Variant report

Variant	nsv559019
Chromosome Location	chr12:57331741-57377509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:427)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:57335445-57335829	HepG2	liver:	n/a	n/a
2	ATF1	chr12:57362833-57363005	K562	blood:	n/a	n/a
3	BACH1	chr12:57335314-57335674	K562	blood:	n/a	n/a
4	BATF	chr12:57335428-57335611	GM12878	blood:	n/a	chr12:57335532-57335543
5	BATF	chr12:57335348-57335706	GM12878	blood:	n/a	chr12:57335532-57335543
6	CBX3	chr12:57337230-57337416	K562	blood:	n/a	n/a
7	CBX3	chr12:57359798-57360321	K562	blood:	n/a	n/a
8	CBX3	chr12:57352149-57352446	K562	blood:	n/a	n/a
9	CBX3	chr12:57337124-57337565	K562	blood:	n/a	n/a
10	CEBPB	chr12:57349345-57349760	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:57335437-57335773	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:57344105-57344290	K562	blood:	n/a	n/a
13	CEBPB	chr12:57344131-57344381	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:57349413-57349754	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:57335495-57335737	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:57349395-57349785	A549	lung:	n/a	n/a
17	CEBPB	chr12:57349273-57349896	A549	lung:	n/a	chr12:57349277-57349289
18	CEBPB	chr12:57349377-57349777	A549	lung:	n/a	n/a
19	CEBPB	chr12:57341747-57341956	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:57372221-57372421	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:57349354-57349829	MCF-7	breast:	n/a	n/a
22	CEBPB	chr12:57349414-57349774	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:57349426-57349758	IMR90	lung:	n/a	n/a
24	CEBPB	chr12:57372206-57372347	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:57344063-57344363	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:57344148-57344348	A549	lung:	n/a	n/a
27	CEBPB	chr12:57349459-57349683	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:57349466-57349757	K562	blood:	n/a	n/a
29	CEBPB	chr12:57349434-57349654	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPD	chr12:57335484-57335715	HepG2	liver:	n/a	n/a
31	CEBPD	chr12:57335487-57335862	HepG2	liver:	n/a	n/a
32	CEBPZ	chr12:57349503-57349558	HepG2	liver:	n/a	n/a
33	CEBPZ	chr12:57335613-57335694	HepG2	liver:	n/a	n/a
34	CHD2	chr12:57335484-57335763	HepG2	liver:	n/a	n/a
35	CREB1	chr12:57335061-57335390	A549	lung:	n/a	n/a
36	CTCF	chr12:57372766-57372848	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr12:57341500-57341650	HFF	foreskin:	n/a	n/a
38	CTCF	chr12:57351160-57351310	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr12:57341477-57341673	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr12:57341460-57341610	GM12872	blood:	n/a	n/a
41	CTCF	chr12:57351212-57351256	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:57341560-57341710	HVMF	connective:	n/a	n/a
43	CTCF	chr12:57341500-57341650	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr12:57341439-57341492	Lung_OC	lung:	n/a	n/a
45	CTCF	chr12:57335220-57335370	HCPEpiC	choroid plexus:	n/a	chr12:57335245-57335263
46	CTCF	chr12:57341540-57341690	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr12:57341560-57341710	A549	lung:	n/a	n/a
48	CTCF	chr12:57341468-57341755	GM12878	blood:	n/a	n/a
49	CTCF	chr12:57335160-57335310	NHEK	skin:	n/a	chr12:57335245-57335263
50	CTCF	chr12:57341557-57341674	NHEK	skin:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57335615-57335665	AG09319	gingival:	n/a
2	chr12:57345934-57345984	HEEpiC	esophagus:	n/a
3	chr12:57351732-57351782	CMK	blood:	n/a
4	chr12:57352514-57352564	AG04449	skin:	fetal
5	chr12:57345934-57345984	GM12891	blood:	n/a
6	chr12:57345407-57345457	SAEC	small airway:	n/a
7	chr12:57345407-57345457	RPTEC	kidney:	n/a
8	chr12:57335615-57335665	AG10803	skin:	n/a
9	chr12:57335615-57335665	Hela-S3	cervix:	n/a
10	chr12:57335615-57335665	MCF10A-Er-Src	breast:	n/a
11	chr12:57351732-57351782	AG09309	skin:	n/a
12	chr12:57335615-57335665	HIPEpiC	eye:	n/a
13	chr12:57351191-57351241	MCF10A-Er-Src	breast:	n/a
14	chr12:57335615-57335665	AG04449	skin:	fetal
15	chr12:57351191-57351241	NB4	blood:	n/a
16	chr12:57345407-57345457	GM06990	blood:	n/a
17	chr12:57351191-57351241	HUVEC	blood vessel:	n/a
18	chr12:57335615-57335665	BJ	skin:	n/a
19	chr12:57351732-57351782	HEK293	kidney:	embryo
20	chr12:57345407-57345457	Hepatocyte	liver:	n/a
