Variant report

Variant	esv2753719
Chromosome Location	chr1:151337788-151373200
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1156)
CpG islands
(count:1343)
Chromatin interactive
region (count:114)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1156 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151371751-151372339	K562	blood:	n/a	chr1:151372120-151372135
2	ARID3A	chr1:151345015-151345215	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:151371733-151372165	HepG2	liver:	n/a	chr1:151372120-151372135
4	ATF1	chr1:151371742-151372196	K562	blood:	n/a	n/a
5	ATF1	chr1:151357084-151357455	K562	blood:	n/a	n/a
6	ATF2	chr1:151371732-151372222	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:151371634-151372180	GM12878	blood:	n/a	n/a
8	ATF2	chr1:151371724-151372171	GM12878	blood:	n/a	n/a
9	ATF2	chr1:151371626-151372256	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:151368851-151369032	K562	blood:	n/a	n/a
11	ATF3	chr1:151371725-151372346	A549	lung:	n/a	n/a
12	BACH1	chr1:151371808-151372310	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr1:151345733-151346070	GM12878	blood:	n/a	n/a
14	BCL3	chr1:151371693-151373473	A549	lung:	n/a	chr1:151372009-151372018
15	BCL3	chr1:151371666-151372235	A549	lung:	n/a	chr1:151372009-151372018
16	BCL3	chr1:151372480-151372962	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:151371605-151372282	GM12878	blood:	n/a	chr1:151372009-151372018
18	BCLAF1	chr1:151371705-151372350	GM12878	blood:	n/a	chr1:151372009-151372018
19	BHLHE40	chr1:151344946-151345289	K562	blood:	n/a	n/a
20	BHLHE40	chr1:151342372-151343265	K562	blood:	n/a	n/a
21	BHLHE40	chr1:151345650-151345906	HepG2	liver:	n/a	n/a
22	BHLHE40	chr1:151356747-151357326	K562	blood:	n/a	n/a
23	BRCA1	chr1:151345169-151345211	HepG2	liver:	n/a	n/a
24	BRCA1	chr1:151371813-151372175	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr1:151372596-151372778	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr1:151360096-151360428	K562	blood:	n/a	n/a
27	CBX3	chr1:151358593-151358947	K562	blood:	n/a	n/a
28	CBX3	chr1:151342983-151343411	K562	blood:	n/a	n/a
29	CBX3	chr1:151371662-151372200	K562	blood:	n/a	n/a
30	CCNT2	chr1:151343082-151343282	K562	blood:	n/a	n/a
31	CCNT2	chr1:151372277-151372477	K562	blood:	n/a	n/a
32	CCNT2	chr1:151357075-151357435	K562	blood:	n/a	n/a
33	CEBPB	chr1:151343793-151344161	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr1:151371706-151372643	MCF-7	breast:	n/a	chr1:151371884-151371895
35	CEBPB	chr1:151368776-151369077	A549	lung:	n/a	chr1:151368942-151368953
36	CEBPB	chr1:151343717-151344423	MCF-7	breast:	n/a	n/a
37	CEBPB	chr1:151343887-151344177	A549	lung:	n/a	n/a
38	CEBPB	chr1:151368768-151369104	IMR90	lung:	n/a	chr1:151368942-151368953
39	CEBPB	chr1:151343727-151344343	A549	lung:	n/a	n/a
40	CEBPB	chr1:151371694-151372147	IMR90	lung:	n/a	chr1:151371884-151371895
41	CEBPB	chr1:151371691-151372192	K562	blood:	n/a	chr1:151371884-151371895
42	CEBPB	chr1:151351919-151352047	HepG2	liver:	n/a	chr1:151351985-151351996
43	CEBPB	chr1:151371734-151372082	K562	blood:	n/a	chr1:151371884-151371895
44	CEBPB	chr1:151368794-151369106	H1-hESC	embryonic stem cell:	n/a	chr1:151368942-151368953
45	CEBPB	chr1:151372556-151372600	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:151345110-151345191	HepG2	liver:	n/a	n/a
47	CEBPB	chr1:151371698-151372133	A549	lung:	n/a	chr1:151371884-151371895
48	CEBPB	chr1:151371698-151372161	HepG2	liver:	n/a	chr1:151371884-151371895
49	CEBPB	chr1:151371700-151372167	Hela-S3	cervix:	n/a	chr1:151371884-151371895
50	CEBPB	chr1:151371745-151372043	HepG2	liver:	n/a	chr1:151371884-151371895

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151346048-151346098	PFSK-1	brain:	n/a
2	chr1:151346048-151346098	PFSK-1	brain:	n/a
3	chr1:151345771-151345821	HNPCEpiC	eye:	n/a
4	chr1:151371972-151372022	NH-A	brain:	n/a
5	chr1:151372335-151372385	AG04449	skin:	fetal
6	chr1:151372228-151372278	A549	lung:	n/a
7	chr1:151346122-151346172	HNPCEpiC	eye:	n/a
8	chr1:151345173-151345223	ProgFib	skin:	n/a
9	chr1:151372572-151372622	A549	lung:	n/a
10	chr1:151345248-151345298	HUVEC	blood vessel:	n/a
11	chr1:151372652-151372702	LNCaP	prostate:	n/a
12	chr1:151346048-151346098	SK-N-SH	brain:	n/a
13	chr1:151370645-151370695	HRCEpiC	kidney:	n/a
14	chr1:151371972-151372022	NT2-D1	testis:	n/a
15	chr1:151371944-151371994	T-47D	breast:	n/a
16	chr1:151371944-151371994	AG09319	gingival:	n/a
17	chr1:151369469-151369519	CMK	blood:	n/a
18	chr1:151372572-151372622	HUVEC	blood vessel:	n/a
19	chr1:151372147-151372197	HL-60	blood:	n/a
20	chr1:151371285-151371335	HRE	kidney:	n/a
21	chr1:151345248-151345298	HAEpiC	amniotic membrane:	n/a
22	chr1:151372147-151372197	HepG2	liver:	n/a
23	chr1:151369469-151369519	HL-60	blood:	n/a
24	chr1:151370645-151370695	MCF-7	breast:	n/a
