Variant report

Variant	esv3395217
Chromosome Location	chr1:146784718-146932376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:645)
CpG islands
(count:122)
Chromatin interactive
region (count:51)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:146848855-146850777	K562	blood:	n/a	n/a
2	ARID3A	chr1:146851502-146852003	K562	blood:	n/a	n/a
3	ARID3A	chr1:146861769-146862001	HepG2	liver:	n/a	n/a
4	ATF1	chr1:146851640-146852020	K562	blood:	n/a	n/a
5	ATF1	chr1:146908268-146908309	K562	blood:	n/a	n/a
6	ATF1	chr1:146838281-146838313	K562	blood:	n/a	n/a
7	ATF1	chr1:146848936-146850093	K562	blood:	n/a	n/a
8	ATF1	chr1:146856653-146856731	K562	blood:	n/a	n/a
9	ATF3	chr1:146851605-146852038	K562	blood:	n/a	n/a
10	BACH1	chr1:146848828-146849217	K562	blood:	n/a	n/a
11	BHLHE40	chr1:146848904-146849288	K562	blood:	n/a	n/a
12	BRCA1	chr1:146810425-146810519	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr1:146809453-146809605	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr1:146861769-146861997	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr1:146849314-146850084	K562	blood:	n/a	n/a
16	CCNT2	chr1:146848949-146850069	K562	blood:	n/a	n/a
17	CCNT2	chr1:146851714-146851966	K562	blood:	n/a	n/a
18	CEBPB	chr1:146826701-146826897	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:146851596-146852074	K562	blood:	n/a	n/a
20	CEBPB	chr1:146851674-146852010	K562	blood:	n/a	n/a
21	CEBPB	chr1:146801401-146801445	A549	lung:	n/a	n/a
22	CEBPB	chr1:146861745-146862014	K562	blood:	n/a	n/a
23	CEBPB	chr1:146849497-146850196	K562	blood:	n/a	n/a
24	CEBPB	chr1:146851405-146852071	K562	blood:	n/a	chr1:146851508-146851521 chr1:146851510-146851521
25	CEBPB	chr1:146849583-146850143	K562	blood:	n/a	n/a
26	CEBPB	chr1:146826798-146826887	K562	blood:	n/a	n/a
27	CEBPB	chr1:146891751-146891948	A549	lung:	n/a	n/a
28	CEBPB	chr1:146891745-146891945	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:146861690-146862028	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:146849641-146849999	K562	blood:	n/a	n/a
31	CEBPB	chr1:146792919-146793071	A549	lung:	n/a	n/a
32	CEBPD	chr1:146851557-146852128	K562	blood:	n/a	n/a
33	CEBPD	chr1:146851473-146852055	K562	blood:	n/a	n/a
34	CEBPD	chr1:146849391-146850045	K562	blood:	n/a	n/a
35	CEBPD	chr1:146849479-146850128	K562	blood:	n/a	n/a
36	CHD1	chr1:146808199-146808588	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr1:146808807-146809266	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:146786721-146786945	K562	blood:	n/a	n/a
39	CTCF	chr1:146815200-146815350	K562	blood:	n/a	n/a
40	CTCF	chr1:146861655-146862003	K562	blood:	n/a	n/a
41	CTCF	chr1:146861800-146861950	SAEC	small airway:	n/a	n/a
42	CTCF	chr1:146862121-146862192	GM12878	blood:	n/a	n/a
43	CTCF	chr1:146861686-146861845	GM12891	blood:	n/a	n/a
44	CTCF	chr1:146861739-146861978	Lung_OC	lung:	n/a	n/a
45	CTCF	chr1:146861380-146861530	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr1:146800183-146800279	LNCaP	prostate:	n/a	n/a
47	CTCF	chr1:146861420-146861570	GM12867	blood:	n/a	n/a
48	CTCF	chr1:146861737-146862008	ECC-1	luminal epithelium:	n/a	n/a
49	CTCF	chr1:146865110-146865179	LNCaP	prostate:	n/a	n/a
50	CTCF	chr1:146861760-146861910	GM12865	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146895247-146895297	AG04450	lung:	fetal
2	chr1:146807706-146807756	HCF	heart:	n/a
3	chr1:146807706-146807756	NT2-D1	testis:	n/a
4	chr1:146895247-146895297	PrEC	prostate:	n/a
5	chr1:146807706-146807756	Hela-S3	cervix:	n/a
6	chr1:146807706-146807756	HNPCEpiC	eye:	n/a
7	chr1:146807706-146807756	AG10803	skin:	n/a
8	chr1:146895247-146895297	GM12891	blood:	n/a
9	chr1:146807706-146807756	HepG2	liver:	n/a
10	chr1:146895247-146895297	IMR90	lung:	fetal
11	chr1:146895247-146895297	MCF10A-Er-Src	breast:	n/a
12	chr1:146895247-146895297	BE2_C	brain:	n/a
13	chr1:146807706-146807756	GM19239	blood:	n/a
14	chr1:146895247-146895297	HUVEC	blood vessel:	n/a
15	chr1:146807706-146807756	AoSMC	blood vessel:	n/a
16	chr1:146895247-146895297	HAEpiC	amniotic membrane:	n/a
17	chr1:146895247-146895297	NH-A	brain:	n/a
18	chr1:146895247-146895297	K562	blood:	n/a
19	chr1:146807706-146807756	NHDF-neo	bronchial:	n/a
20	chr1:146807706-146807756	HCT-116	colon:	n/a
21	chr1:146895247-146895297	PANC-1	pancreas:	n/a
22	chr1:146895247-146895297	AG04449	skin:	fetal
23	chr1:146807706-146807756	HUVEC	blood vessel:	n/a
24	chr1:146895247-146895297	NB4	blood:	n/a
25	chr1:146807706-146807756	AG09309	skin:	n/a
