Variant report

Variant	nsv1049665
Chromosome Location	chr12:50705715-50871542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2002)
CpG islands
(count:1647)
Chromatin interactive
region (count:98)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2002 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:50784138-50784465	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:50796701-50796789	K562	blood:	n/a	n/a
3	ARID3A	chr12:50794120-50794800	K562	blood:	n/a	n/a
4	ARID3A	chr12:50788445-50788751	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:50796058-50797279	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:50781712-50782043	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:50711203-50711252	K562	blood:	n/a	n/a
8	ARID3A	chr12:50798847-50799198	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:50760317-50760322	K562	blood:	n/a	n/a
10	ARID3A	chr12:50758915-50759307	K562	blood:	n/a	n/a
11	ARID3A	chr12:50781816-50781917	K562	blood:	n/a	n/a
12	ARID3A	chr12:50790005-50790738	HepG2	liver:	n/a	n/a
13	ARID3A	chr12:50719928-50720204	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:50804946-50804977	K562	blood:	n/a	n/a
15	ARID3A	chr12:50793878-50794885	HepG2	liver:	n/a	n/a
16	ARID3A	chr12:50789021-50789046	HepG2	liver:	n/a	n/a
17	ARID3A	chr12:50759671-50759672	K562	blood:	n/a	n/a
18	ATF1	chr12:50794326-50794813	K562	blood:	n/a	n/a
19	ATF2	chr12:50794270-50794918	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr12:50871123-50871618	GM12878	blood:	n/a	n/a
21	ATF2	chr12:50794178-50794831	GM12878	blood:	n/a	n/a
22	ATF2	chr12:50794136-50794810	GM12878	blood:	n/a	n/a
23	ATF3	chr12:50735830-50736079	K562	blood:	n/a	n/a
24	ATF3	chr12:50794146-50794845	A549	lung:	n/a	chr12:50794650-50794663 chr12:50794728-50794737
25	ATF3	chr12:50794266-50795129	A549	lung:	n/a	chr12:50794650-50794663 chr12:50794728-50794737
26	BACH1	chr12:50794088-50794528	K562	blood:	n/a	n/a
27	BACH1	chr12:50794338-50795080	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr12:50836293-50836580	GM12878	blood:	n/a	chr12:50836468-50836479
29	BATF	chr12:50871244-50871586	GM12878	blood:	n/a	n/a
30	BATF	chr12:50834327-50834526	GM12878	blood:	n/a	n/a
31	BCL3	chr12:50794195-50795003	A549	lung:	n/a	chr12:50794757-50794766
32	BCL3	chr12:50794155-50795231	A549	lung:	n/a	chr12:50794757-50794766
33	BCLAF1	chr12:50794219-50794805	GM12878	blood:	n/a	chr12:50794757-50794766
34	BCLAF1	chr12:50794130-50795042	GM12878	blood:	n/a	chr12:50794757-50794766
35	BHLHE40	chr12:50794102-50794939	HepG2	liver:	n/a	chr12:50794635-50794651
36	BHLHE40	chr12:50790292-50790618	HepG2	liver:	n/a	n/a
37	BHLHE40	chr12:50836448-50836607	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:50794058-50795077	K562	blood:	n/a	chr12:50794635-50794651
39	BHLHE40	chr12:50794094-50795010	GM12878	blood:	n/a	chr12:50794635-50794651
40	BHLHE40	chr12:50794250-50794625	A549	lung:	n/a	n/a
41	BRCA1	chr12:50794927-50794981	GM12878	blood:	n/a	n/a
42	BRCA1	chr12:50795393-50796727	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr12:50794231-50794785	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr12:50794476-50794717	HepG2	liver:	n/a	n/a
45	BRCA1	chr12:50795066-50795121	HepG2	liver:	n/a	n/a
46	BRCA1	chr12:50793898-50795115	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr12:50812364-50812767	K562	blood:	n/a	n/a
48	CBX3	chr12:50793981-50795103	K562	blood:	n/a	n/a
49	CBX3	chr12:50794290-50794884	K562	blood:	n/a	n/a
50	CBX3	chr12:50783928-50784630	HCT-116	colon:	n/a	n/a

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:50790423-50790473	MCF-7	breast:	n/a
2	chr12:50819810-50819860	AG09309	skin:	n/a
3	chr12:50794919-50794969	MCF-7	breast:	n/a
4	chr12:50794494-50794544	HAEpiC	amniotic membrane:	n/a
5	chr12:50790101-50790151	BJ	skin:	n/a
6	chr12:50793961-50794011	GM12878	blood:	n/a
7	chr12:50795330-50795380	GM06990	blood:	n/a
8	chr12:50794550-50794600	RPTEC	kidney:	n/a
9	chr12:50798901-50798951	H1-hESC	embryonic stem cell:	embryo
10	chr12:50790101-50790151	HNPCEpiC	eye:	n/a
11	chr12:50794308-50794358	K562	blood:	n/a
12	chr12:50870720-50870770	GM06990	blood:	n/a
13	chr12:50870720-50870770	Jurkat	blood:	n/a
14	chr12:50794088-50794138	HCF	heart:	n/a
15	chr12:50781534-50781584	AoSMC	blood vessel:	n/a
16	chr12:50794975-50795025	NHDF-neo	bronchial:	n/a
17	chr12:50794975-50795025	Hela-S3	cervix:	n/a
18	chr12:50794555-50794605	MCF-7	breast:	n/a
19	chr12:50794919-50794969	SK-N-MC	brain:	n/a
20	chr12:50794555-50794605	SAEC	small airway:	n/a
21	chr12:50793961-50794011	HAEpiC	amniotic membrane:	n/a
22	chr12:50794552-50794602	HCPEpiC	choroid plexus:	n/a
23	chr12:50707901-50707951	K562	blood:	n/a
24	chr12:50790423-50790473	GM12892	blood:	n/a
25	chr12:50794550-50794600	AG04450	lung:	fetal
26	chr12:50793961-50794011	SAEC	small airway:	n/a
