Variant report

Variant	nsv535140
Chromosome Location	chr1:146850449-146930319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:459)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:146861769-146862001	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:146848855-146850777	K562	blood:	n/a	n/a
3	ARID3A	chr1:146851502-146852003	K562	blood:	n/a	n/a
4	ATF1	chr1:146908268-146908309	K562	blood:	n/a	n/a
5	ATF1	chr1:146851640-146852020	K562	blood:	n/a	n/a
6	ATF1	chr1:146856653-146856731	K562	blood:	n/a	n/a
7	ATF3	chr1:146851605-146852038	K562	blood:	n/a	n/a
8	BRCA1	chr1:146861769-146861997	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr1:146851714-146851966	K562	blood:	n/a	n/a
10	CEBPB	chr1:146851596-146852074	K562	blood:	n/a	n/a
11	CEBPB	chr1:146851674-146852010	K562	blood:	n/a	n/a
12	CEBPB	chr1:146891745-146891945	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:146861745-146862014	K562	blood:	n/a	n/a
14	CEBPB	chr1:146861690-146862028	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:146891751-146891948	A549	lung:	n/a	n/a
16	CEBPB	chr1:146851405-146852071	K562	blood:	n/a	chr1:146851508-146851521 chr1:146851510-146851521
17	CEBPD	chr1:146851557-146852128	K562	blood:	n/a	n/a
18	CEBPD	chr1:146851473-146852055	K562	blood:	n/a	n/a
19	CTCF	chr1:146901100-146901180	Fibrobl	skin:	n/a	n/a
20	CTCF	chr1:146861700-146861850	A549	lung:	n/a	n/a
21	CTCF	chr1:146861800-146861950	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr1:146861060-146861210	RPTEC	kidney:	n/a	n/a
23	CTCF	chr1:146861800-146861950	GM12870	blood:	n/a	n/a
24	CTCF	chr1:146861760-146861910	HCM	heart:	n/a	n/a
25	CTCF	chr1:146861760-146861910	GM12874	blood:	n/a	n/a
26	CTCF	chr1:146861780-146861930	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr1:146861760-146861910	GM12869	blood:	n/a	n/a
28	CTCF	chr1:146861780-146861930	AG04449	skin:	n/a	n/a
29	CTCF	chr1:146861460-146861610	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr1:146861780-146861930	HPF	lung:	n/a	n/a
31	CTCF	chr1:146861740-146861890	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:146861520-146862060	K562	blood:	n/a	n/a
33	CTCF	chr1:146861724-146861867	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:146861720-146861870	GM12867	blood:	n/a	n/a
35	CTCF	chr1:146861780-146861930	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr1:146861698-146862007	Medullo	brain:	n/a	n/a
37	CTCF	chr1:146861780-146861930	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr1:146861739-146861978	Lung_OC	lung:	n/a	n/a
39	CTCF	chr1:146861740-146861890	HEK293	kidney:	n/a	n/a
40	CTCF	chr1:146861400-146861550	GM12871	blood:	n/a	n/a
41	CTCF	chr1:146861760-146861910	HMEC	breast:	n/a	n/a
42	CTCF	chr1:146860380-146860530	GM12871	blood:	n/a	n/a
43	CTCF	chr1:146861739-146861956	GM10248	blood:	n/a	n/a
