Variant report

Variant	nsv431389
Chromosome Location	chr15:50795835-50979738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1867)
CpG islands
(count:1223)
Chromatin interactive
region (count:180)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1867 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:50885990-50886949	K562	blood:	n/a	n/a
2	ARID3A	chr15:50914579-50914778	K562	blood:	n/a	n/a
3	ARID3A	chr15:50967665-50968053	K562	blood:	n/a	n/a
4	ARID3A	chr15:50979052-50979685	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:50888476-50888556	K562	blood:	n/a	n/a
6	ARID3A	chr15:50978609-50978827	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:50967684-50968037	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:50802172-50802236	K562	blood:	n/a	n/a
9	ARID3A	chr15:50834985-50835658	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:50969340-50969620	K562	blood:	n/a	n/a
11	ATF1	chr15:50916939-50917053	K562	blood:	n/a	n/a
12	ATF1	chr15:50886574-50886849	K562	blood:	n/a	n/a
13	ATF1	chr15:50969291-50969654	K562	blood:	n/a	n/a
14	ATF1	chr15:50837432-50837566	K562	blood:	n/a	n/a
15	ATF2	chr15:50978203-50979513	GM12878	blood:	n/a	n/a
16	ATF2	chr15:50946651-50947033	GM12878	blood:	n/a	n/a
17	ATF2	chr15:50844379-50844831	GM12878	blood:	n/a	n/a
18	ATF3	chr15:50978593-50979400	A549	lung:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
19	ATF3	chr15:50978739-50979258	H1-hESC	embryonic stem cell:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
20	ATF3	chr15:50978792-50979297	K562	blood:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
21	ATF3	chr15:50978715-50979288	HepG2	liver:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
22	ATF3	chr15:50978747-50979244	K562	blood:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
23	ATF3	chr15:50978870-50979254	K562	blood:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
24	ATF3	chr15:50978856-50979230	HepG2	liver:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
25	ATF3	chr15:50978854-50979160	GM12878	blood:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
26	ATF3	chr15:50969292-50969671	K562	blood:	n/a	n/a
27	ATF3	chr15:50978754-50979263	GM12878	blood:	n/a	chr15:50979056-50979065 chr15:50979046-50979066 chr15:50979046-50979055 chr15:50978958-50978967
28	BACH1	chr15:50869845-50869896	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr15:50978557-50979488	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr15:50978030-50978129	K562	blood:	n/a	n/a
31	BACH1	chr15:50869823-50869907	K562	blood:	n/a	n/a
32	BATF	chr15:50946619-50946969	GM12878	blood:	n/a	n/a
33	BATF	chr15:50946645-50947003	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:50978678-50978973	GM12878	blood:	n/a	chr15:50978779-50978788
35	BCL3	chr15:50978293-50979004	A549	lung:	n/a	chr15:50978779-50978788
36	BCL3	chr15:50978853-50979404	GM12878	blood:	n/a	n/a
37	BCL3	chr15:50978427-50979656	A549	lung:	n/a	chr15:50978779-50978788
38	BCLAF1	chr15:50978234-50979510	GM12878	blood:	n/a	chr15:50978779-50978788
39	BCLAF1	chr15:50978372-50979531	GM12878	blood:	n/a	chr15:50978779-50978788
40	BHLHE40	chr15:50978793-50979274	A549	lung:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978960-50978976
41	BHLHE40	chr15:50978197-50979635	HepG2	liver:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978960-50978976
42	BHLHE40	chr15:50978064-50979738	K562	blood:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978960-50978976
43	BHLHE40	chr15:50967736-50967982	GM12878	blood:	n/a	n/a
44	BHLHE40	chr15:50978902-50979208	HepG2	liver:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50979046-50979055 chr15:50978960-50978976
45	BHLHE40	chr15:50977862-50979784	GM12878	blood:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978960-50978976
46	BHLHE40	chr15:50978898-50979243	HepG2	liver:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50979046-50979055 chr15:50978960-50978976
47	BRCA1	chr15:50978339-50979870	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:50978679-50979332	HepG2	liver:	n/a	n/a
49	BRCA1	chr15:50978749-50979344	H1-hESC	embryonic stem cell:	n/a	n/a
