Variant report

Variant	esv3431664
Chromosome Location	chr1:146890997-146917617
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:146908268-146908309	K562	blood:	n/a	n/a
2	CEBPB	chr1:146891745-146891945	HepG2	liver:	n/a	n/a
3	CEBPB	chr1:146891751-146891948	A549	lung:	n/a	n/a
4	CTCF	chr1:146906555-146906565	GM20000	blood:	n/a	n/a
5	CTCF	chr1:146906185-146906243	GM20000	blood:	n/a	n/a
6	CTCF	chr1:146901100-146901180	Fibrobl	skin:	n/a	n/a
7	E2F4	chr1:146911020-146911148	MCF10A-Er-Src	breast:	n/a	n/a
8	EBF1	chr1:146906688-146907086	GM12878	blood:	n/a	chr1:146906892-146906903 chr1:146906894-146906903
9	FOS	chr1:146910831-146911013	MCF10A-Er-Src	breast:	n/a	n/a
10	FOSL2	chr1:146895259-146895471	HepG2	liver:	n/a	n/a
11	FOXA1	chr1:146895307-146895480	T-47D	breast:	n/a	n/a
12	FOXA1	chr1:146895084-146895502	HepG2	liver:	n/a	n/a
13	FOXA2	chr1:146895183-146895531	A549	lung:	n/a	n/a
14	FOXA2	chr1:146895137-146895586	A549	lung:	n/a	n/a
15	GTF2F1	chr1:146894767-146894897	K562	blood:	n/a	n/a
16	HEY1	chr1:146894808-146895099	K562	blood:	n/a	n/a
17	HEY1	chr1:146895142-146895447	K562	blood:	n/a	n/a
18	HEY1	chr1:146895190-146895465	K562	blood:	n/a	n/a
19	MAFK	chr1:146905324-146905564	HepG2	liver:	n/a	chr1:146905398-146905409 chr1:146905397-146905408
20	MAX	chr1:146894816-146895022	MCF-7	breast:	n/a	n/a
21	MYC	chr1:146891287-146891291	MCF-7	breast:	n/a	n/a
22	MYC	chr1:146891258-146891285	MCF-7	breast:	n/a	n/a
23	MYC	chr1:146891248-146891257	MCF-7	breast:	n/a	n/a
24	POLR2A	chr1:146893492-146893679	MCF-7	breast:	n/a	n/a
25	POLR2A	chr1:146895184-146895456	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr1:146910151-146910234	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr1:146902135-146902292	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr1:146904319-146904415	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr1:146895181-146895450	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr1:146895183-146895484	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr1:146910242-146910356	ProgFib	skin:	n/a	n/a
32	POLR2A	chr1:146894943-146895610	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr1:146894797-146894999	K562	blood:	n/a	n/a
34	SETDB1	chr1:146916155-146916379	U2OS	brain:	n/a	n/a
35	SRF	chr1:146895312-146895429	GM12878	blood:	n/a	n/a
36	TAF1	chr1:146895112-146895459	H1-hESC	embryonic stem cell:	n/a	n/a
37	TAF1	chr1:146895102-146895505	H1-hESC	embryonic stem cell:	n/a	n/a
38	TBL1XR1	chr1:146894733-146894846	K562	blood:	n/a	n/a
39	TBP	chr1:146894811-146894962	K562	blood:	n/a	n/a
40	USF2	chr1:146893697-146893724	GM12878	blood:	n/a	n/a
41	YY1	chr1:146894743-146895054	H1-hESC	embryonic stem cell:	n/a	n/a
42	YY1	chr1:146894779-146894986	K562	blood:	n/a	n/a
43	YY1	chr1:146894793-146895014	ECC-1	luminal epithelium:	n/a	n/a
44	YY1	chr1:146894770-146895016	ECC-1	luminal epithelium:	n/a	n/a
45	YY1	chr1:146894811-146895022	K562	blood:	n/a	n/a
46	YY1	chr1:146894786-146895001	SK-N-SH_RA	brain:	n/a	n/a
47	YY1	chr1:146894760-146895009	H1-hESC	embryonic stem cell:	n/a	n/a
48	ZNF274	chr1:146915999-146916876	K562	blood:	n/a	n/a
49	ZNF274	chr1:146916090-146916498	NT2-D1	testis:	n/a	n/a
50	ZNF274	chr1:146916110-146916778	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146895247-146895297	HL-60	blood:	n/a
2	chr1:146895247-146895297	SAEC	small airway:	n/a
3	chr1:146895247-146895297	AoSMC	blood vessel:	n/a
4	chr1:146895247-146895297	NB4	blood:	n/a
5	chr1:146895247-146895297	HRE	kidney:	n/a
6	chr1:146895247-146895297	HMEC	breast:	n/a
