Variant report

Variant	nsv899554
Chromosome Location	chr12:120389613-120513625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1308)
CpG islands
(count:795)
Chromatin interactive
region (count:124)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:120451657-120451980	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:120493209-120493847	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:120500834-120501227	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:120426272-120426439	K562	blood:	n/a	n/a
5	ARID3A	chr12:120436842-120437081	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:120479136-120479526	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:120426946-120426970	K562	blood:	n/a	n/a
8	ARID3A	chr12:120438265-120438607	HepG2	liver:	n/a	n/a
9	ATF1	chr12:120451681-120451957	K562	blood:	n/a	n/a
10	ATF2	chr12:120451567-120452003	GM12878	blood:	n/a	n/a
11	ATF2	chr12:120449794-120450531	GM12878	blood:	n/a	n/a
12	ATF2	chr12:120449882-120450611	GM12878	blood:	n/a	n/a
13	ATF3	chr12:120451715-120451985	K562	blood:	n/a	n/a
14	BACH1	chr12:120427640-120427818	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr12:120393976-120394069	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr12:120426133-120427103	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr12:120448774-120449016	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:120426289-120426464	K562	blood:	n/a	n/a
19	BATF	chr12:120428278-120428463	GM12878	blood:	n/a	n/a
20	BATF	chr12:120451649-120451931	GM12878	blood:	n/a	n/a
21	BATF	chr12:120449863-120450390	GM12878	blood:	n/a	n/a
22	BATF	chr12:120451643-120451954	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:120451667-120451867	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:120451600-120451988	GM12878	blood:	n/a	n/a
25	BCL3	chr12:120449786-120450372	A549	lung:	n/a	n/a
26	BCL3	chr12:120449745-120450330	A549	lung:	n/a	n/a
27	BCLAF1	chr12:120426645-120426999	GM12878	blood:	n/a	chr12:120426812-120426825 chr12:120426755-120426768 chr12:120426814-120426827
28	BCLAF1	chr12:120451558-120452103	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:120449821-120450443	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:120426388-120427256	K562	blood:	n/a	chr12:120426819-120426835 chr12:120426595-120426611 chr12:120426812-120426828 chr12:120426992-120427008 chr12:120426807-120426823
31	BHLHE40	chr12:120427649-120427835	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:120426527-120427257	GM12878	blood:	n/a	chr12:120426819-120426835 chr12:120426595-120426611 chr12:120426812-120426828 chr12:120426992-120427008 chr12:120426807-120426823
33	BRCA1	chr12:120471657-120471733	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr12:120426757-120426942	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr12:120493113-120493813	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr12:120451607-120451984	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr12:120484302-120484317	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr12:120462005-120462272	K562	blood:	n/a	n/a
39	CBX3	chr12:120427610-120427871	K562	blood:	n/a	n/a
40	CBX3	chr12:120461983-120462356	K562	blood:	n/a	n/a
41	CBX3	chr12:120394885-120395412	HCT-116	colon:	n/a	n/a
42	CCNT2	chr12:120427574-120427848	K562	blood:	n/a	n/a
43	CCNT2	chr12:120426485-120427334	K562	blood:	n/a	chr12:120426959-120426968 chr12:120426571-120426580
44	CEBPB	chr12:120493478-120493820	HepG2	liver:	n/a	chr12:120493667-120493678
45	CEBPB	chr12:120479161-120479581	HepG2	liver:	n/a	n/a
46	CEBPB	chr12:120438345-120438654	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:120493362-120493939	A549	lung:	n/a	chr12:120493667-120493678
48	CEBPB	chr12:120438415-120438578	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:120406043-120406269	HepG2	liver:	n/a	n/a
50	CEBPB	chr12:120493496-120493721	H1-hESC	embryonic stem cell:	n/a	chr12:120493667-120493678

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120427178-120427228	HMEC	breast:	n/a
2	chr12:120428313-120428363	GM06990	blood:	n/a
3	chr12:120427178-120427228	HMEC	breast:	n/a
4	chr12:120428313-120428363	GM06990	blood:	n/a
5	chr12:120445227-120445277	HepG2	liver:	n/a
6	chr12:120427667-120427717	IMR90	lung:	fetal
7	chr12:120426784-120426834	PFSK-1	brain:	n/a
8	chr12:120428313-120428363	K562	blood:	n/a
9	chr12:120475264-120475314	SK-N-SH	brain:	n/a
10	chr12:120428313-120428363	MCF10A-Er-Src	breast:	n/a
11	chr12:120427182-120427232	AG10803	skin:	n/a
12	chr12:120428065-120428115	Caco-2	colon:	n/a
13	chr12:120428065-120428115	HUVEC	blood vessel:	n/a
14	chr12:120427182-120427232	SKMC	muscle:	n/a
15	chr12:120428313-120428363	ProgFib	skin:	n/a
16	chr12:120428065-120428115	Jurkat	blood:	n/a
17	chr12:120426784-120426834	RPTEC	kidney:	n/a
18	chr12:120428065-120428115	H1-hESC	embryonic stem cell:	embryo
19	chr12:120426550-120426600	NHBE	bronchial:	n/a
