Variant report

Variant	nsv1010552
Chromosome Location	chr4:76064415-76325430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:76294711-76294852	K562	blood:	n/a	n/a
2	ATF2	chr4:76097665-76098276	GM12878	blood:	n/a	n/a
3	ATF2	chr4:76097733-76098242	GM12878	blood:	n/a	n/a
4	BACH1	chr4:76282966-76282978	K562	blood:	n/a	n/a
5	BATF	chr4:76097808-76098155	GM12878	blood:	n/a	chr4:76097965-76097976
6	BATF	chr4:76097783-76098119	GM12878	blood:	n/a	chr4:76097965-76097976
7	BCL11A	chr4:76097809-76098050	GM12878	blood:	n/a	n/a
8	BCL3	chr4:76097780-76098198	GM12878	blood:	n/a	n/a
9	BCL3	chr4:76215762-76216089	GM12878	blood:	n/a	n/a
10	BCLAF1	chr4:76214975-76215350	GM12878	blood:	n/a	chr4:76215329-76215338
11	BCLAF1	chr4:76160642-76161160	GM12878	blood:	n/a	n/a
12	BCLAF1	chr4:76097714-76098283	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:76160759-76161128	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:76097826-76098078	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:76162598-76162604	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:76176975-76177159	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:76106466-76106496	GM12878	blood:	n/a	n/a
18	CEBPB	chr4:76064706-76064901	HepG2	liver:	n/a	chr4:76064818-76064829
19	CEBPB	chr4:76264522-76264645	HepG2	liver:	n/a	chr4:76264549-76264560
20	CEBPB	chr4:76319825-76319934	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:76319796-76319943	K562	blood:	n/a	n/a
22	CEBPB	chr4:76321097-76321297	IMR90	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
23	CEBPB	chr4:76155962-76156162	HepG2	liver:	n/a	chr4:76156061-76156072 chr4:76156060-76156073
24	CEBPB	chr4:76321118-76321291	K562	blood:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
25	CEBPB	chr4:76115753-76115953	HepG2	liver:	n/a	chr4:76115809-76115820
26	CEBPB	chr4:76182671-76182956	HepG2	liver:	n/a	chr4:76182813-76182824
27	CEBPB	chr4:76321079-76321193	A549	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
28	CEBPB	chr4:76321013-76321304	HepG2	liver:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
29	CHD2	chr4:76176662-76177028	GM12878	blood:	n/a	n/a
30	CHD2	chr4:76106489-76106715	GM12878	blood:	n/a	n/a
31	CHD2	chr4:76160783-76161070	GM12878	blood:	n/a	n/a
32	CREB1	chr4:76097705-76098333	GM12878	blood:	n/a	n/a
33	CTCF	chr4:76215056-76215336	HepG2	liver:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
34	CTCF	chr4:76215160-76215310	K562	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
35	CTCF	chr4:76215180-76215330	NHEK	skin:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
36	CTCF	chr4:76215120-76215270	HPAF	blood vessel:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
37	CTCF	chr4:76215110-76215327	GM19239	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
38	CTCF	chr4:76215074-76215334	GM12878	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
39	CTCF	chr4:76215114-76215313	HepG2	liver:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
40	CTCF	chr4:76215160-76215310	BE2_C	brain:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
41	CTCF	chr4:76215160-76215310	Caco-2	colon:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
42	CTCF	chr4:76215120-76215270	SAEC	small airway:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
43	CTCF	chr4:76232560-76232710	GM12875	blood:	n/a	n/a
44	CTCF	chr4:76296510-76296576	Lung_OC	lung:	n/a	n/a
45	CTCF	chr4:76215140-76215290	GM12874	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
46	CTCF	chr4:76215084-76215329	LNCaP	prostate:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
47	CTCF	chr4:76215120-76215270	HEK293	kidney:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
48	CTCF	chr4:76215160-76215310	GM12871	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
49	CTCF	chr4:76215094-76215323	LNCaP	prostate:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
50	CTCF	chr4:76215160-76215310	GM12866	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76094406-76094456	NHDF-neo	bronchial:	n/a
2	chr4:76094406-76094456	NHDF-neo	bronchial:	n/a
3	chr4:76317967-76318017	HCPEpiC	choroid plexus:	n/a
4	chr4:76317967-76318017	GM12878	blood:	n/a
5	chr4:76201532-76201582	IMR90	lung:	fetal
6	chr4:76317967-76318017	NT2-D1	testis:	n/a
7	chr4:76201532-76201582	AG04449	skin:	fetal
8	chr4:76317967-76318017	HCF	heart:	n/a
9	chr4:76094406-76094456	U87	brain:	n/a
10	chr4:76201532-76201582	NH-A	brain:	n/a
