Variant report

Variant	nsv1042824
Chromosome Location	chr15:39676039-39757222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1171)
CpG islands
(count:244)
Chromatin interactive
region (count:75)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1171 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:39747732-39747957	K562	blood:	n/a	n/a
2	ARID3A	chr15:39726993-39727601	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:39740665-39740941	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:39686113-39686429	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:39680234-39680556	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:39747583-39748662	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:39746918-39747168	HepG2	liver:	n/a	n/a
8	ATF1	chr15:39746636-39746643	K562	blood:	n/a	n/a
9	ATF1	chr15:39689138-39690402	K562	blood:	n/a	n/a
10	ATF1	chr15:39697043-39697457	K562	blood:	n/a	n/a
11	ATF1	chr15:39695823-39696026	K562	blood:	n/a	n/a
12	ATF1	chr15:39683830-39684016	K562	blood:	n/a	n/a
13	ATF2	chr15:39722020-39722552	GM12878	blood:	n/a	n/a
14	ATF2	chr15:39745878-39746319	GM12878	blood:	n/a	n/a
15	ATF2	chr15:39745859-39746251	GM12878	blood:	n/a	n/a
16	ATF2	chr15:39719232-39719822	GM12878	blood:	n/a	n/a
17	ATF2	chr15:39703840-39704314	GM12878	blood:	n/a	n/a
18	ATF2	chr15:39719284-39719792	GM12878	blood:	n/a	n/a
19	ATF2	chr15:39703805-39704253	GM12878	blood:	n/a	n/a
20	ATF3	chr15:39697207-39697400	K562	blood:	n/a	n/a
21	ATF3	chr15:39689237-39689578	K562	blood:	n/a	chr15:39689397-39689408 chr15:39689397-39689408
22	BACH1	chr15:39747633-39748029	K562	blood:	n/a	n/a
23	BACH1	chr15:39747639-39747989	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr15:39722126-39722419	GM12878	blood:	n/a	n/a
25	BATF	chr15:39745906-39746252	GM12878	blood:	n/a	n/a
26	BATF	chr15:39719251-39719741	GM12878	blood:	n/a	n/a
27	BATF	chr15:39703837-39704269	GM12878	blood:	n/a	n/a
28	BATF	chr15:39745912-39746230	GM12878	blood:	n/a	n/a
29	BATF	chr15:39721949-39722530	GM12878	blood:	n/a	n/a
30	BATF	chr15:39747620-39747876	GM12878	blood:	n/a	n/a
31	BATF	chr15:39736093-39736339	GM12878	blood:	n/a	n/a
32	BATF	chr15:39719291-39719713	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:39703839-39704204	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:39745906-39746214	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:39745955-39746242	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:39719378-39719719	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:39719215-39719727	GM12878	blood:	n/a	n/a
38	BCL11A	chr15:39703767-39704164	GM12878	blood:	n/a	n/a
39	BCL3	chr15:39696961-39697356	A549	lung:	n/a	n/a
40	BCL3	chr15:39719289-39719739	GM12878	blood:	n/a	n/a
41	BCL3	chr15:39719267-39719762	GM12878	blood:	n/a	n/a
42	BCLAF1	chr15:39703772-39704302	GM12878	blood:	n/a	n/a
43	BCLAF1	chr15:39719224-39719849	GM12878	blood:	n/a	n/a
44	BCLAF1	chr15:39719244-39719771	GM12878	blood:	n/a	n/a
45	BHLHE40	chr15:39719389-39719800	K562	blood:	n/a	n/a
46	BHLHE40	chr15:39703781-39704328	GM12878	blood:	n/a	n/a
47	BHLHE40	chr15:39745934-39746244	GM12878	blood:	n/a	n/a
48	BHLHE40	chr15:39721937-39722434	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:39698744-39699063	GM12878	blood:	n/a	n/a
50	BHLHE40	chr15:39719077-39719993	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:39696638-39696688	HCF	heart:	n/a
2	chr15:39696638-39696688	GM19239	blood:	n/a
3	chr15:39696638-39696688	PFSK-1	brain:	n/a
4	chr15:39742079-39742129	HUVEC	blood vessel:	n/a
5	chr15:39726997-39727047	ECC-1	luminal epithelium:	n/a
6	chr15:39696638-39696688	Jurkat	blood:	n/a
7	chr15:39742079-39742129	NH-A	brain:	n/a
8	chr15:39696638-39696688	CMK	blood:	n/a
9	chr15:39726997-39727047	GM06990	blood:	n/a
10	chr15:39726997-39727047	PANC-1	pancreas:	n/a
11	chr15:39696638-39696688	HL-60	blood:	n/a
12	chr15:39713049-39713099	NH-A	brain:	n/a
13	chr15:39713049-39713099	ovcar-3	ovarian:	n/a
14	chr15:39713049-39713099	AG09319	gingival:	n/a
15	chr15:39696638-39696688	HUVEC	blood vessel:	n/a
16	chr15:39713049-39713099	SAEC	small airway:	n/a
17	chr15:39742079-39742129	HCF	heart:	n/a
18	chr15:39713049-39713099	HRPEpiC	eye:	n/a
19	chr15:39726997-39727047	RPTEC	kidney:	n/a
20	chr15:39726997-39727047	AG09319	gingival:	n/a
21	chr15:39742079-39742129	SK-N-SH	brain:	n/a
22	chr15:39742079-39742129	HNPCEpiC	eye:	n/a
23	chr15:39713049-39713099	AoSMC	blood vessel:	n/a
24	chr15:39696638-39696688	U87	brain:	n/a
25	chr15:39696638-39696688	NH-A	brain:	n/a
26	chr15:39713049-39713099	AG04449	skin:	fetal
27	chr15:39713049-39713099	SKMC	muscle:	n/a
28	chr15:39713049-39713099	AG09309	skin:	n/a