25	chr1:151371972-151372022	CMK	blood:	n/a
26	chr1:151343840-151343890	GM12892	blood:	n/a
27	chr1:151345771-151345821	NB4	blood:	n/a
28	chr1:151346048-151346098	NB4	blood:	n/a
29	chr1:151371972-151372022	HCPEpiC	choroid plexus:	n/a
30	chr1:151372652-151372702	HCM	heart:	n/a
31	chr1:151371972-151372022	MCF10A-Er-Src	breast:	n/a
32	chr1:151372147-151372197	HNPCEpiC	eye:	n/a
33	chr1:151372581-151372631	NH-A	brain:	n/a
34	chr1:151344806-151344856	GM19239	blood:	n/a
35	chr1:151343840-151343890	HCM	heart:	n/a
36	chr1:151371309-151371359	NT2-D1	testis:	n/a
37	chr1:151372335-151372385	HCM	heart:	n/a
38	chr1:151371285-151371335	BE2_C	brain:	n/a
39	chr1:151372572-151372622	MCF-7	breast:	n/a
40	chr1:151372572-151372622	NH-A	brain:	n/a
41	chr1:151371944-151371994	HAEpiC	amniotic membrane:	n/a
42	chr1:151343840-151343890	HAEpiC	amniotic membrane:	n/a
43	chr1:151372572-151372622	GM12892	blood:	n/a
44	chr1:151372335-151372385	H1-hESC	embryonic stem cell:	embryo
45	chr1:151371972-151372022	HEEpiC	esophagus:	n/a
46	chr1:151346048-151346098	Hela-S3	cervix:	n/a
47	chr1:151345173-151345223	HepG2	liver:	n/a
48	chr1:151372147-151372197	AG04450	lung:	fetal
49	chr1:151372652-151372702	K562	blood:	n/a
50	chr1:151345771-151345821	HEK293	kidney:	embryo

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:151317584..151319682-chr1:151339209..151341519,2	MCF-7	breast:
2	chr1:151368568..151371370-chr1:151392039..151394565,2	K562	blood:
3	chr1:151371183..151372890-chr1:151431011..151433472,2	MCF-7	breast:
4	1:151254384-151268403..1:151358657-151368243	K562	blood:
5	1:151180715-151199990..1:151358657-151368243	K562	blood:
6	chr1:151340503..151343136-chr1:151343197..151345914,3	K562	blood:
7	chr1:151344758..151345571-chr1:151371234..151372258,3	MCF-7	breast:
8	chr1:151351127..151353952-chr1:151357831..151359391,2	K562	blood:
9	1:151171193-151178589..1:151368336-151375897	Hela-S3	cervix:
10	chr1:151273322..151275078-chr1:151370486..151372389,2	MCF-7	breast:
11	chr1:151335152..151338036-chr1:151343299..151345232,3	MCF-7	breast:
12	chr1:151348371..151350424-chr1:151355194..151357742,2	K562	blood:
13	chr1:151254095..151256385-chr1:151338386..151340753,2	K562	blood:
14	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
15	chr1:151317585..151319121-chr1:151341611..151344384,2	MCF-7	breast:
16	chr1:151252692..151257354-chr1:151370358..151373702,7	K562	blood:
17	chr1:151317602..151320403-chr1:151337333..151341038,5	MCF-7	breast:
18	1:151358657-151368243..1:151516085-151535167	Hela-S3	cervix:
19	chr1:151370719..151373828-chr1:151394792..151398021,4	MCF-7	breast:
20	chr1:151297425..151301136-chr1:151370895..151373723,5	MCF-7	breast:
21	chr1:151352995..151355687-chr1:151371966..151374635,2	MCF-7	breast:
22	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
23	chr1:151319321..151320903-chr1:151345990..151347846,2	MCF-7	breast:
24	chr1:151335378..151338148-chr1:151374572..151377494,3	MCF-7	breast:
25	chr1:151298391..151300174-chr1:151343656..151346785,4	MCF-7	breast:
26	chr1:151340916..151343487-chr1:151343853..151346001,2	MCF-7	breast:
27	chr1:151342180..151345047-chr1:151351203..151353694,2	K562	blood:
28	chr1:151340911..151342650-chr1:151344414..151346132,2	K562	blood:
29	1:151270864-151283078..1:151358657-151368243	K562	blood:
30	chr1:151372028..151374418-chr1:151511841..151514665,2	MCF-7	breast:
31	chr1:151371526..151374105-chr1:151428160..151432357,4	K562	blood:
32	chr1:151298168..151300719-chr1:151365669..151368019,2	MCF-7	breast:
33	chr1:151371973..151373501-chr1:151810861..151813533,2	MCF-7	breast:
34	chr1:151351127..151353952-chr1:151357831..151359391,2	K562	blood:
35	chr1:151348873..151352385-chr1:151370200..151373598,3	MCF-7	breast:
36	chr1:151337330..151339100-chr1:151341997..151344198,2	K562	blood:
37	chr1:151317450..151322791-chr1:151370457..151374000,10	MCF-7	breast:
38	chr1:151337983..151340225-chr1:151340448..151342122,2	K562	blood:
39	chr1:151160213..151162825-chr1:151370506..151372060,2	K562	blood:
40	chr1:151253885..151255517-chr1:151367429..151369154,2	MCF-7	breast:
41	chr1:151318232..151320963-chr1:151353197..151355997,2	MCF-7	breast:
42	chr1:151332835..151334750-chr1:151336636..151339074,2	K562	blood:
43	chr1:151312120..151316742-chr1:151370081..151375586,6	MCF-7	breast:
44	chr1:151334136..151338213-chr1:151347669..151350682,3	MCF-7	breast:
45	chr1:151318980..151319798-chr1:151371884..151372449,2	MCF-7	breast:
46	chr1:151371851..151372388-chr2:46843826..46844603,2	HCT-116	colon:
47	chr1:151311947..151315930-chr1:151341715..151344576,4	K562	blood:
48	chr1:151340911..151342650-chr1:151344414..151346132,2	K562	blood:
49	chr1:151353527..151355666-chr1:151374191..151375959,2	K562	blood:
50	chr1:151336320..151338868-chr1:151344785..151346534,2	K562	blood:

No data

