Variant report

Variant	nsv1019145
Chromosome Location	chr6:44313576-44421440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1229)
CpG islands
(count:1283)
Chromatin interactive
region (count:128)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:1229 , 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	chr6:44398919-44399179	K562	blood:	n/a	n/a
2	ATF1	chr6:44322367-44322468	K562	blood:	n/a	n/a
3	ATF1	chr6:44354462-44355588	K562	blood:	n/a	n/a
4	ATF2	chr6:44354870-44355620	H1-hESC	embryonic stem cell:	n/a	chr6:44355189-44355200
5	ATF2	chr6:44354781-44355624	GM12878	blood:	n/a	chr6:44355189-44355200
6	ATF2	chr6:44354704-44355620	GM12878	blood:	n/a	chr6:44355189-44355200
7	ATF2	chr6:44354963-44355725	H1-hESC	embryonic stem cell:	n/a	chr6:44355189-44355200
8	ATF3	chr6:44416907-44417223	K562	blood:	n/a	n/a
9	ATF3	chr6:44354899-44355774	K562	blood:	n/a	chr6:44355189-44355200 chr6:44355188-44355198 chr6:44355187-44355202 chr6:44355188-44355198 chr6:44355191-44355199 chr6:44355187-44355198 chr6:44355190-44355198 chr6:44355188-44355201 chr6:44355189-44355200 chr6:44355188-44355199 chr6:44355191-44355198 chr6:44355189-44355202 chr6:44355187-44355200
10	ATF3	chr6:44355078-44355859	K562	blood:	n/a	chr6:44355189-44355200 chr6:44355188-44355198 chr6:44355187-44355202 chr6:44355188-44355198 chr6:44355191-44355199 chr6:44355187-44355198 chr6:44355190-44355198 chr6:44355188-44355201 chr6:44355189-44355200 chr6:44355188-44355199 chr6:44355191-44355198 chr6:44355189-44355202 chr6:44355187-44355200
11	ATF3	chr6:44318001-44318305	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:44354817-44355817	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr6:44396560-44396746	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:44354945-44355532	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:44355009-44355672	HepG2	liver:	n/a	chr6:44355620-44355636
16	BHLHE40	chr6:44356030-44356161	K562	blood:	n/a	n/a
17	BRCA1	chr6:44354847-44355615	H1-hESC	embryonic stem cell:	n/a	chr6:44355391-44355400 chr6:44355245-44355254
18	BRCA1	chr6:44376378-44376386	HepG2	liver:	n/a	n/a
19	BRCA1	chr6:44354817-44355685	HepG2	liver:	n/a	chr6:44355391-44355400 chr6:44355245-44355254
20	BRCA1	chr6:44355013-44355666	GM12878	blood:	n/a	chr6:44355391-44355400 chr6:44355245-44355254
21	BRCA1	chr6:44354504-44355790	Hela-S3	cervix:	n/a	chr6:44355391-44355400 chr6:44355245-44355254
22	CBX3	chr6:44324086-44324489	K562	blood:	n/a	n/a
23	CBX3	chr6:44354427-44356105	K562	blood:	n/a	n/a
24	CCNT2	chr6:44355152-44355862	K562	blood:	n/a	n/a
25	CEBPB	chr6:44364859-44365148	HepG2	liver:	n/a	chr6:44365020-44365031
26	CEBPB	chr6:44406548-44406821	IMR90	lung:	n/a	chr6:44406678-44406689
27	CEBPB	chr6:44420458-44420757	HepG2	liver:	n/a	chr6:44420588-44420599
28	CEBPB	chr6:44420394-44421207	IMR90	lung:	n/a	chr6:44420588-44420599
29	CEBPB	chr6:44326309-44326523	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:44420475-44420743	A549	lung:	n/a	chr6:44420588-44420599
31	CEBPB	chr6:44354456-44355567	IMR90	lung:	n/a	chr6:44354724-44354737 chr6:44354724-44354735
32	CEBPB	chr6:44318080-44318424	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr6:44414619-44415124	A549	lung:	n/a	n/a
34	CEBPB	chr6:44414359-44415072	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr6:44414414-44415004	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:44406587-44406859	HepG2	liver:	n/a	chr6:44406678-44406689
37	CEBPB	chr6:44414736-44415000	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:44404150-44404374	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:44349480-44349832	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:44364918-44365153	A549	lung:	n/a	chr6:44365020-44365031
41	CEBPB	chr6:44414882-44414919	K562	blood:	n/a	n/a
42	CEBPB	chr6:44365015-44365070	K562	blood:	n/a	chr6:44365020-44365031
43	CEBPB	chr6:44349466-44349845	MCF-7	breast:	n/a	n/a
44	CEBPB	chr6:44349517-44349833	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr6:44420397-44420863	MCF-7	breast:	n/a	chr6:44420588-44420599
46	CEBPB	chr6:44354544-44355685	HepG2	liver:	n/a	chr6:44354724-44354737 chr6:44354724-44354735
47	CEBPB	chr6:44354490-44355625	K562	blood:	n/a	chr6:44354724-44354737 chr6:44354724-44354735
48	CEBPB	chr6:44407455-44407789	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:44354516-44355688	K562	blood:	n/a	chr6:44354724-44354737 chr6:44354724-44354735
50	CEBPB	chr6:44354397-44355808	Hela-S3	cervix:	n/a	chr6:44354724-44354737 chr6:44354724-44354735

