Variant report

Variant	nsv563124
Chromosome Location	chr13:111261267-111300943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1870)
CpG islands
(count:3970)
Chromatin interactive
region (count:92)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111270041-111270363	K562	blood:	n/a	n/a
2	ARID3A	chr13:111267685-111267885	K562	blood:	n/a	n/a
3	ARID3A	chr13:111267627-111268132	HepG2	liver:	n/a	n/a
4	ATF2	chr13:111263279-111264374	GM12878	blood:	n/a	n/a
5	ATF2	chr13:111297005-111297508	GM12878	blood:	n/a	n/a
6	ATF2	chr13:111269691-111269959	H1-hESC	embryonic stem cell:	n/a	chr13:111269830-111269841
7	ATF2	chr13:111268498-111269019	GM12878	blood:	n/a	n/a
8	ATF2	chr13:111292717-111293400	GM12878	blood:	n/a	n/a
9	ATF2	chr13:111263291-111264210	GM12878	blood:	n/a	n/a
10	ATF2	chr13:111291711-111291958	GM12878	blood:	n/a	n/a
11	ATF2	chr13:111267649-111268098	GM12878	blood:	n/a	n/a
12	ATF2	chr13:111269617-111270029	H1-hESC	embryonic stem cell:	n/a	chr13:111269830-111269841
13	ATF2	chr13:111297171-111297695	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr13:111297197-111297370	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr13:111267862-111268018	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:111262346-111262547	K562	blood:	n/a	n/a
17	BATF	chr13:111268630-111269012	GM12878	blood:	n/a	chr13:111268810-111268821 chr13:111268811-111268821
18	BATF	chr13:111263512-111263938	GM12878	blood:	n/a	n/a
19	BATF	chr13:111268661-111268970	GM12878	blood:	n/a	chr13:111268810-111268821 chr13:111268811-111268821
20	BATF	chr13:111263251-111264016	GM12878	blood:	n/a	n/a
21	BCL11A	chr13:111263531-111263876	GM12878	blood:	n/a	n/a
22	BCL11A	chr13:111263323-111263515	GM12878	blood:	n/a	n/a
23	BCL11A	chr13:111268566-111268980	GM12878	blood:	n/a	n/a
24	BCL11A	chr13:111263261-111263935	GM12878	blood:	n/a	n/a
25	BCL3	chr13:111277242-111277728	GM12878	blood:	n/a	n/a
26	BCL3	chr13:111288436-111289023	GM12878	blood:	n/a	n/a
27	BCL3	chr13:111277242-111277713	GM12878	blood:	n/a	n/a
28	BCL3	chr13:111292574-111293622	GM12878	blood:	n/a	n/a
29	BCL3	chr13:111294690-111295365	GM12878	blood:	n/a	n/a
30	BCL3	chr13:111296950-111297667	GM12878	blood:	n/a	chr13:111297442-111297455 chr13:111297171-111297180
31	BCL3	chr13:111290622-111290977	GM12878	blood:	n/a	n/a
32	BCL3	chr13:111288430-111289017	GM12878	blood:	n/a	n/a
33	BCLAF1	chr13:111268478-111268914	GM12878	blood:	n/a	n/a
34	BCLAF1	chr13:111263193-111264009	GM12878	blood:	n/a	n/a
35	BCLAF1	chr13:111267636-111268153	GM12878	blood:	n/a	n/a
36	BCLAF1	chr13:111297119-111297528	GM12878	blood:	n/a	chr13:111297442-111297455 chr13:111297171-111297180
37	BHLHE40	chr13:111263349-111263865	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:111267508-111267920	K562	blood:	n/a	n/a
39	BHLHE40	chr13:111268565-111268616	K562	blood:	n/a	n/a
40	BHLHE40	chr13:111268661-111269317	GM12878	blood:	n/a	n/a
41	BHLHE40	chr13:111293527-111293717	K562	blood:	n/a	n/a
42	BHLHE40	chr13:111297241-111297508	GM12878	blood:	n/a	n/a
43	BHLHE40	chr13:111267509-111268025	GM12878	blood:	n/a	n/a
44	BHLHE40	chr13:111267534-111268165	HepG2	liver:	n/a	n/a
45	BRCA1	chr13:111267579-111268094	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr13:111267608-111268353	HepG2	liver:	n/a	n/a
47	BRCA1	chr13:111268844-111268989	HepG2	liver:	n/a	n/a
48	BRCA1	chr13:111262345-111262546	HepG2	liver:	n/a	n/a
49	BRCA1	chr13:111297153-111297341	H1-hESC	embryonic stem cell:	n/a	n/a
50	CBX3	chr13:111267451-111268091	K562	blood:	n/a	n/a

(count:3970 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111288822-111288872	HRE	kidney:	n/a
2	chr13:111267667-111267717	HCM	heart:	n/a
3	chr13:111291955-111292005	GM12878	blood:	n/a
4	chr13:111267667-111267717	ProgFib	skin:	n/a
5	chr13:111288822-111288872	SK-N-MC	brain:	n/a
6	chr13:111288822-111288872	HRE	kidney:	n/a
7	chr13:111267667-111267717	HCM	heart:	n/a
8	chr13:111291955-111292005	GM12878	blood:	n/a
9	chr13:111267667-111267717	ProgFib	skin:	n/a
10	chr13:111288822-111288872	SK-N-MC	brain:	n/a
11	chr13:111294747-111294797	HEK293	kidney:	embryo
12	chr13:111290755-111290805	MCF-7	breast:	n/a
13	chr13:111291955-111292005	RPTEC	kidney:	n/a
14	chr13:111287944-111287994	HRE	kidney:	n/a
15	chr13:111291582-111291632	SAEC	small airway:	n/a
16	chr13:111267991-111268041	GM06990	blood:	n/a
17	chr13:111270991-111271041	NHBE	bronchial:	n/a
18	chr13:111287263-111287313	T-47D	breast:	n/a
19	chr13:111287117-111287167	HUVEC	blood vessel:	n/a
20	chr13:111277423-111277473	SK-N-MC	brain:	n/a
21	chr13:111277190-111277240	MCF-7	breast:	n/a
22	chr13:111281144-111281194	H1-hESC	embryonic stem cell:	embryo
23	chr13:111267979-111268029	BJ	skin:	n/a
24	chr13:111267856-111267906	Hepatocyte	liver:	n/a
