Variant report

Variant	nsv1007073
Chromosome Location	chr1:72419858-72734657
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	chr1:72503489-72503650	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72695593-72695955	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:72652447-72652641	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72707055-72707441	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
6	ATF1	chr1:72445759-72445819	K562	blood:	n/a	n/a
7	ATF2	chr1:72433360-72433766	GM12878	blood:	n/a	n/a
8	ATF2	chr1:72433342-72433674	GM12878	blood:	n/a	n/a
9	BACH1	chr1:72616564-72616622	H1-hESC	embryonic stem cell:	n/a	chr1:72616581-72616595
10	BATF	chr1:72433420-72433717	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:72433421-72433695	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:72563429-72563467	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:72519630-72519642	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:72588279-72588474	HepG2	liver:	n/a	chr1:72588315-72588326 chr1:72588317-72588328 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588315-72588328
15	CEBPB	chr1:72707099-72707502	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:72474879-72475236	IMR90	lung:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073 chr1:72474884-72474897
17	CEBPB	chr1:72707111-72707491	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:72707115-72707480	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:72588186-72588499	IMR90	lung:	n/a	chr1:72588315-72588326 chr1:72588317-72588328 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588315-72588328
20	CEBPB	chr1:72707157-72707388	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:72707185-72707435	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:72656927-72657197	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:72474893-72475164	A549	lung:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
24	CEBPB	chr1:72707115-72707489	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:72474965-72475177	K562	blood:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
26	CEBPB	chr1:72707117-72707455	A549	lung:	n/a	n/a
27	CEBPB	chr1:72700769-72701168	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:72663490-72663831	IMR90	lung:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
29	CEBPB	chr1:72568541-72568867	HepG2	liver:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
30	CEBPB	chr1:72568547-72568841	A549	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
31	CEBPB	chr1:72649995-72650046	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:72503347-72503641	HepG2	liver:	n/a	chr1:72503460-72503471 chr1:72503459-72503472
33	CEBPB	chr1:72700769-72701072	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:72707179-72707470	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr1:72568659-72568859	K562	blood:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
36	CEBPB	chr1:72474908-72475232	HepG2	liver:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
37	CEBPB	chr1:72731623-72731775	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr1:72568532-72568868	IMR90	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
39	CEBPB	chr1:72663573-72663744	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
40	CEBPB	chr1:72663467-72663765	H1-hESC	embryonic stem cell:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
41	CEBPB	chr1:72707137-72707455	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:72490316-72490600	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:72700804-72701056	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:72663464-72663828	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
45	CEBPB	chr1:72683845-72684065	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:72731625-72731886	IMR90	lung:	n/a	n/a
47	CEBPD	chr1:72707177-72707369	HepG2	liver:	n/a	n/a
48	CTCF	chr1:72503438-72504004	IMR90	lung:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
49	CTCF	chr1:72503560-72503710	GM12872	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
50	CTCF	chr1:72503540-72503690	HCPEpiC	choroid plexus:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72500866-72500916	LNCaP	prostate:	n/a
2	chr1:72500866-72500916	LNCaP	prostate:	n/a
3	chr1:72500866-72500916	SK-N-SH_RA	brain:	n/a
4	chr1:72566690-72566740	NB4	blood:	n/a
5	chr1:72566690-72566740	HCM	heart:	n/a
6	chr1:72500866-72500916	SKMC	muscle:	n/a
7	chr1:72566690-72566740	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:72500866-72500916	Jurkat	blood:	n/a
9	chr1:72566690-72566740	H1-hESC	embryonic stem cell:	embryo
10	chr1:72566690-72566740	ECC-1	luminal epithelium:	n/a
11	chr1:72500866-72500916	HCPEpiC	choroid plexus:	n/a
12	chr1:72566690-72566740	CMK	blood:	n/a
13	chr1:72566690-72566740	HL-60	blood:	n/a
14	chr1:72500866-72500916	MCF10A-Er-Src	breast:	n/a
15	chr1:72566690-72566740	BJ	skin:	n/a
16	chr1:72500866-72500916	HIPEpiC	eye:	n/a
17	chr1:72566690-72566740	MCF-7	breast:	n/a
18	chr1:72566690-72566740	NH-A	brain:	n/a
19	chr1:72500866-72500916	AG09309	skin:	n/a
20	chr1:72500866-72500916	ovcar-3	ovarian:	n/a
21	chr1:72500866-72500916	NH-A	brain:	n/a
22	chr1:72566690-72566740	NHBE	bronchial:	n/a
23	chr1:72500866-72500916	HMEC	breast:	n/a
24	chr1:72566690-72566740	HAEpiC	amniotic membrane:	n/a
