Variant report

Variant	nsv482873
Chromosome Location	chr6:167521620-167679133
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2977)
CpG islands
(count:4890)
Chromatin interactive
region (count:47)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2977 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167544586-167544925	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167536241-167537214	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167554236-167555094	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
15	ATF1	chr6:167538302-167538600	K562	blood:	n/a	n/a
16	ATF2	chr6:167543402-167543914	GM12878	blood:	n/a	n/a
17	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr6:167560330-167560930	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr6:167564561-167565094	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr6:167531955-167532665	GM12878	blood:	n/a	n/a
21	ATF2	chr6:167576782-167577257	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr6:167526259-167528702	GM12878	blood:	n/a	chr6:167528159-167528170
23	ATF2	chr6:167560274-167560920	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:167566874-167567462	GM12878	blood:	n/a	n/a
25	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
26	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:167526348-167528528	GM12878	blood:	n/a	chr6:167528159-167528170
28	ATF2	chr6:167564311-167565240	GM12878	blood:	n/a	n/a
29	ATF2	chr6:167566134-167567505	GM12878	blood:	n/a	n/a
30	ATF2	chr6:167564501-167565096	GM12878	blood:	n/a	n/a
31	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
32	ATF2	chr6:167566160-167566818	GM12878	blood:	n/a	n/a
33	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr6:167577029-167577525	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
39	BATF	chr6:167566162-167567515	GM12878	blood:	n/a	chr6:167567224-167567234
40	BATF	chr6:167524009-167524326	GM12878	blood:	n/a	n/a
41	BATF	chr6:167566962-167567528	GM12878	blood:	n/a	chr6:167567224-167567234
42	BATF	chr6:167564575-167565075	GM12878	blood:	n/a	n/a
43	BATF	chr6:167527373-167527794	GM12878	blood:	n/a	chr6:167527701-167527714
44	BATF	chr6:167544573-167544836	GM12878	blood:	n/a	chr6:167544714-167544724 chr6:167544713-167544724
45	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
46	BATF	chr6:167527974-167528395	GM12878	blood:	n/a	chr6:167528158-167528171
47	BATF	chr6:167566233-167566665	GM12878	blood:	n/a	n/a
48	BATF	chr6:167526513-167526858	GM12878	blood:	n/a	n/a
49	BATF	chr6:167548004-167548270	GM12878	blood:	n/a	n/a
50	BATF	chr6:167564330-167565128	GM12878	blood:	n/a	n/a

(count:4890 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167634139-167634189	HEEpiC	esophagus:	n/a
2	chr6:167536056-167536106	PrEC	prostate:	n/a
3	chr6:167560347-167560397	AG04449	skin:	fetal
4	chr6:167587692-167587742	SK-N-SH_RA	brain:	n/a
5	chr6:167560347-167560397	NHDF-neo	bronchial:	n/a
6	chr6:167649256-167649306	NHDF-neo	bronchial:	n/a
7	chr6:167571328-167571378	ECC-1	luminal epithelium:	n/a
8	chr6:167587692-167587742	SK-N-MC	brain:	n/a
9	chr6:167529765-167529815	ECC-1	luminal epithelium:	n/a
10	chr6:167596239-167596289	PANC-1	pancreas:	n/a
11	chr6:167634139-167634189	HEEpiC	esophagus:	n/a
12	chr6:167536056-167536106	PrEC	prostate:	n/a
13	chr6:167560347-167560397	AG04449	skin:	fetal
14	chr6:167587692-167587742	SK-N-SH_RA	brain:	n/a
15	chr6:167560347-167560397	NHDF-neo	bronchial:	n/a
16	chr6:167649256-167649306	NHDF-neo	bronchial:	n/a
17	chr6:167571328-167571378	ECC-1	luminal epithelium:	n/a
18	chr6:167587692-167587742	SK-N-MC	brain:	n/a
19	chr6:167529765-167529815	ECC-1	luminal epithelium:	n/a
20	chr6:167596239-167596289	PANC-1	pancreas:	n/a
21	chr6:167622202-167622252	HUVEC	blood vessel:	n/a
22	chr6:167589370-167589420	MCF-7	breast:	n/a
23	chr6:167567203-167567253	H1-hESC	embryonic stem cell:	embryo
24	chr6:167649256-167649306	GM12878	blood:	n/a
25	chr6:167535764-167535814	HCM	heart:	n/a
26	chr6:167535909-167535959	U87	brain:	n/a
27	chr6:167590911-167590961	GM12891	blood:	n/a
28	chr6:167596239-167596289	Hela-S3	cervix:	n/a
29	chr6:167536056-167536106	LNCaP	prostate:	n/a
30	chr6:167550145-167550195	LNCaP	prostate:	n/a
31	chr6:167559851-167559901	Hela-S3	cervix:	n/a
32	chr6:167637331-167637381	HEEpiC	esophagus:	n/a
33	chr6:167530343-167530393	HMEC	breast:	n/a
34	chr6:167622441-167622491	SK-N-SH_RA	brain:	n/a
35	chr6:167591040-167591090	PANC-1	pancreas:	n/a
36	chr6:167529678-167529728	HRPEpiC	eye:	n/a
37	chr6:167529678-167529728	AG04450	lung:	fetal
38	chr6:167653982-167654032	GM12892	blood:	n/a
39	chr6:167632873-167632923	ECC-1	luminal epithelium:	n/a
40	chr6:167535764-167535814	NHBE	bronchial:	n/a
41	chr6:167633955-167634005	Hela-S3	cervix:	n/a
