Variant report

Variant	nsv888004
Chromosome Location	chr7:48028771-48120717
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1221)
CpG islands
(count:1649)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:48081424-48081554	K562	blood:	n/a	n/a
2	ATF2	chr7:48031202-48031940	GM12878	blood:	n/a	n/a
3	ATF2	chr7:48092434-48092849	GM12878	blood:	n/a	n/a
4	ATF3	chr7:48068531-48068790	K562	blood:	n/a	n/a
5	BACH1	chr7:48087994-48088025	K562	blood:	n/a	n/a
6	BACH1	chr7:48031303-48031850	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:48075420-48075727	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:48113196-48113281	K562	blood:	n/a	n/a
9	BATF	chr7:48031171-48031633	GM12878	blood:	n/a	chr7:48031442-48031451
10	BATF	chr7:48031260-48031569	GM12878	blood:	n/a	chr7:48031442-48031451
11	BATF	chr7:48092544-48092727	GM12878	blood:	n/a	chr7:48092613-48092624
12	BATF	chr7:48092436-48092745	GM12878	blood:	n/a	chr7:48092613-48092624
13	BCL11A	chr7:48031197-48031559	GM12878	blood:	n/a	chr7:48031538-48031551 chr7:48031544-48031553
14	BCL3	chr7:48049543-48049925	GM12878	blood:	n/a	n/a
15	BCLAF1	chr7:48031213-48031801	GM12878	blood:	n/a	chr7:48031538-48031551 chr7:48031595-48031608 chr7:48031544-48031553
16	BCLAF1	chr7:48031104-48031717	GM12878	blood:	n/a	chr7:48031538-48031551 chr7:48031595-48031608 chr7:48031544-48031553
17	BHLHE40	chr7:48092403-48092754	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:48031329-48031724	K562	blood:	n/a	n/a
19	BHLHE40	chr7:48031212-48031930	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:48029287-48029582	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:48086238-48086438	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:48029349-48029522	HepG2	liver:	n/a	n/a
23	BRCA1	chr7:48113796-48114262	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr7:48118175-48118391	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:48075032-48075095	HepG2	liver:	n/a	n/a
26	CBX3	chr7:48031292-48031664	K562	blood:	n/a	n/a
27	CBX3	chr7:48039513-48040288	HCT-116	colon:	n/a	n/a
28	CCNT2	chr7:48031403-48031637	K562	blood:	n/a	n/a
29	CEBPB	chr7:48106985-48107475	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:48068547-48068900	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:48068549-48068903	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:48039074-48039302	MCF-7	breast:	n/a	chr7:48039185-48039196
33	CEBPB	chr7:48071788-48072064	HepG2	liver:	n/a	chr7:48071936-48071947
34	CEBPB	chr7:48039043-48039287	A549	lung:	n/a	chr7:48039185-48039196
35	CEBPB	chr7:48039111-48039346	IMR90	lung:	n/a	chr7:48039185-48039196
36	CEBPB	chr7:48092218-48092809	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr7:48074997-48075088	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:48039033-48039347	A549	lung:	n/a	chr7:48039185-48039196
39	CEBPB	chr7:48039080-48039329	Hela-S3	cervix:	n/a	chr7:48039185-48039196
40	CEBPB	chr7:48113512-48114366	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:48117818-48118417	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:48087765-48088082	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:48039108-48039349	HepG2	liver:	n/a	chr7:48039185-48039196
44	CEBPB	chr7:48039040-48039349	H1-hESC	embryonic stem cell:	n/a	chr7:48039185-48039196
45	CEBPB	chr7:48081824-48082161	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:48039836-48040130	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:48031326-48031539	GM12878	blood:	n/a	n/a
48	CEBPB	chr7:48039025-48039342	K562	blood:	n/a	chr7:48039185-48039196
49	CEBPB	chr7:48068543-48068895	K562	blood:	n/a	n/a
50	CEBPB	chr7:48099327-48099495	HepG2	liver:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48075316-48075366	HCPEpiC	choroid plexus:	n/a
2	chr7:48071778-48071828	HNPCEpiC	eye:	n/a
3	chr7:48075316-48075366	HCPEpiC	choroid plexus:	n/a
4	chr7:48071778-48071828	HNPCEpiC	eye:	n/a
5	chr7:48075787-48075837	HRCEpiC	kidney:	n/a
6	chr7:48074771-48074821	LNCaP	prostate:	n/a
7	chr7:48073694-48073744	BJ	skin:	n/a
8	chr7:48081031-48081081	AG09319	gingival:	n/a
9	chr7:48081031-48081081	AG10803	skin:	n/a
10	chr7:48108684-48108734	HNPCEpiC	eye:	n/a
11	chr7:48083826-48083876	U87	brain:	n/a
12	chr7:48031468-48031518	Hepatocyte	liver:	n/a
13	chr7:48031468-48031518	K562	blood:	n/a
14	chr7:48081031-48081081	NHBE	bronchial:	n/a
15	chr7:48031559-48031609	U87	brain:	n/a
16	chr7:48069745-48069795	MCF-7	breast:	n/a
17	chr7:48069745-48069795	SK-N-SH	brain:	n/a
18	chr7:48074093-48074143	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:48108684-48108734	Hepatocyte	liver:	n/a
20	chr7:48075844-48075894	MCF10A-Er-Src	breast:	n/a
21	chr7:48073694-48073744	MCF10A-Er-Src	breast:	n/a
22	chr7:48075568-48075618	HL-60	blood:	n/a
23	chr7:48031468-48031518	AG09319	gingival:	n/a
24	chr7:48109763-48109813	HRCEpiC	kidney:	n/a
25	chr7:48074093-48074143	T-47D	breast:	n/a
26	chr7:48075128-48075178	H1-hESC	embryonic stem cell:	embryo
27	chr7:48068321-48068371	HMEC	breast:	n/a
28	chr7:48069745-48069795	HEK293	kidney:	embryo
29	chr7:48075568-48075618	A549	lung:	n/a
30	chr7:48068728-48068778	HEK293	kidney:	embryo
31	chr7:48075568-48075618	LNCaP	prostate:	n/a
32	chr7:48031559-48031609	HEK293	kidney:	embryo
33	chr7:48074771-48074821	HCM	heart:	n/a
34	chr7:48044273-48044323	Caco-2	colon:	n/a
35	chr7:48076004-48076054	HEK293	kidney:	embryo
36	chr7:48074771-48074821	NB4	blood:	n/a
37	chr7:48073694-48073744	GM12892	blood:	n/a
38	chr7:48075128-48075178	AoSMC	blood vessel:	n/a
39	chr7:48075128-48075178	ovcar-3	ovarian:	n/a
40	chr7:48073694-48073744	LNCaP	prostate:	n/a
