Variant report

Variant	esv3351074
Chromosome Location	chr1:144978295-145093993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4469)
CpG islands
(count:3056)
Chromatin interactive
region (count:295)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4469 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145054062-145056297	K562	blood:	n/a	chr1:145054435-145054451 chr1:145054273-145054289 chr1:145054272-145054288 chr1:145054436-145054452
2	ARID3A	chr1:145014466-145014972	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:145040051-145040226	K562	blood:	n/a	n/a
4	ARID3A	chr1:145023275-145025964	K562	blood:	n/a	n/a
5	ARID3A	chr1:145012025-145018939	K562	blood:	n/a	chr1:145012568-145012584 chr1:145012567-145012583
6	ARID3A	chr1:145089768-145090509	K562	blood:	n/a	n/a
7	ARID3A	chr1:145005457-145007401	K562	blood:	n/a	n/a
8	ARID3A	chr1:144989106-144991213	K562	blood:	n/a	n/a
9	ARID3A	chr1:145061354-145062417	K562	blood:	n/a	n/a
10	ARID3A	chr1:145007845-145011203	K562	blood:	n/a	n/a
11	ARID3A	chr1:144994237-144996744	K562	blood:	n/a	n/a
12	ARID3A	chr1:145000157-145004850	K562	blood:	n/a	chr1:145001553-145001569 chr1:145004748-145004764
13	ARID3A	chr1:145039806-145040082	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:144991522-144993662	K562	blood:	n/a	n/a
15	ARID3A	chr1:145058588-145061058	K562	blood:	n/a	n/a
16	ARID3A	chr1:144997084-144999662	K562	blood:	n/a	n/a
17	ARID3A	chr1:145040639-145043538	K562	blood:	n/a	n/a
18	ARID3A	chr1:145027372-145031947	K562	blood:	n/a	n/a
19	ARID3A	chr1:144988785-144990011	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:145083440-145084471	K562	blood:	n/a	n/a
21	ARID3A	chr1:145091964-145092746	HepG2	liver:	n/a	n/a
22	ATF1	chr1:145027502-145029034	K562	blood:	n/a	n/a
23	ATF1	chr1:145074748-145075398	K562	blood:	n/a	n/a
24	ATF1	chr1:145023255-145025928	K562	blood:	n/a	n/a
25	ATF1	chr1:144991677-144992162	K562	blood:	n/a	n/a
26	ATF1	chr1:145083579-145084451	K562	blood:	n/a	n/a
27	ATF1	chr1:145070839-145072121	K562	blood:	n/a	n/a
28	ATF1	chr1:144988840-144990055	K562	blood:	n/a	n/a
29	ATF1	chr1:145077527-145078634	K562	blood:	n/a	n/a
30	ATF1	chr1:145029752-145031659	K562	blood:	n/a	n/a
31	ATF1	chr1:145014382-145016089	K562	blood:	n/a	n/a
32	ATF1	chr1:145082093-145082887	K562	blood:	n/a	n/a
33	ATF1	chr1:145078844-145078995	K562	blood:	n/a	n/a
34	ATF1	chr1:144998715-144999351	K562	blood:	n/a	n/a
35	ATF1	chr1:145008736-145009963	K562	blood:	n/a	n/a
36	ATF1	chr1:145080812-145081067	K562	blood:	n/a	n/a
37	ATF1	chr1:145073353-145074236	K562	blood:	n/a	n/a
38	ATF1	chr1:145090189-145090575	K562	blood:	n/a	n/a
39	ATF1	chr1:145012108-145014066	K562	blood:	n/a	n/a
40	ATF1	chr1:144994316-144996366	K562	blood:	n/a	n/a
41	ATF1	chr1:145032820-145034366	K562	blood:	n/a	n/a
42	ATF1	chr1:145054709-145055914	K562	blood:	n/a	n/a
43	ATF1	chr1:145018078-145018857	K562	blood:	n/a	n/a
44	ATF1	chr1:145068286-145068723	K562	blood:	n/a	n/a
45	ATF1	chr1:145020634-145021790	K562	blood:	n/a	n/a
46	ATF1	chr1:145037166-145037364	K562	blood:	n/a	n/a
47	ATF1	chr1:145042745-145043636	K562	blood:	n/a	n/a
48	ATF1	chr1:145069602-145070170	K562	blood:	n/a	n/a
49	ATF1	chr1:145001703-145004761	K562	blood:	n/a	n/a
50	ATF1	chr1:145086819-145087312	K562	blood:	n/a	n/a

