Variant report

Variant	rs17166507
Chromosome Location	chr7:12951622-12951623
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:12724922..12727661-chr7:12949470..12951778,2	K562	blood:
2	chr7:12941736..12945870-chr7:12950835..12954445,3	K562	blood:
3	chr7:12947440..12949017-chr7:12950414..12952410,2	K562	blood:

Variant related genes	Relation type
ENSG00000122644	Chromatin interaction
ENSG00000271253	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10264460	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10264633	0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10269136	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10269685	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10278146	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10278405	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10488238	0.93[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10488241	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10488242	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11514702	0.97[ASN][1000 genomes]
rs12532561	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12666515	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12673139	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13230205	0.97[ASN][1000 genomes]
rs13240554	0.94[ASN][1000 genomes]
rs17166499	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs17166503	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs17166504	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17166509	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17166510	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17166514	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17166515	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17626895	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2024190	0.97[ASN][1000 genomes]
rs28611315	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs34743284	0.94[ASN][1000 genomes]
rs35319380	0.94[ASN][1000 genomes]
rs41377448	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4373427	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4570037	0.97[ASN][1000 genomes]
rs4591916	0.97[ASN][1000 genomes]
rs4719341	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4721154	0.80[AMR][1000 genomes]
rs4721157	0.88[ASN][1000 genomes]
rs4721158	0.97[ASN][1000 genomes]
rs57052689	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57923104	0.82[AMR][1000 genomes]
rs58376191	0.97[ASN][1000 genomes]
rs61050317	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6957008	0.97[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73061960	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73061961	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73061966	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73061970	0.93[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73061974	0.93[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73063838	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063839	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063840	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063841	0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063842	0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063844	0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063846	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063847	0.97[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73063848	0.97[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7795262	0.97[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7802804	0.88[ASN][1000 genomes]
rs9718616	0.97[ASN][1000 genomes]
rs975205	0.97[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs975206	0.97[AMR][1000 genomes];0.97[ASN][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	nsv1024554	chr7:12214722-12967418	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv538735	chr7:12214722-12967418	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv932020	chr7:12676890-13239551	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv868830	chr7:12712753-13517417	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv606235	chr7:12781381-13205950	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1020568	chr7:12802640-13183737	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv464382	chr7:12907178-12972685	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv606237	chr7:12907178-12972685	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv464384	chr7:12907178-13077065	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv606238	chr7:12907178-13077065	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	esv2763624	chr7:12917029-12951820	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv1029771	chr7:12927648-13153855	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv538736	chr7:12927648-13153855	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv1026908	chr7:12944128-12959702	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12948800-12952000	Enhancers	NHEK	skin
2	chr7:12950000-12951800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:12951000-12951800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:12951200-12961600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:12951400-12951800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:12951600-12951800	Enhancers	HMEC	breast

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