29	chr15:39696638-39696688	Caco-2	colon:	n/a
30	chr15:39696638-39696688	HRPEpiC	eye:	n/a
31	chr15:39726997-39727047	NB4	blood:	n/a
32	chr15:39742079-39742129	HL-60	blood:	n/a
33	chr15:39742079-39742129	T-47D	breast:	n/a
34	chr15:39726997-39727047	H1-hESC	embryonic stem cell:	embryo
35	chr15:39713049-39713099	NB4	blood:	n/a
36	chr15:39696638-39696688	HRE	kidney:	n/a
37	chr15:39726997-39727047	HCT-116	colon:	n/a
38	chr15:39696638-39696688	HMEC	breast:	n/a
39	chr15:39713049-39713099	HNPCEpiC	eye:	n/a
40	chr15:39696638-39696688	NT2-D1	testis:	n/a
41	chr15:39713049-39713099	NHBE	bronchial:	n/a
42	chr15:39696638-39696688	ProgFib	skin:	n/a
43	chr15:39713049-39713099	H1-hESC	embryonic stem cell:	embryo
44	chr15:39696638-39696688	NHDF-neo	bronchial:	n/a
45	chr15:39726997-39727047	AoSMC	blood vessel:	n/a
46	chr15:39742079-39742129	Hepatocyte	liver:	n/a
47	chr15:39713049-39713099	Jurkat	blood:	n/a
48	chr15:39713049-39713099	HUVEC	blood vessel:	n/a
49	chr15:39726997-39727047	HNPCEpiC	eye:	n/a
50	chr15:39713049-39713099	HEK293	kidney:	embryo

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:39693671..39697771-chr15:39871894..39873705,4	MCF-7	breast:
2	chr15:39694167..39696674-chr15:39698967..39702842,3	K562	blood:
3	chr15:39693251..39695685-chr15:39695839..39698387,3	K562	blood:
4	chr15:39733381..39735588-chr15:39737180..39739166,2	MCF-7	breast:
5	chr15:39679859..39682267-chr15:39688446..39690917,2	K562	blood:
6	chr15:39732986..39734871-chr9:127020115..127022303,2	MCF-7	breast:
7	chr15:39724107..39725948-chr15:39841990..39843603,2	MCF-7	breast:
8	chr15:39680767..39685014-chr15:39686318..39690917,5	K562	blood:
9	chr1:149223091..149225186-chr15:39684235..39686134,2	MCF-7	breast:
10	chr15:39688689..39690644-chr15:39690686..39693111,2	MCF-7	breast:
11	chr15:39733791..39736088-chr15:39738338..39740014,2	K562	blood:
12	chr15:39680767..39685014-chr15:39686318..39690917,5	K562	blood:
13	chr15:39694167..39696674-chr15:39698967..39702842,3	K562	blood:
14	chr15:39712002..39713506-chr15:39725005..39726661,2	MCF-7	breast:
15	chr15:39719049..39721581-chr15:39729488..39731125,2	MCF-7	breast:
16	chr15:39694348..39696610-chr15:39874084..39875864,2	MCF-7	breast:
17	chr15:39731790..39738265-chr15:39871818..39875275,7	MCF-7	breast:
18	chr15:39687930..39690603-chr15:39694421..39696812,2	MCF-7	breast:
19	chr15:39739352..39742846-chr15:39745277..39748876,4	MCF-7	breast:
20	chr15:39705799..39707909-chr15:39873297..39874835,2	MCF-7	breast:
21	chr15:39686331..39688222-chr15:39874533..39876316,2	MCF-7	breast:
22	chr15:39688689..39690644-chr15:39690686..39693111,2	MCF-7	breast:
23	chr15:39693251..39695685-chr15:39695839..39697787,2	K562	blood:
24	chr15:39724781..39729630-chr15:39730304..39736268,5	MCF-7	breast:
25	chr15:39741167..39743297-chr15:39871792..39873904,2	MCF-7	breast:
26	chr15:39723566..39727788-chr15:39872507..39874775,4	MCF-7	breast:
27	chr15:39689811..39692581-chr15:39692665..39695062,3	K562	blood:
28	chr15:39683407..39685977-chr15:39689632..39691631,2	MCF-7	breast:
29	chr15:39560119..39564394-chr15:39727167..39731091,3	MCF-7	breast:
30	chr15:39745636..39749475-chr15:39752031..39754404,4	K562	blood:
31	chr15:39739352..39742846-chr15:39745277..39748876,4	MCF-7	breast:
32	chr15:39684874..39687815-chr15:39688159..39690874,2	MCF-7	breast:
33	chr15:39746552..39749195-chr15:39826550..39828305,2	MCF-7	breast:
34	chr15:39721562..39724453-chr15:39734811..39737253,2	MCF-7	breast:
35	chr15:39744731..39747916-chr15:39873044..39877161,3	MCF-7	breast:
36	chr15:39698653..39701088-chr15:39877017..39879720,2	MCF-7	breast:
37	chr15:39735362..39737088-chr15:39871158..39872700,2	MCF-7	breast:
38	chr15:39666611..39670026-chr15:39675209..39676771,3	K562	blood:
39	chr15:39721051..39725636-chr15:39870055..39875310,7	MCF-7	breast:
40	chr15:39733791..39736088-chr15:39738338..39740014,2	K562	blood:
41	chr15:39721562..39724453-chr15:39734811..39737253,2	MCF-7	breast:
42	chr15:39696668..39698687-chr15:39702884..39705384,2	MCF-7	breast:
43	chr15:39684874..39687815-chr15:39688159..39690874,2	MCF-7	breast:
44	chr15:39693251..39695685-chr15:39695839..39697787,2	K562	blood:
45	chr15:39462704..39465639-chr15:39730089..39732672,2	MCF-7	breast:
46	chr15:39679668..39681537-chr15:39681975..39684409,2	K562	blood:
47	chr15:39463804..39465395-chr15:39742405..39744124,2	MCF-7	breast:
48	chr15:39683407..39685977-chr15:39689632..39691631,2	MCF-7	breast:
49	chr15:39464240..39465905-chr15:39723603..39725817,2	MCF-7	breast:
50	chr15:39722154..39722685-chr15:39960642..39961199,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSIP1-8	chr15:39688872-39689442	l_1148_chr15:39688871-39700983_testes