50	CBX3	chr15:50978109-50979754	K562	blood:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:50838805-50838855	CMK	blood:	n/a
2	chr15:50979486-50979536	AG09319	gingival:	n/a
3	chr15:50979198-50979248	SK-N-SH_RA	brain:	n/a
4	chr15:50838805-50838855	CMK	blood:	n/a
5	chr15:50979486-50979536	AG09319	gingival:	n/a
6	chr15:50979198-50979248	SK-N-SH_RA	brain:	n/a
7	chr15:50978903-50978953	AG04449	skin:	fetal
8	chr15:50979137-50979187	HMEC	breast:	n/a
9	chr15:50797795-50797845	HL-60	blood:	n/a
10	chr15:50979137-50979187	NHBE	bronchial:	n/a
11	chr15:50975608-50975658	HRCEpiC	kidney:	n/a
12	chr15:50920452-50920502	HepG2	liver:	n/a
13	chr15:50853806-50853856	AG09319	gingival:	n/a
14	chr15:50979137-50979187	GM12878	blood:	n/a
15	chr15:50978903-50978953	SK-N-SH	brain:	n/a
16	chr15:50838905-50838955	AG04450	lung:	fetal
17	chr15:50978344-50978394	ProgFib	skin:	n/a
18	chr15:50978344-50978394	Caco-2	colon:	n/a
19	chr15:50979356-50979406	HRPEpiC	eye:	n/a
20	chr15:50979172-50979222	AG09309	skin:	n/a
21	chr15:50839463-50839513	AG10803	skin:	n/a
22	chr15:50979172-50979222	HCT-116	colon:	n/a
23	chr15:50979172-50979222	AG04449	skin:	fetal
24	chr15:50853806-50853856	SKMC	muscle:	n/a
25	chr15:50978887-50978937	HepG2	liver:	n/a
26	chr15:50978624-50978674	AG09319	gingival:	n/a
27	chr15:50978624-50978674	ovcar-3	ovarian:	n/a
28	chr15:50979175-50979225	IMR90	lung:	fetal
29	chr15:50797795-50797845	SKMC	muscle:	n/a
30	chr15:50839326-50839376	Jurkat	blood:	n/a
31	chr15:50978903-50978953	GM19239	blood:	n/a
32	chr15:50920452-50920502	HCF	heart:	n/a
33	chr15:50978903-50978953	ECC-1	luminal epithelium:	n/a
34	chr15:50979356-50979406	PrEC	prostate:	n/a
35	chr15:50979172-50979222	ovcar-3	ovarian:	n/a
36	chr15:50979137-50979187	ovcar-3	ovarian:	n/a
37	chr15:50978903-50978953	HMEC	breast:	n/a
38	chr15:50920452-50920502	SKMC	muscle:	n/a
39	chr15:50978903-50978953	CMK	blood:	n/a
40	chr15:50979486-50979536	SK-N-SH_RA	brain:	n/a
41	chr15:50838805-50838855	T-47D	breast:	n/a
42	chr15:50839463-50839513	HEK293	kidney:	embryo
43	chr15:50797795-50797845	AG04450	lung:	fetal
44	chr15:50978344-50978394	HIPEpiC	eye:	n/a
45	chr15:50979175-50979225	HCT-116	colon:	n/a
46	chr15:50979172-50979222	PrEC	prostate:	n/a
47	chr15:50978903-50978953	IMR90	lung:	fetal
48	chr15:50838805-50838855	HRPEpiC	eye:	n/a
49	chr15:50838805-50838855	PFSK-1	brain:	n/a
50	chr15:50979172-50979222	BJ	skin:	n/a

(count:180 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr15:50644948..50647496-chr15:50903184..50905724,2	MCF-7	breast:
2	chr15:50960793..50963238-chr15:50977313..50978978,2	K562	blood:
3	chr15:50872498..50875116-chr15:50878753..50881368,3	K562	blood:
4	chr15:50978805..50979560-chr9:131940463..131940977,2	Hela-S3	cervix:
5	chr15:50897808..50900573-chr15:50902086..50904020,3	K562	blood:
6	chr15:50978559..50979416-chr16:69166261..69166935,2	Hela-S3	cervix:
7	chr15:50977419..50980911-chr15:51055926..51058477,4	K562	blood:
8	chr15:50838341..50841082-chr15:50844328..50846854,3	MCF-7	breast:
9	chr15:50897808..50900573-chr15:50902086..50904020,3	K562	blood:
10	chr15:50900703..50903174-chr15:51177027..51179659,2	K562	blood:
11	chr15:50917148..50919923-chr15:50927346..50929750,2	MCF-7	breast:
12	chr15:50859308..50861522-chr15:50879370..50881097,2	K562	blood:
13	chr15:50966474..50968190-chr15:51199130..51200749,2	K562	blood:
14	chr15:50864188..50868322-chr15:50872346..50875460,4	MCF-7	breast:
15	chr15:50977319..50980700-chr15:51053372..51060901,7	MCF-7	breast:
16	chr15:50973045..50977004-chr15:50977096..50981509,8	MCF-7	breast:
17	chr15:50978981..50979771-chr5:102897847..102898677,2	Hela-S3	cervix:
18	chr15:50967034..50970898-chr15:50976195..50981538,7	MCF-7	breast:
19	chr15:50966292..50969121-chr15:50972031..50974489,2	MCF-7	breast:
20	chr15:50965673..50968390-chr15:50973534..50976519,4	MCF-7	breast:
21	chr15:50865607..50867294-chr15:50870808..50872374,2	K562	blood:
22	chr15:50855242..50858331-chr15:50858835..50863040,3	MCF-7	breast:
23	chr15:50977199..50979864-chr15:51198670..51201821,3	K562	blood:
24	chr15:50967599..50968454-chr15:51200392..51201306,2	MCF-7	breast:
25	chr15:50649293..50650992-chr15:50796880..50798462,2	K562	blood:
26	chr15:50646500..50650701-chr15:50853140..50859875,5	MCF-7	breast:
27	chr15:50855242..50858331-chr15:50858835..50863040,3	MCF-7	breast:
28	chr15:50850389..50851956-chr15:50856015..50858567,2	MCF-7	breast:
29	chr1:185286540..185287260-chr15:50978376..50979105,2	Hela-S3	cervix:
30	chr15:50824175..50826190-chr15:50832683..50834926,2	K562	blood:
31	chr15:50968075..50970371-chr15:50973125..50975063,3	K562	blood:
32	chr15:50952539..50954101-chr15:50965400..50967818,2	MCF-7	breast:
33	chr15:50977014..50979307-chr16:3505643..3508008,2	MCF-7	breast:
34	chr11:62572414..62573039-chr15:50978738..50979496,2	HCT-116	colon:
35	chr15:50967262..50968901-chr15:51168741..51169920,12	MCF-7	breast:
36	chr15:50909782..50912270-chr15:50977423..50980353,2	MCF-7	breast:
37	chr15:50894679..50897378-chr15:50902879..50904659,2	MCF-7	breast:
38	chr15:50952143..50955128-chr15:50963357..50965554,2	MCF-7	breast:
39	chr15:50958513..50961028-chr15:50962323..50965128,2	MCF-7	breast:
40	chr15:50832514..50835250-chr15:50836851..50839622,2	MCF-7	breast:
41	chr15:50950841..50953949-chr15:50977256..50979811,4	MCF-7	breast:
42	chr15:50842951..50845112-chr15:50852235..50854464,2	MCF-7	breast:
43	chr15:50869586..50872138-chr15:50874488..50876598,3	K562	blood:
44	chr15:50970140..50972080-chr15:50972168..50973694,2	MCF-7	breast:
45	chr15:50944212..50946075-chr15:50977425..50980194,3	K562	blood:
46	chr11:46368370..46369020-chr15:50978346..50979082,2	NB4	blood:
47	chr15:50970140..50972080-chr15:50972168..50973694,2	MCF-7	breast:
48	chr15:50977313..50978812-chr15:51169055..51169789,4	MCF-7	breast:
49	chr15:50978732..50980573-chr15:51017236..51021857,4	K562	blood:
50	chr15:50978167..50979033-chr3:171757700..171758531,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP50-5	chr15:50883698-50883786	l_1156_chr15:50879698-50884434_liver
2	lnc-USP8-3	chr15:50873840-50874894	l_1155_chr15:50872073-50874894_testes
3	lnc-USP8-1	chr15:50852196-50852697	ENSG00000259684.1
4	lnc-USP8-1	chr15:50850820-50850825	ENSG00000259684.1
5	lnc-USP8-1	chr15:50849798-50849895	ENSG00000259684.1
6	lnc-USP8-3	chr15:50872074-50872178	l_1155_chr15:50872073-50874894_testes
7	lnc-USP50-5	chr15:50883983-50884434	l_1156_chr15:50879698-50884434_liver
8	lnc-USP50-5	chr15:50879699-50880406	l_1156_chr15:50879698-50884434_liver
9	lnc-USP50-5	chr15:50882478-50883336	l_1156_chr15:50879698-50884434_liver

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	TRPM7	hsa-miR-21-5p	chr15:50852616-50852636
2	TRPM7	hsa-miR-21-5p	chr15:50852622-50852616
3	TRPM7	hsa-miR-9-5p	chr15:50853537-50853560
4	TRPM7	hsa-miR-9-5p	chr15:50853004-50853026
5	TRPM7	hsa-miR-10a-5p	chr15:50853328-50853352
6	TRPM7	hsa-miR-9-5p	chr15:50853009-50853003
7	TRPM7	hsa-miR-9-5p	chr15:50853543-50853537
8	TRPM7	hsa-miR-10a-5p	chr15:50896505-50896530
9	TRPM7	hsa-miR-10a-5p	chr15:50896593-50896615

Variant related genes	Relation type
RN7SL354P	TF binding region
USP50	TF binding region
TRPM7	TF binding region
ENSG00000259298	TF binding region
ENSG00000259684	TF binding region
RN7SL354P	CpG island
USP50	CpG island
TRPM7	CpG island
ENSG00000259298	CpG island
ENSG00000259684	CpG island
ENSG00000116161	chromatin interactions
ENSG00000170236	chromatin interactions
ENSG00000259684	chromatin interactions
ENSG00000138592	chromatin interactions
ENSG00000243027	chromatin interactions
ENSG00000081014	chromatin interactions
ENSG00000141076	chromatin interactions
ENSG00000262621	chromatin interactions
ENSG00000259773	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000162231	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000130726	chromatin interactions
ENSG00000259715	chromatin interactions
ENSG00000092439	chromatin interactions
ENSG00000264109	chromatin interactions
ENSG00000075420	chromatin interactions
ENSG00000122390	chromatin interactions
ENSG00000061273	chromatin interactions
ENSG00000273004	chromatin interactions
ENSG00000100348	chromatin interactions
ENSG00000179218	chromatin interactions
ENSG00000168802	chromatin interactions
ENSG00000259298	chromatin interactions
ENSG00000112874	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000104064	chromatin interactions

