Variant report

Variant	nsv1039515
Chromosome Location	chr12:119085196-119218918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:788)
CpG islands
(count:611)
Chromatin interactive
region (count:13)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:119218845-119219045	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:119118260-119118469	K562	blood:	n/a	n/a
3	ARID3A	chr12:119151817-119153000	HepG2	liver:	n/a	n/a
4	ATF2	chr12:119127458-119127977	GM12878	blood:	n/a	n/a
5	BACH1	chr12:119188512-119188757	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:119127653-119127993	GM12878	blood:	n/a	n/a
7	BATF	chr12:119180926-119181178	GM12878	blood:	n/a	n/a
8	BATF	chr12:119119048-119119439	GM12878	blood:	n/a	n/a
9	BATF	chr12:119127656-119127969	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:119127579-119127974	GM12878	blood:	n/a	chr12:119127860-119127869
11	BCL11A	chr12:119120439-119120774	GM12878	blood:	n/a	n/a
12	BCLAF1	chr12:119127654-119128060	GM12878	blood:	n/a	chr12:119127860-119127869
13	BHLHE40	chr12:119118288-119118471	K562	blood:	n/a	n/a
14	BHLHE40	chr12:119151813-119152777	HepG2	liver:	n/a	n/a
15	BHLHE40	chr12:119152330-119152673	HepG2	liver:	n/a	n/a
16	CBX3	chr12:119151712-119152327	HCT-116	colon:	n/a	n/a
17	CBX3	chr12:119145668-119146026	K562	blood:	n/a	n/a
18	CBX3	chr12:119145694-119146135	K562	blood:	n/a	n/a
19	CEBPB	chr12:119165332-119165608	A549	lung:	n/a	chr12:119165453-119165466 chr12:119165453-119165464 chr12:119165455-119165466
20	CEBPB	chr12:119091771-119092037	HepG2	liver:	n/a	chr12:119091919-119091932 chr12:119091919-119091930 chr12:119091920-119091931 chr12:119091919-119091930 chr12:119091919-119091932
21	CEBPB	chr12:119186288-119186571	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:119102668-119102936	A549	lung:	n/a	chr12:119102803-119102814
23	CEBPB	chr12:119151856-119152766	HepG2	liver:	n/a	n/a
24	CEBPB	chr12:119148971-119149135	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:119127619-119127890	GM12878	blood:	n/a	n/a
26	CEBPB	chr12:119087973-119088334	K562	blood:	n/a	n/a
27	CEBPB	chr12:119152410-119152670	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:119088110-119088169	A549	lung:	n/a	n/a
29	CEBPB	chr12:119151783-119152115	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:119173442-119173644	K562	blood:	n/a	n/a
31	CEBPB	chr12:119151955-119152790	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:119102643-119102951	HepG2	liver:	n/a	chr12:119102803-119102814
33	CEBPB	chr12:119088288-119088297	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr12:119218589-119218899	HepG2	liver:	n/a	n/a
35	CEBPB	chr12:119135315-119135531	HepG2	liver:	n/a	chr12:119135430-119135441
36	CEBPB	chr12:119165300-119165603	HepG2	liver:	n/a	chr12:119165453-119165466 chr12:119165453-119165464 chr12:119165455-119165466
37	CEBPB	chr12:119215016-119215164	HepG2	liver:	n/a	chr12:119215058-119215069
38	CEBPB	chr12:119091824-119091967	K562	blood:	n/a	chr12:119091919-119091932 chr12:119091919-119091930 chr12:119091920-119091931 chr12:119091919-119091930 chr12:119091919-119091932
39	CEBPB	chr12:119152274-119152739	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:119165379-119165619	K562	blood:	n/a	chr12:119165453-119165466 chr12:119165453-119165464 chr12:119165455-119165466
41	CHD1	chr12:119212065-119212298	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr12:119120596-119120725	GM12878	blood:	n/a	n/a
43	CHD2	chr12:119211886-119212428	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr12:119152322-119152727	HepG2	liver:	n/a	n/a
45	CREB1	chr12:119152010-119152871	HepG2	liver:	n/a	n/a
46	CTCF	chr12:119151766-119152113	H1-hESC	embryonic stem cell:	n/a	chr12:119151988-119152006 chr12:119151991-119152004 chr12:119151991-119152004 chr12:119151989-119152005 chr12:119151990-119152011
47	CTCF	chr12:119152300-119152450	GM12872	blood:	n/a	n/a
48	CTCF	chr12:119151880-119152030	RPTEC	kidney:	n/a	chr12:119151988-119152006 chr12:119151991-119152004 chr12:119151991-119152004 chr12:119151989-119152005 chr12:119151990-119152011
49	CTCF	chr12:119151880-119152030	GM12874	blood:	n/a	chr12:119151988-119152006 chr12:119151991-119152004 chr12:119151991-119152004 chr12:119151989-119152005 chr12:119151990-119152011
50	CTCF	chr12:119151784-119152250	MCF-7	breast:	n/a	chr12:119151988-119152006 chr12:119151991-119152004 chr12:119151991-119152004 chr12:119151989-119152005 chr12:119151990-119152011

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119211794-119211844	AG09309	skin:	n/a
2	chr12:119211794-119211844	AG09309	skin:	n/a
3	chr12:119216236-119216286	AG09309	skin:	n/a