(count:3056 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145059467-145059517	NHBE	bronchial:	n/a
2	chr1:145028465-145028515	SKMC	muscle:	n/a
3	chr1:145089017-145089067	GM06990	blood:	n/a
4	chr1:145073743-145073793	NHBE	bronchial:	n/a
5	chr1:144989624-144989674	GM12891	blood:	n/a
6	chr1:145015987-145016037	ECC-1	luminal epithelium:	n/a
7	chr1:145059467-145059517	NHBE	bronchial:	n/a
8	chr1:145028465-145028515	SKMC	muscle:	n/a
9	chr1:145089017-145089067	GM06990	blood:	n/a
10	chr1:145073743-145073793	NHBE	bronchial:	n/a
11	chr1:144989624-144989674	GM12891	blood:	n/a
12	chr1:145015987-145016037	ECC-1	luminal epithelium:	n/a
13	chr1:145028465-145028515	IMR90	lung:	fetal
14	chr1:145039882-145039932	SAEC	small airway:	n/a
15	chr1:144995682-144995732	HEEpiC	esophagus:	n/a
16	chr1:144994826-144994876	CMK	blood:	n/a
17	chr1:145021703-145021753	HEK293	kidney:	embryo
18	chr1:145079447-145079497	NHBE	bronchial:	n/a
19	chr1:144995682-144995732	HRCEpiC	kidney:	n/a
20	chr1:145076239-145076289	SKMC	muscle:	n/a
21	chr1:145012822-145012872	Jurkat	blood:	n/a
22	chr1:145004305-145004355	LNCaP	prostate:	n/a
23	chr1:145039929-145039979	SK-N-MC	brain:	n/a
24	chr1:145003040-145003090	T-47D	breast:	n/a
25	chr1:144995101-144995151	HAEpiC	amniotic membrane:	n/a
26	chr1:144995682-144995732	NHDF-neo	bronchial:	n/a
27	chr1:145075538-145075588	GM06990	blood:	n/a
28	chr1:145040506-145040556	HRE	kidney:	n/a
29	chr1:145023679-145023729	U87	brain:	n/a
30	chr1:145079447-145079497	Jurkat	blood:	n/a
31	chr1:145039929-145039979	LNCaP	prostate:	n/a
32	chr1:145004468-145004518	IMR90	lung:	fetal
33	chr1:145054067-145054117	LNCaP	prostate:	n/a
34	chr1:145040160-145040210	NB4	blood:	n/a
35	chr1:145013480-145013530	MCF-7	breast:	n/a
36	chr1:145003040-145003090	HEK293	kidney:	embryo
37	chr1:145021703-145021753	H1-hESC	embryonic stem cell:	embryo
38	chr1:145015987-145016037	HRE	kidney:	n/a
39	chr1:145076221-145076271	ProgFib	skin:	n/a
40	chr1:145039893-145039943	H1-hESC	embryonic stem cell:	embryo
41	chr1:145013480-145013530	MCF10A-Er-Src	breast:	n/a
42	chr1:145040886-145040936	HepG2	liver:	n/a
43	chr1:145073743-145073793	SKMC	muscle:	n/a
44	chr1:145079447-145079497	NH-A	brain:	n/a
45	chr1:145013480-145013530	SK-N-SH	brain:	n/a
46	chr1:144989624-144989674	HEK293	kidney:	embryo
47	chr1:144989624-144989674	K562	blood:	n/a
48	chr1:145012822-145012872	Hela-S3	cervix:	n/a
49	chr1:145017064-145017114	HUVEC	blood vessel:	n/a
50	chr1:145079447-145079497	HNPCEpiC	eye:	n/a

