Variant report

Variant	nsv470746
Chromosome Location	chr1:174150850-174469905
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2214)
CpG islands
(count:427)
Chromatin interactive
region (count:175)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2214 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174382888-174383024	K562	blood:	n/a	n/a
2	ARID3A	chr1:174174087-174174394	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:174208511-174209005	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:174231891-174232149	K562	blood:	n/a	n/a
5	ARID3A	chr1:174239214-174239484	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:174227162-174227507	K562	blood:	n/a	n/a
7	ARID3A	chr1:174235526-174236877	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:174227171-174227530	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:174199624-174199775	K562	blood:	n/a	n/a
10	ARID3A	chr1:174243609-174243996	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:174396120-174396181	K562	blood:	n/a	n/a
12	ARID3A	chr1:174231871-174232199	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:174186896-174187175	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:174186888-174187188	K562	blood:	n/a	n/a
15	ARID3A	chr1:174160161-174160263	K562	blood:	n/a	n/a
16	ARID3A	chr1:174174954-174175051	K562	blood:	n/a	n/a
17	ATF1	chr1:174397299-174397520	K562	blood:	n/a	n/a
18	ATF1	chr1:174235618-174235768	K562	blood:	n/a	n/a
19	ATF1	chr1:174169246-174169307	K562	blood:	n/a	n/a
20	ATF1	chr1:174263197-174263318	K562	blood:	n/a	n/a
21	ATF1	chr1:174428850-174428929	K562	blood:	n/a	n/a
22	ATF1	chr1:174201924-174202155	K562	blood:	n/a	n/a
23	ATF1	chr1:174199566-174199927	K562	blood:	n/a	n/a
24	ATF1	chr1:174448222-174448255	K562	blood:	n/a	n/a
25	ATF1	chr1:174277912-174277913	K562	blood:	n/a	n/a
26	ATF1	chr1:174173860-174174306	K562	blood:	n/a	n/a
27	ATF2	chr1:174367318-174367778	GM12878	blood:	n/a	n/a
28	ATF2	chr1:174173746-174174313	GM12878	blood:	n/a	n/a
29	ATF2	chr1:174175487-174176060	GM12878	blood:	n/a	n/a
30	ATF2	chr1:174178688-174179318	GM12878	blood:	n/a	n/a
31	ATF2	chr1:174367341-174367790	GM12878	blood:	n/a	n/a
32	ATF2	chr1:174245148-174245601	GM12878	blood:	n/a	n/a
33	ATF2	chr1:174173585-174174478	GM12878	blood:	n/a	n/a
34	BACH1	chr1:174270567-174271092	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr1:174397283-174397435	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr1:174159638-174159721	K562	blood:	n/a	n/a
37	BACH1	chr1:174181908-174182084	K562	blood:	n/a	n/a
38	BACH1	chr1:174186513-174186786	K562	blood:	n/a	n/a
39	BACH1	chr1:174174011-174174379	K562	blood:	n/a	n/a
40	BACH1	chr1:174414983-174415353	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr1:174192832-174192848	K562	blood:	n/a	n/a
42	BACH1	chr1:174180646-174180687	K562	blood:	n/a	n/a
43	BATF	chr1:174366370-174366656	GM12878	blood:	n/a	n/a
44	BATF	chr1:174173782-174174370	GM12878	blood:	n/a	n/a
45	BATF	chr1:174159749-174160060	GM12878	blood:	n/a	n/a
46	BATF	chr1:174178797-174179135	GM12878	blood:	n/a	n/a
47	BATF	chr1:174367368-174367758	GM12878	blood:	n/a	n/a
48	BATF	chr1:174367311-174367749	GM12878	blood:	n/a	n/a
49	BATF	chr1:174178446-174179100	GM12878	blood:	n/a	n/a
50	BATF	chr1:174191294-174191553	GM12878	blood:	n/a	chr1:174191451-174191462 chr1:174191348-174191357

