Variant report

Variant	nsv1030744
Chromosome Location	chr6:5328012-5458222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5329295-5329331	K562	blood:	n/a	n/a
2	ARID3A	chr6:5333915-5334256	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:5351954-5352010	K562	blood:	n/a	n/a
4	ARID3A	chr6:5380018-5380168	K562	blood:	n/a	n/a
5	ATF1	chr6:5329106-5329358	K562	blood:	n/a	n/a
6	ATF1	chr6:5400979-5401008	K562	blood:	n/a	n/a
7	ATF1	chr6:5398731-5399051	K562	blood:	n/a	n/a
8	ATF2	chr6:5338294-5338813	GM12878	blood:	n/a	n/a
9	ATF2	chr6:5335131-5335747	GM12878	blood:	n/a	n/a
10	BACH1	chr6:5380041-5380208	K562	blood:	n/a	n/a
11	BATF	chr6:5335214-5335580	GM12878	blood:	n/a	n/a
12	BATF	chr6:5338449-5338757	GM12878	blood:	n/a	n/a
13	BATF	chr6:5335227-5335571	GM12878	blood:	n/a	n/a
14	BATF	chr6:5338444-5338732	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:5439210-5439426	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCLAF1	chr6:5338441-5338757	GM12878	blood:	n/a	chr6:5338528-5338537
17	BCLAF1	chr6:5335203-5335640	GM12878	blood:	n/a	chr6:5335547-5335556
18	BHLHE40	chr6:5329195-5329272	K562	blood:	n/a	n/a
19	BHLHE40	chr6:5379969-5380169	GM12878	blood:	n/a	n/a
20	BRCA1	chr6:5411934-5412037	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:5351871-5352211	ECC-1	luminal epithelium:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
22	CEBPB	chr6:5351830-5352207	IMR90	lung:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
23	CEBPB	chr6:5351735-5352196	K562	blood:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
24	CEBPB	chr6:5452057-5452363	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:5333392-5333476	HepG2	liver:	n/a	chr6:5333414-5333427 chr6:5333415-5333426 chr6:5333414-5333427 chr6:5333414-5333425
26	CEBPB	chr6:5402661-5402938	K562	blood:	n/a	n/a
27	CEBPB	chr6:5351840-5352205	A549	lung:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
28	CEBPB	chr6:5351706-5352213	K562	blood:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
29	CEBPB	chr6:5394562-5394950	MCF-7	breast:	n/a	chr6:5394716-5394727
30	CEBPB	chr6:5394603-5394931	MCF-7	breast:	n/a	chr6:5394716-5394727
31	CEBPB	chr6:5351845-5352248	MCF-7	breast:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
32	CEBPB	chr6:5439238-5439539	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr6:5394553-5394878	Hela-S3	cervix:	n/a	chr6:5394716-5394727
34	CEBPB	chr6:5351911-5352159	K562	blood:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
35	CEBPB	chr6:5351842-5352195	H1-hESC	embryonic stem cell:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
36	CEBPB	chr6:5394537-5394883	HepG2	liver:	n/a	chr6:5394716-5394727
37	CEBPB	chr6:5351835-5352143	A549	lung:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
38	CEBPB	chr6:5351852-5352213	ECC-1	luminal epithelium:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
39	CEBPB	chr6:5426867-5426988	HepG2	liver:	n/a	chr6:5426914-5426925
40	CEBPB	chr6:5394513-5394800	K562	blood:	n/a	chr6:5394716-5394727
41	CEBPB	chr6:5444631-5444694	K562	blood:	n/a	n/a
42	CEBPB	chr6:5351826-5352209	HepG2	liver:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
43	CEBPB	chr6:5398872-5399134	A549	lung:	n/a	n/a
44	CEBPB	chr6:5351711-5352308	A549	lung:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
45	CEBPB	chr6:5394562-5394904	A549	lung:	n/a	chr6:5394716-5394727
46	CEBPB	chr6:5412316-5412616	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr6:5333912-5334216	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:5394543-5394882	K562	blood:	n/a	chr6:5394716-5394727
49	CEBPB	chr6:5351895-5352236	MCF-7	breast:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
50	CEBPB	chr6:5394541-5394893	IMR90	lung:	n/a	chr6:5394716-5394727

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5431669-5431719	NB4	blood:	n/a
2	chr6:5406020-5406070	AG09319	gingival:	n/a
3	chr6:5378917-5378967	HMEC	breast:	n/a
4	chr6:5442953-5443003	ovcar-3	ovarian:	n/a
5	chr6:5404958-5405008	HAEpiC	amniotic membrane:	n/a
6	chr6:5404958-5405008	A549	lung:	n/a
7	chr6:5442953-5443003	BE2_C	brain:	n/a
8	chr6:5412087-5412137	GM12892	blood:	n/a
9	chr6:5412087-5412137	Jurkat	blood:	n/a
10	chr6:5439460-5439510	U87	brain:	n/a
11	chr6:5425832-5425882	BE2_C	brain:	n/a
12	chr6:5431669-5431719	PANC-1	pancreas:	n/a
13	chr6:5404958-5405008	HCPEpiC	choroid plexus:	n/a
