Variant report

Variant	nsv462944
Chromosome Location	chr6:49869448-49948059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:793)
Chromatin interactive
region (count:46)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:49907440-49908227	K562	blood:	n/a	n/a
2	ARID3A	chr6:49916784-49917409	K562	blood:	n/a	chr6:49916881-49916897
3	ARID3A	chr6:49918023-49918580	K562	blood:	n/a	chr6:49918352-49918368
4	ATF1	chr6:49917862-49918300	K562	blood:	n/a	n/a
5	ATF1	chr6:49907747-49908219	K562	blood:	n/a	n/a
6	ATF3	chr6:49914621-49914956	K562	blood:	n/a	n/a
7	BACH1	chr6:49919377-49919505	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:49907365-49908014	K562	blood:	n/a	n/a
9	BACH1	chr6:49886415-49886769	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:49918531-49918536	K562	blood:	n/a	n/a
11	BHLHE40	chr6:49947324-49947611	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:49907281-49908230	K562	blood:	n/a	n/a
13	BHLHE40	chr6:49882811-49883032	K562	blood:	n/a	n/a
14	CBX3	chr6:49907233-49908301	K562	blood:	n/a	n/a
15	CCNT2	chr6:49902603-49902719	K562	blood:	n/a	n/a
16	CCNT2	chr6:49907207-49908157	K562	blood:	n/a	n/a
17	CEBPB	chr6:49918049-49918454	K562	blood:	n/a	chr6:49918245-49918256
18	CEBPB	chr6:49918129-49918307	A549	lung:	n/a	chr6:49918245-49918256
19	CEBPB	chr6:49919740-49920010	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:49914604-49914909	Hela-S3	cervix:	n/a	chr6:49914749-49914760
21	CEBPB	chr6:49914573-49914905	K562	blood:	n/a	chr6:49914749-49914760
22	CEBPB	chr6:49914603-49914928	A549	lung:	n/a	chr6:49914749-49914760
23	CEBPB	chr6:49933245-49933270	K562	blood:	n/a	n/a
24	CEBPB	chr6:49934575-49934897	A549	lung:	n/a	chr6:49934730-49934741
25	CEBPB	chr6:49918105-49918411	K562	blood:	n/a	chr6:49918245-49918256
26	CEBPB	chr6:49919690-49920014	K562	blood:	n/a	n/a
27	CEBPB	chr6:49934572-49934876	K562	blood:	n/a	chr6:49934730-49934741
28	CEBPB	chr6:49934640-49934807	HepG2	liver:	n/a	chr6:49934730-49934741
29	CEBPB	chr6:49933202-49933427	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr6:49887983-49888295	K562	blood:	n/a	chr6:49888145-49888156
31	CEBPB	chr6:49887998-49888332	HepG2	liver:	n/a	chr6:49888145-49888156
32	CEBPB	chr6:49914565-49914950	K562	blood:	n/a	chr6:49914749-49914760
33	CEBPB	chr6:49914582-49914893	H1-hESC	embryonic stem cell:	n/a	chr6:49914749-49914760
34	CEBPB	chr6:49907739-49908039	K562	blood:	n/a	n/a
35	CEBPB	chr6:49897106-49897439	HepG2	liver:	n/a	chr6:49897256-49897267 chr6:49897255-49897268 chr6:49897255-49897268 chr6:49897255-49897268
36	CEBPB	chr6:49914582-49914928	HepG2	liver:	n/a	chr6:49914749-49914760
37	CEBPB	chr6:49897157-49897355	H1-hESC	embryonic stem cell:	n/a	chr6:49897256-49897267 chr6:49897255-49897268 chr6:49897255-49897268 chr6:49897255-49897268
38	CEBPB	chr6:49887972-49888331	IMR90	lung:	n/a	chr6:49888145-49888156
39	CEBPB	chr6:49897160-49897425	K562	blood:	n/a	chr6:49897256-49897267 chr6:49897255-49897268 chr6:49897255-49897268 chr6:49897255-49897268
40	CEBPB	chr6:49914606-49914863	K562	blood:	n/a	chr6:49914749-49914760
41	CEBPB	chr6:49934561-49934924	Hela-S3	cervix:	n/a	chr6:49934730-49934741
42	CEBPB	chr6:49934545-49934928	K562	blood:	n/a	chr6:49934730-49934741
43	CEBPB	chr6:49918105-49918390	HepG2	liver:	n/a	chr6:49918245-49918256
44	CEBPB	chr6:49914585-49914930	IMR90	lung:	n/a	chr6:49914749-49914760
45	CEBPB	chr6:49918036-49918441	K562	blood:	n/a	chr6:49918245-49918256
46	CEBPB	chr6:49887984-49888296	A549	lung:	n/a	chr6:49888145-49888156
47	CEBPB	chr6:49874186-49874819	Hela-S3	cervix:	n/a	chr6:49874464-49874477 chr6:49874464-49874475
48	CEBPD	chr6:49907652-49908202	K562	blood:	n/a	n/a
49	CHD2	chr6:49907568-49908238	K562	blood:	n/a	n/a
50	CHD2	chr6:49879168-49879377	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:49901607-49901657	U87	brain:	n/a
2	chr6:49937814-49937864	HAEpiC	amniotic membrane:	n/a
3	chr6:49917881-49917931	T-47D	breast:	n/a
4	chr6:49937814-49937864	PrEC	prostate:	n/a
5	chr6:49901607-49901657	HUVEC	blood vessel:	n/a
6	chr6:49877534-49877584	HAEpiC	amniotic membrane:	n/a
7	chr6:49916931-49916981	Jurkat	blood:	n/a
8	chr6:49917881-49917931	MCF10A-Er-Src	breast:	n/a
9	chr6:49886324-49886374	BE2_C	brain:	n/a
10	chr6:49917145-49917195	PANC-1	pancreas:	n/a
11	chr6:49937814-49937864	HRPEpiC	eye:	n/a
12	chr6:49917175-49917225	AG10803	skin:	n/a
13	chr6:49917254-49917304	CMK	blood:	n/a
14	chr6:49917145-49917195	BE2_C	brain:	n/a
15	chr6:49917145-49917195	Caco-2	colon:	n/a
16	chr6:49877534-49877584	PrEC	prostate:	n/a
17	chr6:49917881-49917931	AG09309	skin:	n/a
