Variant report

Variant	esv1803379
Chromosome Location	chr4:79661618-79704210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1428)
CpG islands
(count:793)
Chromatin interactive
region (count:70)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79696224-79697077	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:79694777-79694832	K562	blood:	n/a	n/a
3	ARID3A	chr4:79699840-79700080	K562	blood:	n/a	chr4:79699924-79699940
4	ARID3A	chr4:79700977-79701585	K562	blood:	n/a	n/a
5	ARID3A	chr4:79689726-79690080	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:79689602-79689708	K562	blood:	n/a	n/a
7	ARID3A	chr4:79685558-79686702	K562	blood:	n/a	n/a
8	ARID3A	chr4:79695555-79695925	K562	blood:	n/a	n/a
9	ARID3A	chr4:79700464-79700642	K562	blood:	n/a	n/a
10	ARID3A	chr4:79693490-79694234	K562	blood:	n/a	n/a
11	ARID3A	chr4:79698079-79698400	HepG2	liver:	n/a	n/a
12	ATF1	chr4:79685646-79686170	K562	blood:	n/a	n/a
13	ATF1	chr4:79670624-79670828	K562	blood:	n/a	n/a
14	ATF2	chr4:79663360-79663930	GM12878	blood:	n/a	n/a
15	ATF2	chr4:79695320-79695991	GM12878	blood:	n/a	n/a
16	ATF2	chr4:79696278-79697078	GM12878	blood:	n/a	n/a
17	ATF2	chr4:79674124-79674784	GM12878	blood:	n/a	n/a
18	ATF2	chr4:79671040-79671805	GM12878	blood:	n/a	n/a
19	ATF2	chr4:79696448-79696978	GM12878	blood:	n/a	n/a
20	ATF2	chr4:79695539-79695963	GM12878	blood:	n/a	n/a
21	ATF2	chr4:79670946-79671866	GM12878	blood:	n/a	n/a
22	ATF2	chr4:79687611-79688091	GM12878	blood:	n/a	n/a
23	ATF3	chr4:79696936-79697176	H1-hESC	embryonic stem cell:	n/a	chr4:79697136-79697145 chr4:79696955-79696975
24	ATF3	chr4:79696914-79697196	H1-hESC	embryonic stem cell:	n/a	chr4:79697136-79697145 chr4:79696955-79696975
25	ATF3	chr4:79696803-79697243	HepG2	liver:	n/a	chr4:79697136-79697145 chr4:79696955-79696975
26	ATF3	chr4:79696969-79697245	GM12878	blood:	n/a	chr4:79697136-79697145
27	ATF3	chr4:79696845-79697321	GM12878	blood:	n/a	chr4:79697136-79697145 chr4:79696955-79696975
28	ATF3	chr4:79696931-79697257	K562	blood:	n/a	chr4:79697136-79697145 chr4:79696955-79696975
29	ATF3	chr4:79696926-79697242	HepG2	liver:	n/a	chr4:79697136-79697145 chr4:79696955-79696975
30	BACH1	chr4:79696692-79697359	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr4:79702720-79702954	K562	blood:	n/a	n/a
32	BACH1	chr4:79703709-79703904	K562	blood:	n/a	n/a
33	BACH1	chr4:79699402-79699407	K562	blood:	n/a	n/a
34	BATF	chr4:79670399-79670725	GM12878	blood:	n/a	n/a
35	BATF	chr4:79695438-79695865	GM12878	blood:	n/a	n/a
36	BATF	chr4:79688494-79688765	GM12878	blood:	n/a	n/a
37	BATF	chr4:79693793-79693913	GM12878	blood:	n/a	n/a
38	BATF	chr4:79663472-79663842	GM12878	blood:	n/a	n/a
39	BATF	chr4:79693698-79694009	GM12878	blood:	n/a	n/a
40	BATF	chr4:79671173-79671798	GM12878	blood:	n/a	n/a
41	BATF	chr4:79671133-79671851	GM12878	blood:	n/a	n/a
42	BCL11A	chr4:79687824-79687990	GM12878	blood:	n/a	n/a
43	BCL11A	chr4:79671108-79671572	GM12878	blood:	n/a	chr4:79671262-79671271
44	BCL11A	chr4:79663412-79663842	GM12878	blood:	n/a	n/a
45	BCL11A	chr4:79671066-79671781	GM12878	blood:	n/a	chr4:79671262-79671271
46	BCL11A	chr4:79670458-79670760	GM12878	blood:	n/a	n/a
47	BCL11A	chr4:79695553-79695908	GM12878	blood:	n/a	chr4:79695761-79695770
48	BCL11A	chr4:79674372-79674594	GM12878	blood:	n/a	chr4:79674546-79674555
49	BCL3	chr4:79674310-79674693	GM12878	blood:	n/a	chr4:79674546-79674555
50	BCL3	chr4:79663431-79663873	GM12878	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79700688-79700738	GM12891	blood:	n/a
2	chr4:79696555-79696605	AoSMC	blood vessel:	n/a
3	chr4:79698168-79698218	LNCaP	prostate:	n/a
4	chr4:79698201-79698251	GM12891	blood:	n/a
5	chr4:79689621-79689671	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:79700688-79700738	Jurkat	blood:	n/a
7	chr4:79697329-79697379	CMK	blood:	n/a
8	chr4:79689621-79689671	AoSMC	blood vessel:	n/a
9	chr4:79697742-79697792	HUVEC	blood vessel:	n/a
10	chr4:79697739-79697789	AG09319	gingival:	n/a
11	chr4:79693986-79694036	ECC-1	luminal epithelium:	n/a
12	chr4:79697739-79697789	GM19239	blood:	n/a
13	chr4:79696708-79696758	HMEC	breast:	n/a
14	chr4:79697329-79697379	ECC-1	luminal epithelium:	n/a
15	chr4:79689621-79689671	NHDF-neo	bronchial:	n/a
16	chr4:79696555-79696605	BJ	skin:	n/a
17	chr4:79698168-79698218	HCF	heart:	n/a
18	chr4:79697739-79697789	HCT-116	colon:	n/a
19	chr4:79696708-79696758	K562	blood:	n/a
20	chr4:79696555-79696605	NT2-D1	testis:	n/a
21	chr4:79700688-79700738	HCT-116	colon:	n/a
22	chr4:79697583-79697633	HEK293	kidney:	embryo
