Variant report

Variant	nsv1009742
Chromosome Location	chr1:180342203-180385459
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	chr1:180379529-180379568	K562	blood:	n/a	n/a
2	ATF1	chr1:180361304-180361367	K562	blood:	n/a	n/a
3	BATF	chr1:180372837-180373078	GM12878	blood:	n/a	n/a
4	CBX3	chr1:180348586-180348968	K562	blood:	n/a	n/a
5	CBX3	chr1:180349374-180349774	K562	blood:	n/a	n/a
6	CBX3	chr1:180385127-180385514	K562	blood:	n/a	n/a
7	CCNT2	chr1:180385308-180385408	K562	blood:	n/a	n/a
8	CEBPB	chr1:180371284-180371457	H1-hESC	embryonic stem cell:	n/a	chr1:180371352-180371361
9	CEBPB	chr1:180376010-180376276	HepG2	liver:	n/a	chr1:180376122-180376134 chr1:180376161-180376172
10	CEBPB	chr1:180381754-180382062	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:180381745-180382056	A549	lung:	n/a	n/a
12	CEBPB	chr1:180381719-180382060	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:180381698-180382027	A549	lung:	n/a	n/a
14	CEBPB	chr1:180381744-180382095	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:180366355-180366681	A549	lung:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
16	CEBPB	chr1:180366360-180366690	IMR90	lung:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
17	CEBPB	chr1:180381696-180382185	MCF-7	breast:	n/a	n/a
18	CEBPB	chr1:180381735-180382093	K562	blood:	n/a	n/a
19	CEBPB	chr1:180366366-180366686	HepG2	liver:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
20	CEBPB	chr1:180351493-180351641	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:180381765-180382042	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:180366370-180366611	MCF-7	breast:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
23	CEBPB	chr1:180366394-180366645	Hela-S3	cervix:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
24	CEBPB	chr1:180366365-180366698	K562	blood:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
25	CEBPB	chr1:180381737-180382098	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr1:180376043-180376273	A549	lung:	n/a	chr1:180376122-180376134 chr1:180376161-180376172
27	CEBPB	chr1:180376077-180376264	K562	blood:	n/a	chr1:180376122-180376134 chr1:180376161-180376172
28	CEBPB	chr1:180381711-180382074	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr1:180381782-180382051	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr1:180381716-180382102	K562	blood:	n/a	n/a
31	CTCF	chr1:180385280-180385430	GM12864	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
32	CTCF	chr1:180385230-180385439	MCF-7	breast:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
33	CTCF	chr1:180371303-180371364	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:180385166-180385497	A549	lung:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
35	CTCF	chr1:180385200-180385350	RPTEC	kidney:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
36	CTCF	chr1:180385260-180385410	AG04450	lung:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
37	CTCF	chr1:180385300-180385450	GM12874	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
38	CTCF	chr1:180385260-180385410	GM12874	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
39	CTCF	chr1:180385200-180385350	GM12872	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
40	CTCF	chr1:180385106-180385591	MCF-7	breast:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
41	CTCF	chr1:180385242-180385455	Kidney_OC	kidney:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
42	CTCF	chr1:180385108-180385568	A549	lung:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
43	CTCF	chr1:180385224-180385482	Lung_OC	lung:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
44	CTCF	chr1:180385300-180385450	BE2_C	brain:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
45	CTCF	chr1:180385240-180385390	HMF	breast:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
46	CTCF	chr1:180385254-180385404	HepG2	liver:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
47	CTCF	chr1:180385300-180385450	GM12872	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
48	CTCF	chr1:180371280-180371430	GM12878	blood:	n/a	n/a
49	CTCF	chr1:180385260-180385410	AG10803	skin:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
50	CTCF	chr1:180356640-180356790	HEEpiC	esophagus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180374455-180374505	HNPCEpiC	eye:	n/a
2	chr1:180374455-180374505	HL-60	blood:	n/a
3	chr1:180374455-180374505	LNCaP	prostate:	n/a
4	chr1:180374455-180374505	AG09319	gingival:	n/a
5	chr1:180374455-180374505	GM12891	blood:	n/a
6	chr1:180374455-180374505	SAEC	small airway:	n/a
7	chr1:180374455-180374505	HCM	heart:	n/a
8	chr1:180374455-180374505	NH-A	brain:	n/a
9	chr1:180374455-180374505	ProgFib	skin:	n/a
10	chr1:180374455-180374505	AG09309	skin:	n/a
11	chr1:180374455-180374505	HEEpiC	esophagus:	n/a
12	chr1:180374455-180374505	SK-N-MC	brain:	n/a
13	chr1:180374455-180374505	HCPEpiC	choroid plexus:	n/a
14	chr1:180374455-180374505	GM12892	blood:	n/a
15	chr1:180374455-180374505	MCF-7	breast:	n/a
16	chr1:180374455-180374505	HEK293	kidney:	embryo
17	chr1:180374455-180374505	SK-N-SH_RA	brain:	n/a
18	chr1:180374455-180374505	NHBE	bronchial:	n/a
19	chr1:180374455-180374505	AG10803	skin:	n/a
20	chr1:180374455-180374505	HCT-116	colon:	n/a
21	chr1:180374455-180374505	AG04449	skin:	fetal
22	chr1:180374455-180374505	GM06990	blood:	n/a
23	chr1:180374455-180374505	MCF10A-Er-Src	breast:	n/a
24	chr1:180374455-180374505	RPTEC	kidney:	n/a
25	chr1:180374455-180374505	Caco-2	colon:	n/a
26	chr1:180374455-180374505	NB4	blood:	n/a
27	chr1:180374455-180374505	NHDF-neo	bronchial:	n/a
28	chr1:180374455-180374505	NT2-D1	testis:	n/a
29	chr1:180374455-180374505	SKMC	muscle:	n/a
30	chr1:180374455-180374505	HRPEpiC	eye:	n/a
31	chr1:180374455-180374505	PANC-1	pancreas:	n/a
32	chr1:180374455-180374505	HAEpiC	amniotic membrane:	n/a
33	chr1:180374455-180374505	HRE	kidney:	n/a
