Variant report

Variant	nsv514011
Chromosome Location	chr1:155189136-155197120
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1033)
CpG islands
(count:122)
Chromatin interactive
region (count:108)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155196578-155196994	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:155196486-155197271	K562	blood:	n/a	n/a
3	ATF1	chr1:155194483-155194805	K562	blood:	n/a	n/a
4	ATF1	chr1:155192881-155193170	K562	blood:	n/a	n/a
5	ATF2	chr1:155196944-155197904	GM12878	blood:	n/a	n/a
6	ATF2	chr1:155196936-155197811	GM12878	blood:	n/a	n/a
7	ATF2	chr1:155196208-155196851	GM12878	blood:	n/a	n/a
8	ATF2	chr1:155196290-155196702	GM12878	blood:	n/a	n/a
9	ATF3	chr1:155194392-155194847	K562	blood:	n/a	n/a
10	ATF3	chr1:155189353-155189656	H1-hESC	embryonic stem cell:	n/a	chr1:155189481-155189490
11	ATF3	chr1:155189276-155189599	K562	blood:	n/a	chr1:155189481-155189490
12	ATF3	chr1:155189186-155189737	H1-hESC	embryonic stem cell:	n/a	chr1:155189481-155189490
13	ATF3	chr1:155189316-155189697	GM12878	blood:	n/a	chr1:155189481-155189490
14	ATF3	chr1:155189415-155189608	GM12878	blood:	n/a	chr1:155189481-155189490
15	BACH1	chr1:155196500-155196997	K562	blood:	n/a	n/a
16	BACH1	chr1:155196510-155197939	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr1:155196164-155198121	A549	lung:	n/a	n/a
18	BCLAF1	chr1:155196322-155197414	GM12878	blood:	n/a	n/a
19	BDP1	chr1:155196158-155197032	Hela-S3	cervix:	n/a	n/a
20	BDP1	chr1:155193690-155194244	Hela-S3	cervix:	n/a	chr1:155193724-155193737
21	BHLHE40	chr1:155197067-155197817	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:155189313-155189626	K562	blood:	n/a	n/a
23	BHLHE40	chr1:155196870-155197655	HepG2	liver:	n/a	n/a
24	BHLHE40	chr1:155194516-155194887	K562	blood:	n/a	n/a
25	BHLHE40	chr1:155196322-155196799	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:155193025-155193187	K562	blood:	n/a	n/a
27	BHLHE40	chr1:155196326-155197943	K562	blood:	n/a	n/a
28	BRCA1	chr1:155196161-155198275	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr1:155193712-155193748	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr1:155196488-155197307	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRF1	chr1:155194594-155195036	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr1:155196179-155198094	K562	blood:	n/a	n/a
33	CCNT2	chr1:155196761-155197454	K562	blood:	n/a	n/a
34	CEBPB	chr1:155196229-155197908	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:155190034-155190118	K562	blood:	n/a	n/a
36	CEBPB	chr1:155188711-155189263	ECC-1	luminal epithelium:	n/a	chr1:155189137-155189148
37	CEBPB	chr1:155194555-155194883	A549	lung:	n/a	n/a
38	CEBPB	chr1:155189997-155190081	A549	lung:	n/a	n/a
39	CEBPB	chr1:155188822-155189250	HepG2	liver:	n/a	chr1:155189137-155189148
40	CEBPB	chr1:155188701-155189193	H1-hESC	embryonic stem cell:	n/a	chr1:155189137-155189148
41	CEBPB	chr1:155194534-155194882	K562	blood:	n/a	n/a
42	CEBPB	chr1:155194010-155195055	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr1:155194507-155194902	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:155188725-155189757	K562	blood:	n/a	chr1:155189137-155189148
45	CEBPB	chr1:155188676-155190182	Hela-S3	cervix:	n/a	chr1:155189137-155189148
46	CEBPB	chr1:155188739-155189534	IMR90	lung:	n/a	chr1:155189137-155189148
47	CEBPB	chr1:155188777-155189230	A549	lung:	n/a	chr1:155189137-155189148
48	CEBPD	chr1:155196381-155197697	K562	blood:	n/a	n/a
49	CHD1	chr1:155196392-155197241	H1-hESC	embryonic stem cell:	n/a	chr1:155197234-155197241
50	CHD1	chr1:155196293-155198009	GM12878	blood:	n/a	chr1:155197234-155197241

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155195300-155195350	GM12891	blood:	n/a
2	chr1:155194782-155194832	CMK	blood:	n/a
3	chr1:155194782-155194832	Jurkat	blood:	n/a
4	chr1:155194782-155194832	HEK293	kidney:	embryo
5	chr1:155195300-155195350	HCF	heart:	n/a
6	chr1:155194782-155194832	K562	blood:	n/a
7	chr1:155195300-155195350	HEEpiC	esophagus:	n/a
8	chr1:155194782-155194832	NT2-D1	testis:	n/a
9	chr1:155195300-155195350	PFSK-1	brain:	n/a
10	chr1:155194782-155194832	HCF	heart:	n/a
11	chr1:155195300-155195350	HRPEpiC	eye:	n/a
12	chr1:155195300-155195350	AG04449	skin:	fetal
13	chr1:155194782-155194832	IMR90	lung:	fetal
14	chr1:155195300-155195350	MCF-7	breast:	n/a
15	chr1:155195300-155195350	SK-N-MC	brain:	n/a
16	chr1:155195300-155195350	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:155195300-155195350	ProgFib	skin:	n/a
18	chr1:155195300-155195350	IMR90	lung:	fetal
19	chr1:155194782-155194832	A549	lung:	n/a
20	chr1:155195300-155195350	AG09309	skin:	n/a
21	chr1:155195300-155195350	NHDF-neo	bronchial:	n/a
22	chr1:155194782-155194832	HRE	kidney:	n/a
23	chr1:155195300-155195350	AG09319	gingival:	n/a
24	chr1:155195300-155195350	Jurkat	blood:	n/a
25	chr1:155195300-155195350	ovcar-3	ovarian:	n/a
26	chr1:155195300-155195350	NHBE	bronchial:	n/a
