs6870632
Chromosome Location	chr5:58753267-58753268
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1156028	0.88[CHB][hapmap];0.93[JPT][hapmap];0.89[YRI][hapmap];0.90[ASN][1000 genomes]
rs12518641	0.96[CEU][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1551564	0.88[CEU][hapmap];0.81[CHD][hapmap];0.91[GIH][hapmap];0.93[JPT][hapmap];0.86[MEX][hapmap];0.85[MKK][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16889853	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.85[MKK][hapmap];0.89[YRI][hapmap];0.96[ASN][1000 genomes]
rs16889865	0.89[LWK][hapmap];0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs16889892	0.81[CHB][hapmap];0.93[JPT][hapmap];0.82[YRI][hapmap];0.90[ASN][1000 genomes]
rs16889901	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs16889903	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs16889904	0.81[TSI][hapmap]
rs174039	0.88[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1902610	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2112910	0.87[CEU][hapmap];0.93[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35450986	0.90[ASN][1000 genomes]
rs3852147	0.88[CHB][hapmap];0.93[JPT][hapmap];0.89[YRI][hapmap];0.90[ASN][1000 genomes]
rs41447947	0.93[JPT][hapmap]
rs73097356	0.90[ASN][1000 genomes]
rs7704141	0.96[ASN][1000 genomes]
rs988827	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs988828	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023628	chr5:58557950-58757438	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv917274	chr5:58565291-58814374	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1028022	chr5:58673780-58786468	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1034656	chr5:58674724-58755580	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv598253	chr5:58675538-58754510	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv598254	chr5:58715782-58923601	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv881706	chr5:58730111-58865857	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv881707	chr5:58741491-58784102	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58709800-58756800	Weak transcription	Aorta	Aorta
2	chr5:58716000-58756600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr5:58731800-58764800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr5:58735800-58756400	Weak transcription	Psoas Muscle	Psoas
5	chr5:58746000-58754200	Weak transcription	Fetal Brain Female	brain
6	chr5:58750400-58756200	Weak transcription	Fetal Stomach	stomach
7	chr5:58750600-58754800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:58751400-58753400	Weak transcription	Liver	Liver
9	chr5:58751600-58755400	Weak transcription	Fetal Kidney	kidney
10	chr5:58752200-58753600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr5:58752200-58756600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr5:58752400-58753400	ZNF genes & repeats	A549	lung
13	chr5:58752400-58753800	Weak transcription	Fetal Intestine Small	intestine
14	chr5:58752400-58756400	Weak transcription	Fetal Muscle Leg	muscle
15	chr5:58752600-58754600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:58753200-58753600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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