Variant report

Variant	nsv981604
Chromosome Location	chr7:145773003-145935052
allele	n/a
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	ARID3A	chr7:145787264-145787483	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:145878136-145878188	K562	blood:	n/a	n/a
3	ARID3A	chr7:145787152-145787489	K562	blood:	n/a	n/a
4	ATF1	chr7:145775000-145775187	K562	blood:	n/a	n/a
5	BACH1	chr7:145842137-145842377	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:145813392-145814179	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:145845611-145845615	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:145812851-145813178	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr7:145824603-145824809	K562	blood:	n/a	chr7:145824732-145824741 chr7:145824733-145824742 chr7:145824732-145824741
10	BHLHE40	chr7:145812888-145813075	K562	blood:	n/a	n/a
11	BHLHE40	chr7:145793673-145793674	K562	blood:	n/a	n/a
12	BRCA1	chr7:145887640-145887719	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:145787246-145787465	H1-hESC	embryonic stem cell:	n/a	chr7:145787445-145787452
14	CBX3	chr7:145888491-145888877	K562	blood:	n/a	n/a
15	CBX3	chr7:145812824-145813236	K562	blood:	n/a	n/a
16	CBX3	chr7:145888550-145888786	K562	blood:	n/a	n/a
17	CBX3	chr7:145812871-145813165	K562	blood:	n/a	n/a
18	CCNT2	chr7:145796377-145796527	K562	blood:	n/a	n/a
19	CCNT2	chr7:145813050-145813510	K562	blood:	n/a	n/a
20	CCNT2	chr7:145892339-145892539	K562	blood:	n/a	n/a
21	CCNT2	chr7:145808087-145808172	K562	blood:	n/a	n/a
22	CCNT2	chr7:145838134-145838337	K562	blood:	n/a	n/a
23	CCNT2	chr7:145813815-145814042	K562	blood:	n/a	n/a
24	CCNT2	chr7:145789588-145789669	K562	blood:	n/a	n/a
25	CEBPB	chr7:145882969-145883274	K562	blood:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143
26	CEBPB	chr7:145897657-145897977	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:145929924-145930202	IMR90	lung:	n/a	chr7:145930070-145930081 chr7:145930068-145930079 chr7:145930068-145930081
28	CEBPB	chr7:145779720-145780002	HepG2	liver:	n/a	chr7:145779860-145779871
29	CEBPB	chr7:145872819-145873166	HepG2	liver:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
30	CEBPB	chr7:145881435-145881595	A549	lung:	n/a	chr7:145881497-145881508 chr7:145881496-145881507 chr7:145881498-145881507
31	CEBPB	chr7:145838848-145839167	HepG2	liver:	n/a	chr7:145838922-145838931 chr7:145838921-145838932 chr7:145838920-145838931
32	CEBPB	chr7:145914271-145914588	HepG2	liver:	n/a	chr7:145914411-145914422
33	CEBPB	chr7:145882935-145883521	K562	blood:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143
34	CEBPB	chr7:145883007-145883209	K562	blood:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143
35	CEBPB	chr7:145882944-145883364	MCF-7	breast:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143
36	CEBPB	chr7:145872838-145873169	A549	lung:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
37	CEBPB	chr7:145897673-145897960	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:145882948-145883323	A549	lung:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143
39	CEBPB	chr7:145881370-145881627	HepG2	liver:	n/a	chr7:145881497-145881508 chr7:145881496-145881507 chr7:145881498-145881507
40	CEBPB	chr7:145818808-145819059	K562	blood:	n/a	chr7:145818945-145818958
41	CEBPB	chr7:145882944-145883329	HepG2	liver:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143
42	CEBPB	chr7:145882888-145883407	H1-hESC	embryonic stem cell:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143
43	CEBPB	chr7:145872800-145873072	H1-hESC	embryonic stem cell:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
44	CEBPB	chr7:145850014-145850299	HepG2	liver:	n/a	chr7:145850146-145850157
45	CEBPB	chr7:145881325-145881626	IMR90	lung:	n/a	chr7:145881497-145881508 chr7:145881496-145881507 chr7:145881498-145881507
46	CEBPB	chr7:145847394-145847598	HepG2	liver:	n/a	chr7:145847573-145847590 chr7:145847576-145847589
47	CEBPB	chr7:145929938-145930208	HepG2	liver:	n/a	chr7:145930070-145930081 chr7:145930068-145930079 chr7:145930068-145930081
48	CEBPB	chr7:145850024-145850278	A549	lung:	n/a	chr7:145850146-145850157
49	CEBPB	chr7:145872821-145873202	MCF-7	breast:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
50	CEBPB	chr7:145882949-145883315	ECC-1	luminal epithelium:	n/a	chr7:145883132-145883141 chr7:145883130-145883143 chr7:145883132-145883141 chr7:145883132-145883141 chr7:145883130-145883141 chr7:145883109-145883120 chr7:145883130-145883143

