Variant report

Variant	nsv886303
Chromosome Location	chr6:80147225-80252423
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1222)
CpG islands
(count:1038)
Chromatin interactive
region (count:65)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:80175985-80176324	K562	blood:	n/a	n/a
2	ARID3A	chr6:80235184-80235825	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:80246852-80247644	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:80235204-80235757	K562	blood:	n/a	n/a
5	ARID3A	chr6:80173407-80174028	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:80175976-80176290	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:80246977-80248592	K562	blood:	n/a	n/a
8	ARID3A	chr6:80170896-80171200	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:80214200-80214430	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:80246024-80246629	K562	blood:	n/a	n/a
11	ARID3A	chr6:80187067-80187087	K562	blood:	n/a	n/a
12	ARID3A	chr6:80177250-80177813	K562	blood:	n/a	n/a
13	ATF1	chr6:80177466-80177791	K562	blood:	n/a	n/a
14	ATF1	chr6:80235408-80235651	K562	blood:	n/a	n/a
15	ATF1	chr6:80246943-80247490	K562	blood:	n/a	n/a
16	ATF2	chr6:80247164-80247510	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:80246763-80247512	GM12878	blood:	n/a	n/a
18	ATF3	chr6:80235349-80235792	K562	blood:	n/a	n/a
19	BACH1	chr6:80246673-80246985	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:80247333-80247344	K562	blood:	n/a	n/a
21	BCL3	chr6:80204659-80204921	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:80150457-80150645	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:80246825-80247663	K562	blood:	n/a	n/a
24	BHLHE40	chr6:80177438-80178009	K562	blood:	n/a	n/a
25	BHLHE40	chr6:80247171-80247805	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:80235402-80235724	K562	blood:	n/a	n/a
27	BRCA1	chr6:80161996-80162010	GM12878	blood:	n/a	n/a
28	BRCA1	chr6:80247315-80247614	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr6:80246730-80246733	GM12878	blood:	n/a	n/a
30	BRCA1	chr6:80247172-80247728	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr6:80246816-80247002	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr6:80163443-80163814	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr6:80235303-80235750	K562	blood:	n/a	n/a
34	CBX3	chr6:80247081-80247752	K562	blood:	n/a	n/a
35	CBX3	chr6:80235311-80235703	K562	blood:	n/a	n/a
36	CCNT2	chr6:80246722-80247548	K562	blood:	n/a	n/a
37	CCNT2	chr6:80235381-80235676	K562	blood:	n/a	n/a
38	CEBPB	chr6:80180946-80181075	H1-hESC	embryonic stem cell:	n/a	chr6:80181013-80181024 chr6:80181013-80181022
39	CEBPB	chr6:80150876-80151273	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:80179981-80180265	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr6:80177403-80177776	K562	blood:	n/a	n/a
42	CEBPB	chr6:80235422-80235826	K562	blood:	n/a	chr6:80235671-80235682
43	CEBPB	chr6:80233509-80233856	K562	blood:	n/a	n/a
44	CEBPB	chr6:80208604-80208911	IMR90	lung:	n/a	chr6:80208737-80208748
45	CEBPB	chr6:80171019-80171144	HepG2	liver:	n/a	chr6:80171091-80171102
46	CEBPB	chr6:80163518-80163758	A549	lung:	n/a	n/a
47	CEBPB	chr6:80235598-80235776	Hela-S3	cervix:	n/a	chr6:80235671-80235682
48	CEBPB	chr6:80235329-80235842	K562	blood:	n/a	chr6:80235671-80235682
49	CEBPB	chr6:80163183-80163961	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr6:80235526-80235828	HepG2	liver:	n/a	chr6:80235671-80235682

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:80247339-80247389	MCF10A-Er-Src	breast:	n/a
2	chr6:80247339-80247389	MCF10A-Er-Src	breast:	n/a
3	chr6:80247339-80247389	Jurkat	blood:	n/a
4	chr6:80196224-80196274	HepG2	liver:	n/a
5	chr6:80247037-80247087	HEK293	kidney:	embryo
6	chr6:80233633-80233683	ECC-1	luminal epithelium:	n/a
