Variant report

Variant	nsv536731
Chromosome Location	chr3:140017168-140186984
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:543)
CpG islands
(count:185)
Chromatin interactive
region (count:67)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr3:140060548-140061178	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:140060561-140061106	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	chr3:140105613-140105923	K562	blood:	n/a	n/a
6	BACH1	chr3:140105607-140105925	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:140017435-140017740	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:140103201-140103454	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:140060704-140060857	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr3:140060670-140060952	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr3:140079255-140079476	GM12878	blood:	n/a	n/a
12	BCL3	chr3:140103779-140104304	GM12878	blood:	n/a	chr3:140104056-140104065 chr3:140104055-140104064
13	BCL3	chr3:140165971-140166296	GM12878	blood:	n/a	n/a
14	BCL3	chr3:140125671-140125920	GM12878	blood:	n/a	n/a
15	BCL3	chr3:140166068-140166305	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:140185894-140186269	K562	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	chr3:140186061-140186261	A549	lung:	n/a	n/a
21	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
22	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
23	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
24	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
25	CEBPB	chr3:140181509-140181811	HepG2	liver:	n/a	chr3:140181646-140181657
26	CEBPB	chr3:140181568-140181687	Hela-S3	cervix:	n/a	chr3:140181646-140181657
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	chr3:140166670-140166705	HepG2	liver:	n/a	chr3:140166681-140166692
29	CEBPB	chr3:140031394-140031698	HepG2	liver:	n/a	chr3:140031512-140031523
30	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
31	CEBPB	chr3:140031392-140031691	K562	blood:	n/a	chr3:140031512-140031523
32	CEBPD	chr3:140052919-140053306	K562	blood:	n/a	n/a
33	CHD2	chr3:140088972-140088977	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr3:140060333-140061059	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTBP2	chr3:140017356-140017994	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr3:140060780-140062059	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:140096620-140096770	HRE	kidney:	n/a	n/a
38	CTCF	chr3:140107220-140107370	GM12878	blood:	n/a	n/a
39	CTCF	chr3:140152994-140153054	GM19238	blood:	n/a	n/a
40	CTCF	chr3:140160120-140160270	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr3:140107220-140107370	RPTEC	kidney:	n/a	n/a
42	CTCF	chr3:140079340-140079490	HVMF	connective:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
43	CTCF	chr3:140079307-140079512	MCF-7	breast:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
44	CTCF	chr3:140020640-140020790	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:140079366-140079467	MCF-7	breast:	n/a	chr3:140079404-140079422 chr3:140079406-140079427 chr3:140079405-140079421
46	CTCF	chr3:140096560-140096710	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr3:140128100-140128173	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:140096565-140096804	GM12878	blood:	n/a	n/a
49	CTCF	chr3:140156200-140156350	GM12868	blood:	n/a	n/a
50	CTCF	chr3:140096600-140096750	HMF	breast:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140017225-140017275	LNCaP	prostate:	n/a
2	chr3:140102647-140102697	AG04449	skin:	fetal
3	chr3:140017225-140017275	LNCaP	prostate:	n/a
4	chr3:140102647-140102697	AG04449	skin:	fetal
5	chr3:140102647-140102697	PANC-1	pancreas:	n/a
6	chr3:140102647-140102697	HIPEpiC	eye:	n/a
7	chr3:140017225-140017275	MCF10A-Er-Src	breast:	n/a
8	chr3:140102647-140102697	NB4	blood:	n/a
9	chr3:140017225-140017275	BE2_C	brain:	n/a
10	chr3:140017225-140017275	MCF-7	breast:	n/a
11	chr3:140071429-140071479	NB4	blood:	n/a
12	chr3:140102647-140102697	GM12891	blood:	n/a
13	chr3:140102647-140102697	U87	brain:	n/a
14	chr3:140017225-140017275	U87	brain:	n/a
15	chr3:140071429-140071479	GM12892	blood:	n/a
16	chr3:140071429-140071479	HCM	heart:	n/a
17	chr3:140017225-140017275	HL-60	blood:	n/a
18	chr3:140071429-140071479	PrEC	prostate:	n/a
19	chr3:140017225-140017275	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:140102647-140102697	HRPEpiC	eye:	n/a
21	chr3:140017225-140017275	HRCEpiC	kidney:	n/a
22	chr3:140017225-140017275	A549	lung:	n/a
23	chr3:140017225-140017275	GM06990	blood:	n/a
24	chr3:140017225-140017275	HRE	kidney:	n/a
25	chr3:140102647-140102697	NHBE	bronchial:	n/a
26	chr3:140071429-140071479	NH-A	brain:	n/a
27	chr3:140071429-140071479	HepG2	liver:	n/a