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44355163-44355213	PFSK-1	brain:	n/a
2	chr6:44344842-44344892	ECC-1	luminal epithelium:	n/a
3	chr6:44355163-44355213	PFSK-1	brain:	n/a
4	chr6:44344842-44344892	ECC-1	luminal epithelium:	n/a
5	chr6:44329051-44329101	NT2-D1	testis:	n/a
6	chr6:44420555-44420605	HIPEpiC	eye:	n/a
7	chr6:44396701-44396751	GM12878	blood:	n/a
8	chr6:44352236-44352286	SK-N-SH	brain:	n/a
9	chr6:44420555-44420605	HepG2	liver:	n/a
10	chr6:44355287-44355337	CMK	blood:	n/a
11	chr6:44354883-44354933	PFSK-1	brain:	n/a
12	chr6:44355541-44355591	BJ	skin:	n/a
13	chr6:44355199-44355249	SK-N-SH_RA	brain:	n/a
14	chr6:44355287-44355337	GM12891	blood:	n/a
15	chr6:44359274-44359324	AoSMC	blood vessel:	n/a
16	chr6:44344842-44344892	HCF	heart:	n/a
17	chr6:44396701-44396751	HCT-116	colon:	n/a
18	chr6:44355287-44355337	AoSMC	blood vessel:	n/a
19	chr6:44329051-44329101	Jurkat	blood:	n/a
20	chr6:44420555-44420605	ECC-1	luminal epithelium:	n/a
21	chr6:44354883-44354933	HAEpiC	amniotic membrane:	n/a
22	chr6:44355163-44355213	CMK	blood:	n/a
23	chr6:44355287-44355337	HRCEpiC	kidney:	n/a
24	chr6:44354646-44354696	SK-N-SH_RA	brain:	n/a
25	chr6:44383329-44383379	HCT-116	colon:	n/a
26	chr6:44355163-44355213	NHBE	bronchial:	n/a
27	chr6:44355541-44355591	GM12892	blood:	n/a
28	chr6:44354883-44354933	T-47D	breast:	n/a
29	chr6:44352236-44352286	AG09319	gingival:	n/a
30	chr6:44355950-44356000	SAEC	small airway:	n/a
31	chr6:44355161-44355211	H1-hESC	embryonic stem cell:	embryo
32	chr6:44420555-44420605	AG09309	skin:	n/a
33	chr6:44354883-44354933	ECC-1	luminal epithelium:	n/a
34	chr6:44355199-44355249	CMK	blood:	n/a
35	chr6:44355777-44355827	AG04450	lung:	fetal
36	chr6:44329051-44329101	GM06990	blood:	n/a
37	chr6:44413609-44413659	HNPCEpiC	eye:	n/a
38	chr6:44355950-44356000	SK-N-MC	brain:	n/a
39	chr6:44355777-44355827	SK-N-SH	brain:	n/a
40	chr6:44353839-44353889	MCF10A-Er-Src	breast:	n/a
41	chr6:44396701-44396751	HRPEpiC	eye:	n/a
42	chr6:44354883-44354933	MCF10A-Er-Src	breast:	n/a
43	chr6:44355135-44355185	HAEpiC	amniotic membrane:	n/a
44	chr6:44352236-44352286	NB4	blood:	n/a
45	chr6:44420555-44420605	GM12878	blood:	n/a
46	chr6:44354883-44354933	SK-N-MC	brain:	n/a
47	chr6:44413609-44413659	SKMC	muscle:	n/a
48	chr6:44396701-44396751	GM12891	blood:	n/a
49	chr6:44383329-44383379	PrEC	prostate:	n/a
50	chr6:44383329-44383379	ProgFib	skin:	n/a

