Variant report

Variant	nsv904213
Chromosome Location	chr15:51011402-51119731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1145)
CpG islands
(count:1037)
Chromatin interactive
region (count:128)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:51059347-51059688	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:51057083-51058225	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:51058735-51059038	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:51069432-51069509	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:51045651-51046001	K562	blood:	n/a	n/a
6	ARID3A	chr15:51057958-51058011	K562	blood:	n/a	n/a
7	ARID3A	chr15:51102246-51102334	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:51056462-51056754	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:51056430-51057534	K562	blood:	n/a	n/a
10	ARID3A	chr15:51110747-51110790	K562	blood:	n/a	n/a
11	ATF1	chr15:51090944-51091269	K562	blood:	n/a	n/a
12	ATF1	chr15:51045773-51045996	K562	blood:	n/a	n/a
13	ATF2	chr15:51057209-51058191	GM12878	blood:	n/a	n/a
14	ATF3	chr15:51090913-51091271	K562	blood:	n/a	n/a
15	ATF3	chr15:51045700-51045997	K562	blood:	n/a	n/a
16	ATF3	chr15:51057123-51057710	A549	lung:	n/a	n/a
17	ATF3	chr15:51057183-51057646	K562	blood:	n/a	n/a
18	BCL11A	chr15:51057810-51058299	GM12878	blood:	n/a	chr15:51058009-51058022
19	BCL3	chr15:51057076-51058175	A549	lung:	n/a	chr15:51058009-51058022 chr15:51057801-51057814
20	BCL3	chr15:51090917-51091281	GM12878	blood:	n/a	n/a
21	BCL3	chr15:51057102-51058408	A549	lung:	n/a	chr15:51058009-51058022 chr15:51057801-51057814
22	BCLAF1	chr15:51057573-51058194	GM12878	blood:	n/a	chr15:51058009-51058022 chr15:51057801-51057814
23	BCLAF1	chr15:51056598-51057205	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:51056542-51057226	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:51066644-51067308	K562	blood:	n/a	n/a
26	BHLHE40	chr15:51057125-51058312	K562	blood:	n/a	n/a
27	BHLHE40	chr15:51058775-51059006	HepG2	liver:	n/a	n/a
28	BRCA1	chr15:51057677-51057834	HepG2	liver:	n/a	n/a
29	BRCA1	chr15:51108340-51108820	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr15:51045608-51045972	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr15:51058134-51058305	HepG2	liver:	n/a	n/a
32	CBX3	chr15:51057190-51057517	K562	blood:	n/a	n/a
33	CBX3	chr15:51090131-51090504	HCT-116	colon:	n/a	n/a
34	CBX3	chr15:51057024-51058404	K562	blood:	n/a	n/a
35	CCNT2	chr15:51115557-51115616	K562	blood:	n/a	n/a
36	CCNT2	chr15:51057370-51058205	K562	blood:	n/a	chr15:51057613-51057622
37	CCNT2	chr15:51045653-51046083	K562	blood:	n/a	chr15:51045942-51045962
38	CEBPB	chr15:51056868-51057622	K562	blood:	n/a	n/a
39	CEBPB	chr15:51010838-51011435	HepG2	liver:	n/a	chr15:51011413-51011425
40	CEBPB	chr15:51116741-51117067	Hela-S3	cervix:	n/a	chr15:51116903-51116914
41	CEBPB	chr15:51057932-51058275	IMR90	lung:	n/a	n/a
42	CEBPB	chr15:51090092-51090657	MCF-7	breast:	n/a	n/a
43	CEBPB	chr15:51098898-51099228	A549	lung:	n/a	chr15:51099051-51099062 chr15:51099051-51099064 chr15:51099052-51099063
44	CEBPB	chr15:51057168-51057631	A549	lung:	n/a	n/a
45	CEBPB	chr15:51057145-51057655	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr15:51108185-51108885	MCF-7	breast:	n/a	n/a
47	CEBPB	chr15:51045591-51046047	IMR90	lung:	n/a	chr15:51045815-51045826 chr15:51045875-51045886 chr15:51045875-51045888
48	CEBPB	chr15:51057829-51058244	A549	lung:	n/a	n/a
49	CEBPB	chr15:51116743-51117092	IMR90	lung:	n/a	chr15:51116903-51116914
50	CEBPB	chr15:51078632-51079087	MCF-7	breast:	n/a	chr15:51078837-51078848

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51058014-51058064	NHDF-neo	bronchial:	n/a
2	chr15:51057417-51057467	BE2_C	brain:	n/a
3	chr15:51058100-51058150	SK-N-SH_RA	brain:	n/a
4	chr15:51044672-51044722	NHDF-neo	bronchial:	n/a