25	chr1:72566690-72566740	HIPEpiC	eye:	n/a
26	chr1:72500866-72500916	PFSK-1	brain:	n/a
27	chr1:72500866-72500916	PrEC	prostate:	n/a
28	chr1:72500866-72500916	HAEpiC	amniotic membrane:	n/a
29	chr1:72500866-72500916	MCF-7	breast:	n/a
30	chr1:72500866-72500916	K562	blood:	n/a
31	chr1:72566690-72566740	AG04449	skin:	fetal
32	chr1:72500866-72500916	AG09319	gingival:	n/a
33	chr1:72566690-72566740	GM06990	blood:	n/a
34	chr1:72566690-72566740	GM12891	blood:	n/a
35	chr1:72566690-72566740	BE2_C	brain:	n/a
36	chr1:72566690-72566740	HCF	heart:	n/a
37	chr1:72500866-72500916	GM19239	blood:	n/a
38	chr1:72500866-72500916	U87	brain:	n/a
39	chr1:72500866-72500916	ProgFib	skin:	n/a
40	chr1:72566690-72566740	SKMC	muscle:	n/a
41	chr1:72566690-72566740	HCT-116	colon:	n/a
42	chr1:72566690-72566740	Jurkat	blood:	n/a
43	chr1:72500866-72500916	HUVEC	blood vessel:	n/a
44	chr1:72566690-72566740	Caco-2	colon:	n/a
45	chr1:72566690-72566740	SK-N-SH_RA	brain:	n/a
46	chr1:72566690-72566740	HRCEpiC	kidney:	n/a
47	chr1:72500866-72500916	Hela-S3	cervix:	n/a
48	chr1:72566690-72566740	T-47D	breast:	n/a
49	chr1:72566690-72566740	NT2-D1	testis:	n/a
50	chr1:72566690-72566740	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72053665..72054637-chr1:72503102..72503767,2	MCF-7	breast:
2	chr1:72472788..72474801-chr1:72492789..72495541,2	K562	blood:
3	chr1:72488016..72488819-chr1:72503014..72503883,2	K562	blood:
4	chr1:72708937..72709709-chr2:107409969..107410778,2	MCF-7	breast:
5	chr1:72467998..72470410-chr1:72472067..72474561,2	K562	blood:
6	chr1:72463115..72465700-chr1:72466215..72468715,2	K562	blood:
7	chr1:72487764..72489951-chr1:72495667..72497783,2	K562	blood:
8	chr1:72495707..72498590-chr1:72500903..72503366,2	K562	blood:
9	chr1:72488016..72488819-chr1:72503014..72503883,2	K562	blood:
10	chr1:72487764..72489951-chr1:72495667..72497783,2	K562	blood:
11	chr1:72495707..72498590-chr1:72500903..72503366,2	K562	blood:
12	chr1:72497090..72498877-chr1:72501866..72504493,2	K562	blood:
13	chr1:72497090..72498877-chr1:72501866..72504493,2	K562	blood:
14	chr1:72467998..72470410-chr1:72472067..72474561,2	K562	blood:
15	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:
16	chr1:71559221..71560259-chr1:72503170..72503778,3	MCF-7	breast:
17	chr1:72472788..72474801-chr1:72492789..72495541,2	K562	blood:
18	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:
19	chr1:72483188..72484849-chr1:72487728..72489377,2	K562	blood:
20	chr1:72463115..72465700-chr1:72466215..72468715,2	K562	blood:
21	chr1:72483188..72484849-chr1:72487728..72489377,2	K562	blood:

Variant related genes	Relation type
NEGR1	TF binding region
NEGR1	CpG island

Extended variants
information (count: 8899 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:8899 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541449310	chr1:72419868-72419869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149050458	chr1:72419877-72419878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532966357	chr1:72419888-72419889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551141097	chr1:72419938-72419939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543604004	chr1:72419955-72419956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145882460	chr1:72419962-72419963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532746629	chr1:72419968-72419969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552547867	chr1:72419984-72419985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560015836	chr1:72420062-72420063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528441158	chr1:72420126-72420127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17091980	chr1:72420131-72420132	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568546181	chr1:72420171-72420172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182138727	chr1:72420185-72420186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12078579	chr1:72420288-72420289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs142692491	chr1:72420301-72420302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539626992	chr1:72420323-72420324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552966449	chr1:72420357-72420358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549769522	chr1:72420400-72420401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566776343	chr1:72420495-72420496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200677494	chr1:72420515-72420516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201505047	chr1:72420516-72420517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535069485	chr1:72420565-72420566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187139524	chr1:72420569-72420570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574983695	chr1:72420583-72420584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531219930	chr1:72420590-72420591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543860516	chr1:72420599-72420600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191632649	chr1:72420621-72420622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577339270	chr1:72420634-72420635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544473396	chr1:72420654-72420655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184493931	