27	chr12:50794975-50795025	HCM	heart:	n/a
28	chr12:50795366-50795416	HUVEC	blood vessel:	n/a
29	chr12:50855257-50855307	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:50794308-50794358	NB4	blood:	n/a
31	chr12:50794485-50794535	AoSMC	blood vessel:	n/a
32	chr12:50793961-50794011	HNPCEpiC	eye:	n/a
33	chr12:50748524-50748574	SKMC	muscle:	n/a
34	chr12:50794700-50794750	ovcar-3	ovarian:	n/a
35	chr12:50794494-50794544	HIPEpiC	eye:	n/a
36	chr12:50793961-50794011	AG04449	skin:	fetal
37	chr12:50720139-50720189	AG09309	skin:	n/a
38	chr12:50794552-50794602	PrEC	prostate:	n/a
39	chr12:50794758-50794808	LNCaP	prostate:	n/a
40	chr12:50794308-50794358	SK-N-SH	brain:	n/a
41	chr12:50794088-50794138	HEEpiC	esophagus:	n/a
42	chr12:50794555-50794605	AoSMC	blood vessel:	n/a
43	chr12:50794758-50794808	HMEC	breast:	n/a
44	chr12:50819810-50819860	BE2_C	brain:	n/a
45	chr12:50790638-50790688	NH-A	brain:	n/a
46	chr12:50790423-50790473	BE2_C	brain:	n/a
47	chr12:50790423-50790473	GM06990	blood:	n/a
48	chr12:50720139-50720189	GM12878	blood:	n/a
49	chr12:50794700-50794750	HRE	kidney:	n/a
50	chr12:50794494-50794544	HCPEpiC	choroid plexus:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:50801905..50804539-chr12:50808374..50809962,2	K562	blood:
2	chr12:50812613..50814185-chr12:50823081..50825818,2	MCF-7	breast:
3	chr12:50793235..50796567-chr12:50807744..50811456,6	K562	blood:
4	chr10:90639968..90640523-chr12:50794439..50795346,2	Hela-S3	cervix:
5	chr12:50560048..50562244-chr12:50793488..50796318,2	MCF-7	breast:
6	chr12:50803668..50806425-chr12:50809332..50811405,2	K562	blood:
7	chr12:50416797..50419367-chr12:50793748..50795984,3	K562	blood:
8	chr12:50614138..50615726-chr12:50704917..50707484,2	MCF-7	breast:
9	chr12:50825190..50827072-chr12:50827327..50828879,2	K562	blood:
10	chr12:50720749..50723312-chr12:50808337..50810670,2	MCF-7	breast:
11	chr12:50504921..50507290-chr12:50793420..50795913,2	K562	blood:
12	chr12:50797471..50799671-chr12:50813461..50817013,3	K562	blood:
13	chr12:50838041..50839748-chr12:50842685..50844805,2	K562	blood:
14	chr12:50805941..50808167-chr12:50815030..50816604,2	K562	blood:
15	chr12:50575985..50576844-chr12:50708187..50709140,4	K562	blood:
16	chr12:50794108..50796567-chr12:50808356..50811014,3	K562	blood:
17	chr12:50797616..50799826-chr12:50802454..50804004,2	K562	blood:
18	chr12:50728708..50730581-chr12:50746052..50748839,2	K562	blood:
19	chr12:50834513..50836638-chr12:50838122..50840024,2	K562	blood:
20	chr12:50834513..50836638-chr12:50838122..50840024,2	K562	blood:
21	chr12:50793377..50796191-chr12:50802408..50807418,5	K562	blood:
22	chr12:50575251..50576960-chr12:50708135..50709374,12	MCF-7	breast:
23	chr12:50468671..50469657-chr12:50708194..50709149,5	K562	blood:
24	chr12:50794531..50796202-chr12:50898772..50900284,2	MCF-7	breast:
25	chr1:27188967..27189716-chr12:50794394..50795151,2	Hela-S3	cervix:
26	chr12:50768661..50771049-chr12:50788858..50791669,2	MCF-7	breast:
27	chr12:50792642..50794335-chr12:50796337..50798839,2	MCF-7	breast:
28	chr12:50795980..50797892-chr12:50802971..50805412,2	MCF-7	breast:
29	chr12:50794772..50796988-chr12:50826297..50828190,2	K562	blood:
30	chr12:50698148..50700297-chr12:50709647..50711373,2	K562	blood:
31	chr12:50795879..50797710-chr12:50805639..50808628,2	MCF-7	breast:
32	chr12:50794445..50796158-chr12:50811858..50814422,2	K562	blood:
33	chr12:50495184..50497904-chr12:50792002..50794811,2	K562	blood:
34	chr12:50744030..50745748-chr12:50793472..50795953,2	K562	blood:
35	chr12:50804657..50806853-chr12:50839732..50842092,2	K562	blood:
36	chr12:50819049..50821406-chr12:50835260..50836787,2	MCF-7	breast:
37	chr12:50526029..50526560-chr12:50708191..50708705,2	K562	blood:
38	chr12:50855792..50857540-chr12:50858968..50861259,2	K562	blood:
39	chr12:50794762..50796457-chr12:50796893..50799781,4	K562	blood:
40	chr12:50792642..50794335-chr12:50796337..50798839,2	MCF-7	breast:
41	chr12:50782728..50784449-chr12:50792559..50794993,2	K562	blood:
42	chr12:50793053..50795901-chr12:51566225..51568182,2	K562	blood:
43	chr12:50728708..50730581-chr12:50746052..50748839,2	K562	blood:
44	chr12:50504921..50507362-chr12:50794413..50796105,2	K562	blood:
45	chr12:50812613..50814185-chr12:50823081..50825818,2	MCF-7	breast:
46	chr12:50830783..50832348-chr12:50832808..50834539,2	K562	blood:
47	chr12:50838041..50839748-chr12:50842685..50844805,2	K562	blood:
48	chr12:50825190..50827072-chr12:50827327..50828879,2	K562	blood:
49	chr11:62609053..62609617-chr12:50794323..50794873,2	Hela-S3	cervix:
50	chr12:50575888..50577120-chr12:50707949..50709207,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LARP4-2	chr12:50759435-50759869	NONHSAT028208

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LARP4	hsa-miR-30a-5p	chr12:50870845-50870852
