Variant report

Variant	nsv600883
Chromosome Location	chr6:5302619-5400658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1264)
CpG islands
(count:183)
Chromatin interactive
region (count:73)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5351954-5352010	K562	blood:	n/a	n/a
2	ARID3A	chr6:5380018-5380168	K562	blood:	n/a	n/a
3	ARID3A	chr6:5333915-5334256	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:5329295-5329331	K562	blood:	n/a	n/a
5	ARID3A	chr6:5302507-5302854	K562	blood:	n/a	n/a
6	ATF1	chr6:5302305-5302992	K562	blood:	n/a	n/a
7	ATF1	chr6:5398731-5399051	K562	blood:	n/a	n/a
8	ATF1	chr6:5329106-5329358	K562	blood:	n/a	n/a
9	ATF2	chr6:5338294-5338813	GM12878	blood:	n/a	n/a
10	ATF2	chr6:5303469-5303900	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:5302721-5303188	GM12878	blood:	n/a	n/a
12	ATF2	chr6:5335131-5335747	GM12878	blood:	n/a	n/a
13	ATF2	chr6:5302657-5303223	GM12878	blood:	n/a	n/a
14	BACH1	chr6:5309454-5309486	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:5380041-5380208	K562	blood:	n/a	n/a
16	BACH1	chr6:5303473-5303784	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr6:5335227-5335571	GM12878	blood:	n/a	n/a
18	BATF	chr6:5302751-5303177	GM12878	blood:	n/a	n/a
19	BATF	chr6:5338444-5338732	GM12878	blood:	n/a	n/a
20	BATF	chr6:5335214-5335580	GM12878	blood:	n/a	n/a
21	BATF	chr6:5302740-5303111	GM12878	blood:	n/a	n/a
22	BATF	chr6:5338449-5338757	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:5302827-5303127	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:5302695-5303166	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:5338441-5338757	GM12878	blood:	n/a	chr6:5338528-5338537
26	BCLAF1	chr6:5302694-5303208	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:5335203-5335640	GM12878	blood:	n/a	chr6:5335547-5335556
28	BHLHE40	chr6:5379969-5380169	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:5303479-5303817	K562	blood:	n/a	n/a
30	BHLHE40	chr6:5302378-5303223	K562	blood:	n/a	chr6:5303157-5303173
31	BHLHE40	chr6:5302700-5303149	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:5303415-5303850	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:5303460-5303853	HepG2	liver:	n/a	n/a
34	BHLHE40	chr6:5329195-5329272	K562	blood:	n/a	n/a
35	CBX3	chr6:5324140-5324580	K562	blood:	n/a	n/a
36	CBX3	chr6:5324194-5324573	K562	blood:	n/a	n/a
37	CCNT2	chr6:5302407-5303003	K562	blood:	n/a	n/a
38	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
39	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
40	CEBPB	chr6:5394562-5394950	MCF-7	breast:	n/a	chr6:5394716-5394727
41	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
42	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
43	CEBPB	chr6:5394541-5394893	IMR90	lung:	n/a	chr6:5394716-5394727
44	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
45	CEBPB	chr6:5306244-5306591	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:5394543-5394882	K562	blood:	n/a	chr6:5394716-5394727
47	CEBPB	chr6:5394553-5394878	Hela-S3	cervix:	n/a	chr6:5394716-5394727
48	CEBPB	chr6:5333392-5333476	HepG2	liver:	n/a	chr6:5333414-5333427 chr6:5333415-5333426 chr6:5333414-5333427 chr6:5333414-5333425
49	CEBPB	chr6:5333912-5334216	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:5306298-5306468	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5378917-5378967	SKMC	muscle:	n/a
2	chr6:5378917-5378967	HepG2	liver:	n/a
3	chr6:5316922-5316972	AG04449	skin:	fetal
4	chr6:5313645-5313695	HUVEC	blood vessel:	n/a
5	chr6:5313645-5313695	HRPEpiC	eye:	n/a
6	chr6:5313645-5313695	HCM	heart:	n/a
7	chr6:5313645-5313695	ECC-1	luminal epithelium:	n/a
8	chr6:5378917-5378967	PANC-1	pancreas:	n/a
9	chr6:5316922-5316972	HCPEpiC	choroid plexus:	n/a
10	chr6:5316922-5316972	HCM	heart:	n/a
11	chr6:5316922-5316972	HCF	heart:	n/a
12	chr6:5313645-5313695	HMEC	breast:	n/a
13	chr6:5313645-5313695	HRCEpiC	kidney:	n/a
14	chr6:5378917-5378967	HCT-116	colon:	n/a
15	chr6:5378917-5378967	HNPCEpiC	eye:	n/a
16	chr6:5313645-5313695	HCPEpiC	choroid plexus:	n/a
17	chr6:5313645-5313695	HEEpiC	esophagus:	n/a
18	chr6:5313645-5313695	K562	blood:	n/a
19	chr6:5316922-5316972	HRE	kidney:	n/a
