Variant report

Variant	nsv563162
Chromosome Location	chr13:111583422-111660113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1470)
CpG islands
(count:1099)
Chromatin interactive
region (count:57)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111637930-111638336	K562	blood:	n/a	n/a
2	ARID3A	chr13:111596653-111596866	K562	blood:	n/a	n/a
3	ARID3A	chr13:111616552-111617111	K562	blood:	n/a	n/a
4	ARID3A	chr13:111607771-111607785	K562	blood:	n/a	n/a
5	ARID3A	chr13:111634350-111634590	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:111629139-111629731	K562	blood:	n/a	n/a
7	ARID3A	chr13:111613503-111613506	K562	blood:	n/a	n/a
8	ARID3A	chr13:111633500-111633698	K562	blood:	n/a	n/a
9	ARID3A	chr13:111617591-111618111	K562	blood:	n/a	n/a
10	ARID3A	chr13:111617717-111618019	HepG2	liver:	n/a	n/a
11	ARID3A	chr13:111609938-111610171	K562	blood:	n/a	n/a
12	ATF1	chr13:111609847-111610217	K562	blood:	n/a	n/a
13	ATF1	chr13:111617592-111618059	K562	blood:	n/a	n/a
14	ATF1	chr13:111616538-111617184	K562	blood:	n/a	n/a
15	ATF1	chr13:111633797-111634135	K562	blood:	n/a	n/a
16	ATF2	chr13:111594338-111595038	GM12878	blood:	n/a	n/a
17	ATF2	chr13:111617433-111618175	GM12878	blood:	n/a	n/a
18	ATF2	chr13:111594506-111595157	GM12878	blood:	n/a	n/a
19	ATF2	chr13:111617446-111618193	GM12878	blood:	n/a	n/a
20	ATF3	chr13:111617547-111618071	K562	blood:	n/a	n/a
21	ATF3	chr13:111616603-111616969	K562	blood:	n/a	n/a
22	ATF3	chr13:111607634-111607841	K562	blood:	n/a	n/a
23	ATF3	chr13:111617630-111618014	A549	lung:	n/a	n/a
24	ATF3	chr13:111617522-111618114	HCT-116	colon:	n/a	n/a
25	ATF3	chr13:111617574-111618068	A549	lung:	n/a	n/a
26	ATF3	chr13:111607565-111607923	K562	blood:	n/a	n/a
27	ATF3	chr13:111617515-111618130	HCT-116	colon:	n/a	n/a
28	ATF3	chr13:111617695-111617957	K562	blood:	n/a	n/a
29	BACH1	chr13:111616727-111617031	K562	blood:	n/a	n/a
30	BACH1	chr13:111596762-111596900	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr13:111659219-111659426	H1-hESC	embryonic stem cell:	n/a	chr13:111659308-111659322
32	BACH1	chr13:111657084-111657105	K562	blood:	n/a	n/a
33	BATF	chr13:111617529-111618103	GM12878	blood:	n/a	n/a
34	BATF	chr13:111604447-111604752	GM12878	blood:	n/a	n/a
35	BATF	chr13:111594624-111594904	GM12878	blood:	n/a	chr13:111594793-111594804
36	BATF	chr13:111594637-111594939	GM12878	blood:	n/a	chr13:111594793-111594804
37	BATF	chr13:111596652-111596920	GM12878	blood:	n/a	n/a
38	BATF	chr13:111617146-111618178	GM12878	blood:	n/a	n/a
39	BATF	chr13:111607581-111607894	GM12878	blood:	n/a	n/a
40	BATF	chr13:111604411-111604849	GM12878	blood:	n/a	n/a
41	BCL11A	chr13:111604392-111604833	GM12878	blood:	n/a	n/a
42	BCL11A	chr13:111607486-111607916	GM12878	blood:	n/a	n/a
43	BCL11A	chr13:111594587-111594903	GM12878	blood:	n/a	n/a
44	BCL11A	chr13:111617174-111618094	GM12878	blood:	n/a	n/a
45	BCL11A	chr13:111594523-111594957	GM12878	blood:	n/a	n/a
46	BCL11A	chr13:111617660-111618038	GM12878	blood:	n/a	n/a
47	BCL3	chr13:111596649-111597617	GM12878	blood:	n/a	n/a
48	BCL3	chr13:111597173-111597614	GM12878	blood:	n/a	n/a
49	BCL3	chr13:111594664-111594920	GM12878	blood:	n/a	n/a
50	BCL3	chr13:111617634-111618052	GM12878	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111589153-111589203	HCPEpiC	choroid plexus:	n/a
2	chr13:111589153-111589203	HCPEpiC	choroid plexus:	n/a
3	chr13:111596806-111596856	NHDF-neo	bronchial:	n/a
4	chr13:111642660-111642710	ProgFib	skin:	n/a
5	chr13:111642147-111642197	SK-N-SH_RA	brain:	n/a
6	chr13:111589973-111590023	LNCaP	prostate:	n/a
7	chr13:111642147-111642197	U87	brain:	n/a
8	chr13:111589153-111589203	NHBE	bronchial:	n/a
9	chr13:111644790-111644840	HepG2	liver:	n/a
10	chr13:111589090-111589140	H1-hESC	embryonic stem cell:	embryo
11	chr13:111589973-111590023	GM19239	blood:	n/a
12	chr13:111644279-111644329	A549	lung:	n/a
13	chr13:111607174-111607224	MCF10A-Er-Src	breast:	n/a
14	chr13:111589040-111589090	T-47D	breast:	n/a
15	chr13:111642660-111642710	GM12892	blood:	n/a
16	chr13:111639733-111639783	GM12891	blood:	n/a
17	chr13:111607174-111607224	BJ	skin:	n/a
18	chr13:111644790-111644840	HNPCEpiC	eye:	n/a
19	chr13:111589153-111589203	MCF10A-Er-Src	breast:	n/a
20	chr13:111658907-111658957	HCM	heart:	n/a
21	chr13:111589153-111589203	SK-N-SH_RA	brain:	n/a
22	chr13:111589973-111590023	H1-hESC	embryonic stem cell:	embryo
23	chr13:111658907-111658957	GM12878	blood:	n/a
24	chr13:111642465-111642515	NHDF-neo	bronchial:	n/a
25	chr13:111642443-111642493	AG10803	skin:	n/a
26	chr13:111607174-111607224	GM12891	blood:	n/a
27	chr13:111642646-111642696	NB4	blood:	n/a
28	chr13:111658907-111658957	NT2-D1	testis:	n/a
29	chr13:111642660-111642710	BJ	skin:	n/a
30	chr13:111589040-111589090	A549	lung:	n/a