2	lnc-THBS1-2	chr15:39739845-39739940	NONHSAT041746
3	lnc-FSIP1-5	chr15:39712745-39712910	ENSG00000259345.1
4	lnc-THBS1-2	chr15:39737149-39737401	NONHSAT041746
5	lnc-C15orf54-2	chr15:39680863-39680961	XLOC_011215
6	lnc-C15orf54-2	chr15:39676212-39676327	XLOC_011215
7	lnc-FSIP1-5	chr15:39719299-39719396	ENSG00000259345.1
8	lnc-FSIP1-5	chr15:39713110-39713176	ENSG00000259345.1
9	lnc-FSIP1-8	chr15:39689634-39689690	l_1148_chr15:39688871-39700983_testes
10	lnc-THBS1-2	chr15:39739846-39739940	XLOC_011216
11	lnc-FSIP1-8	chr15:39699803-39700983	l_1148_chr15:39688871-39700983_testes
12	lnc-FSIP1-5	chr15:39711231-39711853	ENSG00000259345.1
13	lnc-C15orf54-2	chr15:39676212-39676327	XLOC_011215
14	lnc-THBS1-2	chr15:39737150-39737401	XLOC_011216
15	lnc-C15orf54-2	chr15:39680836-39680961	XLOC_011215
16	lnc-C15orf54-2	chr15:39684805-39684838	XLOC_011215
17	lnc-C15orf54-2	chr15:39680887-39681108	XLOC_011215
18	lnc-FSIP1-8	chr15:39692025-39692273	l_1148_chr15:39688871-39700983_testes
19	lnc-C15orf54-2	chr15:39676042-39676327	XLOC_011215

No data

Variant related genes	Relation type
ENSG00000259345	TF binding region
ENSG00000259345	CpG island
ENSG00000119408	chromatin interactions
ENSG00000259345	chromatin interactions
ENSG00000137801	chromatin interactions
ENSG00000206737	chromatin interactions
MIER2	miRNA target sites
BTG3	miRNA target sites

Extended variants
information (count: 3298 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3298 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7169602	chr15:39676070-39676071	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs191165988	chr15:39676095-39676096	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs562024019	chr15:39676107-39676108	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs9944226	chr15:39676108-39676109	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs182534409	chr15:39676126-39676127	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs550591659	chr15:39676143-39676144	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs564411457	chr15:39676170-39676171	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs147549271	chr15:39676180-39676181	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs536983749	chr15:39676196-39676197	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs549939453	chr15:39676239-39676240	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs569887844	chr15:39676240-39676241	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs186264201	chr15:39676258-39676259	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs569600939	chr15:39676272-39676273	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs142111026	chr15:39676346-39676347	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143074081	chr15:39676356-39676357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs151204708	chr15:39676366-39676367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77261869	chr15:39676384-39676385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150342372	chr15:39676413-39676414	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75824021	chr15:39676430-39676431	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138096789	chr15:39676461-39676462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143136538	chr15:39676471-39676472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556308193	chr15:39676505-39676506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576263734	chr15:39676511-39676512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142625440	chr15:39676527-39676528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190786652	chr15:39676557-39676558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73393432	chr15:39676668-39676669	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572342898	chr15:39676680-39676681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541050414	chr15:39676702-39676703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564531772	chr15:39676719-39676720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574013580	chr15:39676720-39676721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377096345	chr15:39676766-39676767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533175780	chr15:39676778-39676779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375668917	chr15:39676806-39676807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370281293	chr15:39676842-39676843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145640517	chr15:39676861-39676862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536992424	chr15:39676864-39676865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138212280	