Variant report

Variant	esv2758711
Chromosome Location	chr18:6762909-6943645
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1098)
CpG islands
(count:1223)
Chromatin interactive
region (count:44)
LncRNA
region (count:59)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:6901518-6901528	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:6923285-6923498	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:6920040-6920394	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:6943357-6943415	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:6940589-6940652	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:6920031-6920290	K562	blood:	n/a	n/a
7	ARID3A	chr18:6835362-6835608	HepG2	liver:	n/a	n/a
8	ATF1	chr18:6767665-6767865	K562	blood:	n/a	n/a
9	ATF1	chr18:6836325-6836793	K562	blood:	n/a	n/a
10	ATF1	chr18:6868113-6868297	K562	blood:	n/a	n/a
11	ATF1	chr18:6875852-6876055	K562	blood:	n/a	n/a
12	ATF1	chr18:6927279-6927556	K562	blood:	n/a	n/a
13	ATF3	chr18:6836359-6836675	K562	blood:	n/a	n/a
14	BACH1	chr18:6895411-6895426	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr18:6884931-6885196	K562	blood:	n/a	n/a
16	BACH1	chr18:6920173-6920426	K562	blood:	n/a	n/a
17	BACH1	chr18:6879515-6879935	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr18:6922974-6923150	K562	blood:	n/a	n/a
19	BACH1	chr18:6886241-6886532	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr18:6781274-6781391	K562	blood:	n/a	n/a
21	BHLHE40	chr18:6872104-6872229	K562	blood:	n/a	n/a
22	BHLHE40	chr18:6920038-6920467	K562	blood:	n/a	n/a
23	BHLHE40	chr18:6929692-6930013	K562	blood:	n/a	n/a
24	BHLHE40	chr18:6876253-6876302	K562	blood:	n/a	n/a
25	BHLHE40	chr18:6836478-6836689	K562	blood:	n/a	n/a
26	BHLHE40	chr18:6927365-6927545	K562	blood:	n/a	n/a
27	BHLHE40	chr18:6920055-6920382	GM12878	blood:	n/a	n/a
28	BHLHE40	chr18:6879548-6879846	K562	blood:	n/a	n/a
29	BHLHE40	chr18:6910062-6910211	K562	blood:	n/a	n/a
30	BRCA1	chr18:6920124-6920350	HepG2	liver:	n/a	n/a
31	BRCA1	chr18:6920245-6920373	GM12878	blood:	n/a	n/a
32	BRCA1	chr18:6919994-6920371	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr18:6886317-6886559	H1-hESC	embryonic stem cell:	n/a	n/a
34	CBX3	chr18:6929597-6930073	K562	blood:	n/a	n/a
35	CCNT2	chr18:6929760-6930392	K562	blood:	n/a	chr18:6930021-6930030 chr18:6930056-6930065
36	CEBPB	chr18:6821359-6821719	IMR90	lung:	n/a	n/a
37	CEBPB	chr18:6835343-6835732	IMR90	lung:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
38	CEBPB	chr18:6835386-6835693	Hela-S3	cervix:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
39	CEBPB	chr18:6839244-6839438	K562	blood:	n/a	n/a
40	CEBPB	chr18:6867159-6867359	HepG2	liver:	n/a	n/a
41	CEBPB	chr18:6836363-6836585	K562	blood:	n/a	n/a
42	CEBPB	chr18:6886121-6886162	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr18:6835398-6835674	K562	blood:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
44	CEBPB	chr18:6798199-6798398	K562	blood:	n/a	n/a
45	CEBPB	chr18:6821409-6821614	HepG2	liver:	n/a	n/a
46	CEBPB	chr18:6837943-6838254	A549	lung:	n/a	chr18:6838112-6838123 chr18:6838082-6838095 chr18:6838084-6838093 chr18:6838084-6838093 chr18:6838082-6838095 chr18:6838084-6838095 chr18:6838084-6838093 chr18:6838082-6838093 chr18:6838084-6838093
47	CEBPB	chr18:6830942-6831227	IMR90	lung:	n/a	n/a
48	CEBPB	chr18:6906252-6906484	HepG2	liver:	n/a	chr18:6906352-6906363
49	CEBPB	chr18:6835350-6835719	HepG2	liver:	n/a	chr18:6835526-6835539 chr18:6835527-6835538
50	CEBPB	chr18:6837936-6838263	IMR90	lung:	n/a	chr18:6838112-6838123 chr18:6838082-6838095 chr18:6838084-6838093 chr18:6838084-6838093 chr18:6838082-6838095 chr18:6838084-6838095 chr18:6838084-6838093 chr18:6838082-6838093 chr18:6838084-6838093

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:6930087-6930137	MCF10A-Er-Src	breast:	n/a
2	chr18:6930452-6930502	GM12891	blood:	n/a
3	chr18:6920624-6920674	HCF	heart:	n/a
4	chr18:6930087-6930137	MCF10A-Er-Src	breast:	n/a
5	chr18:6930452-6930502	GM12891	blood:	n/a
6	chr18:6920624-6920674	HCF	heart:	n/a
7	chr18:6920686-6920736	RPTEC	kidney:	n/a
8	chr18:6834653-6834703	HMEC	breast:	n/a
9	chr18:6929476-6929526	K562	blood:	n/a
