Variant report

Variant	rs12794145
Chromosome Location	chr11:64006484-64006485
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:64006427-64006784	U87	brain:	n/a	n/a
2	POLR2A	chr11:64006129-64006940	K562	blood:	n/a	n/a
3	POLR2A	chr11:64005406-64006932	K562	blood:	n/a	n/a
4	POLR2A	chr11:64006253-64006492	HUVEC	blood vessel:	n/a	n/a
5	POLR2A	chr11:64005542-64006874	K562	blood:	n/a	n/a
6	POLR2A	chr11:64006166-64006946	HL-60	blood:	n/a	n/a
7	REST	chr11:64006387-64006963	HL-60	blood:	n/a	n/a
8	POLR2A	chr11:64005176-64006643	HepG2	liver:	n/a	n/a
9	POLR2A	chr11:64006271-64006831	GM12891	blood:	n/a	n/a
10	POLR2A	chr11:64006414-64006788	GM12878	blood:	n/a	n/a
11	POLR2A	chr11:64006299-64006859	GM12891	blood:	n/a	n/a
12	POLR2A	chr11:64006420-64006907	HL-60	blood:	n/a	n/a
13	POLR2A	chr11:64005612-64006867	GM12891	blood:	n/a	n/a
14	SPI1	chr11:64006261-64006941	HL-60	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64005251..64012775-chr11:64065543..64076594,19	MCF-7	breast:
2	chr11:64004816..64010809-chr11:64048058..64057254,13	MCF-7	breast:
3	chr11:64006376..64009542-chr11:64085352..64088265,3	K562	blood:
4	chr11:64003628..64022712-chr11:64064086..64078429,56	MCF-7	breast:
5	chr11:64006100..64009452-chr11:64096947..64099274,3	K562	blood:
6	chr11:64006071..64007767-chr11:64081275..64082893,2	MCF-7	breast:
7	chr11:63933271..63935059-chr11:64002653..64006652,3	MCF-7	breast:

No data

Variant related genes	Relation type
FKBP2	TF binding region
ENSG00000256116	TF binding region
ENSG00000182450	Chromatin interaction
ENSG00000236935	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000173153	Chromatin interaction

Extended variants
information (count: 98 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1058735	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1059440	1.00[ASW][hapmap];0.93[CEU][hapmap];0.93[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];0.92[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11231701	0.86[EUR][1000 genomes]
rs11600867	0.82[YRI][hapmap]
rs11601024	0.89[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs11601577	0.90[EUR][1000 genomes]
rs11602181	1.00[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.86[MEX][hapmap];0.83[MKK][hapmap];0.96[TSI][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes]
rs11603042	0.82[CHB][hapmap]
rs11603212	1.00[ASW][hapmap];0.86[CEU][hapmap];0.93[CHB][hapmap];0.84[CHD][hapmap];0.93[GIH][hapmap];0.81[MEX][hapmap];0.96[TSI][hapmap];0.90[EUR][1000 genomes]
rs11605738	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11606544	0.86[EUR][1000 genomes]
rs11607007	1.00[CEU][hapmap];0.86[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11607144	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11607165	1.00[ASW][hapmap];0.93[CEU][hapmap];0.93[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.86[MEX][hapmap];0.85[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12418035	0.86[MEX][hapmap];0.83[TSI][hapmap]
rs12574258	0.85[EUR][1000 genomes]
rs12575642	1.00[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.87[CHD][hapmap];0.81[MEX][hapmap];0.87[TSI][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12787852	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs12797120	0.86[EUR][1000 genomes]
rs12798333	0.82[CEU][hapmap];0.86[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.91[LWK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12802950	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2001003	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2015226	0.86[CEU][hapmap];0.93[CHB][hapmap];0.91[YRI][hapmap];0.86[EUR][1000 genomes]
rs2070765	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2282490	1.00[ASW][hapmap];0.93[CEU][hapmap];0.93[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.86[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2286614	1.00[ASW][hapmap]
rs2875749	0.86[EUR][1000 genomes]
rs34089806	0.83[EUR][1000 genomes]
rs34113693	0.86[EUR][1000 genomes]
rs34358026	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35090903	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35095324	0.80[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs35458188	0.89[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs35524387	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35858916	0.89[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs3741404	0.82[CHB][hapmap]
rs3802933	0.93[CEU][hapmap];0.93[CHB][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3824854	0.86[CEU][hapmap];0.87[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.84[EUR][1000 genomes]
rs58632573	0.86[EUR][1000 genomes]
rs604203	0.87[CHB][hapmap]
rs6591837	0.92[EUR][1000 genomes]
rs66648159	0.86[EUR][1000 genomes]
rs67546972	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7102327	0.86[CEU][hapmap];0.93[CHB][hapmap];0.83[YRI][hapmap];0.85[EUR][1000 genomes]
rs7111278	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7112277	0.93[EUR][1000 genomes]
rs7130030	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs71479474	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs72918475	0.82[EUR][1000 genomes]
rs72920332	0.89[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs72922039	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7478730	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7939784	1.00[ASW][hapmap];0.86[CEU][hapmap];0.93[CHB][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.86[MEX][hapmap];0.83[MKK][hapmap];0.96[TSI][hapmap];0.91[YRI][hapmap];0.86[EUR][1000 genomes]
rs7944061	0.86[EUR][1000 genomes]
rs7952318	0.82[EUR][1000 genomes]
rs882146	1.00[ASW][hapmap];0.93[CEU][hapmap];0.93[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.84[LWK][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.91[YRI][hapmap];0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
11	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
12	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
13	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
14	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
15	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
16	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
17	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
18	nsv468595	chr11:63953121-64027888	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
19	nsv555187	chr11:63953121-64027888	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
20	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
21	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
22	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
23	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
24	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
25	nsv541061	chr11:63970174-64010995	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
26	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
27	nsv897672	chr11:63979643-64082807	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
28	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
29	nsv897673	chr11:63991581-64018687	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
30	nsv897675	chr11:63994692-64018687	Strong transcription Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	82 gene(s)	inside rSNPs	diseases
31	nsv897676	chr11:63994692-64022459	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	85 gene(s)	inside rSNPs	diseases
32	nsv897677	chr11:63994692-64023971	Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	85 gene(s)	inside rSNPs	diseases
33	nsv897678	chr11:63994692-64026144	Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	85 gene(s)	inside rSNPs	diseases
34	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
35	nsv897680	chr11:63997338-64022459	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	82 gene(s)	inside rSNPs	diseases
36	nsv897681	chr11:63998240-64022459	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	82 gene(s)	inside rSNPs	diseases
37	nsv541062	chr11:63998625-64015834	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
38	nsv541063	chr11:63998625-64020906	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
39	nsv541064	chr11:63998625-64036450	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases
40	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
41	esv18564	chr11:64001265-64018114	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
42	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs12794145	FKBP2	cis	parietal	SCAN
rs12794145	CDK2AP2	cis	parietal	SCAN
rs12794145	PRDX5	cis	parietal	SCAN
rs12794145	FAU	cis	parietal	SCAN
rs12794145	TRPT1	cis	Muscle Skeletal	GTEx
rs12794145	CD248	cis	parietal	SCAN
rs12794145	FLRT1	cis	cerebellum	SCAN
rs12794145	ASRGL1	cis	parietal	SCAN
rs12794145	PPP1R14B	Cis_1M	lymphoblastoid	RTeQTL
rs12794145	FKBP2	cis	lymphoblastoid	seeQTL
rs12794145	PPP1R14B	cis	Heart Left Ventricle	GTEx
rs12794145	FAM89B	cis	parietal	SCAN
rs12794145	PPP1R14B	cis	multi-tissue	Pritchard