4	chr12:119212319-119212369	NHDF-neo	bronchial:	n/a
5	chr12:119212313-119212363	HL-60	blood:	n/a
6	chr12:119214021-119214071	AG09309	skin:	n/a
7	chr12:119214021-119214071	BJ	skin:	n/a
8	chr12:119119725-119119775	AG10803	skin:	n/a
9	chr12:119212319-119212369	HUVEC	blood vessel:	n/a
10	chr12:119187794-119187844	U87	brain:	n/a
11	chr12:119214021-119214071	PrEC	prostate:	n/a
12	chr12:119187794-119187844	ECC-1	luminal epithelium:	n/a
13	chr12:119212160-119212210	Caco-2	colon:	n/a
14	chr12:119212160-119212210	SK-N-SH_RA	brain:	n/a
15	chr12:119211794-119211844	HEEpiC	esophagus:	n/a
16	chr12:119119725-119119775	IMR90	lung:	fetal
17	chr12:119119725-119119775	AG04450	lung:	fetal
18	chr12:119214021-119214071	U87	brain:	n/a
19	chr12:119214021-119214071	HepG2	liver:	n/a
20	chr12:119119725-119119775	NB4	blood:	n/a
21	chr12:119212313-119212363	SKMC	muscle:	n/a
22	chr12:119208234-119208284	AoSMC	blood vessel:	n/a
23	chr12:119211794-119211844	PANC-1	pancreas:	n/a
24	chr12:119216236-119216286	HMEC	breast:	n/a
25	chr12:119119725-119119775	GM19239	blood:	n/a
26	chr12:119216236-119216286	MCF10A-Er-Src	breast:	n/a
27	chr12:119214021-119214071	ECC-1	luminal epithelium:	n/a
28	chr12:119211794-119211844	HEK293	kidney:	embryo
29	chr12:119212319-119212369	AG04450	lung:	fetal
30	chr12:119208234-119208284	SKMC	muscle:	n/a
31	chr12:119216236-119216286	GM12891	blood:	n/a
32	chr12:119211794-119211844	NB4	blood:	n/a
33	chr12:119212160-119212210	PrEC	prostate:	n/a
34	chr12:119119725-119119775	HEK293	kidney:	embryo
35	chr12:119212160-119212210	AG09309	skin:	n/a
36	chr12:119212160-119212210	HIPEpiC	eye:	n/a
37	chr12:119187794-119187844	Hepatocyte	liver:	n/a
38	chr12:119212160-119212210	AG09319	gingival:	n/a
39	chr12:119211794-119211844	MCF10A-Er-Src	breast:	n/a
40	chr12:119211794-119211844	SKMC	muscle:	n/a
41	chr12:119216236-119216286	NH-A	brain:	n/a
42	chr12:119211794-119211844	HCT-116	colon:	n/a
43	chr12:119208234-119208284	GM12891	blood:	n/a
44	chr12:119212313-119212363	PANC-1	pancreas:	n/a
45	chr12:119119725-119119775	HEEpiC	esophagus:	n/a
46	chr12:119212319-119212369	SK-N-SH	brain:	n/a
47	chr12:119212319-119212369	BJ	skin:	n/a
48	chr12:119208234-119208284	AG04449	skin:	fetal
49	chr12:119216236-119216286	RPTEC	kidney:	n/a
50	chr12:119212313-119212363	AoSMC	blood vessel:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:119115880..119117499-chr12:119118007..119120826,2	MCF-7	breast:
2	chr12:119160414..119163209-chr12:119163501..119166217,2	MCF-7	breast:
3	chr12:119137290..119138837-chr12:119141047..119142658,2	MCF-7	breast:
4	chr12:119151580..119152192-chr12:119474698..119475328,2	MCF-7	breast:
5	chr12:119151694..119152462-chr12:119850745..119851652,2	MCF-7	breast:
6	chr12:119160414..119163209-chr12:119163501..119166217,2	MCF-7	breast:
7	chr12:119150767..119153153-chr12:119153929..119156219,2	K562	blood:
8	chr12:119137290..119138837-chr12:119141047..119142658,2	MCF-7	breast:
9	chr12:119150767..119153153-chr12:119153929..119156219,2	K562	blood:
10	chr12:119212868..119215248-chr12:119216097..119217975,2	K562	blood:
11	chr12:118842861..118843440-chr12:119151910..119152659,2	MCF-7	breast:
12	chr12:119117331..119119543-chr12:119272928..119275663,2	K562	blood:
13	chr12:119115880..119117499-chr12:119118007..119120826,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAOK3-4	chr12:119210878-119211112	NONHSAT031051
2	lnc-TAOK3-4	chr12:119211416-119211580	NONHSAT031051
3	lnc-TAOK3-4	chr12:119211416-119211611	XLOC_010215
4	lnc-TAOK3-10	chr12:119143047-119143452	expReg_chr12_10611_-
5	lnc-TAOK3-3	chr12:119199397-119199469	XLOC_010214
6	lnc-SRRM4-5	chr12:119213844-119214031	l_739_chr12:119213843-119215417_liver
7	lnc-TAOK3-3	chr12:119196362-119196836	XLOC_010214
8	lnc-TAOK3-3	chr12:119196218-119196836	NONHSAT031046
9	lnc-TAOK3-3	chr12:119199397-119199484	ENSG00000256750
10	lnc-TAOK3-3	chr12:119197779-119197872	XLOC_010214
11	lnc-TAOK3-4	chr12:119212291-119212323	ENSG00000255618
12	lnc-SRRM4-5	chr12:119215330-119215417	l_739_chr12:119213843-119215417_liver
13	lnc-TAOK3-3	chr12:119197779-119197872	ENSG00000256750
14	lnc-TAOK3-11	chr12:119175769-119176316	NONHSAT031045
15	lnc-TAOK3-4	chr12:119211416-119211580	XLOC_010215
16	lnc-TAOK3-3	chr12:119196559-119196836	ENSG00000256750
17	lnc-TAOK3-3	chr12:119199397-119199458	NONHSAT031046
18	lnc-TAOK3-4	chr12:119212291-119212397	XLOC_010215
19	lnc-TAOK3-3	chr12:119199397-119199462	ENSG00000256750
20	lnc-TAOK3-3	chr12:119196362-119196836	XLOC_010214
21	lnc-TAOK3-4	chr12:119210837-119211107	ENSG00000255618
22	lnc-TAOK3-3	chr12:119197779-119197872	NONHSAT031046
23	lnc-TAOK3-2	chr12:119085680-119085759	ENSG00000255714