42	chr6:167571172-167571222	Caco-2	colon:	n/a
43	chr6:167536521-167536571	BE2_C	brain:	n/a
44	chr6:167554790-167554840	HCPEpiC	choroid plexus:	n/a
45	chr6:167536056-167536106	SK-N-SH	brain:	n/a
46	chr6:167595418-167595468	K562	blood:	n/a
47	chr6:167622441-167622491	GM12878	blood:	n/a
48	chr6:167560504-167560554	GM12878	blood:	n/a
49	chr6:167530343-167530393	Hepatocyte	liver:	n/a
50	chr6:167589878-167589928	RPTEC	kidney:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167530846..167533349-chr6:167533846..167535491,2	K562	blood:
2	chr6:167188403..167189352-chr6:167555280..167555897,4	K562	blood:
3	chr6:167185783..167186302-chr6:167555369..167556350,2	K562	blood:
4	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
5	chr6:167550499..167553471-chr6:167563406..167565855,2	K562	blood:
6	chr6:167533573..167534443-chr6:167549334..167550301,3	MCF-7	breast:
7	chr6:167543795..167547055-chr6:167549259..167552787,3	K562	blood:
8	chr6:167533318..167534107-chr6:167555281..167555885,2	MCF-7	breast:
9	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
10	chr6:167530415..167533348-chr6:167542772..167545436,2	K562	blood:
11	chr6:167199917..167200852-chr6:167555354..167555927,2	MCF-7	breast:
12	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
13	chr6:167533925..167534442-chr6:167554372..167555227,2	MCF-7	breast:
14	chr6:167514002..167514845-chr6:167533614..167534539,2	MCF-7	breast:
15	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
16	chr6:167533318..167534107-chr6:167555281..167555885,2	MCF-7	breast:
17	chr6:167182263..167184637-chr6:167557115..167559460,2	K562	blood:
18	chr6:167459004..167459905-chr6:167555024..167555917,3	MCF-7	breast:
19	chr6:167533573..167534443-chr6:167549334..167550301,3	MCF-7	breast:
20	chr6:167188755..167189454-chr6:167555413..167556221,2	MCF-7	breast:
21	chr6:167513997..167514603-chr6:167533661..167534449,3	MCF-7	breast:
22	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
23	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
24	chr6:167559575..167562153-chr6:167565310..167566996,3	K562	blood:
25	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
26	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
27	chr6:167543795..167547055-chr6:167549259..167552787,3	K562	blood:
28	chr6:167411045..167411873-chr6:167555413..167555930,2	MCF-7	breast:
29	chr6:167547071..167549495-chr6:167560421..167562886,2	K562	blood:
30	chr6:167536255..167537788-chr6:167539934..167541454,2	K562	blood:
31	chr6:167547071..167549495-chr6:167560421..167562886,2	K562	blood:
32	chr6:167410903..167412089-chr6:167555232..167556268,5	MCF-7	breast:
33	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
34	chr6:167187969..167188996-chr6:167555512..167556325,4	MCF-7	breast:
35	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
36	chr6:167571310..167572911-chr6:167574419..167576239,2	K562	blood:
37	chr6:167530846..167533349-chr6:167533846..167535491,2	K562	blood:
38	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
39	chr6:167573482..167576354-chr6:167702662..167705429,2	K562	blood:
40	chr6:167186547..167188661-chr6:167553295..167555799,2	K562	blood:
41	chr6:167533925..167534442-chr6:167554372..167555227,2	MCF-7	breast:
42	chr6:167516694..167518621-chr6:167521648..167524357,2	K562	blood:
43	chr6:167200031..167200812-chr6:167555407..167555996,2	K562	blood:
44	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
45	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
46	chr6:167550499..167553471-chr6:167563406..167565855,2	K562	blood:
47	chr6:167530415..167533348-chr6:167542772..167545436,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCR6-2	chr6:167591872-167592248	NONHSAT116087
2	lnc-GPR31-3	chr6:167582786-167583034	FPKM1_group_28907_transcript_1
3	lnc-CCR6-2	chr6:167585632-167586297	NONHSAT116086
4	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
5	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
6	lnc-GPR31-3	chr6:167583039-167583124	FPKM1_group_28907_transcript_1
7	lnc-CCR6-1	chr6:167575369-167575443	NONHSAT116084
8	lnc-TCP10L2-1	chr6:167577889-167578048	NONHSAT116082
9	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
10	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
11	lnc-CCR6-2	chr6:167590485-167590622	NONHSAT116087
12	lnc-GPR31-2	chr6:167573626-167573961	l_3324_chr6:167571212-167573961_ovary
13	lnc-GPR31-2	chr6:167571213-167571283	l_3324_chr6:167571212-167573961_ovary
14	lnc-TCP10L2-1	chr6:167559902-167560143	NONHSAT116082
15	lnc-GPR31-3	chr6:167583147-167583385	FPKM1_group_28907_transcript_1
16	lnc-CCR6-1	chr6:167579265-167579394	NONHSAT116084
17	lnc-GPR31-3	chr6:167583147-167583385	NONHSAT116085
