Variant report

Variant	nsv904386
Chromosome Location	chr15:75655819-75673209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1206)
CpG islands
(count:915)
Chromatin interactive
region (count:66)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1206 , 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	chr15:75660272-75660552	K562	blood:	n/a	n/a
2	ARID3A	chr15:75660257-75660533	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:75660744-75661420	HepG2	liver:	n/a	n/a
4	ATF1	chr15:75660110-75660538	K562	blood:	n/a	n/a
5	ATF2	chr15:75660161-75661608	GM12878	blood:	n/a	n/a
6	ATF2	chr15:75660738-75661306	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:75660019-75661276	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:75659989-75660699	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:75660097-75661229	GM12878	blood:	n/a	n/a
10	ATF3	chr15:75660002-75661404	A549	lung:	n/a	n/a
11	ATF3	chr15:75660690-75661149	K562	blood:	n/a	n/a
12	ATF3	chr15:75660080-75661379	A549	lung:	n/a	n/a
13	ATF3	chr15:75660106-75660407	K562	blood:	n/a	n/a
14	BACH1	chr15:75660075-75661069	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:75660493-75660715	K562	blood:	n/a	n/a
16	BATF	chr15:75660825-75661127	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:75660716-75661116	GM12878	blood:	n/a	chr15:75660795-75660808
18	BCL3	chr15:75660151-75661676	GM12878	blood:	n/a	chr15:75660795-75660808 chr15:75660365-75660374
19	BCL3	chr15:75659658-75661620	A549	lung:	n/a	chr15:75660795-75660808 chr15:75660365-75660374
20	BCL3	chr15:75659848-75661730	A549	lung:	n/a	chr15:75660795-75660808 chr15:75660365-75660374
21	BCLAF1	chr15:75660578-75661435	K562	blood:	n/a	chr15:75660795-75660808
22	BCLAF1	chr15:75660109-75661616	GM12878	blood:	n/a	chr15:75660795-75660808 chr15:75660365-75660374
23	BCLAF1	chr15:75660176-75661303	K562	blood:	n/a	chr15:75660795-75660808 chr15:75660365-75660374
24	BCLAF1	chr15:75660091-75661555	GM12878	blood:	n/a	chr15:75660795-75660808 chr15:75660365-75660374
25	BHLHE40	chr15:75660202-75661129	GM12878	blood:	n/a	chr15:75660790-75660806
26	BHLHE40	chr15:75660125-75661460	K562	blood:	n/a	chr15:75661241-75661257 chr15:75661252-75661268 chr15:75660790-75660806
27	BHLHE40	chr15:75660177-75661420	HepG2	liver:	n/a	chr15:75661241-75661257 chr15:75661252-75661268 chr15:75660790-75660806
28	BRCA1	chr15:75660258-75660446	HepG2	liver:	n/a	n/a
29	BRCA1	chr15:75660115-75661531	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr15:75660815-75661118	HepG2	liver:	n/a	n/a
31	BRCA1	chr15:75660640-75661137	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr15:75660503-75661053	GM12878	blood:	n/a	n/a
33	CBX3	chr15:75660016-75661418	K562	blood:	n/a	n/a
34	CBX3	chr15:75659897-75661309	HCT-116	colon:	n/a	n/a
35	CBX3	chr15:75660831-75661164	K562	blood:	n/a	n/a
36	CCNT2	chr15:75660206-75661168	K562	blood:	n/a	chr15:75660690-75660699
37	CEBPB	chr15:75662574-75662900	HepG2	liver:	n/a	n/a
38	CEBPB	chr15:75660120-75661257	A549	lung:	n/a	n/a
39	CEBPB	chr15:75662597-75662896	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr15:75660826-75661633	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:75662598-75662886	K562	blood:	n/a	n/a
42	CEBPB	chr15:75662530-75662826	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:75662587-75662828	HepG2	liver:	n/a	n/a
44	CEBPB	chr15:75661319-75661644	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:75662570-75662900	A549	lung:	n/a	n/a
46	CEBPB	chr15:75660808-75661194	K562	blood:	n/a	n/a
47	CEBPB	chr15:75660227-75660578	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr15:75662554-75662923	HepG2	liver:	n/a	n/a
49	CEBPB	chr15:75660665-75661292	GM12878	blood:	n/a	n/a
50	CEBPB	chr15:75660680-75661187	ECC-1	luminal epithelium:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75661059-75661109	MCF10A-Er-Src	breast:	n/a
2	chr15:75661090-75661140	BJ	skin:	n/a
3	chr15:75661003-75661053	IMR90	lung:	fetal
4	chr15:75661240-75661290	HEEpiC	esophagus:	n/a
5	chr15:75661354-75661404	U87	brain:	n/a
6	chr15:75660322-75660372	HPAEpiC	pulmonary alveolar:	n/a
7	chr15:75660780-75660830	HAEpiC	amniotic membrane:	n/a
8	chr15:75661354-75661404	BE2_C	brain:	n/a
9	chr15:75660389-75660439	LNCaP	prostate:	n/a
10	chr15:75656960-75657010	GM19239	blood:	n/a
11	chr15:75660973-75661023	HCT-116	colon:	n/a
12	chr15:75660780-75660830	HCF	heart:	n/a
13	chr15:75661014-75661064	NB4	blood:	n/a
14	chr15:75661003-75661053	SK-N-SH	brain:	n/a
15	chr15:75661014-75661064	ECC-1	luminal epithelium:	n/a
16	chr15:75656960-75657010	HCPEpiC	choroid plexus:	n/a
17	chr15:75660780-75660830	U87	brain:	n/a
18	chr15:75661240-75661290	SKMC	muscle:	n/a
19	chr15:75661014-75661064	PANC-1	pancreas:	n/a
20	chr15:75661000-75661050	GM12892	blood:	n/a
21	chr15:75661240-75661290	HCPEpiC	choroid plexus:	n/a
22	chr15:75661059-75661109	Caco-2	colon:	n/a
23	chr15:75661014-75661064	Jurkat	blood:	n/a