11	chr4:76264560-76264610	HRCEpiC	kidney:	n/a
12	chr4:76201532-76201582	AG10803	skin:	n/a
13	chr4:76094406-76094456	HEEpiC	esophagus:	n/a
14	chr4:76201532-76201582	CMK	blood:	n/a
15	chr4:76317967-76318017	PANC-1	pancreas:	n/a
16	chr4:76264560-76264610	HepG2	liver:	n/a
17	chr4:76264560-76264610	ovcar-3	ovarian:	n/a
18	chr4:76094406-76094456	SAEC	small airway:	n/a
19	chr4:76094406-76094456	T-47D	breast:	n/a
20	chr4:76094406-76094456	HNPCEpiC	eye:	n/a
21	chr4:76201532-76201582	HMEC	breast:	n/a
22	chr4:76094406-76094456	PrEC	prostate:	n/a
23	chr4:76094406-76094456	HIPEpiC	eye:	n/a
24	chr4:76264560-76264610	AG04449	skin:	fetal
25	chr4:76264560-76264610	HNPCEpiC	eye:	n/a
26	chr4:76264560-76264610	SAEC	small airway:	n/a
27	chr4:76094406-76094456	PANC-1	pancreas:	n/a
28	chr4:76264560-76264610	PrEC	prostate:	n/a
29	chr4:76264560-76264610	IMR90	lung:	fetal
30	chr4:76264560-76264610	AG04450	lung:	fetal
31	chr4:76317967-76318017	SK-N-SH	brain:	n/a
32	chr4:76317967-76318017	RPTEC	kidney:	n/a
33	chr4:76317967-76318017	AG09309	skin:	n/a
34	chr4:76264560-76264610	ProgFib	skin:	n/a
35	chr4:76264560-76264610	HUVEC	blood vessel:	n/a
36	chr4:76201532-76201582	Hepatocyte	liver:	n/a
37	chr4:76317967-76318017	LNCaP	prostate:	n/a
38	chr4:76317967-76318017	HEEpiC	esophagus:	n/a
39	chr4:76201532-76201582	Caco-2	colon:	n/a
40	chr4:76317967-76318017	GM12891	blood:	n/a
41	chr4:76264560-76264610	A549	lung:	n/a
42	chr4:76264560-76264610	HRPEpiC	eye:	n/a
43	chr4:76094406-76094456	AG04449	skin:	fetal
44	chr4:76094406-76094456	AoSMC	blood vessel:	n/a
45	chr4:76264560-76264610	HCF	heart:	n/a
46	chr4:76317967-76318017	HepG2	liver:	n/a
47	chr4:76094406-76094456	HepG2	liver:	n/a
48	chr4:76094406-76094456	NH-A	brain:	n/a
49	chr4:76094406-76094456	RPTEC	kidney:	n/a
50	chr4:76201532-76201582	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:76278035..76280636-chr4:76286764..76289463,2	K562	blood:
2	chr4:75857312..75858654-chr4:76214491..76215648,6	MCF-7	breast:
3	chr4:76157900..76160186-chr4:76160189..76163164,2	MCF-7	breast:
4	chr4:75718643..75719283-chr4:76213272..76214122,2	MCF-7	breast:
5	chr4:76178186..76180045-chr4:76183353..76185602,2	K562	blood:
6	chr4:75185612..75186157-chr4:76214776..76215513,2	MCF-7	breast:
7	chr4:76210768..76213178-chr4:76214495..76216137,2	K562	blood:
8	chr4:76066196..76069531-chr4:76069851..76072934,4	K562	blood:
9	chr4:76229171..76231861-chr4:76436993..76438920,2	MCF-7	breast:
10	chr4:76214761..76215324-chr4:76498679..76499192,2	MCF-7	breast:
11	chr4:76277770..76280636-chr4:76287963..76290651,3	K562	blood:
12	chr4:76066196..76069531-chr4:76069851..76072934,4	K562	blood:
13	chr4:76157900..76160186-chr4:76160189..76163164,2	MCF-7	breast:
14	chr4:75799685..75800426-chr4:76215952..76216615,2	MCF-7	breast:
15	chr4:76115478..76117516-chr4:76118088..76119671,2	MCF-7	breast:
16	chr4:76115478..76117516-chr4:76118088..76119671,2	MCF-7	breast:
17	chr4:76178186..76180045-chr4:76183353..76185602,2	K562	blood:
18	chr4:76210768..76213178-chr4:76214495..76216137,2	K562	blood:
19	chr4:75799924..75800563-chr4:76214703..76215703,2	MCF-7	breast:
20	chr4:75857716..75858592-chr4:76214836..76215509,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THAP6-2	chr4:76286934-76287774	XLOC_003576
2	lnc-RCHY1-7	chr4:76113725-76113875	ucscGeneNc_uc003hii_2
3	lnc-PARM1-5	chr4:76120077-76120289	NONHSAT096914
4	lnc-RCHY1-1	chr4:76286417-76286557	XLOC_003988
5	lnc-RCHY1-2	chr4:76272507-76272663	XLOC_003987
6	lnc-RCHY1-2	chr4:76266672-76266847	XLOC_003987
7	lnc-THAP6-2	chr4:76279286-76279325	ENSG00000251383
8	lnc-THAP6-2	chr4:76283191-76283380	XLOC_003576
9	lnc-THAP6-2	chr4:76286934-76287776	ENSG00000251383
10	lnc-RCHY1-7	chr4:76114521-76114596	ucscGeneNc_uc003hii_2
11	lnc-THAP6-2	chr4:76283191-76283380	ENSG00000251383
12	lnc-THAP6-2	chr4:76279286-76279325	XLOC_003576
13	lnc-RCHY1-6	chr4:76322898-76323124	l_2668_chr4:76322897-76324689_adipose
14	lnc-RCHY1-3	chr4:76286352-76286392	XLOC_003986
15	lnc-RCHY1-7	chr4:76110978-76111910	ucscGeneNc_uc003hii_2
16	lnc-RCHY1-7	chr4:76100209-76101593	ucscGeneNc_uc003hii_2
17	lnc-THAP6-2	chr4:76280531-76280597	XLOC_003576
18	lnc-RCHY1-3	chr4:76194278-76194705	XLOC_003986
19	lnc-THAP6-2	chr4:76283191-76283545	XLOC_003576
20	lnc-THAP6-2	chr4:76280528-76280597	ENSG00000251383
21	lnc-THAP6-2	chr4:76280528-76280597	XLOC_003576
22	lnc-RCHY1-6	chr4:76324645-76324689	l_2668_chr4:76322897-76324689_adipose
