Variant report

Variant	nsv536533
Chromosome Location	chr3:34149575-34437701
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1460)
CpG islands
(count:244)
Chromatin interactive
region (count:67)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1460 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:34403250-34403806	GM12878	blood:	n/a	n/a
2	ATF2	chr3:34403255-34403813	GM12878	blood:	n/a	n/a
3	ATF2	chr3:34303410-34303948	GM12878	blood:	n/a	n/a
4	ATF2	chr3:34241982-34242432	GM12878	blood:	n/a	n/a
5	ATF2	chr3:34303467-34303985	GM12878	blood:	n/a	n/a
6	ATF2	chr3:34149051-34149663	GM12878	blood:	n/a	n/a
7	ATF3	chr3:34326480-34326757	K562	blood:	n/a	n/a
8	ATF3	chr3:34326453-34326813	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr3:34326461-34326801	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr3:34326533-34326735	GM12878	blood:	n/a	n/a
11	BACH1	chr3:34206927-34206938	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr3:34219742-34220166	GM12878	blood:	n/a	chr3:34219968-34219979 chr3:34220049-34220058
13	BATF	chr3:34149253-34149592	GM12878	blood:	n/a	n/a
14	BATF	chr3:34403397-34403777	GM12878	blood:	n/a	n/a
15	BATF	chr3:34365038-34365416	GM12878	blood:	n/a	n/a
16	BATF	chr3:34192469-34192865	GM12878	blood:	n/a	chr3:34192682-34192692 chr3:34192681-34192692
17	BATF	chr3:34405806-34406223	GM12878	blood:	n/a	chr3:34405981-34405992
18	BATF	chr3:34192498-34192837	GM12878	blood:	n/a	chr3:34192682-34192692 chr3:34192681-34192692
19	BATF	chr3:34403394-34403840	GM12878	blood:	n/a	n/a
20	BATF	chr3:34365115-34365321	GM12878	blood:	n/a	n/a
21	BATF	chr3:34242122-34242396	GM12878	blood:	n/a	n/a
22	BATF	chr3:34399037-34399335	GM12878	blood:	n/a	chr3:34399205-34399216
23	BCL11A	chr3:34192502-34192826	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:34364988-34365281	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:34289893-34290172	GM12878	blood:	n/a	chr3:34290071-34290080
26	BCL11A	chr3:34403308-34403809	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:34403401-34403766	GM12878	blood:	n/a	n/a
28	BCL3	chr3:34303485-34303869	GM12878	blood:	n/a	chr3:34303488-34303497
29	BCL3	chr3:34424419-34424686	GM12878	blood:	n/a	n/a
30	BCLAF1	chr3:34241952-34242458	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:34403276-34403876	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:34403335-34403847	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:34219753-34219767	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:34326466-34326817	K562	blood:	n/a	n/a
35	BHLHE40	chr3:34258266-34258834	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:34364965-34365446	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:34151376-34151761	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:34242129-34242387	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:34303292-34304065	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:34406128-34406159	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:34304617-34304729	GM12878	blood:	n/a	n/a
42	BHLHE40	chr3:34403373-34403856	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:34284758-34284957	K562	blood:	n/a	chr3:34284872-34284881 chr3:34284866-34284887 chr3:34284870-34284883 chr3:34284873-34284882
44	BHLHE40	chr3:34303290-34303520	K562	blood:	n/a	n/a
45	BRCA1	chr3:34188847-34188852	GM12878	blood:	n/a	n/a
46	BRCA1	chr3:34196963-34197124	GM12878	blood:	n/a	n/a
47	CCNT2	chr3:34186444-34186527	K562	blood:	n/a	n/a
48	CEBPB	chr3:34296765-34297003	IMR90	lung:	n/a	chr3:34296846-34296857 chr3:34296846-34296859
49	CEBPB	chr3:34260239-34260515	HepG2	liver:	n/a	chr3:34260363-34260374
50	CEBPB	chr3:34152517-34152788	Hela-S3	cervix:	n/a	chr3:34152664-34152675

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:34298905-34298955	NHBE	bronchial:	n/a
2	chr3:34298905-34298955	NB4	blood:	n/a
3	chr3:34187750-34187800	LNCaP	prostate:	n/a
4	chr3:34342358-34342408	HUVEC	blood vessel:	n/a