28	chr3:140102647-140102697	SK-N-SH	brain:	n/a
29	chr3:140102647-140102697	CMK	blood:	n/a
30	chr3:140017225-140017275	HCT-116	colon:	n/a
31	chr3:140017225-140017275	PANC-1	pancreas:	n/a
32	chr3:140017225-140017275	ovcar-3	ovarian:	n/a
33	chr3:140102647-140102697	HCPEpiC	choroid plexus:	n/a
34	chr3:140017225-140017275	SKMC	muscle:	n/a
35	chr3:140102647-140102697	HAEpiC	amniotic membrane:	n/a
36	chr3:140071429-140071479	IMR90	lung:	fetal
37	chr3:140071429-140071479	HEK293	kidney:	embryo
38	chr3:140017225-140017275	IMR90	lung:	fetal
39	chr3:140102647-140102697	SK-N-SH_RA	brain:	n/a
40	chr3:140102647-140102697	HMEC	breast:	n/a
41	chr3:140102647-140102697	BE2_C	brain:	n/a
42	chr3:140017225-140017275	PFSK-1	brain:	n/a
43	chr3:140102647-140102697	MCF10A-Er-Src	breast:	n/a
44	chr3:140017225-140017275	Hela-S3	cervix:	n/a
45	chr3:140071429-140071479	HAEpiC	amniotic membrane:	n/a
46	chr3:140102647-140102697	HepG2	liver:	n/a
47	chr3:140071429-140071479	HRCEpiC	kidney:	n/a
48	chr3:140071429-140071479	Hepatocyte	liver:	n/a
49	chr3:140017225-140017275	HCF	heart:	n/a
50	chr3:140017225-140017275	HepG2	liver:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:140049779..140051880-chr3:140060017..140062705,2	K562	blood:
2	chr3:140022731..140026345-chr3:140027266..140029721,3	MCF-7	breast:
3	chr3:140081813..140083413-chr3:140085226..140088185,2	MCF-7	breast:
4	chr3:140105349..140107747-chr3:140133928..140135787,2	K562	blood:
5	chr3:140062953..140066461-chr3:140067922..140071078,3	K562	blood:
6	chr3:140065591..140067586-chr3:140072017..140074131,2	K562	blood:
7	chr3:140022731..140026345-chr3:140027266..140029721,3	MCF-7	breast:
8	chr3:140093026..140095347-chr3:140098280..140100023,2	K562	blood:
9	chr3:140111455..140114445-chr3:140122370..140124734,2	MCF-7	breast:
10	chr3:140077666..140079764-chr3:140083559..140086376,4	MCF-7	breast:
11	chr3:140158384..140160631-chr3:140165568..140168187,2	MCF-7	breast:
12	chr3:140082092..140083700-chr3:140090829..140092486,2	K562	blood:
13	chr3:140073823..140075665-chr3:140078588..140080836,2	K562	blood:
14	chr3:140083102..140085240-chr3:140088764..140091078,2	MCF-7	breast:
15	chr3:140177139..140178947-chr3:140181576..140183907,2	K562	blood:
16	chr3:140160036..140161866-chr3:140164735..140166930,2	K562	blood:
17	chr3:140081086..140083326-chr3:140088654..140090769,2	K562	blood:
18	chr3:140109684..140112139-chr3:140116614..140119489,2	MCF-7	breast:
19	chr3:140068811..140071526-chr3:140072491..140074846,2	MCF-7	breast:
20	chr3:140111455..140114445-chr3:140122370..140124734,2	MCF-7	breast:
21	chr3:140078938..140079524-chr3:140218046..140218560,2	MCF-7	breast:
22	chr3:140105349..140107747-chr3:140133928..140135787,2	K562	blood:
23	chr3:140082092..140083700-chr3:140090829..140092486,2	K562	blood:
24	chr3:140048554..140050507-chr3:140068162..140070278,2	MCF-7	breast:
25	chr3:140058099..140061175-chr3:140062263..140065784,3	MCF-7	breast:
26	chr3:140153110..140155513-chr3:140157177..140159656,3	K562	blood:
27	chr3:140058084..140060936-chr3:140070317..140072868,2	K562	blood:
28	chr3:140145580..140147650-chr3:140148018..140150573,2	MCF-7	breast:
29	chr3:140062953..140066461-chr3:140067922..140071078,3	K562	blood:
30	chr3:140077666..140079764-chr3:140083559..140086376,4	MCF-7	breast:
31	chr17:41380303..41382086-chr3:140048912..140050412,2	K562	blood:
32	chr3:140078608..140080678-chr3:140081046..140083141,2	MCF-7	breast:
33	chr3:140160036..140161866-chr3:140164735..140166930,2	K562	blood:
34	chr3:140073823..140075665-chr3:140078588..140080836,2	K562	blood:
35	chr3:140185147..140188078-chr3:140189944..140194087,5	MCF-7	breast:
36	chr3:140035247..140037628-chr3:140039267..140042194,2	K562	blood:
37	chr3:140058084..140060936-chr3:140070317..140072868,2	K562	blood:
38	chr3:140078608..140080678-chr3:140081046..140083141,2	MCF-7	breast:
39	chr3:140081086..140083326-chr3:140088654..140090769,2	K562	blood:
40	chr3:140173675..140176130-chr3:140184523..140186142,2	MCF-7	breast:
41	chr3:140087589..140090297-chr3:140098054..140099606,2	MCF-7	breast:
42	chr3:140109684..140112139-chr3:140116614..140119489,2	MCF-7	breast:
43	chr3:140153110..140155513-chr3:140157177..140159656,3	K562	blood:
44	chr3:140087589..140090297-chr3:140098054..140099606,2	MCF-7	breast:
45	chr17:41399109..41402008-chr3:140047432..140050412,2	MCF-7	breast:
46	chr3:140081813..140083413-chr3:140085226..140088185,2	MCF-7	breast:
47	chr3:140058099..140061175-chr3:140062263..140065784,3	MCF-7	breast:
48	chr3:140173675..140176130-chr3:140184523..140186142,2	MCF-7	breast:
49	chr3:140096590..140099574-chr3:140099849..140101936,2	K562	blood:
50	chr3:140083102..140085240-chr3:140088764..140091078,2	MCF-7	breast:

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

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

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
ENSG00000236383	chromatin interactions
ENSG00000251058	chromatin interactions
SRPR	miRNA target sites
BCL2L11	miRNA target sites

Extended variants
information (count: 6861 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:6861 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527719830	chr3:140017181-140017182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370929556	chr3:140017212-140017213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545426839	chr3:140017225-140017226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563744000	chr3:140017246-140017247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575665896	chr3:140017255-140017256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547649674	chr3:140017312-140017313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543191156	chr3:140017358-140017359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141403711	chr3:140017368-140017369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528777326	chr3:140017399-140017400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373849592	chr3:140017416-140017417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546929341	chr3:140017433-140017434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530024762	chr3:140017452-140017453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565245854	chr3:140017459-140017460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532720397	chr3:140017463-140017464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550981946	chr3:140017486-140017487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4142785	chr3:140017571-140017572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77958616	chr3:140017680-140017681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114085670	chr3:140017684-140017685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567390893	chr3:140017705-140017706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143562617	chr3:140017706-140017707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148021899	chr3:140017723-140017724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569885121	chr3:140017762-140017763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538690016	chr3:140017833-140017834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530909984	chr3:140017870-140017871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs578017955	chr3:140017917-140017918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141688790	chr3:140017979-140017980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150534514	chr3:140018006-140018007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554255081	chr3:140018085-140018086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs12633096	chr3:140018129-140018130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552020092	chr3:140018150-140018151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185846022	chr3:140018168-140018169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544324823	chr3:140018197-140018198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542802150	chr3:140018247-140018248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76105388	chr3:140018259-140018260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138007122	chr3:140018280-140018281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138415570	chr3:140018281-140018282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540429552	chr3:140018291-140018292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113107652	chr3:140018304-140018305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375024415	chr3:140018334-140018335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190562971	chr3:140018335-140018336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149601952	chr3:140018343-140018344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113314600	chr3:140018344-140018345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1383021	chr3:140018368-140018369	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs577514389	chr3:140018413-140018414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548765321	chr3:140018468-140018469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567360648	chr3:140018470-140018471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528270276	chr3:140018478-140018479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370978049	chr3:140018481-140018482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9858663	chr3:140018489-140018490	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs183202556	chr3:140018501-140018502	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:789 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140009800-140017800	Weak transcription	Right Atrium	heart
2	chr3:140012200-140018600	Weak transcription	HSMMtube	muscle
3	chr3:140012400-140018000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:140015000-140019200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:140015200-140020600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:140015400-140019000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr3:140015600-140019000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:140015600-140019400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:140015600-140019400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr3:140015600-140020000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr3:140016200-140017200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr3:140016200-140017400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:140016400-140017600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr3:140016600-140018600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:140017000-140017400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:140017000-140017400	Weak transcription	Ovary	ovary
17	chr3:140017200-140019000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr3:140017400-140017600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:140017400-140018200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr3:140017400-140018800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr3:140017400-140020000	Enhancers	Ovary	ovary
22	chr3:140017600-140017800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:140017600-140018400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr3:140017800-140018000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:140017800-140018000	Enhancers	Right Atrium	heart
26	chr3:140018000-140018800	Enhancers	Fetal Brain Male	brain
27	chr3:140018200-140019800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:140018400-140019000	Enhancers	Fetal Brain Female	brain
29	chr3:140018600-140019200	Enhancers	HSMMtube	muscle
30	chr3:140018600-140019400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:140018600-140021600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:140018800-140034200	Weak transcription	Fetal Brain Male	brain
33	chr3:140019000-140019400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr3:140019800-140020000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr3:140020000-140020600	Weak transcription	Ovary	ovary
36	chr3:140020600-140020800	Enhancers	Ovary	ovary
37	chr3:140020800-140021600	Weak transcription	Ovary	ovary
38	chr3:140021600-140021800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:140021600-140022800	Enhancers	Ovary	ovary
40	chr3:140021800-140028800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:140022800-140026800	Weak transcription	Ovary	ovary
42	chr3:140024200-140024400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:140025000-140025400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr3:140025400-140025600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr3:140026400-140027400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:140026800-140027200	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr3:140026800-140029400	Enhancers	Ovary	ovary
48	chr3:140027000-140027600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:140027400-140027800	Enhancers	K562	blood
50	chr3:140027600-140027800	Enhancers	Fetal Stomach	stomach

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