5	chr15:51058050-51058100	HNPCEpiC	eye:	n/a
6	chr15:51058100-51058150	Jurkat	blood:	n/a
7	chr15:51115739-51115789	AG10803	skin:	n/a
8	chr15:51057768-51057818	Caco-2	colon:	n/a
9	chr15:51057714-51057764	HNPCEpiC	eye:	n/a
10	chr15:51057417-51057467	AoSMC	blood vessel:	n/a
11	chr15:51057768-51057818	U87	brain:	n/a
12	chr15:51058035-51058085	NHBE	bronchial:	n/a
13	chr15:51058035-51058085	H1-hESC	embryonic stem cell:	embryo
14	chr15:51115739-51115789	U87	brain:	n/a
15	chr15:51057714-51057764	SK-N-SH_RA	brain:	n/a
16	chr15:51058084-51058134	SK-N-SH_RA	brain:	n/a
17	chr15:51056548-51056598	Caco-2	colon:	n/a
18	chr15:51058114-51058164	BE2_C	brain:	n/a
19	chr15:51054077-51054127	ProgFib	skin:	n/a
20	chr15:51060843-51060893	SK-N-SH_RA	brain:	n/a
21	chr15:51057417-51057467	HRE	kidney:	n/a
22	chr15:51057768-51057818	HRE	kidney:	n/a
23	chr15:51058084-51058134	NHBE	bronchial:	n/a
24	chr15:51057714-51057764	HCT-116	colon:	n/a
25	chr15:51054077-51054127	HCPEpiC	choroid plexus:	n/a
26	chr15:51058035-51058085	A549	lung:	n/a
27	chr15:51058042-51058092	AoSMC	blood vessel:	n/a
28	chr15:51115739-51115789	AG09309	skin:	n/a
29	chr15:51115739-51115789	T-47D	breast:	n/a
30	chr15:51058084-51058134	RPTEC	kidney:	n/a
31	chr15:51057859-51057909	IMR90	lung:	fetal
32	chr15:51057417-51057467	NHDF-neo	bronchial:	n/a
33	chr15:51115739-51115789	H1-hESC	embryonic stem cell:	embryo
34	chr15:51058050-51058100	HL-60	blood:	n/a
35	chr15:51058042-51058092	MCF10A-Er-Src	breast:	n/a
36	chr15:51104216-51104266	AG10803	skin:	n/a
37	chr15:51104216-51104266	PrEC	prostate:	n/a
38	chr15:51044672-51044722	H1-hESC	embryonic stem cell:	embryo
39	chr15:51058114-51058164	RPTEC	kidney:	n/a
40	chr15:51060843-51060893	HCT-116	colon:	n/a
41	chr15:51058050-51058100	HCT-116	colon:	n/a
42	chr15:51058114-51058164	GM06990	blood:	n/a
43	chr15:51057768-51057818	GM12878	blood:	n/a
44	chr15:51057768-51057818	AG09319	gingival:	n/a
45	chr15:51104216-51104266	NB4	blood:	n/a
46	chr15:51058114-51058164	NB4	blood:	n/a
47	chr15:51058114-51058164	SK-N-SH	brain:	n/a
48	chr15:51058114-51058164	HCF	heart:	n/a
49	chr15:51057714-51057764	GM12891	blood:	n/a
50	chr15:51054077-51054127	MCF10A-Er-Src	breast:	n/a

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:51025715..51027452-chr15:51057581..51060241,2	MCF-7	breast:
2	chr15:51083211..51087261-chr15:51087532..51090501,5	MCF-7	breast:
3	chr15:51005061..51007555-chr15:51010952..51013855,2	MCF-7	breast:
4	chr15:51057644..51058522-chr18:61089470..61090340,2	NB4	blood:
5	chr15:50918354..50921026-chr15:51021586..51024072,2	MCF-7	breast:
6	chr15:51056930..51057470-chr15:51070200..51070963,2	MCF-7	breast:
7	chr15:51033137..51038584-chr15:51056604..51059356,6	MCF-7	breast:
8	chr15:51057652..51059901-chr15:51083890..51085609,2	K562	blood:
9	chr15:51056515..51059362-chr15:51088829..51092887,6	MCF-7	breast:
10	chr15:51039062..51042009-chr15:51057876..51060168,3	MCF-7	breast:
11	chr11:62608308..62609295-chr15:51057415..51058362,2	MCF-7	breast:
12	chr15:51056441..51059423-chr15:51081156..51083300,2	K562	blood:
13	chr15:51046404..51048794-chr15:51049414..51052213,2	K562	blood:
14	chr15:51110106..51113018-chr15:51115605..51118067,2	K562	blood:
15	chr15:51056930..51057470-chr15:51070200..51070963,2	MCF-7	breast:
16	chr15:51032315..51034610-chr15:51041268..51043342,2	MCF-7	breast:
17	chr15:50977075..50980199-chr15:51027449..51029550,3	MCF-7	breast:
18	chr15:51014164..51017311-chr15:51023770..51026173,3	MCF-7	breast:
19	chr15:51032315..51034610-chr15:51041268..51043342,2	MCF-7	breast:
20	chr15:50978318..50980031-chr15:51108674..51110331,2	MCF-7	breast:
21	chr15:50644661..50647207-chr15:51058214..51061180,2	MCF-7	breast:
22	chr15:51117159..51119186-chr15:51119416..51121611,3	MCF-7	breast:
23	chr15:51056319..51059244-chr15:51115290..51117379,3	MCF-7	breast:
24	chr15:51051434..51054342-chr15:51055658..51057830,3	K562	blood:
25	chr15:50978465..50980068-chr15:51103686..51105331,2	MCF-7	breast:
26	chr15:51039307..51042785-chr15:51044008..51048436,3	MCF-7	breast:
27	chr15:51075505..51077245-chr15:51077633..51079343,2	MCF-7	breast:
28	chr15:51056750..51061263-chr15:51087602..51092500,6	MCF-7	breast:
29	chr15:51080266..51082238-chr17:56734970..56736664,2	MCF-7	breast:
30	chr15:51057579..51059770-chr15:51078366..51080013,2	K562	blood:
31	chr1:37940054..37940679-chr15:51057582..51058263,2	Hela-S3	cervix:
32	chr11:60926802..60929238-chr15:51056528..51059041,2	MCF-7	breast:
33	chr15:51036668..51038336-chr15:51056622..51058914,2	MCF-7	breast:
34	chr15:50977709..50979057-chr15:51056941..51058049,3	MCF-7	breast:
35	chr15:51107261..51109801-chr15:51111049..51113590,2	MCF-7	breast:
36	chr15:50976295..50981465-chr15:51052766..51059546,15	MCF-7	breast:
37	chr15:51023962..51026987-chr15:51030777..51033771,3	MCF-7	breast:
38	chr15:51014164..51017311-chr15:51023770..51026173,3	MCF-7	breast:
39	chr15:51039062..51042009-chr15:51057876..51060168,3	MCF-7	breast:
40	chr15:51039545..51042117-chr15:51054834..51058033,5	MCF-7	breast:
41	chr15:50982616..50983161-chr15:51070119..51071029,2	MCF-7	breast:
42	chr15:51056091..51061159-chr15:51107004..51114924,11	MCF-7	breast:
43	chr15:51054229..51056382-chr15:51058543..51060392,2	K562	blood:
44	chr15:51101484..51104365-chr15:51107028..51109009,2	K562	blood:
45	chr15:51037199..51038791-chr15:51054779..51056301,2	K562	blood:
46	chr15:51026959..51028755-chr15:51050841..51052469,2	MCF-7	breast:
47	chr15:51045886..51047999-chr15:51058293..51060374,2	K562	blood:
48	chr15:50982278..50983197-chr15:51056944..51057802,4	MCF-7	breast:
49	chr15:51059873..51062365-chr15:51065766..51068595,2	K562	blood:
50	chr15:51061121..51063253-chr15:51148478..51150115,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRPM7-3	chr15:51034900-51035473	NONHSAT042435
2	lnc-AP4E1-1	chr15:51041845-51042026	ENSG00000259773.1
3	lnc-AP4E1-1	chr15:51038906-51039027	ENSG00000259773.1
4	lnc-TRPM7-1	chr15:51025117-51025495	ENSG00000250395
5	lnc-TRPM7-2	chr15:51014370-51014398	NONHSAT042433
6	lnc-AP4E1-5	chr15:51090867-51091148	NONHSAT042437
7	lnc-TRPM7-2	chr15:51017418-51017716	NONHSAT042433

No data

Variant related genes	Relation type
ENSG00000241130	TF binding region
ENSG00000259773	TF binding region
SPPL2A	TF binding region
ENSG00000241130	CpG island
ENSG00000259773	CpG island
SPPL2A	CpG island
ENSG00000179818	chromatin interactions
ENSG00000196176	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000272086	chromatin interactions
ENSG00000259773	chromatin interactions
ENSG00000113384	chromatin interactions
ENSG00000119541	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000092439	chromatin interactions
ENSG00000266559	chromatin interactions
ENSG00000081014	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000241130	chromatin interactions
ENSG00000163874	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000154429	chromatin interactions
ENSG00000198366	chromatin interactions
ENSG00000077150	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000243027	chromatin interactions
ENSG00000167987	chromatin interactions
PITPNA	miRNA target sites

Extended variants