Variant related genes	Relation type
SELENBP1	TF binding region
PSMB4	TF binding region
SELENBP1	CpG island
PSMB4	CpG island
ENSG00000159377	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000163159	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000225556	chromatin interactions
ENSG00000143393	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000151665	chromatin interactions
ENSG00000119878	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000237976	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000159352	chromatin interactions
ENSG00000224645	chromatin interactions
ENSG00000163141	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000273481	chromatin interactions
ENSG00000265753	chromatin interactions
ENSG00000143416	chromatin interactions

Extended variants
information (count: 1422 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1422 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10788804	chr1:151337788-151337789	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78815720	chr1:151337792-151337793	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs185714774	chr1:151337833-151337834	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs115799503	chr1:151337903-151337904	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs535036247	chr1:151337913-151337914	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs146007727	chr1:151337919-151337920	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs190259138	chr1:151337949-151337950	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs139909868	chr1:151337967-151337968	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs200741855	chr1:151337983-151337984	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs376094498	chr1:151338028-151338029	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs201872159	chr1:151338030-151338031	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs577797586	chr1:151338052-151338053	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs114570747	chr1:151338054-151338055	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs374791130	chr1:151338092-151338093	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs200387556	chr1:151338113-151338114	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs369369505	chr1:151338124-151338125	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs369459403	chr1:151338125-151338126	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs559934158	chr1:151338138-151338139	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs181909137	chr1:151338149-151338150	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs373594176	chr1:151338150-151338151	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs138507038	chr1:151338151-151338152	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs186498127	chr1:151338171-151338172	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs373440909	chr1:151338175-151338176	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs75460835	chr1:151338176-151338177	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs531212967	chr1:151338181-151338182	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs551024605	chr1:151338184-151338185	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs370107730	chr1:151338231-151338232	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs143408960	chr1:151338243-151338244	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs372709598	chr1:151338247-151338248	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs571013649	chr1:151338253-151338254	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs377145077	chr1:151338254-151338255	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs539688714	chr1:151338286-151338287	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs370612586	chr1:151338347-151338348	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs115463556	chr1:151338383-151338384	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs566187933	chr1:151338413-151338414	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs535192659	chr1:151338453-151338454	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs552697613	chr1:151338483-151338484	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs2800953	chr1:151338570-151338571	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs145497953	chr1:151338578-151338579	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs148403735	chr1:151338654-151338655	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs557809383	chr1:151338665-151338666	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs577765128	chr1:151338666-151338667	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs540384013	chr1:151338669-151338670	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs552180362	chr1:151338702-151338703	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs375056484	chr1:151338709-151338710	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs368338290	chr1:151338719-151338720	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs539358067	chr1:151338741-151338742	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs371127500	chr1:151338742-151338743	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs141611452	chr1:151338753-151338754	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs573345696	chr1:151338754-151338755	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	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
