Variant report

Variant	nsv1011146
Chromosome Location	chr3:145859022-145911429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1646)
CpG islands
(count:1102)
Chromatin interactive
region (count:64)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

(count:1646 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:145881409-145881740	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:145905111-145905471	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:145866291-145866894	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:145907384-145907759	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:145905102-145905388	K562	blood:	n/a	n/a
6	ARID3A	chr3:145878060-145878370	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:145878807-145879683	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:145871872-145872857	HepG2	liver:	n/a	chr3:145872347-145872363
9	ATF3	chr3:145884074-145884786	A549	lung:	n/a	n/a
10	ATF3	chr3:145881178-145881929	A549	lung:	n/a	n/a
11	ATF3	chr3:145878768-145879437	A549	lung:	n/a	chr3:145879029-145879038 chr3:145879022-145879031
12	ATF3	chr3:145883039-145883561	A549	lung:	n/a	n/a
13	ATF3	chr3:145884110-145884736	A549	lung:	n/a	n/a
14	ATF3	chr3:145881251-145881898	A549	lung:	n/a	n/a
15	BACH1	chr3:145877746-145879300	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:145860505-145860803	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr3:145881242-145882194	A549	lung:	n/a	n/a
18	BCL3	chr3:145884072-145884734	A549	lung:	n/a	n/a
19	BCL3	chr3:145883950-145884783	A549	lung:	n/a	n/a
20	BCL3	chr3:145881165-145882063	A549	lung:	n/a	n/a
21	BCL3	chr3:145879045-145879892	A549	lung:	n/a	chr3:145879065-145879078 chr3:145879062-145879075 chr3:145879564-145879573 chr3:145879061-145879074 chr3:145879061-145879070
22	BCL3	chr3:145877875-145879857	A549	lung:	n/a	chr3:145878879-145878892 chr3:145878816-145878829 chr3:145878912-145878925 chr3:145879065-145879078 chr3:145879062-145879075 chr3:145878817-145878830 chr3:145879564-145879573 chr3:145879061-145879074 chr3:145879061-145879070 chr3:145878616-145878629
23	BCL3	chr3:145882798-145883742	A549	lung:	n/a	n/a
24	BHLHE40	chr3:145878763-145879434	HepG2	liver:	n/a	chr3:145879070-145879086 chr3:145879064-145879080 chr3:145878903-145878919 chr3:145878975-145878991 chr3:145878968-145878984
25	BRCA1	chr3:145877526-145879027	Hela-S3	cervix:	n/a	chr3:145878834-145878843
26	BRCA1	chr3:145907095-145907688	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr3:145878647-145879379	HepG2	liver:	n/a	chr3:145878834-145878843
28	BRCA1	chr3:145884019-145884965	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr3:145907921-145907927	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr3:145881384-145882143	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr3:145878644-145879148	H1-hESC	embryonic stem cell:	n/a	chr3:145878834-145878843
32	CCNT2	chr3:145878882-145879094	K562	blood:	n/a	n/a
33	CEBPB	chr3:145882618-145883740	A549	lung:	n/a	n/a
34	CEBPB	chr3:145883042-145883535	A549	lung:	n/a	n/a
35	CEBPB	chr3:145881286-145881932	MCF-7	breast:	n/a	chr3:145881574-145881585 chr3:145881594-145881605
36	CEBPB	chr3:145881255-145882206	MCF-7	breast:	n/a	chr3:145881574-145881585 chr3:145881594-145881605
37	CEBPB	chr3:145906760-145907681	A549	lung:	n/a	chr3:145907081-145907092
38	CEBPB	chr3:145878030-145879797	A549	lung:	n/a	n/a
39	CEBPB	chr3:145866309-145866832	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:145866386-145866758	A549	lung:	n/a	n/a
41	CEBPB	chr3:145882861-145885527	Hela-S3	cervix:	n/a	chr3:145884293-145884304 chr3:145885330-145885341 chr3:145885330-145885341 chr3:145885328-145885341
42	CEBPB	chr3:145881274-145882183	A549	lung:	n/a	chr3:145881574-145881585 chr3:145881594-145881605
43	CEBPB	chr3:145907003-145907698	MCF-7	breast:	n/a	chr3:145907081-145907092
44	CEBPB	chr3:145881349-145881918	HCT-116	colon:	n/a	chr3:145881574-145881585 chr3:145881594-145881605
45	CEBPB	chr3:145884056-145884731	A549	lung:	n/a	chr3:145884293-145884304