25	chr13:111268441-111268491	PFSK-1	brain:	n/a
26	chr13:111294747-111294797	NH-A	brain:	n/a
27	chr13:111295728-111295778	HCM	heart:	n/a
28	chr13:111291316-111291366	NB4	blood:	n/a
29	chr13:111297400-111297450	HL-60	blood:	n/a
30	chr13:111288822-111288872	HCPEpiC	choroid plexus:	n/a
31	chr13:111297400-111297450	RPTEC	kidney:	n/a
32	chr13:111277423-111277473	HRCEpiC	kidney:	n/a
33	chr13:111281384-111281434	LNCaP	prostate:	n/a
34	chr13:111268705-111268755	Hela-S3	cervix:	n/a
35	chr13:111268673-111268723	GM19239	blood:	n/a
36	chr13:111277501-111277551	PFSK-1	brain:	n/a
37	chr13:111287117-111287167	SAEC	small airway:	n/a
38	chr13:111284778-111284828	HRE	kidney:	n/a
39	chr13:111281037-111281087	GM12892	blood:	n/a
40	chr13:111267793-111267843	AG04450	lung:	fetal
41	chr13:111291248-111291298	Caco-2	colon:	n/a
42	chr13:111278058-111278108	HRE	kidney:	n/a
43	chr13:111288822-111288872	T-47D	breast:	n/a
44	chr13:111267935-111267985	BJ	skin:	n/a
45	chr13:111267935-111267985	HAEpiC	amniotic membrane:	n/a
46	chr13:111290755-111290805	Hepatocyte	liver:	n/a
47	chr13:111268673-111268723	PrEC	prostate:	n/a
48	chr13:111267849-111267899	A549	lung:	n/a
49	chr13:111284778-111284828	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:111280738-111280788	HCPEpiC	choroid plexus:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:111267955..111269613-chr13:111288415..111289925,2	K562	blood:
2	chr13:111267921..111270163-chr13:111289347..111290890,2	MCF-7	breast:
3	chr13:111266587..111269692-chr13:111357018..111359356,4	K562	blood:
4	chr13:111280796..111283636-chr13:111367642..111369332,2	K562	blood:
5	chr13:111267252..111268156-chr8:144635373..144636016,2	HCT-116	colon:
6	chr13:111248805..111250322-chr13:111277318..111279178,2	MCF-7	breast:
7	chr13:111287423..111289848-chr13:111365878..111368153,2	MCF-7	breast:
8	chr13:111158551..111160525-chr13:111267801..111269585,2	MCF-7	breast:
9	chr13:111260500..111264112-chr13:111364498..111367166,4	K562	blood:
10	chr13:111282173..111283948-chr13:111364006..111365721,2	K562	blood:
11	chr13:111299507..111301801-chr13:111367049..111369699,2	K562	blood:
12	chr13:111299129..111300874-chr13:111356502..111358469,2	K562	blood:
13	chr13:111281708..111283812-chr13:111291061..111293411,2	K562	blood:
14	chr13:111292549..111296522-chr13:111365011..111368169,4	MCF-7	breast:
15	chr13:111295643..111300120-chr13:111365518..111369026,8	MCF-7	breast:
16	chr13:111289947..111291840-chr13:111364201..111367983,3	MCF-7	breast:
17	chr13:111294769..111302902-chr13:111363368..111369699,14	K562	blood:
18	chr13:111245045..111250011-chr13:111292249..111295847,5	MCF-7	breast:
19	chr13:111271645..111274603-chr13:111290397..111292824,3	MCF-7	breast:
20	chr13:111270148..111271814-chr13:111272109..111273731,2	K562	blood:
21	chr13:111293993..111296064-chr13:111303671..111305521,2	K562	blood:
22	chr13:111267350..111267981-chr17:56756502..56757440,2	NB4	blood:
23	chr13:111297577..111299513-chr13:111565470..111567515,2	MCF-7	breast:
24	chr13:111266655..111268705-chr13:111294879..111298471,3	K562	blood:
25	chr13:111211377..111214970-chr13:111273880..111276435,4	MCF-7	breast:
26	chr13:111266965..111271727-chr13:111364973..111369025,9	MCF-7	breast:
27	chr13:111266678..111269187-chr13:111295319..111298212,3	MCF-7	breast:
28	chr13:111285638..111287730-chr13:111364678..111367940,3	MCF-7	breast:
29	chr13:111284778..111286525-chr13:111522479..111525295,2	K562	blood:
30	chr13:111288106..111291537-chr13:111365021..111367152,3	K562	blood:
31	chr13:111294769..111296453-chr13:111366037..111368687,3	K562	blood:
32	chr13:111286170..111289373-chr13:111362877..111366767,3	K562	blood:
33	chr13:111266314..111268979-chr13:111280505..111282766,2	K562	blood:
34	chr13:111267596..111269197-chr13:111364131..111366094,2	K562	blood:
35	chr13:111268194..111268777-chr6:12010640..12011635,2	Hela-S3	cervix:
36	chr13:111287003..111289809-chr13:111566070..111568939,2	K562	blood:
37	chr13:111267631..111268254-chr5:108083564..108084113,2	Hela-S3	cervix:
38	chr13:111268040..111269954-chr13:111270156..111273298,3	K562	blood:
39	chr10:124768484..124768999-chr13:111291105..111291975,2	NB4	blood:
40	chr13:111266678..111269187-chr13:111295319..111298212,3	MCF-7	breast:
41	chr13:111266306..111273367-chr13:111274094..111280494,12	K562	blood:
42	chr13:111270127..111273388-chr13:111363315..111367711,4	MCF-7	breast:
43	chr13:111278124..111281264-chr13:111364873..111369262,5	MCF-7	breast:
44	chr13:111265756..111270693-chr13:111363417..111370660,10	K562	blood:
45	chr13:111266944..111268705-chr13:111296076..111298471,2	K562	blood:
46	chr13:111271154..111277326-chr13:111363993..111367812,9	K562	blood:
47	chr13:111300252..111302823-chr17:62160230..62162389,2	MCF-7	breast:
48	chr13:111268021..111270238-chr13:111291368..111294151,2	MCF-7	breast:
49	chr13:111292709..111295545-chr13:111300565..111303424,2	MCF-7	breast:
50	chr13:111107824..111108748-chr13:111297271..111297854,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARKD-1	chr13:111291555-111292340	NONHSAT035156

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CARS2	hsa-miR-155-5p	chr13:111293778-111293799

Variant related genes	Relation type
CARS2	TF binding region
ENSG00000255831	TF binding region
CARKD	TF binding region
CARS2	CpG island
ENSG00000255831	CpG island
CARKD	CpG island
ENSG00000050405	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000104518	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000132510	chromatin interactions
ENSG00000213995	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000181929	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000134871	chromatin interactions
ENSG00000139832	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000255831	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000196177	chromatin interactions

Extended variants
information (count: 2155 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2155 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4771699	chr13:111261267-111261268	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74456576	chr13:111261268-111261269	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs9583515	chr13:111261291-111261292	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs577003977	chr13:111261311-111261312	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs145266822	chr13:111261344-111261345	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562591581	chr13:111261379-111261380	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs9559855	chr13:111261403-111261404	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs189643473	chr13:111261433-111261434	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs111546695	chr13:111261492-111261493	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs560150673	chr13:111261496-111261497	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs201984386	chr13:111261520-111261521	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs200177308	chr13:111261525-111261526	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs181630258	chr13:111261550-111261551	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201104596	chr13:111261551-111261552	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs185179786	chr13:111261553-111261554	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs111634402	chr13:111261554-111261555	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs571017983	chr13:111261560-111261561	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs202020974	chr13:111261567-111261568	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs550353478	chr13:111261578-111261579	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs568633598	chr13:111261585-111261586	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs536172388	chr13:111261587-111261588	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs547903435	chr13:111261598-111261599	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs4293240	chr13:111261613-111261614	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs566518297	chr13:111261627-111261628	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs190403954	chr13:111261632-111261633	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs113492720	chr13:111261637-111261638	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs371071685	chr13:111261639-111261640	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558328621	chr13:111261644-111261645	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs146147919	chr13:111261647-111261648	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs181832916	chr13:111261651-111261652	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs544046612	chr13:111261674-111261675	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs368600154	chr13:111261675-111261676	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs574372371	chr13:111261703-111261704	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs541752801	chr13:111261713-111261714	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs560113162	chr13:111261715-111261716	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs372334331	chr13:111261747-111261748	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs534659457	chr13:111261773-111261774	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs546190164	chr13:111261800-111261801	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs564378826	chr13:111261818-111261819	