10	chr18:6927133-6927183	NH-A	brain:	n/a
11	chr18:6933223-6933273	NT2-D1	testis:	n/a
12	chr18:6920873-6920923	LNCaP	prostate:	n/a
13	chr18:6920686-6920736	Hela-S3	cervix:	n/a
14	chr18:6920624-6920674	AG04449	skin:	fetal
15	chr18:6833417-6833467	GM19239	blood:	n/a
16	chr18:6920686-6920736	HRCEpiC	kidney:	n/a
17	chr18:6924586-6924636	GM12892	blood:	n/a
18	chr18:6929701-6929751	IMR90	lung:	fetal
19	chr18:6885601-6885651	H1-hESC	embryonic stem cell:	embryo
20	chr18:6928912-6928962	NHDF-neo	bronchial:	n/a
21	chr18:6834653-6834703	NHDF-neo	bronchial:	n/a
22	chr18:6924586-6924636	U87	brain:	n/a
23	chr18:6898679-6898729	Hepatocyte	liver:	n/a
24	chr18:6930087-6930137	HPAEpiC	pulmonary alveolar:	n/a
25	chr18:6930087-6930137	SK-N-MC	brain:	n/a
26	chr18:6929476-6929526	ECC-1	luminal epithelium:	n/a
27	chr18:6913353-6913403	CMK	blood:	n/a
28	chr18:6929476-6929526	GM19239	blood:	n/a
29	chr18:6933223-6933273	AG09319	gingival:	n/a
30	chr18:6834653-6834703	HepG2	liver:	n/a
31	chr18:6927133-6927183	K562	blood:	n/a
32	chr18:6833417-6833467	GM12891	blood:	n/a
33	chr18:6913353-6913403	HCPEpiC	choroid plexus:	n/a
34	chr18:6933223-6933273	HNPCEpiC	eye:	n/a
35	chr18:6920624-6920674	NHBE	bronchial:	n/a
36	chr18:6898679-6898729	K562	blood:	n/a
37	chr18:6930452-6930502	NH-A	brain:	n/a
38	chr18:6929701-6929751	SK-N-SH	brain:	n/a
39	chr18:6927133-6927183	AoSMC	blood vessel:	n/a
40	chr18:6927133-6927183	NHBE	bronchial:	n/a
41	chr18:6920873-6920923	T-47D	breast:	n/a
42	chr18:6920686-6920736	A549	lung:	n/a
43	chr18:6924586-6924636	NH-A	brain:	n/a
44	chr18:6920686-6920736	HMEC	breast:	n/a
45	chr18:6834653-6834703	HUVEC	blood vessel:	n/a
46	chr18:6920624-6920674	HCT-116	colon:	n/a
47	chr18:6885601-6885651	HRPEpiC	eye:	n/a
48	chr18:6930452-6930502	PANC-1	pancreas:	n/a
49	chr18:6929476-6929526	IMR90	lung:	fetal
50	chr18:6929476-6929526	Hela-S3	cervix:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:6918888..6920537-chr18:7038978..7041847,2	K562	blood:
2	chr18:6685911..6687499-chr18:6763330..6765130,2	K562	blood:
3	chr18:6770718..6772411-chr18:6775406..6777040,2	K562	blood:
4	chr18:6866880..6869867-chr18:6872709..6875099,2	K562	blood:
5	chr18:6780742..6782495-chr18:6812998..6814877,2	K562	blood:
6	chr18:6922138..6924082-chr18:6966857..6969342,2	K562	blood:
7	chr18:6920128..6920680-chr18:7000388..7001151,3	K562	blood:
8	chr18:6770718..6772411-chr18:6775406..6777040,2	K562	blood:
9	chr18:6933466..6936177-chr18:6946950..6949519,2	K562	blood:
10	chr18:6742579..6744550-chr18:6848151..6850631,2	K562	blood:
11	chr18:6919750..6920695-chr18:6999880..7001157,6	MCF-7	breast:
12	chr18:6914921..6917851-chr18:6920099..6922160,2	MCF-7	breast:
13	chr18:6919738..6920523-chr18:6999141..7000038,2	MCF-7	breast:
14	chr18:6919577..6920920-chr18:7021120..7022839,20	MCF-7	breast:
15	chr10:26729577..26730181-chr18:6919937..6920582,2	MCF-7	breast:
16	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:
17	chr18:6914921..6917851-chr18:6920099..6922160,2	MCF-7	breast:
18	chr18:6891111..6892679-chr18:6894919..6896460,2	K562	blood:
19	chr18:6834903..6836491-chr18:6842166..6845111,2	K562	blood:
20	chr18:6543450..6543991-chr18:6885879..6886587,3	K562	blood:
21	chr18:6919159..6921375-chr18:6929681..6931506,2	K562	blood:
22	chr18:6834903..6836491-chr18:6842166..6845111,2	K562	blood:
23	chr18:6919702..6920513-chr18:7174601..7175401,4	MCF-7	breast:
24	chr18:6919673..6920655-chr18:7000229..7001035,3	MCF-7	breast:
25	chr18:5867564..5868499-chr18:6886791..6887501,2	MCF-7	breast:
26	chr18:6891111..6892679-chr18:6894919..6896460,2	K562	blood:
27	chr18:6874182..6876297-chr18:6877806..6879396,2	K562	blood:
28	chr18:6920149..6920730-chr18:7177289..7177849,2	K562	blood:
29	chr18:6939568..6940350-chr18:6999902..7000774,2	MCF-7	breast:
30	chr18:6886014..6886839-chr18:7176913..7177416,2	MCF-7	breast:
31	chr18:6543609..6544152-chr18:6886204..6886860,2	MCF-7	breast:
32	chr18:6919725..6920665-chr18:6999108..6999714,2	MCF-7	breast:
33	chr12:81713189..81713852-chr18:6928781..6929781,2	MCF-7	breast:
34	chr18:5879266..5880057-chr18:6885918..6886780,2	K562	blood:
35	chr18:6919688..6921091-chr18:7021888..7022978,20	MCF-7	breast:
36	chr18:6780742..6782495-chr18:6812998..6814877,2	K562	blood:
37	chr18:6542623..6543373-chr18:6885965..6886489,2	K562	blood:
38	chr18:6886369..6888549-chr18:6889680..6892697,3	K562	blood:
39	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:
40	chr18:6886369..6888549-chr18:6889680..6892697,3	K562	blood:
41	chr18:5073073..5073584-chr18:6886172..6886885,2	MCF-7	breast:
42	chr18:6919703..6920702-chr18:7022006..7023092,6	K562	blood:
43	chr18:5868211..5868845-chr18:6885936..6886486,2	MCF-7	breast:
44	chr18:5867840..5868663-chr18:6885979..6886909,3	K562	blood:

(count:59 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-1	chr18:6929496-6929559	ENSG00000265933.1
2	lnc-LAMA1-1	chr18:6928348-6928718	ENSG00000265933.1
3	lnc-LRRC30-3	chr18:6778921-6779022	XLOC_012619
4	lnc-ARHGAP28-7	chr18:6927615-6928209	NONHSAT057133
5	lnc-ARHGAP28-7	chr18:6926943-6927447	NONHSAT057133
6	lnc-LAMA1-1	chr18:6928119-6928218	NONHSAT057128
7	lnc-LAMA1-1	chr18:6928119-6928234	ENSG00000248723
8	lnc-LAMA1-1	chr18:6925473-6925717	NONHSAT057125
9	lnc-LAMA1-1	chr18:6926656-6927583	ENSG00000248723
10	lnc-LAMA1-1	chr18:6925484-6927583	NONHSAT057128
11	lnc-LAMA1-1	chr18:6925477-6925717	ENSG00000248723
12	lnc-LAMA1-1	chr18:6929782-6929868	ENSG00000248723
13	lnc-LAMA1-1	chr18:6928850-6928967	ENSG00000248723
14	lnc-LRRC30-5	chr18:6896759-6898718	NONHSAT057123
15	lnc-LAMA1-1	chr18:6925477-6927583	ENSG00000248723
16	lnc-LAMA1-1	chr18:6926656-6927583	NONHSAT057125
17	lnc-LAMA1-1	chr18:6925476-6925717	ENSG00000265933.1
18	lnc-LAMA1-1	chr18:6928850-6928967	ENSG00000265933.1
19	lnc-LAMA1-1	chr18:6928850-6928967	NONHSAT057125
20	lnc-LAMA1-1	chr18:6929496-6929559	ENSG00000265933.1
21	lnc-LAMA1-1	chr18:6928850-6928964	NONHSAT057135
22	lnc-LAMA1-1	chr18:6929782-6929804	ENSG00000265933.1
23	lnc-LAMA1-1	chr18:6926071-6926224	NONHSAT057125
24	lnc-LAMA1-1	chr18:6928119-6928218	ENSG00000248723
25	lnc-LAMA1-1	chr18:6928119-6928218	NONHSAT057135
26	lnc-LAMA1-1	chr18:6928850-6928967	ENSG00000265933.1
27	lnc-LAMA1-1	chr18:6926071-6926224	ENSG00000248723
28	lnc-LAMA1-1	chr18:6926439-6926557	ENSG00000248723
29	lnc-LAMA1-1	chr18:6928119-6928218	ENSG00000265933.1
30	lnc-LAMA1-1	chr18:6928119-6928218	ENSG00000265933.1
31	lnc-LAMA1-1	chr18:6926656-6926989	ENSG00000265933.1
32	lnc-LAMA1-1	chr18:6928119-6928218	ENSG00000248723
33	lnc-LAMA1-1	chr18:6926439-6926557	ENSG00000265933.1
34	lnc-LAMA1-1	chr18:6929250-6929835	ENSG00000265933.1
35	lnc-LAMA1-1	chr18:6929782-6929868	NONHSAT057125
36	lnc-LAMA1-1	chr18:6927305-6927583	ENSG00000265933.1
37	lnc-LAMA1-1	chr18:6928850-6928967	ENSG00000248723
38	lnc-LAMA1-1	chr18:6925264-6925324	ENSG00000248723
39	lnc-LAMA1-1	chr18:6919495-6920931	ENSG00000248723
40	lnc-LAMA1-1	chr18:6925484-6927583	NONHSAT057129
41	lnc-LAMA1-1	chr18:6929496-6929520	NONHSAT057135
42	lnc-LAMA1-1	chr18:6929914-6929943	NONHSAT057128
43	lnc-LAMA1-1	chr18:6928850-6928964	NONHSAT057128
44	lnc-LAMA1-1	chr18:6925477-6927583	ENSG00000265933.1
45	lnc-LAMA1-1	chr18:6928119-6928218	ENSG00000265933.1
46	lnc-LAMA1-1	chr18:6927372-6927583	NONHSAT057135
47	lnc-LRRC30-3	chr18:6774030-6774233	XLOC_012619
48	lnc-LAMA1-1	chr18:6927307-6927583	ENSG00000265933.1
49	lnc-LAMA1-1	chr18:6929738-6929804	ENSG00000248723
50	lnc-LAMA1-1	chr18:6928850-6928967	ENSG00000265933.1

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ARHGAP28	hsa-miR-124-3p	chr18:6913758-6913777
2	ARHGAP28	hsa-miR-196a-5p	chr18:6914951-6914957
3	ARHGAP28	hsa-miR-98-5p	chr18:6914952-6914959
4	ARHGAP28	hsa-miR-98-5p	chr18:6914936-6914959
5	ARHGAP28	hsa-miR-196a-5p	chr18:6914938-6914958
6	ARHGAP28	hsa-miR-124-3p	chr18:6915352-6915368

Variant related genes	Relation type
ENSG00000263797	TF binding region
SCML2P1	TF binding region
ARHGAP28	TF binding region
RNU6-916P	TF binding region
LINC00668	TF binding region
ENSG00000263797	CpG island
SCML2P1	CpG island
ARHGAP28	CpG island
RNU6-916P	CpG island
LINC00668	CpG island
ENSG00000101680	chromatin interactions
ENSG00000265933	chromatin interactions
ENSG00000263797	chromatin interactions
ENSG00000088756	chromatin interactions
ERGIC3	miRNA target sites
ADAR	miRNA target sites
MPND	miRNA target sites
NAA15	miRNA target sites
