Variant report

Variant	esv3437569
Chromosome Location	chr15:52367063-52372248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:52370520-52371354	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:52369286-52369388	K562	blood:	n/a	n/a
3	ATF1	chr15:52369187-52369507	K562	blood:	n/a	n/a
4	ATF2	chr15:52369038-52369763	GM12878	blood:	n/a	n/a
5	BATF	chr15:52369158-52369534	GM12878	blood:	n/a	chr15:52369343-52369353 chr15:52369342-52369353
6	BATF	chr15:52369125-52369570	GM12878	blood:	n/a	chr15:52369343-52369353 chr15:52369342-52369353
7	BCL3	chr15:52369201-52369583	GM12878	blood:	n/a	n/a
8	BCL3	chr15:52369085-52369663	GM12878	blood:	n/a	n/a
9	BCLAF1	chr15:52371018-52371527	GM12878	blood:	n/a	n/a
10	BHLHE40	chr15:52369230-52369519	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:52369182-52369781	K562	blood:	n/a	n/a
12	BHLHE40	chr15:52371162-52371448	K562	blood:	n/a	n/a
13	CEBPB	chr15:52370561-52370815	HepG2	liver:	n/a	chr15:52370711-52370722 chr15:52370709-52370722 chr15:52370709-52370720
14	CEBPB	chr15:52368826-52369075	Hela-S3	cervix:	n/a	chr15:52368960-52368971
15	CEBPB	chr15:52368797-52369636	IMR90	lung:	n/a	chr15:52368960-52368971
16	CEBPB	chr15:52370429-52370914	HepG2	liver:	n/a	chr15:52370711-52370722 chr15:52370709-52370722 chr15:52370709-52370720
17	CEBPB	chr15:52368820-52369132	HepG2	liver:	n/a	chr15:52368960-52368971
18	CEBPB	chr15:52368810-52369133	A549	lung:	n/a	chr15:52368960-52368971
19	CEBPB	chr15:52368808-52369123	K562	blood:	n/a	chr15:52368960-52368971
20	CEBPB	chr15:52370383-52370950	HepG2	liver:	n/a	chr15:52370711-52370722 chr15:52370709-52370722 chr15:52370709-52370720
21	CEBPB	chr15:52370600-52370778	Hela-S3	cervix:	n/a	chr15:52370711-52370722 chr15:52370709-52370722 chr15:52370709-52370720
22	CEBPB	chr15:52368917-52368970	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr15:52370504-52370897	HepG2	liver:	n/a	chr15:52370711-52370722 chr15:52370709-52370722 chr15:52370709-52370720
24	CEBPB	chr15:52370552-52370829	A549	lung:	n/a	chr15:52370711-52370722 chr15:52370709-52370722 chr15:52370709-52370720
25	CEBPD	chr15:52370584-52370980	HepG2	liver:	n/a	n/a
26	CHD2	chr15:52370881-52370946	HepG2	liver:	n/a	n/a
27	CHD2	chr15:52369383-52369472	GM12878	blood:	n/a	n/a
28	CHD2	chr15:52369153-52369408	HepG2	liver:	n/a	n/a
29	CREB1	chr15:52368947-52369417	A549	lung:	n/a	n/a
30	CTCF	chr15:52371180-52371330	GM12875	blood:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
31	CTCF	chr15:52369440-52369590	GM12878	blood:	n/a	n/a
32	CTCF	chr15:52371159-52371361	ECC-1	luminal epithelium:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
33	CTCF	chr15:52370720-52370870	HCM	heart:	n/a	n/a
34	CTCF	chr15:52371220-52371370	AG04450	lung:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
35	CTCF	chr15:52371120-52371405	A549	lung:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
36	CTCF	chr15:52371240-52371390	GM12867	blood:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
37	CTCF	chr15:52369520-52369670	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr15:52371113-52371429	Medullo	brain:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
39	CTCF	chr15:52371180-52371330	HepG2	liver:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
40	CTCF	chr15:52369580-52369730	HVMF	connective:	n/a	n/a
41	CTCF	chr15:52369461-52369628	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr15:52371200-52371350	WI-38	lung:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
43	CTCF	chr15:52371240-52371390	GM12801	blood:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
44	CTCF	chr15:52371137-52371397	MCF-7	breast:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
45	CTCF	chr15:52370620-52370770	GM06990	blood:	n/a	n/a
46	CTCF	chr15:52371167-52371385	GM10248	blood:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
47	CTCF	chr15:52371132-52371399	MCF-7	breast:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
48	CTCF	chr15:52371200-52371350	GM12872	blood:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270
49	CTCF	chr15:52369540-52369690	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr15:52371160-52371310	HFF-Myc	foreskin:	n/a	chr15:52371257-52371275 chr15:52371252-52371273 chr15:52371259-52371272 chr15:52371258-52371274 chr15:52371259-52371272 chr15:52371260-52371270

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:52369237-52369287	U87	brain:	n/a
2	chr15:52369237-52369287	NHBE	bronchial:	n/a
3	chr15:52369237-52369287	PANC-1	pancreas:	n/a
4	chr15:52369237-52369287	AG04450	lung:	fetal