information (count: 4064 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4064 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12911753	chr15:51011402-51011403	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532852003	chr15:51011414-51011415	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs8039710	chr15:51011442-51011443	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs564282345	chr15:51011473-51011474	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576867369	chr15:51011515-51011516	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534569692	chr15:51011518-51011519	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs553046468	chr15:51011595-51011596	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574782467	chr15:51011596-51011597	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140943112	chr15:51011602-51011603	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563456876	chr15:51011632-51011633	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575479752	chr15:51011648-51011649	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571671734	chr15:51011661-51011662	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546597995	chr15:51011678-51011679	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs545704365	chr15:51011693-51011694	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144672306	chr15:51011722-51011723	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs186663428	chr15:51011767-51011768	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs147905528	chr15:51011818-51011819	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs191057878	chr15:51011830-51011831	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559348040	chr15:51011840-51011841	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs76487336	chr15:51011919-51011920	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs75382874	chr15:51011920-51011921	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs398078180	chr15:51011929-51011930	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs398027249	chr15:51011930-51011931	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs139327370	chr15:51011964-51011965	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112895715	chr15:51012032-51012033	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570035019	chr15:51012039-51012040	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs145508805	chr15:51012067-51012068	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs537604248	chr15:51012084-51012085	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs552504974	chr15:51012100-51012101	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112694947	chr15:51012101-51012102	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs191335196	chr15:51012105-51012106	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs377103924	chr15:51012115-51012116	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182926903	chr15:51012137-51012138	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370526290	chr15:51012145-51012146	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs145209254	chr15:51012201-51012202	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200436388	chr15:51012202-51012203	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs574519922	chr15:51012223-51012224	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs137902988	chr15:51012245-51012246	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs140685887	chr15:51012256-51012257	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201715278	chr15:51012316-51012317	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373935509	chr15:51012331-51012332	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371436864	chr15:51012346-51012347	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557267576	chr15:51012355-51012356	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs62018798	chr15:51012430-51012431	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs570962397	chr15:51012457-51012458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149106991	chr15:51012466-51012467	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376042190	chr15:51012488-51012489	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144897129	chr15:51012489-51012490	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78666809	chr15:51012501-51012502	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146712557	chr15:51012514-51012515	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1989 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50979800-51014000	Weak transcription	Right Ventricle	heart
