Variant report

Variant	nsv539118
Chromosome Location	chr7:125897362-126225444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:807)
CpG islands
(count:122)
Chromatin interactive
region (count:50)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:126148916-126149043	K562	blood:	n/a	n/a
2	ATF1	chr7:126019383-126019479	K562	blood:	n/a	n/a
3	BACH1	chr7:125897717-125897800	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:126171883-126172029	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:126120721-126120800	K562	blood:	n/a	n/a
6	BATF	chr7:126197396-126197676	GM12878	blood:	n/a	n/a
7	BATF	chr7:126084070-126084326	GM12878	blood:	n/a	chr7:126084174-126084185
8	BATF	chr7:126141768-126142023	GM12878	blood:	n/a	n/a
9	BATF	chr7:126197301-126197638	GM12878	blood:	n/a	n/a
10	BATF	chr7:125970249-125970459	GM12878	blood:	n/a	n/a
11	BCL3	chr7:126210938-126211178	GM12878	blood:	n/a	n/a
12	BCL3	chr7:126214341-126214807	A549	lung:	n/a	chr7:126214764-126214773 chr7:126214576-126214585
13	BCLAF1	chr7:126090235-126090798	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:126090272-126090898	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:125939440-125939499	HepG2	liver:	n/a	n/a
16	BHLHE40	chr7:126018785-126018989	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:126051887-126051999	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:126185104-126185110	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:126089835-126090907	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:125970725-125970731	GM12878	blood:	n/a	n/a
21	BRCA1	chr7:126090013-126090032	GM12878	blood:	n/a	n/a
22	BRCA1	chr7:126090538-126090546	GM12878	blood:	n/a	n/a
23	CCNT2	chr7:126134074-126134168	K562	blood:	n/a	n/a
24	CCNT2	chr7:126151253-126151311	K562	blood:	n/a	n/a
25	CCNT2	chr7:126099340-126099539	K562	blood:	n/a	n/a
26	CEBPB	chr7:126035277-126035444	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:126122640-126122937	K562	blood:	n/a	chr7:126122780-126122791
28	CEBPB	chr7:126084073-126084284	Hela-S3	cervix:	n/a	chr7:126084085-126084096
29	CEBPB	chr7:126159627-126159904	HepG2	liver:	n/a	chr7:126159770-126159781 chr7:126159769-126159782
30	CEBPB	chr7:126042044-126042349	Hela-S3	cervix:	n/a	chr7:126042182-126042193
31	CEBPB	chr7:126100594-126100794	H1-hESC	embryonic stem cell:	n/a	chr7:126100653-126100666 chr7:126100655-126100664 chr7:126100653-126100664 chr7:126100655-126100666
32	CEBPB	chr7:125940807-125941138	IMR90	lung:	n/a	chr7:125940980-125940991
33	CEBPB	chr7:126039435-126039635	A549	lung:	n/a	n/a
34	CEBPB	chr7:126100471-126100834	HepG2	liver:	n/a	chr7:126100653-126100666 chr7:126100655-126100664 chr7:126100653-126100664 chr7:126100655-126100666
35	CEBPB	chr7:126042119-126042350	H1-hESC	embryonic stem cell:	n/a	chr7:126042182-126042193
36	CEBPB	chr7:125940813-125941159	A549	lung:	n/a	chr7:125940980-125940991
37	CEBPB	chr7:126042010-126042361	HepG2	liver:	n/a	chr7:126042182-126042193
38	CEBPB	chr7:126077316-126077456	HepG2	liver:	n/a	chr7:126077404-126077415
39	CEBPB	chr7:126122603-126122918	IMR90	lung:	n/a	chr7:126122780-126122791
40	CEBPB	chr7:125901758-125901932	HepG2	liver:	n/a	chr7:125901796-125901807
41	CEBPB	chr7:125948022-125948265	HepG2	liver:	n/a	chr7:125948111-125948124 chr7:125948111-125948122 chr7:125948111-125948124 chr7:125948113-125948124
42	CEBPB	chr7:126100510-126100809	K562	blood:	n/a	chr7:126100653-126100666 chr7:126100655-126100664 chr7:126100653-126100664 chr7:126100655-126100666
43	CEBPB	chr7:125931700-125931980	HepG2	liver:	n/a	chr7:125931849-125931860
44	CEBPB	chr7:126122626-126122947	HepG2	liver:	n/a	chr7:126122780-126122791
45	CEBPB	chr7:126068332-126068651	IMR90	lung:	n/a	chr7:126068481-126068492
46	CEBPB	chr7:126024630-126024852	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:125982558-125982859	HepG2	liver:	n/a	chr7:125982678-125982691 chr7:125982679-125982690
48	CEBPB	chr7:126159752-126159820	K562	blood:	n/a	chr7:126159770-126159781 chr7:126159769-126159782
49	CEBPB	chr7:126122653-126122853	H1-hESC	embryonic stem cell:	n/a	chr7:126122780-126122791
50	CEBPB	chr7:125940858-125941152	HepG2	liver:	n/a	chr7:125940980-125940991

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126165242-126165292	LNCaP	prostate:	n/a
2	chr7:126165242-126165292	IMR90	lung:	fetal
3	chr7:126079083-126079133	NH-A	brain:	n/a
4	chr7:126079083-126079133	HCPEpiC	choroid plexus:	n/a
5	chr7:126079083-126079133	AG09319	gingival:	n/a
6	chr7:126165242-126165292	ovcar-3	ovarian:	n/a
7	chr7:126079083-126079133	AG04450	lung:	fetal
8	chr7:126165242-126165292	NH-A	brain:	n/a
9	chr7:126165242-126165292	AG09309	skin:	n/a
10	chr7:126165242-126165292	SK-N-MC	brain:	n/a
11	chr7:126165242-126165292	NHBE	bronchial:	n/a
12	chr7:126165242-126165292	NHDF-neo	bronchial:	n/a
13	chr7:126165242-126165292	Caco-2	colon:	n/a
