Variant report

Variant	nsv535160
Chromosome Location	chr1:152031280-152050179
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:83)
CpG islands
(count:61)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:83 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:152043490-152043995	K562	blood:	n/a	n/a
2	ATF1	chr1:152042097-152042261	K562	blood:	n/a	n/a
3	BACH1	chr1:152047735-152047756	K562	blood:	n/a	n/a
4	BHLHE40	chr1:152043476-152043885	K562	blood:	n/a	n/a
5	CBX3	chr1:152043446-152044040	K562	blood:	n/a	n/a
6	CCNT2	chr1:152043465-152043906	K562	blood:	n/a	n/a
7	CEBPB	chr1:152043525-152043833	K562	blood:	n/a	n/a
8	CREB1	chr1:152043421-152044012	K562	blood:	n/a	chr1:152043680-152043693
9	CREB1	chr1:152043328-152044087	K562	blood:	n/a	chr1:152043680-152043693
10	CTCF	chr1:152034460-152034610	NHEK	skin:	n/a	n/a
11	CTCF	chr1:152034484-152034694	MCF-7	breast:	n/a	n/a
12	CTCF	chr1:152034540-152034690	MCF-7	breast:	n/a	n/a
13	CTCF	chr1:152034523-152034673	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:152034499-152034672	K562	blood:	n/a	n/a
15	CTCF	chr1:152034543-152034644	GM12878	blood:	n/a	n/a
16	CTCF	chr1:152034420-152034570	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:152034540-152034690	GM06990	blood:	n/a	n/a
18	CTCF	chr1:152034431-152034751	K562	blood:	n/a	n/a
19	CTCF	chr1:152034561-152034598	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr1:152034400-152034947	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:152038000-152038150	GM12866	blood:	n/a	n/a
22	CTCF	chr1:152043387-152043513	K562	blood:	n/a	n/a
23	CTCF	chr1:152034565-152034603	GM10266	blood:	n/a	n/a
24	CTCF	chr1:152034587-152034672	NHEK	skin:	n/a	n/a
25	CTCF	chr1:152034560-152034710	HMEC	breast:	n/a	n/a
26	CTCF	chr1:152048080-152048230	AG10803	skin:	n/a	n/a
27	CTCF	chr1:152034571-152034602	LNCaP	prostate:	n/a	n/a
28	CUX1	chr1:152043427-152043608	K562	blood:	n/a	n/a
29	E2F6	chr1:152043507-152043742	K562	blood:	n/a	n/a
30	EGR1	chr1:152042103-152042367	K562	blood:	n/a	n/a
31	EGR1	chr1:152042108-152042310	K562	blood:	n/a	n/a
32	ELF1	chr1:152043496-152043944	K562	blood:	n/a	n/a
33	ELK1	chr1:152043633-152043832	K562	blood:	n/a	n/a
34	EP300	chr1:152043558-152043918	K562	blood:	n/a	n/a
35	HCFC1	chr1:152043202-152043905	K562	blood:	n/a	n/a
36	HEY1	chr1:152043475-152043783	K562	blood:	n/a	n/a
37	JUND	chr1:152043491-152044127	K562	blood:	n/a	chr1:152043980-152043991
38	MAFK	chr1:152043533-152044023	K562	blood:	n/a	n/a
39	MAX	chr1:152043464-152043976	K562	blood:	n/a	n/a
40	MAX	chr1:152043460-152043970	K562	blood:	n/a	n/a
41	MAX	chr1:152043485-152043819	K562	blood:	n/a	n/a
42	MAZ	chr1:152043479-152044099	K562	blood:	n/a	n/a
43	MXI1	chr1:152031408-152031438	GM12878	blood:	n/a	n/a
44	MYC	chr1:152043441-152044067	K562	blood:	n/a	n/a
45	MYC	chr1:152043507-152043635	H1-hESC	embryonic stem cell:	n/a	n/a
46	MYC	chr1:152043521-152044022	K562	blood:	n/a	n/a
47	MYC	chr1:152045710-152045742	K562	blood:	n/a	n/a
48	NFE2	chr1:152034896-152034913	GM12878	blood:	n/a	n/a
49	NFYA	chr1:152043519-152044057	K562	blood:	n/a	chr1:152043823-152043841
50	POLR2A	chr1:152041695-152042347	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152040891-152040941	SK-N-SH	brain:	n/a
2	chr1:152040891-152040941	SK-N-SH_RA	brain:	n/a
3	chr1:152040891-152040941	MCF10A-Er-Src	breast:	n/a
4	chr1:152040891-152040941	AG10803	skin:	n/a
5	chr1:152040891-152040941	H1-hESC	embryonic stem cell:	embryo
6	chr1:152040891-152040941	HCT-116	colon:	n/a
7	chr1:152040891-152040941	GM06990	blood:	n/a
8	chr1:152040891-152040941	HRE	kidney:	n/a
9	chr1:152040891-152040941	Hela-S3	cervix:	n/a
10	chr1:152040891-152040941	GM19239	blood:	n/a
11	chr1:152040891-152040941	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:152040891-152040941	CMK	blood:	n/a
