Variant report

Variant	rs10518170
Chromosome Location	chr4:78193913-78193914
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 199 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:165)

rs_ID	r²[population]
rs10000241	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs10002514	0.82[YRI][hapmap]
rs10002520	0.82[YRI][hapmap]
rs10002804	0.82[YRI][hapmap]
rs10010146	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs10010526	0.82[YRI][hapmap]
rs10011183	0.82[YRI][hapmap]
rs10012774	0.81[MKK][hapmap]
rs10012879	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs10015460	0.84[YRI][hapmap]
rs10016991	0.86[YRI][hapmap]
rs10017165	0.83[ASW][hapmap];0.82[MKK][hapmap];0.82[YRI][hapmap]
rs10018841	0.86[YRI][hapmap]
rs10023087	0.81[YRI][hapmap]
rs10026063	0.85[YRI][hapmap]
rs10026632	0.86[YRI][hapmap]
rs10026918	0.95[YRI][hapmap]
rs10033519	0.82[YRI][hapmap]
rs10034292	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs10440383	0.82[YRI][hapmap]
rs10470969	0.82[YRI][hapmap]
rs10470970	0.82[YRI][hapmap]
rs10470971	0.82[YRI][hapmap]
rs10518169	0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs10518171	0.94[ASW][hapmap];1.00[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];0.95[MKK][hapmap];1.00[TSI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10518173	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs10518175	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11536332	0.82[YRI][hapmap]
rs12499084	0.82[YRI][hapmap]
rs12510942	0.81[YRI][hapmap]
rs12640931	0.83[ASW][hapmap];0.82[YRI][hapmap]
rs12643078	0.81[ASW][hapmap];0.82[YRI][hapmap]
rs12644949	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs12645407	0.83[ASW][hapmap];0.82[YRI][hapmap]
rs12645827	0.86[YRI][hapmap]
rs12646036	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12646196	0.82[YRI][hapmap]
rs12649781	0.82[YRI][hapmap]
rs12650240	0.82[YRI][hapmap]
rs12651366	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13434612	0.85[YRI][hapmap]
rs17002493	0.88[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.83[YRI][hapmap]
rs17002495	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[TSI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17002506	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17394817	0.83[AFR][1000 genomes]
rs17394978	0.83[AFR][1000 genomes]
rs17395041	0.83[AFR][1000 genomes]
rs17395298	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs17395353	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17397057	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs17397262	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs17399165	0.83[AFR][1000 genomes]
rs17401246	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17401714	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1862359	0.94[ASW][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs1988614	0.82[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs2007495	0.80[YRI][hapmap]
rs2016783	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2042229	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs2042231	0.81[MKK][hapmap]
rs2042232	0.81[YRI][hapmap]
rs2042233	0.82[YRI][hapmap]
rs2059102	0.94[ASW][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs2059103	0.94[ASW][hapmap];0.92[MKK][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs2059104	0.94[ASW][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs2059105	0.94[ASW][hapmap];0.87[MKK][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs2059106	0.88[ASW][hapmap];0.91[MKK][hapmap]
rs2059108	0.81[YRI][hapmap]
rs2194116	0.82[YRI][hapmap]
rs2194117	0.83[ASW][hapmap];0.82[YRI][hapmap]
rs2194118	0.83[ASW][hapmap];0.82[YRI][hapmap]
rs2194122	0.83[AFR][1000 genomes]
rs2194123	0.83[AFR][1000 genomes]
rs2194126	0.81[MKK][hapmap]
rs2194127	0.82[YRI][hapmap]
rs2194129	0.82[YRI][hapmap]
rs2216633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28440089	0.83[AFR][1000 genomes]
rs28482007	0.83[AFR][1000 genomes]
rs28501511	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28629307	0.83[AFR][1000 genomes]
rs2866044	0.81[YRI][hapmap]
rs2866045	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs2866047	0.82[YRI][hapmap]
rs28741683	0.83[AFR][1000 genomes]
rs28869537	0.83[AFR][1000 genomes]
rs34234821	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4241615	0.82[YRI][hapmap]
rs4241616	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs4241617	0.82[YRI][hapmap]
rs4241618	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs4298160	0.89[CHD][hapmap];0.91[JPT][hapmap]
rs4330372	0.82[YRI][hapmap]
rs4340815	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4412015	0.90[YRI][hapmap];0.83[AFR][1000 genomes]
rs4416501	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4444852	1.00[CHB][hapmap];0.91[JPT][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs4460017	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4475169	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs4484325	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs4501251	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4529080	0.88[ASW][hapmap];0.91[MKK][hapmap]
rs4538516	0.83[AFR][1000 genomes]
rs4590066	0.83[AFR][1000 genomes]
rs4594746	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4608831	0.81[MKK][hapmap];0.82[YRI][hapmap]
rs4859479	0.83[AFR][1000 genomes]
rs4859480	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4859481	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs4859488	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs4859489	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4859764	0.83[AFR][1000 genomes]