2	chr15:50980400-51013600	Weak transcription	Fetal Lung	lung
3	chr15:50988000-51056800	Weak transcription	Esophagus	oesophagus
4	chr15:50988200-51021600	Weak transcription	Pancreas	Pancrea
5	chr15:50990000-51013600	Weak transcription	A549	lung
6	chr15:50990000-51015400	Weak transcription	NH-A	brain
7	chr15:50990000-51038800	Weak transcription	NHLF	lung
8	chr15:50990200-51021600	Weak transcription	Psoas Muscle	Psoas
9	chr15:50991200-51013200	Weak transcription	Lung	lung
10	chr15:50991600-51033600	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr15:50994600-51011600	Weak transcription	Fetal Brain Female	brain
12	chr15:50995000-51026400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr15:50995400-51011600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:50995400-51011800	Weak transcription	Primary hematopoietic stem cells	blood
15	chr15:50995400-51011800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr15:50995400-51012200	Weak transcription	Colon Smooth Muscle	Colon
17	chr15:50995400-51017800	Weak transcription	HUVEC	blood vessel
18	chr15:50995600-51011600	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr15:50995600-51012000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr15:50995600-51013200	Weak transcription	Aorta	Aorta
21	chr15:50995600-51046000	Weak transcription	Small Intestine	intestine
22	chr15:50995800-51012000	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr15:50995800-51013200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:50996000-51012800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:50996200-51011600	Weak transcription	Colonic Mucosa	Colon
26	chr15:50996400-51011600	Weak transcription	Fetal Kidney	kidney
27	chr15:50997000-51017200	Weak transcription	Brain Anterior Caudate	brain
28	chr15:50997000-51044800	Weak transcription	K562	blood
29	chr15:50997200-51011800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:50997400-51025000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr15:50997600-51033600	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr15:50998200-51026800	Weak transcription	HMEC	breast
33	chr15:50998800-51011600	Weak transcription	Brain Hippocampus Middle	brain
34	chr15:50998800-51043200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr15:50999000-51012200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr15:50999000-51021600	Weak transcription	Dnd41	blood
37	chr15:50999200-51027400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr15:50999200-51041600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr15:50999600-51021600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr15:50999800-51043400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr15:51000000-51045000	Weak transcription	NHEK	skin
42	chr15:51000400-51011600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr15:51000600-51013000	Weak transcription	Brain Germinal Matrix	brain
44	chr15:51000600-51013200	Weak transcription	Thymus	Thymus
45	chr15:51000600-51039200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr15:51001800-51011800	Weak transcription	Hela-S3	cervix
47	chr15:51002000-51013200	Weak transcription	Spleen	Spleen
48	chr15:51004000-51056200	Weak transcription	Brain Angular Gyrus	brain
49	chr15:51004800-51028800	Weak transcription	Gastric	stomach
50	chr15:51005400-51018600	Weak transcription	Stomach Mucosa	stomach

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