13	chr1:152040891-152040941	K562	blood:	n/a
14	chr1:152040891-152040941	HAEpiC	amniotic membrane:	n/a
15	chr1:152040891-152040941	SAEC	small airway:	n/a
16	chr1:152040891-152040941	ECC-1	luminal epithelium:	n/a
17	chr1:152040891-152040941	Hepatocyte	liver:	n/a
18	chr1:152040891-152040941	NHBE	bronchial:	n/a
19	chr1:152040891-152040941	HCPEpiC	choroid plexus:	n/a
20	chr1:152040891-152040941	AG09309	skin:	n/a
21	chr1:152040891-152040941	NT2-D1	testis:	n/a
22	chr1:152040891-152040941	ProgFib	skin:	n/a
23	chr1:152040891-152040941	AG04449	skin:	fetal
24	chr1:152040891-152040941	PFSK-1	brain:	n/a
25	chr1:152040891-152040941	IMR90	lung:	fetal
26	chr1:152040891-152040941	T-47D	breast:	n/a
27	chr1:152040891-152040941	LNCaP	prostate:	n/a
28	chr1:152040891-152040941	A549	lung:	n/a
29	chr1:152040891-152040941	HRCEpiC	kidney:	n/a
30	chr1:152040891-152040941	MCF-7	breast:	n/a
31	chr1:152040891-152040941	SKMC	muscle:	n/a
32	chr1:152040891-152040941	HEK293	kidney:	embryo
33	chr1:152040891-152040941	AoSMC	blood vessel:	n/a
34	chr1:152040891-152040941	HRPEpiC	eye:	n/a
35	chr1:152040891-152040941	GM12892	blood:	n/a
36	chr1:152040891-152040941	Caco-2	colon:	n/a
37	chr1:152040891-152040941	NB4	blood:	n/a
38	chr1:152040891-152040941	PrEC	prostate:	n/a
39	chr1:152040891-152040941	RPTEC	kidney:	n/a
40	chr1:152040891-152040941	HEEpiC	esophagus:	n/a
41	chr1:152040891-152040941	NH-A	brain:	n/a
42	chr1:152040891-152040941	SK-N-MC	brain:	n/a
43	chr1:152040891-152040941	BE2_C	brain:	n/a
44	chr1:152040891-152040941	HMEC	breast:	n/a
45	chr1:152040891-152040941	PANC-1	pancreas:	n/a
46	chr1:152040891-152040941	GM12878	blood:	n/a
47	chr1:152040891-152040941	HNPCEpiC	eye:	n/a
48	chr1:152040891-152040941	U87	brain:	n/a
49	chr1:152040891-152040941	HIPEpiC	eye:	n/a
50	chr1:152040891-152040941	GM12891	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:152035307..152036993-chr1:152090240..152092063,2	MCF-7	breast:
2	chr1:152037743..152041105-chr1:152057855..152061211,4	MCF-7	breast:
3	chr1:152032483..152034728-chr1:152036696..152039223,2	MCF-7	breast:
4	chr1:152032363..152034553-chr1:152034554..152037486,2	K562	blood:
5	chr1:152028981..152031946-chr1:152086373..152089708,3	MCF-7	breast:
6	chr1:152009006..152012599-chr1:152042652..152045260,3	MCF-7	breast:
7	chr1:152035579..152037505-chr1:152066956..152069151,2	MCF-7	breast:
8	chr1:152039144..152040996-chr1:152081393..152082940,2	MCF-7	breast:
9	chr1:152036988..152039717-chr1:152040863..152043429,2	MCF-7	breast:
10	chr1:152043286..152045269-chr1:152045806..152047940,2	MCF-7	breast:
11	chr1:151964883..151966894-chr1:152045649..152048031,2	MCF-7	breast:
12	chr1:152015038..152017960-chr1:152041369..152043398,2	K562	blood:
13	chr1:152034771..152037700-chr1:152041582..152044104,2	K562	blood:
14	chr1:152043286..152045269-chr1:152045806..152047940,2	MCF-7	breast:
15	chr1:152032483..152034728-chr1:152036696..152039223,2	MCF-7	breast:
16	chr1:152033237..152035148-chr1:152105108..152107220,2	MCF-7	breast:
17	chr1:152025442..152027599-chr1:152031049..152032717,2	MCF-7	breast:
18	chr1:152039926..152042632-chr20:45914039..45916359,2	MCF-7	breast:
19	chr1:152043433..152046409-chr1:152058160..152060472,2	MCF-7	breast:
20	chr1:152034771..152037700-chr1:152041582..152044104,2	K562	blood:
21	chr1:152017063..152020496-chr1:152029370..152032673,3	MCF-7	breast:
22	chr1:152034269..152035066-chr1:152153200..152153993,2	MCF-7	breast:
23	chr1:152030113..152032608-chr1:152130508..152132764,2	MCF-7	breast:
24	chr1:152025453..152028368-chr1:152034422..152037316,2	MCF-7	breast:
25	chr1:152030574..152033939-chr1:152036045..152039626,3	MCF-7	breast:
26	chr1:152003216..152005599-chr1:152046745..152048519,2	MCF-7	breast:
27	chr1:152033820..152035009-chr1:152157797..152158750,5	MCF-7	breast:
28	chr1:152034141..152035088-chr1:152154621..152155465,4	MCF-7	breast:
29	chr1:152030574..152033939-chr1:152036045..152039626,3	MCF-7	breast:
30	chr1:151963478..151966164-chr1:152034613..152037123,3	MCF-7	breast:
31	chr1:152032812..152034753-chr1:152098910..152100474,2	MCF-7	breast:
32	chr1:152042308..152047029-chr1:152081777..152083465,4	MCF-7	breast:
33	chr1:152032363..152034553-chr1:152034554..152037486,2	K562	blood:
34	chr1:152020471..152023395-chr1:152032705..152034549,2	MCF-7	breast:
35	chr1:152025929..152027831-chr1:152031273..152033941,2	K562	blood:
36	chr1:152036988..152039717-chr1:152040863..152043429,2	MCF-7	breast:
37	chr1:151963049..151965685-chr1:152040873..152042644,2	MCF-7	breast:
38	chr1:152024848..152026371-chr1:152036045..152037587,2	MCF-7	breast:
39	chr1:151958341..151960703-chr1:152042436..152044270,2	MCF-7	breast:
40	chr1:152043416..152046211-chr1:152074806..152077684,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPTLC1P4	TF binding region
SPTLC1P4	CpG island
ENSG00000159450	chromatin interactions
ENSG00000197747	chromatin interactions
ENSG00000215853	chromatin interactions
ENSG00000163191	chromatin interactions

Extended variants
information (count: 349 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142930264	chr1:152031306-152031307	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs146117265	chr1:152031375-152031376	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs563034192	chr1:152031389-152031390	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs571701709	chr1:152031537-152031538	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs191516977	chr1:152031547-152031548	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs149375551	chr1:152031588-152031589	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs567124745	chr1:152031589-152031590	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs199929137	chr1:152031602-152031603	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs144679071	chr1:152031604-152031605	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs374806318	chr1:152031619-152031620	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs550400108	chr1:152031628-152031629	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs556052143	chr1:152031655-152031656	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs77526288	chr1:152031734-152031735	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs182441098	chr1:152031852-152031853	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs376049901	chr1:152031878-152031879	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs558302092	chr1:152031911-152031912	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs117070220	chr1:152031958-152031959	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540774191	chr1:152032004-152032005	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554367217	chr1:152032038-152032039	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371546248	chr1:152032057-152032058	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs574300926	chr1:152032089-152032090	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543316446	chr1:152032176-152032177	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563156557	chr1:152032302-152032303	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs576702092	chr1:152032343-152032344	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs545378765	chr1:152032391-152032392	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs142908973	chr1:152032400-152032401	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs527735777	chr1:152032420-152032421	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547493059	chr1:152032435-152032436	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs560712094	chr1:152032470-152032471	