Variant report

Variant	nsv1032268
Chromosome Location	chr6:167569519-167838993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3648)
CpG islands
(count:7995)
Chromatin interactive
region (count:43)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3648 , 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	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167834911-167835243	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167837621-167838022	HepG2	liver:	n/a	n/a
20	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
21	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
22	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
23	ARID3A	chr6:167702230-167702578	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	chr6:167641353-167641826	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	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
30	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr6:167576782-167577257	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
33	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167577029-167577525	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr6:167631950-167632087	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	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
42	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
43	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
44	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
45	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
46	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
47	BATF	chr6:167596405-167596715	GM12878	blood:	n/a	n/a
48	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
49	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
50	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a

(count:7995 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167836221-167836271	MCF10A-Er-Src	breast:	n/a
2	chr6:167571630-167571680	HRCEpiC	kidney:	n/a
3	chr6:167710360-167710410	PrEC	prostate:	n/a
4	chr6:167703591-167703641	AG09319	gingival:	n/a
5	chr6:167836221-167836271	MCF10A-Er-Src	breast:	n/a
6	chr6:167571630-167571680	HRCEpiC	kidney:	n/a
7	chr6:167710360-167710410	PrEC	prostate:	n/a
8	chr6:167703591-167703641	AG09319	gingival:	n/a
9	chr6:167581988-167582038	MCF-7	breast:	n/a
10	chr6:167834866-167834916	GM06990	blood:	n/a
11	chr6:167571328-167571378	HEK293	kidney:	embryo
12	chr6:167595418-167595468	PANC-1	pancreas:	n/a
13	chr6:167592570-167592620	K562	blood:	n/a
14	chr6:167814314-167814364	CMK	blood:	n/a
15	chr6:167814397-167814447	PrEC	prostate:	n/a
16	chr6:167680447-167680497	GM12892	blood:	n/a
17	chr6:167834866-167834916	HRPEpiC	eye:	n/a
18	chr6:167592570-167592620	U87	brain:	n/a
19	chr6:167704188-167704238	Hepatocyte	liver:	n/a
20	chr6:167838138-167838188	NH-A	brain:	n/a
21	chr6:167753807-167753857	U87	brain:	n/a
22	chr6:167700000-167700050	CMK	blood:	n/a
23	chr6:167571324-167571374	PFSK-1	brain:	n/a
24	chr6:167833940-167833990	BJ	skin:	n/a
25	chr6:167763819-167763869	PrEC	prostate:	n/a
26	chr6:167616968-167617018	U87	brain:	n/a
27	chr6:167571172-167571222	HIPEpiC	eye:	n/a
28	chr6:167709237-167709287	PANC-1	pancreas:	n/a
29	chr6:167595418-167595468	NH-A	brain:	n/a
30	chr6:167762783-167762833	AG04449	skin:	fetal
31	chr6:167704769-167704819	PrEC	prostate:	n/a
32	chr6:167738342-167738392	BE2_C	brain:	n/a
33	chr6:167592854-167592904	LNCaP	prostate:	n/a
34	chr6:167709237-167709287	HNPCEpiC	eye:	n/a
35	chr6:167756099-167756149	A549	lung:	n/a
36	chr6:167814257-167814307	NB4	blood:	n/a
37	chr6:167616968-167617018	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:167765110-167765160	H1-hESC	embryonic stem cell:	embryo
39	chr6:167717313-167717363	CMK	blood:	n/a
40	chr6:167737937-167737987	AG09309	skin:	n/a
41	chr6:167808366-167808416	HEK293	kidney:	embryo
42	chr6:167700000-167700050	HEK293	kidney:	embryo
43	chr6:167810395-167810445	GM06990	blood:	n/a
44	chr6:167810343-167810393	SAEC	small airway:	n/a
45	chr6:167571584-167571634	GM06990	blood:	n/a
46	chr6:167703591-167703641	ProgFib	skin:	n/a
47	chr6:167649539-167649589	SK-N-MC	brain:	n/a
48	chr6:167633955-167634005	HCF	heart:	n/a
49	chr6:167789195-167789245	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:167652028-167652078	RPTEC	kidney:	n/a

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

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

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
2	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
3	lnc-CCR6-2	chr6:167584159-167584210	NONHSAT116087
4	lnc-CCR6-1	chr6:167575369-167575443	NONHSAT116084
5	lnc-CCR6-2	chr6:167591872-167592248	NONHSAT116087
6	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
7	lnc-GPR31-3	chr6:167583147-167583385	FPKM1_group_28907_transcript_1
8	lnc-CCR6-1	chr6:167579265-167579394	NONHSAT116084
9	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
10	lnc-GPR31-2	chr6:167571213-167571283	l_3324_chr6:167571212-167573961_ovary
11	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
12	lnc-TTLL2-2	chr6:167837702-167837948	NONHSAT116104
13	lnc-CCR6-2	chr6:167585632-167586297	NONHSAT116086
14	lnc-TCP10-2	chr6:167821589-167821728	ucscGeneNc_uc003qvx_1
15	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
16	lnc-CCR6-2	chr6:167590485-167590622	NONHSAT116087
17	lnc-GPR31-3	chr6:167582786-167583124	NONHSAT116085
18	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
19	lnc-TCP10-3	chr6:167826637-167827774	ucscGeneNc_uc003qvy_1
20	lnc-GPR31-3	chr6:167583039-167583124	FPKM1_group_28907_transcript_1
21	lnc-GPR31-3	chr6:167583147-167583385	NONHSAT116085
22	lnc-TCP10L2-1	chr6:167578697-167578796	NONHSAT116082
23	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
24	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
25	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
26	lnc-GPR31-3	chr6:167582786-167583034	FPKM1_group_28907_transcript_1
27	lnc-GPR31-2	chr6:167573626-167573961	l_3324_chr6:167571212-167573961_ovary
28	lnc-TCP10-3	chr6:167838864-167838906	ucscGeneNc_uc003qvy_1
29	lnc-TCP10-3	chr6:167825862-167825976	ucscGeneNc_uc003qvy_1
30	lnc-CCR6-2	chr6:167584146-167584210	NONHSAT116086
31	lnc-TCP10-2	chr6:167822441-167822752	ucscGeneNc_uc003qvx_1
32	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
33	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
34	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
35	lnc-TCP10L2-1	chr6:167577889-167578048	NONHSAT116082
36	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
37	lnc-TCP10-3	chr6:167823155-167825466	ucscGeneNc_uc003qvy_1

