Variant report

Variant	rs6968319
Chromosome Location	chr7:97406736-97406737
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:97399083..97401485-chr7:97404504..97407058,2	K562	blood:

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11763921	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11767488	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12113519	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13230541	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13231214	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13232045	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13232142	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13238313	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1397203	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1397204	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1397205	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1510306	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131823	0.86[EUR][1000 genomes]
rs17169082	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17169102	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17169185	0.86[EUR][1000 genomes]
rs17169186	0.86[EUR][1000 genomes]
rs17169191	0.86[EUR][1000 genomes]
rs17344752	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28505181	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34727943	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34815427	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34832720	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35190368	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35337801	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35378128	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35424999	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35500839	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35532973	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35700925	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35950761	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36076129	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36123498	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36198307	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36199127	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41278833	0.86[EUR][1000 genomes]
rs60876280	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67157089	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67877395	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6950092	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6952335	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6952362	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6960541	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6960981	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6966189	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6967582	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6967590	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6968035	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6968079	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6968597	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71561640	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71563535	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563539	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563540	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7787070	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7800135	0.86[EUR][1000 genomes]
rs7801604	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9690584	0.82[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	nsv888757	chr7:97003503-97461115	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv888759	chr7:97283118-97422195	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv1031371	chr7:97312452-98070538	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv508473	chr7:97385368-97407164	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1034752	chr7:97385561-97422926	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2764049	chr7:97385573-97407061	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv6	chr7:97385573-97423298	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv5858	chr7:97385573-97423298	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1017392	chr7:97385921-97438035	Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv516307	chr7:97389030-97422926	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv436563	chr7:97392165-97420411	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1030644	chr7:97395448-97407049	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1017302	chr7:97395448-97422926	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv428178	chr7:97402756-97648029	Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97406600-97407200	Enhancers	Fetal Intestine Large	intestine

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