20	chr6:5313645-5313695	HEK293	kidney:	embryo
21	chr6:5313645-5313695	HepG2	liver:	n/a
22	chr6:5313645-5313695	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:5313645-5313695	NHBE	bronchial:	n/a
24	chr6:5316922-5316972	SK-N-SH	brain:	n/a
25	chr6:5316922-5316972	HMEC	breast:	n/a
26	chr6:5378917-5378967	ovcar-3	ovarian:	n/a
27	chr6:5316922-5316972	NHDF-neo	bronchial:	n/a
28	chr6:5316922-5316972	HEEpiC	esophagus:	n/a
29	chr6:5313645-5313695	Jurkat	blood:	n/a
30	chr6:5378917-5378967	NT2-D1	testis:	n/a
31	chr6:5378917-5378967	AG09319	gingival:	n/a
32	chr6:5378917-5378967	MCF-7	breast:	n/a
33	chr6:5316922-5316972	AoSMC	blood vessel:	n/a
34	chr6:5378917-5378967	Jurkat	blood:	n/a
35	chr6:5316922-5316972	SK-N-SH_RA	brain:	n/a
36	chr6:5313645-5313695	PANC-1	pancreas:	n/a
37	chr6:5313645-5313695	MCF-7	breast:	n/a
38	chr6:5378917-5378967	HRPEpiC	eye:	n/a
39	chr6:5313645-5313695	IMR90	lung:	fetal
40	chr6:5313645-5313695	SK-N-SH	brain:	n/a
41	chr6:5378917-5378967	A549	lung:	n/a
42	chr6:5313645-5313695	Hepatocyte	liver:	n/a
43	chr6:5378917-5378967	PFSK-1	brain:	n/a
44	chr6:5378917-5378967	HEEpiC	esophagus:	n/a
45	chr6:5316922-5316972	BJ	skin:	n/a
46	chr6:5313645-5313695	LNCaP	prostate:	n/a
47	chr6:5316922-5316972	GM12891	blood:	n/a
48	chr6:5316922-5316972	HRCEpiC	kidney:	n/a
49	chr6:5313645-5313695	AG10803	skin:	n/a
50	chr6:5313645-5313695	HRE	kidney:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:5259458..5263167-chr6:5378329..5381459,4	K562	blood:
2	chr6:5299459..5300981-chr6:5301727..5303514,2	MCF-7	breast:
3	chr6:5214744..5215638-chr6:5398420..5399368,7	K562	blood:
4	chr6:5302902..5305704-chr6:5324020..5325616,2	K562	blood:
5	chr6:5324825..5326784-chr6:5328920..5331743,2	K562	blood:
6	chr6:5371917..5373549-chr6:5379735..5382475,2	K562	blood:
7	chr6:5143322..5144392-chr6:5398327..5399283,4	MCF-7	breast:
8	chr6:5352377..5354120-chr6:5360443..5362372,2	K562	blood:
9	chr6:5376489..5378009-chr6:5378380..5380035,2	MCF-7	breast:
10	chr6:5220721..5222969-chr6:5379273..5381024,2	K562	blood:
11	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
12	chr6:5356672..5358762-chr6:5360755..5363627,2	K562	blood:
13	chr6:5056624..5057532-chr6:5398465..5398983,2	K562	blood:
14	chr6:5143575..5144138-chr6:5398465..5399339,2	K562	blood:
15	chr6:5285714..5287859-chr6:5301778..5303462,2	K562	blood:
16	chr6:5143540..5144964-chr6:5379399..5380247,6	K562	blood:
17	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
18	chr6:5316201..5319010-chr6:5321352..5323470,3	K562	blood:
19	chr6:5380009..5381908-chr6:5391068..5392911,2	K562	blood:
20	chr6:5364826..5367079-chr6:5385611..5387966,2	K562	blood:
21	chr6:5324825..5326784-chr6:5328920..5331743,2	K562	blood:
22	chr6:5214746..5216032-chr6:5379652..5380557,3	K562	blood:
23	chr6:5360554..5362439-chr6:5363496..5365484,2	K562	blood:
24	chr6:5316219..5318124-chr6:5321436..5323216,2	K562	blood:
25	chr6:5364063..5366771-chr6:5369592..5371297,2	K562	blood:
26	chr6:5308101..5310755-chr6:5313510..5315565,2	K562	blood:
27	chr6:5337400..5339933-chr6:5352570..5354341,2	K562	blood:
28	chr6:5285977..5287695-chr6:5316657..5318764,2	MCF-7	breast:
29	chr6:5376489..5378009-chr6:5378380..5380035,2	MCF-7	breast:
30	chr6:5354142..5357037-chr6:5358520..5360420,2	K562	blood:
31	chr6:5259536..5262981-chr6:5378329..5381673,4	K562	blood:
32	chr6:5323707..5326276-chr6:5329133..5331071,2	K562	blood:
33	chr15:91040281..91042340-chr6:5395615..5398410,2	MCF-7	breast:
34	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
35	chr6:5351636..5353650-chr6:5354468..5356338,2	K562	blood:
36	chr6:5314865..5316963-chr6:5319263..5320833,2	K562	blood:
37	chr6:5143921..5144506-chr6:5398809..5399361,2	MCF-7	breast:
38	chr6:5323707..5326276-chr6:5329133..5331071,2	K562	blood:
39	chr6:5316201..5319010-chr6:5321352..5323470,3	K562	blood:
40	chr6:5371917..5373549-chr6:5379735..5382475,2	K562	blood:
41	chr6:5364063..5366771-chr6:5369592..5371297,2	K562	blood:
42	chr6:5333079..5335354-chr6:5335769..5338319,2	K562	blood:
43	chr6:5383058..5384884-chr6:5386592..5388274,2	K562	blood:
44	chr6:5214761..5215392-chr6:5379547..5380560,3	MCF-7	breast:
45	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
46	chr6:5259574..5262375-chr6:5317058..5319115,2	K562	blood:
47	chr6:5360554..5362439-chr6:5363496..5365484,2	K562	blood:
48	chr6:5351636..5353650-chr6:5354468..5356338,2	K562	blood:
49	chr6:5308101..5310755-chr6:5313510..5315565,2	K562	blood:
50	chr6:5255894..5257705-chr6:5381224..5383041,2	K562	blood:

No data

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

Extended variants
information (count: 3815 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3815 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17140145	chr6:5302619-5302620	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79138485	chr6:5302639-5302640	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs17140150	chr6:5302676-5302677	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs528458015	chr6:5302688-5302689	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs114871463	chr6:5302699-5302700	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs182908893	chr6:5302705-5302706	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs79663075	chr6:5302722-5302723	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs73365082	chr6:5302777-5302778	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs148923066	chr6:5302814-5302815	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs9392670	chr6:5302844-5302845	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs540031866	chr6:5302921-5302922	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs58857565	chr6:5302922-5302923	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs143673579	chr6:5302971-5302972	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs541004408	chr6:5302990-5302991	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs75236806	chr6:5302993-5302994	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs574499368	chr6:5303027-5303028	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs541917574	chr6:5303053-5303054	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs80099511	chr6:5303054-5303055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs373798186	chr6:5303077-5303078	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs530580015	chr6:5303110-5303111	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs376469991	chr6:5303167-5303168	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs187637350	chr6:5303193-5303194	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs530735858	chr6:5303214-5303215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs74623110	chr6:5303234-5303235	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs528400238	chr6:5303246-5303247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs546576164	chr6:5303341-5303342	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs568081737	chr6:5303382-5303383	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs560588821	chr6:5303412-5303413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs553485065	chr6:5303420-5303421	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs192128790	chr6:5303424-5303425	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs550754895	chr6:5303442-5303443	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs533503856	chr6:5303467-5303468	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs370190249	chr6:5303468-5303469	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs114815658	chr6:5303540-5303541	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs539639851	chr6:5303541-5303542	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs368866745	chr6:5303547-5303548	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs558358341	chr6:5303615-5303616	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs78272230	chr6:5303616-5303617	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs544464917	chr6:5303680-5303681	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs534459716	chr6:5303726-5303727	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs556116675	chr6:5303812-5303813	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs115624504	chr6:5303843-5303844	