14	chr7:126165242-126165292	K562	blood:	n/a
15	chr7:126079083-126079133	PFSK-1	brain:	n/a
16	chr7:126165242-126165292	Hepatocyte	liver:	n/a
17	chr7:126079083-126079133	HCF	heart:	n/a
18	chr7:126165242-126165292	NT2-D1	testis:	n/a
19	chr7:126079083-126079133	T-47D	breast:	n/a
20	chr7:126079083-126079133	HEK293	kidney:	embryo
21	chr7:126079083-126079133	NB4	blood:	n/a
22	chr7:126079083-126079133	SK-N-SH	brain:	n/a
23	chr7:126079083-126079133	SK-N-SH_RA	brain:	n/a
24	chr7:126079083-126079133	Hela-S3	cervix:	n/a
25	chr7:126165242-126165292	HAEpiC	amniotic membrane:	n/a
26	chr7:126079083-126079133	HAEpiC	amniotic membrane:	n/a
27	chr7:126165242-126165292	CMK	blood:	n/a
28	chr7:126165242-126165292	HMEC	breast:	n/a
29	chr7:126165242-126165292	Jurkat	blood:	n/a
30	chr7:126079083-126079133	CMK	blood:	n/a
31	chr7:126079083-126079133	PANC-1	pancreas:	n/a
32	chr7:126165242-126165292	AG10803	skin:	n/a
33	chr7:126165242-126165292	T-47D	breast:	n/a
34	chr7:126165242-126165292	GM12878	blood:	n/a
35	chr7:126165242-126165292	Hela-S3	cervix:	n/a
36	chr7:126165242-126165292	HIPEpiC	eye:	n/a
37	chr7:126079083-126079133	SK-N-MC	brain:	n/a
38	chr7:126079083-126079133	HL-60	blood:	n/a
39	chr7:126165242-126165292	HNPCEpiC	eye:	n/a
40	chr7:126079083-126079133	NT2-D1	testis:	n/a
41	chr7:126165242-126165292	AG04449	skin:	fetal
42	chr7:126079083-126079133	HMEC	breast:	n/a
43	chr7:126165242-126165292	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:126165242-126165292	HCT-116	colon:	n/a
45	chr7:126165242-126165292	HEEpiC	esophagus:	n/a
46	chr7:126165242-126165292	AoSMC	blood vessel:	n/a
47	chr7:126165242-126165292	GM06990	blood:	n/a
48	chr7:126165242-126165292	RPTEC	kidney:	n/a
49	chr7:126165242-126165292	SK-N-SH	brain:	n/a
50	chr7:126079083-126079133	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:126104127..126105778-chr7:126106556..126109113,2	K562	blood:
2	7:126177569-126189146..7:127221502-127225864	Hela-S3	cervix:
3	chr7:126206442..126209218-chr7:126210188..126212895,2	K562	blood:
4	chr7:126028745..126031381-chr7:126035464..126038065,3	K562	blood:
5	chr7:125990319..125992216-chr7:125992809..125995290,2	K562	blood:
6	chr7:125938484..125941094-chr7:125943803..125945713,2	K562	blood:
7	chr7:126206442..126209218-chr7:126210188..126212895,2	K562	blood:
8	chr7:126121758..126123459-chr7:126162475..126164735,2	K562	blood:
9	chr7:126028745..126031381-chr7:126035464..126038065,3	K562	blood:
10	7:126177569-126189146..7:126890676-126899918	K562	blood:
11	chr7:126181175..126183818-chr7:126200228..126202608,2	K562	blood:
12	7:126177569-126189146..7:127225864-127233104	GM12878	blood:
13	chr7:125961680..125963760-chr7:125965307..125968021,2	K562	blood:
14	7:126148685-126150023..7:126733290-126737485	GM12878	blood:
15	chr1:17231179..17231930-chr7:126210642..126211162,2	MCF-7	breast:
16	chr7:126028745..126031381-chr7:126035464..126037060,2	K562	blood:
17	7:126130122-126133705..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
18	chr7:126121758..126123459-chr7:126162475..126164735,2	K562	blood:
19	chr7:126210096..126212275-chr7:126283884..126286217,2	K562	blood:
20	7:126189146-126195230..7:127221502-127225864	Hela-S3	cervix:
21	chr7:125990319..125992216-chr7:125992809..125995290,2	K562	blood:
22	chr7:125970925..125973009-chr7:125973551..125976319,2	K562	blood:
23	chr7:126198359..126200482-chr7:126202205..126203879,2	K562	blood:
24	chr7:125981506..125983615-chr7:125985975..125988885,2	K562	blood:
25	chr7:125981506..125983615-chr7:125985975..125988885,2	K562	blood:
26	7:126195230-126202280..7:127221502-127225864	Hela-S3	cervix:
27	chr7:125961680..125963760-chr7:125965307..125968021,2	K562	blood:
28	chr7:125970152..125973009-chr7:125974819..125977190,2	K562	blood:
29	7:126177569-126189146..7:127233104-127239235	K562	blood:
30	chr7:126127310..126130214-chr7:126150191..126152367,2	K562	blood:
31	7:126154600-126176992..7:127221502-127225864	Hela-S3	cervix:
32	chr7:125970925..125973009-chr7:125973551..125976319,2	K562	blood:
33	7:126154600-126176992..7:126756671-126761022	H1-hESC	embryonic stem cell:	embryo
34	7:126177569-126189146..7:127070190-127076279	Hela-S3	cervix:
35	chr7:126198359..126200482-chr7:126202205..126203879,2	K562	blood:
36	chr7:126147698..126150261-chr7:126203102..126205183,2	K562	blood:
37	7:126177569-126189146..7:126756671-126761022	K562	blood:
38	7:126154600-126176992..7:127009457-127018926	H1-hESC	embryonic stem cell:	embryo
39	chr1:17231377..17231960-chr7:126210642..126211142,3	MCF-7	breast:
40	chr7:126082404..126082904-chr9:129703018..129703561,2	MCF-7	breast:
41	7:126203116-126207963..7:126880504-126885902	GM12878	blood:
42	chr7:125970152..125973009-chr7:125974819..125977190,2	K562	blood:
43	7:126085913-126088095..7:126213565-126217000	H1-hESC	embryonic stem cell:	embryo
