Variant report

Variant	rs2241468
Chromosome Location	chr4:10113905-10113906
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:10113697..10116764-chr4:10457912..10460573,3	K562	blood:
2	chr4:10112946..10115430-chr4:10181535..10185097,4	K562	blood:
3	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
4	chr4:10089838..10092130-chr4:10112314..10114162,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251296	Chromatin interaction
ENSG00000178163	Chromatin interaction

Extended variants
information (count: 176 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:135)

rs_ID	r²[population]
rs10012288	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs10015403	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs10015494	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs10015872	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs10028503	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs10028937	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs10031453	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs1009144	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs10489079	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs10489080	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs10516201	0.87[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1076017	0.85[ASN][1000 genomes]
rs10805356	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs10939722	0.92[CHB][hapmap];0.82[JPT][hapmap]
rs10939730	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs10939732	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs11732828	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs12374229	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12374294	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12498152	0.84[AMR][1000 genomes]
rs12498256	0.84[AMR][1000 genomes]
rs12499772	0.83[AMR][1000 genomes]
rs12499782	0.81[AMR][1000 genomes]
rs12500891	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs12501336	0.86[AMR][1000 genomes]
rs12501597	1.00[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs12501855	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12502556	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12504600	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12506893	0.88[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12507586	0.83[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes]
rs12507725	0.83[AMR][1000 genomes]
rs12508413	0.83[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes]
rs12513165	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs12513376	0.84[AMR][1000 genomes]
rs17198113	1.00[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs17410735	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs17450260	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs17450372	0.83[CHB][hapmap];0.85[JPT][hapmap]
rs17450434	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs1860903	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs2192094	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs2241467	0.84[AMR][1000 genomes]
rs2241472	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2241473	0.81[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2241488	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35758343	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3756215	0.87[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3756227	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3756230	0.90[CEU][hapmap];0.90[EUR][1000 genomes]
rs3796818	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3796825	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3796826	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3822246	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3886038	0.87[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41268389	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4168	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4401449	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4456954	1.00[CHB][hapmap];0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs4484300	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4574408	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4619888	0.92[AMR][1000 genomes]
rs4697711	0.92[CHB][hapmap];0.82[JPT][hapmap]
rs4697713	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4697715	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4697927	0.92[CHB][hapmap];0.82[JPT][hapmap]
rs4697930	0.85[JPT][hapmap]
rs4697931	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4697934	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4697936	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs4697937	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs4697940	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs55683032	0.84[AMR][1000 genomes]
rs55692720	0.84[AMR][1000 genomes]
rs55848383	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55973727	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56146302	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56154234	0.91[ASN][1000 genomes]
rs56393964	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56403947	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61335146	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs62286600	0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs62286604	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs62287521	0.86[AMR][1000 genomes]
rs62287522	0.83[AMR][1000 genomes]
rs62287523	0.81[AMR][1000 genomes]
rs62287538	0.81[AMR][1000 genomes]
rs62287552	0.86[AMR][1000 genomes]
rs62288520	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62288521	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62288546	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6449289	0.91[ASN][1000 genomes]
rs6449300	0.84[CEU][hapmap];0.92[CHB][hapmap]
rs6813334	0.88[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes]
rs6825888	0.87[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6827496	0.92[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes]
rs6834574	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs6838644	0.85[JPT][hapmap]
rs6840883	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs6846402	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs6847379	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs6850516	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs6855657	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs715260	0.93[ASN][1000 genomes]
rs715979	0.83[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs731069	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs731070	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs73212808	0.84[AMR][1000 genomes]
rs73212817	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73212828	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73212853	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73212863	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73212864	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73212886	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73212889	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73212890	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73212891	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73212899	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73216820	0.84[AMR][1000 genomes]
rs73218753	0.81[AMR][1000 genomes]
rs73218771	0.83[AMR][1000 genomes]
rs735527	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs747356	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs747357	0.92[CHB][hapmap];0.86[JPT][hapmap]
rs7662229	0.89[ASN][1000 genomes]
