Variant report

Variant	rs4078242
Chromosome Location	chr14:105148536-105148537
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAZ	chr14:105148038-105148989	Hela-S3	cervix:	n/a	chr14:105148821-105148831 chr14:105148098-105148108 chr14:105148306-105148316
2	PBX3	chr14:105147937-105148612	SK-N-SH	brain:	n/a	chr14:105148283-105148292
3	CEBPB	chr14:105147609-105148928	Hela-S3	cervix:	n/a	n/a
4	RAD21	chr14:105148368-105148952	H1-hESC	embryonic stem cell:	n/a	n/a
5	TBP	chr14:105146948-105149480	Hela-S3	cervix:	n/a	n/a
6	SP1	chr14:105146482-105148999	A549	lung:	n/a	chr14:105148302-105148316 chr14:105146490-105146500 chr14:105148098-105148108 chr14:105147978-105147987 chr14:105148305-105148316 chr14:105148090-105148099 chr14:105148305-105148317 chr14:105148098-105148108 chr14:105148099-105148108 chr14:105147295-105147304 chr14:105147227-105147237 chr14:105147227-105147237 chr14:105148883-105148893 chr14:105148305-105148317 chr14:105148097-105148109 chr14:105148596-105148605 chr14:105148097-105148109 chr14:105148331-105148342 chr14:105147226-105147238 chr14:105148358-105148369 chr14:105148115-105148129 chr14:105148098-105148107 chr14:105148306-105148316 chr14:105148816-105148830
7	POLR2A	chr14:105146737-105149054	Hela-S3	cervix:	n/a	n/a
8	RFX5	chr14:105146913-105148914	Hela-S3	cervix:	n/a	n/a
9	ZBTB7A	chr14:105147888-105148673	ECC-1	luminal epithelium:	n/a	n/a
10	SMC3	chr14:105146768-105149777	Hela-S3	cervix:	n/a	chr14:105147465-105147479 chr14:105148010-105148020 chr14:105148817-105148827 chr14:105148557-105148567
11	POLR2A	chr14:105146698-105148557	HUVEC	blood vessel:	n/a	n/a
12	POLR2A	chr14:105146213-105148996	A549	lung:	n/a	n/a
13	SIN3AK20	chr14:105148399-105148698	A549	lung:	n/a	n/a
14	JUND	chr14:105148464-105148891	H1-hESC	embryonic stem cell:	n/a	n/a
15	MAZ	chr14:105146114-105149283	IMR90	lung:	n/a	chr14:105147697-105147707 chr14:105148821-105148831 chr14:105147699-105147706 chr14:105147373-105147382 chr14:105147696-105147704 chr14:105148098-105148108 chr14:105147698-105147707 chr14:105146998-105147007 chr14:105148306-105148316
16	POLR2A	chr14:105147496-105148929	Hela-S3	cervix:	n/a	n/a
17	CTBP2	chr14:105147801-105149037	H1-hESC	embryonic stem cell:	n/a	n/a
18	TBP	chr14:105148186-105148983	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr14:105146773-105148813	PANC-1	pancreas:	n/a	n/a
20	MAX	chr14:105146682-105149045	Hela-S3	cervix:	n/a	chr14:105147697-105147707 chr14:105148821-105148831 chr14:105147699-105147706 chr14:105147373-105147382 chr14:105147696-105147704 chr14:105148098-105148108 chr14:105147698-105147707 chr14:105146998-105147007 chr14:105148306-105148316
21	FOSL2	chr14:105146367-105148546	A549	lung:	n/a	chr14:105147393-105147403 chr14:105147395-105147406 chr14:105146998-105147005 chr14:105146998-105147006 chr14:105147393-105147403 chr14:105146997-105147007 chr14:105146998-105147006 chr14:105146737-105146748 chr14:105147008-105147020 chr14:105147394-105147402 chr14:105147392-105147404
22	ZNF143	chr14:105148099-105148716	Hela-S3	cervix:	n/a	n/a
23	TEAD4	chr14:105148059-105148911	H1-hESC	embryonic stem cell:	n/a	n/a
24	GATA3	chr14:105146254-105149461	A549	lung:	n/a	chr14:105148762-105148769 chr14:105147395-105147404 chr14:105146711-105146724 chr14:105147520-105147530 chr14:105148760-105148769 chr14:105148760-105148770 chr14:105148454-105148466 chr14:105146713-105146721 chr14:105147392-105147399 chr14:105148456-105148464
25	MAX	chr14:105146352-105149178	A549	lung:	n/a	chr14:105147697-105147707 chr14:105148821-105148831 chr14:105147699-105147706 chr14:105147373-105147382 chr14:105147696-105147704 chr14:105148098-105148108 chr14:105147698-105147707 chr14:105146998-105147007 chr14:105148306-105148316
26	TCF12	chr14:105146041-105149248	A549	lung:	n/a	chr14:105146346-105146356 chr14:105148249-105148257 chr14:105148829-105148839 chr14:105146678-105146688
27	NFIC	chr14:105147931-105148576	ECC-1	luminal epithelium:	n/a	n/a
28	TFAP2C	chr14:105147764-105149938	Hela-S3	cervix:	n/a	chr14:105148730-105148745