18	chr6:49901607-49901657	SK-N-SH	brain:	n/a
19	chr6:49917145-49917195	NH-A	brain:	n/a
20	chr6:49901607-49901657	NB4	blood:	n/a
21	chr6:49901645-49901695	PFSK-1	brain:	n/a
22	chr6:49901607-49901657	NHBE	bronchial:	n/a
23	chr6:49917254-49917304	GM19239	blood:	n/a
24	chr6:49917145-49917195	RPTEC	kidney:	n/a
25	chr6:49917254-49917304	MCF-7	breast:	n/a
26	chr6:49901607-49901657	SAEC	small airway:	n/a
27	chr6:49937814-49937864	AG04450	lung:	fetal
28	chr6:49916931-49916981	SAEC	small airway:	n/a
29	chr6:49877534-49877584	PANC-1	pancreas:	n/a
30	chr6:49881441-49881491	GM12878	blood:	n/a
31	chr6:49937814-49937864	HL-60	blood:	n/a
32	chr6:49877534-49877584	RPTEC	kidney:	n/a
33	chr6:49877534-49877584	HepG2	liver:	n/a
34	chr6:49937814-49937864	GM19239	blood:	n/a
35	chr6:49917872-49917922	HRPEpiC	eye:	n/a
36	chr6:49917145-49917195	HUVEC	blood vessel:	n/a
37	chr6:49917145-49917195	Hela-S3	cervix:	n/a
38	chr6:49917145-49917195	H1-hESC	embryonic stem cell:	embryo
39	chr6:49901645-49901695	AG09309	skin:	n/a
40	chr6:49917145-49917195	HRCEpiC	kidney:	n/a
41	chr6:49928115-49928165	HEK293	kidney:	embryo
42	chr6:49901607-49901657	T-47D	breast:	n/a
43	chr6:49881441-49881491	CMK	blood:	n/a
44	chr6:49916931-49916981	PrEC	prostate:	n/a
45	chr6:49917175-49917225	BE2_C	brain:	n/a
46	chr6:49916931-49916981	GM12892	blood:	n/a
47	chr6:49881441-49881491	Hepatocyte	liver:	n/a
48	chr6:49928115-49928165	GM06990	blood:	n/a
49	chr6:49877534-49877584	AG04449	skin:	fetal
50	chr6:49881441-49881491	ovcar-3	ovarian:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:49900625..49902191-chr6:49908372..49911289,2	K562	blood:
2	chr6:49918423..49920298-chr6:49924382..49926655,2	K562	blood:
3	chr6:49495608..49498128-chr6:49917488..49919733,2	K562	blood:
4	chr6:49919355..49921346-chr6:49947869..49950695,2	K562	blood:
5	chr6:49916297..49920485-chr6:49927814..49931575,4	K562	blood:
6	chr6:49918423..49920298-chr6:49924382..49926655,2	K562	blood:
7	chr6:49917812..49920215-chr6:49938804..49940384,2	K562	blood:
8	chr6:49881812..49884281-chr6:49911673..49914091,2	K562	blood:
9	chr6:49915511..49918385-chr6:49942159..49944582,2	K562	blood:
10	chr6:49872988..49875937-chr6:49910979..49912773,2	K562	blood:
11	chr6:49905732..49908013-chr6:49909471..49912088,3	K562	blood:
12	chr6:49917125..49919923-chr6:49925155..49927283,3	K562	blood:
13	chr6:49896737..49899736-chr6:49902521..49904667,2	K562	blood:
14	chr6:49920570..49922665-chr6:49946320..49948617,2	K562	blood:
15	chr6:49876196..49877993-chr6:49880837..49882746,2	K562	blood:
16	chr6:49863191..49865414-chr6:49879620..49881945,2	K562	blood:
17	chr6:49922102..49925301-chr6:49927046..49930079,3	K562	blood:
18	chr6:49944298..49946329-chr6:49946911..49948837,2	K562	blood:
19	chr6:49865009..49867621-chr6:49871225..49873987,3	K562	blood:
20	chr6:49943600..49946329-chr6:49946911..49949558,2	K562	blood:
21	chr6:49930677..49932249-chr6:49932732..49935281,2	K562	blood:
22	chr6:49919355..49921346-chr6:49947869..49950695,2	K562	blood:
23	chr6:49881812..49884281-chr6:49911673..49914091,2	K562	blood:
24	chr6:49890458..49893246-chr6:49899000..49901989,2	K562	blood:
25	chr6:49900625..49902191-chr6:49908372..49911289,2	K562	blood:
26	chr6:49876196..49877993-chr6:49880837..49882746,2	K562	blood:
27	chr6:49943600..49946329-chr6:49946911..49949558,2	K562	blood:
28	chr6:49939274..49941275-chr6:49942084..49943998,2	K562	blood:
29	chr6:49918496..49920485-chr6:49927814..49930518,2	K562	blood:
30	chr6:49817546..49820511-chr6:49881787..49884354,2	MCF-7	breast:
31	chr6:49889650..49891163-chr6:49896885..49899615,2	MCF-7	breast:
32	chr6:49939274..49941275-chr6:49942084..49943998,2	K562	blood:
33	chr6:49920570..49922665-chr6:49946320..49948617,2	K562	blood:
34	chr6:49905732..49908013-chr6:49909471..49912088,3	K562	blood:
35	chr6:49870740..49872633-chr6:49875508..49879726,3	K562	blood:
36	chr6:49917812..49920215-chr6:49938804..49940384,2	K562	blood:
37	chr6:49936013..49938927-chr6:49939519..49941883,2	K562	blood:
38	chr6:49896737..49899736-chr6:49902521..49904667,2	K562	blood:
39	chr6:49870740..49872633-chr6:49875508..49879726,3	K562	blood:
40	chr6:49890458..49893246-chr6:49899000..49901989,2	K562	blood:
41	chr6:49922102..49925301-chr6:49927046..49930079,3	K562	blood:
42	chr6:49944298..49946329-chr6:49946911..49948837,2	K562	blood:
43	chr6:49918496..49920485-chr6:49927814..49930518,2	K562	blood:
44	chr6:49889650..49891163-chr6:49896885..49899615,2	MCF-7	breast:
45	chr6:49864639..49868104-chr6:49870222..49873987,4	K562	blood:
46	chr6:49872988..49875937-chr6:49910979..49912773,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB133-1	chr6:49899608-49899715	NONHSAT113069
