Variant report

Variant	nsv539080
Chromosome Location	chr7:111049419-111274664
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2399)
CpG islands
(count:1040)
Chromatin interactive
region (count:183)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2399 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
2	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
4	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
7	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
8	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
9	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
11	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
13	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
14	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
15	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
16	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
18	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
19	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
20	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
21	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
22	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
23	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
24	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
25	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
26	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
27	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
28	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
29	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
32	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
33	ATF3	chr7:111156586-111157138	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
34	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
35	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
36	ATF3	chr7:111201918-111202678	K562	blood:	n/a	n/a
37	ATF3	chr7:111156585-111157142	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
38	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a
39	BACH1	chr7:111201779-111202839	K562	blood:	n/a	n/a
40	BACH1	chr7:111188905-111189076	K562	blood:	n/a	n/a
41	BACH1	chr7:111202015-111202410	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr7:111160755-111160869	K562	blood:	n/a	n/a
43	BACH1	chr7:111169257-111169277	K562	blood:	n/a	n/a
44	BACH1	chr7:111172186-111172416	K562	blood:	n/a	n/a
45	BATF	chr7:111228155-111228552	GM12878	blood:	n/a	chr7:111228280-111228290 chr7:111228384-111228394 chr7:111228383-111228394
46	BCL11A	chr7:111168484-111168730	GM12878	blood:	n/a	n/a
47	BCL3	chr7:111138913-111139703	A549	lung:	n/a	chr7:111138981-111138990
48	BCL3	chr7:111139024-111139659	A549	lung:	n/a	n/a
49	BCL3	chr7:111156597-111157052	A549	lung:	n/a	n/a
50	BCL3	chr7:111201738-111202909	A549	lung:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111202222-111202272	AG10803	skin:	n/a
2	chr7:111249924-111249974	SK-N-SH_RA	brain:	n/a
3	chr7:111249924-111249974	Hela-S3	cervix:	n/a
4	chr7:111202222-111202272	AG10803	skin:	n/a
5	chr7:111249924-111249974	SK-N-SH_RA	brain:	n/a
6	chr7:111249924-111249974	Hela-S3	cervix:	n/a
7	chr7:111202222-111202272	AG04449	skin:	fetal
8	chr7:111202682-111202732	HMEC	breast:	n/a
9	chr7:111249576-111249626	HAEpiC	amniotic membrane:	n/a
10	chr7:111200944-111200994	HCM	heart:	n/a
11	chr7:111202755-111202805	AG09319	gingival:	n/a
12	chr7:111202222-111202272	IMR90	lung:	fetal
13	chr7:111202222-111202272	HRPEpiC	eye:	n/a
14	chr7:111202389-111202439	H1-hESC	embryonic stem cell:	embryo
15	chr7:111202679-111202729	Jurkat	blood:	n/a
16	chr7:111202457-111202507	IMR90	lung:	fetal
17	chr7:111249924-111249974	AG09319	gingival:	n/a
18	chr7:111202389-111202439	HL-60	blood:	n/a
19	chr7:111202755-111202805	HCF	heart:	n/a
20	chr7:111202450-111202500	ProgFib	skin:	n/a
21	chr7:111202457-111202507	ProgFib	skin:	n/a
22	chr7:111249576-111249626	HCPEpiC	choroid plexus:	n/a
23	chr7:111202755-111202805	HUVEC	blood vessel:	n/a
24	chr7:111086055-111086105	HUVEC	blood vessel:	n/a
25	chr7:111200944-111200994	NHBE	bronchial:	n/a
26	chr7:111202450-111202500	GM19239	blood:	n/a
27	chr7:111249576-111249626	GM06990	blood:	n/a
28	chr7:111204826-111204876	K562	blood:	n/a
29	chr7:111202222-111202272	HEK293	kidney:	embryo
30	chr7:111202666-111202716	AG04450	lung:	fetal
31	chr7:111249924-111249974	GM06990	blood:	n/a
32	chr7:111202666-111202716	HRPEpiC	eye:	n/a
33	chr7:111249924-111249974	HAEpiC	amniotic membrane:	n/a
34	chr7:111202666-111202716	Hepatocyte	liver:	n/a
35	chr7:111203008-111203058	NHDF-neo	bronchial:	n/a
36	chr7:111249924-111249974	MCF-7	breast:	n/a
37	chr7:111202755-111202805	SK-N-SH	brain:	n/a
38	chr7:111249924-111249974	HRPEpiC	eye:	n/a
39	chr7:111200944-111200994	K562	blood:	n/a
40	chr7:111202395-111202445	HAEpiC	amniotic membrane:	n/a
41	chr7:111204826-111204876	H1-hESC	embryonic stem cell:	embryo
42	chr7:111086055-111086105	SK-N-MC	brain:	n/a
43	chr7:111202682-111202732	RPTEC	kidney:	n/a
44	chr7:111086055-111086105	BJ	skin:	n/a
45	chr7:111202679-111202729	HEK293	kidney:	embryo
46	chr7:111202457-111202507	Hela-S3	cervix:	n/a
47	chr7:111202389-111202439	SK-N-SH	brain:	n/a
48	chr7:111202679-111202729	ovcar-3	ovarian:	n/a
49	chr7:111200944-111200994	HCT-116	colon:	n/a
50	chr7:111202389-111202439	NHDF-neo	bronchial:	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:111163636..111166513-chr7:111167048..111171015,5	K562	blood:
2	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
3	chr7:111168569..111170226-chr7:111188051..111190882,2	K562	blood:
4	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
5	chr7:111165046..111169719-chr7:111171827..111173771,4	K562	blood:
6	chr7:111164149..111166792-chr7:111174165..111176807,3	K562	blood:
7	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
8	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
9	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
10	chr7:111226016..111229076-chr7:111232229..111235664,3	K562	blood:
11	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
12	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
13	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
14	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
15	chr7:111164149..111167742-chr7:111173784..111176807,4	K562	blood:
16	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
17	chr7:111222849..111225723-chr7:111230601..111232352,2	K562	blood:
18	chr7:111227327..111229119-chr7:111232502..111234968,2	K562	blood:
19	chr7:111254948..111257286-chr7:111263356..111265549,2	K562	blood:
20	chr7:111149350..111150943-chr7:111156315..111157965,2	K562	blood:
21	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
22	chr12:108200986..108203742-chr7:111052172..111055145,3	MCF-7	breast:
23	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
24	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
25	chr7:111257306..111261237-chr7:111261907..111264448,3	K562	blood:
26	chr7:111252721..111255749-chr7:111259045..111261451,3	K562	blood:
27	chr7:111176200..111178839-chr7:111180322..111182875,3	K562	blood:
28	chr7:111114124..111115929-chr7:111199099..111201690,2	K562	blood:
29	chr7:111162292..111164581-chr7:111182567..111185234,2	K562	blood:
30	chr7:110975357..110976070-chr7:111125914..111126817,2	K562	blood:
31	chr7:111201240..111203723-chr7:111208743..111211882,3	K562	blood:
32	chr6:31639869..31641695-chr7:111180406..111182806,2	MCF-7	breast:
33	chr7:111132967..111134732-chr7:111137505..111139653,3	MCF-7	breast:
34	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
35	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
36	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
37	chr7:111167719..111169526-chr7:111174940..111178460,3	K562	blood:
38	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:
39	chr7:111182436..111184713-chr7:111201121..111202847,2	MCF-7	breast:
40	chr7:111252721..111255749-chr7:111259045..111261451,3	K562	blood:
41	chr7:111167719..111169526-chr7:111174940..111178460,3	K562	blood:
42	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
43	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
44	chr7:111154283..111157202-chr7:111157997..111159947,2	MCF-7	breast:
45	chr7:111154283..111157202-chr7:111157997..111159947,2	MCF-7	breast:
46	chr7:111222849..111225723-chr7:111230601..111232352,2	K562	blood:
47	chr7:111172655..111174823-chr7:111200872..111202478,2	MCF-7	breast:
48	chr7:111114124..111115929-chr7:111199099..111201690,2	K562	blood:
49	chr7:111136494..111138259-chr7:111146295..111147835,2	K562	blood:
50	chr7:111166819..111169168-chr7:111191445..111193799,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRN3-2	chr7:111246670-111249064	ucscGeneNc_uc003vfz_2
2	lnc-LRRN3-2	chr7:111235830-111235905	ucscGeneNc_uc003vfz_2

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
IMMP2L	TF binding region
ENSG00000227948	CpG island
IMMP2L	CpG island
ENSG00000143643	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000178951	chromatin interactions

Extended variants
information (count: 6680 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:6680 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145891423	chr7:111049444-111049445	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs10250608	chr7:111049537-111049538	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192014203	chr7:111049545-111049546	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs35677841	chr7:111049589-111049590	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs183336283	chr7:111049634-111049635	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs563139658	chr7:111049647-111049648	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs187937506	chr7:111049659-111049660	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs543190896	chr7:111049660-111049661	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs138502898	chr7:111049663-111049664	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567236508	chr7:111049700-111049701	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs534678873	chr7:111049723-111049724	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs17158563	chr7:111049775-111049776	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs571594027	chr7:111049842-111049843	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs192444975	chr7:111049889-111049890	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs139688179	chr7:111049895-111049896	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs557496087	chr7:111049937-111049938	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs182224198	chr7:111049938-111049939	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75411971	chr7:111049952-111049953	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs555273755	chr7:111049962-111049963	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs186462372	chr7:111050029-111050030	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs192744189	chr7:111050063-111050064	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs559290921	chr7:111050067-111050068	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375303957	chr7:111050069-111050070	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs571421746	chr7:111050083-111050084	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs563050722	chr7:111050121-111050122	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs530584481	chr7:111050151-111050152	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs369040847	