31	chr13:111596806-111596856	NHBE	bronchial:	n/a
32	chr13:111658907-111658957	H1-hESC	embryonic stem cell:	embryo
33	chr13:111589040-111589090	HCPEpiC	choroid plexus:	n/a
34	chr13:111589973-111590023	Caco-2	colon:	n/a
35	chr13:111644279-111644329	SAEC	small airway:	n/a
36	chr13:111596806-111596856	HRE	kidney:	n/a
37	chr13:111637435-111637485	HCT-116	colon:	n/a
38	chr13:111589040-111589090	BE2_C	brain:	n/a
39	chr13:111639733-111639783	PFSK-1	brain:	n/a
40	chr13:111642660-111642710	HRPEpiC	eye:	n/a
41	chr13:111642465-111642515	Caco-2	colon:	n/a
42	chr13:111590042-111590092	Hela-S3	cervix:	n/a
43	chr13:111589040-111589090	MCF-7	breast:	n/a
44	chr13:111644279-111644329	PrEC	prostate:	n/a
45	chr13:111642646-111642696	A549	lung:	n/a
46	chr13:111642147-111642197	SKMC	muscle:	n/a
47	chr13:111589969-111590019	Hepatocyte	liver:	n/a
48	chr13:111589040-111589090	AG10803	skin:	n/a
49	chr13:111590042-111590092	GM12891	blood:	n/a
50	chr13:111590042-111590092	Hepatocyte	liver:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:111610789..111612726-chr13:111615344..111617491,2	K562	blood:
2	chr13:111596342..111598319-chr13:111607475..111610357,3	K562	blood:
3	chr13:111627233..111629052-chr13:111683921..111686653,2	K562	blood:
4	chr13:111622129..111626964-chr13:111627433..111631976,8	K562	blood:
5	chr10:85883373..85884342-chr13:111619087..111619728,2	MCF-7	breast:
6	chr13:111589374..111593348-chr13:111595009..111596753,3	K562	blood:
7	chr13:111593882..111596003-chr13:111601487..111604119,2	MCF-7	breast:
8	chr13:111596388..111597279-chr13:111699232..111699797,2	K562	blood:
9	chr13:111629819..111632773-chr13:111658056..111660364,2	K562	blood:
10	chr13:111610789..111612726-chr13:111615344..111617491,2	K562	blood:
11	chr13:111596690..111597257-chr13:111659947..111660486,2	MCF-7	breast:
12	chr13:111625086..111627236-chr13:111632715..111635613,2	K562	blood:
13	chr13:111363897..111368034-chr13:111615655..111620129,4	K562	blood:
14	chr13:111622129..111626964-chr13:111627433..111631976,8	K562	blood:
15	chr13:111616685..111618480-chr13:111634399..111636568,2	K562	blood:
16	chr13:111589463..111592120-chr13:111592601..111596549,3	K562	blood:
17	chr13:111567471..111569469-chr13:111585277..111587944,2	MCF-7	breast:
18	chr13:111565745..111568365-chr13:111597876..111600865,2	K562	blood:
19	chr13:111585239..111587971-chr13:111587983..111589782,2	MCF-7	breast:
20	chr13:111595026..111596884-chr13:111600669..111603295,2	K562	blood:
21	chr13:111589463..111592120-chr13:111592601..111596549,3	K562	blood:
22	chr13:111596301..111597417-chr13:111701936..111703237,11	MCF-7	breast:
23	chr13:111562582..111564420-chr13:111633008..111634665,2	K562	blood:
24	chr13:111596412..111597239-chr13:111702359..111703278,4	MCF-7	breast:
25	chr13:111617540..111619381-chr13:111622818..111625539,2	K562	blood:
26	chr13:111623364..111627680-chr13:111627764..111631976,4	K562	blood:
27	chr13:111629819..111632773-chr13:111658056..111660364,2	K562	blood:
28	chr13:111589374..111593348-chr13:111595009..111596753,3	K562	blood:
29	chr13:111596307..111597526-chr13:111702246..111703284,7	K562	blood:
30	chr13:111595026..111596884-chr13:111600669..111603295,2	K562	blood:
31	chr13:111623288..111624991-chr13:111703272..111705702,2	K562	blood:
32	chr13:111596690..111597257-chr13:111659947..111660486,2	MCF-7	breast:
33	chr13:111617540..111619381-chr13:111622818..111625539,2	K562	blood:
34	chr13:111633005..111636046-chr13:111639587..111642234,3	K562	blood:
35	chr13:111596221..111596849-chr13:111868318..111869035,2	MCF-7	breast:
36	chr13:111593882..111596003-chr13:111601487..111604119,2	MCF-7	breast:
37	chr13:111623364..111627680-chr13:111627764..111631976,4	K562	blood:
38	chr13:111633502..111635898-chr13:111636673..111639447,3	K562	blood:
39	chr13:111522180..111524317-chr13:111617817..111619868,2	K562	blood:
40	chr13:111601035..111603243-chr13:111609725..111611968,2	K562	blood:
41	chr13:111588465..111590963-chr13:111592154..111594101,2	K562	blood:
42	chr13:111627406..111630257-chr13:111633038..111635405,3	MCF-7	breast:
43	chr13:111601035..111603243-chr13:111609725..111611968,2	K562	blood:
44	chr13:111615932..111619555-chr13:111625653..111628328,3	K562	blood:
45	chr13:111600843..111602804-chr13:111656285..111658237,2	K562	blood:
46	chr13:111626589..111629513-chr13:111696541..111699181,2	K562	blood:
47	chr13:111625086..111627236-chr13:111632715..111635613,2	K562	blood:
48	chr13:111520805..111523582-chr13:111615947..111617685,2	K562	blood:
49	chr13:111595257..111596791-chr13:111692860..111695650,2	K562	blood:
50	chr13:111589860..111591714-chr13:111804092..111806384,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGEF7-5	chr13:111603001-111603173	l_920_chr13:111602257-111603531_testes