2	lnc-DEFB133-1	chr6:49894078-49894117	ucscGeneNc_uc003ozv_1
3	lnc-C6orf141-5	chr6:49895998-49896114	NONHSAT113068
4	lnc-C6orf141-5	chr6:49894795-49894994	l_3190_chr6:49863110-49896172_testes
5	lnc-DEFB133-1	chr6:49900282-49900454	NONHSAT113069
6	lnc-DEFB133-1	chr6:49891165-49892478	ucscGeneNc_uc003ozv_1
7	lnc-C6orf141-5	chr6:49894797-49894996	NONHSAT113068
8	lnc-C6orf141-5	chr6:49893063-49893168	l_3190_chr6:49863110-49896172_testes
9	lnc-C6orf141-5	chr6:49896000-49896173	l_3190_chr6:49863110-49896172_testes
10	lnc-C6orf141-5	chr6:49893102-49893165	NONHSAT113068
11	lnc-DEFB133-1	chr6:49899384-49899502	NONHSAT113069
12	lnc-DEFB133-1	chr6:49900282-49900438	ucscGeneNc_uc003ozv_1
13	lnc-DEFB133-1	chr6:49899608-49899715	ucscGeneNc_uc003ozv_1
14	lnc-DEFB133-1	chr6:49899384-49899502	ucscGeneNc_uc003ozv_1

No data

Variant related genes	Relation type
DEFB133	TF binding region
DEFB113	TF binding region
DEFB114	TF binding region
DEFB133	CpG island
DEFB113	CpG island
DEFB114	CpG island
ENSG00000177684	chromatin interactions
ENSG00000214642	chromatin interactions
ENSG00000214643	chromatin interactions

Extended variants
information (count: 2238 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2238 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7764242	chr6:49869448-49869449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76689129	chr6:49869507-49869508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs17664012	chr6:49869536-49869537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562161880	chr6:49869553-49869554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570679560	chr6:49869556-49869557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564376977	chr6:49869570-49869571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142389123	chr6:49869585-49869586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539362048	chr6:49869605-49869606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs151330031	chr6:49869644-49869645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116643518	chr6:49869662-49869663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536192020	chr6:49869678-49869679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139777200	chr6:49869704-49869705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144482678	chr6:49869710-49869711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541142851	chr6:49869758-49869759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146437944	chr6:49869785-49869786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9349507	chr6:49869801-49869802	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs377461751	chr6:49869825-49869826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140788445	chr6:49869856-49869857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193292164	chr6:49869893-49869894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556364028	chr6:49869899-49869900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576256943	chr6:49869921-49869922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530036925	chr6:49869936-49869937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542137861	chr6:49869943-49869944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533580784	chr6:49869957-49869958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185572275	chr6:49869964-49869965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150116050	chr6:49869973-49869974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145486156	chr6:49869986-49869987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190084395	chr6:49870018-49870019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533288779	chr6:49870029-49870030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550102016	chr6:49870081-49870082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575429077	chr6:49870106-49870107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529544339	chr6:49870162-49870163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12207683	chr6:49870164-49870165	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs370325963	chr6:49870202-49870203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568032583	chr6:49870218-49870219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533774326	chr6:49870238-49870239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553862837	chr6:49870244-49870245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570553089	chr6:49870248-49870249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539566642	