Variant report

Variant	nsv879852
Chromosome Location	chr4:121108734-121768496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2230)
CpG islands
(count:489)
Chromatin interactive
region (count:59)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2230 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:121297907-121297919	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:121614174-121614541	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:121588574-121588579	K562	blood:	n/a	n/a
4	ATF2	chr4:121387504-121388036	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:121252954-121253319	GM12878	blood:	n/a	n/a
6	ATF2	chr4:121765601-121766141	GM12878	blood:	n/a	n/a
7	ATF2	chr4:121482693-121483215	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:121670498-121670947	GM12878	blood:	n/a	n/a
9	ATF2	chr4:121387529-121388007	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr4:121252922-121253430	GM12878	blood:	n/a	n/a
11	ATF2	chr4:121765662-121766071	GM12878	blood:	n/a	n/a
12	ATF2	chr4:121248398-121248789	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr4:121478440-121478964	HCT-116	colon:	n/a	n/a
14	BACH1	chr4:121642846-121642911	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:121158096-121158364	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:121594017-121594053	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:121640212-121640444	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr4:121252898-121253394	GM12878	blood:	n/a	n/a
19	BATF	chr4:121765635-121766159	GM12878	blood:	n/a	chr4:121765916-121765927
20	BATF	chr4:121765654-121766090	GM12878	blood:	n/a	chr4:121765916-121765927
21	BCL11A	chr4:121765689-121766051	GM12878	blood:	n/a	n/a
22	BCL3	chr4:121344997-121345240	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:121670672-121671060	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:121765706-121766156	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:121686870-121687098	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:121402998-121403202	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr4:121644141-121644145	GM12878	blood:	n/a	n/a
28	BRCA1	chr4:121690199-121690775	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr4:121252523-121252606	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr4:121651232-121651259	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr4:121236020-121236194	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr4:121482921-121483432	HCT-116	colon:	n/a	n/a
33	CCNT2	chr4:121573758-121573939	K562	blood:	n/a	n/a
34	CCNT2	chr4:121310347-121310670	K562	blood:	n/a	n/a
35	CCNT2	chr4:121754428-121754544	K562	blood:	n/a	n/a
36	CEBPB	chr4:121478566-121478903	IMR90	lung:	n/a	chr4:121478740-121478751
37	CEBPB	chr4:121387580-121387934	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr4:121146760-121147063	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:121750290-121751025	Hela-S3	cervix:	n/a	chr4:121750852-121750863
40	CEBPB	chr4:121182334-121182551	K562	blood:	n/a	chr4:121182442-121182453
41	CEBPB	chr4:121606918-121607260	IMR90	lung:	n/a	chr4:121607082-121607093
42	CEBPB	chr4:121460955-121461138	IMR90	lung:	n/a	chr4:121461075-121461086
43	CEBPB	chr4:121420255-121420416	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:121478553-121478945	HCT-116	colon:	n/a	chr4:121478740-121478751
45	CEBPB	chr4:121238946-121239302	IMR90	lung:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
46	CEBPB	chr4:121238898-121239307	ECC-1	luminal epithelium:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
47	CEBPB	chr4:121676743-121677031	HepG2	liver:	n/a	chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676918-121676929
48	CEBPB	chr4:121387574-121388036	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr4:121182369-121182486	HepG2	liver:	n/a	chr4:121182442-121182453
50	CEBPB	chr4:121239010-121239220	MCF-7	breast:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:121471886-121471936	SK-N-MC	brain:	n/a
2	chr4:121471886-121471936	SK-N-MC	brain:	n/a
3	chr4:121569769-121569819	HCPEpiC	choroid plexus:	n/a
4	chr4:121387400-121387450	ProgFib	skin:	n/a
5	chr4:121763322-121763372	SK-N-MC	brain:	n/a
6	chr4:121569769-121569819	AG04450	lung:	fetal
7	chr4:121569769-121569819	AG04449	skin:	fetal
8	chr4:121471886-121471936	Hela-S3	cervix:	n/a
9	chr4:121471496-121471546	RPTEC	kidney:	n/a
10	chr4:121387400-121387450	Hela-S3	cervix:	n/a
11	chr4:121471288-121471338	AG09309	skin:	n/a
12	chr4:121471496-121471546	A549	lung:	n/a
13	chr4:121763322-121763372	PANC-1	pancreas:	n/a
14	chr4:121569769-121569819	RPTEC	kidney:	n/a
15	chr4:121471886-121471936	Jurkat	blood:	n/a
16	chr4:121387400-121387450	SAEC	small airway:	n/a
17	chr4:121185048-121185098	HepG2	liver:	n/a
18	chr4:121613795-121613845	LNCaP	prostate:	n/a
19	chr4:121569769-121569819	HepG2	liver:	n/a