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
ENSG00000216966	chromatin interactions
ENSG00000101166	chromatin interactions
ENSG00000112494	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000120436	chromatin interactions
CYB5R4	miRNA target sites
CYBASC3	miRNA target sites

Extended variants
information (count: 12162 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:12162 , 50 per page) page: 1 2 3 4 5 6 7 ... 244

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6907629	chr6:167569519-167569520	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34603635	chr6:167569520-167569521	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs374734313	chr6:167569534-167569535	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs565992307	chr6:167569691-167569692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570069115	chr6:167569737-167569738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532910126	chr6:167569740-167569741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537415273	chr6:167569748-167569749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558610051	chr6:167569814-167569815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571526984	chr6:167569821-167569822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538925743	chr6:167569869-167569870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182437725	chr6:167569983-167569984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs397695294	chr6:167569984-167569985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572182694	chr6:167570000-167570001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536091983	chr6:167570010-167570011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147517147	chr6:167570029-167570030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576077780	chr6:167570054-167570055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536734182	chr6:167570059-167570060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564547037	chr6:167570063-167570064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559304000	chr6:167570144-167570145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117446901	chr6:167570189-167570190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113611809	chr6:167570201-167570202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138262241	chr6:167570221-167570222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555464869	chr6:167570223-167570224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149598520	chr6:167570246-167570247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144263520	chr6:167570247-167570248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185145891	chr6:167570249-167570250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563757277	chr6:167570254-167570255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372233666	chr6:167570340-167570341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375648716	chr6:167570348-167570349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368186408	chr6:167570355-167570356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372047373	chr6:167570409-167570410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552746226	chr6:167570418-167570419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148093951	chr6:167570419-167570420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375031842	chr6:167570440-167570441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202061256	chr6:167570473-167570474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528524969	chr6:167570483-167570484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199731205	chr6:167570484-167570485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138110561	chr6:167570520-167570521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35182330	chr6:167570528-167570529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147194973	chr6:167570529-167570530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554469681	chr6:167570551-167570552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369042833	chr6:167570559-167570560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569690384	chr6:167570576-167570577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536737881	chr6:167570580-167570581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148720450	chr6:167570584-167570585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535333186	chr6:167570589-167570590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372266197	chr6:167570594-167570595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576406275	chr6:167570598-167570599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375293717	chr6:167570606-167570607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369535042	chr6:167570632-167570633	Weak transcription Enhancers	n/a	n/a	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:2211 , 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	chr6:167566800-167570600	Enhancers	Fetal Brain Male	brain
5	chr6:167567800-167571600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:167568000-167571000	Weak transcription	Spleen	Spleen
7	chr6:167568200-167569600	Enhancers	Fetal Muscle Leg	muscle
8	chr6:167568200-167570800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr6:167568200-167571000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr6:167568200-167571000	Weak transcription	GM12878-XiMat	blood
11	chr6:167568400-167570400	Enhancers	Fetal Brain Female	brain
12	chr6:167568800-167569600	Enhancers	Brain Angular Gyrus	brain
13	chr6:167568800-167569600	Enhancers	Brain Hippocampus Middle	brain
14	chr6:167569000-167570400	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr6:167569000-167571000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr6:167569200-167569600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:167569200-167569600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167569200-167569600	Enhancers	Brain Substantia Nigra	brain
19	chr6:167569200-167569600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr6:167569200-167570000	Enhancers	Brain Germinal Matrix	brain
21	chr6:167569200-167571000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr6:167569400-167569600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr6:167569400-167569600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:167569400-167569600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr6:167569400-167569600	Flanking Bivalent TSS/Enh	HepG2	liver
26	chr6:167569400-167570200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr6:167569600-167570400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:167569600-167571400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:167570200-167571000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr6:167570400-167571400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:167570800-167571400	Enhancers	Esophagus	oesophagus
32	chr6:167570800-167571600	Enhancers	Primary B cells from cord blood	blood
33	chr6:167570800-167572200	Enhancers	Primary B cells from peripheral blood	blood
34	chr6:167571000-167571400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr6:167571000-167571400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr6:167571000-167571400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr6:167571000-167571400	Enhancers	Spleen	Spleen
38	chr6:167571000-167571600	Enhancers	GM12878-XiMat	blood
39	chr6:167571000-167571800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr6:167571400-167571600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr6:167571400-167572400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:167571400-167575800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:167572400-167573400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr6:167573400-167573800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:167573600-167573800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:167573800-167576200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr6:167573800-167577000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:167575400-167576600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr6:167575400-167576800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:167575400-167577200	Enhancers	Fetal Intestine Small	intestine

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