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs140416717	chr6:5303857-5303858	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs556771776	chr6:5303965-5303966	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs146970678	chr6:5303981-5303982	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs73718059	chr6:5304008-5304009	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs564342831	chr6:5304047-5304048	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143496920	chr6:5304048-5304049	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs540111455	chr6:5304068-5304069	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs6597125	chr6:5304085-5304086	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5280800-5308200	Weak transcription	Primary T cells from cord blood	blood
2	chr6:5287800-5313600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:5288000-5303000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr6:5288000-5316200	Weak transcription	Fetal Stomach	stomach
5	chr6:5288400-5302800	Weak transcription	Esophagus	oesophagus
6	chr6:5288400-5324000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:5288400-5331000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr6:5288600-5302800	Weak transcription	HMEC	breast
9	chr6:5288600-5303000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr6:5288600-5303200	Weak transcription	NHEK	skin
11	chr6:5292200-5303200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:5292800-5334400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr6:5293800-5306200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:5295200-5302800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr6:5295200-5306000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:5295200-5311600	Weak transcription	Small Intestine	intestine
17	chr6:5295400-5303000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr6:5295400-5305800	Weak transcription	Fetal Intestine Large	intestine
19	chr6:5295400-5325000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:5296200-5302800	Weak transcription	Brain Anterior Caudate	brain
21	chr6:5296200-5302800	Weak transcription	Right Ventricle	heart
22	chr6:5296200-5316000	Weak transcription	Lung	lung
23	chr6:5296400-5306000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:5298200-5303400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr6:5298400-5303200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:5298600-5303200	Weak transcription	HepG2	liver
27	chr6:5298600-5305000	Weak transcription	Fetal Intestine Small	intestine
28	chr6:5300400-5302800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr6:5300600-5303800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr6:5300800-5302800	Weak transcription	HSMMtube	muscle
31	chr6:5301000-5315400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:5301600-5303800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr6:5301600-5304200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:5301800-5322200	Weak transcription	Ovary	ovary
35	chr6:5302000-5303200	Enhancers	Fetal Heart	heart
36	chr6:5302000-5304000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr6:5302000-5313000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr6:5302200-5302800	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr6:5302200-5303200	Enhancers	Fetal Kidney	kidney
40	chr6:5302200-5303600	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr6:5302200-5303600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr6:5302200-5303600	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr6:5302200-5303600	Enhancers	Psoas Muscle	Psoas
44	chr6:5302200-5304000	Enhancers	Primary B cells from peripheral blood	blood
45	chr6:5302200-5304000	Enhancers	Primary T cells fromperipheralblood	blood
46	chr6:5302200-5304000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr6:5302200-5304000	Flanking Active TSS	GM12878-XiMat	blood
48	chr6:5302400-5302800	Enhancers	Aorta	Aorta
49	chr6:5302400-5303000	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr6:5302400-5303000	Enhancers	Colon Smooth Muscle	Colon

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