Variant report

Variant	nsv1002086
Chromosome Location	chr2:50912161-51405061
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	chr2:51330523-51330544	HepG2	liver:	n/a	n/a
2	ATF2	chr2:51259020-51259511	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:51259057-51259636	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:50955596-50955702	K562	blood:	n/a	n/a
6	BACH1	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:51330505-51330576	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr2:51330297-51330702	HepG2	liver:	n/a	n/a
11	BRCA1	chr2:51330435-51330474	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr2:51185262-51185455	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
17	CCNT2	chr2:51398751-51398851	K562	blood:	n/a	n/a
18	CEBPB	chr2:51392842-51393189	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:51255964-51256336	MCF-7	breast:	n/a	chr2:51256172-51256183
20	CEBPB	chr2:51185005-51185419	IMR90	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
21	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
22	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
23	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
24	CEBPB	chr2:51185023-51185436	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
25	CEBPB	chr2:51185008-51185377	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
26	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
27	CEBPB	chr2:51324687-51324910	HepG2	liver:	n/a	chr2:51324819-51324830
28	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
29	CEBPB	chr2:51163520-51163763	A549	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
30	CEBPB	chr2:51330496-51330704	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:51335946-51336285	A549	lung:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
32	CEBPB	chr2:51172595-51172790	HepG2	liver:	n/a	chr2:51172679-51172690
33	CEBPB	chr2:51255984-51256364	HepG2	liver:	n/a	chr2:51256172-51256183
34	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
35	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
36	CEBPB	chr2:51255980-51256366	H1-hESC	embryonic stem cell:	n/a	chr2:51256172-51256183
37	CEBPB	chr2:51256026-51256305	HepG2	liver:	n/a	chr2:51256172-51256183
38	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
39	CEBPB	chr2:51255896-51256399	A549	lung:	n/a	chr2:51256172-51256183
40	CEBPB	chr2:51184080-51184410	A549	lung:	n/a	chr2:51184131-51184142
41	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:51196130-51196480	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
45	CEBPB	chr2:51184978-51185335	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
46	CEBPB	chr2:51259207-51259533	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:51314497-51314768	A549	lung:	n/a	chr2:51314679-51314692 chr2:51314681-51314692 chr2:51314679-51314692 chr2:51314681-51314692
48	CEBPB	chr2:51255989-51256366	IMR90	lung:	n/a	chr2:51256172-51256183
49	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
50	CEBPB	chr2:51236313-51236416	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51057548-51057598	SAEC	small airway:	n/a
2	chr2:51057548-51057598	SAEC	small airway:	n/a
3	chr2:51259786-51259836	BE2_C	brain:	n/a
4	chr2:51255324-51255374	Caco-2	colon:	n/a
5	chr2:51056884-51056934	HEEpiC	esophagus:	n/a
6	chr2:51254021-51254071	Caco-2	colon:	n/a
7	chr2:51259703-51259753	AG09309	skin:	n/a
8	chr2:51255306-51255356	T-47D	breast:	n/a
9	chr2:51259493-51259543	H1-hESC	embryonic stem cell:	embryo
10	chr2:50992829-50992879	AG09309	skin:	n/a
11	chr2:51074939-51074989	CMK	blood:	n/a
12	chr2:51001003-51001053	A549	lung:	n/a
13	chr2:51254170-51254220	PrEC	prostate:	n/a
14	chr2:51228125-51228175	AG09309	skin:	n/a
15	chr2:51259493-51259543	SKMC	muscle:	n/a
16	chr2:51240310-51240360	HIPEpiC	eye:	n/a
17	chr2:51259807-51259857	PFSK-1	brain:	n/a
18	chr2:51378948-51378998	ovcar-3	ovarian:	n/a
19	chr2:51252301-51252351	ProgFib	skin:	n/a
20	chr2:51259807-51259857	AoSMC	blood vessel:	n/a
21	chr2:51240310-51240360	NT2-D1	testis:	n/a
22	chr2:51252301-51252351	PrEC	prostate:	n/a
23	chr2:51228125-51228175	HL-60	blood:	n/a
24	chr2:51255306-51255356	ProgFib	skin:	n/a
25	chr2:51254981-51255031	PANC-1	pancreas:	n/a
26	chr2:51057218-51057268	ovcar-3	ovarian:	n/a
27	chr2:51259807-51259857	GM12892	blood:	n/a
28	chr2:51378948-51378998	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:51240310-51240360	A549	lung:	n/a
30	chr2:51260399-51260449	HL-60	blood:	n/a
31	chr2:51378948-51378998	AG04450	lung:	fetal
32	chr2:51259552-51259602	ECC-1	luminal epithelium:	n/a
33	chr2:51254170-51254220	HMEC	breast:	n/a
34	chr2:51065673-51065723	HNPCEpiC	eye:	n/a
35	chr2:51260739-51260789	GM12878	blood:	n/a
36	chr2:51378948-51378998	HMEC	breast:	n/a
37	chr2:51057548-51057598	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:51260003-51260053	HCF	heart:	n/a
39	chr2:51378948-51378998	HAEpiC	amniotic membrane:	n/a
40	chr2:51231649-51231699	BE2_C	brain:	n/a
41	chr2:51074881-51074931	LNCaP	prostate:	n/a
42	chr2:51255306-51255356	ECC-1	luminal epithelium:	n/a
43	chr2:51228125-51228175	U87	brain:	n/a
44	chr2:51378948-51378998	AG09319	gingival:	n/a
45	chr2:51218880-51218930	RPTEC	kidney:	n/a
46	chr2:51260739-51260789	HRCEpiC	kidney:	n/a
47	chr2:51259697-51259747	Hela-S3	cervix:	n/a
48	chr2:51254021-51254071	GM12891	blood:	n/a
49	chr2:51259493-51259543	GM06990	blood:	n/a
50	chr2:51259786-51259836	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