7	chr6:80178612-80178662	LNCaP	prostate:	n/a
8	chr6:80233633-80233683	ProgFib	skin:	n/a
9	chr6:80247907-80247957	U87	brain:	n/a
10	chr6:80247259-80247309	NB4	blood:	n/a
11	chr6:80251197-80251247	Hela-S3	cervix:	n/a
12	chr6:80247259-80247309	PANC-1	pancreas:	n/a
13	chr6:80247368-80247418	MCF-7	breast:	n/a
14	chr6:80247286-80247336	SK-N-MC	brain:	n/a
15	chr6:80247907-80247957	HCM	heart:	n/a
16	chr6:80247368-80247418	RPTEC	kidney:	n/a
17	chr6:80247339-80247389	Caco-2	colon:	n/a
18	chr6:80247134-80247184	PANC-1	pancreas:	n/a
19	chr6:80233633-80233683	HCPEpiC	choroid plexus:	n/a
20	chr6:80247368-80247418	ProgFib	skin:	n/a
21	chr6:80246421-80246471	CMK	blood:	n/a
22	chr6:80246572-80246622	PANC-1	pancreas:	n/a
23	chr6:80247368-80247418	AG09309	skin:	n/a
24	chr6:80178612-80178662	MCF10A-Er-Src	breast:	n/a
25	chr6:80247286-80247336	HMEC	breast:	n/a
26	chr6:80246421-80246471	IMR90	lung:	fetal
27	chr6:80224471-80224521	PANC-1	pancreas:	n/a
28	chr6:80178612-80178662	HAEpiC	amniotic membrane:	n/a
29	chr6:80247339-80247389	NB4	blood:	n/a
30	chr6:80233633-80233683	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:80247368-80247418	SKMC	muscle:	n/a
32	chr6:80251197-80251247	ECC-1	luminal epithelium:	n/a
33	chr6:80247259-80247309	NT2-D1	testis:	n/a
34	chr6:80246572-80246622	AoSMC	blood vessel:	n/a
35	chr6:80247339-80247389	PANC-1	pancreas:	n/a
36	chr6:80247134-80247184	RPTEC	kidney:	n/a
37	chr6:80178612-80178662	Hepatocyte	liver:	n/a
38	chr6:80247037-80247087	HCM	heart:	n/a
39	chr6:80247339-80247389	HCPEpiC	choroid plexus:	n/a
40	chr6:80247286-80247336	GM06990	blood:	n/a
41	chr6:80196224-80196274	K562	blood:	n/a
42	chr6:80247134-80247184	PrEC	prostate:	n/a
43	chr6:80247037-80247087	AG09309	skin:	n/a
44	chr6:80251197-80251247	NT2-D1	testis:	n/a
45	chr6:80247344-80247394	GM12878	blood:	n/a
46	chr6:80251197-80251247	Hepatocyte	liver:	n/a
47	chr6:80247259-80247309	HRE	kidney:	n/a
48	chr6:80246421-80246471	HCT-116	colon:	n/a
49	chr6:80247368-80247418	LNCaP	prostate:	n/a
50	chr6:80196224-80196274	HRPEpiC	eye:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:79784764..79788097-chr6:80246158..80249987,4	MCF-7	breast:
2	chr6:80234104..80236785-chr6:80239338..80241775,2	K562	blood:
3	chr6:80215719..80218658-chr6:80221222..80223898,3	K562	blood:
4	chr6:80218148..80219970-chr6:80220759..80223148,2	K562	blood:
5	chr6:80227058..80229732-chr6:80232396..80234486,2	MCF-7	breast:
6	chr6:79942688..79944316-chr6:80174273..80176094,2	MCF-7	breast:
7	chr6:80220196..80223373-chr6:80227964..80230707,4	K562	blood:
8	chr6:80245821..80247636-chr6:80249028..80251095,2	K562	blood:
9	chr6:80237991..80239545-chr6:80240324..80243252,2	K562	blood:
10	chr6:80141316..80143852-chr6:80149873..80151786,2	MCF-7	breast:
11	chr6:80175533..80178362-chr6:80187176..80190126,2	K562	blood:
12	chr6:80200398..80203034-chr6:80246678..80249374,3	K562	blood:
13	chr6:80140948..80141831-chr6:80176082..80176626,3	MCF-7	breast:
14	chr6:79911023..79911795-chr6:80175584..80176322,2	MCF-7	breast:
15	chr6:79787145..79789750-chr6:80179461..80181373,2	MCF-7	breast:
16	chr6:79910795..79911579-chr6:80175671..80176696,3	MCF-7	breast:
17	chr6:80251123..80253109-chr6:80259738..80262557,2	K562	blood:
18	chr6:80178503..80181005-chr6:80182070..80184026,2	K562	blood:
19	chr6:79786335..79788138-chr6:80172586..80175202,2	MCF-7	breast:
20	chr6:80237991..80239545-chr6:80240324..80243252,2	K562	blood:
21	chr6:80227058..80229732-chr6:80232396..80234486,2	MCF-7	breast:
22	chr6:79786800..79789680-chr6:80184366..80188325,3	MCF-7	breast:
23	chr6:80225254..80226799-chr6:80227104..80230022,2	K562	blood:
24	chr6:80186377..80188286-chr6:80190241..80192504,2	MCF-7	breast:
25	chr6:80225254..80226799-chr6:80227104..80230022,2	K562	blood:
26	chr6:80212286..80214570-chr6:80222627..80224495,2	K562	blood:
27	chr6:80193082..80195834-chr6:80196342..80199250,3	K562	blood:
28	chr6:80233762..80237001-chr6:80242844..80245026,3	K562	blood:
29	chr6:80203346..80206046-chr6:80245933..80247472,2	K562	blood:
30	chr6:80234104..80236785-chr6:80239338..80241775,2	K562	blood:
31	chr6:80221232..80224610-chr6:80224901..80227580,3	K562	blood:
32	chr6:80212286..80214570-chr6:80222627..80224495,2	K562	blood:
33	chr6:80247904..80250067-chr6:80253206..80255779,2	MCF-7	breast:
34	chr6:80193082..80195834-chr6:80196342..80199250,3	K562	blood:
35	chr6:79786363..79788392-chr6:80226877..80228992,2	K562	blood:
36	chr6:79784565..79790401-chr6:80174482..80177325,6	MCF-7	breast:
37	chr6:79785608..79789213-chr6:80161960..80164790,3	MCF-7	breast:
38	chr6:79789634..79791337-chr6:80176211..80178981,2	K562	blood:
39	chr6:80233762..80237001-chr6:80242844..80245026,3	K562	blood:
40	chr6:79786974..79789353-chr6:80246033..80249654,3	K562	blood:
41	chr6:80229075..80231339-chr6:80247082..80250716,3	K562	blood:
42	chr6:80233273..80237296-chr6:80243465..80250344,8	K562	blood:
43	chr6:80242321..80244974-chr6:80252815..80254989,3	K562	blood:
44	chr6:80237991..80239810-chr6:80240324..80243252,3	K562	blood:
45	chr6:80211479..80218062-chr6:80218996..80224127,6	K562	blood:
46	chr6:80221232..80223663-chr6:80223749..80226401,2	K562	blood:
47	chr6:80215719..80218658-chr6:80221222..80223898,3	K562	blood:
48	chr6:80211479..80218062-chr6:80218996..80224127,6	K562	blood:
49	chr6:80186377..80188286-chr6:80190241..80192504,2	MCF-7	breast:
50	chr6:80218148..80219970-chr6:80220759..80223148,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3BGRL2-9	chr6:80181141-80181234	NONHSAT113692
2	lnc-SH3BGRL2-8	chr6:80187474-80187741	NONHSAT113694
3	lnc-SH3BGRL2-9	chr6:80190967-80191157	NONHSAT113692
4	lnc-SH3BGRL2-1	chr6:80251234-80251677	XLOC_005361
5	lnc-SH3BGRL2-9	chr6:80195902-80196367	NONHSAT113692
6	lnc-SH3BGRL2-1	chr6:80247342-80247429	XLOC_005361
7	lnc-SH3BGRL2-1	chr6:80248445-80248560	XLOC_005361
8	lnc-SH3BGRL2-1	chr6:80251234-80251672	NONHSAT113702
9	lnc-SH3BGRL2-1	chr6:80248445-80248560	XLOC_005361
10	lnc-SH3BGRL2-8	chr6:80186976-80187073	NONHSAT113694
11	lnc-SH3BGRL2-1	chr6:80248445-80248560	XLOC_005361
12	lnc-SH3BGRL2-1	chr6:80247342-80247601	XLOC_005361
13	lnc-SH3BGRL2-1	chr6:80251234-80251481	XLOC_005361
14	lnc-SH3BGRL2-1	chr6:80248445-80248562	NONHSAT113702
15	lnc-SH3BGRL2-9	chr6:80190973-80191157	NONHSAT113695
16	lnc-SH3BGRL2-8	chr6:80186733-80186840	NONHSAT113694
17	lnc-SH3BGRL2-1	chr6:80247547-80247601	XLOC_005361
18	lnc-SH3BGRL2-1	chr6:80248445-80248560	XLOC_005361
19	lnc-SH3BGRL2-9	chr6:80228485-80228894	NONHSAT113695
20	lnc-SH3BGRL2-1	chr6:80247285-80247429	XLOC_005361

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	LCA5	hsa-miR-335-5p	chr6:80196025-80196049
2	LCA5	hsa-miR-10a-5p	chr6:80194781-80194803
3	LCA5	hsa-miR-10a-5p	chr6:80194808-80194829
4	LCA5	hsa-miR-132-3p	chr6:80222799-80222819

Variant related genes	Relation type
LCA5	TF binding region
DBIP1	TF binding region
LCA5	CpG island
DBIP1	CpG island
ENSG00000135338	chromatin interactions
ENSG00000270362	chromatin interactions
ENSG00000146247	chromatin interactions
ENSG00000261970	chromatin interactions
ENSG00000218748	chromatin interactions
EYS	miRNA target sites
OCA2	miRNA target sites
SETD7	miRNA target sites
ANGEL2	miRNA target sites

Extended variants