46	CEBPB	chr3:145907044-145907156	K562	blood:	n/a	chr3:145907081-145907092
47	CEBPB	chr3:145872776-145873081	K562	blood:	n/a	chr3:145872911-145872923
48	CEBPB	chr3:145866356-145866830	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:145866266-145866810	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr3:145881178-145882375	A549	lung:	n/a	chr3:145881574-145881585 chr3:145881594-145881605

(count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145879430-145879480	HCM	heart:	n/a
2	chr3:145879084-145879134	AG09319	gingival:	n/a
3	chr3:145879430-145879480	LNCaP	prostate:	n/a
4	chr3:145878431-145878481	HL-60	blood:	n/a
5	chr3:145879430-145879480	HCM	heart:	n/a
6	chr3:145879084-145879134	AG09319	gingival:	n/a
7	chr3:145879430-145879480	LNCaP	prostate:	n/a
8	chr3:145878431-145878481	HL-60	blood:	n/a
9	chr3:145871392-145871442	NB4	blood:	n/a
10	chr3:145879710-145879760	SKMC	muscle:	n/a
11	chr3:145875907-145875957	AoSMC	blood vessel:	n/a
12	chr3:145875907-145875957	CMK	blood:	n/a
13	chr3:145860909-145860959	HEK293	kidney:	embryo
14	chr3:145878539-145878589	HCT-116	colon:	n/a
15	chr3:145875907-145875957	ProgFib	skin:	n/a
16	chr3:145879686-145879736	GM12892	blood:	n/a
17	chr3:145879084-145879134	PrEC	prostate:	n/a
18	chr3:145879642-145879692	HEK293	kidney:	embryo
19	chr3:145871392-145871442	HEEpiC	esophagus:	n/a
20	chr3:145860909-145860959	K562	blood:	n/a
21	chr3:145878979-145879029	PFSK-1	brain:	n/a
22	chr3:145879686-145879736	HNPCEpiC	eye:	n/a
23	chr3:145879430-145879480	NHBE	bronchial:	n/a
24	chr3:145879277-145879327	NHDF-neo	bronchial:	n/a
25	chr3:145860909-145860959	T-47D	breast:	n/a
26	chr3:145879626-145879676	HCT-116	colon:	n/a
27	chr3:145878177-145878227	ECC-1	luminal epithelium:	n/a
28	chr3:145860909-145860959	IMR90	lung:	fetal
29	chr3:145879084-145879134	SKMC	muscle:	n/a
30	chr3:145881800-145881850	CMK	blood:	n/a
31	chr3:145879710-145879760	AoSMC	blood vessel:	n/a
32	chr3:145879568-145879618	HCF	heart:	n/a
33	chr3:145883489-145883539	AG09309	skin:	n/a
34	chr3:145878539-145878589	HUVEC	blood vessel:	n/a
35	chr3:145879686-145879736	SKMC	muscle:	n/a
36	chr3:145879430-145879480	Hepatocyte	liver:	n/a
37	chr3:145879710-145879760	LNCaP	prostate:	n/a
38	chr3:145878979-145879029	HEK293	kidney:	embryo
39	chr3:145879642-145879692	MCF10A-Er-Src	breast:	n/a
40	chr3:145883489-145883539	BJ	skin:	n/a
41	chr3:145878979-145879029	K562	blood:	n/a
42	chr3:145878539-145878589	H1-hESC	embryonic stem cell:	embryo
43	chr3:145879568-145879618	MCF-7	breast:	n/a
44	chr3:145879686-145879736	HRE	kidney:	n/a
45	chr3:145883489-145883539	NT2-D1	testis:	n/a
46	chr3:145879626-145879676	HRE	kidney:	n/a
47	chr3:145879084-145879134	Jurkat	blood:	n/a
48	chr3:145878177-145878227	HEEpiC	esophagus:	n/a
49	chr3:145860909-145860959	AoSMC	blood vessel:	n/a
50	chr3:145879568-145879618	NT2-D1	testis:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:145783388..145783946-chr3:145902245..145902938,2	MCF-7	breast:
2	chr3:145907272..145908250-chr3:146358720..146359373,2	MCF-7	breast:
3	chr3:145886536..145888429-chr3:145902390..145904087,2	MCF-7	breast:
4	chr3:145897285..145900091-chr3:145902174..145904427,2	MCF-7	breast:
5	chr3:145883004..145884526-chr3:145908906..145911614,2	MCF-7	breast:
6	chr3:145885862..145887990-chr3:145898381..145900841,2	MCF-7	breast:
7	chr3:145877161..145880633-chr3:145902263..145906629,5	MCF-7	breast:
8	chr3:145881041..145885690-chr3:145886054..145890900,6	MCF-7	breast:
9	chr3:145877078..145879512-chr3:145896928..145899546,3	MCF-7	breast:
10	chr3:145843855..145845524-chr3:145864168..145866252,2	MCF-7	breast:
11	chr3:145878954..145881409-chr3:145891982..145893775,2	MCF-7	breast:
12	chr3:145870477..145872332-chr3:145872492..145874567,2	MCF-7	breast:
13	chr3:145782122..145785411-chr3:145878106..145882365,5	MCF-7	breast:
14	chr3:145878063..145880102-chr6:43735669..43738313,2	MCF-7	breast:
15	chr3:145804083..145806262-chr3:145874178..145876137,2	MCF-7	breast:
16	chr3:145783076..145784215-chr3:145904959..145906020,4	MCF-7	breast:
17	chr3:145783058..145783996-chr3:145865459..145867166,7	MCF-7	breast:
18	chr3:145897285..145900091-chr3:145902174..145904427,2	MCF-7	breast:
19	chr3:63896385..63899379-chr3:145877518..145879661,2	MCF-7	breast:
20	chr3:145864521..145866275-chr3:145870715..145872248,2	MCF-7	breast:
21	chr20:56286022..56288671-chr3:145875051..145877020,2	MCF-7	breast:
22	chr3:145779679..145784840-chr3:145877412..145880527,5	MCF-7	breast:
23	chr3:145779537..145781361-chr3:145905477..145907451,2	MCF-7	breast:
24	chr3:145860639..145862586-chr3:145877075..145878969,2	MCF-7	breast:
25	chr3:145736816..145738594-chr3:145881561..145884475,2	MCF-7	breast:
26	chr3:145781835..145785011-chr3:145902581..145906704,4	MCF-7	breast:
27	chr3:145876765..145880789-chr3:145885972..145889074,4	MCF-7	breast:
28	chr3:145883004..145884526-chr3:145908906..145911614,2	MCF-7	breast:
29	chr3:145865509..145867074-chr3:145870719..145872599,2	K562	blood:
30	chr3:145863564..145865449-chr3:145867210..145869807,2	MCF-7	breast:
31	chr3:145862765..145866552-chr3:145878072..145880810,4	MCF-7	breast:
32	chr11:67889304..67890106-chr3:145878724..145879660,2	Hela-S3	cervix:
33	chr3:145884303..145885954-chr3:145902265..145904653,2	MCF-7	breast:
34	chr3:145878599..145881384-chr3:145968449..145970595,2	MCF-7	breast:
35	chr3:145880474..145882151-chr3:145882740..145884446,2	K562	blood:
36	chr17:66031764..66032335-chr3:145878797..145879348,2	Hela-S3	cervix:
37	chr3:145738494..145739375-chr3:145904889..145905776,3	MCF-7	breast:
38	chr3:145865509..145867074-chr3:145870719..145872599,2	K562	blood:
39	chr3:145884303..145885954-chr3:145902265..145904653,2	MCF-7	breast:
40	chr3:145787365..145792721-chr3:145875341..145880381,7	MCF-7	breast:
41	chr11:58245426..58248139-chr3:145902493..145905033,2	MCF-7	breast:
42	chr3:145783014..145783624-chr3:145865958..145866776,2	MCF-7	breast:
43	chr3:145832179..145836696-chr3:145881447..145885871,6	MCF-7	breast:
44	chr3:145879440..145881243-chr3:146138706..146140785,2	MCF-7	breast:
45	chr3:145870477..145872332-chr3:145872492..145874567,2	MCF-7	breast:
46	chr3:145874654..145883964-chr3:145902489..145908084,13	MCF-7	breast:
47	chr3:145886536..145888429-chr3:145902390..145904087,2	MCF-7	breast:
48	chr3:145877632..145880246-chrX:55477813..55479806,2	MCF-7	breast:
49	chr3:145856481..145858828-chr3:145868804..145871513,3	MCF-7	breast:
50	chr3:145783270..145783989-chr3:145904824..145905816,4	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC107021.1-6	chr3:145881383-145881588	NONHSAT092552
2	lnc-PLOD2-3	chr3:145884655-145884915	NONHSAT092553
3	lnc-AC107021.1-6	chr3:145880657-145880745	NONHSAT092552

No data

(count:10 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PLSCR4	hsa-miR-103a-3p	chr3:145910624-145910647
2	PLSCR4	hsa-miR-16-5p	chr3:145910796-145910817
3	PLSCR4	hsa-miR-124-3p	chr3:145910564-145910583
4	PLSCR4	hsa-miR-16-5p	chr3:145910629-145910622
5	PLSCR4	hsa-miR-16-5p	chr3:145910623-145910644
6	PLSCR4	hsa-miR-15b-5p	chr3:145910623-145910644
7	PLSCR4	hsa-miR-15b-5p	chr3:145910629-145910622
8	PLSCR4	hsa-miR-15b-5p	chr3:145910793-145910815
9	PLSCR4	hsa-miR-16-5p	chr3:145910585-145910607
10	PLSCR4	hsa-miR-15b-5p	chr3:145910585-145910606

Variant related genes	Relation type
PLOD2	TF binding region
PLOD2	CpG island
ENSG00000114698	chromatin interactions
ENSG00000232013	chromatin interactions
ENSG00000255236	chromatin interactions
ENSG00000112715	chromatin interactions
ENSG00000243415	chromatin interactions
ENSG00000187601	chromatin interactions
ENSG00000266328	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000163932	chromatin interactions
ENSG00000152952	chromatin interactions
ENSG00000124225	chromatin interactions
ENSG00000182481	chromatin interactions

Extended variants