20	chr4:121387400-121387450	Caco-2	colon:	n/a
21	chr4:121763322-121763372	AG09319	gingival:	n/a
22	chr4:121471886-121471936	AoSMC	blood vessel:	n/a
23	chr4:121471496-121471546	SK-N-SH	brain:	n/a
24	chr4:121185048-121185098	K562	blood:	n/a
25	chr4:121387400-121387450	SK-N-SH_RA	brain:	n/a
26	chr4:121471496-121471546	HCF	heart:	n/a
27	chr4:121185048-121185098	HNPCEpiC	eye:	n/a
28	chr4:121471496-121471546	NHBE	bronchial:	n/a
29	chr4:121387400-121387450	AG10803	skin:	n/a
30	chr4:121471288-121471338	NB4	blood:	n/a
31	chr4:121387400-121387450	PFSK-1	brain:	n/a
32	chr4:121763322-121763372	AG10803	skin:	n/a
33	chr4:121471886-121471936	HEEpiC	esophagus:	n/a
34	chr4:121569769-121569819	NHBE	bronchial:	n/a
35	chr4:121569769-121569819	SK-N-MC	brain:	n/a
36	chr4:121613795-121613845	AoSMC	blood vessel:	n/a
37	chr4:121471886-121471936	HCPEpiC	choroid plexus:	n/a
38	chr4:121569769-121569819	HEEpiC	esophagus:	n/a
39	chr4:121387400-121387450	SK-N-SH	brain:	n/a
40	chr4:121387400-121387450	BJ	skin:	n/a
41	chr4:121763322-121763372	SKMC	muscle:	n/a
42	chr4:121471886-121471936	SKMC	muscle:	n/a
43	chr4:121613795-121613845	NHDF-neo	bronchial:	n/a
44	chr4:121763322-121763372	HMEC	breast:	n/a
45	chr4:121471288-121471338	HUVEC	blood vessel:	n/a
46	chr4:121763322-121763372	GM06990	blood:	n/a
47	chr4:121185048-121185098	NHDF-neo	bronchial:	n/a
48	chr4:121471288-121471338	SKMC	muscle:	n/a
49	chr4:121471886-121471936	Caco-2	colon:	n/a
50	chr4:121471496-121471546	SK-N-SH_RA	brain:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:121561336..121562974-chr4:121568163..121571035,2	MCF-7	breast:
2	chr3:122274439..122275125-chr4:121523467..121524237,2	MCF-7	breast:
3	chr4:121189633..121192348-chr4:121208319..121209845,2	K562	blood:
4	chr4:121396849..121398573-chr4:121700140..121702182,2	K562	blood:
5	chr4:121768312..121769256-chr5:10250360..10250922,2	NB4	blood:
6	chr4:121574015..121575886-chr4:121579540..121581895,2	MCF-7	breast:
7	chr4:121228431..121230743-chr4:121233140..121235922,2	K562	blood:
8	chr4:23802609..23803478-chr4:121273037..121273864,2	MCF-7	breast:
9	chr4:121514733..121517411-chr4:121540771..121542429,2	K562	blood:
10	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:
11	chr17:58501463..58503848-chr4:121259806..121262242,2	MCF-7	breast:
12	chr4:121228431..121230743-chr4:121233140..121235922,2	K562	blood:
13	chr4:121764972..121765670-chr4:121898848..121899366,2	MCF-7	breast:
14	chr4:121303352..121305526-chr4:121306861..121309621,3	K562	blood:
15	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:
16	chr4:121526673..121529460-chr4:121534400..121537130,2	MCF-7	breast:
17	chr4:121575389..121577725-chr4:121580963..121583228,2	K562	blood:
18	chr4:121561336..121562974-chr4:121568163..121571035,2	MCF-7	breast:
19	chr4:121646983..121649694-chr4:121650404..121652066,2	K562	blood:
20	chr4:121167566..121169623-chr4:121176920..121179543,2	MCF-7	breast:
21	chr4:121130697..121133786-chr4:121135139..121137341,3	K562	blood:
22	chr4:121522532..121523424-chr4:122017550..122018444,2	MCF-7	breast:
23	chr4:121130697..121133786-chr4:121135139..121137341,3	K562	blood:
24	chr4:121575389..121577725-chr4:121580963..121583228,2	K562	blood:
25	chr4:121763712..121766459-chr4:121767957..121770236,3	MCF-7	breast:
26	chr4:121361067..121362763-chr4:121362852..121365271,2	MCF-7	breast:
27	chr4:121185242..121187871-chr4:121188856..121190633,2	K562	blood:
28	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:
29	chr4:121309932..121311519-chr4:121313046..121315204,2	K562	blood:
30	chr4:120985495..120988183-chr4:121111194..121113222,2	K562	blood:
31	chr4:121189633..121192348-chr4:121208319..121209845,2	K562	blood:
32	chr4:121574015..121575886-chr4:121579540..121581895,2	MCF-7	breast:
33	chr4:121257279..121258865-chr4:121260585..121262446,2	K562	blood:
34	chr4:121593641..121594483-chr9:126875138..126875779,2	MCF-7	breast:
35	chr4:121303352..121305526-chr4:121306861..121309621,3	K562	blood:
36	chr4:121514733..121517411-chr4:121540771..121542429,2	K562	blood:
37	chr2:162678536..162680855-chr4:121354549..121356105,2	MCF-7	breast:
38	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
39	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:
40	chr4:121526673..121529460-chr4:121534400..121537130,2	MCF-7	breast:
41	chr4:121341832..121344209-chr4:121346289..121348125,2	K562	blood:
42	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:
43	chr4:121622815..121625386-chr4:121625794..121628188,2	K562	blood:
44	chr4:121341832..121344209-chr4:121346289..121348125,2	K562	blood:
45	chr4:121639899..121640642-chr4:121840005..121841112,3	MCF-7	breast:
46	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:
47	chr4:121763712..121766459-chr4:121767957..121770236,3	MCF-7	breast:
48	chr4:121185242..121187871-chr4:121188856..121190633,2	K562	blood:
49	chr4:121077068..121077961-chr4:121639964..121640817,3	MCF-7	breast:
50	chr4:121361067..121362763-chr4:121362852..121365271,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-6	chr4:121256793-121256886	ENSG00000250938.1
2	lnc-AC079341.1-4	chr4:121571665-121571951	XLOC_003671
3	lnc-AC079341.1-4	chr4:121560264-121560506	XLOC_003671
4	lnc-AC110373.1-6	chr4:121314655-121314877	ENSG00000250938.1
5	lnc-NDNF-4	chr4:121751724-121752408	NONHSAT098129
6	lnc-AC110373.1-6	chr4:121249688-121249741	ENSG00000250938.1
7	lnc-AC110373.1-13	chr4:121263211-121263802	NONHSAT098122
8	lnc-AC079341.1-4	chr4:121560245-121560506	XLOC_003671
9	lnc-AC110373.1-6	chr4:121337705-121337921	ENSG00000250938.1
10	lnc-AC110373.1-6	chr4:121314655-121314709	ENSG00000250938.1
11	lnc-AC079341.1-4	chr4:121571662-121571943	XLOC_003671
12	lnc-AC110373.1-6	chr4:121249688-121249741	ENSG00000250938.1
13	lnc-AC110373.1-13	chr4:121263212-121263784	NONHSAT098123
14	lnc-AC110373.1-6	chr4:121256793-121256886	ENSG00000250938.1

No data

Variant related genes	Relation type
RNU6-550P	TF binding region
PRDM5	TF binding region
ENSG00000225665	TF binding region
ENSG00000249409	TF binding region
RNU6-550P	CpG island
PRDM5	CpG island
ENSG00000225665	CpG island
ENSG00000249409	CpG island
ENSG00000150753	chromatin interactions
ENSG00000164109	chromatin interactions
ENSG00000250938	chromatin interactions
ELF3	miRNA target sites
ELAVL4	miRNA target sites

Extended variants
information (count: 17203 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:17203 , 50 per page) page: 1 2 3 4 5 6 7 ... 345

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6822059	chr4:121111237-121111238	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571448046	chr4:121111255-121111256	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376296507	chr4:121111284-121111285	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs13108603	chr4:121111308-121111309	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs2662755	chr4:121111336-121111337	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs548142613	chr4:121111342-121111343	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs536470306	chr4:121111402-121111403	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs555961890	chr4:121111456-121111457	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs13109047	chr4:121111497-121111498	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs369885878	chr4:121111512-121111513	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs558484490	chr4:121111520-121111521	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190228935	chr4:121111589-121111590	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs6822879	chr4:121111601-121111602	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs561268625	chr4:121111649-121111650	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530839141	chr4:121111671-121111672	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544029597	chr4:121111679-121111680	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs78007050	chr4:121111682-121111683	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553555379	chr4:121111754-121111755	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs181109645	chr4:121111797-121111798	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552392222	chr4:121111910-121111911	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185352190	chr4:121111939-121111940	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs116068308	chr4:121112029-121112030	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558522949	chr4:121112036-121112037	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs547684946	chr4:121112109-121112110	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs191934023	chr4:121112141-121112142	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575413885	chr4:121112267-121112268	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs551036175	chr4:121112325-121112326	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144097523	chr4:121112356-121112357	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs75058964	chr4:121112371-121112372	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs532700424	chr4:121112488-121112489	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141134402	chr4:121112497-121112498	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs183253837	chr4:121112542-121112543	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs189250381	chr4:121112550-121112551	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571679758	chr4:121112662-121112663	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2716003	chr4:121112669-121112670	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs554827992	chr4:121112702-121112703	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574833325	