Variant report

Variant	rs4288933
Chromosome Location	chr14:105534009-105534010
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	WRNIP1	chr14:105533645-105534101	GM12878	blood:	n/a	n/a
2	PAX5	chr14:105533491-105534104	GM12878	blood:	n/a	n/a
3	BHLHE40	chr14:105533688-105534015	HepG2	liver:	n/a	chr14:105533847-105533868 chr14:105533852-105533861 chr14:105533853-105533862 chr14:105533854-105533863 chr14:105533690-105533706 chr14:105533853-105533862 chr14:105533851-105533864
4	USF1	chr14:105533701-105534071	SK-N-SH	brain:	n/a	chr14:105533847-105533868 chr14:105533852-105533861 chr14:105533853-105533862 chr14:105533854-105533863 chr14:105533853-105533862 chr14:105533851-105533864 chr14:105533851-105533862
5	POLR2A	chr14:105530960-105534026	GM18526	blood:	n/a	n/a
6	IRF4	chr14:105533510-105534091	GM12878	blood:	n/a	n/a
7	STAT5A	chr14:105533668-105534058	GM12878	blood:	n/a	chr14:105533824-105533831
8	ZEB1	chr14:105533826-105534090	GM12878	blood:	n/a	chr14:105533949-105533957
9	MTA3	chr14:105533579-105534010	GM12878	blood:	n/a	n/a
10	NFIC	chr14:105533545-105534101	GM12878	blood:	n/a	n/a
11	SP1	chr14:105533664-105534030	GM12878	blood:	n/a	n/a
12	SPI1	chr14:105533569-105534086	HL-60	blood:	n/a	chr14:105533651-105533664
13	RELA	chr14:105533604-105534053	GM18951	blood:	n/a	n/a
14	CEBPB	chr14:105533548-105534147	GM12878	blood:	n/a	n/a
15	EBF1	chr14:105532784-105534042	GM12878	blood:	n/a	chr14:105533066-105533077 chr14:105533497-105533507 chr14:105533498-105533507
16	USF1	chr14:105533706-105534017	GM12878	blood:	n/a	chr14:105533847-105533868 chr14:105533852-105533861 chr14:105533853-105533862 chr14:105533854-105533863 chr14:105533853-105533862 chr14:105533851-105533864 chr14:105533851-105533862
17	RCOR1	chr14:105532890-105534082	GM12878	blood:	n/a	n/a
18	MAX	chr14:105533630-105534095	SK-N-SH	brain:	n/a	chr14:105533853-105533862
19	POLR2A	chr14:105529905-105534031	GM19099	blood:	n/a	n/a
20	POLR2A	chr14:105524037-105534209	GM12878	blood:	n/a	n/a
21	POLR2A	chr14:105533536-105534018	GM12891	blood:	n/a	n/a
22	NFIC	chr14:105533574-105534027	GM12878	blood:	n/a	n/a
23	IKZF1	chr14:105533475-105534244	GM12878	blood:	n/a	n/a
24	PML	chr14:105533461-105534094	GM12878	blood:	n/a	n/a
25	STAT5A	chr14:105530796-105534132	GM12878	blood:	n/a	chr14:105533482-105533493 chr14:105532716-105532728 chr14:105533824-105533831 chr14:105532312-105532324
26	IRF4	chr14:105533522-105534047	GM12878	blood:	n/a	n/a
27	MXI1	chr14:105533512-105534009	GM12878	blood:	n/a	n/a
28	SP1	chr14:105533569-105534020	GM12878	blood:	n/a	chr14:105533636-105533646
29	FOXM1	chr14:105533593-105534051	GM12878	blood:	n/a	n/a
30	MAX	chr14:105533664-105534067	NB4	blood:	n/a	chr14:105533853-105533862
31	FOXM1	chr14:105533559-105534111	GM12878	blood:	n/a	n/a
32	POLR2A	chr14:105529865-105534212	GM12892	blood:	n/a	n/a
33	USF1	chr14:105533696-105534059	SK-N-SH_RA	brain:	n/a	chr14:105533847-105533868 chr14:105533852-105533861 chr14:105533853-105533862 chr14:105533854-105533863 chr14:105533853-105533862 chr14:105533851-105533864 chr14:105533851-105533862
34	BHLHE40	chr14:105530959-105534300	GM12878	blood:	n/a	chr14:105533847-105533868 chr14:105531209-105531218 chr14:105533852-105533861 chr14:105533853-105533862 chr14:105531206-105531219 chr14:105533854-105533863 chr14:105533690-105533706 chr14:105531208-105531217 chr14:105531207-105531216 chr14:105531202-105531223 chr14:105531987-105532003 chr14:105533853-105533862 chr14:105531208-105531217 chr14:105533851-105533864
35	RUNX3	chr14:105533367-105534193	GM12878	blood:	n/a	n/a
36	POLR2A	chr14:105530939-105534080	GM18951	blood:	n/a	n/a
37	MAX	chr14:105533537-105534031	GM12878	blood:	n/a	chr14:105533853-105533862
38	USF2	chr14:105533658-105534038	GM12878	blood:	n/a	chr14:105533847-105533868 chr14:105533852-105533861 chr14:105533853-105533862 chr14:105533851-105533862 chr14:105533854-105533863 chr14:105533690-105533706 chr14:105533853-105533862 chr14:105533851-105533864
39	ELK1	chr14:105533515-105534029	GM12878	blood:	n/a	n/a
40	ELF1	chr14:105530851-105534229	GM12878	blood:	n/a	chr14:105531770-105531783 chr14:105533818-105533831
41	POLR2A	chr14:105524257-105534197	GM12878	blood:	n/a	n/a
42	USF1	chr14:105533733-105534009	K562	blood:	n/a	chr14:105533847-105533868 chr14:105533852-105533861 chr14:105533853-105533862 chr14:105533854-105533863 chr14:105533853-105533862 chr14:105533851-105533864 chr14:105533851-105533862
43	TBL1XR1	chr14:105533520-105534153	GM12878	blood:	n/a	n/a
44	RUNX3	chr14:105533532-105534089	GM12878	blood:	n/a	n/a