26	chr1:146895247-146895297	HL-60	blood:	n/a
27	chr1:146895247-146895297	AG09319	gingival:	n/a
28	chr1:146895247-146895297	LNCaP	prostate:	n/a
29	chr1:146895247-146895297	H1-hESC	embryonic stem cell:	embryo
30	chr1:146895247-146895297	A549	lung:	n/a
31	chr1:146895247-146895297	Caco-2	colon:	n/a
32	chr1:146895247-146895297	HEEpiC	esophagus:	n/a
33	chr1:146895247-146895297	HRCEpiC	kidney:	n/a
34	chr1:146807706-146807756	GM12878	blood:	n/a
35	chr1:146895247-146895297	NT2-D1	testis:	n/a
36	chr1:146807706-146807756	BE2_C	brain:	n/a
37	chr1:146895247-146895297	AG09309	skin:	n/a
38	chr1:146807706-146807756	HRE	kidney:	n/a
39	chr1:146895247-146895297	BJ	skin:	n/a
40	chr1:146807706-146807756	NHBE	bronchial:	n/a
41	chr1:146895247-146895297	SK-N-SH	brain:	n/a
42	chr1:146895247-146895297	HCM	heart:	n/a
43	chr1:146807706-146807756	Jurkat	blood:	n/a
44	chr1:146895247-146895297	ovcar-3	ovarian:	n/a
45	chr1:146807706-146807756	Hepatocyte	liver:	n/a
46	chr1:146807706-146807756	H1-hESC	embryonic stem cell:	embryo
47	chr1:146895247-146895297	AoSMC	blood vessel:	n/a
48	chr1:146807706-146807756	GM06990	blood:	n/a
49	chr1:146895247-146895297	U87	brain:	n/a
50	chr1:146895247-146895297	SAEC	small airway:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
2	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
3	chr1:146902129..146904025-chr1:146907523..146909259,2	MCF-7	breast:
4	chr1:146904930..146907237-chr1:146910258..146912746,2	MCF-7	breast:
5	chr1:146919316..146922658-chr1:146922805..146926781,4	MCF-7	breast:
6	chr1:146744019..146745756-chr1:146860547..146863397,2	MCF-7	breast:
7	chr1:146907560..146910519-chr1:146910936..146913596,2	K562	blood:
8	chr1:146907560..146910519-chr1:146910936..146913596,2	K562	blood:
9	chr1:146889760..146891342-chr1:146892775..146894723,2	K562	blood:
10	chr1:146904036..146904863-chr6:92344357..92345281,2	MCF-7	breast:
11	chr1:146861647..146862210-chr1:146963967..146964711,2	MCF-7	breast:
12	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
13	chr1:146899574..146902487-chr1:146902750..146904367,2	K562	blood:
14	chr1:146643870..146644650-chr1:146861592..146862107,2	MCF-7	breast:
15	chr1:146902569..146904865-chr1:146917610..146920209,2	MCF-7	breast:
16	chr1:146902129..146904025-chr1:146907523..146909259,2	MCF-7	breast:
17	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
18	chr1:146841177..146844214-chr1:146848195..146851017,3	K562	blood:
19	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
20	chr1:146841177..146844214-chr1:146848195..146851017,3	K562	blood:
21	chr1:146903700..146906235-chr1:146908558..146911092,2	MCF-7	breast:
22	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
23	chr1:146806520..146809758-chr1:146812607..146814433,3	K562	blood:
24	chr1:146745161..146746194-chr1:146861354..146862246,9	MCF-7	breast:
25	chr1:146714335..146717266-chr1:146861810..146864638,2	K562	blood:
26	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
27	chr1:146829897..146832000-chr1:146834771..146837746,2	K562	blood:
28	chr1:146785986..146788702-chr1:146789697..146791855,2	MCF-7	breast:
29	chr1:146892685..146894306-chr1:146902333..146904733,2	K562	blood:
30	chr1:146924006..146926238-chr1:146927310..146929768,2	K562	blood:
31	chr1:146714725..146717432-chr1:146860214..146861781,2	MCF-7	breast:
32	chr1:146745473..146746108-chr1:146861600..146862389,4	K562	blood:
33	chr1:146892606..146894867-chr1:146909100..146911293,2	MCF-7	breast:
34	chr1:146806520..146809758-chr1:146812607..146814433,3	K562	blood:
35	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
36	chr1:146904930..146907237-chr1:146910258..146912746,2	MCF-7	breast:
37	chr1:146745103..146745868-chr1:146861342..146862193,4	MCF-7	breast:
38	chr1:146553543..146556468-chr1:146848913..146851805,2	K562	blood:
39	chr1:146902569..146904865-chr1:146917610..146920209,2	MCF-7	breast:
40	chr1:146829897..146832000-chr1:146834771..146837746,2	K562	blood:
41	chr1:146899574..146902487-chr1:146902750..146904367,2	K562	blood:
42	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
43	chr1:146900267..146901994-chr1:146917876..146920490,2	MCF-7	breast:
44	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
45	chr1:146900267..146901994-chr1:146917876..146920490,2	MCF-7	breast:
46	chr1:146886806..146889082-chr1:146891750..146894750,3	K562	blood:
47	chr1:146924006..146926238-chr1:146927310..146929768,2	K562	blood:
48	chr1:146892606..146894867-chr1:146909100..146911293,2	MCF-7	breast:
49	chr1:146892685..146894306-chr1:146902333..146904733,2	K562	blood:
50	chr1:146903700..146906235-chr1:146908558..146911092,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
OR13Z2P	TF binding region
ENSG00000213226	TF binding region
OR13Z1P	TF binding region
ENSG00000207209	TF binding region
OR13Z2P	CpG island
ENSG00000213226	CpG island
OR13Z1P	CpG island
ENSG00000207209	CpG island
ENSG00000207209	chromatin interactions
ENSG00000237188	chromatin interactions
ENSG00000226653	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000131791	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000213226	chromatin interactions

Extended variants
information (count: 2079 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138596458	chr1:146786024-146786025	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs885305	chr1:146786080-146786081	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs587605334	chr1:146786134-146786135	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372632610	chr1:146786186-146786187	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587664832	chr1:146786187-146786188	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12046626	chr1:146786210-146786211	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs587630332	chr1:146786212-146786213	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587685812	chr1:146786252-146786253	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs587742812	chr1:146786288-146786289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587615786	chr1:146786301-146786302	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587689237	chr1:146786317-146786318	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35618507	chr1:146786336-146786337	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs587641244	chr1:146786341-146786342	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587680208	chr1:146786426-146786427	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587776212	chr1:146786434-146786435	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs143774410	chr1:146786448-146786449	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587745926	chr1:146786460-146786461	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148130325	chr1:146786471-146786472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587654722	chr1:146786492-146786493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201346941	chr1:146786493-146786494	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372890878	chr1:146786494-146786495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs386368258	chr1:146786495-146786496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs386354278	chr1:146786506-146786507	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78463664	chr1:146786507-146786508	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372102166	chr1:146786508-146786509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587705705	chr1:146786564-146786565	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs55694029	chr1:146786571-146786572	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs117639888	chr1:146786606-146786607	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs139055093	chr1:146786607-146786608	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587609387	chr1:146786622-146786623	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587661395	chr1:146786633-146786634	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587742863	chr1:146786635-146786636	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs386635245	chr1:146786640-146786641	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4415628	chr1:146786641-146786642	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs587721855	chr1:146786683-146786684	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150687920	chr1:146786685-146786686	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368304615	chr1:146786713-146786714	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186344411	chr1:146786718-146786719	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76371289	chr1:146786726-146786727	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587776168	chr1:146786733-146786734	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587641696	chr1:146786738-146786739	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587721748	chr1:146786780-146786781	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587755299	