Variant report

Variant	nsv537845
Chromosome Location	chr5:104360192-104615766
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	chr5:104565880-104566023	K562	blood:	n/a	n/a
2	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
3	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
4	ARID3A	chr5:104369169-104369636	K562	blood:	n/a	n/a
5	ATF1	chr5:104370024-104370214	K562	blood:	n/a	n/a
6	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
7	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
8	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
9	ATF1	chr5:104373680-104373755	K562	blood:	n/a	n/a
10	BACH1	chr5:104541248-104541265	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr5:104369418-104369675	K562	blood:	n/a	n/a
13	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
15	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
16	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
17	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
18	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
19	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
20	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
21	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
22	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
23	CEBPB	chr5:104534357-104534498	HepG2	liver:	n/a	chr5:104534396-104534407
24	CEBPB	chr5:104437246-104437795	MCF-7	breast:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
25	CEBPB	chr5:104593448-104593544	K562	blood:	n/a	chr5:104593456-104593469 chr5:104593456-104593469 chr5:104593458-104593469 chr5:104593456-104593469 chr5:104593458-104593469
26	CEBPB	chr5:104437345-104437662	A549	lung:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
27	CEBPB	chr5:104575759-104576055	K562	blood:	n/a	chr5:104575897-104575908 chr5:104575896-104575907
28	CEBPB	chr5:104370063-104370467	A549	lung:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
29	CEBPB	chr5:104423448-104423672	K562	blood:	n/a	chr5:104423566-104423577
30	CEBPB	chr5:104613257-104613341	K562	blood:	n/a	n/a
31	CEBPB	chr5:104437342-104437688	Hela-S3	cervix:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
32	CEBPB	chr5:104370069-104370367	H1-hESC	embryonic stem cell:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
33	CEBPB	chr5:104369173-104369683	K562	blood:	n/a	chr5:104369288-104369301
34	CEBPB	chr5:104391916-104392212	A549	lung:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
35	CEBPB	chr5:104575874-104575947	HepG2	liver:	n/a	chr5:104575897-104575908 chr5:104575896-104575907
36	CEBPB	chr5:104510149-104510395	H1-hESC	embryonic stem cell:	n/a	chr5:104510228-104510239
37	CEBPB	chr5:104475581-104475765	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr5:104423406-104423707	A549	lung:	n/a	chr5:104423566-104423577
39	CEBPB	chr5:104437313-104437709	MCF-7	breast:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
40	CEBPB	chr5:104370011-104370528	HepG2	liver:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
41	CEBPB	chr5:104485721-104485921	K562	blood:	n/a	n/a
42	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:104437340-104437708	ECC-1	luminal epithelium:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
44	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:104526203-104526286	K562	blood:	n/a	n/a
46	CEBPB	chr5:104437386-104437647	IMR90	lung:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
47	CEBPB	chr5:104369987-104370554	Hela-S3	cervix:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
48	CEBPB	chr5:104437422-104437706	ECC-1	luminal epithelium:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
49	CEBPB	chr5:104613163-104613370	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:104484312-104484512	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104433849-104433899	K562	blood:	n/a
2	chr5:104433849-104433899	K562	blood:	n/a
3	chr5:104435608-104435658	HAEpiC	amniotic membrane:	n/a
4	chr5:104434827-104434877	HEK293	kidney:	embryo
5	chr5:104433849-104433899	GM12891	blood:	n/a
6	chr5:104434827-104434877	AG04449	skin:	fetal
7	chr5:104433849-104433899	HAEpiC	amniotic membrane:	n/a
8	chr5:104433849-104433899	HL-60	blood:	n/a
9	chr5:104434864-104434914	MCF10A-Er-Src	breast:	n/a
10	chr5:104434827-104434877	SK-N-SH	brain:	n/a
11	chr5:104434864-104434914	ECC-1	luminal epithelium:	n/a
12	chr5:104433849-104433899	BE2_C	brain:	n/a
13	chr5:104434827-104434877	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:104433849-104433899	PANC-1	pancreas:	n/a
15	chr5:104433849-104433899	Jurkat	blood:	n/a
16	chr5:104433849-104433899	U87	brain:	n/a
17	chr5:104433849-104433899	NHDF-neo	bronchial:	n/a
18	chr5:104435608-104435658	SKMC	muscle:	n/a
19	chr5:104434864-104434914	NHDF-neo	bronchial:	n/a
20	chr5:104435608-104435658	HIPEpiC	eye:	n/a
21	chr5:104435062-104435112	HNPCEpiC	eye:	n/a
22	chr5:104435062-104435112	ovcar-3	ovarian:	n/a
23	chr5:104435608-104435658	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:104433849-104433899	GM12892	blood:	n/a
25	chr5:104435608-104435658	A549	lung:	n/a
26	chr5:104434827-104434877	GM12878	blood:	n/a
27	chr5:104435608-104435658	NHDF-neo	bronchial:	n/a
28	chr5:104434827-104434877	BJ	skin:	n/a
29	chr5:104434864-104434914	K562	blood:	n/a
30	chr5:104433849-104433899	GM12878	blood:	n/a
31	chr5:104435062-104435112	HMEC	breast:	n/a
32	chr5:104435608-104435658	NT2-D1	testis:	n/a
33	chr5:104434864-104434914	NT2-D1	testis:	n/a
34	chr5:104435062-104435112	Hepatocyte	liver:	n/a
35	chr5:104435062-104435112	LNCaP	prostate:	n/a
36	chr5:104435062-104435112	Hela-S3	cervix:	n/a
37	chr5:104434827-104434877	HL-60	blood:	n/a
38	chr5:104433849-104433899	AoSMC	blood vessel:	n/a
39	chr5:104434864-104434914	HRPEpiC	eye:	n/a
40	chr5:104435608-104435658	NB4	blood:	n/a
41	chr5:104435608-104435658	CMK	blood:	n/a
42	chr5:104434827-104434877	NB4	blood:	n/a
43	chr5:104433849-104433899	AG04450	lung:	fetal
44	chr5:104434864-104434914	CMK	blood:	n/a
45	chr5:104435608-104435658	HRCEpiC	kidney:	n/a
46	chr5:104434827-104434877	Hepatocyte	liver:	n/a
47	chr5:104435062-104435112	RPTEC	kidney:	n/a
48	chr5:104434864-104434914	SKMC	muscle:	n/a
49	chr5:104435062-104435112	AG04449	skin:	fetal
50	chr5:104435062-104435112	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
2	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
3	chr12:23105697..23106553-chr5:104539343..104540254,2	MCF-7	breast:
4	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
5	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
6	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
7	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
8	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
9	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
10	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
11	chr19:12903711..12905991-chr5:104578289..104580216,2	MCF-7	breast:
12	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
13	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
14	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
15	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
16	chr5:104369671..104371200-chr5:104727235..104729208,2	K562	blood:
17	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
18	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
19	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
20	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
21	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
22	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
23	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
24	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
25	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
26	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
27	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
28	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:
29	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
30	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
31	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
32	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
33	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
34	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
35	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
36	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
37	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
38	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
39	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:
40	chr5:104586940..104589611-chr5:104727738..104729575,2	K562	blood:
41	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
42	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
43	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
44	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
45	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
46	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
47	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
48	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
49	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
50	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf30-8	chr5:104435175-104435799	NR_000039
2	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584
3	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097
4	lnc-C5orf30-8	chr5:104435174-104435799	NONHSAT103096