2	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
3	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
4	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
5	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
6	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
7	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
8	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
9	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
10	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
11	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
12	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
13	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
14	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
15	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
16	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
17	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
18	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
19	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
20	chr2:51288072..51290967-chr2:232569534..232571521,2	MCF-7	breast:
21	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
22	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
23	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
24	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
25	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
26	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
27	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
28	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
29	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
30	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
31	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
32	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
33	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
2	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
3	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1
4	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648
5	lnc-CHAC2-4	chr2:51279495-51279592	ENSG00000231918.1
6	lnc-NRXN1-3	chr2:51283579-51283793	l_1833_chr2:51283578-51306188_testes
7	lnc-NRXN1-3	chr2:51283633-51283791	NONHSAT070652
8	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
9	lnc-NRXN1-3	chr2:51282723-51282956	NONHSAT070652
10	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000231918	TF binding region
NRXN1	TF binding region
ENSG00000216011	TF binding region
ENSG00000272385	TF binding region
ENSG00000216191	CpG island
ENSG00000238165	CpG island
ENSG00000215968	CpG island
ENSG00000231918	CpG island
NRXN1	CpG island
ENSG00000216011	CpG island
ENSG00000272385	CpG island
ENSG00000216191	chromatin interactions

Extended variants
information (count: 15970 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:15970 , 50 per page) page: 1 2 3 4 5 6 7 ... 320

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10197512	chr2:50912161-50912162	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574358206	chr2:50912168-50912169	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547590133	chr2:50912173-50912174	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567481968	chr2:50912186-50912187	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186934841	chr2:50912246-50912247	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563084120	chr2:50912286-50912287	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532916600	chr2:50912304-50912305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545086406	chr2:50912312-50912313	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs34039928	chr2:50912339-50912340	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550499475	chr2:50912355-50912356	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559933838	chr2:50912356-50912357	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370269760	chr2:50912360-50912361	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190577666	chr2:50912364-50912365	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372455224	chr2:50913422-50913423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547605650	chr2:50913430-50913431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559567065	chr2:50913476-50913477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527836604	chr2:50913477-50913478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549492395	chr2:50913484-50913485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527791488	chr2:50913500-50913501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567721113	chr2:50913548-50913549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375765513	chr2:50913563-50913564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541171285	chr2:50913585-50913586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11900164	chr2:50913616-50913617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs571925324	chr2:50913625-50913626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150555075	chr2:50913667-50913668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183894670	chr2:50913675-50913676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139626633	chr2:50913734-50913735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187646462	chr2:50913753-50913754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11900221	chr2:50913760-50913761	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs78225701	