Variant report

Variant	nsv469376
Chromosome Location	chr12:50792846-50856613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1079)
CpG islands
(count:1159)
Chromatin interactive
region (count:73)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:50796058-50797279	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:50794120-50794800	K562	blood:	n/a	n/a
3	ARID3A	chr12:50804946-50804977	K562	blood:	n/a	n/a
4	ARID3A	chr12:50793878-50794885	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:50796701-50796789	K562	blood:	n/a	n/a
6	ARID3A	chr12:50798847-50799198	HepG2	liver:	n/a	n/a
7	ATF1	chr12:50794326-50794813	K562	blood:	n/a	n/a
8	ATF2	chr12:50794178-50794831	GM12878	blood:	n/a	n/a
9	ATF2	chr12:50794270-50794918	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr12:50794136-50794810	GM12878	blood:	n/a	n/a
11	ATF3	chr12:50794146-50794845	A549	lung:	n/a	chr12:50794650-50794663 chr12:50794728-50794737
12	ATF3	chr12:50794266-50795129	A549	lung:	n/a	chr12:50794650-50794663 chr12:50794728-50794737
13	BACH1	chr12:50794088-50794528	K562	blood:	n/a	n/a
14	BACH1	chr12:50794338-50795080	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr12:50834327-50834526	GM12878	blood:	n/a	n/a
16	BATF	chr12:50836293-50836580	GM12878	blood:	n/a	chr12:50836468-50836479
17	BCL3	chr12:50794155-50795231	A549	lung:	n/a	chr12:50794757-50794766
18	BCL3	chr12:50794195-50795003	A549	lung:	n/a	chr12:50794757-50794766
19	BCLAF1	chr12:50794219-50794805	GM12878	blood:	n/a	chr12:50794757-50794766
20	BCLAF1	chr12:50794130-50795042	GM12878	blood:	n/a	chr12:50794757-50794766
21	BHLHE40	chr12:50794094-50795010	GM12878	blood:	n/a	chr12:50794635-50794651
22	BHLHE40	chr12:50794102-50794939	HepG2	liver:	n/a	chr12:50794635-50794651
23	BHLHE40	chr12:50794058-50795077	K562	blood:	n/a	chr12:50794635-50794651
24	BHLHE40	chr12:50836448-50836607	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:50794250-50794625	A549	lung:	n/a	n/a
26	BRCA1	chr12:50793898-50795115	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr12:50795393-50796727	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr12:50795066-50795121	HepG2	liver:	n/a	n/a
29	BRCA1	chr12:50794927-50794981	GM12878	blood:	n/a	n/a
30	BRCA1	chr12:50794476-50794717	HepG2	liver:	n/a	n/a
31	BRCA1	chr12:50794231-50794785	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr12:50812364-50812767	K562	blood:	n/a	n/a
33	CBX3	chr12:50794290-50794884	K562	blood:	n/a	n/a
34	CBX3	chr12:50793981-50795103	K562	blood:	n/a	n/a
35	CCNT2	chr12:50794293-50795441	K562	blood:	n/a	chr12:50795125-50795134
36	CEBPB	chr12:50795266-50795899	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:50854085-50854299	MCF-7	breast:	n/a	chr12:50854166-50854177
38	CEBPB	chr12:50810015-50810188	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr12:50804979-50805126	H1-hESC	embryonic stem cell:	n/a	chr12:50805024-50805035
40	CEBPB	chr12:50841645-50841738	K562	blood:	n/a	chr12:50841706-50841717
41	CEBPB	chr12:50809927-50810228	K562	blood:	n/a	n/a
42	CEBPB	chr12:50804900-50805186	IMR90	lung:	n/a	chr12:50805024-50805035
43	CEBPB	chr12:50847691-50848062	MCF-7	breast:	n/a	chr12:50847879-50847888
44	CEBPB	chr12:50847731-50848075	ECC-1	luminal epithelium:	n/a	chr12:50847879-50847888
45	CEBPB	chr12:50809912-50810288	MCF-7	breast:	n/a	n/a
46	CEBPB	chr12:50813000-50813190	K562	blood:	n/a	chr12:50813059-50813070
47	CEBPB	chr12:50800458-50800555	A549	lung:	n/a	chr12:50800462-50800473
48	CEBPB	chr12:50847699-50848073	K562	blood:	n/a	chr12:50847879-50847888
49	CEBPB	chr12:50804916-50805106	K562	blood:	n/a	chr12:50805024-50805035
50	CEBPB	chr12:50854081-50854327	HepG2	liver:	n/a	chr12:50854166-50854177

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:50795330-50795380	Jurkat	blood:	n/a
2	chr12:50794494-50794544	HEK293	kidney:	embryo
3	chr12:50798901-50798951	U87	brain:	n/a
4	chr12:50794574-50794624	PrEC	prostate:	n/a
5	chr12:50795366-50795416	NB4	blood:	n/a
6	chr12:50794919-50794969	GM12892	blood:	n/a
7	chr12:50794550-50794600	HEEpiC	esophagus:	n/a
8	chr12:50794700-50794750	ECC-1	luminal epithelium:	n/a
9	chr12:50819810-50819860	ProgFib	skin:	n/a
10	chr12:50819810-50819860	NHBE	bronchial:	n/a
11	chr12:50855257-50855307	Hela-S3	cervix:	n/a
12	chr12:50794574-50794624	SK-N-MC	brain:	n/a
13	chr12:50798901-50798951	HEK293	kidney:	embryo
14	chr12:50794485-50794535	HNPCEpiC	eye:	n/a
15	chr12:50794975-50795025	K562	blood:	n/a
16	chr12:50793981-50794031	HCF	heart:	n/a
17	chr12:50794308-50794358	GM19239	blood:	n/a
18	chr12:50795366-50795416	HUVEC	blood vessel:	n/a
19	chr12:50793961-50794011	HRCEpiC	kidney:	n/a
20	chr12:50798901-50798951	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:50795330-50795380	NH-A	brain:	n/a