rs4859767	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4859768	0.83[AFR][1000 genomes]
rs4859769	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4859771	0.82[YRI][hapmap]
rs4859776	0.86[YRI][hapmap]
rs4859778	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4859783	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs4859784	0.82[YRI][hapmap]
rs4859786	0.82[YRI][hapmap]
rs4859787	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs4859790	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs4859794	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs4859796	0.83[ASW][hapmap]
rs4859797	0.89[YRI][hapmap]
rs4859799	0.81[YRI][hapmap]
rs4859802	0.81[YRI][hapmap]
rs4859805	0.81[YRI][hapmap]
rs4859806	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4859809	0.83[ASW][hapmap]
rs4859816	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4859822	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56942936	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57035249	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57123831	0.83[AFR][1000 genomes]
rs57885133	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60011597	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61454994	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6843119	0.82[YRI][hapmap]
rs723972	0.85[YRI][hapmap]
rs72866448	0.83[AFR][1000 genomes]
rs72866450	0.81[AFR][1000 genomes]
rs736601	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7375828	0.82[YRI][hapmap]
rs7375829	0.82[YRI][hapmap]
rs7376348	0.82[ASW][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes]
rs7376994	0.82[YRI][hapmap]
rs73827328	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73827341	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7435398	0.83[ASW][hapmap];0.83[MKK][hapmap];0.82[YRI][hapmap]
rs752062	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs752064	0.88[ASW][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.81[MKK][hapmap];0.81[TSI][hapmap];0.82[YRI][hapmap]
rs888981	0.83[AFR][1000 genomes]
rs918497	0.81[YRI][hapmap]
rs9307260	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs9307261	0.81[MKK][hapmap]
rs960507	0.81[MKK][hapmap];0.82[YRI][hapmap]
rs960508	0.82[YRI][hapmap]
rs9884375	0.81[YRI][hapmap]
rs9884379	0.95[YRI][hapmap]
rs9884380	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs9991953	0.83[ASW][hapmap];0.81[MKK][hapmap];0.82[YRI][hapmap]
rs9992191	0.82[YRI][hapmap]
rs9997026	0.90[YRI][hapmap];0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000730	chr4:78109138-78210296	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1011551	chr4:78120872-78204224	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1012298	chr4:78120872-78255427	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv997743	chr4:78126462-78217004	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1014055	chr4:78132200-78255427	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1013602	chr4:78133566-78217004	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1007726	chr4:78133566-78255427	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1001852	chr4:78135874-78260269	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv998972	chr4:78139780-78240303	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1010406	chr4:78139780-78255427	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv1014305	chr4:78139780-78260269	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1006017	chr4:78139780-78312974	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv1003755	chr4:78145279-78255427	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv1014450	chr4:78157527-78255427	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv1014839	chr4:78167603-78255427	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv1001987	chr4:78168857-78217004	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv1011073	chr4:78168857-78255427	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv432613	chr4:78169507-78234279	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
19	nsv1009917	chr4:78169507-78255427	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
20	nsv1003098	chr4:78170317-78255427	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv998039	chr4:78170317-78258022	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
22	nsv1003383	chr4:78170317-78265687	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	nsv1002683	chr4:78170317-78281331	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
24	nsv1014906	chr4:78171206-78205171	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv1006633	chr4:78171825-78211882	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
26	nsv1002490	chr4:78172216-78209182	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
27	esv3417866	chr4:78173063-78200157	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv1003935	chr4:78181108-78255427	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
29	nsv1009375	chr4:78182037-78255427	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
30	nsv1010450	chr4:78182037-78317840	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
31	nsv1003399	chr4:78186343-78255427	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
32	nsv1003000	chr4:78188691-78255427	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
33	nsv1004824	chr4:78188691-78312974	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
34	nsv1000447	chr4:78191608-78291173	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78191000-78200000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:78193600-78205400	Weak transcription	Placenta	Placenta

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