29	MAX	chr14:105146686-105149042	Hela-S3	cervix:	n/a	chr14:105147697-105147707 chr14:105148821-105148831 chr14:105147699-105147706 chr14:105147373-105147382 chr14:105147696-105147704 chr14:105148098-105148108 chr14:105147698-105147707 chr14:105146998-105147007 chr14:105148306-105148316
30	CHD2	chr14:105148481-105148886	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr14:105146579-105148744	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr14:105148448-105148601	A549	lung:	n/a	n/a
33	SMARCC1	chr14:105148235-105149982	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr14:105145662-105148567	U87	brain:	n/a	n/a
35	BACH1	chr14:105147832-105149057	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr14:105148520-105148670	NHEK	skin:	n/a	n/a
37	SP1	chr14:105147953-105148736	H1-hESC	embryonic stem cell:	n/a	chr14:105148302-105148316 chr14:105148098-105148108 chr14:105147978-105147987 chr14:105148305-105148316 chr14:105148090-105148099 chr14:105148305-105148317 chr14:105148098-105148108 chr14:105148099-105148108 chr14:105148305-105148317 chr14:105148097-105148109 chr14:105148596-105148605 chr14:105148097-105148109 chr14:105148331-105148342 chr14:105148358-105148369 chr14:105148115-105148129 chr14:105148098-105148107 chr14:105148306-105148316
38	POLR2A	chr14:105145798-105149415	Hela-S3	cervix:	n/a	n/a
39	TFAP2A	chr14:105147934-105149218	Hela-S3	cervix:	n/a	chr14:105148614-105148626 chr14:105148614-105148626 chr14:105148732-105148742 chr14:105148730-105148744 chr14:105148614-105148626 chr14:105148730-105148744 chr14:105148728-105148743 chr14:105148732-105148742 chr14:105148732-105148742 chr14:105148732-105148742
40	POLR2A	chr14:105148435-105148880	H1-hESC	embryonic stem cell:	n/a	n/a
41	RCOR1	chr14:105147840-105149390	Hela-S3	cervix:	n/a	n/a
42	REST	chr14:105147989-105148870	A549	lung:	n/a	chr14:105148839-105148852 chr14:105148529-105148542 chr14:105148529-105148542
43	CHD1	chr14:105146642-105148566	IMR90	lung:	n/a	chr14:105147533-105147543
44	CTCF	chr14:105148440-105148590	A549	lung:	n/a	n/a
45	POLR2A	chr14:105147762-105148550	HUVEC	blood vessel:	n/a	n/a
46	E2F6	chr14:105146740-105148926	A549	lung:	n/a	chr14:105148820-105148832 chr14:105147160-105147174
47	MAFK	chr14:105147915-105149385	Hela-S3	cervix:	n/a	chr14:105148448-105148458
48	POLR2A	chr14:105146463-105149852	Hela-S3	cervix:	n/a	n/a
49	MAX	chr14:105143454-105149192	A549	lung:	n/a	chr14:105147697-105147707 chr14:105148821-105148831 chr14:105143577-105143587 chr14:105147699-105147706 chr14:105147373-105147382 chr14:105145703-105145713 chr14:105147696-105147704 chr14:105148098-105148108 chr14:105143491-105143501 chr14:105147698-105147707 chr14:105146998-105147007 chr14:105148306-105148316 chr14:105144497-105144507
50	ZKSCAN1	chr14:105148219-105148893	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105131134..105134373-chr14:105146178..105149539,6	MCF-7	breast:
2	chr14:105132267..105134426-chr14:105148392..105150808,3	MCF-7	breast:
3	chr14:105148182..105148999-chr16:46723270..46723980,2	Hela-S3	cervix:
4	chr14:105145208..105149817-chr14:105259856..105263393,4	MCF-7	breast:
5	chr14:105146944..105148675-chr14:105240764..105242693,2	MCF-7	breast:

Variant related genes	Relation type
MIR4710	TF binding region
ENSG00000069329	Chromatin interaction
ENSG00000142208	Chromatin interaction
ENSG00000260792	Chromatin interaction
ENSG00000091651	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10135029	0.96[ASN][1000 genomes]
rs10139247	1.00[ASN][1000 genomes]
rs10143904	0.96[ASN][1000 genomes]
rs28661507	0.93[ASN][1000 genomes]
rs28676628	0.96[ASN][1000 genomes]
rs28729119	0.96[ASN][1000 genomes]
rs3935916	0.93[ASN][1000 genomes]
rs4075355	0.96[ASN][1000 genomes]
rs5015594	0.96[ASN][1000 genomes]
rs56275181	0.80[ASN][1000 genomes]
rs56385415	0.80[ASN][1000 genomes]
rs7145744	1.00[ASN][1000 genomes]
rs7147744	1.00[ASN][1000 genomes]
rs72713850	0.80[ASN][1000 genomes]
rs72713852	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530812	chr14:104775571-105364883	Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1051647	chr14:104983302-105153720	Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
