Variant report

Variant	rs10226672
Chromosome Location	chr7:86457755-86457756
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:86455859..86457813-chr7:86459522..86462357,2	K562	blood:
2	chr7:86457573..86460345-chr7:86463468..86465258,2	K562	blood:
3	chr7:86456097..86458760-chr7:86462488..86464768,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10224033	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10245069	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10259486	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10952891	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11772755	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs16888204	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17161024	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17161223	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2190299	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs55776729	1.00[ASN][1000 genomes]
rs57384334	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58178461	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6465086	1.00[ASN][1000 genomes]
rs6465087	1.00[CHB][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6465089	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6947778	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6950123	1.00[ASN][1000 genomes]
rs6954573	1.00[CHB][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6955452	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6955565	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6955917	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6957842	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6958245	1.00[ASN][1000 genomes]
rs6958716	1.00[ASN][1000 genomes]
rs6960053	1.00[CHB][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6967992	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6974073	1.00[ASN][1000 genomes]
rs6974507	1.00[CHB][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6977048	1.00[ASN][1000 genomes]
rs6978155	1.00[CHB][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73382326	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73382367	1.00[ASN][1000 genomes]
rs73398484	1.00[ASN][1000 genomes]
rs7781922	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7800616	1.00[ASN][1000 genomes]
rs7801050	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7801589	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7804469	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7812155	1.00[ASN][1000 genomes]
rs9655947	1.00[CEU][hapmap];1.00[CHB][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]

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	nsv1025032	chr7:86032479-86642973	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1025277	chr7:86299224-87206007	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv538999	chr7:86299224-87206007	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
4	nsv532147	chr7:86299225-87121975	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86442200-86468400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:86443400-86480600	Weak transcription	Brain Angular Gyrus	brain
3	chr7:86453400-86468400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:86456000-86459600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:86456400-86460200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:86456400-86460200	Weak transcription	Brain Substantia Nigra	brain
7	chr7:86456600-86460200	Weak transcription	Brain Hippocampus Middle	brain
8	chr7:86456600-86461200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr7:86457600-86459000	Enhancers	Brain Anterior Caudate	brain

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