information (count: 1859 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1859 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535117282	chr3:145859035-145859036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368926359	chr3:145859055-145859056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553232078	chr3:145859079-145859080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145892330	chr3:145859122-145859123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376169918	chr3:145859153-145859154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539064151	chr3:145859161-145859162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564865019	chr3:145859170-145859171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532192128	chr3:145859175-145859176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552082656	chr3:145859223-145859224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73865325	chr3:145859230-145859231	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531129997	chr3:145859235-145859236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557414230	chr3:145859278-145859279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549507473	chr3:145859350-145859351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187055368	chr3:145859364-145859365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377745580	chr3:145859414-145859415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191861871	chr3:145859458-145859459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555667872	chr3:145859469-145859470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575974141	chr3:145859643-145859644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1170388	chr3:145859715-145859716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138616359	chr3:145859716-145859717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536161518	chr3:145859739-145859740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141133805	chr3:145859842-145859843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184399375	chr3:145859874-145859875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369091189	chr3:145859895-145859896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555099016	chr3:145859901-145859902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374170834	chr3:145859936-145859937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573404417	chr3:145859944-145859945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565002278	chr3:145859976-145859977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576893389	chr3:145860065-145860066	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9856304	chr3:145860245-145860246	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544194570	chr3:145860247-145860248	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34392701	chr3:145860271-145860272	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs531194247	chr3:145860273-145860274	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549451317	chr3:145860274-145860275	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146943957	chr3:145860287-145860288	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189326207	chr3:145860326-145860327	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546670485	chr3:145860327-145860328	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571371866	chr3:145860341-145860342	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538770856	chr3:145860486-145860487	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550907467	chr3:145860526-145860527	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77073087	chr3:145860545-145860546	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539090101	chr3:145860574-145860575	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559054368	chr3:145860582-145860583	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149546020	chr3:145860585-145860586	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144017913	chr3:145860594-145860595	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566812925	chr3:145860618-145860619	