7	chr1:146895247-146895297	IMR90	lung:	fetal
8	chr1:146895247-146895297	HepG2	liver:	n/a
9	chr1:146895247-146895297	Caco-2	colon:	n/a
10	chr1:146895247-146895297	AG04449	skin:	fetal
11	chr1:146895247-146895297	ovcar-3	ovarian:	n/a
12	chr1:146895247-146895297	ECC-1	luminal epithelium:	n/a
13	chr1:146895247-146895297	RPTEC	kidney:	n/a
14	chr1:146895247-146895297	NHDF-neo	bronchial:	n/a
15	chr1:146895247-146895297	HEK293	kidney:	embryo
16	chr1:146895247-146895297	PrEC	prostate:	n/a
17	chr1:146895247-146895297	SKMC	muscle:	n/a
18	chr1:146895247-146895297	PANC-1	pancreas:	n/a
19	chr1:146895247-146895297	CMK	blood:	n/a
20	chr1:146895247-146895297	PFSK-1	brain:	n/a
21	chr1:146895247-146895297	AG10803	skin:	n/a
22	chr1:146895247-146895297	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:146895247-146895297	HUVEC	blood vessel:	n/a
24	chr1:146895247-146895297	HEEpiC	esophagus:	n/a
25	chr1:146895247-146895297	GM12892	blood:	n/a
26	chr1:146895247-146895297	BE2_C	brain:	n/a
27	chr1:146895247-146895297	GM12878	blood:	n/a
28	chr1:146895247-146895297	Jurkat	blood:	n/a
29	chr1:146895247-146895297	HAEpiC	amniotic membrane:	n/a
30	chr1:146895247-146895297	SK-N-MC	brain:	n/a
31	chr1:146895247-146895297	MCF10A-Er-Src	breast:	n/a
32	chr1:146895247-146895297	K562	blood:	n/a
33	chr1:146895247-146895297	H1-hESC	embryonic stem cell:	embryo
34	chr1:146895247-146895297	ProgFib	skin:	n/a
35	chr1:146895247-146895297	HRPEpiC	eye:	n/a
36	chr1:146895247-146895297	AG04450	lung:	fetal
37	chr1:146895247-146895297	GM06990	blood:	n/a
38	chr1:146895247-146895297	U87	brain:	n/a
39	chr1:146895247-146895297	BJ	skin:	n/a
40	chr1:146895247-146895297	A549	lung:	n/a
41	chr1:146895247-146895297	AG09309	skin:	n/a
42	chr1:146895247-146895297	HCT-116	colon:	n/a
43	chr1:146895247-146895297	AG09319	gingival:	n/a
44	chr1:146895247-146895297	HCM	heart:	n/a
45	chr1:146895247-146895297	HCPEpiC	choroid plexus:	n/a
46	chr1:146895247-146895297	Hela-S3	cervix:	n/a
47	chr1:146895247-146895297	MCF-7	breast:	n/a
48	chr1:146895247-146895297	LNCaP	prostate:	n/a
49	chr1:146895247-146895297	NHBE	bronchial:	n/a
50	chr1:146895247-146895297	NH-A	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:146892606..146894867-chr1:146909100..146911293,2	MCF-7	breast:
2	chr1:146904930..146907237-chr1:146910258..146912746,2	MCF-7	breast:
3	chr1:146889760..146891342-chr1:146892775..146894723,2	K562	blood:
4	chr1:146899574..146902487-chr1:146902750..146904367,2	K562	blood:
5	chr1:146907560..146910519-chr1:146910936..146913596,2	K562	blood:
6	chr1:146903700..146906235-chr1:146908558..146911092,2	MCF-7	breast:
7	chr1:146892606..146894867-chr1:146909100..146911293,2	MCF-7	breast:
8	chr1:146902569..146904865-chr1:146917610..146920209,2	MCF-7	breast:
9	chr1:146902569..146904865-chr1:146917610..146920209,2	MCF-7	breast:
10	chr1:146907560..146910519-chr1:146910936..146913596,2	K562	blood:
11	chr1:146892685..146894306-chr1:146902333..146904733,2	K562	blood:
12	chr1:146902129..146904025-chr1:146907523..146909259,2	MCF-7	breast:
13	chr1:146904930..146907237-chr1:146910258..146912746,2	MCF-7	breast:
14	chr1:146892685..146894306-chr1:146902333..146904733,2	K562	blood:
15	chr1:146902129..146904025-chr1:146907523..146909259,2	MCF-7	breast:
16	chr1:146899574..146902487-chr1:146902750..146904367,2	K562	blood:
17	chr1:146904036..146904863-chr6:92344357..92345281,2	MCF-7	breast:
18	chr1:146903700..146906235-chr1:146908558..146911092,2	MCF-7	breast:
19	chr1:146900267..146901994-chr1:146917876..146920490,2	MCF-7	breast:

No data

Variant related genes	Relation type
OR13Z2P	TF binding region
ENSG00000207209	TF binding region
OR13Z2P	CpG island
ENSG00000207209	CpG island
ENSG00000226653	chromatin interactions

Extended variants
information (count: 220 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:220 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587695284	chr1:146892794-146892795	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs587755322	chr1:146892829-146892830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs76512254	chr1:146892869-146892870	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77951311	chr1:146892871-146892872	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587771255	chr1:146892872-146892873	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs80200999	chr1:146892874-146892875	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587706027	chr1:146892938-146892939	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4600098	chr1:146892956-146892957	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs370707208	chr1:146892986-146892987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587638187	chr1:146893011-146893012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374454391	chr1:146893017-146893018	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587711703	chr1:146893044-146893045	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs587596500	chr1:146893058-146893059	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587693005	chr1:146893080-146893081	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587752273	chr1:146893081-146893082	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190234483	chr1:146893108-146893109	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587684699	chr1:146893111-146893112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587766662	chr1:146893128-146893129	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs182304583	chr1:146893153-146893154	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376087353	chr1:146893211-146893212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370767244	chr1:146893258-146893259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187278173	chr1:146893267-146893268	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587730164	chr1:146893318-146893319	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587635913	chr1:146893346-146893347	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375091685	chr1:146893349-146893350	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2883315	chr1:146893365-146893366	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs190860832	chr1:146893368-146893369	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74123843	chr1:146893373-146893374	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs587683785	chr1:146893396-146893397	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs371835787	chr1:146893405-146893406	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs180720636	chr1:146893492-146893493	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs140759006	chr1:146893541-146893542	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs111705387	chr1:146893548-146893549	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs2353969	chr1:146893554-146893555	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs587597841	chr1:146893560-146893561	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs115043206	chr1:146893572-146893573	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs587731582	chr1:146893580-146893581	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs115797762	chr1:146893590-146893591	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs587686823	chr1:146893598-146893599	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs587740388	chr1:146893609-146893610	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs587602600	chr1:146893613-146893614	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs587672031	chr1:146893629-146893630	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs145127233	chr1:146893689-146893690	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs74123844	chr1:146893691-146893692	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs76891200	chr1:146893705-146893706	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs587728517	chr1:146893706-146893707	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs587628243	chr1:146893767-146893768	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs185507410	chr1:146893781-146893782	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587683740	chr1:146893850-146893851	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs12084073	chr1:146893860-146893861	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:157)

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
small cell lung cancer	20016488	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	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
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	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
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146894000-146894600	Enhancers	K562	blood
2	chr1:146894600-146894800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:146894600-146894800	Active TSS	K562	blood
4	chr1:146894800-146895000	Flanking Active TSS	K562	blood
5	chr1:146894800-146895400	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr1:146895000-146895400	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr1:146895000-146895400	Active TSS	Rectal Mucosa Donor 31	rectum
8	chr1:146910000-146910600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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