41	chr7:48068758-48068808	HCT-116	colon:	n/a
42	chr7:48073694-48073744	IMR90	lung:	fetal
43	chr7:48075316-48075366	MCF10A-Er-Src	breast:	n/a
44	chr7:48071778-48071828	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:48044273-48044323	HCT-116	colon:	n/a
46	chr7:48075787-48075837	HEK293	kidney:	embryo
47	chr7:48031468-48031518	GM19239	blood:	n/a
48	chr7:48068728-48068778	HRCEpiC	kidney:	n/a
49	chr7:48076004-48076054	HL-60	blood:	n/a
50	chr7:48075950-48076000	AG09309	skin:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:48030749..48032126-chr7:48149476..48150428,18	MCF-7	breast:
2	chr7:48032161..48032696-chr7:48149524..48150293,2	MCF-7	breast:
3	chr7:48029675..48031702-chr7:48142721..48144419,2	MCF-7	breast:
4	chr7:48103688..48106218-chr7:48110783..48112306,2	K562	blood:
5	chr7:48099152..48101253-chr7:48106756..48108759,2	K562	blood:
6	chr7:48080536..48082874-chr7:48084498..48087203,2	MCF-7	breast:
7	chr7:48031095..48033453-chr7:48087493..48089900,2	K562	blood:
8	chr7:48017886..48020914-chr7:48029520..48034474,4	K562	blood:
9	chr7:48102695..48105188-chr7:48109404..48112283,2	K562	blood:
10	chr7:48084214..48085770-chr7:48090694..48092571,2	K562	blood:
11	chr7:48016931..48018822-chr7:48064700..48066889,2	K562	blood:
12	chr7:48017992..48020587-chr7:48035794..48038277,2	K562	blood:
13	chr7:48031086..48031966-chr7:48194039..48195056,3	MCF-7	breast:
14	chr7:48016950..48019113-chr7:48039129..48042039,2	K562	blood:
15	chr7:48072450..48075424-chr7:48078443..48080669,2	K562	blood:
16	chr7:48031394..48031943-chr7:48194189..48194981,3	MCF-7	breast:
17	chr7:48031501..48032431-chr7:48127706..48128521,2	MCF-7	breast:
18	chr7:48066136..48067682-chr7:48095170..48098073,2	K562	blood:
19	chr7:48084214..48085770-chr7:48090694..48092571,2	K562	blood:
20	chr7:48099152..48101253-chr7:48106756..48108759,2	K562	blood:
21	chr7:48044680..48047190-chr7:48067195..48070779,3	K562	blood:
22	chr7:48031057..48031968-chr7:48149640..48150841,6	MCF-7	breast:
23	chr7:48016045..48020914-chr7:48030569..48033658,6	K562	blood:
24	chr7:48076129..48077793-chr7:48082998..48085969,2	K562	blood:
25	chr7:48102695..48105188-chr7:48109404..48112283,2	K562	blood:
26	chr7:48066136..48067682-chr7:48095170..48098073,2	K562	blood:
27	chr7:48080536..48082874-chr7:48084498..48087203,2	MCF-7	breast:
28	chr7:48017992..48020478-chr7:48035794..48038589,2	K562	blood:
29	chr7:48044680..48047190-chr7:48067195..48070779,3	K562	blood:
30	chr7:48076129..48077793-chr7:48082998..48085969,2	K562	blood:
31	chr7:48031095..48033453-chr7:48087493..48089900,2	K562	blood:
32	chr7:48103688..48106218-chr7:48110783..48112306,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUN3-1	chr7:48120412-48120592	XLOC_006436

No data

Variant related genes	Relation type
SUN3	TF binding region
C7orf57	TF binding region
SUN3	CpG island
C7orf57	CpG island
ENSG00000136273	chromatin interactions
ENSG00000164746	chromatin interactions
ENSG00000164744	chromatin interactions
ENSG00000183696	chromatin interactions

Extended variants
information (count: 3112 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:3112 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10279520	chr7:48028771-48028772	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112520622	chr7:48028808-48028809	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs575607898	chr7:48028856-48028857	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs544537192	chr7:48028886-48028887	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs148713585	chr7:48028925-48028926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142289282	chr7:48028926-48028927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547203569	chr7:48028975-48028976	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146747972	chr7:48028976-48028977	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs528165656	chr7:48029040-48029041	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555141958	chr7:48029083-48029084	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs548322342	chr7:48029175-48029176	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs187790589	chr7:48029185-48029186	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs537055646	chr7:48029204-48029205	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs140411371	chr7:48029314-48029315	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs11763527	chr7:48029426-48029427	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs543526357	chr7:48029427-48029428	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs75516317	chr7:48029440-48029441	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs540971004	chr7:48029445-48029446	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs79431398	chr7:48029483-48029484	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs202168101	chr7:48029572-48029573	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200361492	chr7:48029585-48029586	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572719697	chr7:48029605-48029606	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535520982	chr7:48029607-48029608	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201381543	chr7:48029642-48029643	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs386712950	chr7:48029646-48029647	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs146484547	chr7:48029647-48029648	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370112531	chr7:48029659-48029660	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs28880325	chr7:48029668-48029669	