23	lnc-RCHY1-2	chr4:76266489-76266522	XLOC_003987
24	lnc-RCHY1-2	chr4:76284180-76284234	XLOC_003987

Variant related genes	Relation type
ENSG00000250560	TF binding region
ENSG00000250735	TF binding region
ENSG00000251383	TF binding region
ENSG00000251185	TF binding region
ENSG00000251454	TF binding region
ENSG00000250560	CpG island
ENSG00000250735	CpG island
ENSG00000251383	CpG island
ENSG00000251185	CpG island
ENSG00000251454	CpG island
ENSG00000251383	chromatin interactions
ENSG00000169116	chromatin interactions
ESYT1	miRNA target sites
ANXA5	miRNA target sites
IL6R	miRNA target sites
ESRRA	miRNA target sites

Extended variants
information (count: 5355 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5355 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550006988	chr4:76067004-76067005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374869778	chr4:76067035-76067036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149673148	chr4:76067053-76067054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545765326	chr4:76067055-76067056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560612198	chr4:76067147-76067148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535411350	chr4:76067167-76067168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547396649	chr4:76067183-76067184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565817951	chr4:76067217-76067218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539532596	chr4:76067218-76067219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147759693	chr4:76067220-76067221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141241461	chr4:76067259-76067260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577321690	chr4:76067327-76067328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538166774	chr4:76067360-76067361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556782789	chr4:76067390-76067391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1497223	chr4:76067391-76067392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72662465	chr4:76067419-76067420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541855129	chr4:76067424-76067425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116388975	chr4:76067444-76067445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572251436	chr4:76067448-76067449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546230549	chr4:76067451-76067452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564132961	chr4:76067507-76067508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531498078	chr4:76067547-76067548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542110178	chr4:76067555-76067556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549825789	chr4:76067563-76067564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79037464	chr4:76067564-76067565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371321000	chr4:76067574-76067575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527870005	chr4:76067575-76067576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541173619	chr4:76067597-76067598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565677617	chr4:76067599-76067600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146954314	chr4:76067629-76067630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551415693	chr4:76067632-76067633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147731139	chr4:76067672-76067673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190508510	chr4:76067673-76067674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556463833	chr4:76067682-76067683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149185031	chr4:76067696-76067697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75728055	chr4:76067704-76067705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553753037	chr4:76067721-76067722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572066048	chr4:76067777-76067778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143410181	chr4:76067791-76067792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564572905	chr4:76067794-76067795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182329494	chr4:76067844-76067845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543638752	chr4:76067897-76067898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141560562	