Variant report

Variant	nsv470873
Chromosome Location	chr6:167572542-167844264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3632)
CpG islands
(count:7704)
Chromatin interactive
region (count:43)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3632 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167837621-167838022	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167834911-167835243	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
20	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
21	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
22	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
23	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
24	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
25	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
26	ATF2	chr6:167576782-167577257	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
29	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
34	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr6:167577029-167577525	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
41	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
42	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
43	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
44	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
45	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
46	BATF	chr6:167596405-167596715	GM12878	blood:	n/a	n/a
47	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
48	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
49	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
50	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a

(count:7704 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167680447-167680497	HL-60	blood:	n/a
2	chr6:167589878-167589928	HRPEpiC	eye:	n/a
3	chr6:167764146-167764196	PrEC	prostate:	n/a
4	chr6:167622441-167622491	GM12892	blood:	n/a
5	chr6:167658907-167658957	HRPEpiC	eye:	n/a
6	chr6:167814397-167814447	HRPEpiC	eye:	n/a
7	chr6:167680447-167680497	GM19239	blood:	n/a
8	chr6:167718461-167718511	AG09309	skin:	n/a
9	chr6:167653907-167653957	AoSMC	blood vessel:	n/a
10	chr6:167717313-167717363	NHBE	bronchial:	n/a
11	chr6:167631788-167631838	HIPEpiC	eye:	n/a
12	chr6:167587558-167587608	NHBE	bronchial:	n/a
13	chr6:167634139-167634189	HEEpiC	esophagus:	n/a
14	chr6:167617119-167617169	SAEC	small airway:	n/a
15	chr6:167717196-167717246	RPTEC	kidney:	n/a
16	chr6:167768382-167768432	AG09319	gingival:	n/a
17	chr6:167717196-167717246	SK-N-MC	brain:	n/a
18	chr6:167710360-167710410	SK-N-MC	brain:	n/a
19	chr6:167680447-167680497	HL-60	blood:	n/a
20	chr6:167589878-167589928	HRPEpiC	eye:	n/a
21	chr6:167764146-167764196	PrEC	prostate:	n/a
22	chr6:167622441-167622491	GM12892	blood:	n/a
23	chr6:167658907-167658957	HRPEpiC	eye:	n/a
24	chr6:167814397-167814447	HRPEpiC	eye:	n/a
25	chr6:167680447-167680497	GM19239	blood:	n/a
26	chr6:167718461-167718511	AG09309	skin:	n/a
27	chr6:167653907-167653957	AoSMC	blood vessel:	n/a
28	chr6:167717313-167717363	NHBE	bronchial:	n/a
29	chr6:167631788-167631838	HIPEpiC	eye:	n/a
30	chr6:167587558-167587608	NHBE	bronchial:	n/a
31	chr6:167634139-167634189	HEEpiC	esophagus:	n/a
32	chr6:167617119-167617169	SAEC	small airway:	n/a
33	chr6:167717196-167717246	RPTEC	kidney:	n/a
34	chr6:167768382-167768432	AG09319	gingival:	n/a
35	chr6:167717196-167717246	SK-N-MC	brain:	n/a
36	chr6:167710360-167710410	SK-N-MC	brain:	n/a
37	chr6:167649749-167649799	LNCaP	prostate:	n/a
38	chr6:167768382-167768432	SAEC	small airway:	n/a
39	chr6:167655290-167655340	PrEC	prostate:	n/a
40	chr6:167789539-167789589	NHDF-neo	bronchial:	n/a
41	chr6:167809876-167809926	ProgFib	skin:	n/a
42	chr6:167631788-167631838	NHBE	bronchial:	n/a
43	chr6:167838138-167838188	GM12878	blood:	n/a
44	chr6:167705253-167705303	Hela-S3	cervix:	n/a
45	chr6:167763975-167764025	AG04449	skin:	fetal
46	chr6:167761204-167761254	RPTEC	kidney:	n/a
47	chr6:167633022-167633072	SAEC	small airway:	n/a
48	chr6:167839518-167839568	SK-N-MC	brain:	n/a
49	chr6:167700000-167700050	Hela-S3	cervix:	n/a
50	chr6:167710360-167710410	GM12892	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
2	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
3	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
4	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
5	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
6	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