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs531854906	chr13:111261832-111261833	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550073207	chr13:111261842-111261843	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs137858499	chr13:111261882-111261883	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs112612168	chr13:111261913-111261914	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs186384294	chr13:111261920-111261921	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs371110891	chr13:111261921-111261922	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs548148916	chr13:111261962-111261963	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs566385223	chr13:111261985-111261986	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs557786676	chr13:111262032-111262033	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs117743080	chr13:111262081-111262082	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs533722134	chr13:111262095-111262096	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	21364760	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2110 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111249800-111262400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:111254000-111262600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:111255800-111262600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr13:111259600-111262600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr13:111260000-111262600	Weak transcription	Placenta	Placenta
6	chr13:111260600-111261600	Enhancers	Ovary	ovary
7	chr13:111260600-111262400	Weak transcription	GM12878-XiMat	blood
8	chr13:111260600-111262600	Weak transcription	HepG2	liver
9	chr13:111260800-111264000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr13:111261800-111262200	Weak transcription	Ovary	ovary
11	chr13:111262000-111263200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr13:111262000-111263200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr13:111262000-111263400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr13:111262000-111263400	Enhancers	NHEK	skin
15	chr13:111262000-111264200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr13:111262200-111263200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr13:111262400-111262600	Enhancers	HSMM	muscle
18	chr13:111262400-111262600	Bivalent/Poised TSS	NH-A	brain
19	chr13:111262400-111263200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr13:111262400-111263400	Flanking Active TSS	GM12878-XiMat	blood
21	chr13:111262600-111263000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr13:111262600-111263000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr13:111262600-111263000	Enhancers	H9 Cell Line	embryonic stem cell
24	chr13:111262600-111263000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr13:111262600-111263000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
26	chr13:111262600-111263000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr13:111262600-111263000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr13:111262600-111263000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:111262600-111263000	Enhancers	Brain Anterior Caudate	brain
30	chr13:111262600-111263000	Enhancers	Esophagus	oesophagus
31	chr13:111262600-111263000	Enhancers	Fetal Kidney	kidney
32	chr13:111262600-111263000	Enhancers	HMEC	breast
33	chr13:111262600-111263200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:111262600-111263400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr13:111262600-111263400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr13:111262600-111263400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr13:111262600-111263400	Enhancers	Placenta	Placenta
38	chr13:111262600-111263400	Enhancers	HepG2	liver
39	chr13:111262600-111265200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr13:111262600-111267200	Weak transcription	HSMM	muscle
41	chr13:111262800-111263200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr13:111263000-111263200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr13:111263000-111263200	Enhancers	Duodenum Mucosa	Duodenum
44	chr13:111263000-111263800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr13:111263000-111263800	Weak transcription	Brain Anterior Caudate	brain
46	chr13:111263000-111267000	Weak transcription	Esophagus	oesophagus
47	chr13:111263000-111267200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr13:111263000-111267200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr13:111263000-111267400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr13:111263000-111267400	Weak transcription	Fetal Kidney	kidney

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