RBM47	miRNA target sites
C7orf58	miRNA target sites
CCNF	miRNA target sites
DOT1L	miRNA target sites
PSMB2	miRNA target sites
ATP2A2	miRNA target sites
CYP1A2	miRNA target sites
ARMC8	miRNA target sites
RPS24	miRNA target sites
LIN28B	miRNA target sites
GORASP2	miRNA target sites

Extended variants
information (count: 7051 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:7051 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546307059	chr18:6762910-6762911	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4486986	chr18:6762959-6762960	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4522478	chr18:6762971-6762972	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs542013553	chr18:6763016-6763017	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561744346	chr18:6763058-6763059	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142968549	chr18:6763080-6763081	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370839493	chr18:6763081-6763082	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371377619	chr18:6763103-6763104	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs57953826	chr18:6763106-6763107	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527535902	chr18:6763141-6763142	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371473158	chr18:6763150-6763151	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547423305	chr18:6763166-6763167	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564099724	chr18:6763185-6763186	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532798370	chr18:6763201-6763202	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142686893	chr18:6763240-6763241	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113510877	chr18:6763302-6763303	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528970656	chr18:6763323-6763324	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529022511	chr18:6763342-6763343	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548721496	chr18:6763366-6763367	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568562952	chr18:6763382-6763383	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534501358	chr18:6763415-6763416	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs8089354	chr18:6763438-6763439	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs570841105	chr18:6763451-6763452	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140697099	chr18:6763539-6763540	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556615238	chr18:6763553-6763554	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369626618	chr18:6763586-6763587	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576567738	chr18:6763587-6763588	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191003073	chr18:6763637-6763638	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555536243	chr18:6763789-6763790	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144584370	chr18:6763822-6763823	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541304139	chr18:6763825-6763826	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181493432	chr18:6763834-6763835	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533079515	chr18:6763849-6763850	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542979027	chr18:6763872-6763873	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185829431	chr18:6763896-6763897	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147881983	chr18:6763944-6763945	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4798492	chr18:6764063-6764064	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs568626981	chr18:6764101-6764102	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79642222	chr18:6764128-6764129	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547994753	chr18:6764147-6764148	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190933983	chr18:6764181-6764182	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540148385	chr18:6764201-6764202	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556553010	chr18:6764221-6764222	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570112611	chr18:6764234-6764235	