14	chr6:5412087-5412137	SAEC	small airway:	n/a
15	chr6:5412087-5412137	Caco-2	colon:	n/a
16	chr6:5431669-5431719	NHDF-neo	bronchial:	n/a
17	chr6:5425832-5425882	PFSK-1	brain:	n/a
18	chr6:5406020-5406070	PANC-1	pancreas:	n/a
19	chr6:5431669-5431719	HepG2	liver:	n/a
20	chr6:5431669-5431719	AG04449	skin:	fetal
21	chr6:5406020-5406070	NT2-D1	testis:	n/a
22	chr6:5404958-5405008	HCF	heart:	n/a
23	chr6:5404958-5405008	HRCEpiC	kidney:	n/a
24	chr6:5439460-5439510	HCPEpiC	choroid plexus:	n/a
25	chr6:5378917-5378967	SK-N-MC	brain:	n/a
26	chr6:5439460-5439510	HCM	heart:	n/a
27	chr6:5404958-5405008	GM19239	blood:	n/a
28	chr6:5431669-5431719	AG09319	gingival:	n/a
29	chr6:5406020-5406070	HL-60	blood:	n/a
30	chr6:5442953-5443003	HRE	kidney:	n/a
31	chr6:5378917-5378967	HL-60	blood:	n/a
32	chr6:5406020-5406070	Hepatocyte	liver:	n/a
33	chr6:5378917-5378967	SK-N-SH_RA	brain:	n/a
34	chr6:5412087-5412137	HIPEpiC	eye:	n/a
35	chr6:5404958-5405008	AG04449	skin:	fetal
36	chr6:5439460-5439510	AG04450	lung:	fetal
37	chr6:5404958-5405008	HRE	kidney:	n/a
38	chr6:5439460-5439510	GM12891	blood:	n/a
39	chr6:5431669-5431719	LNCaP	prostate:	n/a
40	chr6:5378917-5378967	HUVEC	blood vessel:	n/a
41	chr6:5442953-5443003	ProgFib	skin:	n/a
42	chr6:5406020-5406070	HEK293	kidney:	embryo
43	chr6:5439460-5439510	SKMC	muscle:	n/a
44	chr6:5425832-5425882	MCF-7	breast:	n/a
45	chr6:5412087-5412137	IMR90	lung:	fetal
46	chr6:5439460-5439510	HNPCEpiC	eye:	n/a
47	chr6:5404958-5405008	NHBE	bronchial:	n/a
48	chr6:5406020-5406070	HCM	heart:	n/a
49	chr6:5412087-5412137	HL-60	blood:	n/a
50	chr6:5425832-5425882	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:5214746..5216032-chr6:5379652..5380557,3	K562	blood:
2	chr6:5438413..5441149-chr6:5444124..5446462,2	K562	blood:
3	chr6:5351636..5353650-chr6:5354468..5356338,2	K562	blood:
4	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
5	chr6:5422389..5423223-chr6:5898415..5898938,2	MCF-7	breast:
6	chr6:5455034..5457596-chr6:5459159..5460952,3	K562	blood:
7	chr6:5378846..5381566-chr6:5383901..5386296,2	K562	blood:
8	chr6:5143614..5144581-chr6:5379550..5380557,6	MCF-7	breast:
9	chr6:5434559..5437034-chr6:5438817..5440512,2	MCF-7	breast:
10	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
11	chr6:5337400..5339933-chr6:5352570..5354341,2	K562	blood:
12	chr6:5434559..5437034-chr6:5438817..5440512,2	MCF-7	breast:
13	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
14	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
15	chr6:5356672..5358762-chr6:5360755..5363627,2	K562	blood:
16	chr6:5422309..5423241-chr6:6547390..6547945,3	MCF-7	breast:
17	chr6:5295190..5297508-chr6:5331125..5333153,2	K562	blood:
18	chr6:5143921..5144506-chr6:5398809..5399361,2	MCF-7	breast:
19	chr6:5376489..5378009-chr6:5378380..5380035,2	MCF-7	breast:
20	chr6:5431881..5436604-chr6:5436753..5441713,4	K562	blood:
21	chr6:5380009..5381908-chr6:5391068..5392911,2	K562	blood:
22	chr6:5143546..5144516-chr6:5402052..5403264,7	K562	blood:
23	chr6:5259458..5263167-chr6:5378329..5381459,4	K562	blood:
24	chr6:5255894..5257705-chr6:5381224..5383041,2	K562	blood:
25	chr6:5135691..5136262-chr6:5402310..5402817,2	K562	blood:
26	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
27	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
28	chr6:5056624..5057532-chr6:5398465..5398983,2	K562	blood:
29	chr6:5143540..5144964-chr6:5379399..5380247,6	K562	blood:
30	chr6:5143607..5144647-chr6:5402160..5403231,5	MCF-7	breast:
31	chr6:5383058..5384884-chr6:5386592..5388274,2	K562	blood:
32	chr6:5324825..5326784-chr6:5328920..5331743,2	K562	blood:
33	chr6:5214761..5215392-chr6:5379547..5380560,3	MCF-7	breast:
34	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
35	chr6:5259536..5262981-chr6:5378329..5381673,4	K562	blood:
36	chr6:5220721..5222969-chr6:5379273..5381024,2	K562	blood:
37	chr6:5354142..5357037-chr6:5358520..5360420,2	K562	blood:
38	chr6:5214686..5215658-chr6:5401229..5403280,10	K562	blood:
39	chr6:5378846..5381566-chr6:5383901..5386296,2	K562	blood:
40	chr6:5380009..5381908-chr6:5391068..5392911,2	K562	blood:
41	chr6:5360554..5362439-chr6:5363496..5365484,2	K562	blood:
42	chr6:5356672..5358762-chr6:5360755..5363627,2	K562	blood:
43	chr6:5371917..5373549-chr6:5379735..5382475,2	K562	blood:
44	chr6:5435025..5437230-chr6:5438877..5440438,2	MCF-7	breast:
45	chr6:5214744..5215638-chr6:5398420..5399368,7	K562	blood:
46	chr6:5378186..5380144-chr6:5383015..5385414,2	K562	blood:
47	chr6:5143322..5144392-chr6:5398327..5399283,4	MCF-7	breast:
48	chr6:5445214..5446148-chr7:141145714..141146573,2	MCF-7	breast:
49	chr6:5431881..5436604-chr6:5436753..5441713,4	K562	blood:
50	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYRM4-3	chr6:5458127-5458308	ENSG00000269985.1
2	lnc-LYRM4-3	chr6:5457186-5457261	ENSG00000269985.1
3	lnc-LYRM4-3	chr6:5452701-5452990	ENSG00000269985.1
4	lnc-LYRM4-3	chr6:5457093-5457261	NONHSAT107520
5	lnc-LYRM4-3	chr6:5458127-5458278	NONHSAT107520
6	lnc-LYRM4-3	chr6:5458127-5458266	ENSG00000269985.1
7	lnc-LYRM4-3	chr6:5451916-5452990	ENSG00000269985.1

Variant related genes	Relation type
FARS2	TF binding region
FARS2	CpG island
ENSG00000145982	chromatin interactions
ENSG00000214113	chromatin interactions

Extended variants
information (count: 5316 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:5316 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561071221	chr6:5328023-5328024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368213825	chr6:5328033-5328034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138213368	chr6:5328038-5328039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549825967	chr6:5328098-5328099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565246591	chr6:5328099-5328100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149589339	chr6:5328147-5328148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547464207	chr6:5328148-5328149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs61482411	chr6:5328172-5328173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565880998	chr6:5328181-5328182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373866067	chr6:5328189-5328190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182596711	chr6:5328218-5328219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34868184	chr6:5328221-5328222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540917087	chr6:5328235-5328236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372494692	chr6:5328253-5328254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575651025	chr6:5328270-5328271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112440193	chr6:5328286-5328287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs58845080	chr6:5328290-5328291	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570177247	chr6:5328349-5328350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187635929	chr6:5328365-5328366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs386696495	chr6:5328404-5328405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs797127	chr6:5328406-5328407	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs114800922	chr6:5328500-5328501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532128900	chr6:5328503-5328504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538304780	chr6:5328512-5328513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78184173	chr6:5328519-5328520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377481142	chr6:5328569-5328570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113881657	chr6:5328620-5328621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191804392	chr6:5328812-5328813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148302352	chr6:5328823-5328824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368941122	chr6:5328856-5328857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116353839	chr6:5328900-5328901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565059910	chr6:5328965-5328966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184092853	chr6:5329012-5329013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189074343	chr6:5329036-5329037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs193025920	chr6:5329138-5329139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115742527	chr6:5329151-5329152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183679387	chr6:5329201-5329202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142635610	chr6:5329278-5329279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186554327	chr6:5329289-5329290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531042964	