24	lnc-TAOK3-4	chr12:119211416-119211580	ENSG00000255618
25	lnc-TAOK3-4	chr12:119212732-119212942	ENSG00000255618
26	lnc-TAOK3-4	chr12:119210845-119211107	XLOC_010215
27	lnc-TAOK3-3	chr12:119196610-119196836	ENSG00000256750
28	lnc-TAOK3-4	chr12:119210855-119211107	XLOC_010215
29	lnc-SUDS3-2	chr12:119133324-119134955	ncRnaDb_ncrna_FR048197_1
30	lnc-TAOK3-2	chr12:119086289-119086529	ENSG00000255714
31	lnc-TAOK3-4	chr12:119212061-119212087	NONHSAT031051
32	lnc-TAOK3-3	chr12:119199397-119199469	XLOC_010214

No data

Variant related genes	Relation type
ENSG00000256750	TF binding region
ENSG00000255714	TF binding region
RPL17P37	TF binding region
ENSG00000255618	TF binding region
ENSG00000256750	CpG island
ENSG00000255714	CpG island
RPL17P37	CpG island
ENSG00000255618	CpG island
ENSG00000255618	chromatin interactions
CSNK1G1	miRNA target sites

Extended variants
information (count: 2957 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2957 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566310036	chr12:119085708-119085709	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs577957811	chr12:119085728-119085729	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs116295583	chr12:119085734-119085735	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs568012313	chr12:119085747-119085748	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs61944066	chr12:119086304-119086305	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs74768163	chr12:119086351-119086352	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs7958804	chr12:119086357-119086358	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs532202337	chr12:119086434-119086435	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs543397399	chr12:119086455-119086456	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs148786350	chr12:119086487-119086488	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs114778333	chr12:119086555-119086556	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547638587	chr12:119086559-119086560	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs113065491	chr12:119086606-119086607	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374468943	chr12:119086637-119086638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs73413464	chr12:119086769-119086770	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs528687426	chr12:119086866-119086867	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs78145201	chr12:119086902-119086903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs12309659	chr12:119086914-119086915	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs548764996	chr12:119087977-119087978	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs568751834	chr12:119087995-119087996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs145434449	chr12:119087998-119087999	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs189238452	chr12:119088006-119088007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570729070	chr12:119088015-119088016	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs539835149	chr12:119088020-119088021	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs553125806	chr12:119088025-119088026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs569878954	chr12:119088052-119088053	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs573458989	chr12:119088078-119088079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs542589941	chr12:119088120-119088121	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs555984012	chr12:119088162-119088163	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs575916007	chr12:119088176-119088177	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552441991	chr12:119088181-119088182	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs564188381	chr12:119088198-119088199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs549063882	chr12:119088220-119088221	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs532920939	chr12:119088227-119088228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs545181327	chr12:119088242-119088243	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs559940030	chr12:119088289-119088290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs182325596	chr12:119088322-119088323	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs147280752	chr12:119088372-119088373	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs2730717	chr12:119088378-119088379	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs79736298	chr12:119088415-119088416	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs55677348	