Variant report

Variant	nsv1030863
Chromosome Location	chr6:26371006-26405990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:836)
CpG islands
(count:855)
Chromatin interactive
region (count:78)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26389651-26389753	K562	blood:	n/a	n/a
2	ARID3A	chr6:26388282-26388592	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:26383245-26383472	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:26379721-26379968	K562	blood:	n/a	n/a
5	ARID3A	chr6:26372942-26373010	K562	blood:	n/a	n/a
6	ATF1	chr6:26402234-26402914	K562	blood:	n/a	n/a
7	ATF1	chr6:26383091-26383465	K562	blood:	n/a	n/a
8	ATF1	chr6:26379681-26379920	K562	blood:	n/a	n/a
9	ATF1	chr6:26384288-26384605	K562	blood:	n/a	n/a
10	ATF1	chr6:26389555-26389824	K562	blood:	n/a	n/a
11	ATF3	chr6:26389548-26389958	K562	blood:	n/a	n/a
12	ATF3	chr6:26384220-26384567	K562	blood:	n/a	n/a
13	BATF	chr6:26378427-26378675	GM12878	blood:	n/a	n/a
14	BATF	chr6:26393290-26393652	GM12878	blood:	n/a	n/a
15	BATF	chr6:26398309-26398646	GM12878	blood:	n/a	chr6:26398493-26398504 chr6:26398513-26398524
16	BHLHE40	chr6:26402307-26402786	HepG2	liver:	n/a	n/a
17	BHLHE40	chr6:26400981-26401160	K562	blood:	n/a	n/a
18	BHLHE40	chr6:26383051-26383475	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:26385594-26385771	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:26402305-26402843	K562	blood:	n/a	n/a
21	BHLHE40	chr6:26372951-26372953	K562	blood:	n/a	n/a
22	BHLHE40	chr6:26383196-26383520	HepG2	liver:	n/a	n/a
23	BHLHE40	chr6:26389616-26389894	K562	blood:	n/a	n/a
24	BHLHE40	chr6:26402290-26402595	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:26383124-26383727	K562	blood:	n/a	n/a
26	BRCA1	chr6:26383338-26383539	GM12878	blood:	n/a	n/a
27	BRCA1	chr6:26383197-26383433	HepG2	liver:	n/a	n/a
28	BRCA1	chr6:26383245-26383595	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr6:26383156-26383464	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr6:26383574-26384637	K562	blood:	n/a	chr6:26384271-26384282
31	CCNT2	chr6:26379819-26379837	K562	blood:	n/a	n/a
32	CCNT2	chr6:26384407-26384584	K562	blood:	n/a	n/a
33	CEBPB	chr6:26394658-26394984	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:26398819-26399148	HepG2	liver:	n/a	chr6:26398983-26398994 chr6:26398982-26398993 chr6:26398984-26398993
35	CEBPB	chr6:26390793-26391031	A549	lung:	n/a	n/a
36	CEBPB	chr6:26390830-26390987	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr6:26389480-26389826	A549	lung:	n/a	n/a
38	CEBPB	chr6:26389383-26389976	K562	blood:	n/a	n/a
39	CEBPB	chr6:26399843-26399971	K562	blood:	n/a	n/a
40	CEBPB	chr6:26394478-26394974	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr6:26398864-26399130	IMR90	lung:	n/a	chr6:26398983-26398994 chr6:26398982-26398993 chr6:26398984-26398993
42	CEBPB	chr6:26389434-26389917	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:26390776-26391098	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:26389455-26389872	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:26372133-26372288	HepG2	liver:	n/a	chr6:26372235-26372246
46	CEBPB	chr6:26388692-26388972	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:26398825-26399127	K562	blood:	n/a	chr6:26398983-26398994 chr6:26398982-26398993 chr6:26398984-26398993
48	CEBPB	chr6:26398753-26399178	K562	blood:	n/a	chr6:26398983-26398994 chr6:26398982-26398993 chr6:26398984-26398993
49	CEBPB	chr6:26389554-26389831	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:26398841-26399110	A549	lung:	n/a	chr6:26398983-26398994 chr6:26398982-26398993 chr6:26398984-26398993

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26402310-26402360	BJ	skin:	n/a
2	chr6:26402310-26402360	BJ	skin:	n/a
3	chr6:26402310-26402360	HCM	heart:	n/a
4	chr6:26383297-26383347	H1-hESC	embryonic stem cell:	embryo
5	chr6:26383374-26383424	PrEC	prostate:	n/a
6	chr6:26383297-26383347	HL-60	blood:	n/a
7	chr6:26402511-26402561	HEEpiC	esophagus:	n/a
8	chr6:26383374-26383424	SK-N-MC	brain:	n/a
9	chr6:26401691-26401741	CMK	blood:	n/a
10	chr6:26375990-26376040	SAEC	small airway:	n/a
11	chr6:26383004-26383054	HepG2	liver:	n/a
12	chr6:26393253-26393303	NHBE	bronchial:	n/a
13	chr6:26375990-26376040	AG10803	skin:	n/a
14	chr6:26382695-26382745	AG09319	gingival:	n/a
15	chr6:26401793-26401843	ECC-1	luminal epithelium:	n/a
16	chr6:26383374-26383424	HRE	kidney:	n/a
17	chr6:26383297-26383347	A549	lung:	n/a
18	chr6:26375990-26376040	BE2_C	brain:	n/a
19	chr6:26383673-26383723	HNPCEpiC	eye:	n/a
20	chr6:26401691-26401741	SAEC	small airway:	n/a
21	chr6:26375990-26376040	H1-hESC	embryonic stem cell:	embryo
22	chr6:26382695-26382745	AG04449	skin:	fetal