34	chr1:180374455-180374505	HepG2	liver:	n/a
35	chr1:180374455-180374505	HUVEC	blood vessel:	n/a
36	chr1:180374455-180374505	PrEC	prostate:	n/a
37	chr1:180374455-180374505	ECC-1	luminal epithelium:	n/a
38	chr1:180374455-180374505	T-47D	breast:	n/a
39	chr1:180374455-180374505	Hela-S3	cervix:	n/a
40	chr1:180374455-180374505	GM19239	blood:	n/a
41	chr1:180374455-180374505	IMR90	lung:	fetal
42	chr1:180374455-180374505	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:180374455-180374505	HCF	heart:	n/a
44	chr1:180374455-180374505	U87	brain:	n/a
45	chr1:180374455-180374505	HIPEpiC	eye:	n/a
46	chr1:180374455-180374505	BJ	skin:	n/a
47	chr1:180374455-180374505	K562	blood:	n/a
48	chr1:180374455-180374505	A549	lung:	n/a
49	chr1:180374455-180374505	H1-hESC	embryonic stem cell:	embryo
50	chr1:180374455-180374505	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:180374275..180378586-chr1:180383335..180386300,4	K562	blood:
2	chr1:180373412..180375725-chr1:180377296..180379670,2	MCF-7	breast:
3	chr1:180385266..180387346-chr1:180425240..180427346,2	K562	blood:
4	chr1:180374275..180377221-chr1:180383343..180386300,2	K562	blood:
5	chr1:180353732..180356120-chr1:180367249..180368760,2	MCF-7	breast:
6	chr1:180384412..180386137-chr1:180393141..180396163,3	K562	blood:
7	chr1:180156740..180157798-chr1:180384923..180385820,3	MCF-7	breast:
8	chr1:180345449..180347535-chr1:180362052..180364147,2	MCF-7	breast:
9	chr1:180345449..180347535-chr1:180362052..180364147,2	MCF-7	breast:
10	chr1:180383756..180385501-chr1:180395011..180397819,2	K562	blood:
11	chr1:180374275..180378586-chr1:180383335..180386300,4	K562	blood:
12	chr1:180221511..180222402-chr1:180384611..180385850,8	K562	blood:
13	chr1:180338679..180340699-chr1:180366769..180368773,2	K562	blood:
14	chr1:180373412..180375725-chr1:180377296..180379670,2	MCF-7	breast:
15	chr1:180342071..180344205-chr1:180346633..180349074,2	K562	blood:
16	chr1:180383396..180385405-chr1:180470493..180472141,2	MCF-7	breast:
17	chr1:180222556..180224240-chr1:180362387..180364458,2	MCF-7	breast:
18	chr1:180353732..180356120-chr1:180367249..180368760,2	MCF-7	breast:
19	chr1:180349414..180351217-chr1:180352650..180354645,2	K562	blood:
20	chr1:180381265..180383323-chr1:180383973..180385553,2	K562	blood:
21	chr1:180374275..180377221-chr1:180383343..180386300,2	K562	blood:
22	chr1:180333279..180333792-chr1:180384823..180385385,2	MCF-7	breast:
23	chr1:180342071..180344205-chr1:180346633..180349074,2	K562	blood:
24	chr1:180338174..180341966-chr1:180380791..180382462,3	MCF-7	breast:
25	chr1:180156865..180157706-chr1:180384959..180385623,2	K562	blood:
26	chr1:180354979..180356991-chr1:180360915..180363474,2	MCF-7	breast:
27	chr1:180221010..180222431-chr1:180384882..180385873,4	MCF-7	breast:
28	chr1:180349414..180351217-chr1:180352650..180354645,2	K562	blood:
29	chr1:180333422..180334593-chr1:180384864..180385775,6	MCF-7	breast:
30	chr1:180354979..180356991-chr1:180360915..180363474,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOR1AIP2-7	chr1:180364163-180364423	NONHSAT008259
2	lnc-TOR1AIP2-7	chr1:180363055-180363304	NONHSAT008259
3	lnc-LHX4-3	chr1:180353449-180353586	l_154_chr1:180351088-180353586_testes
4	lnc-LHX4-3	chr1:180353269-180353407	l_154_chr1:180351088-180353586_testes
5	lnc-LHX4-3	chr1:180351089-180351110	l_154_chr1:180351088-180353586_testes
6	lnc-TOR1AIP2-7	chr1:180363569-180363685	NONHSAT008259

Variant related genes	Relation type
ACBD6	TF binding region
ACBD6	CpG island
ENSG00000135847	chromatin interactions

Extended variants
information (count: 1612 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1612 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548261342	chr1:180342203-180342204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115000463	chr1:180342281-180342282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537397575	chr1:180342312-180342313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563406145	chr1:180342331-180342332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570798455	chr1:180342338-180342339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539774054	chr1:180342402-180342403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6678216	chr1:180342417-180342418	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs573142429	chr1:180342466-180342467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74132480	chr1:180342482-180342483	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs570847825	chr1:180342490-180342491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555630667	chr1:180342551-180342552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185023208	chr1:180342616-180342617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544019105	chr1:180342653-180342654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116338918	chr1:180342734-180342735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532790141	chr1:180342783-180342784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189485358	chr1:180342938-180342939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182067258	chr1:180342973-180342974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528729809	chr1:180343013-180343014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373624680	chr1:180343040-180343041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185727763	chr1:180343172-180343173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76287980	chr1:180343201-180343202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568349011	chr1:180343284-180343285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10913972	chr1:180343288-180343289	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs200267655	chr1:180343375-180343376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550842461	chr1:180343390-180343391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570884873	