18	lnc-TCP10L2-1	chr6:167578697-167578796	NONHSAT116082
19	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
20	lnc-CCR6-2	chr6:167584159-167584210	NONHSAT116087
21	lnc-CCR6-2	chr6:167584146-167584210	NONHSAT116086
22	lnc-GPR31-3	chr6:167582786-167583124	NONHSAT116085
23	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
24	lnc-TCP10L2-1	chr6:167562878-167562972	NONHSAT116082

No data

Variant related genes	Relation type
ENSG00000228648	TF binding region
CCR6	TF binding region
ENSG00000231720	TF binding region
GPR31	TF binding region
ENSG00000216966	TF binding region
TCP10L2	TF binding region
ENSG00000228648	CpG island
CCR6	CpG island
ENSG00000231720	CpG island
GPR31	CpG island
ENSG00000216966	CpG island
TCP10L2	CpG island
ENSG00000112494	chromatin interactions
ENSG00000166984	chromatin interactions
ENSG00000216966	chromatin interactions
ENSG00000265828	chromatin interactions
ENSG00000120436	chromatin interactions
ENSG00000112486	chromatin interactions
CYBASC3	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 6719 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:6719 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6905911	chr6:167521624-167521625	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543472087	chr6:167521650-167521651	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117255907	chr6:167521657-167521658	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs4709148	chr6:167521676-167521677	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs574210868	chr6:167521724-167521725	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559431879	chr6:167521728-167521729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189802025	chr6:167521785-167521786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548628872	chr6:167521786-167521787	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs535509377	chr6:167521789-167521790	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs531026414	chr6:167521796-167521797	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552210617	chr6:167521827-167521828	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs60856896	chr6:167521835-167521836	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs180986539	chr6:167521882-167521883	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs534834964	chr6:167521889-167521890	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs546576462	chr6:167521919-167521920	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185218176	chr6:167522002-167522003	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs117034557	chr6:167522115-167522116	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs28695374	chr6:167522125-167522126	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs531715702	chr6:167522138-167522139	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs146192583	chr6:167522172-167522173	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs576362879	chr6:167522176-167522177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543936962	chr6:167522219-167522220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565024237	chr6:167522220-167522221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62436800	chr6:167522231-167522232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575140662	chr6:167522279-167522280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114251390	chr6:167522283-167522284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6456156	chr6:167522300-167522301	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs148396645	chr6:167522301-167522302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541161592	chr6:167522310-167522311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142999841	chr6:167522337-167522338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374423209	chr6:167522358-167522359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4710185	chr6:167522386-167522387	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs76096437	chr6:167522388-167522389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189735070	chr6:167522425-167522426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531084648	chr6:167522444-167522445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183447402	chr6:167522456-167522457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564376483	chr6:167522462-167522463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371039752	chr6:167522465-167522466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186300874	chr6:167522472-167522473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546713183	chr6:167522505-167522506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191588343	