45	ATF2	chr14:105533544-105534046	GM12878	blood:	n/a	n/a
46	POU2F2	chr14:105533448-105534061	GM12878	blood:	n/a	n/a
47	MTA3	chr14:105530839-105534396	GM12878	blood:	n/a	n/a
48	POLR2A	chr14:105530375-105534010	GM19193	blood:	n/a	n/a
49	POLR2A	chr14:105529442-105534045	GM18505	blood:	n/a	n/a
50	POLR2A	chr14:105524880-105534106	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105532364..105534245-chr14:105540275..105543125,2	K562	blood:
2	chr14:105442748..105444564-chr14:105532745..105535377,2	MCF-7	breast:
3	chr14:105531056..105532748-chr14:105533772..105537041,3	K562	blood:
4	chr14:105532364..105534497-chr14:105539681..105543125,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR132-1	chr14:105533801-105534066	XLOC_011152

Variant related genes	Relation type
GPR132	TF binding region
ENSG00000183484	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10151777	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11627133	0.97[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12433746	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12436511	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12889428	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12890396	0.83[ASN][1000 genomes]
rs12895274	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs28664663	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34116292	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34878850	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34882611	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs35886229	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35966880	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3803294	0.86[JPT][hapmap]
rs3809464	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3809465	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3809466	1.00[CEU][hapmap];0.90[CHB][hapmap];0.82[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3809469	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3809470	0.84[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[GIH][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3825765	0.94[EUR][1000 genomes]
rs4265748	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4391998	0.91[CEU][hapmap];0.97[TSI][hapmap];0.94[EUR][1000 genomes]
rs4457938	0.91[EUR][1000 genomes]
rs4464021	0.88[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4581644	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4635277	0.86[JPT][hapmap]
rs55780149	0.87[AMR][1000 genomes]
rs55951335	0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs56159244	0.82[EUR][1000 genomes]
rs56275808	0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs60562761	0.86[EUR][1000 genomes]
rs61997788	0.81[AMR][1000 genomes]
rs61997789	0.81[AMR][1000 genomes]
rs7144647	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7145885	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7147439	0.83[CEU][hapmap];0.97[TSI][hapmap];0.95[EUR][1000 genomes]
rs7147669	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7152235	0.91[CEU][hapmap];0.90[CHB][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7152401	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7157567	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7158479	1.00[CHB][hapmap];0.87[CHD][hapmap];0.87[GIH][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap]
rs7159920	0.86[JPT][hapmap]
rs7160811	0.89[CHB][hapmap];0.81[CHD][hapmap];0.96[MEX][hapmap]
rs72703887	0.93[ASN][1000 genomes]
rs8011909	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8015942	0.89[CHB][hapmap];0.81[CHD][hapmap];0.85[JPT][hapmap];0.92[MEX][hapmap]
rs8018607	0.92[MEX][hapmap]
rs8020062	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9743945	0.89[CHB][hapmap];0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv456457	chr14:105404384-105555396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	nsv566141	chr14:105404384-105555396	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
7	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
8	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
9	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
10	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
11	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
12	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
14	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
15	nsv566151	chr14:105459140-105555396	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
16	nsv456459	chr14:105459140-105617891	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