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63999400-64007200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:64003000-64007600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:64003000-64007600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:64003000-64007800	Genic enhancers	Fetal Muscle Trunk	muscle
5	chr11:64003200-64006800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:64003200-64007600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:64003200-64007600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr11:64003400-64006600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr11:64003400-64007200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr11:64003400-64007200	Weak transcription	Brain Substantia Nigra	brain
11	chr11:64003400-64007200	Strong transcription	NHLF	lung
12	chr11:64003400-64007400	Weak transcription	Brain Angular Gyrus	brain
13	chr11:64003400-64007400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr11:64003400-64007600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr11:64003400-64007600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr11:64003400-64007600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr11:64003400-64007600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr11:64003400-64007600	Weak transcription	Fetal Kidney	kidney
19	chr11:64003400-64007600	Weak transcription	Fetal Lung	lung
20	chr11:64003400-64007600	Weak transcription	HSMM	muscle
21	chr11:64003400-64007600	Weak transcription	NH-A	brain
22	chr11:64003400-64007800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr11:64003400-64008000	Weak transcription	Fetal Brain Male	brain
24	chr11:64003600-64006800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:64003600-64007200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:64003600-64007200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr11:64003600-64007400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:64003600-64007400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr11:64003600-64007400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr11:64003600-64007400	Strong transcription	Fetal Stomach	stomach
31	chr11:64003600-64007400	Weak transcription	Psoas Muscle	Psoas
32	chr11:64003600-64007400	Weak transcription	Hela-S3	cervix
33	chr11:64003600-64007600	Weak transcription	Osteobl	bone
34	chr11:64003600-64007800	Weak transcription	Right Atrium	heart
35	chr11:64003800-64006800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr11:64003800-64007200	Weak transcription	Fetal Heart	heart
37	chr11:64003800-64007200	Weak transcription	K562	blood
38	chr11:64003800-64007600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr11:64003800-64007600	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr11:64004400-64006800	Strong transcription	Thymus	Thymus
41	chr11:64004400-64007600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr11:64004400-64007600	Enhancers	Stomach Mucosa	stomach
43	chr11:64004400-64007800	Genic enhancers	Placenta	Placenta
44	chr11:64004600-64006600	Genic enhancers	Primary B cells from cord blood	blood
45	chr11:64004600-64006800	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr11:64004600-64006800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:64004600-64006800	Strong transcription	Primary T cells from cord blood	blood
48	chr11:64004600-64006800	Strong transcription	Adipose Nuclei	Adipose
49	chr11:64004600-64006800	Genic enhancers	Fetal Thymus	thymus
50	chr11:64004600-64006800	Strong transcription	Stomach Smooth Muscle	stomach

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