44	CTCF	chr1:146861420-146861570	HAc	cerebellar:	n/a	n/a
45	CTCF	chr1:146861760-146861910	GM12872	blood:	n/a	n/a
46	CTCF	chr1:146861633-146862062	K562	blood:	n/a	n/a
47	CTCF	chr1:146861723-146861964	HepG2	liver:	n/a	n/a
48	CTCF	chr1:146861593-146861597	GM19238	blood:	n/a	n/a
49	CTCF	chr1:146861693-146861913	HepG2	liver:	n/a	n/a
50	CTCF	chr1:146860620-146860770	WERI-Rb-1	eye:	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	HCPEpiC	choroid plexus:	n/a
2	chr1:146895247-146895297	HEEpiC	esophagus:	n/a
3	chr1:146895247-146895297	HMEC	breast:	n/a
4	chr1:146895247-146895297	SKMC	muscle:	n/a
5	chr1:146895247-146895297	AG09319	gingival:	n/a
6	chr1:146895247-146895297	NH-A	brain:	n/a
7	chr1:146895247-146895297	HIPEpiC	eye:	n/a
8	chr1:146895247-146895297	ECC-1	luminal epithelium:	n/a
9	chr1:146895247-146895297	NB4	blood:	n/a
10	chr1:146895247-146895297	HUVEC	blood vessel:	n/a
11	chr1:146895247-146895297	AG04449	skin:	fetal
12	chr1:146895247-146895297	SK-N-SH	brain:	n/a
13	chr1:146895247-146895297	SK-N-MC	brain:	n/a
14	chr1:146895247-146895297	GM12891	blood:	n/a
15	chr1:146895247-146895297	NHBE	bronchial:	n/a
16	chr1:146895247-146895297	A549	lung:	n/a
17	chr1:146895247-146895297	K562	blood:	n/a
18	chr1:146895247-146895297	AG09309	skin:	n/a
19	chr1:146895247-146895297	HRE	kidney:	n/a
20	chr1:146895247-146895297	GM12878	blood:	n/a
21	chr1:146895247-146895297	SAEC	small airway:	n/a
22	chr1:146895247-146895297	HEK293	kidney:	embryo
23	chr1:146895247-146895297	HRCEpiC	kidney:	n/a
24	chr1:146895247-146895297	NHDF-neo	bronchial:	n/a
25	chr1:146895247-146895297	SK-N-SH_RA	brain:	n/a
26	chr1:146895247-146895297	AoSMC	blood vessel:	n/a
27	chr1:146895247-146895297	HCM	heart:	n/a
28	chr1:146895247-146895297	HRPEpiC	eye:	n/a
29	chr1:146895247-146895297	LNCaP	prostate:	n/a
30	chr1:146895247-146895297	ovcar-3	ovarian:	n/a
31	chr1:146895247-146895297	U87	brain:	n/a
32	chr1:146895247-146895297	Hepatocyte	liver:	n/a
33	chr1:146895247-146895297	PFSK-1	brain:	n/a
34	chr1:146895247-146895297	MCF-7	breast:	n/a
35	chr1:146895247-146895297	BE2_C	brain:	n/a
36	chr1:146895247-146895297	PANC-1	pancreas:	n/a
37	chr1:146895247-146895297	AG04450	lung:	fetal
38	chr1:146895247-146895297	GM06990	blood:	n/a
39	chr1:146895247-146895297	HepG2	liver:	n/a
40	chr1:146895247-146895297	CMK	blood:	n/a
41	chr1:146895247-146895297	HNPCEpiC	eye:	n/a
42	chr1:146895247-146895297	HCT-116	colon:	n/a
43	chr1:146895247-146895297	ProgFib	skin:	n/a
44	chr1:146895247-146895297	HL-60	blood:	n/a
45	chr1:146895247-146895297	PrEC	prostate:	n/a
46	chr1:146895247-146895297	T-47D	breast:	n/a
47	chr1:146895247-146895297	BJ	skin:	n/a
48	chr1:146895247-146895297	IMR90	lung:	fetal
49	chr1:146895247-146895297	HAEpiC	amniotic membrane:	n/a
50	chr1:146895247-146895297	H1-hESC	embryonic stem cell:	embryo

