Variant report

Variant	rs13118272
Chromosome Location	chr4:10122722-10122723
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:0)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SMC3	chr4:10122648-10123707	HepG2	liver:	n/a	n/a
2	HNF4A	chr4:10122513-10122925	HepG2	liver:	n/a	chr4:10122782-10122794 chr4:10122780-10122795
3	HNF4A	chr4:10122634-10122854	HepG2	liver:	n/a	chr4:10122782-10122794 chr4:10122780-10122795
4	FOXA1	chr4:10122616-10122947	HepG2	liver:	n/a	n/a
5	NFIC	chr4:10122504-10123726	HepG2	liver:	n/a	n/a
6	FOXA2	chr4:10122549-10122901	HepG2	liver:	n/a	n/a
7	HEY1	chr4:10122544-10123756	HepG2	liver:	n/a	n/a
8	HNF4A	chr4:10122612-10123691	HepG2	liver:	n/a	chr4:10123501-10123516 chr4:10123431-10123446 chr4:10123091-10123099 chr4:10123431-10123446 chr4:10122782-10122794 chr4:10122780-10122795
9	HEY1	chr4:10122518-10123958	HepG2	liver:	n/a	n/a
10	MYBL2	chr4:10122520-10123604	HepG2	liver:	n/a	chr4:10122684-10122698
11	MAZ	chr4:10122687-10123743	HepG2	liver:	n/a	n/a
12	MAX	chr4:10122656-10123507	HepG2	liver:	n/a	n/a
13	POLR2A	chr4:10122505-10123008	HepG2	liver:	n/a	n/a
14	RFX5	chr4:10122672-10123632	HepG2	liver:	n/a	chr4:10123450-10123465
15	POLR2A	chr4:10122679-10122871	HepG2	liver:	n/a	n/a
16	RCOR1	chr4:10122384-10122904	HepG2	liver:	n/a	n/a
17	MYC	chr4:10122687-10122899	HepG2	liver:	n/a	n/a
18	POLR2A	chr4:10122574-10123681	HepG2	liver:	n/a	n/a
19	FOXA1	chr4:10122565-10122946	HepG2	liver:	n/a	n/a
20	POLR2A	chr4:10107879-10124513	HepG2	liver:	n/a	n/a
21	TBP	chr4:10122677-10123731	HepG2	liver:	n/a	n/a
22	MAX	chr4:10122531-10123721	HepG2	liver:	n/a	n/a
23	POLR2A	chr4:10122582-10123011	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:10122605-10123542	HepG2	liver:	n/a	n/a
25	FOXA1	chr4:10122562-10123008	HepG2	liver:	n/a	n/a
26	CREB1	chr4:10122514-10123748	HepG2	liver:	n/a	n/a
27	SP1	chr4:10122519-10123748	HepG2	liver:	n/a	chr4:10122760-10122770 chr4:10123076-10123088
28	HDAC2	chr4:10122550-10122894	HepG2	liver:	n/a	n/a
29	TEAD4	chr4:10122404-10123512	HepG2	liver:	n/a	n/a
30	MAX	chr4:10122484-10123799	HepG2	liver:	n/a	n/a
31	POLR2A	chr4:10122555-10123869	HepG2	liver:	n/a	n/a
32	POLR2A	chr4:10122662-10123481	HepG2	liver:	n/a	n/a
33	ARID3A	chr4:10122672-10123968	HepG2	liver:	n/a	n/a
34	MYBL2	chr4:10122533-10123688	HepG2	liver:	n/a	chr4:10122684-10122698
35	HNF4G	chr4:10122591-10122921	HepG2	liver:	n/a	chr4:10122782-10122794 chr4:10122781-10122796
36	EP300	chr4:10122695-10123778	HepG2	liver:	n/a	chr4:10123463-10123477 chr4:10123281-10123294
37	MXI1	chr4:10122543-10123660	HepG2	liver:	n/a	n/a
38	EP300	chr4:10122488-10122965	HepG2	liver:	n/a	n/a
39	HDAC2	chr4:10122555-10122965	HepG2	liver:	n/a	n/a