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145813421-145813471	HRE	kidney:	n/a
2	chr7:145813421-145813471	HRE	kidney:	n/a
3	chr7:145813915-145813965	AoSMC	blood vessel:	n/a
4	chr7:145814152-145814202	HCM	heart:	n/a
5	chr7:145813421-145813471	HCF	heart:	n/a
6	chr7:145814003-145814053	AG10803	skin:	n/a
7	chr7:145813031-145813081	HRPEpiC	eye:	n/a
8	chr7:145812842-145812892	Hepatocyte	liver:	n/a
9	chr7:145814152-145814202	IMR90	lung:	fetal
10	chr7:145813915-145813965	SK-N-MC	brain:	n/a
11	chr7:145813413-145813463	HRCEpiC	kidney:	n/a
12	chr7:145875026-145875076	NT2-D1	testis:	n/a
13	chr7:145812842-145812892	NHBE	bronchial:	n/a
14	chr7:145813413-145813463	T-47D	breast:	n/a
15	chr7:145813494-145813544	CMK	blood:	n/a
16	chr7:145875026-145875076	Jurkat	blood:	n/a
17	chr7:145813008-145813058	Hepatocyte	liver:	n/a
18	chr7:145813413-145813463	HCF	heart:	n/a
19	chr7:145813432-145813482	NHDF-neo	bronchial:	n/a
20	chr7:145813439-145813489	Jurkat	blood:	n/a
21	chr7:145814152-145814202	ECC-1	luminal epithelium:	n/a
22	chr7:145813432-145813482	Caco-2	colon:	n/a
23	chr7:145812842-145812892	HRE	kidney:	n/a
24	chr7:145813915-145813965	HCF	heart:	n/a
25	chr7:145812871-145812921	GM06990	blood:	n/a
26	chr7:145813439-145813489	HEEpiC	esophagus:	n/a
27	chr7:145813008-145813058	SKMC	muscle:	n/a
28	chr7:145875026-145875076	MCF10A-Er-Src	breast:	n/a
29	chr7:145813417-145813467	BJ	skin:	n/a
30	chr7:145813008-145813058	IMR90	lung:	fetal
31	chr7:145813494-145813544	GM06990	blood:	n/a
32	chr7:145813437-145813487	AG10803	skin:	n/a
33	chr7:145875026-145875076	PFSK-1	brain:	n/a
34	chr7:145814306-145814356	BE2_C	brain:	n/a
35	chr7:145813066-145813116	GM06990	blood:	n/a
36	chr7:145875026-145875076	A549	lung:	n/a
37	chr7:145813439-145813489	BJ	skin:	n/a
38	chr7:145813494-145813544	H1-hESC	embryonic stem cell:	embryo
39	chr7:145813008-145813058	PFSK-1	brain:	n/a
40	chr7:145813437-145813487	HCPEpiC	choroid plexus:	n/a
41	chr7:145814003-145814053	Hepatocyte	liver:	n/a
42	chr7:145813066-145813116	CMK	blood:	n/a
43	chr7:145813417-145813467	HCT-116	colon:	n/a
44	chr7:145814306-145814356	HCT-116	colon:	n/a
45	chr7:145813946-145813996	NT2-D1	testis:	n/a
46	chr7:145813031-145813081	ovcar-3	ovarian:	n/a
47	chr7:145812871-145812921	T-47D	breast:	n/a
48	chr7:145813066-145813116	T-47D	breast:	n/a
49	chr7:145814003-145814053	MCF-7	breast:	n/a
50	chr7:145814306-145814356	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:145806708..145809039-chr7:145812340..145814652,2	K562	blood:
2	chr7:145782508..145785032-chr7:145801785..145804184,2	K562	blood:
3	chr7:145774442..145776114-chr7:145776448..145779399,2	K562	blood:
4	chr7:145879679..145882297-chr7:145885152..145887234,2	K562	blood:
5	chr7:145879679..145882297-chr7:145885152..145887234,2	K562	blood:
6	chr7:145931221..145934684-chr7:145937680..145940356,3	K562	blood:
7	chr7:145816235..145818075-chr7:145818635..145820633,2	K562	blood:
8	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:
9	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:
10	chr7:145794339..145796121-chr7:145802069..145803645,2	K562	blood:
11	chr7:145782097..145783756-chr7:145785466..145787437,2	K562	blood:
12	chr7:145349967..145350847-chr7:145786768..145787358,3	MCF-7	breast:
13	chr7:145757899..145760042-chr7:145772123..145774268,2	K562	blood:
14	chr7:145788344..145790564-chr7:145791387..145793910,2	K562	blood:
15	chr7:145870161..145872926-chr7:145874663..145877386,2	K562	blood:
16	chr7:145771822..145774419-chr7:145775630..145778255,2	K562	blood:
17	chr7:145805690..145807503-chr7:145809091..145811939,2	K562	blood:
18	chr7:145782097..145783756-chr7:145785466..145787437,2	K562	blood:
19	chr7:145782508..145785032-chr7:145801785..145804184,2	K562	blood:
20	chr7:118909733..118910708-chr7:145816212..145816735,2	MCF-7	breast:
21	chr7:144712868..144713384-chr7:145787231..145787880,2	MCF-7	breast:
22	chr7:145771822..145774419-chr7:145775630..145778255,2	K562	blood:
23	chr7:144551617..144552520-chr7:145786903..145787735,4	MCF-7	breast:
24	chr7:145870161..145872926-chr7:145874663..145877386,2	K562	blood:
25	chr7:145805690..145807503-chr7:145809091..145811939,2	K562	blood:
26	chr7:144733417..144734684-chr7:145786550..145787817,10	MCF-7	breast:
27	chr7:145449251..145450121-chr7:145786995..145787798,2	K562	blood:
28	chr7:145800703..145803223-chr7:145808125..145812343,3	K562	blood:
29	chr7:144733716..144734359-chr7:145787136..145787836,2	MCF-7	breast:
30	chr7:145816235..145818075-chr7:145818635..145820633,2	K562	blood:
31	chr7:145800703..145803223-chr7:145808125..145812343,3	K562	blood:
32	chr7:145794339..145796121-chr7:145802069..145803645,2	K562	blood:
33	chr7:145774442..145776114-chr7:145776448..145779399,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP2-3	chr7:145777121-145777289	NONHSAT123945
2	lnc-CNTNAP2-2	chr7:145793180-145793471	NONHSAT123946

Variant related genes	Relation type
CNTNAP2	TF binding region
RN7SL207P	TF binding region
CNTNAP2	CpG island
RN7SL207P	CpG island
ENSG00000264018	chromatin interactions
ENSG00000174469	chromatin interactions

Extended variants
information (count: 3530 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3530 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567450210	chr7:145777159-145777160	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs577810903	chr7:145777166-145777167	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs371829585	chr7:145777192-145777193	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs190427698	chr7:145777236-145777237	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs113186121	chr7:145787408-145787409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12703763	chr7:145787476-145787477	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs560251620	chr7:145787477-145787478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527287801	chr7:145787547-145787548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7455178	chr7:145787584-145787585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576343421	chr7:145787589-145787590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552176676	chr7:145787642-145787643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543666739	chr7:145787654-145787655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185457134	chr7:145787672-145787673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532728441	chr7:145787696-145787697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551233782	chr7:145787787-145787788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34220788	chr7:145787793-145787794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150563927	chr7:145787882-145787883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554651927	chr7:145787896-145787897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115485437	chr7:145787921-145787922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191583888	chr7:145787956-145787957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140777107	chr7:145787996-145787997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143127807	chr7:145787999-145788000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368307589	chr7:145788001-145788002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369823631	chr7:145788005-145788006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537800081	chr7:145788036-145788037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556417049	chr7:145788053-145788054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542771862	chr7:145788066-145788067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574557643	chr7:145788070-145788071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542001270	chr7:145788072-145788073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560312823	chr7:145788108-145788109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377240242	chr7:145788132-145788133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1880597	chr7:145788161-145788162	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs545899259	chr7:145788215-145788216	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563954458	chr7:145788231-145788232	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566830662	chr7:145788252-145788253	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs531332883	chr7:145788254-145788255	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559779633	chr7:145788256-145788257	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs182508999	chr7:145788263-145788264	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs527703396	chr7:145788335-145788336	