27	chr1:155195300-155195350	HIPEpiC	eye:	n/a
28	chr1:155195300-155195350	HEK293	kidney:	embryo
29	chr1:155195300-155195350	SKMC	muscle:	n/a
30	chr1:155195300-155195350	SK-N-SH_RA	brain:	n/a
31	chr1:155194782-155194832	BJ	skin:	n/a
32	chr1:155194782-155194832	HAEpiC	amniotic membrane:	n/a
33	chr1:155194782-155194832	HUVEC	blood vessel:	n/a
34	chr1:155194782-155194832	U87	brain:	n/a
35	chr1:155194782-155194832	GM19239	blood:	n/a
36	chr1:155195300-155195350	AG04450	lung:	fetal
37	chr1:155195300-155195350	HMEC	breast:	n/a
38	chr1:155194782-155194832	T-47D	breast:	n/a
39	chr1:155194782-155194832	NB4	blood:	n/a
40	chr1:155195300-155195350	SAEC	small airway:	n/a
41	chr1:155194782-155194832	AG04449	skin:	fetal
42	chr1:155194782-155194832	HCM	heart:	n/a
43	chr1:155195300-155195350	U87	brain:	n/a
44	chr1:155194782-155194832	GM12892	blood:	n/a
45	chr1:155194782-155194832	BE2_C	brain:	n/a
46	chr1:155194782-155194832	MCF10A-Er-Src	breast:	n/a
47	chr1:155194782-155194832	ProgFib	skin:	n/a
48	chr1:155195300-155195350	HCPEpiC	choroid plexus:	n/a
49	chr1:155194782-155194832	Caco-2	colon:	n/a
50	chr1:155195300-155195350	HL-60	blood:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:155176293..155177732-chr1:155196164..155197059,7	MCF-7	breast:
2	chr1:155178151..155179039-chr1:155196306..155197423,3	Hela-S3	cervix:
3	chr1:155192655..155194574-chr1:155230487..155232931,2	MCF-7	breast:
4	chr1:155193188..155195403-chr1:155211959..155214156,2	K562	blood:
5	chr1:155195600..155203152-chr1:155209955..155216515,9	MCF-7	breast:
6	chr1:155196978..155198560-chr1:155209319..155211586,2	K562	blood:
7	chr1:155174590..155181850-chr1:155192419..155201858,28	K562	blood:
8	chr1:155196524..155199471-chr1:155205933..155208728,2	MCF-7	breast:
9	chr1:148241110..148242082-chr1:155197046..155197929,2	Hela-S3	cervix:
10	chr1:155162028..155164533-chr1:155190701..155192344,2	MCF-7	breast:
11	chr1:155196402..155197362-chr16:89557375..89557938,2	Hela-S3	cervix:
12	chr1:155196728..155197629-chr22:36924753..36925288,2	HCT-116	colon:
13	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
14	chr1:94312249..94313217-chr1:155197097..155198051,2	Hela-S3	cervix:
15	chr1:155169679..155172666-chr1:155186873..155189391,3	MCF-7	breast:
16	chr1:45987235..45987946-chr1:155196847..155197356,2	Hela-S3	cervix:
17	chr1:155196897..155198047-chr10:112064528..112065330,3	NB4	blood:
18	chr1:155195512..155198962-chr1:155200125..155202735,3	MCF-7	breast:
19	chr1:155191881..155194028-chr1:155195597..155197149,2	MCF-7	breast:
20	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
21	chr1:155196643..155197439-chr16:89988732..89989242,2	Hela-S3	cervix:
22	chr1:155194687..155197665-chr1:155223228..155225374,3	MCF-7	breast:
23	chr1:155187581..155189617-chr1:155195998..155199387,4	MCF-7	breast:
24	chr1:155195691..155197531-chr1:155658226..155660788,2	K562	blood:
25	chr1:155144282..155146428-chr1:155196994..155199261,3	K562	blood:
26	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
27	chr1:155196517..155197108-chr12:46384125..46384821,2	Hela-S3	cervix:
28	chr1:155148823..155149771-chr1:155196116..155196635,2	K562	blood:
29	chr1:155196797..155197673-chr7:99698835..99699797,2	Hela-S3	cervix:
30	chr1:155145152..155147163-chr1:155193032..155194544,2	K562	blood:
31	chr1:155098008..155101008-chr1:155194682..155198746,4	MCF-7	breast:
32	chr1:145381905..145382698-chr1:155196540..155197297,2	Hela-S3	cervix:
33	chr1:155195759..155198427-chr1:155276824..155279493,2	K562	blood:
34	chr1:155196803..155197423-chr12:6862306..6863139,2	Hela-S3	cervix:
35	chr1:155195599..155199380-chr1:155211353..155216703,7	MCF-7	breast:
36	chr1:155165613..155168147-chr1:155195516..155197930,3	K562	blood:
37	chr1:117602404..117603075-chr1:155196850..155197424,2	Hela-S3	cervix:
38	chr1:155186477..155191173-chr1:155191711..155194571,4	MCF-7	breast:
39	chr1:155196887..155197681-chr11:126173810..126174418,2	Hela-S3	cervix:
40	chr1:155197037..155198006-chr19:18392015..18392606,2	Hela-S3	cervix:
41	chr1:155155866..155157645-chr1:155191595..155193213,2	MCF-7	breast:
42	chr1:155196583..155198165-chr11:66405632..66407790,2	MCF-7	breast:
43	chr1:155196808..155197366-chr3:49448953..49449687,2	Hela-S3	cervix:
44	chr1:155170199..155172108-chr1:155187853..155191276,3	MCF-7	breast:
45	chr1:155196696..155197276-chr13:99738346..99738910,2	Hela-S3	cervix:
46	chr1:155196805..155197397-chr1:244998371..244999084,2	Hela-S3	cervix:
47	chr1:155196805..155197610-chr9:131486404..131487395,2	Hela-S3	cervix:
48	chr1:155196871..155197993-chr1:155213605..155215251,6	Hela-S3	cervix:
49	chr1:155187302..155192095-chr1:155195846..155198767,7	MCF-7	breast:
50	chr1:155106515..155109128-chr1:155196131..155198130,2	K562	blood:

No data

Variant related genes	Relation type
MTX1P1	TF binding region
GBAP1	TF binding region
MTX1P1	CpG island
GBAP1	CpG island
ENSG00000160446	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000223478	chromatin interactions