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:44356394..44359367-chr6:44380277..44384190,3	K562	blood:
2	chr6:44390673..44392350-chr6:44396444..44398249,2	K562	blood:
3	chr6:44368851..44370605-chr6:44376077..44377814,2	K562	blood:
4	chr6:44405048..44409188-chr6:44409781..44413783,5	K562	blood:
5	chr6:44368851..44370605-chr6:44376077..44377814,2	K562	blood:
6	chr6:44354618..44355305-chr7:150065512..150066433,2	NB4	blood:
7	chr6:44237431..44239577-chr6:44323185..44324985,2	K562	blood:
8	chr6:44406091..44407637-chr6:44410068..44412209,2	K562	blood:
9	chr6:44213933..44216610-chr6:44311528..44314415,2	K562	blood:
10	chr6:44420357..44422515-chr6:44433684..44436230,2	K562	blood:
11	chr6:44333775..44335329-chr6:44340756..44342946,2	K562	blood:
12	chr6:44398980..44399515-chr6:44437258..44438078,2	MCF-7	breast:
13	chr6:44387232..44389973-chr6:44398026..44400145,2	K562	blood:
14	chr6:44279410..44281730-chr6:44319275..44322107,2	K562	blood:
15	chr6:44340013..44342443-chr6:44347687..44349600,2	K562	blood:
16	chr6:44333775..44335329-chr6:44340756..44342946,2	K562	blood:
17	chr6:44315264..44318217-chr6:44339899..44341797,2	K562	blood:
18	chr6:44352373..44357409-chr6:44366084..44371174,7	K562	blood:
19	chr6:44356556..44360481-chr6:44380097..44385414,6	K562	blood:
20	chr10:74397336..74398116-chr6:44355396..44356191,2	Hela-S3	cervix:
21	chr6:44371835..44373897-chr6:44382894..44384925,2	MCF-7	breast:
22	chr6:44396473..44398052-chr6:44398079..44400521,2	K562	blood:
23	chr6:44279048..44280754-chr6:44413022..44414721,2	MCF-7	breast:
24	chr6:44410364..44415906-chr6:44416897..44422592,7	K562	blood:
25	chr6:44345933..44348931-chr6:44350479..44354332,6	K562	blood:
26	chr6:44402998..44404546-chr6:44407688..44409189,2	K562	blood:
27	chr6:44320113..44321810-chr6:44322763..44325227,2	K562	blood:
28	chr6:44410364..44415906-chr6:44416897..44422592,7	K562	blood:
29	chr6:44391748..44393635-chr6:44395811..44398462,2	MCF-7	breast:
30	chr6:44365878..44368641-chr6:44383402..44385534,2	K562	blood:
31	chr5:172197837..172198617-chr6:44355209..44356148,2	Hela-S3	cervix:
32	chr6:44398528..44400400-chr6:44423668..44424679,12	K562	blood:
33	chr6:44097271..44099374-chr6:44352380..44355163,2	K562	blood:
34	chr6:44370773..44372443-chr6:44426552..44428315,2	K562	blood:
35	chr6:44320113..44321810-chr6:44322763..44325227,2	K562	blood:
36	chr6:44243596..44246439-chr6:44318248..44320876,2	K562	blood:
37	chr6:44398593..44399479-chr6:44423901..44425088,5	MCF-7	breast:
38	chr6:44357790..44359510-chr6:44364205..44366302,2	K562	blood:
39	chr6:44350111..44351913-chr6:44352677..44355083,2	MCF-7	breast:
40	chr12:120729344..120729897-chr6:44355147..44356131,2	HCT-116	colon:
41	chr6:44339222..44342779-chr6:44344698..44347140,3	K562	blood:
42	chr6:44231291..44234957-chr6:44353668..44356659,3	K562	blood:
43	chr6:44355078..44355968-chrX:47696084..47696843,2	Hela-S3	cervix:
44	chr6:44342784..44345720-chr6:44353458..44355449,2	K562	blood:
45	chr6:44373289..44375679-chr6:44378205..44380978,2	K562	blood:
46	chr6:44213880..44217687-chr6:44354177..44357164,5	K562	blood:
47	chr6:44398603..44399105-chr6:44423995..44424580,2	MCF-7	breast:
48	chr6:44355391..44357263-chr6:44358949..44363275,4	MCF-7	breast:
49	chr6:44326030..44327611-chr6:44332225..44334880,2	MCF-7	breast:
50	chr6:44396473..44398052-chr6:44398079..44400521,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC5L-3	chr6:44418311-44418898	NONHSAT112963
2	lnc-AARS2-1	chr6:44338508-44338780	expReg_chr6_5009_-

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4642	chr6:44403387-44403408	MIMAT0019702

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDC5L	hsa-miR-16-5p	chr6:44414719-44414740