7	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
8	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
9	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
10	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
11	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
12	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
13	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
14	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
15	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
16	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
17	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
18	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
19	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
20	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
21	chr6:167571310..167572911-chr6:167574419..167576239,2	K562	blood:
22	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
23	chr20:57615578..57617834-chr6:167831422..167833295,2	MCF-7	breast:
24	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
25	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
26	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
27	chr6:167573482..167576354-chr6:167702662..167705429,2	K562	blood:
28	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
29	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
30	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
31	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
32	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
33	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
34	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
35	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
36	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
37	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
38	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
39	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
40	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
41	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
42	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
43	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCR6-1	chr6:167575369-167575443	NONHSAT116084
2	lnc-TTLL2-2	chr6:167837702-167837948	NONHSAT116104
3	lnc-GPR31-3	chr6:167583039-167583124	FPKM1_group_28907_transcript_1
4	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
5	lnc-TCP10-3	chr6:167826637-167827774	ucscGeneNc_uc003qvy_1
6	lnc-GPR31-2	chr6:167573626-167573961	l_3324_chr6:167571212-167573961_ovary
7	lnc-TCP10-3	chr6:167838864-167838906	ucscGeneNc_uc003qvy_1
8	lnc-TCP10-3	chr6:167839445-167839616	ucscGeneNc_uc003qvy_1
9	lnc-TCP10-3	chr6:167839733-167839819	ucscGeneNc_uc003qvy_1
10	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
11	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
12	lnc-CCR6-2	chr6:167591872-167592248	NONHSAT116087
13	lnc-GPR31-3	chr6:167582786-167583124	NONHSAT116085
14	lnc-TTLL2-2	chr6:167840757-167840858	NONHSAT116104
15	lnc-TCP10L2-1	chr6:167577889-167578048	NONHSAT116082
16	lnc-CCR6-2	chr6:167584146-167584210	NONHSAT116086
17	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
18	lnc-GPR31-3	chr6:167583147-167583385	FPKM1_group_28907_transcript_1
19	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
20	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
21	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
22	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
23	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
24	lnc-TCP10-3	chr6:167823155-167825466	ucscGeneNc_uc003qvy_1
25	lnc-TCP10L2-1	chr6:167578697-167578796	NONHSAT116082
26	lnc-CCR6-1	chr6:167579265-167579394	NONHSAT116084
27	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
28	lnc-CCR6-2	chr6:167584159-167584210	NONHSAT116087
29	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
30	lnc-CCR6-2	chr6:167590485-167590622	NONHSAT116087
31	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
32	lnc-TCP10-2	chr6:167821589-167821728	ucscGeneNc_uc003qvx_1
33	lnc-GPR31-3	chr6:167582786-167583034	FPKM1_group_28907_transcript_1
34	lnc-CCR6-2	chr6:167585632-167586297	NONHSAT116086
35	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
36	lnc-TCP10-3	chr6:167825862-167825976	ucscGeneNc_uc003qvy_1
37	lnc-GPR31-3	chr6:167583147-167583385	NONHSAT116085
38	lnc-TCP10-2	chr6:167822441-167822752	ucscGeneNc_uc003qvx_1
39	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095

