Variant report

Variant	rs17128172
Chromosome Location	chr12:40840467-40840468
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:40840275-40840508	HUVEC	blood vessel:	n/a	n/a
2	CTCF	chr12:40840320-40840470	NHEK	skin:	n/a	n/a
3	CTCF	chr12:40840320-40840470	AoAF	blood vessel:	n/a	n/a
4	CTCF	chr12:40840340-40840490	HRE	kidney:	n/a	n/a
5	CTCF	chr12:40840340-40840490	GM12864	blood:	n/a	n/a
6	SMC3	chr12:40840183-40840574	GM12878	blood:	n/a	n/a
7	CTCF	chr12:40840211-40840478	HepG2	liver:	n/a	n/a
8	CTCF	chr12:40840295-40840472	GM20000	blood:	n/a	n/a
9	RAD21	chr12:40840236-40840548	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:40840286-40840484	LNCaP	prostate:	n/a	n/a
11	CTCF	chr12:40840400-40840550	NB4	blood:	n/a	n/a
12	CTCF	chr12:40840320-40840470	GM12866	blood:	n/a	n/a
13	CTCF	chr12:40840202-40840518	SK-N-SH_RA	brain:	n/a	n/a
14	RAD21	chr12:40840235-40840485	GM12878	blood:	n/a	n/a
15	CTCF	chr12:40840291-40840476	K562	blood:	n/a	n/a
16	RAD21	chr12:40840236-40840541	GM12878	blood:	n/a	n/a
17	CTCF	chr12:40840320-40840470	HEK293	kidney:	n/a	n/a
18	CTCF	chr12:40840380-40840530	HMEC	breast:	n/a	n/a
19	CTCF	chr12:40840101-40840731	SK-N-SH	brain:	n/a	n/a
20	CTCF	chr12:40840340-40840490	HMF	breast:	n/a	n/a
21	CTCF	chr12:40840340-40840490	HA-sp	spinal cord:	n/a	n/a
22	SMC3	chr12:40840220-40840523	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr12:40840360-40840510	GM12872	blood:	n/a	n/a
24	CTCF	chr12:40840320-40840470	GM12865	blood:	n/a	n/a
25	ZNF143	chr12:40840247-40840557	GM12878	blood:	n/a	chr12:40840261-40840276
26	CTCF	chr12:40840320-40840470	GM12874	blood:	n/a	n/a
27	RAD21	chr12:40840243-40840534	GM12878	blood:	n/a	n/a
28	JUN	chr12:40840228-40840490	HepG2	liver:	n/a	chr12:40840376-40840389
29	CTCF	chr12:40840320-40840470	Caco-2	colon:	n/a	n/a
30	CTCF	chr12:40840292-40840483	LNCaP	prostate:	n/a	n/a
31	CTCF	chr12:40840320-40840470	Hela-S3	cervix:	n/a	n/a
32	RAD21	chr12:40840225-40840500	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr12:40840380-40840530	HCM	heart:	n/a	n/a
34	CTCF	chr12:40840320-40840470	HFF	foreskin:	n/a	n/a
35	CTCF	chr12:40840320-40840470	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:40840320-40840470	HRPEpiC	eye:	n/a	n/a
37	JUND	chr12:40840245-40840541	K562	blood:	n/a	n/a
38	CTCF	chr12:40840320-40840470	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr12:40840259-40840508	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr12:40840320-40840470	GM12878	blood:	n/a	n/a
41	CTCF	chr12:40840380-40840530	RPTEC	kidney:	n/a	n/a
42	CTCF	chr12:40840340-40840490	GM12871	blood:	n/a	n/a
43	CTCF	chr12:40840340-40840490	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr12:40840340-40840490	HPF	lung:	n/a	n/a
45	RAD21	chr12:40840192-40840536	HepG2	liver:	n/a	n/a
46	RAD21	chr12:40840292-40840519	IMR90	lung:	n/a	n/a
47	CTCF	chr12:40840340-40840490	AG09309	skin:	n/a	n/a
48	CTCF	chr12:40840320-40840470	GM12875	blood:	n/a	n/a
49	CTCF	chr12:40840420-40840570	A549	lung:	n/a	n/a
50	CTCF	chr12:40840340-40840490	HVMF	connective:	n/a	n/a

No data

Variant related genes	Relation type
ENSG00000258167	TF binding region

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11564134	1.00[CEU][hapmap]
rs11564174	1.00[CEU][hapmap]
rs11564186	1.00[CEU][hapmap]
rs11564208	1.00[CEU][hapmap]
rs11564254	1.00[CEU][hapmap]
rs11564257	1.00[CEU][hapmap]
rs17128169	1.00[CEU][hapmap]
rs17128301	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17128396	1.00[CEU][hapmap];0.92[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17521316	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56770752	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56778408	1.00[EUR][1000 genomes]
rs57721717	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58104027	1.00[EUR][1000 genomes]
rs7134318	1.00[EUR][1000 genomes]
rs7135212	1.00[EUR][1000 genomes]
rs73100424	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73100433	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73106627	1.00[EUR][1000 genomes]
rs73106651	1.00[EUR][1000 genomes]
rs73110078	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73110086	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73110087	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73110089	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73112010	1.00[EUR][1000 genomes]
rs73112021	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73112024	1.00[EUR][1000 genomes]
rs73116213	1.00[EUR][1000 genomes]
rs73117999	1.00[EUR][1000 genomes]
rs73119906	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7315719	1.00[CEU][hapmap]
rs7315853	1.00[CEU][hapmap]
rs9668092	1.00[CEU][hapmap];1.00[EUR][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	nsv832377	chr12:40704881-40855223	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1039272	chr12:40817585-40841318	Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv558606	chr12:40837331-40863052	Enhancers	TF binding region Chromatin interactive region lncRNA	2 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	chr12:40839000-40841000	Enhancers	Fetal Heart	heart

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