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:146892606..146894867-chr1:146909100..146911293,2	MCF-7	breast:
2	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
3	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
4	chr1:146902569..146904865-chr1:146917610..146920209,2	MCF-7	breast:
5	chr1:146902129..146904025-chr1:146907523..146909259,2	MCF-7	breast:
6	chr1:146899574..146902487-chr1:146902750..146904367,2	K562	blood:
7	chr1:146886806..146889082-chr1:146891750..146894750,3	K562	blood:
8	chr1:146907560..146910519-chr1:146910936..146913596,2	K562	blood:
9	chr1:146907560..146910519-chr1:146910936..146913596,2	K562	blood:
10	chr1:146904930..146907237-chr1:146910258..146912746,2	MCF-7	breast:
11	chr1:146919316..146922658-chr1:146922805..146926781,4	MCF-7	breast:
12	chr1:146904036..146904863-chr6:92344357..92345281,2	MCF-7	breast:
13	chr1:146899574..146902487-chr1:146902750..146904367,2	K562	blood:
14	chr1:146841177..146844214-chr1:146848195..146851017,3	K562	blood:
15	chr1:146900267..146901994-chr1:146917876..146920490,2	MCF-7	breast:
16	chr1:146745161..146746194-chr1:146861354..146862246,9	MCF-7	breast:
17	chr1:146745103..146745868-chr1:146861342..146862193,4	MCF-7	breast:
18	chr1:146892685..146894306-chr1:146902333..146904733,2	K562	blood:
19	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
20	chr1:146553543..146556468-chr1:146848913..146851805,2	K562	blood:
21	chr1:146900267..146901994-chr1:146917876..146920490,2	MCF-7	breast:
22	chr1:146744019..146745756-chr1:146860547..146863397,2	MCF-7	breast:
23	chr1:146924006..146926238-chr1:146927310..146929768,2	K562	blood:
24	chr1:146745473..146746108-chr1:146861600..146862389,4	K562	blood:
25	chr1:146903700..146906235-chr1:146908558..146911092,2	MCF-7	breast:
26	chr1:146714725..146717432-chr1:146860214..146861781,2	MCF-7	breast:
27	chr1:146861647..146862210-chr1:146963967..146964711,2	MCF-7	breast:
28	chr1:146889760..146891342-chr1:146892775..146894723,2	K562	blood:
29	chr1:146903700..146906235-chr1:146908558..146911092,2	MCF-7	breast:
30	chr1:146643870..146644650-chr1:146861592..146862107,2	MCF-7	breast:
31	chr1:146902129..146904025-chr1:146907523..146909259,2	MCF-7	breast:
32	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
33	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
34	chr1:146902569..146904865-chr1:146917610..146920209,2	MCF-7	breast:
35	chr1:146924006..146926238-chr1:146927310..146929768,2	K562	blood:
36	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
37	chr1:146904930..146907237-chr1:146910258..146912746,2	MCF-7	breast:
38	chr1:146714335..146717266-chr1:146861810..146864638,2	K562	blood:
39	chr1:146919316..146922658-chr1:146922805..146926781,4	MCF-7	breast:
40	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
41	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
42	chr1:146892606..146894867-chr1:146909100..146911293,2	MCF-7	breast:
43	chr1:146892685..146894306-chr1:146902333..146904733,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACP6-1	chr1:146853914-146856585	NONHSAT006032
2	lnc-ACP6-1	chr1:146856390-146856585	NONHSAT006008
3	lnc-ACP6-1	chr1:146880322-146880421	NONHSAT006008
4	lnc-ACP6-1	chr1:146880390-146880421	NONHSAT139896