24	chr15:75661014-75661064	AG04450	lung:	fetal
25	chr15:75664343-75664393	HL-60	blood:	n/a
26	chr15:75660322-75660372	HepG2	liver:	n/a
27	chr15:75661240-75661290	HRE	kidney:	n/a
28	chr15:75661014-75661064	BJ	skin:	n/a
29	chr15:75656960-75657010	LNCaP	prostate:	n/a
30	chr15:75661059-75661109	Jurkat	blood:	n/a
31	chr15:75660780-75660830	H1-hESC	embryonic stem cell:	embryo
32	chr15:75664343-75664393	GM12878	blood:	n/a
33	chr15:75661000-75661050	GM12891	blood:	n/a
34	chr15:75660322-75660372	HNPCEpiC	eye:	n/a
35	chr15:75661059-75661109	RPTEC	kidney:	n/a
36	chr15:75661240-75661290	PFSK-1	brain:	n/a
37	chr15:75661240-75661290	HepG2	liver:	n/a
38	chr15:75661184-75661234	SK-N-MC	brain:	n/a
39	chr15:75660389-75660439	BJ	skin:	n/a
40	chr15:75664343-75664393	SKMC	muscle:	n/a
41	chr15:75660973-75661023	GM19239	blood:	n/a
42	chr15:75661000-75661050	Hela-S3	cervix:	n/a
43	chr15:75660389-75660439	GM19239	blood:	n/a
44	chr15:75661240-75661290	NB4	blood:	n/a
45	chr15:75656960-75657010	HRE	kidney:	n/a
46	chr15:75656216-75656266	RPTEC	kidney:	n/a
47	chr15:75661014-75661064	AG09319	gingival:	n/a
48	chr15:75661090-75661140	CMK	blood:	n/a
49	chr15:75656960-75657010	SK-N-MC	brain:	n/a
50	chr15:75661354-75661404	HL-60	blood:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:75660200..75660849-chr8:144679964..144680506,2	Hela-S3	cervix:
2	chr15:75657323..75661859-chr15:75928778..75934895,5	K562	blood:
3	chr15:75628015..75635137-chr15:75659177..75662618,8	MCF-7	breast:
4	chr15:75660298..75660886-chr9:74979501..74980233,2	Hela-S3	cervix:
5	chr15:75320338..75322055-chr15:75659198..75660857,2	K562	blood:
6	chr15:75660995..75662598-chr15:75687412..75689086,2	K562	blood:
7	chr11:61159614..61160370-chr15:75660583..75661085,2	Hela-S3	cervix:
8	chr1:84971286..84972368-chr15:75659986..75660965,3	Hela-S3	cervix:
9	chr15:75660196..75660788-chr3:158519289..158520156,2	Hela-S3	cervix:
10	chr15:75660425..75661076-chr6:36164710..36165398,2	HCT-116	colon:
11	chr15:75659495..75662351-chr15:75705859..75709575,3	MCF-7	breast:
12	chr15:75658228..75661982-chr15:75967267..75971746,4	K562	blood:
13	chr15:75657489..75661684-chr15:75927450..75931877,5	K562	blood:
14	chr15:75660298..75662011-chr15:75917109..75918951,2	MCF-7	breast:
15	chr15:75660469..75660993-chr3:39447877..39448827,2	Hela-S3	cervix:
16	chr15:75660459..75661077-chr19:16435007..16435522,2	Hela-S3	cervix:
17	chr15:75660327..75660863-chr7:92219197..92220073,2	Hela-S3	cervix:
18	chr15:75630795..75633486-chr15:75658867..75660629,2	K562	blood:
19	chr15:75660467..75661982-chr15:75931951..75934210,2	K562	blood:
20	chr15:75661606..75664299-chr15:75683955..75686073,2	MCF-7	breast:
21	chr11:10829821..10830809-chr15:75660199..75660833,2	Hela-S3	cervix:
22	chr15:75658017..75661976-chr15:75870089..75873800,4	K562	blood:
23	chr15:75658930..75662576-chr15:75931399..75933599,5	MCF-7	breast:
24	chr15:75626715..75630609-chr15:75659083..75662163,7	K562	blood:
25	chr10:75757491..75758402-chr15:75660402..75660987,2	Hela-S3	cervix:
26	chr15:75660565..75661351-chr6:35656003..35656976,2	Hela-S3	cervix:
27	chr15:75660482..75662699-chr15:76134018..76135657,2	MCF-7	breast:
28	chr15:75657601..75665504-chr15:75739437..75749700,27	K562	blood:
29	chr14:20800961..20801511-chr15:75660256..75660818,2	Hela-S3	cervix:
30	chr15:75660086..75660899-chrX:71496569..71497174,2	Hela-S3	cervix:
31	chr15:75669231..75671963-chr15:75673071..75675723,3	MCF-7	breast:
32	chr15:75626774..75630064-chr15:75654261..75656966,3	K562	blood:
33	chr15:75630334..75631987-chr15:75656015..75658534,2	MCF-7	breast:
34	chr15:75659887..75662361-chr15:75938355..75942043,7	MCF-7	breast:
35	chr15:75673195..75675877-chr15:75743620..75745869,3	MCF-7	breast:
36	chr15:75661841..75663589-chr15:75672331..75674100,2	K562	blood:
37	chr15:75667630..75669544-chr15:75671089..75672778,2	K562	blood:
38	chr15:75660364..75660914-chr5:40834869..40835784,2	Hela-S3	cervix:
39	chr15:75671213..75673361-chr15:75743963..75746267,3	MCF-7	breast:
40	chr15:75658070..75664945-chr15:75741625..75749756,25	K562	blood:
41	chr15:75658624..75662706-chr15:75930016..75932707,8	MCF-7	breast:
42	chr15:74909806..74912416-chr15:75659270..75660874,2	MCF-7	breast:
43	chr15:75659648..75660390-chrX:153626628..153627266,2	Hela-S3	cervix:
44	chr15:75659986..75660919-chr17:56736480..56737002,2	Hela-S3	cervix:
45	chr15:75656095..75662590-chr15:75739456..75750037,27	MCF-7	breast:
46	chr15:75627175..75629335-chr15:75660124..75661831,2	MCF-7	breast:
47	chr15:75660249..75660980-chr17:57915181..57915748,2	MCF-7	breast:
48	chr15:75662150..75663707-chr15:75759404..75761916,2	K562	blood:
49	chr15:75659436..75662034-chr15:75939431..75941023,2	K562	blood:
50	chr15:75661739..75662424-chr15:75673693..75674236,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEIL1-1	chr15:75660496-75661925	ENSG00000260274.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SIN3A	hsa-miR-1	chr15:75663717-75663739