chr1:146786781-146786782	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369503463	chr1:146786803-146786804	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587710586	chr1:146786816-146786817	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587748634	chr1:146786823-146786824	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs587652548	chr1:146786860-146786861	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs587708197	chr1:146786890-146786891	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587608085	chr1:146786904-146786905	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587661152	chr1:146786943-146786944	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:162)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146787800-146788200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:146788200-146788600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:146788600-146788800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:146798800-146799400	Enhancers	H1 Cell Line	embryonic stem cell
5	chr1:146798800-146799400	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr1:146798800-146799600	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr1:146799400-146803000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:146799600-146803200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:146802600-146803600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:146803000-146803400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr1:146803000-146803400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr1:146803000-146803800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr1:146803200-146803800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr1:146803400-146805600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr1:146803400-146805800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr1:146803600-146806000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:146803800-146806000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr1:146803800-146806000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:146805200-146806800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:146805400-146811200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr1:146805600-146806000	Enhancers	K562	blood
22	chr1:146805600-146807800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr1:146805800-146806200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:146805800-146806400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr1:146805800-146806600	Enhancers	Brain Germinal Matrix	brain
26	chr1:146806000-146806200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr1:146806000-146806400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:146806000-146806400	Flanking Active TSS	K562	blood
29	chr1:146806000-146806600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:146806000-146806800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr1:146806000-146807800	Enhancers	H9 Cell Line	embryonic stem cell
32	chr1:146806000-146808200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:146806000-146808200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:146806200-146806400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr1:146806200-146806400	Enhancers	Brain Anterior Caudate	brain
36	chr1:146806200-146808800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr1:146806200-146809400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr1:146806400-146806800	Enhancers	K562	blood
39	chr1:146806400-146807400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr1:146806400-146807400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:146806400-146808400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr1:146806600-146807600	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:146806800-146807200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:146806800-146807400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:146807200-146808800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr1:146807400-146807600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:146807400-146807600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr1:146807400-146808800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:146807600-146808000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:146807600-146808200	Enhancers	HUES64 Cell Line	embryonic stem cell

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