22	chr12:50794975-50795025	HIPEpiC	eye:	n/a
23	chr12:50794552-50794602	SK-N-SH_RA	brain:	n/a
24	chr12:50794919-50794969	GM12878	blood:	n/a
25	chr12:50819810-50819860	BE2_C	brain:	n/a
26	chr12:50794494-50794544	HL-60	blood:	n/a
27	chr12:50794550-50794600	Jurkat	blood:	n/a
28	chr12:50793961-50794011	K562	blood:	n/a
29	chr12:50795330-50795380	AG10803	skin:	n/a
30	chr12:50795366-50795416	ECC-1	luminal epithelium:	n/a
31	chr12:50794485-50794535	HCT-116	colon:	n/a
32	chr12:50794919-50794969	AoSMC	blood vessel:	n/a
33	chr12:50794550-50794600	MCF10A-Er-Src	breast:	n/a
34	chr12:50794308-50794358	AG04449	skin:	fetal
35	chr12:50793981-50794031	GM12892	blood:	n/a
36	chr12:50819810-50819860	MCF10A-Er-Src	breast:	n/a
37	chr12:50793961-50794011	HEEpiC	esophagus:	n/a
38	chr12:50794700-50794750	K562	blood:	n/a
39	chr12:50794919-50794969	MCF-7	breast:	n/a
40	chr12:50798901-50798951	Jurkat	blood:	n/a
41	chr12:50794555-50794605	NB4	blood:	n/a
42	chr12:50794494-50794544	T-47D	breast:	n/a
43	chr12:50798901-50798951	SK-N-SH	brain:	n/a
44	chr12:50819810-50819860	NH-A	brain:	n/a
45	chr12:50819810-50819860	Jurkat	blood:	n/a
46	chr12:50794555-50794605	LNCaP	prostate:	n/a
47	chr12:50794919-50794969	HCT-116	colon:	n/a
48	chr12:50794919-50794969	GM19239	blood:	n/a
49	chr12:50794975-50795025	ECC-1	luminal epithelium:	n/a
50	chr12:50794308-50794358	GM12891	blood:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:50811830..50813752-chr12:50815622..50818052,2	K562	blood:
2	chr12:50794494..50797062-chr12:50813268..50815522,2	MCF-7	breast:
3	chr12:50794762..50796457-chr12:50796893..50799781,4	K562	blood:
4	chr12:50794755..50795359-chr5:36151589..36152450,2	Hela-S3	cervix:
5	chr12:50794772..50796988-chr12:50826297..50828190,2	K562	blood:
6	chr12:50838041..50839748-chr12:50842685..50844805,2	K562	blood:
7	chr12:50825190..50827072-chr12:50827327..50828879,2	K562	blood:
8	chr12:50804657..50806853-chr12:50839732..50842092,2	K562	blood:
9	chr12:50416797..50419367-chr12:50793748..50795984,3	K562	blood:
10	chr12:50812613..50814185-chr12:50823081..50825818,2	MCF-7	breast:
11	chr12:50614841..50617436-chr12:50793138..50796219,5	K562	blood:
12	chr12:50504921..50507290-chr12:50793420..50795913,2	K562	blood:
13	chr12:50838040..50839651-chr12:50846886..50849566,2	K562	blood:
14	chr12:50795980..50797892-chr12:50802971..50805412,2	MCF-7	breast:
15	chr12:50560048..50562244-chr12:50793488..50796318,2	MCF-7	breast:
16	chr12:50811830..50813752-chr12:50815622..50818052,2	K562	blood:
17	chr12:50797616..50799826-chr12:50802454..50804004,2	K562	blood:
18	chr12:50794419..50795025-chr4:151936304..151937173,2	Hela-S3	cervix:
19	chr12:50794748..50795302-chr2:198318118..198318777,2	Hela-S3	cervix:
20	chr12:50614841..50617436-chr12:50793138..50795396,3	K562	blood:
21	chr12:50797471..50799671-chr12:50813461..50817013,3	K562	blood:
22	chr12:50794445..50796158-chr12:50811858..50814422,2	K562	blood:
23	chr12:50797616..50799826-chr12:50802454..50804004,2	K562	blood:
24	chr12:50838040..50839651-chr12:50846886..50849566,2	K562	blood:
25	chr12:50819049..50821406-chr12:50835260..50836787,2	MCF-7	breast:
26	chr12:50803668..50806425-chr12:50809332..50811405,2	K562	blood:
27	chr12:50792642..50794335-chr12:50796337..50798839,2	MCF-7	breast:
28	chr12:50787607..50792856-chr12:50793045..50797935,10	K562	blood:
29	chr12:50611453..50613308-chr12:50792675..50795177,2	K562	blood:
30	chr12:50830783..50832348-chr12:50832808..50834539,2	K562	blood:
31	chr12:50803668..50806425-chr12:50809332..50811405,2	K562	blood:
32	chr12:50838041..50839748-chr12:50842685..50844805,2	K562	blood:
33	chr12:50720749..50723312-chr12:50808337..50810670,2	MCF-7	breast:
34	chr12:50792642..50794335-chr12:50796337..50798839,2	MCF-7	breast:
35	chr12:50639732..50644182-chr12:50792343..50795361,4	K562	blood:
36	chr12:50805941..50808167-chr12:50815030..50816604,2	K562	blood:
37	chr12:50794531..50796202-chr12:50898772..50900284,2	MCF-7	breast:
38	chr12:50795879..50797710-chr12:50805639..50808628,2	MCF-7	breast:
39	chr12:50787607..50792856-chr12:50793045..50797935,10	K562	blood:
40	chr12:50804657..50806853-chr12:50839732..50842092,2	K562	blood:
41	chr11:62609053..62609617-chr12:50794323..50794873,2	Hela-S3	cervix:
42	chr12:50793377..50796191-chr12:50802408..50807418,5	K562	blood:
43	chr12:50561032..50562687-chr12:50794487..50796124,2	K562	blood:
44	chr12:50834513..50836638-chr12:50838122..50840024,2	K562	blood:
45	chr12:50794468..50798200-chr12:50800215..50802365,3	K562	blood:
46	chr12:50793078..50796292-chr12:50797637..50799893,4	K562	blood:
47	chr12:50793452..50795945-chr12:50811858..50813525,2	K562	blood:
48	chr12:50794108..50796567-chr12:50808356..50811014,3	K562	blood:
49	chr12:50801905..50804539-chr12:50808374..50809962,2	K562	blood:
50	chr12:50793235..50796567-chr12:50807744..50811456,6	K562	blood:

No data

Variant related genes	Relation type
LARP4	TF binding region
FAM186A	TF binding region
LARP4	CpG island
FAM186A	CpG island
ENSG00000135457	chromatin interactions
ENSG00000050405	chromatin interactions
ENSG00000138134	chromatin interactions
ENSG00000257531	chromatin interactions
ENSG00000203433	chromatin interactions
ENSG00000244266	chromatin interactions
ENSG00000115520	chromatin interactions
ENSG00000167588	chromatin interactions
ENSG00000161813	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000272368	chromatin interactions
ENSG00000145604	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000175793	chromatin interactions
ENSG00000166803	chromatin interactions
ENSG00000164187	chromatin interactions
ENSG00000198589	chromatin interactions
ENSG00000139624	chromatin interactions
ENSG00000066084	chromatin interactions
ENSG00000185958	chromatin interactions
ENSG00000161800	chromatin interactions
ENSG00000103966	chromatin interactions
ENSG00000178449	chromatin interactions

Extended variants
information (count: 2379 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2379 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7296212	chr12:50792846-50792847	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140680015	chr12:50792862-50792863	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs536124450	chr12:50792871-50792872	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs534787442	chr12:50792951-50792952	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs7310686	chr12:50792953-50792954	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs566255252	chr12:50792977-50792978	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs144614290	chr12:50792981-50792982	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs534955012	chr12:50793156-50793157	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs138562016	chr12:50793159-50793160	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs554508903	chr12:50793179-50793180	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs148189194	chr12:50793186-50793187	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs68162104	chr12:50793187-50793188	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs56709238	chr12:50793196-50793197	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs577330248	chr12:50793253-50793254	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs4768936	chr12:50793267-50793268	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs145386964	chr12:50793383-50793384	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs556562939	chr12:50793422-50793423	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs573586436	chr12:50793438-50793439	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs542895542	chr12:50793439-50793440	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs372185195	chr12:50793448-50793449	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs572945245	chr12:50793475-50793476	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs565374952	chr12:50793488-50793489	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs182120238	chr12:50793504-50793505	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs367717806	chr12:50793570-50793571	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs79352528	chr12:50793572-50793573	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs533486887	chr12:50793575-50793576	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs550326020	chr12:50793617-50793618	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs150978939	chr12:50793632-50793633	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs529311313	chr12:50793709-50793710	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs559686471	chr12:50793724-50793725	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs549650239	chr12:50793752-50793753	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs192892849	chr12:50793789-50793790	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs75754104	chr12:50793799-50793800	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs147121978	chr12:50793805-50793806	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs529992095	chr12:50793826-50793827	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs535180804	chr12:50793908-50793909	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs551576096	chr12:50793929-50793930	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs28709365	chr12:50793936-50793937	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs570984214	chr12:50793941-50793942	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs536729864	chr12:50793965-50793966	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs117769037	chr12:50793978-50793979	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs149621194	chr12:50793982-50793983	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