ENSG00000251246	chromatin interactions
ENSG00000144579	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000197912	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000203667	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000125967	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000088387	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000137936	chromatin interactions
ENSG00000116830	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000229848	chromatin interactions
ENSG00000173933	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000119953	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000255062	chromatin interactions
ENSG00000056586	chromatin interactions
ENSG00000273088	chromatin interactions
ENSG00000167977	chromatin interactions
ENSG00000231064	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000243364	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000216109	chromatin interactions
ENSG00000089693	chromatin interactions
ENSG00000271748	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000089009	chromatin interactions
ENSG00000211575	chromatin interactions
ENSG00000147124	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000137203	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000118960	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000260464	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000236675	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000139218	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000100353	chromatin interactions
ENSG00000148341	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000160753	chromatin interactions

Extended variants
information (count: 261 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558990026	chr1:155189173-155189174	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs549887169	chr1:155189175-155189176	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs375427780	chr1:155189196-155189197	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs180801877	chr1:155189224-155189225	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs550947168	chr1:155189233-155189234	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs563640942	chr1:155189364-155189365	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs140033404	chr1:155189373-155189374	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs549212855	chr1:155189389-155189390	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs185747263	chr1:155189393-155189394	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs534773684	chr1:155189419-155189420	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs373856500	chr1:155189423-155189424	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs571745118	chr1:155189425-155189426	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs539072343	chr1:155189428-155189429	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs557071648	chr1:155189429-155189430	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs575942400	chr1:155189559-155189560	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs190454108	chr1:155189580-155189581	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs555205479	chr1:155189585-155189586	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs573373698	chr1:155189608-155189609	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs540400686	chr1:155189613-155189614	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs181763081	chr1:155189632-155189633	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs141452721	chr1:155189644-155189645	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs577308071	chr1:155189741-155189742	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs544651111	chr1:155189757-155189758	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs186846830	chr1:155189769-155189770	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs530482906	chr1:155189777-155189778	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs562115395	chr1:155189788-155189789	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs537934304	chr1:155189790-155189791	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs554560135	chr1:155189795-155189796	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs549020901	chr1:155189824-155189825	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs561205382	chr1:155189868-155189869	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs112873385	chr1:155189870-155189871	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs421585	chr1:155189880-155189881	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs570156312	chr1:155189905-155189906	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs371115285	chr1:155189927-155189928	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs546804961	chr1:155189940-155189941	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs571812589	