Variant report

Variant	nsv899076
Chromosome Location	chr12:50770291-50869589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1402)
CpG islands
(count:1403)
Chromatin interactive
region (count:79)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:50789021-50789046	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:50796058-50797279	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:50794120-50794800	K562	blood:	n/a	n/a
4	ARID3A	chr12:50781712-50782043	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:50784138-50784465	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:50804946-50804977	K562	blood:	n/a	n/a
7	ARID3A	chr12:50796701-50796789	K562	blood:	n/a	n/a
8	ARID3A	chr12:50781816-50781917	K562	blood:	n/a	n/a
9	ARID3A	chr12:50798847-50799198	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:50793878-50794885	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:50790005-50790738	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:50788445-50788751	HepG2	liver:	n/a	n/a
13	ATF1	chr12:50794326-50794813	K562	blood:	n/a	n/a
14	ATF2	chr12:50794136-50794810	GM12878	blood:	n/a	n/a
15	ATF2	chr12:50794270-50794918	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr12:50794178-50794831	GM12878	blood:	n/a	n/a
17	ATF3	chr12:50794146-50794845	A549	lung:	n/a	chr12:50794650-50794663 chr12:50794728-50794737
18	ATF3	chr12:50794266-50795129	A549	lung:	n/a	chr12:50794650-50794663 chr12:50794728-50794737
19	BACH1	chr12:50794088-50794528	K562	blood:	n/a	n/a
20	BACH1	chr12:50794338-50795080	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr12:50834327-50834526	GM12878	blood:	n/a	n/a
22	BATF	chr12:50836293-50836580	GM12878	blood:	n/a	chr12:50836468-50836479
23	BCL3	chr12:50794155-50795231	A549	lung:	n/a	chr12:50794757-50794766
24	BCL3	chr12:50794195-50795003	A549	lung:	n/a	chr12:50794757-50794766
25	BCLAF1	chr12:50794130-50795042	GM12878	blood:	n/a	chr12:50794757-50794766
26	BCLAF1	chr12:50794219-50794805	GM12878	blood:	n/a	chr12:50794757-50794766
27	BHLHE40	chr12:50836448-50836607	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:50794058-50795077	K562	blood:	n/a	chr12:50794635-50794651
29	BHLHE40	chr12:50794250-50794625	A549	lung:	n/a	n/a
30	BHLHE40	chr12:50790292-50790618	HepG2	liver:	n/a	n/a
31	BHLHE40	chr12:50794102-50794939	HepG2	liver:	n/a	chr12:50794635-50794651
32	BHLHE40	chr12:50794094-50795010	GM12878	blood:	n/a	chr12:50794635-50794651
33	BRCA1	chr12:50795393-50796727	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr12:50794231-50794785	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr12:50793898-50795115	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr12:50795066-50795121	HepG2	liver:	n/a	n/a
37	BRCA1	chr12:50794927-50794981	GM12878	blood:	n/a	n/a
38	BRCA1	chr12:50794476-50794717	HepG2	liver:	n/a	n/a
39	CBX3	chr12:50793981-50795103	K562	blood:	n/a	n/a
40	CBX3	chr12:50783928-50784630	HCT-116	colon:	n/a	n/a
41	CBX3	chr12:50812364-50812767	K562	blood:	n/a	n/a
42	CBX3	chr12:50794290-50794884	K562	blood:	n/a	n/a
43	CCNT2	chr12:50794293-50795441	K562	blood:	n/a	chr12:50795125-50795134
44	CEBPB	chr12:50841573-50841753	IMR90	lung:	n/a	chr12:50841706-50841717
45	CEBPB	chr12:50847710-50848120	A549	lung:	n/a	chr12:50847879-50847888
46	CEBPB	chr12:50835666-50835842	A549	lung:	n/a	n/a
47	CEBPB	chr12:50771799-50772107	IMR90	lung:	n/a	chr12:50771957-50771968
48	CEBPB	chr12:50788444-50788746	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:50804899-50805178	HepG2	liver:	n/a	chr12:50805024-50805035
50	CEBPB	chr12:50812986-50813189	A549	lung:	n/a	chr12:50813059-50813070

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:50794700-50794750	SK-N-SH_RA	brain:	n/a
2	chr12:50794552-50794602	K562	blood:	n/a
3	chr12:50794574-50794624	HNPCEpiC	eye:	n/a
4	chr12:50793981-50794031	HCM	heart:	n/a
5	chr12:50794975-50795025	GM12878	blood:	n/a
6	chr12:50794758-50794808	SK-N-SH	brain:	n/a
7	chr12:50790638-50790688	ECC-1	luminal epithelium:	n/a
8	chr12:50794919-50794969	NH-A	brain:	n/a
9	chr12:50794088-50794138	MCF-7	breast:	n/a
10	chr12:50790101-50790151	HRCEpiC	kidney:	n/a
11	chr12:50794919-50794969	CMK	blood:	n/a
12	chr12:50794700-50794750	CMK	blood:	n/a
13	chr12:50794494-50794544	NH-A	brain:	n/a
14	chr12:50798901-50798951	HCT-116	colon:	n/a
15	chr12:50795330-50795380	BJ	skin:	n/a
16	chr12:50794088-50794138	HIPEpiC	eye:	n/a
17	chr12:50794700-50794750	GM12892	blood:	n/a