2	LARP4	hsa-miR-30a-5p	chr12:50870831-50870852

Variant related genes	Relation type
ENSG00000203423	TF binding region
LARP4	TF binding region
ENSG00000203424	TF binding region
ENSG00000244266	TF binding region
ENSG00000203421	TF binding region
FAM186A	TF binding region
ENSG00000196082	TF binding region
ENSG00000203425	TF binding region
ENSG00000203422	TF binding region
ENSG00000203423	CpG island
LARP4	CpG island
ENSG00000203424	CpG island
ENSG00000244266	CpG island
ENSG00000203421	CpG island
FAM186A	CpG island
ENSG00000196082	CpG island
ENSG00000203425	CpG island
ENSG00000203422	CpG island
ENSG00000185958	chromatin interactions
ENSG00000272368	chromatin interactions
ENSG00000139624	chromatin interactions
ENSG00000178449	chromatin interactions
ENSG00000050405	chromatin interactions
ENSG00000166803	chromatin interactions
ENSG00000115520	chromatin interactions
ENSG00000203433	chromatin interactions
ENSG00000164187	chromatin interactions
ENSG00000138134	chromatin interactions
ENSG00000203426	chromatin interactions
ENSG00000135457	chromatin interactions
ENSG00000175793	chromatin interactions
ENSG00000145604	chromatin interactions
ENSG00000244266	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000161800	chromatin interactions
ENSG00000167588	chromatin interactions
ENSG00000198589	chromatin interactions
ENSG00000257531	chromatin interactions
ENSG00000103966	chromatin interactions
ENSG00000066084	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000161813	chromatin interactions

Extended variants
information (count: 5882 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5882 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6580738	chr12:50705715-50705716	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542810486	chr12:50705801-50705802	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs553116792	chr12:50705867-50705868	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs11169370	chr12:50705872-50705873	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs182172036	chr12:50705890-50705891	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs564465780	chr12:50705946-50705947	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs533117742	chr12:50705990-50705991	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs139495276	chr12:50706022-50706023	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs563613673	chr12:50706025-50706026	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs149693811	chr12:50706037-50706038	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs549297964	chr12:50706043-50706044	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs566239653	chr12:50706065-50706066	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs569533398	chr12:50706129-50706130	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs551446001	chr12:50706172-50706173	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs539883054	chr12:50706195-50706196	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs187210407	chr12:50706212-50706213	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550611698	chr12:50706217-50706218	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs567304728	chr12:50706247-50706248	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs190868965	chr12:50706268-50706269	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs112090564	chr12:50706272-50706273	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73108263	chr12:50706287-50706288	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538466760	chr12:50706299-50706300	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558188167	chr12:50706331-50706332	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs577739303	chr12:50706336-50706337	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs11169371	chr12:50706346-50706347	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs187307168	chr12:50706355-50706356	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573722852	chr12:50706392-50706393	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543301675	chr12:50706425-50706426	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs559834673	chr12:50706429-50706430	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs190164000	chr12:50706441-50706442	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs551684863	chr12:50706466-50706467	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs564946066	chr12:50706511-50706512	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs530606078	chr12:50706574-50706575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12831176	chr12:50706684-50706685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550723650	chr12:50706706-50706707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546220353	