chr12:119088425-119088426	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570907568	chr12:119088440-119088441	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539576565	chr12:119088478-119088479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs553327034	chr12:119088589-119088590	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs566790431	chr12:119088596-119088597	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs570888223	chr12:119088605-119088606	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs536112992	chr12:119088633-119088634	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs556120555	chr12:119088635-119088636	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs575876332	chr12:119088658-119088659	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs77604507	chr12:119088664-119088665	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Lung cancer	18172305	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119089400-119089600	Bivalent Enhancer	Lung	lung
2	chr12:119091800-119094400	Enhancers	Liver	Liver
3	chr12:119102200-119103000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:119105200-119106200	Enhancers	Fetal Muscle Leg	muscle
5	chr12:119111200-119112000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr12:119112000-119112800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr12:119112000-119112800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:119112800-119118000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:119118000-119118400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr12:119118000-119118400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:119118000-119118400	Enhancers	Fetal Muscle Trunk	muscle
12	chr12:119118000-119118400	Active TSS	K562	blood
13	chr12:119118000-119118800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr12:119118000-119118800	Enhancers	Brain Hippocampus Middle	brain
15	chr12:119118000-119118800	Enhancers	Fetal Muscle Leg	muscle
16	chr12:119118000-119119000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:119118000-119119000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr12:119118000-119119200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:119118000-119120400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr12:119118200-119118400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr12:119118200-119118600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr12:119118200-119118600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr12:119118200-119119000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr12:119118200-119119000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr12:119118200-119119000	Enhancers	Brain Anterior Caudate	brain
26	chr12:119118200-119119000	Enhancers	Brain Substantia Nigra	brain
27	chr12:119118200-119119200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr12:119118400-119118600	Enhancers	GM12878-XiMat	blood
29	chr12:119118400-119118800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr12:119118400-119118800	Enhancers	Brain Angular Gyrus	brain
31	chr12:119118400-119119000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:119118400-119119200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:119118400-119127800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr12:119118400-119131200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr12:119118600-119119600	Weak transcription	GM12878-XiMat	blood
36	chr12:119118600-119119800	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr12:119118600-119119800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr12:119118800-119119000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr12:119118800-119119000	Bivalent Enhancer	Brain Angular Gyrus	brain
40	chr12:119118800-119119800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:119118800-119123800	Weak transcription	Fetal Muscle Leg	muscle
42	chr12:119119000-119119400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr12:119119000-119119400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr12:119119000-119119400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr12:119119000-119119800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr12:119119000-119120000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:119119200-119119600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr12:119119200-119119600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:119119200-119119800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:119119400-119120400	Enhancers	HUES48 Cell Line	embryonic stem cell

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