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr1:144932167..144933314-chr1:145058712..145059472,5	MCF-7	breast:
2	chr1:145058445..145059351-chr12:58299064..58299785,2	MCF-7	breast:
3	chr1:145012523..145015160-chr1:145055357..145057301,2	K562	blood:
4	chr1:144931155..144934615-chr1:145010020..145012641,3	MCF-7	breast:
5	chr1:144917481..144919146-chr1:145058283..145060040,20	MCF-7	breast:
6	chr1:144992586..144994194-chr1:145030165..145032446,2	MCF-7	breast:
7	chr1:145000528..145004410-chr1:145059527..145062479,4	K562	blood:
8	chr1:145013488..145015671-chr1:145056479..145059269,3	MCF-7	breast:
9	chr1:144991605..144996644-chr1:145057606..145061569,4	K562	blood:
10	chr1:145069991..145072792-chr1:145078438..145080718,2	K562	blood:
11	chr1:144534213..144536284-chr1:145054889..145056789,2	MCF-7	breast:
12	chr1:145081885..145085259-chr1:145087352..145090342,5	K562	blood:
13	chr1:145013143..145015357-chr1:145059234..145060924,2	K562	blood:
14	chr1:144992899..144993435-chr1:145029983..145030524,2	MCF-7	breast:
15	chr1:144932512..144934807-chr1:144998183..145000518,2	MCF-7	breast:
16	chr1:145038465..145040335-chr1:145073529..145077328,4	MCF-7	breast:
17	chr1:144917479..144918148-chr1:145066148..145066847,2	K562	blood:
18	chr1:144988447..144988982-chr1:145009629..145010133,2	K562	blood:
19	chr1:144610196..144613113-chr1:144999265..145001595,2	K562	blood:
20	chr1:145009850..145011713-chr1:145053445..145055856,2	K562	blood:
21	chr1:145082860..145085361-chr1:145086854..145088510,5	K562	blood:
22	chr1:145061540..145065119-chr1:145065155..145068193,4	MCF-7	breast:
23	chr1:144919025..144921038-chr1:145058900..145061668,2	K562	blood:
24	chr1:144988330..144990331-chr1:145096274..145097862,2	MCF-7	breast:
25	chr1:144917701..144918598-chr1:145059017..145059574,2	MCF-7	breast:
26	chr1:144993161..144995099-chr1:145058341..145060153,2	MCF-7	breast:
27	chr1:145012804..145013720-chr1:145058918..145059629,3	MCF-7	breast:
28	chr1:145025247..145027949-chr1:145103213..145105927,2	K562	blood:
29	chr1:144532739..144535051-chr1:145058991..145061540,3	K562	blood:
30	chr1:144532329..144535680-chr1:145012343..145016063,5	K562	blood:
31	chr1:145073999..145076164-chr1:145381316..145383485,2	MCF-7	breast:
32	chr1:144987976..144988507-chr1:145060005..145060715,2	MCF-7	breast:
33	chr1:145052713..145055657-chr1:145057659..145059759,3	K562	blood:
34	chr1:145000529..145002356-chr1:145004395..145006145,2	MCF-7	breast:
35	chr1:145079205..145081578-chr1:145083280..145086175,3	K562	blood:
36	chr1:145073882..145075772-chr15:71407192..71409797,2	MCF-7	breast:
37	chr1:145000529..145002356-chr1:145004395..145006145,2	MCF-7	breast:
38	chr1:145013051..145015770-chr1:145381611..145384530,4	K562	blood:
39	chr1:144984721..144986263-chr1:144986371..144987987,2	MCF-7	breast:
40	chr1:145032352..145035242-chr1:145073203..145075747,2	K562	blood:
41	chr1:120510712..120511507-chr1:144989621..144990280,2	MCF-7	breast:
42	chr1:145009850..145011713-chr1:145053445..145055856,2	K562	blood:
43	chr1:144532674..144534262-chr1:145089036..145091259,2	K562	blood:
44	chr1:144997738..145000659-chr1:145007857..145011011,3	MCF-7	breast:
45	chr1:145068824..145071051-chr1:145086179..145089112,2	K562	blood:
46	chr1:145035558..145037358-chr1:145055855..145058557,2	K562	blood:
47	chr1:144999173..145001999-chr1:145037688..145039743,3	MCF-7	breast:
48	chr1:145018409..145019163-chr1:145060589..145061400,2	MCF-7	breast:
49	chr1:145070476..145072137-chr10:116063962..116066541,2	MCF-7	breast:
50	chr1:144992633..144993235-chr1:145029941..145030565,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE4DIP-5	chr1:145088039-145088567	NONHSAT005874
2	lnc-POLR3GL-6	chr1:145021112-145021167	NONHSAT005872
3	lnc-POLR3GL-6	chr1:145039590-145039851	NONHSAT005872
4	lnc-NBPF9-5	chr1:145018395-145018959	ENSG00000272755.1
5	lnc-POLR3GL-6	chr1:145015873-145016011	NONHSAT005872
6	lnc-POLR3GL-6	chr1:145017881-145017999	NONHSAT005872
7	lnc-NOTCH2NL-4	chr1:145044651-145044900	NONHSAT005873
8	lnc-NBPF9-3	chr1:145004781-145005286	NONHSAT005869
9	lnc-NBPF9-4	chr1:145013726-145013828	NONHSAT005870
10	lnc-NBPF9-4	chr1:145016388-145016968	NONHSAT005870

No data

Variant related genes	Relation type
SEC22B	TF binding region
RN7SKP88	TF binding region
ENSG00000272755	TF binding region
PDE4DIP	TF binding region
ENSG00000271546	TF binding region
ENSG00000268172	TF binding region
SEC22B	CpG island
RN7SKP88	CpG island
ENSG00000272755	CpG island
PDE4DIP	CpG island
ENSG00000271546	CpG island
ENSG00000268172	CpG island
ENSG00000212694	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000125347	chromatin interactions
ENSG00000225362	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000174827	chromatin interactions
ENSG00000203843	chromatin interactions
ENSG00000261139	chromatin interactions
ENSG00000188486	chromatin interactions
ENSG00000223491	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000271546	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000079335	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000226446	chromatin interactions
ENSG00000160972	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000255182	chromatin interactions
ENSG00000180370	chromatin interactions
ENSG00000169129	chromatin interactions

