Variant report

Variant	nsv872434
Chromosome Location	chr1:151347820-151413180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1212)
CpG islands
(count:977)
Chromatin interactive
region (count:170)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1212 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151371733-151372165	HepG2	liver:	n/a	chr1:151372120-151372135
2	ARID3A	chr1:151371751-151372339	K562	blood:	n/a	chr1:151372120-151372135
3	ATF1	chr1:151371742-151372196	K562	blood:	n/a	n/a
4	ATF1	chr1:151357084-151357455	K562	blood:	n/a	n/a
5	ATF2	chr1:151371634-151372180	GM12878	blood:	n/a	n/a
6	ATF2	chr1:151371724-151372171	GM12878	blood:	n/a	n/a
7	ATF2	chr1:151371626-151372256	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:151371732-151372222	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr1:151371725-151372346	A549	lung:	n/a	n/a
10	ATF3	chr1:151368851-151369032	K562	blood:	n/a	n/a
11	BACH1	chr1:151371808-151372310	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:151405126-151405250	K562	blood:	n/a	n/a
13	BACH1	chr1:151405549-151405676	K562	blood:	n/a	n/a
14	BCL3	chr1:151375014-151375704	A549	lung:	n/a	n/a
15	BCL3	chr1:151373524-151374156	A549	lung:	n/a	n/a
16	BCL3	chr1:151371666-151372235	A549	lung:	n/a	chr1:151372009-151372018
17	BCL3	chr1:151371693-151373473	A549	lung:	n/a	chr1:151372009-151372018
18	BCL3	chr1:151372480-151372962	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:151371605-151372282	GM12878	blood:	n/a	chr1:151372009-151372018
20	BCLAF1	chr1:151371705-151372350	GM12878	blood:	n/a	chr1:151372009-151372018
21	BHLHE40	chr1:151356747-151357326	K562	blood:	n/a	n/a
22	BRCA1	chr1:151371813-151372175	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr1:151372596-151372778	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr1:151360096-151360428	K562	blood:	n/a	n/a
25	CBX3	chr1:151371662-151372200	K562	blood:	n/a	n/a
26	CBX3	chr1:151358593-151358947	K562	blood:	n/a	n/a
27	CCNT2	chr1:151357075-151357435	K562	blood:	n/a	n/a
28	CCNT2	chr1:151372277-151372477	K562	blood:	n/a	n/a
29	CEBPB	chr1:151371706-151372643	MCF-7	breast:	n/a	chr1:151371884-151371895
30	CEBPB	chr1:151372559-151372585	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:151368768-151369104	IMR90	lung:	n/a	chr1:151368942-151368953
32	CEBPB	chr1:151388726-151389184	ECC-1	luminal epithelium:	n/a	chr1:151388928-151388939
33	CEBPB	chr1:151371684-151372272	GM12878	blood:	n/a	chr1:151371884-151371895
34	CEBPB	chr1:151371615-151372199	K562	blood:	n/a	chr1:151371884-151371895
35	CEBPB	chr1:151388793-151389072	K562	blood:	n/a	chr1:151388928-151388939
36	CEBPB	chr1:151371730-151372070	HepG2	liver:	n/a	chr1:151371884-151371895
37	CEBPB	chr1:151368769-151369117	HepG2	liver:	n/a	chr1:151368942-151368953
38	CEBPB	chr1:151407641-151407943	MCF-7	breast:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
39	CEBPB	chr1:151407724-151407933	A549	lung:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
40	CEBPB	chr1:151368823-151369081	K562	blood:	n/a	chr1:151368942-151368953
41	CEBPB	chr1:151388608-151389348	MCF-7	breast:	n/a	chr1:151388928-151388939
42	CEBPB	chr1:151368769-151369121	K562	blood:	n/a	chr1:151368942-151368953
43	CEBPB	chr1:151388768-151389111	H1-hESC	embryonic stem cell:	n/a	chr1:151388928-151388939
44	CEBPB	chr1:151371700-151372167	Hela-S3	cervix:	n/a	chr1:151371884-151371895
45	CEBPB	chr1:151371691-151372192	K562	blood:	n/a	chr1:151371884-151371895
46	CEBPB	chr1:151392443-151392803	A549	lung:	n/a	chr1:151392614-151392625
47	CEBPB	chr1:151368804-151369023	Hela-S3	cervix:	n/a	chr1:151368942-151368953
48	CEBPB	chr1:151388787-151389075	K562	blood:	n/a	chr1:151388928-151388939
49	CEBPB	chr1:151388780-151389091	A549	lung:	n/a	chr1:151388928-151388939
50	CEBPB	chr1:151371703-151372202	HepG2	liver:	n/a	chr1:151371884-151371895

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151371285-151371335	GM12892	blood:	n/a
2	chr1:151371285-151371335	GM12892	blood:	n/a
3	chr1:151371944-151371994	NT2-D1	testis:	n/a
4	chr1:151372581-151372631	AG09309	skin:	n/a
5	chr1:151399683-151399733	NH-A	brain:	n/a
6	chr1:151399683-151399733	HCT-116	colon:	n/a
7	chr1:151375993-151376043	GM12891	blood:	n/a
8	chr1:151371285-151371335	T-47D	breast:	n/a
9	chr1:151372228-151372278	SAEC	small airway:	n/a
10	chr1:151372335-151372385	NB4	blood:	n/a
11	chr1:151371944-151371994	HMEC	breast:	n/a
12	chr1:151371944-151371994	MCF-7	breast:	n/a
13	chr1:151372581-151372631	HRE	kidney:	n/a
14	chr1:151402121-151402171	LNCaP	prostate:	n/a
15	chr1:151371972-151372022	HMEC	breast:	n/a
16	chr1:151371944-151371994	SKMC	muscle:	n/a
17	chr1:151371285-151371335	RPTEC	kidney:	n/a
18	chr1:151372335-151372385	PrEC	prostate:	n/a
19	chr1:151372147-151372197	GM06990	blood:	n/a
20	chr1:151369469-151369519	SAEC	small airway:	n/a
21	chr1:151371944-151371994	PFSK-1	brain:	n/a
22	chr1:151371309-151371359	LNCaP	prostate:	n/a
23	chr1:151369469-151369519	Caco-2	colon:	n/a
