Variant report

Variant	nsv556886
Chromosome Location	chr12:628236-662448
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	chr12:656149-656351	HepG2	liver:	n/a	n/a
2	ATF3	chr12:656152-656565	A549	lung:	n/a	n/a
3	ATF3	chr12:656100-656281	K562	blood:	n/a	n/a
4	BCLAF1	chr12:656074-656472	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:656137-656470	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:632323-632391	HepG2	liver:	n/a	n/a
7	BHLHE40	chr12:661701-661984	K562	blood:	n/a	chr12:661801-661822 chr12:661807-661816 chr12:661807-661816 chr12:661805-661818 chr12:661808-661817
8	BHLHE40	chr12:656129-656368	K562	blood:	n/a	n/a
9	BRCA1	chr12:656191-656341	HepG2	liver:	n/a	n/a
10	BRCA1	chr12:656068-656439	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr12:656098-656486	K562	blood:	n/a	n/a
12	CBX3	chr12:641490-641751	K562	blood:	n/a	n/a
13	CCNT2	chr12:656103-656402	K562	blood:	n/a	n/a
14	CEBPB	chr12:631954-632154	HepG2	liver:	n/a	chr12:632053-632064
15	CEBPB	chr12:656127-656441	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:656149-656371	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:642021-642363	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:635046-635293	IMR90	lung:	n/a	chr12:635144-635157 chr12:635144-635155 chr12:635144-635157 chr12:635145-635156
19	CEBPB	chr12:637993-638179	HepG2	liver:	n/a	chr12:638080-638091 chr12:638153-638161
20	CEBPB	chr12:656230-656238	K562	blood:	n/a	n/a
21	CEBPB	chr12:631994-632121	HepG2	liver:	n/a	chr12:632053-632064
22	CEBPB	chr12:635038-635327	HepG2	liver:	n/a	chr12:635144-635157 chr12:635144-635155 chr12:635144-635157 chr12:635145-635156
23	CEBPD	chr12:656135-656384	HepG2	liver:	n/a	n/a
24	CHD1	chr12:655991-656867	IMR90	lung:	n/a	n/a
25	CHD2	chr12:656232-656384	K562	blood:	n/a	n/a
26	CHD2	chr12:656144-656438	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr12:656324-656326	HepG2	liver:	n/a	n/a
28	CREB1	chr12:656037-656458	A549	lung:	n/a	n/a
29	CREB1	chr12:646824-647320	ECC-1	luminal epithelium:	n/a	chr12:647157-647170
30	CTCF	chr12:656220-656370	HepG2	liver:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
31	CTCF	chr12:656180-656330	GM12873	blood:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
32	CTCF	chr12:655985-656579	A549	lung:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
33	CTCF	chr12:646840-646990	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:651267-651466	NHEK	skin:	n/a	n/a
35	CTCF	chr12:651340-651490	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr12:656180-656330	WI-38	lung:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
37	CTCF	chr12:648825-648855	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr12:655820-655970	GM12878	blood:	n/a	n/a
39	CTCF	chr12:656160-656310	K562	blood:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
40	CTCF	chr12:656220-656370	GM12873	blood:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
41	CTCF	chr12:656200-656350	BE2_C	brain:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
42	CTCF	chr12:656142-656421	LNCaP	prostate:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
43	CTCF	chr12:656180-656330	SAEC	small airway:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
44	CTCF	chr12:657273-657314	GM19239	blood:	n/a	n/a
45	CTCF	chr12:656559-656564	GM10248	blood:	n/a	n/a
46	CTCF	chr12:656260-656410	NHEK	skin:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
47	CTCF	chr12:656023-656464	K562	blood:	n/a	chr12:656271-656292 chr12:656278-656291 chr12:656277-656293 chr12:656282-656291 chr12:656278-656291 chr12:656276-656294 chr12:656279-656289
48	CTCF	chr12:651260-651410	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr12:651274-651462	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:646940-647090	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:656757-656807	NB4	blood:	n/a
2	chr12:656757-656807	NB4	blood:	n/a
3	chr12:630807-630857	AG04449	skin:	fetal
4	chr12:630892-630942	U87	brain:	n/a
5	chr12:655829-655879	AG09319	gingival:	n/a
6	chr12:658824-658874	GM12891	blood:	n/a
7	chr12:655829-655879	AG04449	skin:	fetal
8	chr12:650711-650761	AG04449	skin:	fetal
9	chr12:655964-656014	PrEC	prostate:	n/a