44	chr7:126028745..126031381-chr7:126035464..126037060,2	K562	blood:
45	chr7:126147698..126150261-chr7:126203102..126205183,2	K562	blood:
46	chr7:126136384..126139302-chr7:126250186..126252685,2	K562	blood:
47	chr7:126181175..126183818-chr7:126200228..126202608,2	K562	blood:
48	7:126195230-126202280..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
49	chr7:125938484..125941094-chr7:125943803..125945713,2	K562	blood:
50	7:126133705-126138790..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-17	chr7:126151189-126152933	NONHSAT123118
2	lnc-ARF5-5	chr7:125924175-125924312	XLOC_006235
3	lnc-ARF5-4	chr7:126019024-126019055	XLOC_006236
4	lnc-ARF5-4	chr7:126058290-126058349	XLOC_006236
5	lnc-ARF5-4	chr7:126061118-126061230	XLOC_006236
6	lnc-ARF5-5	chr7:125924175-125924216	XLOC_006235
7	lnc-ARF5-4	chr7:126059887-126059999	XLOC_006236
8	lnc-ARF5-4	chr7:126064175-126064239	XLOC_006236
9	lnc-ARF5-4	chr7:126055283-126055392	XLOC_006236
10	lnc-ARF5-4	chr7:126061482-126061634	XLOC_006236

No data

Variant related genes	Relation type
ENSG00000241921	TF binding region
ENSG00000227249	TF binding region
GRM8	TF binding region
ENSG00000241921	CpG island
ENSG00000227249	CpG island
GRM8	CpG island
ENSG00000227249	chromatin interactions
ENSG00000179603	chromatin interactions
ENSG00000179562	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000048405	chromatin interactions
ENSG00000106328	chromatin interactions
ENSG00000004059	chromatin interactions
FBXW7	miRNA target sites

Extended variants
information (count: 4901 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:4901 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549815024	chr7:125901857-125901858	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs571528237	chr7:125901859-125901860	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs6960672	chr7:125901871-125901872	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs577226814	chr7:125901909-125901910	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs554077906	chr7:125901937-125901938	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs566338621	chr7:125901969-125901970	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs191848202	chr7:125901974-125901975	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs548035524	chr7:125902003-125902004	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs533596771	chr7:125902024-125902025	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs11766257	chr7:125902025-125902026	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs558517448	chr7:125902052-125902053	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146956345	chr7:125902176-125902177	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs182824529	chr7:125902179-125902180	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs79353532	chr7:125904803-125904804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535058561	chr7:125904804-125904805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142042009	chr7:125904823-125904824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371140969	chr7:125904840-125904841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574732713	chr7:125904887-125904888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541983179	chr7:125904963-125904964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73451625	chr7:125905012-125905013	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs116983587	chr7:125905029-125905030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181535358	chr7:125905040-125905041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77857241	chr7:125905041-125905042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs337909	chr7:125905053-125905054	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs540880285	chr7:125905082-125905083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535652599	chr7:125905084-125905085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559089440	chr7:125905091-125905092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529663602	chr7:125905093-125905094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547895640	chr7:125905094-125905095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555970459	chr7:125905148-125905149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185756677	chr7:125905154-125905155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs207468576	chr7:125905166-125905167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs337910	chr7:125905191-125905192	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs140967678	chr7:125905192-125905193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150430665	chr7:125905221-125905222	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs534619757	chr7:125905262-125905263	