5	chr15:52369237-52369287	HRCEpiC	kidney:	n/a
6	chr15:52369237-52369287	HEEpiC	esophagus:	n/a
7	chr15:52369237-52369287	SK-N-SH	brain:	n/a
8	chr15:52369237-52369287	AoSMC	blood vessel:	n/a
9	chr15:52369237-52369287	HCF	heart:	n/a
10	chr15:52369237-52369287	HAEpiC	amniotic membrane:	n/a
11	chr15:52369237-52369287	HL-60	blood:	n/a
12	chr15:52369237-52369287	HepG2	liver:	n/a
13	chr15:52369237-52369287	Hela-S3	cervix:	n/a
14	chr15:52369237-52369287	HCPEpiC	choroid plexus:	n/a
15	chr15:52369237-52369287	GM19239	blood:	n/a
16	chr15:52369237-52369287	NH-A	brain:	n/a
17	chr15:52369237-52369287	AG09309	skin:	n/a
18	chr15:52369237-52369287	AG09319	gingival:	n/a
19	chr15:52369237-52369287	SK-N-SH_RA	brain:	n/a
20	chr15:52369237-52369287	GM12891	blood:	n/a
21	chr15:52369237-52369287	Jurkat	blood:	n/a
22	chr15:52369237-52369287	NHDF-neo	bronchial:	n/a
23	chr15:52369237-52369287	K562	blood:	n/a
24	chr15:52369237-52369287	PrEC	prostate:	n/a
25	chr15:52369237-52369287	RPTEC	kidney:	n/a
26	chr15:52369237-52369287	HRPEpiC	eye:	n/a
27	chr15:52369237-52369287	NB4	blood:	n/a
28	chr15:52369237-52369287	HNPCEpiC	eye:	n/a
29	chr15:52369237-52369287	SK-N-MC	brain:	n/a
30	chr15:52369237-52369287	AG04449	skin:	fetal
31	chr15:52369237-52369287	HUVEC	blood vessel:	n/a
32	chr15:52369237-52369287	NT2-D1	testis:	n/a
33	chr15:52369237-52369287	IMR90	lung:	fetal
34	chr15:52369237-52369287	Hepatocyte	liver:	n/a
35	chr15:52369237-52369287	ovcar-3	ovarian:	n/a
36	chr15:52369237-52369287	HCT-116	colon:	n/a
37	chr15:52369237-52369287	H1-hESC	embryonic stem cell:	embryo
38	chr15:52369237-52369287	SKMC	muscle:	n/a
39	chr15:52369237-52369287	AG10803	skin:	n/a
40	chr15:52369237-52369287	HPAEpiC	pulmonary alveolar:	n/a
41	chr15:52369237-52369287	MCF10A-Er-Src	breast:	n/a
42	chr15:52369237-52369287	GM12892	blood:	n/a
43	chr15:52369237-52369287	HIPEpiC	eye:	n/a
44	chr15:52369237-52369287	HRE	kidney:	n/a
45	chr15:52369237-52369287	GM12878	blood:	n/a
46	chr15:52369237-52369287	LNCaP	prostate:	n/a
47	chr15:52369237-52369287	HEK293	kidney:	embryo
48	chr15:52369237-52369287	Caco-2	colon:	n/a
49	chr15:52369237-52369287	PFSK-1	brain:	n/a
50	chr15:52369237-52369287	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:52366885..52371007-chr15:52377121..52381657,4	MCF-7	breast:
2	chr15:52367526..52370460-chr15:52373083..52374686,2	K562	blood:
3	chr15:52370890..52371721-chr15:52431328..52432654,3	MCF-7	breast:
4	chr15:52274218..52275165-chr15:52370716..52372312,7	MCF-7	breast:
5	chr15:52367787..52369559-chr15:52372887..52374614,2	MCF-7	breast:
6	chr15:52355832..52357497-chr15:52369964..52372920,2	MCF-7	breast:
7	chr15:52309334..52315760-chr15:52366746..52373412,20	MCF-7	breast:
8	chr15:52267047..52268763-chr15:52371441..52374035,2	K562	blood:
9	chr15:52074652..52075239-chr15:52370872..52371682,3	MCF-7	breast:
10	chr15:52311665..52312617-chr15:52370871..52371422,2	MCF-7	breast:
11	chr15:52370736..52372537-chr15:52471693..52473323,2	MCF-7	breast:
12	chr15:52265430..52265936-chr15:52370586..52371262,2	K562	blood:
13	chr15:52273987..52275289-chr15:52370394..52371967,22	MCF-7	breast:
14	chr15:52274293..52274815-chr15:52372080..52373063,2	MCF-7	breast:
15	chr15:52339947..52342319-chr15:52368984..52372783,3	MCF-7	breast:
16	chr15:52263755..52264751-chr15:52370850..52371704,2	MCF-7	breast:
17	chr15:52264000..52265602-chr15:52369038..52371034,3	MCF-7	breast:
18	chr15:52366411..52367932-chr15:52425830..52428559,2	MCF-7	breast:
19	chr15:52272756..52275955-chr15:52369833..52372310,3	MCF-7	breast:
20	chr15:52365247..52369257-chr15:52370072..52371646,3	MCF-7	breast:
21	chr15:52262830..52265268-chr15:52372078..52374982,4	MCF-7	breast:
22	chr15:52362758..52365823-chr15:52370997..52373206,3	K562	blood:
23	chr15:52359845..52362361-chr15:52369816..52371937,2	MCF-7	breast:
24	chr15:52272788..52276993-chr15:52369760..52371998,4	MCF-7	breast:
25	chr15:52263873..52266562-chr15:52369853..52372558,3	MCF-7	breast:
26	chr15:52365247..52369257-chr15:52370072..52371646,3	MCF-7	breast:
27	chr15:52369845..52371701-chr15:52385019..52386714,2	MCF-7	breast:
28	chr15:52274113..52275112-chr15:52370804..52371366,6	K562	blood:
29	chr15:52362582..52365416-chr15:52366428..52369427,4	MCF-7	breast:
30	chr15:52274413..52275086-chr15:52368881..52369577,2	MCF-7	breast:
31	chr15:52362758..52364447-chr15:52370997..52373206,2	K562	blood:
32	chr15:52346904..52348485-chr15:52369068..52371304,2	MCF-7	breast:
33	chr15:52371404..52373055-chr15:52373147..52374878,2	MCF-7	breast:
34	chr15:52370352..52371596-chr15:52431725..52432958,5	MCF-7	breast:
35	chr15:52308069..52314807-chr15:52359242..52376066,34	MCF-7	breast:
36	chr15:52360023..52361929-chr15:52364183..52367724,3	K562	blood:
37	chr15:52359015..52361742-chr15:52367466..52369559,2	MCF-7	breast:
38	chr15:52371333..52373042-chr15:52391102..52393252,2	MCF-7	breast:
39	chr15:52360405..52361171-chr15:52370393..52371006,2	MCF-7	breast:
40	chr15:52362640..52365502-chr15:52370243..52371813,2	MCF-7	breast:
41	chr15:52371710..52374413-chr15:52385596..52389516,3	MCF-7	breast:
42	chr15:52371129..52371827-chr15:52430855..52431660,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAPK6-13	chr15:52369355-52369810	NONHSAT043908

Variant related genes	Relation type
ENSG00000259178	TF binding region
ENSG00000259178	CpG island
ENSG00000166477	chromatin interactions
ENSG00000259438	chromatin interactions
ENSG00000128872	chromatin interactions
ENSG00000259178	chromatin interactions
ENSG00000259712	chromatin interactions
ENSG00000259577	chromatin interactions
ENSG00000242327	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000069966	chromatin interactions

Extended variants
information (count: 243 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:243 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554098029	chr15:52367076-52367077	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs113988462	chr15:52367083-52367084	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575755289	chr15:52367117-52367118	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs77978555	chr15:52367176-52367177	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs562977013	chr15:52367199-52367200	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs936886	chr15:52367267-52367268	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs545426528	chr15:52367268-52367269	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs560847026	chr15:52367310-52367311	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs377150336	chr15:52367317-52367318	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs572187212	chr15:52367320-52367321	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs556827597	chr15:52367325-52367326	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs386783964	chr15:52367359-52367360	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs732097	chr15:52367368-52367369	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs376969863	chr15:52367380-52367381	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs531876234	chr15:52367425-52367426	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs144193444	chr15:52367433-52367434	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs368939464	chr15:52367459-52367460	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs540789722	chr15:52367488-52367489	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs369399671	chr15:52367512-52367513	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs538816725	chr15:52367539-52367540	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs547235911	chr15:52367555-52367556	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs565642982	chr15:52367558-52367559	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs148658393	chr15:52367573-52367574	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs77700256	chr15:52367594-52367595	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs75875118	chr15:52367595-52367596	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs536776369	chr15:52367610-52367611	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs558619021	chr15:52367637-52367638	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs148653175	chr15:52367801-52367802	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs2414127	chr15:52367808-52367809	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs35940641	chr15:52367846-52367847	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs545585336	chr15:52367915-52367916	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs55813964	chr15:52367963-52367964	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs559105878	chr15:52367964-52367965	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs138424431	chr15:52367974-52367975	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs200054013	chr15:52367975-52367976	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201288604	chr15:52367976-52367977	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs200574133	chr15:52367980-52367981	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs7182643	chr15:52367987-52367988	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs199667391	