18	chr12:50794494-50794544	AG04449	skin:	fetal
19	chr12:50794485-50794535	GM06990	blood:	n/a
20	chr12:50795366-50795416	Hela-S3	cervix:	n/a
21	chr12:50793981-50794031	NB4	blood:	n/a
22	chr12:50794975-50795025	ovcar-3	ovarian:	n/a
23	chr12:50794555-50794605	ProgFib	skin:	n/a
24	chr12:50794574-50794624	GM12892	blood:	n/a
25	chr12:50794552-50794602	HCPEpiC	choroid plexus:	n/a
26	chr12:50855257-50855307	ECC-1	luminal epithelium:	n/a
27	chr12:50855257-50855307	ProgFib	skin:	n/a
28	chr12:50794700-50794750	Caco-2	colon:	n/a
29	chr12:50793981-50794031	GM12892	blood:	n/a
30	chr12:50794494-50794544	PFSK-1	brain:	n/a
31	chr12:50794975-50795025	RPTEC	kidney:	n/a
32	chr12:50794550-50794600	LNCaP	prostate:	n/a
33	chr12:50794975-50795025	AoSMC	blood vessel:	n/a
34	chr12:50790423-50790473	HCPEpiC	choroid plexus:	n/a
35	chr12:50794485-50794535	HRPEpiC	eye:	n/a
36	chr12:50795330-50795380	HNPCEpiC	eye:	n/a
37	chr12:50794555-50794605	AG09309	skin:	n/a
38	chr12:50790423-50790473	RPTEC	kidney:	n/a
39	chr12:50794552-50794602	ovcar-3	ovarian:	n/a
40	chr12:50794700-50794750	AG04449	skin:	fetal
41	chr12:50855257-50855307	GM06990	blood:	n/a
42	chr12:50790101-50790151	HCF	heart:	n/a
43	chr12:50794088-50794138	H1-hESC	embryonic stem cell:	embryo
44	chr12:50794758-50794808	MCF-7	breast:	n/a
45	chr12:50798901-50798951	SK-N-SH_RA	brain:	n/a
46	chr12:50790101-50790151	PrEC	prostate:	n/a
47	chr12:50794485-50794535	AG04449	skin:	fetal
48	chr12:50855257-50855307	T-47D	breast:	n/a
49	chr12:50855257-50855307	AG09319	gingival:	n/a
50	chr12:50795366-50795416	U87	brain:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:50677350..50679861-chr12:50792501..50795030,2	K562	blood:
2	chr12:50812613..50814185-chr12:50823081..50825818,2	MCF-7	breast:
3	chr12:50819049..50821406-chr12:50835260..50836787,2	MCF-7	breast:
4	chr12:50793078..50796292-chr12:50797637..50799893,4	K562	blood:
5	chr12:50793452..50795945-chr12:50811858..50813525,2	K562	blood:
6	chr12:50794748..50795302-chr2:198318118..198318777,2	Hela-S3	cervix:
7	chr12:50838041..50839748-chr12:50842685..50844805,2	K562	blood:
8	chr12:50792642..50794335-chr12:50796337..50798839,2	MCF-7	breast:
9	chr12:50561032..50562687-chr12:50794487..50796124,2	K562	blood:
10	chr12:50838040..50839651-chr12:50846886..50849566,2	K562	blood:
11	chr10:90639968..90640523-chr12:50794439..50795346,2	Hela-S3	cervix:
12	chr12:50797471..50799671-chr12:50813461..50817013,3	K562	blood:
13	chr12:50560048..50562244-chr12:50793488..50796318,2	MCF-7	breast:
14	chr12:50804657..50806853-chr12:50839732..50842092,2	K562	blood:
15	chr12:50838041..50839748-chr12:50842685..50844805,2	K562	blood:
16	chr12:50797471..50799671-chr12:50813461..50817013,3	K562	blood:
17	chr12:50838040..50839651-chr12:50846886..50849566,2	K562	blood:
18	chr12:50812613..50814185-chr12:50823081..50825818,2	MCF-7	breast:
19	chr12:50829934..50834172-chr12:50845502..50848522,3	MCF-7	breast:
20	chr12:50811830..50813752-chr12:50815622..50818052,2	K562	blood:
21	chr12:50819049..50821406-chr12:50835260..50836787,2	MCF-7	breast:
22	chr12:50793235..50796567-chr12:50807744..50811456,6	K562	blood:
23	chr12:50795980..50797892-chr12:50802971..50805412,2	MCF-7	breast:
24	chr11:62609053..62609617-chr12:50794323..50794873,2	Hela-S3	cervix:
25	chr12:50781735..50783474-chr12:51157275..51159680,2	K562	blood:
26	chr12:50794468..50798200-chr12:50800215..50802365,3	K562	blood:
27	chr12:50793377..50796191-chr12:50802408..50807418,5	K562	blood:
28	chr12:50794445..50796158-chr12:50811858..50814422,2	K562	blood:
29	chr12:50794772..50796988-chr12:50826297..50828190,2	K562	blood:
30	chr12:50504921..50507362-chr12:50794413..50796105,2	K562	blood:
31	chr12:50795149..50795970-chr15:42264195..42264775,2	Hela-S3	cervix:
32	chr12:50825190..50827072-chr12:50827327..50828879,2	K562	blood:
33	chr1:27188967..27189716-chr12:50794394..50795151,2	Hela-S3	cervix:
34	chr12:50495184..50497904-chr12:50792002..50794811,2	K562	blood:
35	chr12:50795879..50797710-chr12:50805639..50808628,2	MCF-7	breast:
36	chr12:50720749..50723312-chr12:50808337..50810670,2	MCF-7	breast:
37	chr12:50797616..50799826-chr12:50802454..50804004,2	K562	blood:
38	chr12:50797616..50799826-chr12:50802454..50804004,2	K562	blood:
39	chr12:50787607..50792856-chr12:50793045..50797935,10	K562	blood:
40	chr12:50794445..50795114-chr15:64673256..64673791,2	NB4	blood:
41	chr12:50795980..50797892-chr12:50802971..50805412,2	MCF-7	breast:
42	chr12:50781163..50784058-chr12:50784396..50787586,3	MCF-7	breast:
43	chr12:50639732..50644182-chr12:50792343..50795361,4	K562	blood:
44	chr12:50614841..50617436-chr12:50793138..50796219,5	K562	blood:
45	chr12:50805941..50808167-chr12:50815030..50816604,2	K562	blood:
46	chr12:50834513..50836638-chr12:50838122..50840024,2	K562	blood:
47	chr12:50804657..50806853-chr12:50839732..50842092,2	K562	blood:
48	chr12:50744030..50745748-chr12:50793472..50795953,2	K562	blood:
49	chr12:50794494..50797062-chr12:50813268..50815522,2	MCF-7	breast:
50	chr12:50787607..50792856-chr12:50793045..50797935,10	K562	blood:

No data

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

Extended variants
information (count: 3782 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3782 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4477515	chr12:50770291-50770292	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558542892	chr12:50770298-50770299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184051076	chr12:50770308-50770309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs373745430	chr12:50770427-50770428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570512232	chr12:50770432-50770433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs11169402	chr12:50770461-50770462	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539550267	chr12:50770462-50770463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs55712994	chr12:50770530-50770531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs398019509	chr12:50770542-50770543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34694724	chr12:50770609-50770610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs549771624	chr12:50770700-50770701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569657625	chr12:50770740-50770741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373139176	chr12:50770767-50770768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs535134228	chr12:50770816-50770817	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138922543	chr12:50770825-50770826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572291525	chr12:50770827-50770828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs377651240	chr12:50770848-50770849	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149007719	chr12:50770855-50770856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs59210472	chr12:50770862-50770863	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs545913993	chr12:50770933-50770934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143843921	chr12:50770968-50770969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576367616	chr12:50770984-50770985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148083675	chr12:50771000-50771001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561315087	chr12:50771005-50771006	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562399556	chr12:50771049-50771050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs4340149	chr12:50771090-50771091	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs200473181	chr12:50771140-50771141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35028050	chr12:50771142-50771143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547972072	chr12:50771198-50771199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188494134	chr12:50771203-50771204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371499751	chr12:50771261-50771262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71693683	chr12:50771262-50771263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58320549	chr12:50771264-50771265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142725384	chr12:50771265-50771266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147579453	chr12:50771266-50771267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557728469	chr12:50771289-50771290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533033597	chr12:50771303-50771304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs193184513	chr12:50771304-50771305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11169403	chr12:50771341-50771342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536880770	chr12:50771342-50771343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11609043	