Extended variants
information (count: 7516 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:7516 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12708423	chr15:50795835-50795836	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556490116	chr15:50795899-50795900	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs185136808	chr15:50795918-50795919	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs80113186	chr15:50795919-50795920	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7181536	chr15:50795984-50795985	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs571671554	chr15:50796009-50796010	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189991680	chr15:50796023-50796024	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560802915	chr15:50796067-50796068	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182632086	chr15:50796080-50796081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs3131613	chr15:50796103-50796104	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188311995	chr15:50796147-50796148	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs193201770	chr15:50796154-50796155	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs549828774	chr15:50796181-50796182	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs200410120	chr15:50796182-50796183	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs551890936	chr15:50796214-50796215	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs566988985	chr15:50796240-50796241	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs183441115	chr15:50796263-50796264	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs549404113	chr15:50796314-50796315	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs541570446	chr15:50796325-50796326	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs567908218	chr15:50796415-50796416	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs116345936	chr15:50796422-50796423	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs556864624	chr15:50796437-50796438	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs571728068	chr15:50796524-50796525	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs538862588	chr15:50796526-50796527	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs56023772	chr15:50796530-50796531	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs553421680	chr15:50796535-50796536	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs4581651	chr15:50796554-50796555	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs571811031	chr15:50796601-50796602	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs149008265	chr15:50796656-50796657	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs549216906	chr15:50796663-50796664	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs143845186	chr15:50796711-50796712	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs576033377	chr15:50796749-50796750	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs138471038	chr15:50796767-50796768	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs144026884	chr15:50796773-50796774	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs532176114	chr15:50796783-50796784	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs146504172	chr15:50796816-50796817	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs368842248	chr15:50796818-50796819	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs567162436	chr15:50796833-50796834	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs531380440	chr15:50796852-50796853	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs113184806	chr15:50796894-50796895	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs527797059	chr15:50796903-50796904	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs188898157	chr15:50796904-50796905	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs560535307	chr15:50796941-50796942	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs139162366	chr15:50796948-50796949	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs192570442	chr15:50796993-50796994	