21	chr12:57345407-57345457	GM19239	blood:	n/a
22	chr12:57352514-57352564	HEEpiC	esophagus:	n/a
23	chr12:57351191-57351241	AG09309	skin:	n/a
24	chr12:57351191-57351241	HRPEpiC	eye:	n/a
25	chr12:57335615-57335665	SKMC	muscle:	n/a
26	chr12:57345934-57345984	H1-hESC	embryonic stem cell:	embryo
27	chr12:57345934-57345984	Jurkat	blood:	n/a
28	chr12:57345934-57345984	SK-N-SH	brain:	n/a
29	chr12:57351732-57351782	AG09319	gingival:	n/a
30	chr12:57345407-57345457	IMR90	lung:	fetal
31	chr12:57335615-57335665	NHBE	bronchial:	n/a
32	chr12:57335615-57335665	K562	blood:	n/a
33	chr12:57351732-57351782	NHDF-neo	bronchial:	n/a
34	chr12:57335615-57335665	Hepatocyte	liver:	n/a
35	chr12:57345407-57345457	SK-N-MC	brain:	n/a
36	chr12:57351732-57351782	ProgFib	skin:	n/a
37	chr12:57351191-57351241	ProgFib	skin:	n/a
38	chr12:57345934-57345984	AoSMC	blood vessel:	n/a
39	chr12:57345934-57345984	HCT-116	colon:	n/a
40	chr12:57352514-57352564	HRCEpiC	kidney:	n/a
41	chr12:57351856-57351906	HRPEpiC	eye:	n/a
42	chr12:57352514-57352564	K562	blood:	n/a
43	chr12:57351856-57351906	HRE	kidney:	n/a
44	chr12:57345934-57345984	K562	blood:	n/a
45	chr12:57335615-57335665	T-47D	breast:	n/a
46	chr12:57352514-57352564	HCT-116	colon:	n/a
47	chr12:57352514-57352564	SK-N-SH	brain:	n/a
48	chr12:57345934-57345984	BJ	skin:	n/a
49	chr12:57345407-57345457	HMEC	breast:	n/a
50	chr12:57351191-57351241	NHDF-neo	bronchial:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57347864..57350577-chr12:57381566..57383920,2	MCF-7	breast:
2	chr12:57325236..57327206-chr12:57341575..57344080,3	MCF-7	breast:
3	chr12:57370332..57372734-chr12:57384660..57386537,2	K562	blood:
4	chr12:57350025..57351752-chr12:57359432..57361772,2	MCF-7	breast:
5	chr12:57319872..57321581-chr12:57347777..57350711,2	MCF-7	breast:
6	chr12:57319841..57322040-chr12:57335776..57337907,3	MCF-7	breast:
7	chr12:57326673..57329540-chr12:57347284..57349028,2	MCF-7	breast:
8	chr12:57374244..57376394-chr12:57378626..57381125,2	MCF-7	breast:
9	chr12:57233379..57233935-chr12:57351193..57351985,2	MCF-7	breast:
10	chr12:57341072..57342721-chr12:57384674..57386261,2	K562	blood:
11	chr12:57349241..57352181-chr12:57373731..57375876,2	MCF-7	breast:
12	chr12:57211985..57213673-chr12:57349961..57351583,2	MCF-7	breast:
13	chr12:57351472..57353366-chr12:57371615..57374205,2	MCF-7	breast:
14	chr12:57347827..57349628-chr12:57379616..57381539,3	MCF-7	breast:
15	chr12:57327540..57330418-chr12:57347371..57350395,3	K562	blood:
16	chr12:57349108..57350665-chr12:57479276..57481586,2	MCF-7	breast:
17	chr12:57322265..57324003-chr12:57330480..57332983,2	MCF-7	breast:
18	chr12:57324104..57327319-chr12:57348172..57351129,3	MCF-7	breast:
19	chr12:57342671..57345733-chr12:57481207..57484376,3	MCF-7	breast:
20	chr12:57144393..57147298-chr12:57377477..57379944,2	MCF-7	breast:
21	chr12:57327126..57329472-chr12:57342749..57346552,3	MCF-7	breast:
22	chr12:57341397..57342171-chr12:57399982..57400550,2	MCF-7	breast:
23	chr12:57347630..57349531-chr12:57349740..57351878,2	MCF-7	breast:
24	chr12:57338428..57340285-chr12:57349754..57351660,2	MCF-7	breast:
25	chr12:57327918..57330814-chr12:57348513..57351502,2	MCF-7	breast:
26	chr12:57347630..57349531-chr12:57349740..57351878,2	MCF-7	breast:
27	chr12:57350025..57351752-chr12:57359432..57361772,2	MCF-7	breast:
28	chr12:57347121..57349496-chr12:57383085..57384758,2	MCF-7	breast:
29	chr12:57351085..57351674-chr12:57381073..57381575,2	MCF-7	breast:
30	chr12:57341567..57342147-chr12:57381088..57381948,3	MCF-7	breast:
31	chr12:57328840..57330584-chr12:57335451..57337263,2	MCF-7	breast:
32	chr12:57340605..57343794-chr12:57388280..57390645,3	MCF-7	breast:
33	chr12:57338428..57340285-chr12:57349754..57351660,2	MCF-7	breast:
34	chr12:57330845..57332526-chr12:57336068..57338551,2	MCF-7	breast:
35	chr12:57081337..57084055-chr12:57347595..57351157,3	MCF-7	breast:
36	chr12:57326942..57329124-chr12:57333812..57335374,2	MCF-7	breast:
37	chr12:57326664..57330911-chr12:57334392..57337503,4	K562	blood:
38	chr12:57341090..57342031-chr12:57380872..57381968,6	MCF-7	breast:
39	chr12:57325326..57326887-chr12:57330449..57332916,2	K562	blood:
40	chr12:57323485..57328382-chr12:57328704..57333004,6	K562	blood:
41	chr12:57345020..57348622-chr12:57399414..57401826,4	MCF-7	breast:
42	chr12:57349736..57351385-chr12:57380003..57382609,2	MCF-7	breast:
43	chr12:57321673..57323369-chr12:57347515..57349644,2	MCF-7	breast:
44	chr12:57330845..57332526-chr12:57336068..57338551,2	MCF-7	breast:
45	chr12:57325090..57327714-chr12:57331602..57333568,3	MCF-7	breast:
46	chr12:57333897..57335886-chr12:57347612..57349669,2	MCF-7	breast:
47	chr12:57333897..57335886-chr12:57347612..57349669,2	MCF-7	breast:

No data

Variant related genes	Relation type
SDR9C7	TF binding region
RDH16	TF binding region
SDR9C7	CpG island
RDH16	CpG island
ENSG00000198056	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000166860	chromatin interactions
ENSG00000139547	chromatin interactions
ENSG00000170426	chromatin interactions
ENSG00000025423	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000258442	chromatin interactions

Extended variants
information (count: 1624 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1624 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs725957	chr12:57331741-57331742	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542214909	chr12:57331761-57331762	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs78975029	chr12:57331767-57331768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575699799	chr12:57331795-57331796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543240253	chr12:57331797-57331798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185873290	chr12:57331798-57331799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375991667	chr12:57331816-57331817	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532342663	chr12:57331818-57331819	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190589293	chr12:57331877-57331878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372461525	chr12:57331892-57331893	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs181718050	chr12:57331908-57331909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138568192	chr12:57331919-57331920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549362641	chr12:57331923-57331924	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs725956	chr12:57331936-57331937	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531818795	chr12:57331997-57331998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550432457	chr12:57332116-57332117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2629411	chr12:57332119-57332120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539010624	chr12:57332141-57332142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs725958	chr12:57332158-57332159	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11829786	chr12:57332232-57332233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566204811	chr12:57332245-57332246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs372921009	chr12:57332258-57332259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554118494	chr12:57332272-57332273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575763710	chr12:57332275-57332276	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs71459395	chr12:57332289-57332290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148806077	chr12:57332326-57332327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs61939618	chr12:57332357-57332358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558375533	chr12:57332404-57332405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576968822	chr12:57332490-57332491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540827471	chr12:57332524-57332525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs571218837	chr12:57332559-57332560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559614574	chr12:57332627-57332628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369358548	chr12:57332629-57332630	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574615066	chr12:57332634-57332635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543070541	chr12:57332658-57332659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs561252569	chr12:57332676-57332677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531883892	chr12:57332704-57332705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550295305	chr12:57332732-57332733	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs376852369	chr12:57332806-57332807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532753145	