17	nsv566152	chr14:105459140-105617891	Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
18	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
19	nsv983941	chr14:105485574-105534240	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
20	nsv9175	chr14:105496509-105688941	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
21	nsv902426	chr14:105500760-105537476	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
22	nsv902427	chr14:105508577-105585347	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
23	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
24	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
25	nsv902428	chr14:105531945-105555396	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4288933	AHNAK2	cis	cerebellum	SCAN
rs4288933	TRMT61A	cis	parietal	SCAN

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105525600-105534200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
2	chr14:105528800-105542000	Weak transcription	Right Atrium	heart
3	chr14:105531000-105534400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr14:105531000-105534600	Enhancers	Spleen	Spleen
5	chr14:105531400-105542800	Weak transcription	Gastric	stomach
6	chr14:105531600-105534200	Enhancers	Fetal Muscle Leg	muscle
7	chr14:105531600-105536600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr14:105531600-105536600	Weak transcription	Pancreas	Pancrea
9	chr14:105531800-105534200	Enhancers	Thymus	Thymus
10	chr14:105531800-105534200	Flanking Active TSS	GM12878-XiMat	blood
11	chr14:105532000-105534200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr14:105532200-105534400	Enhancers	Fetal Thymus	thymus
13	chr14:105532200-105535200	Weak transcription	Fetal Intestine Small	intestine
14	chr14:105532400-105534200	Enhancers	Primary hematopoietic stem cells	blood
15	chr14:105532400-105534200	Enhancers	Placenta	Placenta
16	chr14:105532400-105536600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr14:105532600-105534400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr14:105532600-105534400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr14:105532600-105534600	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr14:105532600-105538200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr14:105532600-105538400	Enhancers	Primary B cells from peripheral blood	blood
22	chr14:105532600-105538800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr14:105532800-105534400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr14:105532800-105534400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr14:105532800-105534400	Enhancers	Duodenum Mucosa	Duodenum
26	chr14:105532800-105534600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr14:105532800-105536200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr14:105532800-105536200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:105532800-105537400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr14:105532800-105538200	Enhancers	Primary B cells from cord blood	blood
31	chr14:105533000-105534200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr14:105533000-105534200	Enhancers	HMEC	breast
33	chr14:105533000-105535400	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr14:105533200-105534200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr14:105533200-105534200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:105533200-105534200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr14:105533200-105534200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr14:105533200-105534200	Enhancers	HSMM	muscle
39	chr14:105533200-105534200	Enhancers	NHEK	skin
40	chr14:105533200-105534400	Bivalent Enhancer	Colonic Mucosa	Colon
41	chr14:105533200-105534600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr14:105533200-105534600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr14:105533400-105534200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:105533400-105534200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr14:105533400-105534200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr14:105533400-105534400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:105533400-105534400	Bivalent Enhancer	Adipose Nuclei	Adipose
48	chr14:105533400-105534400	Enhancers	Esophagus	oesophagus
49	chr14:105533400-105534600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr14:105533400-105537800	Enhancers	Primary T helper cells fromperipheralblood	blood

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