3	nsv542223	chr14:104983302-105153720	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
4	nsv902372	chr14:105011436-105200377	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv456445	chr14:105023512-105170003	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
6	nsv566047	chr14:105023512-105170003	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
7	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
8	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
9	esv2830002	chr14:105078251-105348552	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
10	nsv902378	chr14:105086475-105200377	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
11	nsv902379	chr14:105086475-105274093	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
12	nsv902380	chr14:105092479-105166002	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription 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	36 gene(s)	inside rSNPs	diseases
13	nsv902381	chr14:105092479-105168414	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
14	nsv902382	chr14:105092479-105185666	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	nsv902383	chr14:105092479-105200377	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
16	nsv902384	chr14:105092479-105208567	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
17	nsv902385	chr14:105092479-105215351	Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
18	nsv902386	chr14:105092479-105233095	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
19	nsv902387	chr14:105092479-105274093	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
20	nsv902388	chr14:105092479-105311249	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
21	nsv902389	chr14:105092479-105366499	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
22	nsv902390	chr14:105100021-105185666	Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
23	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
24	nsv902391	chr14:105105769-105185666	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
25	nsv902392	chr14:105105769-105274093	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
26	nsv902393	chr14:105116232-105200377	Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
27	nsv902394	chr14:105116232-105274093	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
28	nsv902395	chr14:105119897-105215351	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
29	nsv902396	chr14:105119897-105274093	Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
30	nsv566048	chr14:105126354-105185666	Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
31	nsv456446	chr14:105126354-105189504	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
32	nsv566049	chr14:105126354-105189504	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
33	nsv456447	chr14:105126354-105200377	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
34	nsv566050	chr14:105126354-105200377	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
35	nsv456448	chr14:105126354-105208567	Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
36	nsv566051	chr14:105126354-105208567	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
37	nsv470678	chr14:105126354-105246686	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
38	nsv566052	chr14:105126354-105268228	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
39	nsv470677	chr14:105126354-105348552	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
40	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
41	nsv984482	chr14:105134201-105159338	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
42	nsv566053	chr14:105139894-105268228	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
43	nsv902397	chr14:105139894-105268228	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
44	nsv456449	chr14:105146579-105200377	ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
45	nsv566054	chr14:105146579-105200377	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