20	chr12:120426784-120426834	BJ	skin:	n/a
21	chr12:120428065-120428115	GM19239	blood:	n/a
22	chr12:120426618-120426668	AG10803	skin:	n/a
23	chr12:120426784-120426834	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:120427182-120427232	MCF-7	breast:	n/a
25	chr12:120426784-120426834	CMK	blood:	n/a
26	chr12:120428313-120428363	NH-A	brain:	n/a
27	chr12:120475264-120475314	HL-60	blood:	n/a
28	chr12:120426618-120426668	HCM	heart:	n/a
29	chr12:120426550-120426600	U87	brain:	n/a
30	chr12:120427178-120427228	HEK293	kidney:	embryo
31	chr12:120426529-120426579	H1-hESC	embryonic stem cell:	embryo
32	chr12:120475264-120475314	NH-A	brain:	n/a
33	chr12:120426618-120426668	AG09309	skin:	n/a
34	chr12:120427182-120427232	PrEC	prostate:	n/a
35	chr12:120423883-120423933	HNPCEpiC	eye:	n/a
36	chr12:120426784-120426834	HMEC	breast:	n/a
37	chr12:120426529-120426579	AG04449	skin:	fetal
38	chr12:120426618-120426668	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:120426618-120426668	GM12878	blood:	n/a
40	chr12:120426618-120426668	HMEC	breast:	n/a
41	chr12:120427667-120427717	ECC-1	luminal epithelium:	n/a
42	chr12:120426550-120426600	AG09319	gingival:	n/a
43	chr12:120427178-120427228	GM12891	blood:	n/a
44	chr12:120427667-120427717	MCF-7	breast:	n/a
45	chr12:120426529-120426579	A549	lung:	n/a
46	chr12:120426529-120426579	U87	brain:	n/a
47	chr12:120427667-120427717	AG10803	skin:	n/a
48	chr12:120428313-120428363	Jurkat	blood:	n/a
49	chr12:120426529-120426579	GM12878	blood:	n/a
50	chr12:120427667-120427717	GM19239	blood:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:120471122..120473803-chr12:120553194..120555161,2	MCF-7	breast:
2	chr12:120103322..120105454-chr12:120505057..120506745,2	K562	blood:
3	chr12:120433338..120435447-chr12:120438031..120440080,2	MCF-7	breast:
4	chr12:120462600..120465002-chr12:120472760..120475274,2	MCF-7	breast:
5	chr12:120446709..120448766-chr12:120465189..120467335,2	K562	blood:
6	chr12:120465481..120467971-chr12:120475425..120477605,2	K562	blood:
7	chr12:120425840..120426796-chr20:19097523..19098151,2	MCF-7	breast:
8	chr12:120472651..120475329-chr12:120480082..120481970,2	MCF-7	breast:
9	chr12:120463438..120466010-chr12:120520839..120524838,3	K562	blood:
10	chr12:120425404..120428200-chr12:120435927..120438924,2	K562	blood:
11	chr12:120419275..120421989-chr12:120429002..120431271,2	K562	blood:
12	chr12:120451212..120453577-chr12:120455749..120457974,2	MCF-7	breast:
13	chr12:120425209..120429306-chr12:120552934..120555400,5	MCF-7	breast:
14	chr12:120426002..120427624-chr12:120517341..120518989,2	MCF-7	breast:
15	chr12:120419275..120421989-chr12:120429002..120431271,2	K562	blood:
16	chr12:120442698..120445126-chr12:120517597..120519391,2	MCF-7	breast:
17	chr12:120462029..120464430-chr12:120473662..120476125,2	MCF-7	breast:
18	chr12:120460478..120462636-chr12:120462819..120465138,2	MCF-7	breast:
19	chr12:120479228..120480776-chr12:120492305..120495211,2	MCF-7	breast:
20	chr12:120472651..120475329-chr12:120480082..120481970,2	MCF-7	breast:
21	chr12:120420772..120424084-chr12:120424860..120426963,3	MCF-7	breast:
22	chr12:120425546..120427435-chr12:120477512..120479258,2	MCF-7	breast:
23	chr12:120410929..120415600-chr12:120416913..120420697,4	MCF-7	breast:
24	chr12:120462029..120464430-chr12:120473662..120476125,2	MCF-7	breast:
25	chr12:120513305..120516227-chr12:120637401..120638998,2	MCF-7	breast:
26	chr12:120420772..120424084-chr12:120424860..120426963,3	MCF-7	breast:
27	chr12:120451912..120458058-chr12:120461710..120466479,5	K562	blood:
28	chr12:120395843..120397395-chr12:120398275..120401201,2	MCF-7	breast:
29	chr12:120414941..120417051-chr12:120419035..120420939,2	MCF-7	breast:
30	chr12:120495318..120496991-chr12:120499571..120501871,2	K562	blood:
31	chr12:120504107..120508235-chr12:120509191..120512333,4	MCF-7	breast:
32	chr12:120446709..120448766-chr12:120465189..120467335,2	K562	blood:
33	chr12:120460478..120462636-chr12:120462819..120465138,2	MCF-7	breast:
34	chr12:120471763..120474758-chr12:120482350..120484738,2	K562	blood:
35	chr12:120481268..120483505-chr12:120486033..120487661,2	MCF-7	breast:
36	chr12:120451212..120453577-chr12:120455749..120457974,2	MCF-7	breast:
37	chr12:120427181..120429549-chr12:120460154..120462199,2	K562	blood:
38	chr12:120313729..120318058-chr12:120425281..120428238,3	K562	blood:
39	chr12:120425735..120427312-chr12:120553344..120556119,2	MCF-7	breast:
40	chr12:120426493..120428297-chr12:120534910..120538709,3	MCF-7	breast:
41	chr12:120426318..120428272-chr12:120451574..120453127,2	MCF-7	breast:
42	chr12:120426620..120429059-chr12:120727400..120730169,3	MCF-7	breast:
43	chr12:120425404..120428200-chr12:120435927..120438924,2	K562	blood:
44	chr12:120475158..120477800-chr12:120503210..120505823,2	K562	blood:
45	chr12:120426849..120430098-chr12:120430754..120434744,4	K562	blood:
46	chr12:120513025..120515032-chr12:120727834..120729863,2	MCF-7	breast:
47	chr12:120430661..120432265-chr12:120435208..120438105,2	K562	blood:
48	chr12:120428276..120430346-chr12:120637372..120639264,2	MCF-7	breast:
49	chr12:120426261..120428229-chr12:120638078..120640091,2	MCF-7	breast:
50	chr12:120427220..120428828-chr12:120429667..120432120,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC64-2	chr12:120412822-120412950	NONHSAT031098
2	lnc-RP1-127H14.3.1-4	chr12:120437657-120437716	NONHSAT031101
3	lnc-RP1-127H14.3.1-4	chr12:120438074-120438358	NONHSAT031101

No data

Variant related genes	Relation type
ENSG00000272464	TF binding region
ENSG00000255575	TF binding region
RPL35AP30	TF binding region
CCDC64	TF binding region
ENSG00000272464	CpG island
ENSG00000255575	CpG island
RPL35AP30	CpG island
CCDC64	CpG island
ENSG00000132481	chromatin interactions
ENSG00000267549	chromatin interactions
ENSG00000111737	chromatin interactions
ENSG00000255575	chromatin interactions
ENSG00000176915	chromatin interactions
ENSG00000131848	chromatin interactions
ENSG00000122966	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000255857	chromatin interactions
ENSG00000272464	chromatin interactions
ENSG00000226729	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000135127	chromatin interactions

Extended variants
information (count: 3624 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3624 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557057989	chr12:120393156-120393157	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs375091001	chr12:120393174-120393175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs35430416	chr12:120393183-120393184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs192573235	chr12:120393195-120393196	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs78955224	chr12:120393258-120393259	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559168168	chr12:120393298-120393299	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572793232	chr12:120393299-120393300	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs148867334	chr12:120393313-120393314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs561403707	chr12:120393325-120393326	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs563154299	chr12:120393336-120393337	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs185703473	chr12:120393337-120393338	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563804110	chr12:120393340-120393341	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs145357032	chr12:120393343-120393344	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs185247459	chr12:120393812-120393813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs535231356	chr12:120393859-120393860	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs567957537	chr12:120393900-120393901	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs148188959	chr12:120393947-120393948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs73404500	chr12:120393960-120393961	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs142022463	chr12:120393976-120393977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528062432	chr12:120393988-120393989	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs188587424	chr12:120393989-120393990	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs76743726	chr12:120394010-120394011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545920282	chr12:120394043-120394044	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs181041791	chr12:120394076-120394077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369432488	chr12:120394097-120394098	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs528310227	chr12:120394156-120394157	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs35683384	chr12:120394171-120394172	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs183666474	chr12:120394179-120394180	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs139900340	chr12:120394199-120394200	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs530689170	chr12:120394236-120394237	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs550568498	chr12:120394239-120394240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs188283291	chr12:120394262-120394263	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs149393748	chr12:120394287-120394288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs147485014	chr12:120394296-120394297	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs528098727	chr12:120394306-120394307	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs568587080	chr12:120394729-120394730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs78538196	chr12:120394735-120394736	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs551030526	chr12:120394762-120394763	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs61945800	chr12:120394782-120394783	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs151211056	