chr6:5329295-5329296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552834943	chr6:5329326-5329327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191785182	chr6:5329327-5329328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535349940	chr6:5329359-5329360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34726622	chr6:5329362-5329363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368431616	chr6:5329363-5329364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565699764	chr6:5329364-5329365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544501742	chr6:5329370-5329371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77399042	chr6:5329412-5329413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576163850	chr6:5329429-5329430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372742946	chr6:5329494-5329495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5288400-5331000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:5292800-5334400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:5303200-5368800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:5303600-5332400	Weak transcription	Gastric	stomach
5	chr6:5304000-5337600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr6:5309200-5333400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:5309200-5334000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:5316400-5333800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:5316800-5335200	Weak transcription	NHLF	lung
10	chr6:5318800-5331600	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr6:5319200-5328200	Weak transcription	Thymus	Thymus
12	chr6:5319600-5334600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr6:5320600-5344400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:5321800-5335200	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr6:5322200-5333800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:5322600-5333600	Weak transcription	A549	lung
17	chr6:5323000-5331800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:5324800-5334000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:5325000-5331600	Weak transcription	Right Ventricle	heart
20	chr6:5325200-5335000	Weak transcription	Fetal Lung	lung
21	chr6:5325600-5328600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr6:5325600-5329200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr6:5325800-5328800	Weak transcription	Ovary	ovary
24	chr6:5325800-5331600	Weak transcription	Adipose Nuclei	Adipose
25	chr6:5325800-5331600	Weak transcription	Fetal Muscle Leg	muscle
26	chr6:5325800-5334000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:5325800-5334000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr6:5325800-5339600	Weak transcription	Fetal Intestine Large	intestine
29	chr6:5326000-5333600	Weak transcription	HepG2	liver
30	chr6:5326000-5335400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr6:5326000-5337800	Weak transcription	HSMM	muscle
32	chr6:5326400-5337800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr6:5326600-5328400	Weak transcription	Brain Substantia Nigra	brain
34	chr6:5326600-5349200	Weak transcription	Primary B cells from cord blood	blood
35	chr6:5326600-5385000	Weak transcription	Primary hematopoietic stem cells	blood
36	chr6:5326800-5328400	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr6:5326800-5328400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr6:5326800-5330000	Weak transcription	Brain Cingulate Gyrus	brain
39	chr6:5326800-5334000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:5326800-5337800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr6:5327000-5328800	Weak transcription	Fetal Muscle Trunk	muscle
42	chr6:5327000-5328800	Weak transcription	K562	blood
43	chr6:5327000-5329800	Weak transcription	Pancreas	Pancrea
44	chr6:5327000-5334400	Weak transcription	Fetal Stomach	stomach
45	chr6:5327000-5337400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:5327000-5338000	Weak transcription	Fetal Intestine Small	intestine
47	chr6:5327000-5368800	Weak transcription	Aorta	Aorta
48	chr6:5327200-5329000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr6:5327200-5329400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:5327400-5328600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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