10	chr12:650711-650761	H1-hESC	embryonic stem cell:	embryo
11	chr12:657046-657096	HNPCEpiC	eye:	n/a
12	chr12:656726-656776	AG09309	skin:	n/a
13	chr12:630892-630942	SK-N-SH	brain:	n/a
14	chr12:656757-656807	SAEC	small airway:	n/a
15	chr12:630773-630823	HRPEpiC	eye:	n/a
16	chr12:630773-630823	ProgFib	skin:	n/a
17	chr12:630807-630857	Jurkat	blood:	n/a
18	chr12:650711-650761	SK-N-MC	brain:	n/a
19	chr12:630773-630823	K562	blood:	n/a
20	chr12:650711-650761	U87	brain:	n/a
21	chr12:630807-630857	GM06990	blood:	n/a
22	chr12:630773-630823	HIPEpiC	eye:	n/a
23	chr12:630773-630823	Hepatocyte	liver:	n/a
24	chr12:656423-656473	HCT-116	colon:	n/a
25	chr12:630892-630942	H1-hESC	embryonic stem cell:	embryo
26	chr12:658824-658874	CMK	blood:	n/a
27	chr12:658824-658874	HCT-116	colon:	n/a
28	chr12:630892-630942	SKMC	muscle:	n/a
29	chr12:630773-630823	NT2-D1	testis:	n/a
30	chr12:630892-630942	NT2-D1	testis:	n/a
31	chr12:656423-656473	NHDF-neo	bronchial:	n/a
32	chr12:655964-656014	HCT-116	colon:	n/a
33	chr12:655964-656014	AG10803	skin:	n/a
34	chr12:656703-656753	SK-N-SH_RA	brain:	n/a
35	chr12:630807-630857	PrEC	prostate:	n/a
36	chr12:657046-657096	HCF	heart:	n/a
37	chr12:655964-656014	T-47D	breast:	n/a
38	chr12:630807-630857	AG10803	skin:	n/a
39	chr12:658824-658874	HMEC	breast:	n/a
40	chr12:656726-656776	K562	blood:	n/a
41	chr12:658824-658874	ECC-1	luminal epithelium:	n/a
42	chr12:650711-650761	K562	blood:	n/a
43	chr12:630892-630942	AG09309	skin:	n/a
44	chr12:656423-656473	HRPEpiC	eye:	n/a
45	chr12:650711-650761	HCM	heart:	n/a
46	chr12:656757-656807	NH-A	brain:	n/a
47	chr12:630773-630823	ovcar-3	ovarian:	n/a
48	chr12:656703-656753	HepG2	liver:	n/a
49	chr12:630892-630942	NHDF-neo	bronchial:	n/a
50	chr12:656757-656807	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:562705..564349-chr12:655693..658061,2	MCF-7	breast:
2	chr12:650148..653007-chr12:654069..655622,2	K562	blood:
3	chr12:551206..552180-chr12:655785..656728,9	K562	blood:
4	chr12:626830..629195-chr12:631126..633825,2	K562	blood:
5	chr12:622355..623083-chr12:633209..633927,4	MCF-7	breast:
6	chr12:645596..647518-chr12:650603..652175,2	MCF-7	breast:
7	chr12:632266..634936-chr12:638337..639948,2	MCF-7	breast:
8	chr12:562112..562967-chr12:655719..656711,9	K562	blood:
9	chr12:655824..656332-chr19:54950316..54950832,2	MCF-7	breast:
10	chr12:622277..623146-chr12:632963..633980,6	MCF-7	breast:
11	chr12:559544..561291-chr12:645812..647419,2	K562	blood:
12	chr12:632266..634936-chr12:638337..639948,2	MCF-7	breast:
13	chr12:643233..646020-chr12:647234..650208,4	K562	blood:
14	chr12:549410..550324-chr12:655836..656812,2	K562	blood:
15	chr12:510904..511428-chr12:655804..656333,2	MCF-7	breast:
16	chr12:562205..562756-chr12:650853..651426,2	MCF-7	breast:
17	chr12:561789..563094-chr12:650609..651816,8	MCF-7	breast:
18	chr12:589171..589964-chr12:633097..633983,2	MCF-7	breast:
19	chr12:646530..648692-chr12:654414..656219,2	MCF-7	breast:
20	chr12:656034..658407-chr12:660278..663078,2	MCF-7	breast:
21	chr12:645596..647518-chr12:650603..652175,2	MCF-7	breast:
22	chr12:622362..623146-chr12:632963..633907,2	MCF-7	breast:
23	chr12:562086..563088-chr12:655521..657408,28	MCF-7	breast:
24	chr12:631879..633874-chr12:643555..645936,2	K562	blood:
25	chr12:646530..648692-chr12:654414..656219,2	MCF-7	breast:
26	chr12:561777..563247-chr12:653593..656972,77	MCF-7	breast:
27	chr12:627385..629195-chr12:632325..634029,2	K562	blood:
28	chr12:563544..564514-chr12:655825..656615,2	MCF-7	breast:
29	chr12:623934..625776-chr12:628238..630617,2	MCF-7	breast:
30	chr12:633000..634118-chr12:680824..681736,4	MCF-7	breast:
31	chr12:562103..563075-chr12:634406..635587,3	MCF-7	breast:
32	chr12:651428..654360-chr12:656676..659200,3	MCF-7	breast:
33	chr12:626830..629195-chr12:631126..633825,2	K562	blood:
34	chr12:618074..619807-chr12:641547..643283,2	MCF-7	breast:
35	chr12:617937..620233-chr12:642508..644938,2	MCF-7	breast:
36	chr12:631879..633874-chr12:643555..645936,2	K562	blood:
37	chr12:567792..568717-chr12:633148..633750,3	MCF-7	breast:
38	chr12:567922..570491-chr12:654360..656771,2	MCF-7	breast:
39	chr12:627385..629195-chr12:632325..634029,2	K562	blood:
40	chr12:563547..564241-chr12:655739..656517,2	MCF-7	breast:
41	chr12:643233..646020-chr12:647234..650208,3	K562	blood:
42	chr12:551367..552157-chr12:655845..657279,4	MCF-7	breast:
43	chr12:633000..634015-chr12:680744..681736,4	MCF-7	breast:
44	chr12:611154..613945-chr12:632166..635023,2	MCF-7	breast:
45	chr12:565368..565882-chr12:633415..633928,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC77-3	chr12:654048-654138	NONHSAT025345
2	lnc-CCDC77-3	chr12:652284-652371	NONHSAT025345
3	lnc-CCDC77-3	chr12:654306-654570	NONHSAT025345
4	lnc-CCDC77-3	chr12:653505-653600	NONHSAT025345

Variant related genes	Relation type
B4GALNT3	TF binding region
B4GALNT3	CpG island
ENSG00000267838	chromatin interactions
ENSG00000139044	chromatin interactions

Extended variants
information (count: 1680 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1680 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2286782	chr12:628236-628237	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568558521	chr12:628244-628245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535986892	chr12:628265-628266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548746299	chr12:628379-628380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372875667	chr12:628430-628431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375653796	chr12:628438-628439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368809081	chr12:628464-628465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575370632	chr12:628549-628550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567257105	chr12:628596-628597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71447491	chr12:628608-628609	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs572456473	chr12:628628-628629	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs539837633	chr12:628665-628666	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs2286783	chr12:628669-628670	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528336550	chr12:628670-628671	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs573382198	chr12:628671-628672	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs546211451	chr12:628688-628689	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs34817117	chr12:628698-628699	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs2369282	chr12:628723-628724	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs563873800	chr12:628724-628725	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs570619707	chr12:628763-628764	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs386375356	chr12:628764-628765	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs386375357	chr12:628778-628779	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs33954082	chr12:628779-628780	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs71045070	chr12:628780-628781	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs574464965	chr12:628781-628782	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs531024428	chr12:628817-628818	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs371231754	chr12:628818-628819	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs74341002	chr12:628823-628824	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs528836725	chr12:628885-628886	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs547002073	chr12:628899-628900	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs542898153	chr12:628926-628927	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs568493256	chr12:628939-628940	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs529377149	chr12:628940-628941	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs550811748	chr12:628972-628973	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs61916634	chr12:628983-628984	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs150722154	chr12:628987-628988	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs573491530	chr12:628993-628994	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs4980930	chr12:629054-629055	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557977078	chr12:629055-629056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369101659	chr12:629057-629058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566418709	