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs183689510	chr15:50796994-50796995	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs538799607	chr15:50797021-50797022	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs551271868	chr15:50797022-50797023	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs553953771	chr15:50797060-50797061	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs3131612	chr15:50797061-50797062	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4108 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50738200-50796800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr15:50741800-50797000	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr15:50751000-50796600	Strong transcription	Fetal Thymus	thymus
4	chr15:50754400-50797000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:50757000-50796600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:50757000-50796800	Strong transcription	Liver	Liver
7	chr15:50763600-50796200	Strong transcription	Primary T cells from cord blood	blood
8	chr15:50768000-50796800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:50768400-50797000	Strong transcription	Duodenum Mucosa	Duodenum
10	chr15:50768400-50797000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr15:50768800-50796000	Strong transcription	Hela-S3	cervix
12	chr15:50771200-50796000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr15:50772400-50796000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr15:50772800-50796000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:50774200-50797600	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr15:50776000-50796000	Strong transcription	Fetal Intestine Large	intestine
17	chr15:50776400-50796000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:50777000-50796000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr15:50777400-50796000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:50778400-50796800	Strong transcription	Primary B cells from cord blood	blood
21	chr15:50778800-50796000	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr15:50779400-50796000	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr15:50779400-50796800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr15:50780000-50796200	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr15:50780200-50796000	Strong transcription	Placenta	Placenta
26	chr15:50781000-50796000	Strong transcription	HSMM	muscle
27	chr15:50785800-50797000	Weak transcription	Right Ventricle	heart
28	chr15:50785800-50798400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr15:50786000-50798000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr15:50786200-50797000	Weak transcription	Pancreas	Pancrea
31	chr15:50786200-50797200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr15:50786200-50797200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr15:50786200-50797200	Weak transcription	Esophagus	oesophagus
34	chr15:50786200-50810000	Weak transcription	Psoas Muscle	Psoas
35	chr15:50786400-50796800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr15:50786400-50797400	Weak transcription	Fetal Heart	heart
37	chr15:50786400-50798400	Weak transcription	Gastric	stomach
38	chr15:50787600-50796000	Strong transcription	A549	lung
39	chr15:50789600-50798200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr15:50789600-50798200	Weak transcription	Aorta	Aorta
41	chr15:50789600-50798200	Weak transcription	HepG2	liver
42	chr15:50791000-50796600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr15:50791400-50798000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr15:50791400-50805400	Weak transcription	Small Intestine	intestine
45	chr15:50791800-50797400	Weak transcription	HUVEC	blood vessel
46	chr15:50791800-50798200	Weak transcription	Brain Angular Gyrus	brain
47	chr15:50792000-50797400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr15:50792400-50796000	Strong transcription	Left Ventricle	heart
49	chr15:50792400-50797000	Strong transcription	Fetal Muscle Leg	muscle
50	chr15:50792400-50797200	Weak transcription	Colonic Mucosa	Colon

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