chr12:57332880-57332881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186379132	chr12:57332892-57332893	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs28584593	chr12:57332916-57332917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147153116	chr12:57332930-57332931	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547820624	chr12:57332940-57332941	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs28470625	chr12:57332983-57332984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs28621466	chr12:57332984-57332985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1813815	chr12:57333077-57333078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1813814	chr12:57333114-57333115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192397060	chr12:57333132-57333133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534838130	chr12:57333159-57333160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57325800-57335200	Weak transcription	Fetal Intestine Large	intestine
2	chr12:57326400-57335200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr12:57327000-57335200	Weak transcription	Spleen	Spleen
4	chr12:57328200-57335000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:57329400-57335200	Weak transcription	A549	lung
6	chr12:57329800-57335000	Weak transcription	NHEK	skin
7	chr12:57330000-57334600	Weak transcription	HMEC	breast
8	chr12:57330000-57335200	Weak transcription	K562	blood
9	chr12:57330200-57335200	Weak transcription	Esophagus	oesophagus
10	chr12:57333000-57335000	Weak transcription	Liver	Liver
11	chr12:57333200-57333800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:57333200-57333800	Enhancers	HepG2	liver
13	chr12:57333800-57335000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:57333800-57335000	Weak transcription	HepG2	liver
15	chr12:57334600-57336400	Enhancers	HMEC	breast
16	chr12:57335000-57335200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:57335000-57335200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:57335000-57335200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr12:57335000-57335200	Enhancers	HepG2	liver
20	chr12:57335000-57335200	Enhancers	NHEK	skin
21	chr12:57335000-57335600	Enhancers	GM12878-XiMat	blood
22	chr12:57335000-57336200	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr12:57335000-57336400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:57335000-57336400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr12:57335000-57336400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:57335000-57336400	Enhancers	HSMM	muscle
27	chr12:57335000-57337200	Enhancers	Liver	Liver
28	chr12:57335200-57335400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:57335200-57335400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr12:57335200-57335400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:57335200-57335400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:57335200-57335400	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr12:57335200-57335600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr12:57335200-57335600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr12:57335200-57335600	Enhancers	Duodenum Mucosa	Duodenum
36	chr12:57335200-57335800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:57335200-57335800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:57335200-57335800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr12:57335200-57335800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr12:57335200-57335800	Enhancers	Right Atrium	heart
41	chr12:57335200-57335800	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr12:57335200-57335800	Flanking Active TSS	Hela-S3	cervix
43	chr12:57335200-57335800	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr12:57335200-57335800	Flanking Active TSS	NHEK	skin
45	chr12:57335200-57336000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr12:57335200-57336000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:57335200-57336000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr12:57335200-57336000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:57335200-57336000	Enhancers	Adipose Nuclei	Adipose
50	chr12:57335200-57336000	Enhancers	Brain Inferior Temporal Lobe	brain

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