chr1:180343396-180343397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10798752	chr1:180343400-180343401	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs10798753	chr1:180343406-180343407	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566850894	chr1:180343409-180343410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144073187	chr1:180343421-180343422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79630833	chr1:180343512-180343513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376973019	chr1:180343607-180343608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12403665	chr1:180343664-180343665	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557203437	chr1:180343686-180343687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150298571	chr1:180343713-180343714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112744427	chr1:180343717-180343718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs66801452	chr1:180343718-180343719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71118453	chr1:180343722-180343723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200032122	chr1:180343723-180343724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200734946	chr1:180343725-180343726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371321393	chr1:180343785-180343786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148734278	chr1:180343821-180343822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561219847	chr1:180343829-180343830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557574191	chr1:180343839-180343840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190925641	chr1:180343849-180343850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376535997	chr1:180343880-180343881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7538303	chr1:180343893-180343894	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs7546030	chr1:180343923-180343924	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs144741873	chr1:180343935-180343936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7538219	chr1:180344012-180344013	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180309600-180345400	Weak transcription	Primary T cells from cord blood	blood
2	chr1:180310000-180348200	Weak transcription	Primary B cells from cord blood	blood
3	chr1:180314000-180345800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:180330200-180345400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:180330600-180349000	Weak transcription	HMEC	breast
6	chr1:180333000-180356200	Weak transcription	Ovary	ovary
7	chr1:180333600-180343400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr1:180334200-180348000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr1:180335800-180343200	Weak transcription	Fetal Lung	lung
10	chr1:180335800-180349000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:180336200-180344400	Weak transcription	Psoas Muscle	Psoas
12	chr1:180336200-180347600	Weak transcription	NHDF-Ad	bronchial
13	chr1:180337000-180349000	Weak transcription	Esophagus	oesophagus
14	chr1:180337800-180348000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:180338400-180345000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:180338400-180348400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr1:180338600-180347800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:180338600-180347800	Weak transcription	Aorta	Aorta
19	chr1:180338600-180348000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:180338600-180349000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:180338600-180349000	Weak transcription	Left Ventricle	heart
22	chr1:180339000-180342600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr1:180339600-180343200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr1:180339600-180345400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:180339600-180349000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:180340200-180343200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:180340400-180345400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr1:180340800-180343200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:180340800-180347600	Weak transcription	HSMM	muscle
30	chr1:180341000-180343000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr1:180341200-180401400	Weak transcription	Osteobl	bone
32	chr1:180341600-180343800	Enhancers	Duodenum Mucosa	Duodenum
33	chr1:180341800-180347000	Weak transcription	Fetal Stomach	stomach
34	chr1:180342000-180344200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:180342200-180346800	Weak transcription	Fetal Intestine Small	intestine
36	chr1:180342200-180348000	Weak transcription	Gastric	stomach
37	chr1:180342600-180344000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr1:180343000-180343800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr1:180343200-180343400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr1:180343200-180343400	Enhancers	Fetal Lung	lung
41	chr1:180343200-180343800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:180343200-180344000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr1:180343400-180343800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr1:180343400-180343800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:180343400-180344000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr1:180343400-180348000	Weak transcription	Fetal Lung	lung
47	chr1:180343600-180356400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr1:180343800-180348000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr1:180343800-180348200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:180344000-180344600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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