43	rs535872156	chr12:50793992-50793993	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
44	rs6580749	chr12:50794033-50794034	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs528253816	chr12:50794039-50794040	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
46	rs372412941	chr12:50794092-50794093	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
47	rs144375363	chr12:50794112-50794113	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
48	rs548225957	chr12:50794124-50794125	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
49	rs11374121	chr12:50794256-50794257	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
50	rs397720288	chr12:50794262-50794263	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Breast cancer	21858162	CNVD
Urothelial carcinoma	21177765	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2097 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50781800-50794000	Weak transcription	Fetal Kidney	kidney
2	chr12:50782000-50794000	Weak transcription	Fetal Heart	heart
3	chr12:50782800-50794200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:50785000-50794000	Weak transcription	HUVEC	blood vessel
5	chr12:50790200-50794000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr12:50790400-50793800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr12:50790600-50793600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr12:50790600-50793800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:50790600-50794000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:50790600-50794200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:50790800-50793800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:50790800-50793800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr12:50790800-50793800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:50790800-50793800	Weak transcription	NHEK	skin
15	chr12:50790800-50794000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:50790800-50794000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:50790800-50794200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr12:50791000-50793800	Weak transcription	Osteobl	bone
19	chr12:50791000-50794000	Weak transcription	A549	lung
20	chr12:50791000-50794000	Weak transcription	NHDF-Ad	bronchial
21	chr12:50791200-50793800	Weak transcription	Hela-S3	cervix
22	chr12:50791200-50794000	Weak transcription	HMEC	breast
23	chr12:50791400-50793800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:50791400-50793800	Weak transcription	HepG2	liver
25	chr12:50791400-50794000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:50791400-50794200	Weak transcription	Placenta	Placenta
27	chr12:50793400-50793600	Enhancers	Dnd41	blood
28	chr12:50793600-50794400	Flanking Active TSS	Dnd41	blood
29	chr12:50793600-50796800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr12:50793800-50794000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:50793800-50794000	Enhancers	Primary B cells from cord blood	blood
32	chr12:50793800-50794000	Enhancers	Primary B cells from peripheral blood	blood
33	chr12:50793800-50794000	Enhancers	Primary T cells from cord blood	blood
34	chr12:50793800-50794000	Enhancers	Primary hematopoietic stem cells	blood
35	chr12:50793800-50794000	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr12:50793800-50794000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr12:50793800-50794000	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr12:50793800-50794000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:50793800-50794000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr12:50793800-50794000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:50793800-50794000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr12:50793800-50794000	Enhancers	Liver	Liver
43	chr12:50793800-50794000	Enhancers	Brain Substantia Nigra	brain
44	chr12:50793800-50794000	Enhancers	Colon Smooth Muscle	Colon
45	chr12:50793800-50794000	Enhancers	Fetal Intestine Small	intestine
46	chr12:50793800-50794000	Enhancers	Fetal Thymus	thymus
47	chr12:50793800-50794000	Enhancers	Osteobl	bone
48	chr12:50793800-50794200	Enhancers	Placenta Amnion	Placenta Amnion
49	chr12:50793800-50794400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:50793800-50794800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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