Variant related genes	Relation type
SIN3A	TF binding region
ENSG00000260274	TF binding region
MAN2C1	TF binding region
SIN3A	CpG island
ENSG00000260274	CpG island
MAN2C1	CpG island
ENSG00000260483	chromatin interactions
ENSG00000107372	chromatin interactions
ENSG00000035403	chromatin interactions
ENSG00000198034	chromatin interactions
ENSG00000178761	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000272247	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000179886	chromatin interactions
ENSG00000260892	chromatin interactions
ENSG00000169410	chromatin interactions
ENSG00000138621	chromatin interactions
ENSG00000168028	chromatin interactions
ENSG00000246982	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000118855	chromatin interactions
ENSG00000140367	chromatin interactions
ENSG00000100814	chromatin interactions
ENSG00000187049	chromatin interactions
ENSG00000260235	chromatin interactions
ENSG00000173548	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000267275	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000234545	chromatin interactions
ENSG00000140365	chromatin interactions
ENSG00000174021	chromatin interactions
ENSG00000096070	chromatin interactions
ENSG00000169371	chromatin interactions
ENSG00000261714	chromatin interactions
ENSG00000260206	chromatin interactions
ENSG00000122432	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000231721	chromatin interactions
ENSG00000128585	chromatin interactions
ENSG00000241890	chromatin interactions
ENSG00000203392	chromatin interactions
ENSG00000199347	chromatin interactions

Extended variants
information (count: 676 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112694805	chr15:75655819-75655820	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs138486022	chr15:75655855-75655856	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs372394494	chr15:75655920-75655921	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs375694817	chr15:75655921-75655922	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs56258187	chr15:75655962-75655963	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs145953784	chr15:75655963-75655964	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs538953735	chr15:75655990-75655991	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs371406680	chr15:75655992-75655993	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs547677741	chr15:75656010-75656011	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs565914671	chr15:75656056-75656057	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs536427196	chr15:75656082-75656083	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs371225716	chr15:75656093-75656094	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs554416650	chr15:75656106-75656107	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs576080588	chr15:75656108-75656109	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs536707298	chr15:75656112-75656113	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs545234288	chr15:75656131-75656132	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs374402587	chr15:75656142-75656143	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs548683687	chr15:75656146-75656147	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs10622316	chr15:75656148-75656149	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs576402496	chr15:75656168-75656169	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs541343441	chr15:75656177-75656178	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs559595810	chr15:75656200-75656201	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs574737475	chr15:75656205-75656206	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs565231660	chr15:75656216-75656217	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs542398552	chr15:75656226-75656227	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs371685367	chr15:75656227-75656228	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs532778038	chr15:75656230-75656231	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs185606328	chr15:75656235-75656236	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs531033902	chr15:75656241-75656242	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs375169075	chr15:75656296-75656297	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs140379576	chr15:75656311-75656312	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs552359191	chr15:75656388-75656389	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs566994555	chr15:75656390-75656391	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs144931327	chr15:75656422-75656423	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs367619996	chr15:75656440-75656441	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs79888318	chr15:75656445-75656446	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs371634709	