chr12:120394796-120394797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs539450506	chr12:120394829-120394830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552920897	chr12:120394841-120394842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs140299304	chr12:120394868-120394869	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535611046	chr12:120394891-120394892	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs374301226	chr12:120394925-120394926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575397299	chr12:120394956-120394957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs544388050	chr12:120394964-120394965	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs7964604	chr12:120395002-120395003	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577975946	chr12:120395006-120395007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs571572686	chr12:120395009-120395010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	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
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1461 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120397800-120400200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:120400800-120401200	Bivalent Enhancer	HSMMtube	muscle
3	chr12:120401000-120401400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:120406200-120406400	Enhancers	Primary hematopoietic stem cells	blood
5	chr12:120410800-120411200	Enhancers	Gastric	stomach
6	chr12:120411200-120412400	Weak transcription	Gastric	stomach
7	chr12:120412400-120412600	Enhancers	Gastric	stomach
8	chr12:120415600-120416000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:120417800-120418200	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr12:120417800-120418400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr12:120417800-120418400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr12:120417800-120418400	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr12:120417800-120418400	Enhancers	Stomach Mucosa	stomach
14	chr12:120418000-120418200	Enhancers	NHEK	skin
15	chr12:120418000-120418400	Enhancers	GM12878-XiMat	blood
16	chr12:120424000-120425800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr12:120424600-120426200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr12:120425200-120425800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr12:120425400-120426000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
20	chr12:120425600-120425800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr12:120425600-120425800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
22	chr12:120425600-120425800	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr12:120425600-120425800	Bivalent Enhancer	HepG2	liver
24	chr12:120425600-120426000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
25	chr12:120425600-120426000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr12:120425600-120426000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:120425600-120426200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr12:120425600-120426200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr12:120425800-120426000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr12:120425800-120426000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
31	chr12:120425800-120426000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
32	chr12:120425800-120426000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
33	chr12:120425800-120426000	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr12:120425800-120426000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr12:120425800-120426000	Enhancers	Brain Cingulate Gyrus	brain
36	chr12:120425800-120426000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
37	chr12:120425800-120426000	Bivalent Enhancer	Fetal Brain Female	brain
38	chr12:120425800-120426000	Bivalent Enhancer	A549	lung
39	chr12:120425800-120426200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
40	chr12:120425800-120426200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr12:120425800-120426200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
42	chr12:120425800-120426200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:120425800-120426200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr12:120425800-120426200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:120425800-120426200	Enhancers	Primary B cells from peripheral blood	blood
46	chr12:120425800-120426200	Enhancers	Primary T cells fromperipheralblood	blood
47	chr12:120425800-120426200	Enhancers	Primary hematopoietic stem cells	blood
48	chr12:120425800-120426200	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr12:120425800-120426200	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr12:120425800-120426200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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