information (count: 3865 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3865 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10755387	chr6:80147225-80147226	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192594264	chr6:80147272-80147273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9361534	chr6:80147302-80147303	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs141890177	chr6:80147320-80147321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147032914	chr6:80147338-80147339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548432776	chr6:80147392-80147393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549992021	chr6:80147411-80147412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183542860	chr6:80147436-80147437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529155071	chr6:80147463-80147464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147658988	chr6:80147490-80147491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9294146	chr6:80147506-80147507	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9448710	chr6:80147522-80147523	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs115676957	chr6:80147530-80147531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548919835	chr6:80147531-80147532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150206383	chr6:80147598-80147599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568933181	chr6:80147647-80147648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542132891	chr6:80147700-80147701	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs188424458	chr6:80147714-80147715	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs138811911	chr6:80147728-80147729	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192826406	chr6:80147730-80147731	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs538999088	chr6:80147737-80147738	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs35969627	chr6:80147774-80147775	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs564310785	chr6:80147790-80147791	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs76895290	chr6:80147792-80147793	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs538109965	chr6:80147800-80147801	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs184752159	chr6:80147813-80147814	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs77077119	chr6:80147849-80147850	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs531508721	chr6:80147865-80147866	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs60649362	chr6:80147873-80147874	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571545790	chr6:80147874-80147875	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs113501373	chr6:80147921-80147922	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs188707545	chr6:80147925-80147926	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs557340299	chr6:80147950-80147951	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs149506908	chr6:80147956-80147957	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373369481	chr6:80147972-80147973	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs143155373	chr6:80147982-80147983	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs370954639	chr6:80147990-80147991	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374020397	chr6:80148016-80148017	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570067301	chr6:80148054-80148055	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs111441953	chr6:80148073-80148074	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs368357563	chr6:80148079-80148080	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs377652121	chr6:80148087-80148088	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs566468953	chr6:80148108-80148109	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs555805241	chr6:80148114-80148115	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs75865394	chr6:80148143-80148144	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs138746469	chr6:80148145-80148146	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569400949	chr6:80148242-80148243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572737240	chr6:80148245-80148246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191225119	chr6:80148251-80148252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558145199	chr6:80148310-80148311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80136000-80147600	Weak transcription	Brain Angular Gyrus	brain