chr12:50771367-50771368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535423183	chr12:50771369-50771370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4636745	chr12:50771374-50771375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs558054749	chr12:50771381-50771382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573303542	chr12:50771397-50771398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565920194	chr12:50771454-50771455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577846541	chr12:50771477-50771478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371499668	chr12:50771480-50771481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557502313	chr12:50771532-50771533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114504811	chr12:50771540-50771541	Weak transcription	n/a	n/a	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:2665 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50764800-50774600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:50767200-50780800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr12:50770200-50783400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:50774200-50781200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:50774600-50775000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:50775000-50781400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:50779200-50780000	Enhancers	GM12878-XiMat	blood
8	chr12:50779400-50779800	Enhancers	Primary B cells from peripheral blood	blood
9	chr12:50780000-50781000	Weak transcription	GM12878-XiMat	blood
10	chr12:50780800-50781000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:50780800-50781000	Enhancers	Fetal Lung	lung
12	chr12:50780800-50781000	Enhancers	Osteobl	bone
13	chr12:50780800-50781200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr12:50780800-50781400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr12:50780800-50781600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr12:50780800-50781600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr12:50780800-50781800	Enhancers	H9 Cell Line	embryonic stem cell
18	chr12:50780800-50782000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:50780800-50782000	Enhancers	Fetal Stomach	stomach
20	chr12:50780800-50782000	Enhancers	Hela-S3	cervix
21	chr12:50780800-50782800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr12:50780800-50782800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:50780800-50786200	Enhancers	Placenta	Placenta
24	chr12:50781000-50781200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:50781000-50781200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:50781000-50781200	Flanking Active TSS	Fetal Lung	lung
27	chr12:50781000-50781200	Enhancers	HepG2	liver
28	chr12:50781000-50781200	Flanking Active TSS	NHDF-Ad	bronchial
29	chr12:50781000-50781400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr12:50781000-50781400	Enhancers	Brain Germinal Matrix	brain
31	chr12:50781000-50781400	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr12:50781000-50781600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr12:50781000-50781600	Flanking Active TSS	Osteobl	bone
34	chr12:50781000-50781800	Enhancers	Stomach Mucosa	stomach
35	chr12:50781000-50782000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr12:50781000-50782000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:50781000-50782000	Enhancers	Fetal Intestine Large	intestine
38	chr12:50781000-50782400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr12:50781000-50782800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr12:50781000-50783000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr12:50781000-50783200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr12:50781200-50781400	Enhancers	Fetal Lung	lung
43	chr12:50781200-50781400	Enhancers	GM12878-XiMat	blood
44	chr12:50781200-50781400	Active TSS	NHDF-Ad	bronchial
45	chr12:50781200-50781600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr12:50781200-50781600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr12:50781200-50781600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:50781200-50781600	Enhancers	Brain Hippocampus Middle	brain
49	chr12:50781200-50781800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:50781200-50781800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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