rs7667775	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7681250	0.86[ASN][1000 genomes]
rs7683755	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs881641	0.84[CEU][hapmap];0.92[CHB][hapmap];0.83[AMR][1000 genomes]
rs881642	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs887729	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs887735	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs929577	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs9732	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9926	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
2	nsv530090	chr4:9383695-10165033	Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	nsv1014216	chr4:9713612-10223836	Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
4	nsv878681	chr4:9802853-10397327	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
5	nsv997941	chr4:9805223-10493388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
6	nsv1008649	chr4:9805223-10589802	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
7	nsv1000587	chr4:9805223-10610752	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	nsv537022	chr4:9805223-10610752	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
9	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
10	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
11	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
12	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
13	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
14	nsv537026	chr4:9903566-10262258	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
15	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
16	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
17	esv2752052	chr4:9911872-10313111	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
18	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
19	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
20	nsv532706	chr4:9948018-10451450	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
21	nsv1013022	chr4:9961220-10230042	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
22	nsv537028	chr4:9961220-10230042	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
23	nsv537029	chr4:9961220-10262258	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
24	nsv878691	chr4:9966477-10418078	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
25	nsv1013487	chr4:9972011-10320963	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
26	nsv829857	chr4:9982514-10155835	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
27	nsv469621	chr4:9987670-10142287	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
28	nsv482719	chr4:9987670-10142287	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
29	nsv1008067	chr4:10004664-10262258	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
30	nsv537030	chr4:10004664-10262258	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
31	nsv869057	chr4:10013411-10875454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
32	nsv537031	chr4:10040713-10262258	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
33	nsv997936	chr4:10040713-11009045	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
34	nsv428438	chr4:10058226-10273779	Flanking Active TSS Genic enhancers Strong transcription Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
35	nsv537032	chr4:10069805-10262258	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
36	nsv537033	chr4:10069805-10297561	Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	49 gene(s)	inside rSNPs	diseases
37	nsv524687	chr4:10080462-10159103	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
38	nsv1003286	chr4:10082156-10230606	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
39	esv16807	chr4:10099819-10234566	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
40	nsv537034	chr4:10103058-10262258	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
41	nsv537035	chr4:10103058-10297561	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2241468	WDR1	Cis_1M	lymphoblastoid	RTeQTL
rs2241468	SLC2A9	cis	Artery Tibial	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10084400-10114000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:10084800-10116600	Genic enhancers	Fetal Muscle Leg	muscle
3	chr4:10090400-10116400	Genic enhancers	Primary T cells fromperipheralblood	blood
4	chr4:10091800-10116800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr4:10093000-10116800	Genic enhancers	Fetal Thymus	thymus
6	chr4:10093800-10116000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr4:10101000-10116600	Enhancers	Right Atrium	heart
8	chr4:10102200-10114000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:10104200-10116000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
10	chr4:10105800-10116000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:10106000-10114600	Genic enhancers	Sigmoid Colon	Sigmoid Colon
12	chr4:10106000-10116600	Genic enhancers	Fetal Stomach	stomach
13	chr4:10106000-10116800	Genic enhancers	Rectal Mucosa Donor 31	rectum
14	chr4:10106600-10114400	Genic enhancers	Primary B cells from peripheral blood	blood
15	chr4:10107000-10115800	Enhancers	Fetal Heart	heart
16	chr4:10107200-10116600	Genic enhancers	Thymus	Thymus
17	chr4:10108000-10116800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
18	chr4:10108000-10117000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr4:10108200-10115000	Genic enhancers	NHLF	lung
20	chr4:10108200-10115200	Genic enhancers	Colonic Mucosa	Colon
21	chr4:10108200-10116400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:10108600-10117600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr4:10108800-10116000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:10108800-10116400	Genic enhancers	Duodenum Mucosa	Duodenum
25	chr4:10108800-10116600	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr4:10108800-10116600	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr4:10109000-10115600	Genic enhancers	Muscle Satellite Cultured Cells	--
28	chr4:10109200-10114000	Genic enhancers	Right Ventricle	heart
29	chr4:10109200-10114200	Genic enhancers	HMEC	breast
30	chr4:10109200-10116000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:10109200-10116400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:10109400-10115200	Genic enhancers	NH-A	brain
33	chr4:10109400-10115800	Genic enhancers	HUVEC	blood vessel
34	chr4:10109400-10116400	Genic enhancers	HSMM	muscle
35	chr4:10109600-10114200	Genic enhancers	NHDF-Ad	bronchial
36	chr4:10109600-10115400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr4:10109600-10115400	Genic enhancers	Duodenum Smooth Muscle	Duodenum
38	chr4:10109600-10115800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:10109600-10116800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr4:10109800-10114200	Genic enhancers	Brain Inferior Temporal Lobe	brain
41	chr4:10109800-10115800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr4:10109800-10116600	Genic enhancers	Brain Anterior Caudate	brain
43	chr4:10110000-10114200	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr4:10110000-10115600	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr4:10110000-10115800	Strong transcription	Primary hematopoietic stem cells	blood
46	chr4:10110000-10116400	Genic enhancers	HepG2	liver
47	chr4:10110000-10116600	Weak transcription	Hela-S3	cervix
48	chr4:10110400-10116000	Genic enhancers	Brain Cingulate Gyrus	brain
49	chr4:10110400-10116600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:10110600-10116400	Genic enhancers	Skeletal Muscle Female	skeletal muscle

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