No data

Variant related genes	Relation type
UNC93A	TF binding region
TCP10	TF binding region
TTLL2	TF binding region
ENSG00000231720	TF binding region
GPR31	TF binding region
TCP10L2	TF binding region
ENSG00000228648	TF binding region
ENSG00000216966	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TCP10	CpG island
TTLL2	CpG island
ENSG00000231720	CpG island
GPR31	CpG island
TCP10L2	CpG island
ENSG00000228648	CpG island
ENSG00000216966	CpG island
ENSG00000217447	CpG island
ENSG00000180198	chromatin interactions
ENSG00000120436	chromatin interactions
ENSG00000216966	chromatin interactions
ENSG00000101166	chromatin interactions
ENSG00000112494	chromatin interactions
CYBASC3	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 12224 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:12224 , 50 per page) page: 1 2 3 4 5 6 7 ... 245

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4710191	chr6:167572542-167572543	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534842334	chr6:167572586-167572587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112058757	chr6:167572598-167572599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187265579	chr6:167572628-167572629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs151206519	chr6:167572637-167572638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537949003	chr6:167572706-167572707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556267097	chr6:167572736-167572737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191848632	chr6:167572737-167572738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184027104	chr6:167572770-167572771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557740332	chr6:167572779-167572780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9459898	chr6:167572791-167572792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs546784373	chr6:167572855-167572856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571102865	chr6:167572864-167572865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76377584	chr6:167572868-167572869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149905642	chr6:167572870-167572871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529148496	chr6:167572887-167572888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544300649	chr6:167572898-167572899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144926229	chr6:167572910-167572911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369037832	chr6:167572963-167572964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551416358	chr6:167572967-167572968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189491361	chr6:167572988-167572989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376361878	chr6:167573034-167573035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141975714	chr6:167573066-167573067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74782375	chr6:167573211-167573212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12664448	chr6:167573318-167573319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs67132351	chr6:167573370-167573371	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs80101880	chr6:167573371-167573372	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs556205775	chr6:167573383-167573384	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs571430765	chr6:167573493-167573494	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs538599721	chr6:167573577-167573578	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554145552	chr6:167573637-167573638	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs138632538	chr6:167573657-167573658	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs534089733	chr6:167573663-167573664	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs555400612	chr6:167573727-167573728	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs192303436	chr6:167573737-167573738	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs544433921	chr6:167573815-167573816	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs9348224	chr6:167573830-167573831	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs537064805	chr6:167573890-167573891	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs577824826	chr6:167574006-167574007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544818582	chr6:167574050-167574051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs71571477	chr6:167574064-167574065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560093775	chr6:167574102-167574103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575517343	chr6:167574122-167574123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527319208	chr6:167574130-167574131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200303276	chr6:167574173-167574174	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs536659404	chr6:167574258-167574259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549637996	chr6:167574295-167574296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78957396	chr6:167574312-167574313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12663355	chr6:167574335-167574336	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs549966366	chr6:167574341-167574342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2217 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167534000-167573400	Weak transcription	Right Atrium	heart
2	chr6:167565800-167575600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr6:167566000-167575600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:167571400-167575800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:167572400-167573400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:167573400-167573800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:167573600-167573800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr6:167573800-167576200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:167573800-167577000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr6:167575400-167576600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:167575400-167576800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:167575400-167577200	Enhancers	Fetal Intestine Small	intestine
13	chr6:167575600-167576000	Bivalent Enhancer	HepG2	liver
14	chr6:167575600-167576400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:167575600-167576800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:167575600-167577200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:167575600-167577200	Enhancers	Fetal Intestine Large	intestine
18	chr6:167575600-167579200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr6:167575800-167576400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr6:167575800-167576600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr6:167575800-167576600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:167575800-167576600	Enhancers	Duodenum Mucosa	Duodenum
23	chr6:167575800-167576800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr6:167575800-167577600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr6:167576000-167576600	Flanking Bivalent TSS/Enh	HepG2	liver
26	chr6:167576000-167577200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr6:167576000-167577200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr6:167576200-167576400	Bivalent Enhancer	Thymus	Thymus
29	chr6:167576200-167577200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:167576400-167577000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr6:167576400-167577600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:167576400-167578200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr6:167576600-167576800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr6:167576600-167577000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:167576600-167577200	Bivalent Enhancer	HepG2	liver
36	chr6:167576600-167578200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr6:167576800-167577000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr6:167576800-167577600	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr6:167576800-167577800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr6:167576800-167578200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:167577000-167577200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:167577000-167577200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:167577000-167577600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr6:167577000-167579200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:167577200-167577600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr6:167577200-167577600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr6:167577200-167577600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr6:167577200-167577600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr6:167577200-167577600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr6:167577600-167578000	Weak transcription	H9 Cell Line	embryonic stem cell

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