2	chr6:80141000-80147400	Enhancers	Fetal Intestine Large	intestine
3	chr6:80144200-80147600	Enhancers	Fetal Intestine Small	intestine
4	chr6:80145000-80148200	Enhancers	Hela-S3	cervix
5	chr6:80146000-80148000	Enhancers	Fetal Lung	lung
6	chr6:80146400-80147400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr6:80146400-80147400	Enhancers	Placenta	Placenta
8	chr6:80146400-80147600	Enhancers	HSMMtube	muscle
9	chr6:80146600-80148000	Enhancers	Ovary	ovary
10	chr6:80146800-80147800	Weak transcription	HSMM	muscle
11	chr6:80146800-80148000	Enhancers	Fetal Muscle Leg	muscle
12	chr6:80147200-80147400	Enhancers	Brain Hippocampus Middle	brain
13	chr6:80147400-80147800	Weak transcription	Brain Hippocampus Middle	brain
14	chr6:80147400-80148200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:80147400-80148400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr6:80147400-80148400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr6:80147400-80152600	Weak transcription	Fetal Intestine Large	intestine
18	chr6:80147600-80147800	Enhancers	Fetal Kidney	kidney
19	chr6:80147600-80148000	Enhancers	Brain Cingulate Gyrus	brain
20	chr6:80147600-80148200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:80147600-80148200	Enhancers	Brain Angular Gyrus	brain
22	chr6:80147600-80148400	Enhancers	Adipose Nuclei	Adipose
23	chr6:80147600-80150000	Weak transcription	Fetal Intestine Small	intestine
24	chr6:80147800-80148400	Enhancers	Brain Hippocampus Middle	brain
25	chr6:80148000-80148200	Enhancers	HSMM	muscle
26	chr6:80148000-80148400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:80148000-80148600	Weak transcription	Fetal Lung	lung
28	chr6:80148000-80148600	Weak transcription	Fetal Muscle Leg	muscle
29	chr6:80148200-80150200	Weak transcription	Hela-S3	cervix
30	chr6:80148400-80153000	Weak transcription	Adipose Nuclei	Adipose
31	chr6:80148600-80148800	Enhancers	Fetal Kidney	kidney
32	chr6:80148600-80148800	Enhancers	Fetal Lung	lung
33	chr6:80148600-80148800	Enhancers	Fetal Muscle Leg	muscle
34	chr6:80149600-80151200	Enhancers	Fetal Heart	heart
35	chr6:80150000-80151600	Enhancers	Fetal Intestine Small	intestine
36	chr6:80150200-80151600	Enhancers	Hela-S3	cervix
37	chr6:80151000-80160800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:80151600-80151800	Weak transcription	Fetal Intestine Small	intestine
39	chr6:80151600-80151800	Enhancers	HepG2	liver
40	chr6:80152400-80153200	ZNF genes & repeats	Fetal Intestine Small	intestine
41	chr6:80152600-80152800	Enhancers	Fetal Intestine Large	intestine
42	chr6:80152800-80153000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:80153000-80153800	Enhancers	Adipose Nuclei	Adipose
44	chr6:80153000-80163200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:80154200-80162400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:80158000-80158600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr6:80158600-80162600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr6:80160200-80160400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr6:80160200-80163000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr6:80160400-80161000	Enhancers	HepG2	liver

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