5	chr3:34429403-34429453	Jurkat	blood:	n/a
6	chr3:34342358-34342408	HIPEpiC	eye:	n/a
7	chr3:34187750-34187800	SKMC	muscle:	n/a
8	chr3:34342358-34342408	AoSMC	blood vessel:	n/a
9	chr3:34298905-34298955	Hela-S3	cervix:	n/a
10	chr3:34298905-34298955	GM19239	blood:	n/a
11	chr3:34187750-34187800	HRE	kidney:	n/a
12	chr3:34342358-34342408	A549	lung:	n/a
13	chr3:34342358-34342408	GM12891	blood:	n/a
14	chr3:34298905-34298955	NH-A	brain:	n/a
15	chr3:34429403-34429453	GM19239	blood:	n/a
16	chr3:34429403-34429453	H1-hESC	embryonic stem cell:	embryo
17	chr3:34429403-34429453	SK-N-SH_RA	brain:	n/a
18	chr3:34187750-34187800	MCF10A-Er-Src	breast:	n/a
19	chr3:34187750-34187800	NHBE	bronchial:	n/a
20	chr3:34342358-34342408	AG10803	skin:	n/a
21	chr3:34429403-34429453	IMR90	lung:	fetal
22	chr3:34342358-34342408	NB4	blood:	n/a
23	chr3:34298905-34298955	HIPEpiC	eye:	n/a
24	chr3:34187750-34187800	T-47D	breast:	n/a
25	chr3:34298905-34298955	ovcar-3	ovarian:	n/a
26	chr3:34342358-34342408	SKMC	muscle:	n/a
27	chr3:34342358-34342408	HCM	heart:	n/a
28	chr3:34298905-34298955	HEK293	kidney:	embryo
29	chr3:34429403-34429453	A549	lung:	n/a
30	chr3:34298905-34298955	AG10803	skin:	n/a
31	chr3:34342358-34342408	HepG2	liver:	n/a
32	chr3:34342358-34342408	GM19239	blood:	n/a
33	chr3:34429403-34429453	SKMC	muscle:	n/a
34	chr3:34429403-34429453	HCPEpiC	choroid plexus:	n/a
35	chr3:34342358-34342408	MCF10A-Er-Src	breast:	n/a
36	chr3:34298905-34298955	GM12892	blood:	n/a
37	chr3:34187750-34187800	AoSMC	blood vessel:	n/a
38	chr3:34342358-34342408	HRPEpiC	eye:	n/a
39	chr3:34298905-34298955	RPTEC	kidney:	n/a
40	chr3:34342358-34342408	HAEpiC	amniotic membrane:	n/a
41	chr3:34429403-34429453	NHBE	bronchial:	n/a
42	chr3:34429403-34429453	NT2-D1	testis:	n/a
43	chr3:34298905-34298955	HCM	heart:	n/a
44	chr3:34187750-34187800	MCF-7	breast:	n/a
45	chr3:34298905-34298955	LNCaP	prostate:	n/a
46	chr3:34429403-34429453	HIPEpiC	eye:	n/a
47	chr3:34429403-34429453	NHDF-neo	bronchial:	n/a
48	chr3:34342358-34342408	PANC-1	pancreas:	n/a
49	chr3:34298905-34298955	PANC-1	pancreas:	n/a
50	chr3:34298905-34298955	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:34244429..34246745-chr3:34254432..34256118,2	K562	blood:
2	chr3:34321033..34322833-chr3:34323963..34326820,2	MCF-7	breast:
3	chr3:34188769..34191997-chr3:34195133..34197924,3	MCF-7	breast:
4	chr3:34307945..34310504-chr3:34315183..34316833,2	MCF-7	breast:
5	chr3:34392704..34395066-chr3:34408045..34410350,2	K562	blood:
6	chr3:34187980..34191122-chr3:34195449..34197279,3	K562	blood:
7	chr3:34306531..34307201-chr3:34318306..34319090,2	MCF-7	breast:
8	chr3:34105862..34107737-chr3:34241942..34244433,2	K562	blood:
9	chr3:34238738..34241610-chr3:34244230..34246747,2	K562	blood:
10	chr3:34306937..34309088-chr3:34310627..34313215,3	K562	blood:
11	chr3:34330070..34332074-chr3:34332268..34334733,2	K562	blood:
12	chr3:34021708..34023803-chr3:34147360..34150233,3	MCF-7	breast:
13	chr3:34288854..34291341-chr3:34298518..34300242,2	K562	blood:
14	chr3:34254296..34256628-chr3:34259423..34261115,2	K562	blood:
15	chr3:34302064..34302720-chr3:34415830..34416441,2	MCF-7	breast:
16	chr3:34148303..34148939-chr3:34318312..34319187,3	MCF-7	breast:
17	chr3:34251179..34253231-chr3:34254856..34256423,2	K562	blood:
18	chr3:34268022..34268698-chr3:34276487..34277413,2	MCF-7	breast:
19	chr3:34302064..34302720-chr3:34415830..34416441,2	MCF-7	breast:
20	chr3:34330070..34332074-chr3:34332268..34334733,2	K562	blood:
21	chr3:34325094..34326771-chr3:34500714..34502668,2	K562	blood:
22	chr3:34395435..34397295-chr3:34398899..34400436,2	K562	blood:
23	chr3:34187980..34191122-chr3:34195449..34197279,3	K562	blood:
24	chr3:34302039..34302590-chr3:34415682..34416266,2	MCF-7	breast:
25	chr3:34288854..34291341-chr3:34298518..34300242,2	K562	blood:
26	chr3:34164835..34166730-chr3:34169015..34171649,2	K562	blood:
27	chr3:34164835..34166730-chr3:34169015..34171649,2	K562	blood:
28	chr3:34188769..34191997-chr3:34195133..34197924,3	MCF-7	breast:
29	chr3:34372519..34374395-chr3:34376405..34378291,2	K562	blood:
30	chr3:34254296..34256628-chr3:34259423..34261115,2	K562	blood:
31	chr3:34319221..34321894-chr3:34324307..34326829,2	K562	blood:
32	chr3:34251179..34253231-chr3:34254856..34256423,2	K562	blood:
33	chr3:33925768..33926296-chr3:34301785..34302560,2	MCF-7	breast:
34	chr3:34375056..34377736-chr3:34380092..34383036,2	MCF-7	breast:
35	chr3:34307556..34310522-chr3:34325293..34326875,2	K562	blood:
36	chr3:34302039..34302590-chr3:34415682..34416266,2	MCF-7	breast:
37	chr3:34021551..34022550-chr3:34318530..34319319,6	MCF-7	breast:
38	chr3:34294305..34297993-chr3:34298599..34300564,3	K562	blood:
39	chr3:34321033..34322833-chr3:34323963..34326820,2	MCF-7	breast:
40	chr3:34181281..34183776-chr3:34186988..34188789,2	K562	blood:
41	chr3:33925854..33926364-chr3:34318708..34319375,2	MCF-7	breast:
42	chr3:34319221..34321894-chr3:34324307..34326829,2	K562	blood:
43	chr3:34285723..34288551-chr3:34291607..34294875,3	K562	blood:
44	chr3:34268022..34268698-chr3:34276487..34277413,2	MCF-7	breast:
45	chr3:34375056..34377736-chr3:34380092..34383036,2	MCF-7	breast:
46	chr3:34276733..34278426-chr3:34286932..34289441,2	MCF-7	breast:
47	chr3:34286135..34288097-chr3:34290697..34293518,2	K562	blood:
48	chr3:34237804..34239515-chr3:34306998..34309662,2	K562	blood:
49	chr3:34276733..34278426-chr3:34286932..34289441,2	MCF-7	breast:
50	chr3:34282049..34282764-chr3:156418622..156419493,2	Hela-S3	cervix:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDCD6IP-1	chr3:34244736-34244800	XLOC_002613
2	lnc-PDCD6IP-2	chr3:34200874-34200908	XLOC_002612
3	lnc-PDCD6IP-2	chr3:34401763-34401853	XLOC_002612
4	lnc-PDCD6IP-1	chr3:34242415-34242459	XLOC_002613
5	lnc-PDCD6IP-2	chr3:34387714-34387781	XLOC_002612
6	lnc-PDCD6IP-2	chr3:34340345-34340411	XLOC_002612
7	lnc-PDCD6IP-2	chr3:34340345-34340411	XLOC_002612
8	lnc-PDCD6IP-2	chr3:34387714-34387781	XLOC_002612
9	lnc-PDCD6IP-2	chr3:34365040-34365090	XLOC_002612
10	lnc-PDCD6IP-2	chr3:34340345-34340411	XLOC_002612
11	lnc-PDCD6IP-2	chr3:34212337-34212412	XLOC_002612
12	lnc-PDCD6IP-4	chr3:34250444-34250609	NONHSAT088955
13	lnc-PDCD6IP-4	chr3:34253771-34253924	NONHSAT088955
14	lnc-PDCD6IP-2	chr3:34212337-34212412	XLOC_002612
15	lnc-PDCD6IP-5	chr3:34425757-34425857	l_2344_chr3:34377232-34452128_testes
16	lnc-PDCD6IP-2	chr3:34262110-34262347	NONHSAT088957
17	lnc-PDCD6IP-2	chr3:34428383-34428569	XLOC_002612
18	lnc-PDCD6IP-2	chr3:34201487-34201519	XLOC_002612
19	lnc-PDCD6IP-2	chr3:34401795-34401853	XLOC_002612
20	lnc-PDCD6IP-2	chr3:34309814-34311242	NONHSAT088957
21	lnc-PDCD6IP-2	chr3:34364840-34365090	XLOC_002612
22	lnc-PDCD6IP-2	chr3:34402297-34402513	XLOC_002612
23	lnc-PDCD6IP-2	chr3:34200900-34200908	XLOC_002612
24	lnc-PDCD6IP-2	chr3:34200826-34200908	XLOC_002612
25	lnc-PDCD6IP-5	chr3:34377233-34377517	l_2344_chr3:34377232-34452128_testes
26	lnc-PDCD6IP-2	chr3:34402297-34402551	XLOC_002612
27	lnc-PDCD6IP-4	chr3:34253697-34253924	NONHSAT088956
28	lnc-PDCD6IP-2	chr3:34402262-34402513	XLOC_002612
29	lnc-PDCD6IP-2	chr3:34340345-34340411	XLOC_002612
30	lnc-PDCD6IP-1	chr3:34309814-34310303	XLOC_002613
31	lnc-PDCD6IP-4	chr3:34250444-34250609	NONHSAT088956
32	lnc-PDCD6IP-2	chr3:34387714-34387781	XLOC_002612
33	lnc-PDCD6IP-2	chr3:34212337-34212412	XLOC_002612
34	lnc-PDCD6IP-1	chr3:34309814-34310187	XLOC_002613
35	lnc-PDCD6IP-2	chr3:34364840-34365039	XLOC_002612
36	lnc-PDCD6IP-2	chr3:34387714-34387781	XLOC_002612
37	lnc-PDCD6IP-2	chr3:34212337-34212412	XLOC_002612

No data

Variant related genes	Relation type
ENSG00000226320	TF binding region
ENSG00000236452	TF binding region
ENSG00000226320	CpG island
ENSG00000236452	CpG island
ENSG00000236452	chromatin interactions
SFRS3	miRNA target sites
FBXL3	miRNA target sites
NKRF	miRNA target sites
CHUK	miRNA target sites
CDKN1B	miRNA target sites

Extended variants