chr4:121112725-121112726	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs191938475	chr4:121112741-121112742	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs563857410	chr4:121112854-121112855	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs28610167	chr4:121112887-121112888	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs112562698	chr4:121112901-121112902	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546242372	chr4:121112983-121112984	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576637684	chr4:121112996-121112997	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs150712911	chr4:121113010-121113011	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559727912	chr4:121113032-121113033	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374940063	chr4:121113038-121113039	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528471015	chr4:121113077-121113078	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs369301070	chr4:121113102-121113103	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548635903	chr4:121113114-121113115	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs6858797	chr4:121113118-121113119	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Myelodysplastic syndrome	18508791	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121112800-121113200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:121116000-121118400	Weak transcription	Aorta	Aorta
3	chr4:121118400-121118800	ZNF genes & repeats	Aorta	Aorta
4	chr4:121118800-121119800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr4:121118800-121120200	Enhancers	HMEC	breast
6	chr4:121119200-121119600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:121121600-121121800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:121121800-121122800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr4:121122600-121123000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:121122600-121123000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:121122600-121124000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:121122800-121124000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:121122800-121124000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:121123000-121123400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:121123000-121123400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:121123000-121124000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:121123000-121124000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:121123400-121124000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:121123400-121124200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:121123600-121124000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:121123600-121124000	Enhancers	H9 Cell Line	embryonic stem cell
22	chr4:121123600-121124000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:121126400-121137400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:121133000-121133400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:121133000-121133600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:121133400-121136200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:121136200-121136400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:121139600-121140800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:121140600-121141000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr4:121146600-121147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:121146800-121147200	Enhancers	HepG2	liver
32	chr4:121147400-121148800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:121148800-121150000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:121148800-121151400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:121149200-121149600	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr4:121149200-121151600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:121149400-121150000	Enhancers	Adipose Nuclei	Adipose
38	chr4:121149600-121150000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr4:121149600-121150000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:121150000-121151000	Weak transcription	Adipose Nuclei	Adipose
41	chr4:121150200-121151200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:121151200-121151400	Enhancers	Adipose Nuclei	Adipose
43	chr4:121151200-121152200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:121153000-121153600	Enhancers	Osteobl	bone
45	chr4:121153400-121153600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:121154400-121154800	Enhancers	Pancreas	Pancrea
47	chr4:121154800-121159600	Weak transcription	Pancreas	Pancrea
48	chr4:121159600-121160000	Enhancers	Pancreas	Pancrea
49	chr4:121163000-121165200	Enhancers	Fetal Lung	lung
50	chr4:121163200-121163800	Enhancers	Fetal Kidney	kidney

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