No data

Variant related genes	Relation type
OR13Z2P	TF binding region
OR13Z1P	TF binding region
ENSG00000207209	TF binding region
OR13Z2P	CpG island
OR13Z1P	CpG island
ENSG00000207209	CpG island
ENSG00000226653	chromatin interactions
ENSG00000207209	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000237188	chromatin interactions
ENSG00000131791	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000230832	chromatin interactions

Extended variants
information (count: 1155 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587670253	chr1:146850455-146850456	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs587748172	chr1:146850510-146850511	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587645898	chr1:146850539-146850540	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142157964	chr1:146850566-146850567	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587762320	chr1:146850571-146850572	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs35888923	chr1:146850633-146850634	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367716431	chr1:146850639-146850640	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587617529	chr1:146850643-146850644	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144365693	chr1:146850661-146850662	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587753225	chr1:146850691-146850692	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587645547	chr1:146850693-146850694	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371467284	chr1:146850718-146850719	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147850487	chr1:146850749-146850750	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141405824	chr1:146850751-146850752	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587724600	chr1:146850776-146850777	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374727554	chr1:146850871-146850872	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587599401	chr1:146850967-146850968	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34602039	chr1:146850972-146850973	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs191140491	chr1:146850978-146850979	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587594159	chr1:146850982-146850983	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587663877	chr1:146851003-146851004	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145594804	chr1:146851010-146851011	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587727418	chr1:146851019-146851020	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587623615	chr1:146851031-146851032	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587682534	chr1:146851048-146851049	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146934899	chr1:146851108-146851109	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs76086566	chr1:146851126-146851127	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587674154	chr1:146851165-146851166	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114061235	chr1:146851169-146851170	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs147977273	chr1:146851181-146851182	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587689726	chr1:146851185-146851186	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587769440	chr1:146851195-146851196	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375694792	chr1:146851196-146851197	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140791056	chr1:146851197-146851198	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587702290	chr1:146851198-146851199	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11240013	chr1:146851286-146851287	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs587628948	chr1:146851294-146851295	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150113177	chr1:146851305-146851306	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587746319	chr1:146851306-146851307	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs138913669	chr1:146851326-146851327	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs116208403	chr1:146851328-146851329	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146348715	chr1:146851333-146851334	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182433671	chr1:146851365-146851366	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs116795080	chr1:146851404-146851405	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587599033	chr1:146851435-146851436	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587669818	chr1:146851473-146851474	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138491367	chr1:146851492-146851493	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188297142	chr1:146851497-146851498	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587667401	chr1:146851542-146851543	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs12041474	chr1:146851579-146851580	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:160)

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
Ovarian clear cell carcinoma	21343371	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
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146848800-146850800	Flanking Active TSS	K562	blood
2	chr1:146850800-146852200	Enhancers	K562	blood
3	chr1:146860000-146860800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:146860400-146860800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:146860400-146861800	Enhancers	K562	blood
6	chr1:146860600-146861000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:146860600-146861200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:146860600-146861400	Enhancers	Placenta Amnion	Placenta Amnion
9	chr1:146860800-146862000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:146861000-146861200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:146861200-146861400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:146861400-146861600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:146861400-146861800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr1:146861400-146861800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:146861600-146861800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:146861600-146862200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:146861600-146862200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr1:146861600-146862200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:146861800-146874400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:146862000-146862400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:146873800-146874000	Enhancers	HepG2	liver
22	chr1:146873800-146874200	Enhancers	Liver	Liver
23	chr1:146874000-146874600	Active TSS	HepG2	liver
24	chr1:146874200-146874600	Active TSS	Rectal Smooth Muscle	rectum
25	chr1:146874200-146874800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr1:146874200-146875000	Active TSS	Colonic Mucosa	Colon
27	chr1:146874400-146874800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:146874400-146875000	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr1:146885600-146887400	Enhancers	Liver	Liver
30	chr1:146888000-146889600	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr1:146889600-146890600	Enhancers	Fetal Intestine Small	intestine
32	chr1:146894000-146894600	Enhancers	K562	blood
33	chr1:146894600-146894800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr1:146894600-146894800	Active TSS	K562	blood
35	chr1:146894800-146895000	Flanking Active TSS	K562	blood
36	chr1:146894800-146895400	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr1:146895000-146895400	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr1:146895000-146895400	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr1:146910000-146910600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:146918800-146919000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:146924400-146925000	Enhancers	Pancreatic Islets	Pancreatic Islet

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