24	chr1:151371944-151371994	HCPEpiC	choroid plexus:	n/a
25	chr1:151371285-151371335	MCF10A-Er-Src	breast:	n/a
26	chr1:151372572-151372622	ProgFib	skin:	n/a
27	chr1:151371285-151371335	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:151372652-151372702	PFSK-1	brain:	n/a
29	chr1:151402121-151402171	HEEpiC	esophagus:	n/a
30	chr1:151372147-151372197	NHDF-neo	bronchial:	n/a
31	chr1:151371972-151372022	HIPEpiC	eye:	n/a
32	chr1:151372335-151372385	AG09309	skin:	n/a
33	chr1:151371944-151371994	U87	brain:	n/a
34	chr1:151402121-151402171	T-47D	breast:	n/a
35	chr1:151372652-151372702	ovcar-3	ovarian:	n/a
36	chr1:151371285-151371335	NT2-D1	testis:	n/a
37	chr1:151372147-151372197	LNCaP	prostate:	n/a
38	chr1:151371972-151372022	Hepatocyte	liver:	n/a
39	chr1:151371309-151371359	HepG2	liver:	n/a
40	chr1:151372572-151372622	PFSK-1	brain:	n/a
41	chr1:151371285-151371335	GM19239	blood:	n/a
42	chr1:151372572-151372622	Hepatocyte	liver:	n/a
43	chr1:151372147-151372197	HIPEpiC	eye:	n/a
44	chr1:151400745-151400795	IMR90	lung:	fetal
45	chr1:151372572-151372622	H1-hESC	embryonic stem cell:	embryo
46	chr1:151371944-151371994	CMK	blood:	n/a
47	chr1:151399683-151399733	HRE	kidney:	n/a
48	chr1:151400745-151400795	RPTEC	kidney:	n/a
49	chr1:151400745-151400795	GM12892	blood:	n/a
50	chr1:151399683-151399733	GM12878	blood:	n/a

(count:170 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:151352995..151355687-chr1:151371966..151374635,2	MCF-7	breast:
2	chr1:151348873..151352385-chr1:151370200..151373598,3	MCF-7	breast:
3	1:151203965-151215310..1:151402394-151411623	GM12878	blood:
4	1:151375897-151378579..1:151496437-151509688	Hela-S3	cervix:
5	chr1:151356408..151358278-chr1:151371812..151374330,2	MCF-7	breast:
6	chr1:151394927..151396962-chr1:151399900..151402085,2	K562	blood:
7	chr1:151319505..151321169-chr1:151370320..151372349,2	MCF-7	breast:
8	chr1:151318180..151322621-chr1:151370786..151375600,7	K562	blood:
9	chr1:151268846..151270969-chr1:151374087..151376100,2	MCF-7	breast:
10	chr1:151317696..151319917-chr1:151365664..151368589,2	MCF-7	breast:
11	chr1:151372245..151374554-chr1:151396741..151398920,2	MCF-7	breast:
12	chr1:151318232..151320963-chr1:151353197..151355997,2	MCF-7	breast:
13	1:151381232-151382407..1:151411623-151426875	Hela-S3	cervix:
14	chr1:151370811..151373589-chr1:151512732..151514796,2	K562	blood:
15	chr1:151372236..151373964-chr20:46129058..46130747,2	MCF-7	breast:
16	chr1:151404848..151406397-chr1:151409975..151412744,2	MCF-7	breast:
17	chr1:151298919..151301179-chr1:151402872..151405310,2	MCF-7	breast:
18	chr1:151162193..151163907-chr1:151370731..151372764,2	MCF-7	breast:
19	chr1:151359793..151362779-chr1:151363178..151366342,4	MCF-7	breast:
20	chr1:151344758..151345571-chr1:151371234..151372258,3	MCF-7	breast:
21	chr1:151335378..151338148-chr1:151374572..151377494,3	MCF-7	breast:
22	chr1:151377630..151380310-chr1:151382827..151386169,3	K562	blood:
23	chr1:151225665..151228952-chr1:151371435..151373604,4	MCF-7	breast:
24	chr1:151343293..151346242-chr1:151376581..151379238,2	MCF-7	breast:
25	chr1:151373766..151375598-chr1:151437855..151440411,2	K562	blood:
26	chr1:151298007..151300903-chr1:151353589..151355616,2	MCF-7	breast:
27	chr1:151371183..151372890-chr1:151431011..151433472,2	MCF-7	breast:
28	chr1:151403924..151406134-chr1:151413187..151414813,2	MCF-7	breast:
29	1:151270864-151283078..1:151378579-151379560	H1-hESC	embryonic stem cell:	embryo
30	chr1:151334122..151336931-chr1:151349089..151351816,2	K562	blood:
31	chr1:151389430..151391036-chr1:151431116..151432632,2	MCF-7	breast:
32	chr1:151279190..151281838-chr1:151374219..151376364,2	MCF-7	breast:
33	chr1:151400556..151402238-chr1:151404299..151407025,2	K562	blood:
34	chr1:151353527..151355666-chr1:151374191..151375959,2	K562	blood:
35	1:151402394-151411623..1:151618750-151636526	GM12878	blood:
36	chr1:151372028..151374418-chr1:151511841..151514665,2	MCF-7	breast:
37	1:151393910-151394636..1:151411623-151426875	Hela-S3	cervix:
38	chr1:151348976..151351066-chr1:151352472..151354650,2	K562	blood:
39	chr1:151319321..151320903-chr1:151345990..151347846,2	MCF-7	breast:
40	chr1:151406315..151409257-chr1:151430992..151432763,2	MCF-7	breast:
41	chr1:151371526..151374105-chr1:151428160..151432357,4	K562	blood:
42	chr1:151297425..151301136-chr1:151370895..151373723,5	MCF-7	breast:
43	chr1:151273322..151275078-chr1:151370486..151372389,2	MCF-7	breast:
44	chr1:151343171..151345745-chr1:151364677..151366498,2	MCF-7	breast:
45	chr1:151388224..151390291-chr1:151485508..151488200,2	MCF-7	breast:
46	chr1:151318482..151320695-chr1:151375632..151377570,2	MCF-7	breast:
47	chr1:151397867..151399867-chr1:151430315..151432145,2	MCF-7	breast:
48	chr1:151373885..151375953-chr1:151382352..151386017,5	K562	blood:
49	chr1:151371973..151373501-chr1:151810861..151813533,2	MCF-7	breast:
50	chr1:151253607..151256454-chr1:151374853..151377670,2	MCF-7	breast:

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	POGZ	hsa-miR-34a-5p	chr1:151376091-151376084
2	POGZ	hsa-miR-34a-5p	chr1:151376085-151376106
3	POGZ	hsa-miR-19b-3p	chr1:151376496-151376518
4	POGZ	hsa-miR-130b-3p	chr1:151376495-151376516
5	POGZ	hsa-miR-17-5p	chr1:151376717-151376739
6	POGZ	hsa-miR-221-3p	chr1:151376785-151376779
7	POGZ	hsa-miR-20a-5p	chr1:151376717-151376739
8	POGZ	hsa-miR-9-5p	chr1:151377089-151377112
9	POGZ	hsa-miR-221-3p	chr1:151376779-151376802

Variant related genes	Relation type
SELENBP1	TF binding region
POGZ	TF binding region
PSMB4	TF binding region
RNY4P25	TF binding region
SELENBP1	CpG island
POGZ	CpG island
PSMB4	CpG island
RNY4P25	CpG island
ENSG00000151665	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000197622	chromatin interactions
ENSG00000273481	chromatin interactions
ENSG00000143376	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000143436	chromatin interactions
ENSG00000238711	chromatin interactions
ENSG00000224645	chromatin interactions
ENSG00000143450	chromatin interactions
ENSG00000159377	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000237976	chromatin interactions
ENSG00000143416	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000143393	chromatin interactions
ENSG00000143375	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000163159	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000159352	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000119878	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000225556	chromatin interactions
ENSG00000265753	chromatin interactions
ENSG00000252840	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000143442	chromatin interactions

Extended variants
information (count: 2471 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:2471 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11806477	chr1:151347820-151347821	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149181054	chr1:151347823-151347824	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs553541766	chr1:151347883-151347884	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs529995107	chr1:151347929-151347930	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs550208000	chr1:151347939-151347940	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs143699418	chr1:151347951-151347952	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs539361093	chr1:151347966-151347967	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs146808088	chr1:151347998-151347999	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs373344865	chr1:151348021-151348022	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs116903523	chr1:151348042-151348043	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs534708282	chr1:151348043-151348044	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs370268288	chr1:151348059-151348060	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs554414642	chr1:151348080-151348081	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs373479805	chr1:151348094-151348095	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs78886547	chr1:151348099-151348100	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs71090157	chr1:151348101-151348102	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs397981546	chr1:151348107-151348108	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs12125519	chr1:151348145-151348146	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs557847276	chr1:151348149-151348150	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs536611362	chr1:151348174-151348175	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs540513543	chr1:151348201-151348202	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs145656737	chr1:151348233-151348234	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs576699925	chr1:151348245-151348246	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs183566850	chr1:151348275-151348276	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs12752186	chr1:151348330-151348331	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs35128068	chr1:151348336-151348337	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555968251	chr1:151348361-151348362	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs34540465	chr1:151348376-151348377	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188448531	chr1:151348377-151348378	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs530232993	chr1:151348514-151348515	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs61818030	chr1:151348533-151348534	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs77409040	chr1:151348535-151348536	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs191524267	chr1:151348550-151348551	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs182544134	chr1:151348551-151348552	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs76939749	chr1:151348597-151348598	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs552946410	