chr12:50706707-50706708	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183194629	chr12:50706728-50706729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534259568	chr12:50706750-50706751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369850330	chr12:50706858-50706859	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557866691	chr12:50706889-50706890	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs144430857	chr12:50706917-50706918	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188335671	chr12:50706940-50706941	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs546834367	chr12:50706963-50706964	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs193029037	chr12:50706979-50706980	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146627672	chr12:50707008-50707009	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558491739	chr12:50707042-50707043	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185564893	chr12:50707078-50707079	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532430843	chr12:50707094-50707095	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs188933264	chr12:50707118-50707119	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs557076991	chr12:50707210-50707211	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
low-grade B-cell lymphoma tumor	18367492	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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3102 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50678400-50708600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:50679800-50708600	Weak transcription	Liver	Liver
3	chr12:50690000-50711800	Weak transcription	Ovary	ovary
4	chr12:50692000-50719800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:50692400-50708800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr12:50693600-50722800	Weak transcription	Fetal Intestine Small	intestine
7	chr12:50697200-50707200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr12:50698200-50705800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr12:50698400-50705800	Weak transcription	A549	lung
10	chr12:50698800-50708600	Weak transcription	Hela-S3	cervix
11	chr12:50704400-50705800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:50704600-50707200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:50705000-50707800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:50705400-50707400	Enhancers	Osteobl	bone
15	chr12:50705400-50707600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:50705600-50706000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr12:50705600-50706000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr12:50705600-50706000	Enhancers	HSMM	muscle
19	chr12:50705600-50706000	Enhancers	HSMMtube	muscle
20	chr12:50705600-50706000	Enhancers	K562	blood
21	chr12:50705600-50706000	Enhancers	NHLF	lung
22	chr12:50705600-50706600	Enhancers	NHDF-Ad	bronchial
23	chr12:50705600-50707400	Enhancers	Stomach Mucosa	stomach
24	chr12:50705800-50706400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr12:50705800-50706400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:50705800-50706400	Enhancers	A549	lung
27	chr12:50705800-50706400	Enhancers	NH-A	brain
28	chr12:50705800-50706600	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr12:50706000-50707000	Weak transcription	HSMM	muscle
30	chr12:50706000-50707400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr12:50706000-50708800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:50706000-50708800	Weak transcription	HSMMtube	muscle
33	chr12:50706000-50708800	Weak transcription	NHLF	lung
34	chr12:50706400-50706800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr12:50706400-50707200	Weak transcription	A549	lung
36	chr12:50706400-50720000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:50706600-50707000	Weak transcription	NHDF-Ad	bronchial
38	chr12:50706600-50708800	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr12:50706800-50709000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr12:50707000-50707200	Enhancers	NHEK	skin
41	chr12:50707000-50707600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:50707000-50707600	Enhancers	HMEC	breast
43	chr12:50707000-50707600	Enhancers	HSMM	muscle
44	chr12:50707000-50707600	Enhancers	NHDF-Ad	bronchial
45	chr12:50707200-50707400	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr12:50707200-50707600	Enhancers	A549	lung
47	chr12:50707200-50707600	Flanking Active TSS	NHEK	skin
48	chr12:50707200-50708200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr12:50707400-50708800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr12:50707400-50720000	Weak transcription	Osteobl	bone

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