23	chr6:26401793-26401843	HMEC	breast:	n/a
24	chr6:26393253-26393303	H1-hESC	embryonic stem cell:	embryo
25	chr6:26383374-26383424	GM12891	blood:	n/a
26	chr6:26402310-26402360	AG10803	skin:	n/a
27	chr6:26383297-26383347	HCPEpiC	choroid plexus:	n/a
28	chr6:26402511-26402561	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:26386191-26386241	A549	lung:	n/a
30	chr6:26383374-26383424	SKMC	muscle:	n/a
31	chr6:26401793-26401843	RPTEC	kidney:	n/a
32	chr6:26386191-26386241	SK-N-MC	brain:	n/a
33	chr6:26401691-26401741	AG04450	lung:	fetal
34	chr6:26383374-26383424	GM19239	blood:	n/a
35	chr6:26383297-26383347	MCF10A-Er-Src	breast:	n/a
36	chr6:26383374-26383424	HRCEpiC	kidney:	n/a
37	chr6:26401793-26401843	GM12891	blood:	n/a
38	chr6:26402776-26402826	RPTEC	kidney:	n/a
39	chr6:26383297-26383347	PANC-1	pancreas:	n/a
40	chr6:26386191-26386241	MCF-7	breast:	n/a
41	chr6:26401691-26401741	HCPEpiC	choroid plexus:	n/a
42	chr6:26393253-26393303	HIPEpiC	eye:	n/a
43	chr6:26393253-26393303	SKMC	muscle:	n/a
44	chr6:26383673-26383723	MCF10A-Er-Src	breast:	n/a
45	chr6:26402776-26402826	NHDF-neo	bronchial:	n/a
46	chr6:26375990-26376040	SK-N-MC	brain:	n/a
47	chr6:26402776-26402826	HUVEC	blood vessel:	n/a
48	chr6:26383004-26383054	GM12891	blood:	n/a
49	chr6:26382817-26382867	H1-hESC	embryonic stem cell:	embryo
50	chr6:26383673-26383723	HAEpiC	amniotic membrane:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:26384661..26390027-chr6:26390440..26394308,9	K562	blood:
2	chr6:26391021..26393717-chr6:26396965..26399290,2	K562	blood:
3	chr6:26373194..26374949-chr6:26387423..26389905,2	K562	blood:
4	chr6:26386249..26387977-chr6:26410768..26413470,2	K562	blood:
5	chr6:26384661..26390027-chr6:26390440..26394308,9	K562	blood:
6	chr6:26403327..26405922-chr6:26411445..26413266,2	K562	blood:
7	chr6:26383587..26385903-chr6:26419597..26421640,2	MCF-7	breast:
8	chr6:26382632..26385246-chr6:26444412..26446084,2	K562	blood:
9	chr6:26384869..26386538-chr6:26388093..26389767,2	MCF-7	breast:
10	chr6:26395411..26398038-chr6:26426386..26428479,2	K562	blood:
11	chr6:26373307..26375855-chr6:26376435..26379484,4	K562	blood:
12	chr6:26388091..26389819-chr6:26401316..26403853,2	K562	blood:
13	chr6:26373111..26374832-chr6:26379026..26381530,2	MCF-7	breast:
14	chr6:26158092..26160722-chr6:26391626..26394367,2	MCF-7	breast:
15	chr6:26391021..26393717-chr6:26396965..26399290,2	K562	blood:
16	chr6:26390542..26392521-chr6:26396863..26399641,3	K562	blood:
17	chr6:26402744..26404382-chr6:26575217..26577628,2	K562	blood:
18	chr6:26393733..26396170-chr6:26401086..26404245,3	K562	blood:
19	chr6:26397216..26399740-chr6:26407400..26409263,3	K562	blood:
20	chr6:26398898..26401039-chr6:26402224..26404751,3	K562	blood:
21	chr6:26385663..26388143-chr6:26388160..26389788,2	K562	blood:
22	chr6:26399787..26402548-chr6:26520304..26522588,2	K562	blood:
23	chr6:26365252..26366783-chr6:26384022..26386049,2	K562	blood:
24	chr6:26395454..26397277-chr6:26501383..26504153,2	K562	blood:
25	chr6:26400774..26405587-chr6:26406042..26409897,8	K562	blood:
26	chr6:26363140..26366680-chr6:26382117..26385194,3	MCF-7	breast:
27	chr6:26373111..26374832-chr6:26379026..26381530,2	MCF-7	breast:
28	chr6:26378930..26384775-chr6:26385231..26390850,8	MCF-7	breast:
29	chr6:26374643..26376462-chr6:26381050..26382858,2	K562	blood:
30	chr6:26378690..26380275-chr6:26532676..26534577,2	K562	blood:
31	chr6:26157049..26158999-chr6:26401561..26403598,2	K562	blood:
32	chr6:26378930..26384775-chr6:26385231..26390850,8	MCF-7	breast:
33	chr6:26214943..26217251-chr6:26374280..26376179,2	K562	blood:
34	chr6:26382380..26384957-chr6:26398631..26401172,3	K562	blood:
35	chr6:26374643..26376462-chr6:26381050..26382858,2	K562	blood:
36	chr6:26384982..26386521-chr6:26418535..26421413,2	K562	blood:
37	chr6:26385663..26388143-chr6:26388160..26389788,2	K562	blood:
38	chr6:26370389..26373294-chr6:26375542..26378035,2	K562	blood:
39	chr6:26390074..26392884-chr6:26401508..26403224,2	K562	blood:
40	chr6:26389060..26391838-chr6:26394516..26396204,2	K562	blood:
41	chr6:26400255..26403237-chr6:26521906..26524697,3	K562	blood:
42	chr6:26386609..26388143-chr6:26388160..26389725,2	K562	blood:
43	chr6:26403709..26405372-chr6:26410974..26412511,2	MCF-7	breast:
44	chr6:26231864..26233958-chr6:26385034..26386589,2	K562	blood:
45	chr6:26188276..26190980-chr6:26381179..26383865,2	K562	blood:
46	chr6:26373307..26375855-chr6:26376435..26379484,4	K562	blood:
47	chr6:26376258..26380187-chr6:26381333..26383262,3	K562	blood:
48	chr6:26055082..26056690-chr6:26399620..26401268,2	K562	blood:
49	chr6:26392331..26394717-chr6:26410303..26413058,2	K562	blood:
50	chr6:26283237..26286235-chr6:26387862..26389996,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTN2A2-1	chr6:26404363-26404783	NONHSAT108276
2	lnc-BTN2A2-2	chr6:26374555-26374601	NONHSAT108273
3	lnc-BTN2A2-2	chr6:26374999-26375036	NONHSAT108273
4	lnc-BTN2A2-1	chr6:26402478-26402640	NONHSAT108276
5	lnc-BTN2A2-2	chr6:26372921-26375929	NONHSAT108275
6	lnc-BTN2A2-2	chr6:26373504-26373641	NONHSAT108273

No data

Variant related genes	Relation type
BTN3A2	TF binding region
BTN3A1	TF binding region
BTN2A2	TF binding region
BTN3A2	CpG island
BTN3A1	CpG island
BTN2A2	CpG island
ENSG00000182952	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000228223	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000218281	chromatin interactions
ENSG00000215979	chromatin interactions
ENSG00000124549	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000111801	chromatin interactions
ENSG00000252399	chromatin interactions
ENSG00000188987	chromatin interactions
ENSG00000124508	chromatin interactions
ENSG00000124557	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000026950	chromatin interactions
ENSG00000186470	chromatin interactions
ENSG00000158406	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000196787	chromatin interactions

Extended variants
information (count: 1457 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1457 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10946818	chr6:26371006-26371007	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35857763	chr6:26371028-26371029	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183827833	chr6:26371102-26371103	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72841516	chr6:26371195-26371196	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs150757948	chr6:26371231-26371232	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139089156	chr6:26371262-26371263	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544294385	chr6:26371279-26371280	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536957284	chr6:26371289-26371290	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556827509	chr6:26371318-26371319	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7750384	chr6:26371364-26371365	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs147128089	chr6:26371411-26371412	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72841517	chr6:26371426-26371427	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs572865961	chr6:26371480-26371481	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545058432	chr6:26371484-26371485	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35249543	chr6:26371525-26371526	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140216134	chr6:26371620-26371621	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575870281	chr6:26371627-26371628	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12173854	chr6:26371679-26371680	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs186344544	chr6:26371699-26371700	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530147076	chr6:26371749-26371750	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145628875	chr6:26371795-26371796	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560505424	chr6:26371814-26371815	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532520773	chr6:26371818-26371819	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73736214	chr6:26371831-26371832	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs571391668	chr6:26371900-26371901	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72841519	chr6:26371901-26371902	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs150885158	chr6:26371914-26371915	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78525827	chr6:26371925-26371926	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201066305	chr6:26371926-26371927	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111886880	chr6:26371927-26371928	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145400432	chr6:26371928-26371929	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552713123	chr6:26371939-26371940	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572749558	chr6:26371953-26371954	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs56380525	chr6:26371981-26371982	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs142401480	chr6:26372051-26372052	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369669728	chr6:26372063-26372064	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182143641	chr6:26372107-26372108	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186698391	chr6:26372153-26372154	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs61518529	chr6:26372154-26372155	