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174417375-174417425	HCT-116	colon:	n/a
2	chr1:174186816-174186866	GM12892	blood:	n/a
3	chr1:174186816-174186866	CMK	blood:	n/a
4	chr1:174417967-174418017	T-47D	breast:	n/a
5	chr1:174352684-174352734	HAEpiC	amniotic membrane:	n/a
6	chr1:174186816-174186866	PANC-1	pancreas:	n/a
7	chr1:174208162-174208212	MCF10A-Er-Src	breast:	n/a
8	chr1:174319673-174319723	U87	brain:	n/a
9	chr1:174186816-174186866	HUVEC	blood vessel:	n/a
10	chr1:174208162-174208212	SK-N-SH_RA	brain:	n/a
11	chr1:174417967-174418017	HAEpiC	amniotic membrane:	n/a
12	chr1:174208162-174208212	H1-hESC	embryonic stem cell:	embryo
13	chr1:174208162-174208212	HCF	heart:	n/a
14	chr1:174319673-174319723	HCT-116	colon:	n/a
15	chr1:174417967-174418017	AoSMC	blood vessel:	n/a
16	chr1:174417967-174418017	MCF10A-Er-Src	breast:	n/a
17	chr1:174417175-174417225	CMK	blood:	n/a
18	chr1:174352684-174352734	ProgFib	skin:	n/a
19	chr1:174352684-174352734	NHBE	bronchial:	n/a
20	chr1:174417967-174418017	HCM	heart:	n/a
21	chr1:174186816-174186866	Caco-2	colon:	n/a
22	chr1:174208162-174208212	Jurkat	blood:	n/a
23	chr1:174186816-174186866	T-47D	breast:	n/a
24	chr1:174208162-174208212	GM12892	blood:	n/a
25	chr1:174208162-174208212	K562	blood:	n/a
26	chr1:174352684-174352734	PrEC	prostate:	n/a
27	chr1:174186816-174186866	ProgFib	skin:	n/a
28	chr1:174208162-174208212	AG04449	skin:	fetal
29	chr1:174186816-174186866	AoSMC	blood vessel:	n/a
30	chr1:174186816-174186866	AG09309	skin:	n/a
31	chr1:174186816-174186866	U87	brain:	n/a
32	chr1:174417175-174417225	AG09309	skin:	n/a
33	chr1:174417967-174418017	AG10803	skin:	n/a
34	chr1:174319673-174319723	CMK	blood:	n/a
35	chr1:174417175-174417225	AG10803	skin:	n/a
36	chr1:174319673-174319723	SK-N-SH_RA	brain:	n/a
37	chr1:174319673-174319723	GM12891	blood:	n/a
38	chr1:174208162-174208212	AoSMC	blood vessel:	n/a
39	chr1:174319673-174319723	AG10803	skin:	n/a
40	chr1:174186816-174186866	HNPCEpiC	eye:	n/a
41	chr1:174417175-174417225	GM06990	blood:	n/a
42	chr1:174186816-174186866	GM12891	blood:	n/a
43	chr1:174208162-174208212	SAEC	small airway:	n/a
44	chr1:174417375-174417425	HMEC	breast:	n/a
45	chr1:174417375-174417425	HUVEC	blood vessel:	n/a
46	chr1:174417375-174417425	NT2-D1	testis:	n/a
47	chr1:174352684-174352734	PANC-1	pancreas:	n/a
48	chr1:174417375-174417425	SK-N-SH	brain:	n/a
49	chr1:174319673-174319723	HEK293	kidney:	embryo
50	chr1:174417375-174417425	HRE	kidney:	n/a