chr15:52368002-52368003	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs5812579	chr15:52368010-52368011	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs561122960	chr15:52368011-52368012	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs10444826	chr15:52368013-52368014	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs111705708	chr15:52368015-52368016	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs560638014	chr15:52368056-52368057	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs188881572	chr15:52368114-52368115	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs543326942	chr15:52368115-52368116	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs561293827	chr15:52368131-52368132	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs193235339	chr15:52368154-52368155	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs550046441	chr15:52368156-52368157	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs529560024	chr15:52368269-52368270	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52353200-52370800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr15:52353600-52368800	Weak transcription	HSMMtube	muscle
3	chr15:52356200-52368600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr15:52356200-52368800	Weak transcription	HUVEC	blood vessel
5	chr15:52356200-52369000	Weak transcription	Hela-S3	cervix
6	chr15:52356400-52368600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr15:52357200-52371200	Weak transcription	Spleen	Spleen
8	chr15:52357600-52368600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:52357600-52368600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr15:52357600-52369000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr15:52357600-52373200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:52357800-52368800	Weak transcription	NH-A	brain
13	chr15:52357800-52370800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr15:52358000-52369000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:52358600-52371000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr15:52358800-52368600	Weak transcription	HSMM	muscle
17	chr15:52358800-52368800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:52359200-52368800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:52362200-52367200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:52362400-52371000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr15:52362800-52368400	Weak transcription	A549	lung
22	chr15:52362800-52374600	Weak transcription	Small Intestine	intestine
23	chr15:52363800-52367600	Weak transcription	HMEC	breast
24	chr15:52364000-52368600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr15:52364200-52369000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr15:52364200-52369000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr15:52364400-52369000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr15:52364600-52367600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:52364600-52368600	Weak transcription	HepG2	liver
30	chr15:52364600-52368800	Weak transcription	Fetal Intestine Small	intestine
31	chr15:52364600-52368800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr15:52364600-52374000	Weak transcription	Pancreas	Pancrea
33	chr15:52364800-52368600	Weak transcription	Liver	Liver
34	chr15:52364800-52368600	Weak transcription	Fetal Intestine Large	intestine
35	chr15:52364800-52368800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr15:52365200-52369000	Weak transcription	Esophagus	oesophagus
37	chr15:52366600-52369000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr15:52366600-52369000	Enhancers	NHEK	skin
39	chr15:52366800-52368400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr15:52367200-52367800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr15:52367600-52369000	Enhancers	HMEC	breast
42	chr15:52367600-52373200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr15:52367800-52368400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr15:52368400-52369000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr15:52368400-52369000	Enhancers	A549	lung
46	chr15:52368400-52370600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:52368600-52368800	Enhancers	HepG2	liver
48	chr15:52368600-52369000	Enhancers	Muscle Satellite Cultured Cells	--
49	chr15:52368600-52369000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr15:52368600-52369800	Enhancers	Primary monocytes fromperipheralblood	blood

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