Variant report

Variant	nsv829741
Chromosome Location	chr3:140021063-140183294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:485)
CpG islands
(count:122)
Chromatin interactive
region (count:61)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr3:140105607-140105925	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:140094140-140094192	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:140105613-140105923	K562	blood:	n/a	n/a
7	BATF	chr3:140103201-140103454	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:140060670-140060952	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr3:140060704-140060857	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr3:140165971-140166296	GM12878	blood:	n/a	n/a
11	BCL3	chr3:140125671-140125920	GM12878	blood:	n/a	n/a
12	BCL3	chr3:140166068-140166305	GM12878	blood:	n/a	n/a
13	BCL3	chr3:140079255-140079476	GM12878	blood:	n/a	n/a
14	BCL3	chr3:140103779-140104304	GM12878	blood:	n/a	chr3:140104056-140104065 chr3:140104055-140104064
15	BHLHE40	chr3:140167031-140167061	GM12878	blood:	n/a	n/a
16	CCNT2	chr3:140165492-140165663	K562	blood:	n/a	n/a
17	CCNT2	chr3:140053551-140053720	K562	blood:	n/a	chr3:140053586-140053606
18	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
19	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
20	CEBPB	chr3:140166670-140166705	HepG2	liver:	n/a	chr3:140166681-140166692
21	CEBPB	chr3:140031394-140031698	HepG2	liver:	n/a	chr3:140031512-140031523
22	CEBPB	chr3:140031392-140031691	K562	blood:	n/a	chr3:140031512-140031523
23	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
24	CEBPB	chr3:140181509-140181811	HepG2	liver:	n/a	chr3:140181646-140181657
25	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
26	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
27	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
28	CEBPB	chr3:140181568-140181687	Hela-S3	cervix:	n/a	chr3:140181646-140181657
29	CEBPD	chr3:140052919-140053306	K562	blood:	n/a	n/a
30	CHD2	chr3:140060333-140061059	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr3:140088972-140088977	Hela-S3	cervix:	n/a	n/a
32	CTBP2	chr3:140060780-140062059	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr3:140139660-140139810	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr3:140107220-140107370	GM12878	blood:	n/a	n/a
35	CTCF	chr3:140139700-140139850	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr3:140079320-140079470	HRPEpiC	eye:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
37	CTCF	chr3:140175940-140176090	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr3:140175920-140176070	HBMEC	blood vessel:	n/a	chr3:140175924-140175933
39	CTCF	chr3:140175946-140176077	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:140079260-140079410	RPTEC	kidney:	n/a	n/a
41	CTCF	chr3:140152975-140153060	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr3:140175952-140176061	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:140152969-140153076	GM12878	blood:	n/a	n/a
44	CTCF	chr3:140079368-140079454	MCF-7	breast:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
45	CTCF	chr3:140175975-140176071	K562	blood:	n/a	n/a
46	CTCF	chr3:140128100-140128173	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:140079380-140079530	SAEC	small airway:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
48	CTCF	chr3:140079390-140079450	H1-hESC	embryonic stem cell:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
49	CTCF	chr3:140096620-140096770	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr3:140096660-140096724	NHEK	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140102647-140102697	MCF10A-Er-Src	breast:	n/a
2	chr3:140102647-140102697	HMEC	breast:	n/a
3	chr3:140071429-140071479	AG09309	skin:	n/a
4	chr3:140071429-140071479	PANC-1	pancreas:	n/a
5	chr3:140071429-140071479	Hela-S3	cervix:	n/a
6	chr3:140102647-140102697	SAEC	small airway:	n/a
7	chr3:140071429-140071479	Jurkat	blood:	n/a
8	chr3:140071429-140071479	HEK293	kidney:	embryo
9	chr3:140102647-140102697	BJ	skin:	n/a
10	chr3:140071429-140071479	GM12892	blood:	n/a
11	chr3:140071429-140071479	AG04449	skin:	fetal
12	chr3:140071429-140071479	Caco-2	colon:	n/a
13	chr3:140102647-140102697	HCM	heart:	n/a
14	chr3:140071429-140071479	BJ	skin:	n/a
15	chr3:140102647-140102697	NB4	blood:	n/a
16	chr3:140102647-140102697	PrEC	prostate:	n/a
17	chr3:140102647-140102697	PFSK-1	brain:	n/a
18	chr3:140102647-140102697	HEEpiC	esophagus:	n/a
19	chr3:140102647-140102697	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:140102647-140102697	BE2_C	brain:	n/a
21	chr3:140071429-140071479	PrEC	prostate:	n/a
22	chr3:140071429-140071479	NB4	blood:	n/a
23	chr3:140102647-140102697	Jurkat	blood:	n/a
24	chr3:140071429-140071479	HCT-116	colon:	n/a