chr1:151348627-151348628	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs566259699	chr1:151348653-151348654	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs187186995	chr1:151348668-151348669	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs548775325	chr1:151348684-151348685	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs138038769	chr1:151348685-151348686	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs536773963	chr1:151348756-151348757	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs191250088	chr1:151348763-151348764	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs570152069	chr1:151348778-151348779	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs149497251	chr1:151348817-151348818	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs539342115	chr1:151348831-151348832	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs184488996	chr1:151348952-151348953	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs573099787	chr1:151348987-151348988	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs12123091	chr1:151348996-151348997	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190551424	chr1:151349015-151349016	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs574965172	chr1:151349027-151349028	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	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
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1558 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151346000-151351600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:151346400-151348800	Enhancers	Rectal Mucosa Donor 29	rectum
3	chr1:151346600-151349000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr1:151347200-151349000	Weak transcription	Colonic Mucosa	Colon
5	chr1:151347800-151348000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:151347800-151350600	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr1:151348800-151349200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:151349000-151349200	Enhancers	Colonic Mucosa	Colon
9	chr1:151349000-151349200	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr1:151349200-151349800	Weak transcription	Colonic Mucosa	Colon
11	chr1:151349200-151350200	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr1:151349800-151350600	Enhancers	Colonic Mucosa	Colon
13	chr1:151350200-151350600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
14	chr1:151350600-151350800	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr1:151350600-151353400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr1:151351800-151352000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:151353400-151354000	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr1:151353800-151354400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:151356200-151356800	Enhancers	K562	blood
20	chr1:151356800-151357600	Flanking Active TSS	K562	blood
21	chr1:151357000-151358000	Enhancers	HMEC	breast
22	chr1:151357200-151357400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:151357200-151357600	Enhancers	NHEK	skin
24	chr1:151357200-151357800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:151357400-151358000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:151357600-151358200	Enhancers	K562	blood
27	chr1:151358200-151358800	Weak transcription	K562	blood
28	chr1:151358800-151360600	Enhancers	K562	blood
29	chr1:151362000-151362600	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr1:151362200-151362400	Enhancers	Placenta	Placenta
31	chr1:151362200-151362400	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr1:151362400-151363600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr1:151362600-151363200	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr1:151363400-151364000	Enhancers	Liver	Liver
35	chr1:151363600-151365600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr1:151365600-151371200	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr1:151370200-151370400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:151370200-151370800	Enhancers	Fetal Kidney	kidney
39	chr1:151370200-151370800	Enhancers	HepG2	liver
40	chr1:151370400-151371200	Enhancers	A549	lung
41	chr1:151370600-151370800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:151370600-151371200	Enhancers	Dnd41	blood
43	chr1:151370800-151371400	Enhancers	Primary B cells from peripheral blood	blood
44	chr1:151370800-151371400	Weak transcription	Fetal Kidney	kidney
45	chr1:151370800-151371400	Weak transcription	HepG2	liver
46	chr1:151371000-151371200	Enhancers	Primary T cells fromperipheralblood	blood
47	chr1:151371000-151371200	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr1:151371000-151371400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr1:151371000-151371400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:151371200-151371400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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