46	nsv456450	chr14:105146579-105208567	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
47	nsv566055	chr14:105146579-105208567	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
48	nsv456451	chr14:105146579-105215351	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
49	nsv566056	chr14:105146579-105215351	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
50	nsv902398	chr14:105146579-105215351	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105143400-105149800	Enhancers	Fetal Brain Male	brain
2	chr14:105144400-105149200	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr14:105144600-105149800	Enhancers	Esophagus	oesophagus
4	chr14:105144600-105150000	Enhancers	Spleen	Spleen
5	chr14:105144600-105152000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:105144800-105148800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr14:105144800-105149400	Enhancers	Fetal Intestine Small	intestine
8	chr14:105144800-105149800	Enhancers	Lung	lung
9	chr14:105144800-105149800	Enhancers	Right Ventricle	heart
10	chr14:105144800-105150600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:105145000-105148600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr14:105145000-105148600	Enhancers	Primary hematopoietic stem cells	blood
13	chr14:105145000-105148800	Enhancers	Primary B cells from peripheral blood	blood
14	chr14:105145000-105150400	Enhancers	Fetal Muscle Leg	muscle
15	chr14:105145000-105150800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr14:105145000-105151800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr14:105145000-105152200	Enhancers	Placenta	Placenta
18	chr14:105145000-105153400	Weak transcription	Primary T cells from cord blood	blood
19	chr14:105145200-105148800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr14:105145200-105149400	Enhancers	Fetal Intestine Large	intestine
21	chr14:105145200-105154000	Weak transcription	Aorta	Aorta
22	chr14:105145400-105148800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr14:105145400-105148800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:105145400-105149800	Enhancers	Fetal Muscle Trunk	muscle
25	chr14:105145400-105153000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr14:105145600-105151400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr14:105146200-105148600	Flanking Active TSS	HepG2	liver
28	chr14:105146200-105149400	Enhancers	Left Ventricle	heart
29	chr14:105146200-105149400	Enhancers	Right Atrium	heart
30	chr14:105146400-105149000	Enhancers	Pancreas	Pancrea
31	chr14:105146400-105149000	Flanking Active TSS	Stomach Smooth Muscle	stomach
32	chr14:105146400-105149800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr14:105146600-105148600	Flanking Active TSS	NH-A	brain
34	chr14:105146600-105149000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr14:105146600-105149000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:105146600-105149200	Flanking Active TSS	Brain Anterior Caudate	brain
37	chr14:105146600-105149200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
38	chr14:105146600-105149200	Flanking Active TSS	NHEK	skin
39	chr14:105146800-105148800	Enhancers	Primary B cells from cord blood	blood
40	chr14:105146800-105148800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr14:105146800-105148800	Flanking Active TSS	Osteobl	bone
42	chr14:105146800-105149000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr14:105146800-105149000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:105146800-105149000	Enhancers	Brain Germinal Matrix	brain
45	chr14:105146800-105149200	Flanking Active TSS	HSMM	muscle
46	chr14:105146800-105150000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:105147000-105148600	Enhancers	Fetal Brain Female	brain
48	chr14:105147000-105148800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr14:105147000-105148800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr14:105147000-105148800	Flanking Active TSS	Colonic Mucosa	Colon

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