chr15:39676871-39676872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529400564	chr15:39676886-39676887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549601204	chr15:39676889-39676890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373943827	chr15:39676918-39676919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528818018	chr15:39676928-39676929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142897608	chr15:39676930-39676931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570426725	chr15:39676935-39676936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183088188	chr15:39676936-39676937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556245012	chr15:39676963-39676964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569811083	chr15:39676975-39676976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187065344	chr15:39676991-39676992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555570842	chr15:39677009-39677010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561203410	chr15:39677037-39677038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370638219	chr15:39677042-39677043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39672600-39680400	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr15:39675800-39676800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr15:39675800-39677200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr15:39676400-39676600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr15:39676600-39677600	Enhancers	Fetal Muscle Leg	muscle
6	chr15:39676800-39679800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr15:39677200-39684400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr15:39679800-39680200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr15:39679800-39680600	Enhancers	A549	lung
10	chr15:39679800-39681000	Enhancers	Fetal Intestine Large	intestine
11	chr15:39679800-39681000	Enhancers	HepG2	liver
12	chr15:39680200-39680600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr15:39680200-39681000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr15:39680400-39680600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr15:39680600-39680800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr15:39680600-39681000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr15:39680600-39681000	Enhancers	Primary hematopoietic stem cells	blood
18	chr15:39680600-39681000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr15:39680600-39681200	Enhancers	Fetal Heart	heart
20	chr15:39680600-39685000	Weak transcription	A549	lung
21	chr15:39680800-39681000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr15:39681000-39682800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr15:39681000-39684800	Weak transcription	Fetal Intestine Large	intestine
24	chr15:39681000-39684800	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr15:39681000-39685400	Weak transcription	HepG2	liver
26	chr15:39681000-39688800	Weak transcription	Primary hematopoietic stem cells	blood
27	chr15:39681000-39691800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr15:39681200-39683200	Weak transcription	Fetal Heart	heart
29	chr15:39682400-39687800	Enhancers	Hela-S3	cervix
30	chr15:39682800-39683600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
31	chr15:39682800-39686800	Enhancers	NHEK	skin
32	chr15:39683000-39684200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr15:39683000-39684200	Enhancers	HMEC	breast
34	chr15:39683000-39684400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr15:39683000-39684600	Enhancers	Colon Smooth Muscle	Colon
36	chr15:39683200-39683600	Enhancers	Fetal Heart	heart
37	chr15:39683200-39686600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr15:39683200-39687000	Enhancers	Placenta Amnion	Placenta Amnion
39	chr15:39683400-39683600	Enhancers	Right Atrium	heart
40	chr15:39683400-39684400	Enhancers	Osteobl	bone
41	chr15:39683400-39685000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr15:39683400-39686000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr15:39683600-39684600	Weak transcription	Fetal Heart	heart
44	chr15:39684000-39684400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:39684200-39684400	Enhancers	Right Atrium	heart
46	chr15:39684200-39685200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:39684400-39686200	Weak transcription	Osteobl	bone
48	chr15:39684400-39686600	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr15:39684600-39685200	Weak transcription	Colon Smooth Muscle	Colon
50	chr15:39684600-39685400	Enhancers	Fetal Heart	heart

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