chr6:167522531-167522532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112842456	chr6:167522584-167522585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150690256	chr6:167522595-167522596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529353194	chr6:167522623-167522624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188122561	chr6:167522636-167522637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569849619	chr6:167522657-167522658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537383628	chr6:167522714-167522715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558769221	chr6:167522733-167522734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192870212	chr6:167522784-167522785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6925931	chr6:167522796-167522797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1696 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167503600-167527200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:167509000-167525200	Enhancers	Primary B cells from peripheral blood	blood
3	chr6:167517400-167523800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr6:167517600-167523800	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr6:167517600-167529800	Weak transcription	Spleen	Spleen
6	chr6:167518200-167524600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:167519400-167527800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:167520400-167529800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:167521400-167522400	Enhancers	GM12878-XiMat	blood
10	chr6:167521400-167522600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:167521400-167524000	Enhancers	Primary B cells from cord blood	blood
12	chr6:167522200-167524200	Enhancers	Placenta Amnion	Placenta Amnion
13	chr6:167522400-167523600	Weak transcription	GM12878-XiMat	blood
14	chr6:167522400-167524000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr6:167522600-167523000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:167523000-167524200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:167523200-167524400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:167523400-167524000	Enhancers	Placenta	Placenta
19	chr6:167523600-167525000	Enhancers	GM12878-XiMat	blood
20	chr6:167523800-167524000	Enhancers	Primary T cells fromperipheralblood	blood
21	chr6:167523800-167524000	Enhancers	Fetal Stomach	stomach
22	chr6:167523800-167524800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr6:167524000-167524200	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr6:167524000-167524800	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr6:167524000-167524800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr6:167524000-167525000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr6:167524000-167525200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr6:167524200-167524600	Enhancers	Primary B cells from cord blood	blood
29	chr6:167524200-167525000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr6:167524200-167525200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr6:167524200-167526800	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr6:167524400-167527400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:167524600-167525000	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr6:167524600-167525200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr6:167524600-167525400	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr6:167524800-167525000	Enhancers	Primary T cells fromperipheralblood	blood
37	chr6:167524800-167525000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr6:167524800-167525600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
39	chr6:167525000-167525400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
40	chr6:167525000-167525400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr6:167525000-167525400	Flanking Active TSS	GM12878-XiMat	blood
42	chr6:167525000-167526000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:167525000-167527600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr6:167525000-167529000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr6:167525200-167525400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr6:167525200-167525400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr6:167525200-167525400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr6:167525200-167525400	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr6:167525200-167528600	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr6:167525400-167525600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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