25	chr3:140071429-140071479	HUVEC	blood vessel:	n/a
26	chr3:140102647-140102697	NHDF-neo	bronchial:	n/a
27	chr3:140102647-140102697	HCT-116	colon:	n/a
28	chr3:140071429-140071479	SK-N-SH	brain:	n/a
29	chr3:140102647-140102697	A549	lung:	n/a
30	chr3:140071429-140071479	K562	blood:	n/a
31	chr3:140071429-140071479	MCF10A-Er-Src	breast:	n/a
32	chr3:140071429-140071479	MCF-7	breast:	n/a
33	chr3:140071429-140071479	GM12891	blood:	n/a
34	chr3:140102647-140102697	CMK	blood:	n/a
35	chr3:140102647-140102697	HRE	kidney:	n/a
36	chr3:140071429-140071479	NT2-D1	testis:	n/a
37	chr3:140071429-140071479	HAEpiC	amniotic membrane:	n/a
38	chr3:140071429-140071479	LNCaP	prostate:	n/a
39	chr3:140071429-140071479	HRPEpiC	eye:	n/a
40	chr3:140102647-140102697	AG04449	skin:	fetal
41	chr3:140102647-140102697	ECC-1	luminal epithelium:	n/a
42	chr3:140102647-140102697	GM12878	blood:	n/a
43	chr3:140102647-140102697	SK-N-SH_RA	brain:	n/a
44	chr3:140102647-140102697	K562	blood:	n/a
45	chr3:140071429-140071479	U87	brain:	n/a
46	chr3:140102647-140102697	GM06990	blood:	n/a
47	chr3:140071429-140071479	AG10803	skin:	n/a
48	chr3:140071429-140071479	HEEpiC	esophagus:	n/a
49	chr3:140071429-140071479	AoSMC	blood vessel:	n/a
50	chr3:140071429-140071479	ECC-1	luminal epithelium:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:140082092..140083700-chr3:140090829..140092486,2	K562	blood:
2	chr3:140035247..140037628-chr3:140039267..140042194,2	K562	blood:
3	chr3:140173675..140176130-chr3:140184523..140186142,2	MCF-7	breast:
4	chr3:140158384..140160631-chr3:140165568..140168187,2	MCF-7	breast:
5	chr3:140087589..140090297-chr3:140098054..140099606,2	MCF-7	breast:
6	chr3:140145580..140147650-chr3:140148018..140150573,2	MCF-7	breast:
7	chr3:140160036..140161866-chr3:140164735..140166930,2	K562	blood:
8	chr3:140059548..140062315-chr3:140087730..140089988,2	MCF-7	breast:
9	chr3:140073823..140075665-chr3:140078588..140080836,2	K562	blood:
10	chr3:140111455..140114445-chr3:140122370..140124734,2	MCF-7	breast:
11	chr3:140062953..140066461-chr3:140067922..140071078,3	K562	blood:
12	chr3:140081086..140083326-chr3:140088654..140090769,2	K562	blood:
13	chr3:140068811..140071526-chr3:140072491..140074846,2	MCF-7	breast:
14	chr3:140081813..140083413-chr3:140085226..140088185,2	MCF-7	breast:
15	chr3:140161141..140164298-chr3:140170200..140174173,3	MCF-7	breast:
16	chr3:140022731..140026345-chr3:140027266..140029721,3	MCF-7	breast:
17	chr3:140058084..140060936-chr3:140070317..140072868,2	K562	blood:
18	chr3:140093026..140095347-chr3:140098280..140100023,2	K562	blood:
19	chr3:140087589..140090297-chr3:140098054..140099606,2	MCF-7	breast:
20	chr3:140049779..140051880-chr3:140060017..140062705,2	K562	blood:
21	chr3:140058099..140061175-chr3:140062263..140065784,3	MCF-7	breast:
22	chr3:140109684..140112139-chr3:140116614..140119489,2	MCF-7	breast:
23	chr3:140177139..140178947-chr3:140181576..140183907,2	K562	blood:
24	chr3:140160036..140161866-chr3:140164735..140166930,2	K562	blood:
25	chr3:140105349..140107747-chr3:140133928..140135787,2	K562	blood:
26	chr3:140078608..140080678-chr3:140081046..140083141,2	MCF-7	breast:
27	chr3:140035247..140037628-chr3:140039267..140042194,2	K562	blood:
28	chr3:140077666..140079764-chr3:140083559..140086376,4	MCF-7	breast:
29	chr3:140078397..140079800-chr3:140217706..140218666,5	MCF-7	breast:
30	chr3:140081813..140083413-chr3:140085226..140088185,2	MCF-7	breast:
31	chr3:140048554..140050507-chr3:140068162..140070278,2	MCF-7	breast:
32	chr3:140145580..140147650-chr3:140148018..140150573,2	MCF-7	breast:
33	chr3:140049779..140051880-chr3:140060017..140062705,2	K562	blood:
34	chr3:140083102..140085240-chr3:140088764..140091078,2	MCF-7	breast:
35	chr3:140022731..140026345-chr3:140027266..140029721,3	MCF-7	breast:
36	chr3:140082092..140083700-chr3:140090829..140092486,2	K562	blood:
37	chr3:140077666..140079764-chr3:140083559..140086376,4	MCF-7	breast:
38	chr3:140065591..140067586-chr3:140072017..140074131,2	K562	blood:
39	chr3:140153110..140155513-chr3:140157177..140159656,3	K562	blood:
40	chr3:140058084..140060936-chr3:140070317..140072868,2	K562	blood:
41	chr17:41380303..41382086-chr3:140048912..140050412,2	K562	blood:
42	chr3:140068811..140071526-chr3:140072491..140074846,2	MCF-7	breast:
43	chr3:140048554..140050507-chr3:140068162..140070278,2	MCF-7	breast:
44	chr3:140158384..140160631-chr3:140165568..140168187,2	MCF-7	breast:
45	chr3:140073823..140075665-chr3:140078588..140080836,2	K562	blood:
46	chr3:140078938..140079524-chr3:140218046..140218560,2	MCF-7	breast:
47	chr17:41399109..41402008-chr3:140047432..140050412,2	MCF-7	breast:
48	chr3:140059548..140062315-chr3:140087730..140089988,2	MCF-7	breast:
49	chr3:140058099..140061175-chr3:140062263..140065784,3	MCF-7	breast:
50	chr3:140078608..140080678-chr3:140081046..140083141,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMNAT3-8	chr3:140036153-140036530	expReg_chr3_10285_-
2	lnc-NMNAT3-4	chr3:140179842-140180219	ENSG00000251058.1
3	lnc-NMNAT3-3	chr3:140171295-140171507	ENSG00000249290.1
4	lnc-NMNAT3-4	chr3:140181564-140181667	ENSG00000251058.1
5	lnc-NMNAT3-3	chr3:140168352-140168618	ENSG00000249290.1
6	lnc-NMNAT3-3	chr3:140168784-140168885	ENSG00000249290.1
7	lnc-NMNAT3-3	chr3:140173499-140173595	ENSG00000249290.1
8	lnc-NMNAT3-3	chr3:140172061-140172122	ENSG00000249290.1
9	lnc-NMNAT3-3	chr3:140171295-140171507	ENSG00000249290.1
10	lnc-NMNAT3-3	chr3:140172061-140172122	ENSG00000249290.1
11	lnc-NMNAT3-9	chr3:140143916-140144150	ucscGeneNc_uc003esv_1
12	lnc-NMNAT3-3	chr3:140168784-140168885	ENSG00000249290.1
13	lnc-NMNAT3-3	chr3:140171370-140171507	ENSG00000249290.1
14	lnc-NMNAT3-3	chr3:140173499-140173595	ENSG00000249290.1
15	lnc-NMNAT3-3	chr3:140173204-140173260	ENSG00000249290.1
16	lnc-NMNAT3-3	chr3:140173118-140173260	ENSG00000249290.1
17	lnc-NMNAT3-9	chr3:140145498-140145552	ucscGeneNc_uc003esv_1
18	lnc-NMNAT3-3	chr3:140179094-140179193	ENSG00000249290.1
19	lnc-NMNAT3-3	chr3:140173499-140173573	ENSG00000249290.1
20	lnc-NMNAT3-3	chr3:140168277-140168618	ENSG00000249290.1
21	lnc-NMNAT3-9	chr3:140136721-140139968	ucscGeneNc_uc003esv_1

No data

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

Extended variants
information (count: 6576 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:6576 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368881440	chr3:140021113-140021114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373395199	chr3:140021118-140021119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150365705	chr3:140021204-140021205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564554308	chr3:140021206-140021207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559312522	chr3:140021234-140021235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531706041	chr3:140021273-140021274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552245824	chr3:140021344-140021345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550209706	chr3:140021373-140021374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568467345	chr3:140021388-140021389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7636303	chr3:140021406-140021407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs192080449	chr3:140021424-140021425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528198479	chr3:140021425-140021426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370756783	chr3:140021445-140021446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540162549	chr3:140021462-140021463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11927781	chr3:140021470-140021471	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs567741244	chr3:140021568-140021569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34648747	chr3:140021580-140021581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs16850127	chr3:140021594-140021595	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs556175543	chr3:140021658-140021659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9855259	chr3:140021664-140021665	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs76217602	chr3:140021686-140021687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553579083	chr3:140021763-140021764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572008759	chr3:140021765-140021766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545735580	chr3:140021766-140021767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564234953	chr3:140021774-140021775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531687092	chr3:140021794-140021795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184201808	chr3:140021832-140021833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562175921	chr3:140021859-140021860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113256744	chr3:140021892-140021893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188951599	chr3:140021908-140021909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566323755	chr3:140021934-140021935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149085709	chr3:140021962-140021963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552010064	chr3:140021990-140021991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367721572	chr3:140021991-140021992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538912423	chr3:140022086-140022087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74772609	chr3:140022126-140022127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555921035	