23	chr4:79698168-79698218	SK-N-SH	brain:	n/a
24	chr4:79693986-79694036	K562	blood:	n/a
25	chr4:79697583-79697633	AG04449	skin:	fetal
26	chr4:79697742-79697792	LNCaP	prostate:	n/a
27	chr4:79689621-79689671	T-47D	breast:	n/a
28	chr4:79696647-79696697	HNPCEpiC	eye:	n/a
29	chr4:79698242-79698292	AG04450	lung:	fetal
30	chr4:79696708-79696758	BJ	skin:	n/a
31	chr4:79693986-79694036	Jurkat	blood:	n/a
32	chr4:79698242-79698292	IMR90	lung:	fetal
33	chr4:79697583-79697633	AG10803	skin:	n/a
34	chr4:79700688-79700738	Hela-S3	cervix:	n/a
35	chr4:79697742-79697792	H1-hESC	embryonic stem cell:	embryo
36	chr4:79698242-79698292	AG10803	skin:	n/a
37	chr4:79696708-79696758	SAEC	small airway:	n/a
38	chr4:79689621-79689671	K562	blood:	n/a
39	chr4:79696708-79696758	AG09309	skin:	n/a
40	chr4:79697329-79697379	SK-N-SH	brain:	n/a
41	chr4:79698201-79698251	HEK293	kidney:	embryo
42	chr4:79697329-79697379	SAEC	small airway:	n/a
43	chr4:79698242-79698292	Caco-2	colon:	n/a
44	chr4:79696555-79696605	Hela-S3	cervix:	n/a
45	chr4:79696647-79696697	MCF10A-Er-Src	breast:	n/a
46	chr4:79697742-79697792	ECC-1	luminal epithelium:	n/a
47	chr4:79698242-79698292	NH-A	brain:	n/a
48	chr4:79697329-79697379	GM19239	blood:	n/a
49	chr4:79693986-79694036	HCPEpiC	choroid plexus:	n/a
50	chr4:79693986-79694036	SK-N-SH	brain:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:79548752..79551333-chr4:79698595..79700948,2	K562	blood:
2	chr4:79683262..79685331-chr4:79691098..79694068,3	MCF-7	breast:
3	chr4:79675645..79678606-chr4:79678648..79682266,4	K562	blood:
4	chr4:79670306..79672761-chr4:79674776..79676315,2	K562	blood:
5	chr4:79671491..79675172-chr4:79695694..79700236,6	K562	blood:
6	chr4:79656229..79658092-chr4:79667705..79669486,2	K562	blood:
7	chr4:79589319..79591272-chr4:79690520..79692107,2	K562	blood:
8	chr4:79563120..79566472-chr4:79698388..79700680,4	K562	blood:
9	chr4:79571726..79575122-chr4:79694078..79695730,3	K562	blood:
10	chr4:79652471..79656671-chr4:79657113..79664892,10	K562	blood:
11	chr4:79564080..79567985-chr4:79696414..79698633,7	MCF-7	breast:
12	chr4:79661337..79663411-chr4:79678166..79679666,2	K562	blood:
13	chr4:79562196..79569044-chr4:79695847..79699797,11	MCF-7	breast:
14	chr4:79668400..79670810-chr4:79695190..79697374,3	K562	blood:
15	chr4:79679599..79681509-chr4:79684030..79686056,2	K562	blood:
16	chr12:6309195..6310003-chr4:79696831..79697536,2	Hela-S3	cervix:
17	chr4:79686100..79693924-chr4:79694940..79698947,11	MCF-7	breast:
18	chr4:79666351..79669068-chr4:79669581..79671853,2	K562	blood:
19	chr4:79697991..79698551-chr4:79785291..79786155,2	MCF-7	breast:
20	chr4:79547801..79550163-chr4:79699958..79704022,3	K562	blood:
21	chr4:79561055..79563429-chr4:79700959..79703090,2	K562	blood:
22	chr4:79697362..79698154-chrX:118601587..118602475,2	HCT-116	colon:
23	chr4:79573461..79577118-chr4:79700688..79703892,3	K562	blood:
24	chr4:79668464..79671093-chr4:79675204..79677763,2	K562	blood:
25	chr4:79570295..79572982-chr4:79695014..79699413,6	MCF-7	breast:
26	chr4:79583221..79584780-chr4:79699632..79701353,2	MCF-7	breast:
27	chr4:79679599..79681509-chr4:79684030..79686056,2	K562	blood:
28	chr4:79541751..79544197-chr4:79672798..79674957,2	K562	blood:
29	chr4:79562740..79566241-chr4:79702324..79704926,3	MCF-7	breast:
30	chr4:79670306..79672761-chr4:79674776..79676315,2	K562	blood:
31	chr4:79674995..79676989-chr4:79751851..79754832,2	K562	blood:
32	chr4:79675924..79678633-chr4:79679158..79682139,3	K562	blood:
33	chr4:79676661..79679162-chr4:79694637..79696425,2	K562	blood:
34	chr4:79652422..79657384-chr4:79659734..79665634,7	K562	blood:
35	chr4:79571366..79573433-chr4:79699664..79702069,2	K562	blood:
36	chr4:79522193..79524527-chr4:79697309..79699707,2	MCF-7	breast:
37	chr4:79610837..79614309-chr4:79701098..79703975,3	K562	blood:
38	chr4:79546177..79548904-chr4:79704201..79706828,2	K562	blood:
39	chr4:79697257..79699576-chr4:79770892..79773352,2	MCF-7	breast:
40	chr4:79663586..79665356-chr4:79665502..79667860,2	K562	blood:
41	chr4:79565693..79569294-chr4:79696000..79698136,3	K562	blood:
42	chr4:79531023..79534724-chr4:79692809..79696400,3	K562	blood:
43	chr4:79666351..79669068-chr4:79669581..79671853,2	K562	blood:
44	chr4:79675924..79678633-chr4:79679158..79682139,3	K562	blood:
45	chr4:79566015..79567656-chr4:79699216..79701058,2	MCF-7	breast:
46	chr4:79668464..79671093-chr4:79675204..79677763,2	K562	blood:
47	chr4:79522884..79525832-chr4:79695803..79698616,2	K562	blood:
48	chr4:79676661..79679162-chr4:79694637..79696425,2	K562	blood:
49	chr4:79568346..79573757-chr4:79695931..79699478,7	MCF-7	breast:
50	chr4:79671149..79677345-chr4:79694159..79700053,8	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAQR3-1	chr4:79696609-79697054	NONHSAT097083
2	lnc-PAQR3-1	chr4:79694808-79697127	ENSG00000260278.1
3	lnc-PAQR3-1	chr4:79689637-79689955	NONHSAT097083

No data

Variant related genes	Relation type
ENSG00000239793	TF binding region
ENSG00000260278	TF binding region
BMP2K	TF binding region
ENSG00000239793	CpG island
ENSG00000260278	CpG island
BMP2K	CpG island
ENSG00000138772	chromatin interactions
ENSG00000010278	chromatin interactions
ENSG00000112715	chromatin interactions
ENSG00000251442	chromatin interactions
ENSG00000138756	chromatin interactions
ENSG00000251019	chromatin interactions
ENSG00000260278	chromatin interactions
ENSG00000238816	chromatin interactions
ENSG00000224281	chromatin interactions
ENSG00000239793	chromatin interactions
ENSG00000005022	chromatin interactions
ENSG00000272114	chromatin interactions

Extended variants
information (count: 1439 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1439 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9992277	chr4:79661618-79661619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371941922	chr4:79661659-79661660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35348460	chr4:79661660-79661661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561623403	chr4:79661667-79661668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575071631	chr4:79661691-79661692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552195685	chr4:79661699-79661700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540784018	chr4:79661708-79661709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568984775	chr4:79661739-79661740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538227745	chr4:79661793-79661794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560526865	chr4:79661926-79661927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532443774	chr4:79661999-79662000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552271660	chr4:79662048-79662049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147732078	chr4:79662051-79662052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185458816	chr4:79662074-79662075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531399686	chr4:79662177-79662178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548338546	chr4:79662241-79662242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567540322	chr4:79662282-79662283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34806120	chr4:79662283-79662284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62308354	chr4:79662319-79662320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62308355	chr4:79662323-79662324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539939013	chr4:79662330-79662331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs60572279	chr4:79662331-79662332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376021220	chr4:79662373-79662374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189235638	chr4:79662381-79662382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77287693	chr4:79662403-79662404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536485506	chr4:79662448-79662449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192272060	chr4:79662465-79662466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111836663	chr4:79662489-79662490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368869726	chr4:79662580-79662581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372980676	chr4:79662586-79662587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558665097	chr4:79662594-79662595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9995485	chr4:79662606-79662607	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs368483344	chr4:79662635-79662636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566928924	chr4:79662799-79662800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188292572	chr4:79662817-79662818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142527019	chr4:79662820-79662821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191680111	chr4:79662864-79662865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532843887	chr4:79662874-79662875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541555362	chr4:79662878-79662879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567638207	