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566650808	chr3:145860649-145860650	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141450739	chr3:145860665-145860666	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534291349	chr3:145860672-145860673	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375914557	chr3:145860676-145860677	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1456 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145832000-145870800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:145835800-145874000	Weak transcription	Psoas Muscle	Psoas
3	chr3:145840400-145874000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr3:145843600-145861200	Weak transcription	Right Ventricle	heart
5	chr3:145844600-145860600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:145850400-145860200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr3:145850400-145864400	Weak transcription	HMEC	breast
8	chr3:145851600-145860400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:145851600-145864200	Weak transcription	Right Atrium	heart
10	chr3:145852600-145860400	Weak transcription	NH-A	brain
11	chr3:145852800-145860600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr3:145853200-145860400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:145853200-145861600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr3:145855400-145860400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:145855800-145862000	Enhancers	Fetal Stomach	stomach
16	chr3:145856000-145861400	Enhancers	Rectal Smooth Muscle	rectum
17	chr3:145856200-145859200	Enhancers	Adipose Nuclei	Adipose
18	chr3:145856200-145860200	Enhancers	Colon Smooth Muscle	Colon
19	chr3:145856200-145862200	Enhancers	Fetal Heart	heart
20	chr3:145856400-145861200	Weak transcription	HepG2	liver
21	chr3:145856400-145864200	Weak transcription	Left Ventricle	heart
22	chr3:145856400-145875800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:145856800-145860400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr3:145857000-145859400	Enhancers	Liver	Liver
25	chr3:145857400-145860000	Enhancers	Osteobl	bone
26	chr3:145857800-145860600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:145858000-145860200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:145858000-145860200	Weak transcription	HSMMtube	muscle
29	chr3:145858000-145860200	Weak transcription	NHDF-Ad	bronchial
30	chr3:145858000-145860400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr3:145858000-145860400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr3:145858000-145860400	Weak transcription	Brain Substantia Nigra	brain
33	chr3:145858000-145861800	Enhancers	A549	lung
34	chr3:145858200-145859200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr3:145858200-145859200	Weak transcription	Fetal Intestine Small	intestine
36	chr3:145858200-145859200	Weak transcription	NHLF	lung
37	chr3:145858200-145860200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr3:145858200-145860200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:145858200-145860200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr3:145858200-145860200	Weak transcription	Brain Hippocampus Middle	brain
41	chr3:145858200-145860200	Weak transcription	Ovary	ovary
42	chr3:145858200-145860200	Weak transcription	HSMM	muscle
43	chr3:145858200-145860200	Weak transcription	HUVEC	blood vessel
44	chr3:145858200-145860400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr3:145858200-145860400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr3:145858200-145860400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr3:145858200-145860400	Weak transcription	Fetal Kidney	kidney
48	chr3:145858200-145860600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr3:145858400-145860000	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr3:145858400-145860400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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