chr7:111050159-111050160	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs142934727	chr7:111050196-111050197	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs560952288	chr7:111050206-111050207	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs114086708	chr7:111050226-111050227	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs568400934	chr7:111050231-111050232	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs184753265	chr7:111050308-111050309	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs144356339	chr7:111050310-111050311	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs538664598	chr7:111050425-111050426	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs117867488	chr7:111050591-111050592	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs569398656	chr7:111050721-111050722	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs6966451	chr7:111050725-111050726	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555187635	chr7:111050748-111050749	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs573396251	chr7:111050749-111050750	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs144890009	chr7:111050754-111050755	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs189514677	chr7:111050829-111050830	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs577522852	chr7:111050875-111050876	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs544620512	chr7:111050880-111050881	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs556610387	chr7:111050881-111050882	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs193185444	chr7:111050928-111050929	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs542356748	chr7:111050940-111050941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561133909	chr7:111050948-111050949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184532462	chr7:111051005-111051006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540481374	chr7:111051142-111051143	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs555158217	chr7:111051147-111051148	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111044600-111049800	Weak transcription	HSMMtube	muscle
2	chr7:111046400-111049600	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr7:111047000-111050000	Weak transcription	Aorta	Aorta
4	chr7:111047000-111053800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:111048200-111049600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:111048400-111049800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:111048800-111050800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:111049200-111051000	Enhancers	NHDF-Ad	bronchial
9	chr7:111049400-111050200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:111049400-111050600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:111049400-111051000	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr7:111049400-111051200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:111049600-111050600	Enhancers	Osteobl	bone
14	chr7:111049800-111050200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:111049800-111050200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:111049800-111050200	Enhancers	Ovary	ovary
17	chr7:111049800-111050400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:111049800-111050400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:111049800-111050400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:111049800-111050400	Enhancers	HSMMtube	muscle
21	chr7:111049800-111050800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:111049800-111055400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:111050000-111050200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:111050000-111050200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr7:111050000-111050400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr7:111050000-111050400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:111050000-111050400	Enhancers	Fetal Intestine Large	intestine
28	chr7:111050000-111050400	Enhancers	HepG2	liver
29	chr7:111050000-111050600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:111050000-111050600	Enhancers	Fetal Intestine Small	intestine
31	chr7:111050200-111050400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr7:111050200-111051000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:111050200-111051400	Weak transcription	Ovary	ovary
34	chr7:111050200-111053800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:111050400-111051400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr7:111050400-111053000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:111050400-111053200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:111050400-111053600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr7:111050400-111053800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr7:111050600-111050800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:111050600-111051400	Weak transcription	Fetal Intestine Small	intestine
42	chr7:111050600-111051600	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr7:111050600-111053800	Weak transcription	Left Ventricle	heart
44	chr7:111050800-111051800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:111050800-111052400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr7:111050800-111053800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:111051000-111052200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr7:111051200-111051600	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr7:111051400-111051600	Weak transcription	Aorta	Aorta
50	chr7:111051400-111051800	Enhancers	Lung	lung

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