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs138196281	chr7:125905300-125905301	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs568380596	chr7:125905320-125905321	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs541710768	chr7:125905359-125905360	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs565574307	chr7:125905387-125905388	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs535827091	chr7:125905401-125905402	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs190074851	chr7:125905432-125905433	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs563895771	chr7:125905470-125905471	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs540077649	chr7:125905477-125905478	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs11435812	chr7:125905483-125905484	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs370139237	chr7:125905495-125905496	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs374811471	chr7:125905499-125905500	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs558390568	chr7:125905504-125905505	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs573340250	chr7:125905507-125905508	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs540591904	chr7:125905593-125905594	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Autism	19246517	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:125901800-125902200	Active TSS	GM12878-XiMat	blood
2	chr7:125904800-125905200	Enhancers	Spleen	Spleen
3	chr7:125905200-125905600	Active TSS	Spleen	Spleen
4	chr7:125915200-125916000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:125963800-125964000	Enhancers	Left Ventricle	heart
6	chr7:125966400-125967600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:125967000-125967400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:125999200-125999600	Enhancers	Pancreas	Pancrea
9	chr7:126001200-126001600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:126009800-126010800	ZNF genes & repeats	GM12878-XiMat	blood
11	chr7:126016600-126017200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:126017000-126017400	Enhancers	Adipose Nuclei	Adipose
13	chr7:126017600-126018000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:126018400-126020000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr7:126018600-126019000	Flanking Active TSS	GM12878-XiMat	blood
16	chr7:126038400-126039400	Enhancers	HSMMtube	muscle
17	chr7:126038800-126039600	Enhancers	Fetal Heart	heart
18	chr7:126039000-126039800	Enhancers	GM12878-XiMat	blood
19	chr7:126040800-126041600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:126041600-126042800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:126042800-126043600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:126050200-126050400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr7:126051000-126051600	Active TSS	A549	lung
24	chr7:126051200-126051600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:126051200-126051600	Active TSS	Duodenum Mucosa	Duodenum
26	chr7:126051200-126051800	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr7:126051400-126051600	Active TSS	GM12878-XiMat	blood
28	chr7:126051400-126051600	Enhancers	Hela-S3	cervix
29	chr7:126051400-126052000	Active TSS	Brain Angular Gyrus	brain
30	chr7:126051600-126052000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr7:126051600-126052200	Flanking Active TSS	GM12878-XiMat	blood
32	chr7:126052200-126052400	Enhancers	GM12878-XiMat	blood
33	chr7:126055600-126056000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:126070800-126071200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:126070800-126071400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:126070800-126071600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr7:126071400-126076200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:126076200-126076400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:126076200-126076400	Enhancers	Fetal Heart	heart
40	chr7:126076400-126076600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:126076400-126076800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr7:126076400-126076800	Flanking Active TSS	Fetal Heart	heart
43	chr7:126076400-126077200	Enhancers	Fetal Intestine Large	intestine
44	chr7:126076600-126076800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:126076600-126077200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:126076800-126077000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:126076800-126077400	Enhancers	Fetal Heart	heart
48	chr7:126076800-126081800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr7:126077000-126082000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:126077200-126080200	Weak transcription	Fetal Intestine Large	intestine

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