information (count: 7968 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:7968 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140012681	chr3:34149582-34149583	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs367924136	chr3:34149610-34149611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545534711	chr3:34149623-34149624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564853774	chr3:34149683-34149684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559152863	chr3:34149750-34149751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183336560	chr3:34149775-34149776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550831852	chr3:34149780-34149781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7633784	chr3:34149814-34149815	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs529889826	chr3:34149815-34149816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114697448	chr3:34149830-34149831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566526291	chr3:34149835-34149836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114919795	chr3:34149896-34149897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7622281	chr3:34149980-34149981	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs147418013	chr3:34149989-34149990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148456780	chr3:34149994-34149995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72864468	chr3:34150042-34150043	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs373776824	chr3:34150049-34150050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376925232	chr3:34150084-34150085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527482644	chr3:34150107-34150108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530387949	chr3:34150186-34150187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142595848	chr3:34150239-34150240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553849423	chr3:34150240-34150241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572175394	chr3:34150289-34150290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151014466	chr3:34150292-34150293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564353448	chr3:34150295-34150296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188956975	chr3:34150314-34150315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544221624	chr3:34150334-34150335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562763205	chr3:34150341-34150342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114272598	chr3:34150429-34150430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539121737	chr3:34150467-34150468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78981743	chr3:34150483-34150484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549395621	chr3:34150497-34150498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566586998	chr3:34150509-34150510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139608587	chr3:34150603-34150604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552278955	chr3:34150649-34150650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563491584	chr3:34150684-34150685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570398941	chr3:34150754-34150755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566682197	chr3:34150777-34150778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11290402	chr3:34150778-34150779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533097134	chr3:34150779-34150780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs397989154	chr3:34150791-34150792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62250181	chr3:34150794-34150795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191743751	chr3:34150802-34150803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111803800	chr3:34150821-34150822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568687721	chr3:34150842-34150843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535672386	