chr4:76067939-76067940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76383248	chr4:76067963-76067964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184698209	chr4:76067968-76067969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145639575	chr4:76068008-76068009	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs532924237	chr4:76068011-76068012	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs374270514	chr4:76068031-76068032	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs189065536	chr4:76068040-76068041	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs373416225	chr4:76068064-76068065	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-small cell lung cancer	21829676	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD
Autism	18414403	CNVD

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76067000-76067200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:76067000-76068000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:76067200-76067800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:76067200-76069000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:76067200-76069400	Enhancers	NHDF-Ad	bronchial
6	chr4:76067400-76068400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:76067400-76068800	Enhancers	HSMM	muscle
8	chr4:76067400-76069600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:76067600-76068800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:76067800-76068800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:76068000-76068600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:76068000-76068800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:76068000-76069000	Enhancers	HSMMtube	muscle
14	chr4:76068200-76068400	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr4:76068800-76069000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:76069000-76069200	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr4:76069400-76070400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:76069600-76070400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:76069600-76070400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:76069800-76070600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:76070000-76070400	Enhancers	H9 Cell Line	embryonic stem cell
22	chr4:76070000-76070400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:76071000-76071200	Enhancers	Aorta	Aorta
24	chr4:76071200-76072000	Enhancers	Fetal Heart	heart
25	chr4:76079200-76079600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:76081200-76081800	ZNF genes & repeats	Spleen	Spleen
27	chr4:76083200-76084600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr4:76092400-76092600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr4:76092600-76093200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr4:76092600-76093400	Enhancers	H9 Cell Line	embryonic stem cell
31	chr4:76092600-76093400	Enhancers	Fetal Muscle Leg	muscle
32	chr4:76092600-76094200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr4:76092800-76093000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr4:76092800-76095000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:76093000-76093200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:76093000-76093400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:76093200-76093400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr4:76093200-76094000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:76093200-76094200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:76093200-76094200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:76093400-76093800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr4:76093400-76094400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr4:76093400-76097800	Weak transcription	Fetal Muscle Leg	muscle
44	chr4:76093600-76094600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:76093600-76095000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:76093800-76094000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:76093800-76094000	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr4:76093800-76095600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr4:76094000-76094600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:76094000-76094800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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