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10121764..10123838-chr4:10222085..10224894,2	K562	blood:
2	chr4:10119738..10123155-chr4:10543992..10547634,3	K562	blood:
3	chr4:10119978..10123045-chr4:10320529..10323793,3	K562	blood:
4	chr4:10119529..10122770-chr4:10324822..10328767,4	K562	blood:
5	chr4:10121162..10125014-chr4:10131852..10134322,3	MCF-7	breast:
6	chr4:10120550..10123104-chr4:10488243..10490755,2	K562	blood:
7	chr4:10120460..10123281-chr4:10421587..10423639,2	K562	blood:
8	chr4:10120437..10124442-chr4:10402726..10405362,4	K562	blood:
9	chr4:10121789..10123650-chr4:10877948..10880549,2	K562	blood:
10	chr4:10119097..10123564-chr4:10520690..10524781,5	K562	blood:
11	chr4:10122680..10125562-chr4:10662021..10664504,2	K562	blood:
12	chr4:10122708..10125358-chr4:10375421..10377082,2	K562	blood:
13	chr4:10019909..10022554-chr4:10120525..10123585,3	K562	blood:
14	chr4:10117259..10123841-chr4:10401893..10417202,19	K562	blood:
15	chr4:10120616..10123591-chr4:10237653..10240360,2	K562	blood:
16	chr4:10028896..10030894-chr4:10122706..10125313,2	K562	blood:
17	chr4:10120325..10123218-chr4:10371729..10374334,2	K562	blood:
18	chr4:10121175..10123087-chr4:10143158..10145495,2	MCF-7	breast:
19	chr4:10120021..10122735-chr4:10225048..10229120,3	K562	blood:
20	chr4:10117460..10124392-chr4:10456675..10465032,17	K562	blood:
21	chr4:10122589..10124935-chr4:10442923..10445169,2	K562	blood:
22	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
23	chr4:10121065..10123200-chr4:10609575..10612227,2	K562	blood:
24	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
25	chr4:10120679..10126916-chr4:10412453..10417013,7	K562	blood:
26	chr4:10116325..10123199-chr4:10169149..10177855,21	K562	blood:

No data

Variant related genes	Relation type
WDR1	TF binding region
ENSG00000250613	Chromatin interaction
ENSG00000109667	Chromatin interaction
ENSG00000251296	Chromatin interaction
ENSG00000178163	Chromatin interaction
ENSG00000250393	Chromatin interaction
ENSG00000271544	Chromatin interaction

Extended variants
information (count: 181 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:140)