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535935909	chr18:6764235-6764236	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555615247	chr18:6764238-6764239	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150011261	chr18:6764253-6764254	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567967926	chr18:6764262-6764263	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs8092311	chr18:6764297-6764298	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182344176	chr18:6764387-6764388	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Breast cancer	17133270	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Schizophrenia	20838587	CNVD

Chromatin state (count:1848 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:6752800-6773800	Weak transcription	Right Atrium	heart
2	chr18:6753200-6763600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr18:6757000-6766400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr18:6757000-6768600	Weak transcription	Psoas Muscle	Psoas
5	chr18:6758000-6773400	Weak transcription	Fetal Kidney	kidney
6	chr18:6758200-6770400	Weak transcription	Ovary	ovary
7	chr18:6758400-6764200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr18:6758600-6763600	Weak transcription	Fetal Muscle Leg	muscle
9	chr18:6758600-6764400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr18:6758600-6766400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr18:6758600-6781200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr18:6760000-6764400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr18:6760200-6763600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr18:6760400-6764600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr18:6760600-6764200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr18:6761400-6764400	Genic enhancers	Fetal Lung	lung
17	chr18:6761800-6763600	Weak transcription	Spleen	Spleen
18	chr18:6761800-6766400	Weak transcription	Pancreas	Pancrea
19	chr18:6762800-6763800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr18:6763600-6763800	Enhancers	Fetal Muscle Leg	muscle
21	chr18:6763600-6763800	Enhancers	Fetal Stomach	stomach
22	chr18:6763600-6764600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr18:6763600-6764600	Enhancers	Spleen	Spleen
24	chr18:6763600-6765400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr18:6763800-6766400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr18:6764200-6765000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr18:6764200-6765200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr18:6764400-6764600	Enhancers	Fetal Stomach	stomach
29	chr18:6764400-6764800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr18:6764400-6764800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr18:6764400-6764800	Enhancers	Left Ventricle	heart
32	chr18:6764400-6765000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr18:6764400-6767000	Strong transcription	Fetal Lung	lung
34	chr18:6764600-6765200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr18:6764600-6766400	Weak transcription	Spleen	Spleen
36	chr18:6764600-6773400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr18:6764800-6766400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr18:6764800-6766400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr18:6765000-6766400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr18:6765200-6766400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr18:6765400-6766800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr18:6766000-6766200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr18:6766400-6766600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr18:6766400-6766600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr18:6766400-6766600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr18:6766400-6766600	Enhancers	Gastric	stomach
47	chr18:6766400-6766600	ZNF genes & repeats	Pancreas	Pancrea
48	chr18:6766400-6766600	Enhancers	Spleen	Spleen
49	chr18:6766400-6766800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr18:6766400-6767000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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