chr6:49870255-49870256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563997662	chr6:49870284-49870285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556066057	chr6:49870337-49870338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181592038	chr6:49870367-49870368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532738021	chr6:49870432-49870433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183879821	chr6:49870496-49870497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs62406371	chr6:49870531-49870532	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs188667025	chr6:49870614-49870615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs36067025	chr6:49870656-49870657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576616724	chr6:49870673-49870674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569317353	chr6:49870686-49870687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148883281	chr6:49870718-49870719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49869000-49869600	Weak transcription	Fetal Intestine Large	intestine
2	chr6:49869600-49874600	Enhancers	Fetal Intestine Large	intestine
3	chr6:49869800-49870400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr6:49869800-49870400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr6:49869800-49870800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:49870000-49870200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr6:49870200-49871600	Enhancers	Liver	Liver
8	chr6:49870200-49874000	Enhancers	Fetal Intestine Small	intestine
9	chr6:49870400-49875000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:49870800-49877400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:49873200-49873400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr6:49873200-49875400	Enhancers	Fetal Brain Male	brain
13	chr6:49873400-49873600	Enhancers	Fetal Muscle Leg	muscle
14	chr6:49873400-49879000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:49873600-49873800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:49873600-49873800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:49873600-49874400	Weak transcription	Fetal Muscle Leg	muscle
18	chr6:49874000-49874400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr6:49874000-49874600	Weak transcription	Fetal Intestine Small	intestine
20	chr6:49874000-49875000	Enhancers	Hela-S3	cervix
21	chr6:49874000-49875200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr6:49874000-49876600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:49874400-49874600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr6:49874400-49874600	Enhancers	Fetal Muscle Leg	muscle
25	chr6:49874400-49875000	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr6:49874600-49874800	Enhancers	Fetal Intestine Small	intestine
27	chr6:49874600-49875200	Enhancers	Fetal Brain Female	brain
28	chr6:49874600-49876400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:49874600-49881400	Weak transcription	Fetal Muscle Leg	muscle
30	chr6:49874800-49875000	Enhancers	HSMMtube	muscle
31	chr6:49875000-49875600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr6:49875000-49877400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr6:49875200-49877600	Weak transcription	Fetal Brain Female	brain
34	chr6:49875200-49883800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:49875400-49881000	Weak transcription	Fetal Brain Male	brain
36	chr6:49875600-49876400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr6:49875800-49876000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr6:49876000-49877200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr6:49876400-49876600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr6:49876400-49879000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:49876600-49876800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:49876600-49877000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr6:49876800-49877600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:49877000-49883200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr6:49877200-49877800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr6:49877200-49877800	Enhancers	Fetal Lung	lung
47	chr6:49877200-49878400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr6:49877400-49877800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:49877400-49877800	Enhancers	Fetal Heart	heart
50	chr6:49877400-49877800	Enhancers	Skeletal Muscle Female	skeletal muscle

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