(count:175 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:174236338..174237956-chr1:174241519..174243229,2	K562	blood:
2	chr1:174294663..174296200-chr1:174300746..174303006,2	MCF-7	breast:
3	chr1:174231547..174232813-chr1:174695220..174696649,6	MCF-7	breast:
4	chr1:174158960..174161694-chr1:174164662..174167169,2	K562	blood:
5	chr1:174293187..174295185-chr1:174300416..174302383,2	K562	blood:
6	chr1:174257821..174260787-chr1:174268762..174270773,2	MCF-7	breast:
7	chr1:174178345..174180252-chr1:174182223..174184373,2	K562	blood:
8	chr1:174409687..174411251-chr1:174412999..174415751,2	K562	blood:
9	chr1:174193716..174196579-chr1:174196717..174200011,3	MCF-7	breast:
10	chr1:174460451..174463330-chr1:174468900..174471148,2	K562	blood:
11	chr1:174190274..174193024-chr1:174230012..174232463,2	K562	blood:
12	chr1:174382494..174383374-chr1:174713222..174713791,2	MCF-7	breast:
13	chr1:174178623..174180294-chr1:174184610..174187215,2	K562	blood:
14	chr1:174420323..174421165-chr1:174695373..174696419,3	MCF-7	breast:
15	chr1:174128241..174130281-chr1:174157762..174160299,2	K562	blood:
16	chr1:173989061..173991259-chr1:174208907..174211636,3	MCF-7	breast:
17	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
18	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
19	chr1:174127794..174129583-chr1:174152496..174155394,2	K562	blood:
20	chr1:174186060..174188372-chr1:174193893..174195942,2	K562	blood:
21	chr1:174392997..174395880-chr1:174397869..174401974,3	K562	blood:
22	chr1:174419001..174421193-chr1:174434649..174437565,2	K562	blood:
23	chr1:174208598..174210493-chr1:174218021..174220094,2	MCF-7	breast:
24	chr1:174357412..174359554-chr1:174362221..174364096,2	K562	blood:
25	chr1:174257821..174260787-chr1:174268762..174270773,2	MCF-7	breast:
26	chr1:174236001..174238178-chr1:174240503..174243812,3	K562	blood:
27	chr1:174365587..174367907-chr1:174369349..174371264,2	K562	blood:
28	chr1:174427874..174429422-chr1:174431934..174434699,2	MCF-7	breast:
29	chr1:174134591..174137742-chr1:174149123..174151486,3	K562	blood:
30	chr1:174293187..174295185-chr1:174300416..174302383,2	K562	blood:
31	chr1:174367483..174370019-chr1:174373894..174376540,2	K562	blood:
32	chr1:174188636..174191430-chr1:174968395..174970624,2	K562	blood:
33	chr1:174302180..174304421-chr1:174305573..174307627,2	K562	blood:
34	chr1:174292133..174293963-chr1:174301470..174303626,2	MCF-7	breast:
35	chr1:174460451..174463330-chr1:174468900..174471148,2	K562	blood:
36	chr1:174409687..174411251-chr1:174412999..174415751,2	K562	blood:
37	chr1:174223640..174225967-chr1:174230477..174232706,2	K562	blood:
38	chr1:174134604..174137311-chr1:174161839..174164526,2	K562	blood:
39	chr1:174236001..174238178-chr1:174240503..174243812,3	K562	blood:
40	chr1:174152071..174154187-chr1:174154617..174157580,2	K562	blood:
41	chr1:174246288..174247946-chr1:174254999..174256826,2	K562	blood:
42	chr1:174458959..174461243-chr1:174465302..174467364,3	MCF-7	breast:
43	chr1:174320271..174322217-chr1:174328823..174331200,2	MCF-7	breast:
44	chr1:174420628..174423006-chr1:174424339..174426436,2	K562	blood:
45	chr1:174427874..174429422-chr1:174431934..174434699,2	MCF-7	breast:
46	chr1:173792385..173795057-chr1:174174691..174177146,2	K562	blood:
47	chr1:174152447..174154110-chr1:174154958..174156995,2	K562	blood:
48	chr1:174403554..174404054-chr10:47655569..47656367,2	NB4	blood:
49	chr1:174182976..174185342-chr1:174187527..174191499,3	K562	blood:
50	chr1:174188949..174191911-chr1:174193700..174196292,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RC3H1-4	chr1:174336243-174337177	NONHSAT007733
2	lnc-RC3H1-3	chr1:174156215-174156272	NONHSAT007727

No data

Variant related genes	Relation type
GPR52	TF binding region
ENSG00000238872	TF binding region
ENSG00000237317	TF binding region
RABGAP1L	TF binding region
ENSG00000266125	TF binding region
GPR52	CpG island
ENSG00000238872	CpG island
ENSG00000237317	CpG island
RABGAP1L	CpG island
ENSG00000266125	CpG island
ENSG00000208317	chromatin interactions
ENSG00000117593	chromatin interactions
ENSG00000120334	chromatin interactions
ENSG00000135870	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000224977	chromatin interactions
ENSG00000203737	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000259942	chromatin interactions
ENSG00000227373	chromatin interactions
ENSG00000152061	chromatin interactions

Extended variants
information (count: 11023 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:11023 , 50 per page) page: 1 2 3 4 5 6 7 ... 221