chr1:72420661-72420662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533712170	chr1:72420720-72420721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537207538	chr1:72420727-72420728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147361233	chr1:72420766-72420767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528824503	chr1:72420777-72420778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138184148	chr1:72420780-72420781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377340137	chr1:72420870-72420871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141798253	chr1:72420906-72420907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530938123	chr1:72420919-72420920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550754526	chr1:72421016-72421017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs17091983	chr1:72421032-72421033	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532951103	chr1:72421045-72421046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546809721	chr1:72421055-72421056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188666294	chr1:72421137-72421138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569988576	chr1:72421146-72421147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192820058	chr1:72421180-72421181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150552805	chr1:72421275-72421276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7541380	chr1:72421349-72421350	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs527737501	chr1:72421380-72421381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557533594	chr1:72421398-72421399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185746063	chr1:72421402-72421403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cancer	21272361	CNVD
Obesity	21131291	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72416400-72422800	Weak transcription	Brain Angular Gyrus	brain
2	chr1:72419600-72420000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:72422200-72422400	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr1:72422400-72422800	Enhancers	Fetal Heart	heart
5	chr1:72422400-72422800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr1:72422400-72423000	Active TSS	Brain Substantia Nigra	brain
7	chr1:72422400-72423000	Enhancers	Colon Smooth Muscle	Colon
8	chr1:72422400-72423000	Active TSS	Osteobl	bone
9	chr1:72422400-72423200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:72422600-72423000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:72422600-72423000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:72422600-72423000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:72422600-72423000	Enhancers	Adipose Nuclei	Adipose
14	chr1:72422600-72423000	Active TSS	Brain Anterior Caudate	brain
15	chr1:72422600-72423000	Active TSS	Brain Cingulate Gyrus	brain
16	chr1:72422600-72423000	Active TSS	Right Atrium	heart
17	chr1:72422600-72423000	Active TSS	Stomach Smooth Muscle	stomach
18	chr1:72422800-72423000	Enhancers	Brain Angular Gyrus	brain
19	chr1:72422800-72423000	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr1:72423000-72423200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:72423000-72423200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:72423000-72423400	Weak transcription	Brain Angular Gyrus	brain
23	chr1:72423200-72423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:72427800-72428200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr1:72429800-72430000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:72429800-72430400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:72431400-72433600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr1:72432000-72432800	Enhancers	Brain Substantia Nigra	brain
29	chr1:72432200-72432800	Enhancers	Fetal Heart	heart
30	chr1:72432200-72434200	Enhancers	Dnd41	blood
31	chr1:72432400-72433800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:72432800-72437600	Weak transcription	Fetal Heart	heart
33	chr1:72433200-72434000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:72433400-72434200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:72433600-72434000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr1:72434000-72435200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:72434000-72439400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr1:72435200-72435800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:72435800-72439400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:72437600-72438000	Enhancers	Fetal Heart	heart
41	chr1:72438000-72443600	Weak transcription	Fetal Heart	heart
42	chr1:72439400-72439800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr1:72439400-72440000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:72440800-72441200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:72443600-72446200	Enhancers	Fetal Heart	heart
46	chr1:72444600-72447400	Enhancers	Dnd41	blood
47	chr1:72446200-72446600	Enhancers	Primary T cells from cord blood	blood
48	chr1:72446200-72446600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:72446200-72446600	Flanking Active TSS	Fetal Heart	heart
50	chr1:72446200-72446600	Enhancers	Thymus	Thymus

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