Extended variants
information (count: 4751 )
Associated
traits (count: 181 )

Variant overlapped rSNPs/rCNVs (count:4751 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10910684	chr1:144978306-144978307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587603872	chr1:144978317-144978318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587682847	chr1:144978348-144978349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147568549	chr1:144978366-144978367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs56885006	chr1:144978545-144978546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587731673	chr1:144978603-144978604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12089952	chr1:144978605-144978606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150169195	chr1:144978617-144978618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2985370	chr1:144978652-144978653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139661237	chr1:144978674-144978675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7527238	chr1:144978682-144978683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587686753	chr1:144978687-144978688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200443200	chr1:144978688-144978689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201248094	chr1:144978700-144978701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4649728	chr1:144978739-144978740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111538644	chr1:144978931-144978932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587740291	chr1:144978934-144978935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12087927	chr1:144978993-144978994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143564496	chr1:144979005-144979006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112822676	chr1:144979061-144979062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587622039	chr1:144979089-144979090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587671942	chr1:144979128-144979129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587737246	chr1:144979155-144979156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs60535272	chr1:144979156-144979157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9424644	chr1:144979192-144979193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587772002	chr1:144979221-144979222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61812904	chr1:144979254-144979255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs56687289	chr1:144979311-144979312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112596764	chr1:144979348-144979349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372774334	chr1:144979351-144979352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587683506	chr1:144979379-144979380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587762002	chr1:144979385-144979386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587616081	chr1:144979388-144979389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186159889	chr1:144979416-144979417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587748404	chr1:144979417-144979418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74351604	chr1:144979442-144979443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12039900	chr1:144979479-144979480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587650393	chr1:144979489-144979490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587703589	chr1:144979518-144979519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587763617	chr1:144979552-144979553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369855598	chr1:144979572-144979573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587674857	chr1:144979575-144979576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587733542	chr1:144979616-144979617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587629393	chr1:144979656-144979657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587688711	chr1:144979675-144979676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587723181	chr1:144979689-144979690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371221323	chr1:144979714-144979715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587679926	chr1:144979721-144979722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587722100	chr1:144979751-144979752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367645133	chr1:144979769-144979770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:181)

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
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	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
Breast cancer	17142309	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
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:5386 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144951000-144982400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:144965000-144982400	Weak transcription	Fetal Intestine Large	intestine
3	chr1:144966400-144982400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:144966400-144982400	Weak transcription	Brain Angular Gyrus	brain
5	chr1:144966600-144982400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr1:144966600-144982400	Weak transcription	K562	blood
7	chr1:144967400-144982400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:144967600-144982400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:144968000-144982400	Weak transcription	Brain Hippocampus Middle	brain
10	chr1:144968000-144982400	Weak transcription	HSMM	muscle
11	chr1:144968200-144982400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:144968200-144982600	Weak transcription	Osteobl	bone
13	chr1:144968600-144982400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr1:144970800-144982600	Weak transcription	Placenta	Placenta
15	chr1:144973000-144982400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:144973000-144982600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:144973200-144982400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:144973200-144982600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:144973200-144986000	Weak transcription	Right Atrium	heart
20	chr1:144974000-144982600	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr1:144976400-144982000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:144976400-144982400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr1:144976400-144982400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr1:144976400-144982400	Weak transcription	Fetal Muscle Leg	muscle
25	chr1:144976400-144982400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr1:144976400-144982600	Weak transcription	Left Ventricle	heart
27	chr1:144976600-144982400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr1:144977400-144982400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:144978200-144982400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:144978200-144987800	Weak transcription	Primary B cells from cord blood	blood
31	chr1:144978600-144981200	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr1:144981200-144981400	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr1:144981200-144982600	Weak transcription	Psoas Muscle	Psoas
34	chr1:144981400-144982400	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr1:144981800-144982400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:144982000-144982800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:144982000-144982800	Enhancers	Fetal Kidney	kidney
38	chr1:144982000-144983000	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr1:144982400-144982600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:144982400-144982600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:144982400-144982600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:144982400-144982600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr1:144982400-144982600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:144982400-144982600	Enhancers	Liver	Liver
45	chr1:144982400-144982600	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr1:144982400-144982600	Enhancers	Stomach Smooth Muscle	stomach
47	chr1:144982400-144982600	Enhancers	HMEC	breast
48	chr1:144982400-144982600	Enhancers	HSMM	muscle
49	chr1:144982400-144982600	Enhancers	K562	blood
50	chr1:144982400-144982600	Enhancers	NHEK	skin

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