2	lnc-ARHGEF7-5	chr13:111603001-111603251	NONHSAT035193
3	lnc-ANKRD10-1	chr13:111609527-111609598	XLOC_010724
4	lnc-ANKRD10-1	chr13:111623858-111623935	NONHSAT035195
5	lnc-ARHGEF7-5	chr13:111602303-111602398	NONHSAT035193
6	lnc-ANKRD10-1	chr13:111609527-111609598	NONHSAT035195
7	lnc-ARHGEF7-5	chr13:111602300-111602398	NONHSAT035192
8	lnc-ARHGEF7-6	chr13:111595711-111595763	l_919_chr13:111595710-111597078_testes
9	lnc-ANKRD10-1	chr13:111608813-111608988	XLOC_010724
10	lnc-ANKRD10-1	chr13:111608858-111608988	NONHSAT035195
11	lnc-ARHGEF7-5	chr13:111603215-111603491	NONHSAT035192
12	lnc-ARHGEF7-5	chr13:111602258-111602398	l_920_chr13:111602257-111603531_testes
13	lnc-ANKRD10-1	chr13:111612217-111612429	XLOC_010724
14	lnc-ARHGEF7-5	chr13:111603260-111603531	l_920_chr13:111602257-111603531_testes
15	lnc-ARHGEF7-6	chr13:111596587-111597078	l_919_chr13:111595710-111597078_testes

No data

Variant related genes	Relation type
PARP1P1	TF binding region
LINC00431	TF binding region
PARP1P1	CpG island
LINC00431	CpG island
ENSG00000134905	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000102606	chromatin interactions
ENSG00000227105	chromatin interactions
ENSG00000225760	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000255874	chromatin interactions

Extended variants
information (count: 3321 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3321 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9521997	chr13:111583422-111583423	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187323294	chr13:111583470-111583471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572880928	chr13:111583485-111583486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12429405	chr13:111583517-111583518	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
5	rs115677880	chr13:111583525-111583526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576872299	chr13:111583526-111583527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567479984	chr13:111583559-111583560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190627700	chr13:111583585-111583586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530151838	chr13:111583610-111583611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183780748	chr13:111583679-111583680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77995143	chr13:111583716-111583717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373122511	chr13:111583719-111583720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140106426	chr13:111583802-111583803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527685174	chr13:111583806-111583807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555810935	chr13:111583815-111583816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9555745	chr13:111583938-111583939	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs188722233	chr13:111583947-111583948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370933067	chr13:111583968-111583969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78140877	chr13:111583977-111583978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146868374	chr13:111583991-111583992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554515965	chr13:111583995-111583996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9583554	chr13:111584018-111584019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533602776	chr13:111584020-111584021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558506939	chr13:111584032-111584033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147001982	chr13:111584074-111584075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10663908	chr13:111584075-111584076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139195709	chr13:111584076-111584077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377342566	chr13:111584112-111584113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569134012	chr13:111584146-111584147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193270878	chr13:111584190-111584191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562215198	chr13:111584217-111584218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140127774	chr13:111584232-111584233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567923544	chr13:111584250-111584251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4773280	chr13:111584254-111584255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs554817196	chr13:111584274-111584275	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs374263243	chr13:111584326-111584327	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs4773281	