Variant report

Variant	nsv460867
Chromosome Location	chr3:140007294-140180563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:554)
CpG islands
(count:183)
Chromatin interactive
region (count:68)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:140053022-140053236	K562	blood:	n/a	n/a
2	ATF2	chr3:140060561-140061106	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:140060548-140061178	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:140094140-140094192	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:140017435-140017740	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:140105607-140105925	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:140008950-140009240	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr3:140105613-140105923	K562	blood:	n/a	n/a
9	BATF	chr3:140103201-140103454	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:140060670-140060952	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr3:140060704-140060857	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr3:140166068-140166305	GM12878	blood:	n/a	n/a
13	BCL3	chr3:140125671-140125920	GM12878	blood:	n/a	n/a
14	BCL3	chr3:140103779-140104304	GM12878	blood:	n/a	chr3:140104056-140104065 chr3:140104055-140104064
15	BCL3	chr3:140079255-140079476	GM12878	blood:	n/a	n/a
16	BCL3	chr3:140165971-140166296	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:140167031-140167061	GM12878	blood:	n/a	n/a
18	CCNT2	chr3:140053551-140053720	K562	blood:	n/a	chr3:140053586-140053606
19	CCNT2	chr3:140165492-140165663	K562	blood:	n/a	n/a
20	CEBPB	chr3:140095355-140095714	HepG2	liver:	n/a	chr3:140095529-140095538 chr3:140095527-140095540 chr3:140095529-140095538 chr3:140095529-140095538 chr3:140095527-140095538 chr3:140095529-140095538 chr3:140095528-140095539
21	CEBPB	chr3:140095347-140095719	A549	lung:	n/a	chr3:140095529-140095538 chr3:140095527-140095540 chr3:140095529-140095538 chr3:140095529-140095538 chr3:140095527-140095538 chr3:140095529-140095538 chr3:140095528-140095539
22	CEBPB	chr3:140095354-140095699	K562	blood:	n/a	chr3:140095529-140095538 chr3:140095527-140095540 chr3:140095529-140095538 chr3:140095529-140095538 chr3:140095527-140095538 chr3:140095529-140095538 chr3:140095528-140095539
23	CEBPB	chr3:140031392-140031691	K562	blood:	n/a	chr3:140031512-140031523
24	CEBPB	chr3:140095400-140095690	Hela-S3	cervix:	n/a	chr3:140095529-140095538 chr3:140095527-140095540 chr3:140095529-140095538 chr3:140095529-140095538 chr3:140095527-140095538 chr3:140095529-140095538 chr3:140095528-140095539
25	CEBPB	chr3:140031394-140031698	HepG2	liver:	n/a	chr3:140031512-140031523
26	CEBPB	chr3:140095377-140095687	H1-hESC	embryonic stem cell:	n/a	chr3:140095529-140095538 chr3:140095527-140095540 chr3:140095529-140095538 chr3:140095529-140095538 chr3:140095527-140095538 chr3:140095529-140095538 chr3:140095528-140095539
27	CEBPB	chr3:140166670-140166705	HepG2	liver:	n/a	chr3:140166681-140166692
28	CEBPB	chr3:140095349-140095715	IMR90	lung:	n/a	chr3:140095529-140095538 chr3:140095527-140095540 chr3:140095529-140095538 chr3:140095529-140095538 chr3:140095527-140095538 chr3:140095529-140095538 chr3:140095528-140095539
29	CEBPB	chr3:140014416-140014423	HepG2	liver:	n/a	n/a
30	CEBPD	chr3:140052919-140053306	K562	blood:	n/a	n/a
31	CHD2	chr3:140088972-140088977	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr3:140060333-140061059	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr3:140060780-140062059	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr3:140017356-140017994	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr3:140096644-140096724	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:140175841-140176127	H1-hESC	embryonic stem cell:	n/a	chr3:140175924-140175933 chr3:140175913-140175934
37	CTCF	chr3:140128174-140128177	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:140139780-140139930	HMF	breast:	n/a	n/a
39	CTCF	chr3:140096580-140096730	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr3:140079287-140079591	MCF-7	breast:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
41	CTCF	chr3:140079332-140079478	K562	blood:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