chr1:155190064-155190065	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs181369369	chr1:155190139-155190140	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs374423676	chr1:155190156-155190157	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs551007795	chr1:155190169-155190170	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs369272653	chr1:155190230-155190231	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs2990220	chr1:155190254-155190255	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs113690547	chr1:155190282-155190283	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs554985890	chr1:155190290-155190291	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs566802992	chr1:155190291-155190292	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs185646701	chr1:155190292-155190293	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs565889116	chr1:155190306-155190307	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs558723528	chr1:155190390-155190391	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs576976194	chr1:155190409-155190410	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs574466171	chr1:155190470-155190471	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs190013098	chr1:155190480-155190481	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155179600-155189200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:155179600-155189200	Weak transcription	Colonic Mucosa	Colon
3	chr1:155179600-155189200	Weak transcription	Psoas Muscle	Psoas
4	chr1:155179600-155195400	Weak transcription	Aorta	Aorta
5	chr1:155179600-155195800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:155179600-155196200	Weak transcription	Pancreas	Pancrea
7	chr1:155179600-155196600	Weak transcription	Gastric	stomach
8	chr1:155179600-155196600	Weak transcription	Small Intestine	intestine
9	chr1:155179800-155193800	Weak transcription	HSMMtube	muscle
10	chr1:155180000-155189200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr1:155180000-155194000	Weak transcription	HUVEC	blood vessel
12	chr1:155180000-155195600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr1:155180200-155194000	Weak transcription	HSMM	muscle
14	chr1:155180600-155189600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr1:155180600-155195600	Weak transcription	HepG2	liver
16	chr1:155182200-155189200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:155182200-155195800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr1:155182200-155196400	Weak transcription	Esophagus	oesophagus
19	chr1:155182200-155196600	Weak transcription	Lung	lung
20	chr1:155182400-155189200	Weak transcription	Right Ventricle	heart
21	chr1:155182600-155196200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr1:155182800-155194800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr1:155182800-155194800	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr1:155182800-155196400	Weak transcription	Left Ventricle	heart
25	chr1:155185800-155189200	Weak transcription	Primary B cells from cord blood	blood
26	chr1:155185800-155189400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr1:155186000-155195200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:155186200-155189200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:155186600-155189200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:155186600-155189200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr1:155186600-155189200	Weak transcription	Primary T cells from cord blood	blood
32	chr1:155186600-155193000	Weak transcription	A549	lung
33	chr1:155186800-155193600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:155186800-155193600	Weak transcription	Fetal Muscle Leg	muscle
35	chr1:155186800-155193600	Weak transcription	Thymus	Thymus
36	chr1:155187800-155189200	Weak transcription	Fetal Thymus	thymus
37	chr1:155187800-155190800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:155187800-155196000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:155188000-155189200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:155188000-155189200	Weak transcription	NHLF	lung
41	chr1:155188000-155189600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:155188000-155193800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:155188200-155189400	Flanking Active TSS	Brain Cingulate Gyrus	brain
44	chr1:155188200-155189600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr1:155188200-155189800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr1:155188400-155189200	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr1:155188400-155189200	Active TSS	Fetal Intestine Large	intestine
48	chr1:155188400-155189600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr1:155188400-155191000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:155188600-155189200	Active TSS	ES-I3 Cell Line	embryonic stem cell

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