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs147450530	chr7:145788349-145788350	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs187976120	chr7:145788351-145788352	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs139903109	chr7:145788353-145788354	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs566638123	chr7:145788372-145788373	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs534058896	chr7:145788379-145788380	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150058040	chr7:145788422-145788423	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs570800615	chr7:145788473-145788474	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538202279	chr7:145788564-145788565	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs373985475	chr7:145788575-145788576	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs145429306	chr7:145788602-145788603	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148769768	chr7:145788608-145788609	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145787400-145788400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr7:145790600-145792400	Enhancers	Fetal Lung	lung
3	chr7:145812000-145812600	Enhancers	Brain Germinal Matrix	brain
4	chr7:145812000-145813600	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr7:145812200-145812600	Enhancers	Fetal Brain Male	brain
6	chr7:145812200-145813600	Active TSS	Brain Anterior Caudate	brain
7	chr7:145812200-145815200	Active TSS	Brain Angular Gyrus	brain
8	chr7:145812400-145812600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:145812400-145812600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr7:145812400-145812600	Enhancers	Fetal Lung	lung
11	chr7:145812400-145812800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:145812400-145813600	Active TSS	Brain Hippocampus Middle	brain
13	chr7:145812400-145815200	Active TSS	Fetal Brain Female	brain
14	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
15	chr7:145812600-145812800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:145812600-145812800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
18	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
19	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
20	chr7:145812600-145812800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:145812600-145812800	Enhancers	Primary hematopoietic stem cells	blood
22	chr7:145812600-145812800	Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr7:145812600-145812800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
24	chr7:145812600-145812800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:145812600-145812800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr7:145812600-145812800	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr7:145812600-145812800	Flanking Active TSS	Brain Substantia Nigra	brain
29	chr7:145812600-145812800	Enhancers	Fetal Heart	heart
30	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
31	chr7:145812600-145812800	Enhancers	Fetal Muscle Trunk	muscle
32	chr7:145812600-145812800	Enhancers	Fetal Muscle Leg	muscle
33	chr7:145812600-145812800	Active TSS	Fetal Stomach	stomach
34	chr7:145812600-145812800	Enhancers	Ovary	ovary
35	chr7:145812600-145812800	Enhancers	Pancreas	Pancrea
36	chr7:145812600-145813000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:145812600-145813000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:145812600-145813000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:145812600-145813000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:145812600-145813000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:145812600-145813000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr7:145812600-145813000	Flanking Active TSS	Fetal Lung	lung
43	chr7:145812600-145813000	Bivalent Enhancer	Fetal Thymus	thymus
44	chr7:145812600-145813400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:145812600-145813400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:145812600-145813400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:145812600-145813800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr7:145812600-145814000	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr7:145812600-145814000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:145812600-145814000	Active TSS	Brain Cingulate Gyrus	brain

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