42	CTCF	chr3:140079305-140079449	HepG2	liver:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
43	CTCF	chr3:140096672-140096740	GM19238	blood:	n/a	n/a
44	CTCF	chr3:140139620-140139770	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr3:140175975-140176071	K562	blood:	n/a	n/a
46	CTCF	chr3:140015940-140016090	HFF	foreskin:	n/a	n/a
47	CTCF	chr3:140128136-140128173	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:140079358-140079459	GM19239	blood:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
49	CTCF	chr3:140139660-140139810	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr3:140015856-140015914	NHEK	skin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140071429-140071479	AG04449	skin:	fetal
2	chr3:140071429-140071479	GM12878	blood:	n/a
3	chr3:140017225-140017275	SK-N-SH	brain:	n/a
4	chr3:140102647-140102697	AoSMC	blood vessel:	n/a
5	chr3:140017225-140017275	H1-hESC	embryonic stem cell:	embryo
6	chr3:140017225-140017275	HMEC	breast:	n/a
7	chr3:140017225-140017275	AG09319	gingival:	n/a
8	chr3:140017225-140017275	K562	blood:	n/a
9	chr3:140102647-140102697	MCF-7	breast:	n/a
10	chr3:140017225-140017275	PFSK-1	brain:	n/a
11	chr3:140102647-140102697	ovcar-3	ovarian:	n/a
12	chr3:140102647-140102697	IMR90	lung:	fetal
13	chr3:140017225-140017275	MCF10A-Er-Src	breast:	n/a
14	chr3:140071429-140071479	NB4	blood:	n/a
15	chr3:140071429-140071479	HCF	heart:	n/a
16	chr3:140071429-140071479	PFSK-1	brain:	n/a
17	chr3:140071429-140071479	SKMC	muscle:	n/a
18	chr3:140102647-140102697	NHBE	bronchial:	n/a
19	chr3:140102647-140102697	MCF10A-Er-Src	breast:	n/a
20	chr3:140071429-140071479	HCT-116	colon:	n/a
21	chr3:140102647-140102697	HCT-116	colon:	n/a
22	chr3:140017225-140017275	GM12878	blood:	n/a
23	chr3:140071429-140071479	GM19239	blood:	n/a
24	chr3:140102647-140102697	AG04449	skin:	fetal
25	chr3:140017225-140017275	Jurkat	blood:	n/a
26	chr3:140102647-140102697	HCM	heart:	n/a
27	chr3:140102647-140102697	ECC-1	luminal epithelium:	n/a
28	chr3:140102647-140102697	HNPCEpiC	eye:	n/a
29	chr3:140102647-140102697	LNCaP	prostate:	n/a
30	chr3:140071429-140071479	AG09319	gingival:	n/a
31	chr3:140102647-140102697	SK-N-MC	brain:	n/a
32	chr3:140071429-140071479	SK-N-SH	brain:	n/a
33	chr3:140017225-140017275	HNPCEpiC	eye:	n/a
34	chr3:140102647-140102697	HepG2	liver:	n/a
35	chr3:140071429-140071479	HRPEpiC	eye:	n/a
36	chr3:140017225-140017275	RPTEC	kidney:	n/a
37	chr3:140071429-140071479	A549	lung:	n/a
38	chr3:140017225-140017275	BJ	skin:	n/a
39	chr3:140102647-140102697	NT2-D1	testis:	n/a
40	chr3:140102647-140102697	SK-N-SH	brain:	n/a
41	chr3:140102647-140102697	U87	brain:	n/a
42	chr3:140102647-140102697	HUVEC	blood vessel:	n/a
43	chr3:140102647-140102697	CMK	blood:	n/a
44	chr3:140071429-140071479	AG09309	skin:	n/a
45	chr3:140102647-140102697	HRE	kidney:	n/a
46	chr3:140071429-140071479	HIPEpiC	eye:	n/a
47	chr3:140017225-140017275	HRE	kidney:	n/a
48	chr3:140017225-140017275	Hepatocyte	liver:	n/a
49	chr3:140071429-140071479	HUVEC	blood vessel:	n/a
50	chr3:140017225-140017275	HCT-116	colon:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:41380303..41382086-chr3:140048912..140050412,2	K562	blood:
2	chr3:140058084..140060936-chr3:140070317..140072868,2	K562	blood:
3	chr3:140059548..140062315-chr3:140087730..140089988,2	MCF-7	breast:
4	chr3:140145580..140147650-chr3:140148018..140150573,2	MCF-7	breast:
5	chr3:140173675..140176130-chr3:140184523..140186142,2	MCF-7	breast:
6	chr3:140109684..140112139-chr3:140116614..140119489,2	MCF-7	breast:
7	chr3:140109684..140112139-chr3:140116614..140119489,2	MCF-7	breast:
8	chr3:140081813..140083413-chr3:140085226..140088185,2	MCF-7	breast:
9	chr3:140073823..140075665-chr3:140078588..140080836,2	K562	blood:
10	chr3:140081813..140083413-chr3:140085226..140088185,2	MCF-7	breast:
11	chr3:140158384..140160631-chr3:140165568..140168187,2	MCF-7	breast:
12	chr3:140177139..140178947-chr3:140181576..140183907,2	K562	blood:
13	chr3:140049779..140051880-chr3:140060017..140062705,2	K562	blood:
14	chr3:140161141..140164298-chr3:140170200..140174173,3	MCF-7	breast:
15	chr3:140078397..140079800-chr3:140217706..140218666,5	MCF-7	breast:
16	chr3:140081086..140083326-chr3:140088654..140090769,2	K562	blood:
17	chr3:140073823..140075665-chr3:140078588..140080836,2	K562	blood:
18	chr3:140058084..140060936-chr3:140070317..140072868,2	K562	blood:
19	chr3:140035247..140037628-chr3:140039267..140042194,2	K562	blood:
20	chr3:140009863..140012696-chr3:140014385..140017496,3	K562	blood:
21	chr3:140082092..140083700-chr3:140090829..140092486,2	K562	blood:
22	chr3:140058099..140061175-chr3:140062263..140065784,3	MCF-7	breast:
23	chr3:140111455..140114445-chr3:140122370..140124734,2	MCF-7	breast:
24	chr3:140077666..140079764-chr3:140083559..140086376,4	MCF-7	breast:
25	chr3:140049779..140051880-chr3:140060017..140062705,2	K562	blood:
26	chr3:140065591..140067586-chr3:140072017..140074131,2	K562	blood:
27	chr3:140058099..140061175-chr3:140062263..140065784,3	MCF-7	breast:
28	chr3:140059548..140062315-chr3:140087730..140089988,2	MCF-7	breast:
29	chr3:140068811..140071526-chr3:140072491..140074846,2	MCF-7	breast:
30	chr3:140078608..140080678-chr3:140081046..140083141,2	MCF-7	breast:
31	chr3:140010384..140011884-chr3:140017839..140020263,2	MCF-7	breast:
32	chr17:41399109..41402008-chr3:140047432..140050412,2	MCF-7	breast:
33	chr3:140068811..140071526-chr3:140072491..140074846,2	MCF-7	breast:
34	chr3:140065591..140067586-chr3:140072017..140074131,2	K562	blood:
35	chr3:140145580..140147650-chr3:140148018..140150573,2	MCF-7	breast:
36	chr3:140022731..140026345-chr3:140027266..140029721,3	MCF-7	breast:
37	chr3:140096590..140099574-chr3:140099849..140101936,2	K562	blood:
38	chr3:140010384..140011884-chr3:140017839..140020263,2	MCF-7	breast:
39	chr3:140009863..140011937-chr3:140014588..140017496,2	K562	blood:
40	chr3:140035247..140037628-chr3:140039267..140042194,2	K562	blood:
41	chr3:140004703..140007058-chr3:140009329..140011674,2	MCF-7	breast:
42	chr3:140062953..140066461-chr3:140067922..140071078,3	K562	blood:
43	chr3:140062953..140066461-chr3:140067922..140071078,3	K562	blood:
44	chr3:140160036..140161866-chr3:140164735..140166930,2	K562	blood:
45	chr3:140078938..140079524-chr3:140218046..140218560,2	MCF-7	breast:
46	chr3:140153110..140155513-chr3:140157177..140159656,3	K562	blood:
47	chr3:140009863..140012696-chr3:140014385..140017496,3	K562	blood:
48	chr3:140083102..140085240-chr3:140088764..140091078,2	MCF-7	breast:
49	chr3:140160036..140161866-chr3:140164735..140166930,2	K562	blood:
50	chr3:140081086..140083326-chr3:140088654..140090769,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMNAT3-3	chr3:140168784-140168885	ENSG00000249290.1
2	lnc-NMNAT3-4	chr3:140179842-140180219	ENSG00000251058.1
3	lnc-NMNAT3-3	chr3:140171295-140171507	ENSG00000249290.1
4	lnc-NMNAT3-3	chr3:140171295-140171507	ENSG00000249290.1
5	lnc-NMNAT3-3	chr3:140173499-140173573	ENSG00000249290.1
6	lnc-NMNAT3-3	chr3:140168277-140168618	ENSG00000249290.1
7	lnc-NMNAT3-3	chr3:140179094-140179193	ENSG00000249290.1
8	lnc-NMNAT3-3	chr3:140173118-140173260	ENSG00000249290.1
9	lnc-NMNAT3-3	chr3:140168784-140168885	ENSG00000249290.1
10	lnc-NMNAT3-3	chr3:140173204-140173260	ENSG00000249290.1
11	lnc-NMNAT3-9	chr3:140145498-140145552	ucscGeneNc_uc003esv_1
12	lnc-NMNAT3-3	chr3:140168352-140168618	ENSG00000249290.1
13	lnc-NMNAT3-3	chr3:140173499-140173595	ENSG00000249290.1
14	lnc-NMNAT3-3	chr3:140172061-140172122	ENSG00000249290.1
15	lnc-NMNAT3-3	chr3:140171370-140171507	ENSG00000249290.1
16	lnc-NMNAT3-8	chr3:140036153-140036530	expReg_chr3_10285_-
17	lnc-NMNAT3-9	chr3:140143916-140144150	ucscGeneNc_uc003esv_1
18	lnc-NMNAT3-3	chr3:140173499-140173595	ENSG00000249290.1
19	lnc-NMNAT3-3	chr3:140172061-140172122	ENSG00000249290.1
20	lnc-NMNAT3-9	chr3:140136721-140139968	ucscGeneNc_uc003esv_1

No data

Variant related genes	Relation type
ENSG00000249290	TF binding region
ENSG00000263959	TF binding region
ENSG00000249290	CpG island
ENSG00000263959	CpG island
ENSG00000251058	chromatin interactions
ENSG00000249290	chromatin interactions