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529858828	chr1:152032491-152032492	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs549593512	chr1:152032535-152032536	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569917672	chr1:152032550-152032551	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs187817025	chr1:152032583-152032584	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552145874	chr1:152032641-152032642	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565550701	chr1:152032642-152032643	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147423385	chr1:152032661-152032662	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577303200	chr1:152034699-152034700	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545672034	chr1:152034711-152034712	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs540145391	chr1:152034712-152034713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559547241	chr1:152034755-152034756	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528351799	chr1:152034842-152034843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542156855	chr1:152034977-152034978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150419882	chr1:152035017-152035018	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565133659	chr1:152035055-152035056	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550577006	chr1:152035071-152035072	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188277522	chr1:152035136-152035137	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533088365	chr1:152035141-152035142	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs552492460	chr1:152035160-152035161	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs542538648	chr1:152035178-152035179	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565936509	chr1:152035198-152035199	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152035800-152036000	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
2	chr1:152040000-152041000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr1:152040200-152040400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:152040200-152040800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr1:152040200-152041400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr1:152040200-152041600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr1:152040200-152041800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr1:152040400-152040800	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr1:152040400-152040800	Enhancers	Fetal Intestine Large	intestine
10	chr1:152040800-152041000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
11	chr1:152040800-152041200	Weak transcription	Fetal Intestine Large	intestine
12	chr1:152040800-152041600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:152041000-152041600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
14	chr1:152041200-152041400	Enhancers	Fetal Intestine Large	intestine
15	chr1:152041400-152042800	Weak transcription	Fetal Intestine Large	intestine
16	chr1:152042400-152044000	Enhancers	Stomach Mucosa	stomach
17	chr1:152042800-152044200	Enhancers	Fetal Intestine Large	intestine
18	chr1:152043000-152044000	Enhancers	Placenta	Placenta
19	chr1:152043200-152043400	Enhancers	K562	blood
20	chr1:152043400-152043600	Flanking Active TSS	K562	blood
21	chr1:152043600-152043800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
22	chr1:152043600-152043800	Enhancers	K562	blood
23	chr1:152043600-152044000	ZNF genes & repeats	Aorta	Aorta
24	chr1:152043800-152044000	Flanking Active TSS	K562	blood
25	chr1:152044000-152044400	Enhancers	K562	blood
26	chr1:152047600-152048400	Enhancers	Pancreatic Islets	Pancreatic Islet

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