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
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
Breast cancer	21611746	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
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	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
Follicular lymphoma	18703704	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
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151329400-151340600	Weak transcription	Osteobl	bone
2	chr1:151332200-151340000	Weak transcription	Fetal Heart	heart
3	chr1:151334400-151341600	Strong transcription	Fetal Lung	lung
4	chr1:151334600-151340000	Strong transcription	Skeletal Muscle Male	skeletal muscle
5	chr1:151334800-151339400	Strong transcription	Right Ventricle	heart
6	chr1:151335000-151344600	Weak transcription	Fetal Kidney	kidney
7	chr1:151335400-151340000	Strong transcription	Liver	Liver
8	chr1:151335400-151340000	Weak transcription	Right Atrium	heart
9	chr1:151335400-151340600	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr1:151335400-151340600	Weak transcription	NHDF-Ad	bronchial
11	chr1:151335400-151341200	Weak transcription	Brain Angular Gyrus	brain
12	chr1:151335400-151342000	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:151335400-151342800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr1:151335400-151344400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:151335600-151338600	Strong transcription	Adipose Nuclei	Adipose
16	chr1:151335600-151339400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:151335600-151340000	Strong transcription	Fetal Stomach	stomach
18	chr1:151335600-151340200	Strong transcription	Fetal Muscle Trunk	muscle
19	chr1:151335600-151340200	Strong transcription	Lung	lung
20	chr1:151335600-151340600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:151335600-151341200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:151335600-151344400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr1:151335800-151340000	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr1:151335800-151342200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:151335800-151342400	Weak transcription	Brain Germinal Matrix	brain
26	chr1:151335800-151343000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr1:151336000-151339200	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr1:151336000-151339400	Strong transcription	Left Ventricle	heart
29	chr1:151336000-151339400	Strong transcription	Ovary	ovary
30	chr1:151336000-151339800	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr1:151336000-151339800	Strong transcription	Skeletal Muscle Female	skeletal muscle
32	chr1:151336000-151340400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:151336000-151340600	Strong transcription	Gastric	stomach
34	chr1:151336000-151341400	Strong transcription	Stomach Smooth Muscle	stomach
35	chr1:151336200-151339000	Strong transcription	Placenta	Placenta
36	chr1:151336200-151340000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:151336200-151340000	Strong transcription	Fetal Muscle Leg	muscle
38	chr1:151336200-151341600	Strong transcription	Fetal Intestine Large	intestine
39	chr1:151336200-151344600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr1:151336200-151344600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr1:151336400-151340600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:151336400-151340600	Strong transcription	Duodenum Mucosa	Duodenum
43	chr1:151336600-151337800	Strong transcription	Spleen	Spleen
44	chr1:151336600-151338200	Strong transcription	K562	blood
45	chr1:151336600-151338400	Strong transcription	Brain Inferior Temporal Lobe	brain
46	chr1:151336600-151339400	Strong transcription	Pancreas	Pancrea
47	chr1:151336600-151341600	Strong transcription	Rectal Smooth Muscle	rectum
48	chr1:151336600-151342200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:151336800-151338600	Strong transcription	Placenta Amnion	Placenta Amnion
50	chr1:151336800-151338800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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