ENSG00000236383	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 6963 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:6963 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1479869	chr3:140007294-140007295	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558126281	chr3:140007298-140007299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566738722	chr3:140007317-140007318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147772259	chr3:140007352-140007353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544196760	chr3:140007367-140007368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138993550	chr3:140007418-140007419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555231339	chr3:140007427-140007428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62268001	chr3:140007463-140007464	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541609882	chr3:140007480-140007481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149862260	chr3:140007502-140007503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113452545	chr3:140007507-140007508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527457073	chr3:140007517-140007518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189796970	chr3:140007577-140007578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs967861	chr3:140007588-140007589	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531517703	chr3:140007616-140007617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531094378	chr3:140007643-140007644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182413025	chr3:140007684-140007685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568144411	chr3:140007722-140007723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535550821	chr3:140007737-140007738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369358187	chr3:140007784-140007785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34628786	chr3:140007792-140007793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79913422	chr3:140007794-140007795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs397876866	chr3:140007796-140007797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566172714	chr3:140007841-140007842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539598057	chr3:140007844-140007845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558350226	chr3:140007845-140007846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576772527	chr3:140007868-140007869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs922566	chr3:140007919-140007920	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560220255	chr3:140007937-140007938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145855391	chr3:140007939-140007940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73228924	chr3:140008011-140008012	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs115855932	chr3:140008019-140008020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188110694	chr3:140008031-140008032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148990278	chr3:140008036-140008037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145814392	chr3:140008043-140008044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147405244	chr3:140008170-140008171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372924382	chr3:140008171-140008172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144918835	chr3:140008175-140008176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531482157	chr3:140008176-140008177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386666396	chr3:140008178-140008179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs60116021	chr3:140008179-140008180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1466461	chr3:140008180-140008181	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs114806243	chr3:140008212-140008213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537784028	chr3:140008235-140008236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146598605	chr3:140008282-140008283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547082723	chr3:140008342-140008343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114210864	chr3:140008388-140008389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566011415	chr3:140008405-140008406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539935843	chr3:140008417-140008418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551664447	chr3:140008506-140008507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Ependymoma	20639864	CNVD