Variant related genes	Relation type
CDC5L	TF binding region
MIR4642	TF binding region
ENSG00000267849	TF binding region
CDC5L	CpG island
MIR4642	CpG island
ENSG00000267849	CpG island
ENSG00000096401	chromatin interactions
ENSG00000083720	chromatin interactions
ENSG00000197779	chromatin interactions
ENSG00000124608	chromatin interactions
ENSG00000146232	chromatin interactions
ENSG00000196456	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000267849	chromatin interactions
ENSG00000205138	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000178233	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000266619	chromatin interactions
ENSG00000249481	chromatin interactions
ENSG00000214022	chromatin interactions
ENSG00000272442	chromatin interactions
ENSG00000265700	chromatin interactions
ENSG00000248668	chromatin interactions

Extended variants
information (count: 3824 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3824 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544013823	chr6:44313577-44313578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs367831517	chr6:44313618-44313619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181374434	chr6:44313621-44313622	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs541564407	chr6:44313633-44313634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs77481601	chr6:44313641-44313642	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs28436671	chr6:44313661-44313662	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs116736292	chr6:44313687-44313688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564428426	chr6:44313731-44313732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs527448272	chr6:44313748-44313749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139975372	chr6:44313804-44313805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs377124181	chr6:44313834-44313835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145617558	chr6:44313836-44313837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535952147	chr6:44313885-44313886	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536402168	chr6:44313976-44313977	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114263545	chr6:44313977-44313978	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs1971329	chr6:44313986-44313987	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376246459	chr6:44314015-44314016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370499160	chr6:44314016-44314017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200602469	chr6:44314017-44314018	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs60566028	chr6:44314028-44314029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376526345	chr6:44314029-44314030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1609726	chr6:44314036-44314037	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs368299506	chr6:44314091-44314092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148463919	chr6:44314112-44314113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs142603784	chr6:44314163-44314164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538942995	chr6:44314174-44314175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs9472258	chr6:44314176-44314177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181874257	chr6:44314200-44314201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs571919660	chr6:44314209-44314210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545787924	chr6:44314211-44314212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs150962570	chr6:44314242-44314243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531626642	chr6:44314280-44314281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs550148627	chr6:44314403-44314404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561845693	chr6:44314406-44314407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372714672	chr6:44314460-44314461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529138536	chr6:44314503-44314504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9462981	chr6:44314507-44314508	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs140757970	chr6:44314508-44314509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539402616	chr6:44314520-44314521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551760245	chr6:44314574-44314575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569991131	chr6:44314584-44314585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34413521	chr6:44314586-44314587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537344123	chr6:44314640-44314641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555667887	chr6:44314661-44314662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573879700	chr6:44314662-44314663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371826726	chr6:44314675-44314676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535173597	chr6:44314676-44314677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34719276	chr6:44314766-44314767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79696822	chr6:44314773-44314774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553405335	chr6:44314781-44314782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
Cancer	20164920	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:3233 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44310600-44317600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:44310800-44314400	Weak transcription	Pancreas	Pancrea
3	chr6:44316200-44317400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:44317400-44317800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr6:44317400-44318600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:44317600-44318000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:44317600-44318000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:44317600-44318200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:44317600-44318200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:44317600-44318200	Enhancers	HMEC	breast
11	chr6:44317600-44318400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:44317600-44318600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:44317600-44318600	Enhancers	Liver	Liver
14	chr6:44317800-44318200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr6:44317800-44318200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:44317800-44318400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr6:44317800-44318400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr6:44317800-44318600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr6:44317800-44318600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr6:44317800-44318600	Enhancers	HepG2	liver
21	chr6:44318000-44318400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr6:44318200-44318400	Enhancers	Stomach Mucosa	stomach
23	chr6:44318200-44323400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:44318400-44318600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr6:44318400-44318600	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:44318400-44320600	Weak transcription	Stomach Mucosa	stomach
27	chr6:44318600-44320600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr6:44318600-44320800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr6:44320600-44321200	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr6:44320600-44321600	Enhancers	Stomach Mucosa	stomach
31	chr6:44320800-44321200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr6:44321000-44321200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:44321000-44321200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr6:44328600-44331600	Enhancers	Fetal Brain Male	brain
35	chr6:44329000-44330400	Enhancers	Fetal Brain Female	brain
36	chr6:44329200-44330200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:44329800-44330000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
38	chr6:44330200-44331800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:44331800-44332400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:44332600-44332800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr6:44332600-44332800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr6:44334200-44334800	Enhancers	HepG2	liver
43	chr6:44334200-44335400	Enhancers	Liver	Liver
44	chr6:44335200-44335800	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr6:44335200-44335800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:44335200-44335800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:44335400-44336000	Enhancers	Primary hematopoietic stem cells	blood
48	chr6:44335400-44340800	Weak transcription	Liver	Liver
49	chr6:44335600-44336200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:44335800-44340600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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