chr13:111584374-111584375	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs73623064	chr13:111584385-111584386	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs184205961	chr13:111584389-111584390	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs114678762	chr13:111584390-111584391	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs144969575	chr13:111584401-111584402	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550252632	chr13:111584421-111584422	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs9583555	chr13:111584453-111584454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536096696	chr13:111584468-111584469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149061727	chr13:111584503-111584504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528078982	chr13:111584547-111584548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187871310	chr13:111584569-111584570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533953985	chr13:111584576-111584577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191507060	chr13:111584586-111584587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558134719	chr13:111584594-111584595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111583200-111585800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:111583600-111584000	Enhancers	A549	lung
3	chr13:111584200-111585400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr13:111585400-111586800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr13:111585800-111586200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
6	chr13:111585800-111586200	ZNF genes & repeats	Small Intestine	intestine
7	chr13:111585800-111586600	ZNF genes & repeats	Primary T cells from cord blood	blood
8	chr13:111586000-111586400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:111586000-111586600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr13:111586400-111588000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:111586600-111589000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr13:111589000-111589600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr13:111589800-111590000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr13:111590000-111591200	Enhancers	Primary B cells from peripheral blood	blood
15	chr13:111590200-111590600	Enhancers	K562	blood
16	chr13:111590200-111590800	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr13:111590200-111591000	Enhancers	Primary B cells from cord blood	blood
18	chr13:111590600-111591000	Enhancers	Placenta	Placenta
19	chr13:111590600-111593600	Weak transcription	K562	blood
20	chr13:111591000-111596600	Weak transcription	Placenta	Placenta
21	chr13:111593600-111595600	Enhancers	K562	blood
22	chr13:111594200-111594400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr13:111594200-111594400	Enhancers	HMEC	breast
24	chr13:111594200-111595200	Enhancers	GM12878-XiMat	blood
25	chr13:111594200-111595400	Enhancers	NH-A	brain
26	chr13:111594600-111595200	Enhancers	Primary B cells from peripheral blood	blood
27	chr13:111594600-111595800	Weak transcription	HMEC	breast
28	chr13:111594600-111596400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr13:111594600-111597000	Enhancers	NHEK	skin
30	chr13:111594800-111595000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr13:111594800-111595000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr13:111594800-111595000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:111594800-111595000	Enhancers	Stomach Mucosa	stomach
34	chr13:111595000-111595200	Enhancers	HSMMtube	muscle
35	chr13:111595000-111595600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr13:111595200-111596000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr13:111595200-111596200	Weak transcription	HSMMtube	muscle
38	chr13:111595200-111596600	Weak transcription	GM12878-XiMat	blood
39	chr13:111595400-111595800	Weak transcription	NH-A	brain
40	chr13:111595600-111596000	Weak transcription	K562	blood
41	chr13:111595600-111596800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:111595800-111596200	Enhancers	Left Ventricle	heart
43	chr13:111595800-111596600	Enhancers	HUVEC	blood vessel
44	chr13:111595800-111596600	Enhancers	NH-A	brain
45	chr13:111595800-111596800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr13:111595800-111597000	Enhancers	HMEC	breast
47	chr13:111595800-111597200	Enhancers	NHDF-Ad	bronchial
48	chr13:111595800-111597600	Enhancers	Hela-S3	cervix
49	chr13:111595800-111598600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr13:111596000-111596400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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