chr4:79663006-79663007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140706781	chr4:79663007-79663008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62308356	chr4:79663009-79663010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540594130	chr4:79663023-79663024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116825547	chr4:79663033-79663034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577008969	chr4:79663065-79663066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546014470	chr4:79663110-79663111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28451964	chr4:79663112-79663113	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs531728837	chr4:79663127-79663128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542162511	chr4:79663144-79663145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561939655	chr4:79663212-79663213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	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
lymphocytic leukemia	21291569	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
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
renal disease	20603712	CNVD
Tracheal agenesis	20877625	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79642800-79662000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:79659400-79662200	Weak transcription	GM12878-XiMat	blood
3	chr4:79659400-79663400	Weak transcription	K562	blood
4	chr4:79660400-79669400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr4:79661200-79663800	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr4:79662200-79664000	Enhancers	GM12878-XiMat	blood
7	chr4:79663400-79663800	Enhancers	K562	blood
8	chr4:79663800-79667400	Weak transcription	K562	blood
9	chr4:79667400-79668400	Enhancers	K562	blood
10	chr4:79667600-79668600	Enhancers	NHLF	lung
11	chr4:79668000-79669400	Enhancers	NHDF-Ad	bronchial
12	chr4:79668200-79670000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr4:79668400-79669800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:79668400-79670400	Weak transcription	K562	blood
15	chr4:79668400-79671600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:79668600-79669000	Weak transcription	NHLF	lung
17	chr4:79668600-79669400	Enhancers	HSMMtube	muscle
18	chr4:79668600-79671600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:79668800-79669200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr4:79669000-79670200	Enhancers	NHLF	lung
21	chr4:79669000-79670600	Enhancers	Fetal Heart	heart
22	chr4:79669000-79671600	Enhancers	Osteobl	bone
23	chr4:79669200-79669600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr4:79669400-79669600	Flanking Active TSS	NHDF-Ad	bronchial
25	chr4:79669400-79670400	Weak transcription	HSMMtube	muscle
26	chr4:79669400-79675400	Enhancers	Primary B cells from peripheral blood	blood
27	chr4:79669600-79669800	Enhancers	Fetal Intestine Large	intestine
28	chr4:79669600-79669800	Enhancers	NHDF-Ad	bronchial
29	chr4:79669600-79670000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:79669800-79670000	Flanking Active TSS	NHDF-Ad	bronchial
31	chr4:79669800-79670200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:79669800-79670600	Enhancers	GM12878-XiMat	blood
33	chr4:79669800-79670800	Enhancers	Fetal Muscle Leg	muscle
34	chr4:79669800-79670800	Enhancers	Left Ventricle	heart
35	chr4:79669800-79672600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr4:79670000-79671200	Enhancers	NHDF-Ad	bronchial
37	chr4:79670200-79671200	Weak transcription	NHLF	lung
38	chr4:79670200-79671600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:79670200-79675400	Enhancers	Primary B cells from cord blood	blood
40	chr4:79670400-79670600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr4:79670400-79671800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr4:79670400-79671800	Enhancers	HSMMtube	muscle
43	chr4:79670400-79671800	Enhancers	K562	blood
44	chr4:79670400-79672200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr4:79670600-79670800	Flanking Active TSS	Fetal Heart	heart
46	chr4:79670600-79670800	Enhancers	Small Intestine	intestine
47	chr4:79670600-79671600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:79670600-79671600	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr4:79670600-79671800	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr4:79670600-79672000	Flanking Active TSS	GM12878-XiMat	blood

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