chr3:140022141-140022142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs16850130	chr3:140022146-140022147	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs112136229	chr3:140022165-140022166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572401087	chr3:140022238-140022239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553544331	chr3:140022247-140022248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141597641	chr3:140022283-140022284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539255038	chr3:140022332-140022333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201713889	chr3:140022350-140022351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541533448	chr3:140022374-140022375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576272876	chr3:140022378-140022379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs193048735	chr3:140022379-140022380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117422784	chr3:140022380-140022381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145264721	chr3:140022401-140022402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77662684	chr3:140022444-140022445	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:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140018600-140021600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:140018800-140034200	Weak transcription	Fetal Brain Male	brain
3	chr3:140020800-140021600	Weak transcription	Ovary	ovary
4	chr3:140021600-140021800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:140021600-140022800	Enhancers	Ovary	ovary
6	chr3:140021800-140028800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:140022800-140026800	Weak transcription	Ovary	ovary
8	chr3:140024200-140024400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:140025000-140025400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:140025400-140025600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr3:140026400-140027400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:140026800-140027200	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr3:140026800-140029400	Enhancers	Ovary	ovary
14	chr3:140027000-140027600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:140027400-140027800	Enhancers	K562	blood
16	chr3:140027600-140027800	Enhancers	Fetal Stomach	stomach
17	chr3:140028400-140028600	Enhancers	Fetal Stomach	stomach
18	chr3:140028800-140029400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:140029400-140047200	Weak transcription	Ovary	ovary
20	chr3:140032600-140032800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr3:140033000-140033800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr3:140033800-140034000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr3:140034000-140034800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:140034200-140035200	Enhancers	Fetal Brain Male	brain
25	chr3:140034600-140035000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:140034600-140035200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr3:140034600-140035200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:140034600-140035200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:140034600-140035400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:140034600-140035400	Enhancers	Fetal Brain Female	brain
31	chr3:140034800-140035200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:140034800-140035400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr3:140035000-140035200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr3:140035000-140035600	Enhancers	Pancreas	Pancrea
35	chr3:140035000-140035600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr3:140035200-140035400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr3:140035200-140039000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:140035200-140041200	Weak transcription	Fetal Brain Male	brain
39	chr3:140035400-140036200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr3:140035600-140035800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:140035600-140036400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:140035800-140036400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:140038000-140039000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr3:140038600-140039000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:140038800-140039000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:140041200-140041400	Enhancers	Fetal Brain Male	brain
47	chr3:140041400-140042000	Weak transcription	Fetal Brain Male	brain
48	chr3:140041800-140042400	Enhancers	HSMMtube	muscle
49	chr3:140041800-140043000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:140042000-140042200	Enhancers	Fetal Brain Male	brain

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