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs370242631	chr6:26372173-26372174	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs572836471	chr6:26372186-26372187	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs192375641	chr6:26372191-26372192	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs560289054	chr6:26372202-26372203	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs532528046	chr6:26372222-26372223	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs552436971	chr6:26372237-26372238	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs562619272	chr6:26372238-26372239	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs7765566	chr6:26372349-26372350	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs550374642	chr6:26372392-26372393	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567093342	chr6:26372393-26372394	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111981006	chr6:26372399-26372400	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Autism	22495309	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1767 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26365800-26375200	Weak transcription	Aorta	Aorta
2	chr6:26366000-26373200	Weak transcription	Colonic Mucosa	Colon
3	chr6:26366000-26373800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr6:26366000-26374800	Weak transcription	Esophagus	oesophagus
5	chr6:26366000-26375000	Weak transcription	Brain Anterior Caudate	brain
6	chr6:26366000-26375600	Weak transcription	Gastric	stomach
7	chr6:26366000-26382600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr6:26366000-26383000	Weak transcription	Brain Hippocampus Middle	brain
9	chr6:26366000-26383200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr6:26366000-26383200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:26366000-26383200	Weak transcription	Pancreas	Pancrea
12	chr6:26366000-26383200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr6:26366000-26383200	Weak transcription	HSMMtube	muscle
14	chr6:26366000-26383400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr6:26366200-26371200	Weak transcription	A549	lung
16	chr6:26366200-26374600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr6:26366200-26374800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:26366200-26375000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:26366200-26375200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:26366200-26375800	Weak transcription	NH-A	brain
21	chr6:26366200-26382400	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr6:26366200-26383200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:26366200-26383200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr6:26366400-26372600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr6:26367000-26374400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr6:26367000-26377800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr6:26367000-26383000	Weak transcription	NHEK	skin
28	chr6:26367000-26383200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:26367200-26371600	Weak transcription	Stomach Mucosa	stomach
30	chr6:26367200-26374600	Weak transcription	NHLF	lung
31	chr6:26367400-26375000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:26367600-26372800	Weak transcription	NHDF-Ad	bronchial
33	chr6:26367600-26373400	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr6:26367600-26374600	Weak transcription	Hela-S3	cervix
35	chr6:26367800-26372200	Weak transcription	K562	blood
36	chr6:26367800-26373000	Weak transcription	GM12878-XiMat	blood
37	chr6:26367800-26378600	Weak transcription	Small Intestine	intestine
38	chr6:26368600-26372000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:26368800-26371400	Strong transcription	Fetal Stomach	stomach
40	chr6:26368800-26375200	Strong transcription	Primary B cells from cord blood	blood
41	chr6:26368800-26376000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
42	chr6:26369200-26374800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr6:26369400-26371200	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr6:26369400-26371400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:26369400-26371600	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr6:26369400-26371800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
47	chr6:26369400-26372200	Strong transcription	Fetal Intestine Large	intestine
48	chr6:26369400-26372600	Strong transcription	HepG2	liver
49	chr6:26369400-26373600	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr6:26369400-26375200	Strong transcription	Fetal Lung	lung

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