chr3:34150862-34150863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146661271	chr3:34150935-34150936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532640063	chr3:34150992-34150993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572286019	chr3:34151073-34151074	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs552383859	chr3:34151090-34151091	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Wilms tumour	17204608	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Kartagener syndrome	16639409	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34147800-34151600	Enhancers	Thymus	Thymus
2	chr3:34147800-34152600	Enhancers	Fetal Thymus	thymus
3	chr3:34147800-34153000	Enhancers	Dnd41	blood
4	chr3:34148400-34149600	Enhancers	Primary B cells from peripheral blood	blood
5	chr3:34148400-34149600	Flanking Active TSS	GM12878-XiMat	blood
6	chr3:34148400-34149800	Enhancers	Primary B cells from cord blood	blood
7	chr3:34148400-34149800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:34148600-34149600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr3:34148600-34149800	Enhancers	Primary hematopoietic stem cells	blood
10	chr3:34149200-34149600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr3:34149400-34151000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr3:34149600-34150400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr3:34149600-34150600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:34149600-34151000	Enhancers	GM12878-XiMat	blood
15	chr3:34149600-34151200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr3:34149800-34150200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:34149800-34150800	Weak transcription	Primary B cells from cord blood	blood
18	chr3:34150200-34151200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr3:34150400-34150800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr3:34150600-34150800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr3:34150800-34151000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr3:34151000-34151400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr3:34151000-34151400	Flanking Active TSS	GM12878-XiMat	blood
24	chr3:34151000-34151600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr3:34151200-34151600	Enhancers	Primary B cells from peripheral blood	blood
26	chr3:34151400-34151600	Enhancers	Primary B cells from cord blood	blood
27	chr3:34151400-34151600	Enhancers	Primary hematopoietic stem cells	blood
28	chr3:34151400-34151800	Enhancers	GM12878-XiMat	blood
29	chr3:34151600-34152400	Weak transcription	Thymus	Thymus
30	chr3:34152000-34152800	Enhancers	Brain Germinal Matrix	brain
31	chr3:34152400-34152600	Enhancers	Thymus	Thymus
32	chr3:34152600-34155000	Weak transcription	Thymus	Thymus
33	chr3:34153000-34155200	Weak transcription	Dnd41	blood
34	chr3:34155200-34155400	Enhancers	Thymus	Thymus
35	chr3:34155200-34155800	Enhancers	Dnd41	blood
36	chr3:34159400-34163400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:34163400-34164000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:34165800-34166200	ZNF genes & repeats	Aorta	Aorta
39	chr3:34166200-34166800	ZNF genes & repeats	Dnd41	blood
40	chr3:34166800-34167000	Weak transcription	Aorta	Aorta
41	chr3:34167400-34167800	Weak transcription	Dnd41	blood
42	chr3:34168000-34168200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:34169600-34170600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:34170200-34174800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr3:34171400-34172200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr3:34171400-34174600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:34171600-34171800	Enhancers	Dnd41	blood
48	chr3:34171600-34172200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr3:34171800-34173400	Weak transcription	Dnd41	blood
50	chr3:34172200-34173200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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