Variant report

Variant	rs2190299
Chromosome Location	chr7:86418905-86418906
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	chr7:86416612..86418923-chr7:86419769..86421424,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10224033	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10226672	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10245069	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10259486	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10952891	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11772755	0.93[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16888204	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17161024	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17161223	1.00[ASN][1000 genomes]
rs55776729	1.00[ASN][1000 genomes]
rs57384334	1.00[ASN][1000 genomes]
rs6465085	0.96[EUR][1000 genomes]
rs6465086	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6465087	1.00[CHB][hapmap];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]
rs6954573	1.00[CHB][hapmap];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	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6958716	1.00[ASN][1000 genomes]
rs6960053	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6967992	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6974073	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6974507	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6977048	1.00[ASN][1000 genomes]
rs6978155	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs73382326	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	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7801050	1.00[ASN][1000 genomes]
rs7801589	1.00[ASN][1000 genomes]
rs7804469	1.00[ASN][1000 genomes]
rs7812155	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9655947	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs970186	0.81[YRI][hapmap]

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	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	nsv831053	chr7:86268171-86440999	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86415800-86419400	Weak transcription	Brain Angular Gyrus	brain
2	chr7:86416200-86419200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr7:86416400-86419000	Weak transcription	Fetal Brain Male	brain
4	chr7:86416600-86426200	Weak transcription	Fetal Brain Female	brain
5	chr7:86416800-86419000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr7:86416800-86420800	Weak transcription	Brain Substantia Nigra	brain
7	chr7:86416800-86421200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:86418000-86419400	Enhancers	Brain Anterior Caudate	brain
9	chr7:86418000-86419400	Flanking Active TSS	GM12878-XiMat	blood
10	chr7:86418200-86419600	Enhancers	Brain Cingulate Gyrus	brain
11	chr7:86418200-86420000	Enhancers	Brain Hippocampus Middle	brain
12	chr7:86418400-86419000	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr7:86418400-86423600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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