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs367867478	chr7:48029671-48029672	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs540977831	chr7:48029678-48029679	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs544586734	chr7:48029679-48029680	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs150109888	chr7:48029686-48029687	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs578244659	chr7:48029722-48029723	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs540953111	chr7:48029727-48029728	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs375781336	chr7:48029781-48029782	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs559093565	chr7:48029783-48029784	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs192138558	chr7:48029806-48029807	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs547931139	chr7:48029818-48029819	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561816485	chr7:48029842-48029843	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530559313	chr7:48029865-48029866	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs202192170	chr7:48029915-48029916	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs199803161	chr7:48029926-48029927	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184221947	chr7:48029928-48029929	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570391240	chr7:48029946-48029947	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372731173	chr7:48029947-48029948	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs148816448	chr7:48029952-48029953	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559595102	chr7:48029969-48029970	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200913227	chr7:48029971-48029972	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200346932	chr7:48029972-48029973	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs374873077	chr7:48030023-48030024	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Abnormal phenotypes	18644119	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48019400-48028800	Weak transcription	Fetal Lung	lung
2	chr7:48019800-48031600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:48023200-48031200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:48024200-48030800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:48027600-48029400	Weak transcription	Placenta	Placenta
6	chr7:48028200-48029000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr7:48028200-48029600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:48028400-48031200	Enhancers	HepG2	liver
9	chr7:48028600-48028800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr7:48028600-48029000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:48028600-48029000	Enhancers	A549	lung
12	chr7:48028600-48029400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:48028600-48029800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:48028600-48029800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:48028600-48030000	Enhancers	Fetal Intestine Large	intestine
16	chr7:48028800-48029000	Enhancers	Fetal Lung	lung
17	chr7:48028800-48030000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:48028800-48030000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr7:48028800-48030800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr7:48029000-48030800	Weak transcription	A549	lung
21	chr7:48029000-48031000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr7:48029000-48031200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr7:48029000-48031200	Weak transcription	Fetal Lung	lung
24	chr7:48029400-48029800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr7:48029400-48029800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:48029400-48030200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:48029400-48030200	Enhancers	Placenta	Placenta
28	chr7:48029400-48030800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr7:48029600-48030000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr7:48029600-48030200	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr7:48029800-48030000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr7:48029800-48030000	Enhancers	Fetal Intestine Small	intestine
33	chr7:48029800-48030400	Enhancers	Primary hematopoietic stem cells	blood
34	chr7:48029800-48031000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr7:48029800-48031200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:48029800-48031200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:48030000-48030200	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr7:48030000-48030200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:48030000-48030200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:48030000-48031000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr7:48030000-48031000	Weak transcription	Fetal Intestine Large	intestine
42	chr7:48030000-48031200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr7:48030000-48031200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr7:48030000-48031200	Weak transcription	Fetal Intestine Small	intestine
45	chr7:48030200-48030800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr7:48030200-48030800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr7:48030200-48030800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:48030200-48031000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr7:48030200-48031000	Weak transcription	Placenta	Placenta
50	chr7:48030200-48031200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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