chr15:75656453-75656454	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs144333944	chr15:75656475-75656476	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs141629850	chr15:75656487-75656488	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs374866022	chr15:75656496-75656497	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs112334378	chr15:75656505-75656506	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs190692217	chr15:75656523-75656524	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs373133314	chr15:75656527-75656528	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs147928844	chr15:75656531-75656532	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs201919526	chr15:75656538-75656539	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs376985685	chr15:75656539-75656540	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs536100299	chr15:75656561-75656562	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs373221679	chr15:75656579-75656580	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs548377504	chr15:75656622-75656623	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs75700351	chr15:75656665-75656666	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75641400-75658600	Weak transcription	HUVEC	blood vessel
2	chr15:75641600-75659200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:75641600-75659600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr15:75641800-75659600	Weak transcription	Fetal Heart	heart
5	chr15:75642000-75659600	Strong transcription	Fetal Intestine Small	intestine
6	chr15:75642200-75659800	Weak transcription	Fetal Brain Male	brain
7	chr15:75642400-75659800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:75643000-75659600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr15:75643200-75659800	Weak transcription	Right Atrium	heart
10	chr15:75643400-75656800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr15:75643600-75656200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr15:75643800-75657000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr15:75644200-75659600	Strong transcription	Fetal Muscle Trunk	muscle
14	chr15:75644200-75659800	Strong transcription	Fetal Stomach	stomach
15	chr15:75644400-75657600	Strong transcription	Gastric	stomach
16	chr15:75644400-75658000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr15:75644400-75658800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr15:75644400-75659600	Strong transcription	Colonic Mucosa	Colon
19	chr15:75644400-75659600	Strong transcription	Duodenum Mucosa	Duodenum
20	chr15:75644400-75659800	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr15:75644600-75659600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:75644800-75659600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:75645600-75659800	Strong transcription	Placenta	Placenta
24	chr15:75645800-75659600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:75645800-75659600	Strong transcription	Fetal Intestine Large	intestine
26	chr15:75645800-75660000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:75646000-75659200	Strong transcription	Brain Germinal Matrix	brain
28	chr15:75646000-75659200	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr15:75646000-75659400	Strong transcription	Primary T cells from cord blood	blood
30	chr15:75646000-75659400	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr15:75646000-75659400	Strong transcription	Skeletal Muscle Female	skeletal muscle
32	chr15:75646000-75659800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:75646000-75659800	Strong transcription	NHLF	lung
34	chr15:75646000-75660200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr15:75646200-75659400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:75646200-75659400	Strong transcription	Esophagus	oesophagus
37	chr15:75646200-75659600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr15:75646200-75659600	Strong transcription	Adipose Nuclei	Adipose
39	chr15:75646200-75659600	Strong transcription	NHEK	skin
40	chr15:75646200-75659800	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr15:75646200-75659800	Strong transcription	Fetal Muscle Leg	muscle
42	chr15:75646400-75659800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr15:75646600-75659400	Strong transcription	Stomach Smooth Muscle	stomach
44	chr15:75646600-75659600	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr15:75646800-75657600	Strong transcription	Right Ventricle	heart
46	chr15:75646800-75659400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr15:75646800-75659400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr15:75646800-75659400	Strong transcription	Fetal Brain Female	brain
49	chr15:75646800-75659400	Strong transcription	Left Ventricle	heart
50	chr15:75646800-75659600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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