Variant related genes	Relation type
ENSG00000253584	TF binding region
RAB9BP1	TF binding region
ENSG00000253584	CpG island
RAB9BP1	CpG island
ENSG00000251574	chromatin interactions

Extended variants
information (count: 2544 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2544 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551173771	chr5:104369411-104369412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567724461	chr5:104369424-104369425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80213085	chr5:104369447-104369448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13168070	chr5:104369455-104369456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs567169618	chr5:104369459-104369460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539076977	chr5:104369475-104369476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529169327	chr5:104369491-104369492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558639915	chr5:104369503-104369504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549198741	chr5:104369506-104369507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575697070	chr5:104369514-104369515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568940603	chr5:104369547-104369548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544354833	chr5:104369582-104369583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557137686	chr5:104369592-104369593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369630905	chr5:104369605-104369606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370273956	chr5:104369717-104369718	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573791045	chr5:104369739-104369740	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34567596	chr5:104369804-104369805	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542393671	chr5:104369836-104369837	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7709488	chr5:104369901-104369902	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528326636	chr5:104369906-104369907	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544604571	chr5:104369921-104369922	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564695647	chr5:104369937-104369938	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs62366393	chr5:104369953-104369954	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs550436959	chr5:104369954-104369955	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs118109132	chr5:104369955-104369956	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530364091	chr5:104369956-104369957	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78189970	chr5:104369965-104369966	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571686307	chr5:104369975-104369976	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547207899	chr5:104369990-104369991	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567181919	chr5:104369992-104369993	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs13185910	chr5:104370015-104370016	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145869163	chr5:104370027-104370028	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531771058	chr5:104370028-104370029	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567997437	chr5:104370124-104370125	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569126214	chr5:104370140-104370141	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs13168898	chr5:104370141-104370142	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552575111	chr5:104370157-104370158	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574590942	chr5:104370169-104370170	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369789657	chr5:104370184-104370185	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542422121	chr5:104370267-104370268	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552701931	chr5:104370274-104370275	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs62366394	chr5:104370306-104370307	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs73777388	chr5:104370319-104370320	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565170705	chr5:104370322-104370323	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12518114	chr5:104370486-104370487	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs115934720	chr5:104370516-104370517	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs12518136	chr5:104370570-104370571	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs560862111	chr5:104370605-104370606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529774703	chr5:104370607-104370608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547219910	chr5:104370638-104370639	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104369400-104369800	Enhancers	K562	blood
2	chr5:104369400-104370000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr5:104369400-104370200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr5:104369800-104370200	Flanking Active TSS	K562	blood
5	chr5:104370200-104370400	Enhancers	K562	blood
6	chr5:104370200-104370600	Enhancers	Hela-S3	cervix
7	chr5:104370400-104371600	Weak transcription	K562	blood
8	chr5:104376200-104376600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:104380200-104380600	Enhancers	Fetal Brain Male	brain
10	chr5:104388000-104392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:104389600-104390600	Enhancers	Fetal Lung	lung
12	chr5:104390200-104390800	Active TSS	Fetal Brain Male	brain
13	chr5:104392400-104393200	ZNF genes & repeats	Esophagus	oesophagus
14	chr5:104392400-104394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:104392400-104394000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:104392400-104394000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:104398800-104402000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:104421400-104421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:104421600-104422200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:104422400-104422600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:104422600-104423600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:104423600-104425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:104424000-104424400	Enhancers	Primary hematopoietic stem cells	blood
24	chr5:104425000-104428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:104428000-104428200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:104437400-104438000	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr5:104446800-104447200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr5:104451200-104451400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:104453600-104455000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr5:104459600-104460200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr5:104468200-104468800	Enhancers	Brain Germinal Matrix	brain
32	chr5:104469400-104470600	Enhancers	Liver	Liver
33	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
39	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
40	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
41	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
42	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
43	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
48	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:104512000-104512400	Active TSS	Breast Myoepithelial Primary Cells	Breast

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