Variant report

Variant	rs4697943
Chromosome Location	chr4:10165361-10165362
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:10159186..10164011-chr4:10164137..10169302,8	K562	blood:
2	chr4:10118527..10121179-chr4:10164648..10167186,3	K562	blood:
3	chr4:10140841..10143166-chr4:10164924..10167000,2	K562	blood:
4	chr4:10160529..10162216-chr4:10164137..10166713,2	K562	blood:
5	chr4:10164883..10167477-chr4:10450300..10452643,2	K562	blood:
6	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:

Variant related genes	Relation type
ENSG00000071127	Chromatin interaction
ENSG00000223086	Chromatin interaction

Extended variants
information (count: 154 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs1001218	0.95[JPT][hapmap]
rs10020720	0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10027448	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs10028570	0.89[JPT][hapmap];0.81[MEX][hapmap]
rs10031699	0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs10155145	0.81[ASN][1000 genomes]
rs10489075	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.93[MEX][hapmap]
rs10489077	0.90[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs10516195	0.81[GIH][hapmap]
rs10516202	0.81[CHB][hapmap]
rs10939741	0.90[ASN][1000 genomes]
rs10939762	1.00[JPT][hapmap]
rs10939820	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs11723503	0.80[ASN][1000 genomes]
rs11724141	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs11724641	0.81[JPT][hapmap]
rs11727261	0.90[JPT][hapmap]
rs11727367	0.81[ASN][1000 genomes]
rs11728574	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs11735463	0.89[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs11736560	0.90[ASN][1000 genomes]
rs11945358	0.80[JPT][hapmap]
rs12499527	0.82[ASN][1000 genomes]
rs12502342	0.81[ASN][1000 genomes]
rs12502368	0.81[ASN][1000 genomes]
rs12505722	0.90[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs12509082	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs12511548	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs12642426	1.00[JPT][hapmap]
rs12642543	0.82[ASN][1000 genomes]
rs13101772	0.81[GIH][hapmap]
rs13118272	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs13120791	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs13126688	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap]
rs13127090	0.81[GIH][hapmap]
rs13134726	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs13135578	0.94[CHB][hapmap];0.94[JPT][hapmap]
rs13147600	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13148836	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs1541522	0.90[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap]
rs16891923	0.81[GIH][hapmap]
rs16891926	0.81[GIH][hapmap]
rs16893993	0.80[ASN][1000 genomes]
rs1860892	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs1860912	0.90[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs2068466	0.90[JPT][hapmap]
rs2080076	0.81[JPT][hapmap]
rs2110028	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2110029	0.89[CHB][hapmap];0.94[JPT][hapmap]
rs2192087	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs2192097	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap]
rs2192100	0.95[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs2215687	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2215693	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2241466	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.89[ASN][1000 genomes]
rs2241487	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2303401	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2868419	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs2869214	0.90[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap]
rs34448220	0.82[ASN][1000 genomes]
rs35865690	0.82[ASN][1000 genomes]
rs3733589	0.81[GIH][hapmap]
rs3756217	0.95[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs3756231	1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap]
rs3796840	1.00[CEU][hapmap]
rs4140695	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4235358	0.86[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.88[ASN][1000 genomes]
rs4393996	0.80[ASN][1000 genomes]
rs4406017	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4472137	0.90[CHB][hapmap];0.87[CHD][hapmap];0.95[JPT][hapmap];0.81[MEX][hapmap];0.88[ASN][1000 genomes]
rs4478188	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4572881	0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs4697718	0.81[JPT][hapmap]
rs4697719	0.81[JPT][hapmap]
rs4697723	0.95[CHB][hapmap];0.92[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.81[ASN][1000 genomes]
rs4697725	0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4697733	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs4697734	0.90[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs4697736	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs4697737	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4697942	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4697944	0.92[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.93[MEX][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4697945	0.90[CHB][hapmap];0.87[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4697952	0.81[JPT][hapmap]
rs4697953	0.95[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.83[ASN][1000 genomes]
rs4697954	0.81[JPT][hapmap]
rs4697959	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4697970	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.81[MEX][hapmap]
rs4697976	0.95[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.93[MEX][hapmap]
rs4697985	0.90[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs4697987	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697988	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs4697990	0.90[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs4697995	0.92[JPT][hapmap]
rs4697997	0.90[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap]
rs6449341	0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs6449414	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs6449423	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs6449441	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs6814532	0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.81[MEX][hapmap];0.86[ASN][1000 genomes]
rs6816102	0.90[CHB][hapmap]
rs6850167	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6854212	0.90[JPT][hapmap]
rs715259	0.81[ASN][1000 genomes]
rs737678	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs759032	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7670692	0.90[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap]
rs7688808	0.90[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap]
rs7691156	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs874079	0.81[JPT][hapmap]
rs887726	0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs929576	0.80[AMR][1000 genomes]
rs9991911	0.90[ASN][1000 genomes]
rs9998005	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:40 , 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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	esv2752053	chr4:10124819-10270300	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
38	esv1000327	chr4:10135604-10192545	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
39	nsv593695	chr4:10138470-10345548	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
40	nsv593696	chr4:10140551-10168849	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10158600-10165600	Enhancers	Fetal Thymus	thymus
2	chr4:10159800-10172600	Weak transcription	NHEK	skin
3	chr4:10160200-10169400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:10161600-10166000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:10161800-10167800	Enhancers	K562	blood
6	chr4:10162600-10167000	Weak transcription	Colon Smooth Muscle	Colon
7	chr4:10163200-10166000	Enhancers	Pancreas	Pancrea
8	chr4:10163200-10166400	Weak transcription	HMEC	breast
9	chr4:10163400-10166000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr4:10163400-10168400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:10163600-10165400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr4:10163600-10166800	Enhancers	Liver	Liver
13	chr4:10163600-10167200	Weak transcription	HSMMtube	muscle
14	chr4:10163800-10165400	Enhancers	Stomach Mucosa	stomach
15	chr4:10163800-10165600	Enhancers	Fetal Intestine Large	intestine
16	chr4:10163800-10165600	Enhancers	Fetal Intestine Small	intestine
17	chr4:10163800-10166800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:10164200-10169600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:10164400-10167000	Enhancers	Fetal Heart	heart
20	chr4:10164600-10165400	Enhancers	Stomach Smooth Muscle	stomach
21	chr4:10164600-10166000	Enhancers	Right Ventricle	heart
22	chr4:10164600-10166200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr4:10164600-10166200	Enhancers	Left Ventricle	heart
24	chr4:10164800-10169600	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr4:10165000-10166000	Enhancers	Right Atrium	heart
26	chr4:10165000-10174000	Weak transcription	Gastric	stomach
27	chr4:10165200-10173800	Weak transcription	Rectal Mucosa Donor 31	rectum

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