chr2:50913811-50913812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530255140	chr2:50913836-50913837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544347937	chr2:50913839-50913840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558250954	chr2:50913865-50913866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577099101	chr2:50913873-50913874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540966543	chr2:50913877-50913878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs72887530	chr2:50913894-50913895	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191312748	chr2:50913944-50913945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373248517	chr2:50913945-50913946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376755742	chr2:50913985-50913986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183698338	chr2:50914067-50914068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561390952	chr2:50914083-50914084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531678321	chr2:50914106-50914107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550184833	chr2:50914111-50914112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571546367	chr2:50914166-50914167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532880348	chr2:50914169-50914170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550089223	chr2:50914178-50914179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547693747	chr2:50914190-50914191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565985699	chr2:50914207-50914208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537686983	chr2:50914225-50914226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554705457	chr2:50914242-50914243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Acute myeloid leukemia	20729466	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50913400-50914000	Enhancers	Brain Angular Gyrus	brain
2	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr2:50913600-50914800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:50913600-50916000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:50913600-50916200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr2:50913800-50915800	Enhancers	Brain Anterior Caudate	brain
7	chr2:50913800-50916200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:50914000-50914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:50914000-50914200	Enhancers	Brain Cingulate Gyrus	brain
10	chr2:50914000-50914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:50914000-50917800	Weak transcription	Brain Angular Gyrus	brain
12	chr2:50914200-50915200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:50914200-50916000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:50914200-50918600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:50914400-50918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:50914600-50914800	Enhancers	H9 Cell Line	embryonic stem cell
17	chr2:50914600-50914800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr2:50914600-50915200	Enhancers	Fetal Heart	heart
19	chr2:50914800-50915200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr2:50914800-50915200	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr2:50914800-50915800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr2:50915000-50915200	Enhancers	Brain Substantia Nigra	brain
23	chr2:50915000-50915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr2:50915000-50915600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr2:50915200-50915600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr2:50915200-50915800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:50915200-50916000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:50915600-50915800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr2:50915600-50916000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr2:50915600-50916200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:50915800-50917800	Weak transcription	Brain Anterior Caudate	brain
32	chr2:50915800-50918600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr2:50915800-50918800	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr2:50916000-50918600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr2:50916000-50918800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr2:50916000-50948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:50916200-50923800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr2:50917600-50917800	Enhancers	Brain Hippocampus Middle	brain
39	chr2:50917600-50918000	Weak transcription	Brain Substantia Nigra	brain
40	chr2:50917600-50918400	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr2:50917800-50918400	Enhancers	Brain Angular Gyrus	brain
42	chr2:50917800-50918600	Enhancers	Brain Anterior Caudate	brain
43	chr2:50918000-50918200	Enhancers	Brain Substantia Nigra	brain
44	chr2:50918200-50918800	Weak transcription	Brain Substantia Nigra	brain
45	chr2:50918400-50918600	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr2:50918400-50918800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:50918400-50919200	Active TSS	Brain Angular Gyrus	brain
48	chr2:50918400-50919600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:50918600-50918800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr2:50918600-50919200	Enhancers	HUES48 Cell Line	embryonic stem cell

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