chr12:629060-629061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571112209	chr12:629077-629078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186979421	chr12:629092-629093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554915991	chr12:629108-629109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573319503	chr12:629138-629139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs57974226	chr12:629221-629222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532382693	chr12:629252-629253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555990687	chr12:629253-629254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs61916636	chr12:629255-629256	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546072788	chr12:629257-629258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Autism	22495309	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD

Chromatin state (count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:620200-633200	Weak transcription	NHEK	skin
2	chr12:620400-637600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:620400-638200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr12:620600-630600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr12:620600-632800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:620600-636600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:620600-637800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:620800-648000	Weak transcription	Pancreas	Pancrea
9	chr12:622800-633400	Weak transcription	Gastric	stomach
10	chr12:623000-628800	Weak transcription	Right Atrium	heart
11	chr12:623200-629200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr12:623200-633200	Weak transcription	Right Ventricle	heart
13	chr12:623400-628400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:625400-630200	Enhancers	Fetal Heart	heart
15	chr12:626000-633400	Weak transcription	Stomach Mucosa	stomach
16	chr12:626800-635200	Weak transcription	Aorta	Aorta
17	chr12:627000-628800	Weak transcription	Left Ventricle	heart
18	chr12:627800-628600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr12:627800-628600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr12:628000-628600	Enhancers	Brain Anterior Caudate	brain
21	chr12:628000-628600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr12:628400-629800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:628600-629000	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr12:628600-629200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr12:628600-632000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:628800-629200	Enhancers	Right Atrium	heart
27	chr12:628800-629400	Enhancers	Left Ventricle	heart
28	chr12:629000-629600	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr12:629000-630800	Enhancers	Placenta	Placenta
30	chr12:629200-630600	Weak transcription	Right Atrium	heart
31	chr12:629200-630800	Enhancers	Placenta Amnion	Placenta Amnion
32	chr12:629200-638200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr12:629400-629800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr12:629400-630400	Weak transcription	Left Ventricle	heart
35	chr12:629800-632200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:629800-633000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr12:630200-630400	Flanking Active TSS	Fetal Heart	heart
38	chr12:630400-630600	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr12:630400-630800	Enhancers	Fetal Heart	heart
40	chr12:630400-631800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr12:630400-633800	Enhancers	Left Ventricle	heart
42	chr12:630600-631400	Enhancers	Right Atrium	heart
43	chr12:630600-631800	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr12:630800-631600	Genic enhancers	Fetal Heart	heart
45	chr12:631200-631400	Enhancers	Fetal Thymus	thymus
46	chr12:631200-631800	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr12:631200-632000	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr12:631200-632400	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr12:631200-634000	Enhancers	HepG2	liver
50	chr12:631400-636400	Weak transcription	Right Atrium	heart

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