rs_ID	r²[population]
rs1001218	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs10020720	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10027448	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs10028570	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10031699	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10155145	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10489075	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs10489077	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs10516202	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10516203	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10516204	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10939679	0.81[EUR][1000 genomes]
rs10939680	0.81[EUR][1000 genomes]
rs10939681	0.81[EUR][1000 genomes]
rs10939741	0.85[ASN][1000 genomes]
rs10939762	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs10939820	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10939829	0.81[JPT][hapmap]
rs11722643	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11723250	0.81[EUR][1000 genomes]
rs11723503	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11724141	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs11724184	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11724641	0.82[JPT][hapmap]
rs11727367	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11727418	0.91[EUR][1000 genomes]
rs11728574	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs11735463	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11736560	0.85[ASN][1000 genomes]
rs11945358	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs12108388	0.81[EUR][1000 genomes]
rs12498474	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12498746	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12499527	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12502342	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12502368	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12505722	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs12509082	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12509609	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12511548	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12512525	0.91[EUR][1000 genomes]
rs12642426	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13112782	0.81[EUR][1000 genomes]
rs13120791	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs13126688	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13127630	0.81[EUR][1000 genomes]
rs13134726	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13135578	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs13141629	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13147600	0.82[CHB][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs13148836	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs1541522	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs16893993	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1860892	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs1860912	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2068466	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs2080076	0.81[JPT][hapmap]
rs2098234	0.81[JPT][hapmap]
rs2110028	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2110029	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs2192087	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2192097	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2192100	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2215687	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2215693	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2241466	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2241471	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2241479	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2241487	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2303401	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2868419	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2869214	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs34426660	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34448220	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35411115	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35865690	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3756216	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3756217	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3775931	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3775933	0.85[ASN][1000 genomes]
rs3775936	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3796820	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs3822238	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4140695	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4235358	0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4393996	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4406017	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4472137	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4478188	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4549382	0.91[EUR][1000 genomes]
rs4572881	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4697718	0.81[JPT][hapmap]
rs4697719	0.81[JPT][hapmap]
rs4697721	0.81[JPT][hapmap]
rs4697723	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4697725	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs4697733	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4697734	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697736	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4697737	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697942	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4697943	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697944	0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs4697945	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697952	0.81[JPT][hapmap]
rs4697953	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4697954	0.82[JPT][hapmap]
rs4697959	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697970	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs4697976	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs4697985	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697987	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4697988	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4697990	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4697995	0.93[JPT][hapmap]
rs4697997	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs6449341	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6449414	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs6449423	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6449441	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs6814532	1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs6816102	0.95[CHB][hapmap]
rs6836961	0.83[EUR][1000 genomes]
rs6850167	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs715259	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs71603987	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71603991	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs737678	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs759032	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs7670692	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs7677430	0.91[EUR][1000 genomes]
rs7677939	0.90[EUR][1000 genomes]
rs7678346	0.81[EUR][1000 genomes]
rs7683832	0.83[EUR][1000 genomes]
rs7688808	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs7691156	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs874079	0.81[JPT][hapmap]
rs887726	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9991911	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9998005	0.83[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

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10119400-10122800	Weak transcription	Liver	Liver
2	chr4:10119400-10124000	Enhancers	Fetal Muscle Leg	muscle
3	chr4:10119400-10124600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr4:10119400-10124600	Weak transcription	Pancreas	Pancrea
5	chr4:10119400-10126200	Enhancers	Fetal Intestine Large	intestine
6	chr4:10119600-10124200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:10119600-10124600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:10119600-10124600	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr4:10119600-10124600	Weak transcription	HSMM	muscle
10	chr4:10119600-10124800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr4:10119600-10125400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr4:10119600-10126000	Enhancers	Fetal Stomach	stomach
13	chr4:10119600-10126400	Enhancers	Fetal Intestine Small	intestine
14	chr4:10119800-10123800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr4:10119800-10124800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:10119800-10124800	Weak transcription	Right Atrium	heart
17	chr4:10119800-10125000	Weak transcription	Hela-S3	cervix
18	chr4:10120000-10123000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:10120000-10124200	Weak transcription	HUVEC	blood vessel
20	chr4:10120000-10124800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:10120000-10124800	Weak transcription	Brain Anterior Caudate	brain
22	chr4:10120000-10124800	Weak transcription	Esophagus	oesophagus
23	chr4:10120000-10125000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:10120000-10127200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr4:10120200-10123000	Weak transcription	Colonic Mucosa	Colon
26	chr4:10120200-10124400	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr4:10120200-10124800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr4:10120200-10124800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr4:10120200-10124800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr4:10120200-10124800	Weak transcription	Adipose Nuclei	Adipose
31	chr4:10120200-10124800	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr4:10120200-10125000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr4:10120200-10125000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr4:10120200-10125200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr4:10120200-10126800	Enhancers	Fetal Thymus	thymus
36	chr4:10120400-10122800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:10120400-10124200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:10120400-10124600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:10120400-10125000	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr4:10120400-10125000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr4:10120400-10125200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:10120400-10125200	Weak transcription	Brain Hippocampus Middle	brain
43	chr4:10120400-10125200	Weak transcription	Small Intestine	intestine
44	chr4:10120400-10125400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:10120400-10126200	Enhancers	Duodenum Mucosa	Duodenum
46	chr4:10120600-10123000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr4:10120600-10123200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr4:10120600-10124200	Weak transcription	Lung	lung
49	chr4:10120600-10124800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr4:10120600-10125200	Weak transcription	H1 Cell Line	embryonic stem cell

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