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4652234	chr1:174150850-174150851	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540439380	chr1:174150906-174150907	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs531221638	chr1:174150908-174150909	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs61827906	chr1:174150933-174150934	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542911460	chr1:174151021-174151022	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs9970465	chr1:174151147-174151148	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184159760	chr1:174151251-174151252	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs78223912	chr1:174151260-174151261	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs551970327	chr1:174151262-174151263	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs11365912	chr1:174151290-174151291	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs549399520	chr1:174151352-174151353	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs533057617	chr1:174151370-174151371	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs201091879	chr1:174151375-174151376	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs115021354	chr1:174151376-174151377	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs187281468	chr1:174151391-174151392	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs529241834	chr1:174151418-174151419	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs549280851	chr1:174151439-174151440	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs567550363	chr1:174151476-174151477	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs569305062	chr1:174151513-174151514	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs538217686	chr1:174151520-174151521	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs191377454	chr1:174151541-174151542	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs184323493	chr1:174151543-174151544	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs80051984	chr1:174151594-174151595	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs554118290	chr1:174151602-174151603	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs189269799	chr1:174151634-174151635	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs542948268	chr1:174151677-174151678	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs146093278	chr1:174151759-174151760	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs138768388	chr1:174151775-174151776	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs543818662	chr1:174151837-174151838	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs564209573	chr1:174151847-174151848	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs182213966	chr1:174151863-174151864	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs536602505	chr1:174151885-174151886	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs145489320	chr1:174151891-174151892	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs185584209	chr1:174152005-174152006	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs549034783	chr1:174152027-174152028	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs560120899	chr1:174152041-174152042	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs149359193	chr1:174152126-174152127	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs190195818	chr1:174152133-174152134	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs539143763	chr1:174152165-174152166	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs144665270	chr1:174152180-174152181	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs531749924	chr1:174152242-174152243	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs552959584	chr1:174152259-174152260	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551441564	chr1:174152270-174152271	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs181687904	chr1:174152359-174152360	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs534074297	chr1:174152383-174152384	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs554225230	chr1:174152385-174152386	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs115620585	chr1:174152396-174152397	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs185368619	chr1:174152451-174152452	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556448327	chr1:174152454-174152455	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs6658543	chr1:174152476-174152477	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:100)

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
Intellectual disability	22102821	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
Retinoblastoma	19183342	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
Chordoma	18071362	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
Burkitt''s lymphoma	19759907	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2817 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174129600-174164800	Weak transcription	Gastric	stomach
2	chr1:174129600-174173200	Weak transcription	Pancreas	Pancrea
3	chr1:174130000-174157600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:174130800-174156600	Weak transcription	Primary T cells from cord blood	blood
5	chr1:174134800-174159800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:174136400-174160000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:174137800-174155600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr1:174138400-174160000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr1:174139000-174159800	Weak transcription	Right Atrium	heart
10	chr1:174139400-174153800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr1:174141800-174151200	Weak transcription	Fetal Heart	heart
12	chr1:174142000-174153800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:174144000-174151200	Weak transcription	K562	blood
14	chr1:174144000-174151400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr1:174144000-174178200	Weak transcription	Left Ventricle	heart
16	chr1:174144200-174158000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:174145800-174157600	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr1:174148800-174159600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr1:174150800-174151000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr1:174150800-174151600	Enhancers	Liver	Liver
21	chr1:174150800-174152000	Enhancers	GM12878-XiMat	blood
22	chr1:174150800-174152600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:174151000-174151400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:174151200-174151800	Enhancers	Fetal Heart	heart
25	chr1:174151200-174151800	Enhancers	K562	blood
26	chr1:174151400-174151800	Enhancers	Primary B cells from peripheral blood	blood
27	chr1:174151400-174152000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:174151600-174151800	Enhancers	HepG2	liver
29	chr1:174151800-174153800	Weak transcription	Fetal Heart	heart
30	chr1:174151800-174154000	Weak transcription	HepG2	liver
31	chr1:174151800-174159600	Weak transcription	K562	blood
32	chr1:174152000-174154000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:174152600-174152800	Weak transcription	GM12878-XiMat	blood
34	chr1:174153000-174155400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:174153800-174154000	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr1:174153800-174154200	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr1:174153800-174154200	Enhancers	Fetal Heart	heart
38	chr1:174154000-174154200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr1:174154000-174154400	Enhancers	HepG2	liver
40	chr1:174154200-174173600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr1:174155600-174155800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr1:174155800-174156400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr1:174157000-174157400	Weak transcription	Primary T cells from cord blood	blood
44	chr1:174157600-174158000	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
45	chr1:174157600-174158200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:174157800-174158000	Weak transcription	Primary T cells from cord blood	blood
47	chr1:174157800-174158000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr1:174158000-174158800	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr1:174158200-174159800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:174158400-174158800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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