Dyslexia	22102821	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Cancer	20164919	CNVD
Blepharophimosis syndrome	18726931	CNVD
Blepharophimosis syndrome	18642388	CNVD
Disorders of sex development	22290220	CNVD
Non-syndromic sensorineural hearing loss	19491894	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:849 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139995400-140007400	Weak transcription	HSMMtube	muscle
2	chr3:139999600-140015600	Weak transcription	Pancreas	Pancrea
3	chr3:140003600-140009400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:140003800-140007400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr3:140004400-140009200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:140004400-140015600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:140004600-140008800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr3:140004800-140008800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr3:140004800-140009200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr3:140004800-140015600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr3:140005000-140007800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr3:140006600-140010600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:140006800-140013400	Enhancers	HMEC	breast
14	chr3:140007000-140010600	Enhancers	NHEK	skin
15	chr3:140007000-140012400	Enhancers	NHDF-Ad	bronchial
16	chr3:140007200-140007600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr3:140007200-140008000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:140007200-140008000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:140007200-140008000	Enhancers	NH-A	brain
20	chr3:140007200-140008600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:140007200-140010000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:140007200-140010400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:140007200-140012400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr3:140007400-140007800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr3:140007400-140007800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr3:140007400-140007800	Enhancers	HSMMtube	muscle
27	chr3:140007400-140007800	Enhancers	NHLF	lung
28	chr3:140007400-140008000	Enhancers	HSMM	muscle
29	chr3:140007600-140008000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:140007600-140008800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr3:140007800-140008000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr3:140007800-140008000	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr3:140007800-140008000	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr3:140007800-140008800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr3:140007800-140009200	Enhancers	Osteobl	bone
36	chr3:140007800-140010600	Weak transcription	HSMMtube	muscle
37	chr3:140007800-140010800	Weak transcription	NHLF	lung
38	chr3:140008000-140010000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr3:140008000-140010200	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr3:140008000-140010200	Weak transcription	NH-A	brain
41	chr3:140008000-140010400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:140008000-140010400	Weak transcription	HSMM	muscle
43	chr3:140008000-140010600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr3:140008000-140010600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr3:140008000-140010800	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr3:140008600-140010800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr3:140008800-140009000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr3:140008800-140009200	Enhancers	Placenta Amnion	Placenta Amnion
49	chr3:140008800-140009400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr3:140008800-140009400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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