Variant report

Variant	nsv553588
Chromosome Location	chr11:17713507-17791822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2171)
CpG islands
(count:3055)
Chromatin interactive
region (count:85)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2171 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17791527-17791963	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:17752734-17752850	HepG2	liver:	n/a	n/a
3	ATF1	chr11:17738453-17738597	K562	blood:	n/a	n/a
4	ATF1	chr11:17783928-17784200	K562	blood:	n/a	n/a
5	ATF3	chr11:17725592-17725911	GM12878	blood:	n/a	n/a
6	ATF3	chr11:17725652-17725838	K562	blood:	n/a	n/a
7	ATF3	chr11:17721100-17721405	K562	blood:	n/a	n/a
8	BACH1	chr11:17743545-17743911	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:17781684-17782192	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:17743740-17743870	K562	blood:	n/a	n/a
11	BACH1	chr11:17756192-17756315	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:17741849-17741864	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:17735827-17736024	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:17717654-17717769	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr11:17740034-17740383	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr11:17781712-17781838	K562	blood:	n/a	n/a
17	BHLHE40	chr11:17791512-17792072	HepG2	liver:	n/a	n/a
18	BHLHE40	chr11:17781973-17782310	K562	blood:	n/a	n/a
19	BHLHE40	chr11:17791514-17791889	K562	blood:	n/a	n/a
20	BHLHE40	chr11:17784019-17784137	K562	blood:	n/a	n/a
21	BHLHE40	chr11:17756573-17756763	GM12878	blood:	n/a	chr11:17756644-17756660
22	BHLHE40	chr11:17721100-17721426	K562	blood:	n/a	chr11:17721107-17721123
23	BHLHE40	chr11:17756580-17756727	K562	blood:	n/a	chr11:17756644-17756660
24	BHLHE40	chr11:17782021-17782165	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:17756560-17756818	HepG2	liver:	n/a	chr11:17756644-17756660
26	BHLHE40	chr11:17752607-17752898	GM12878	blood:	n/a	n/a
27	BRCA1	chr11:17752773-17752833	GM12878	blood:	n/a	n/a
28	BRCA1	chr11:17781963-17782291	HepG2	liver:	n/a	n/a
29	BRCA1	chr11:17752729-17752836	HepG2	liver:	n/a	n/a
30	BRCA1	chr11:17741781-17741867	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr11:17752601-17752887	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr11:17721090-17721463	K562	blood:	n/a	n/a
33	CBX3	chr11:17791632-17791866	K562	blood:	n/a	n/a
34	CBX3	chr11:17781908-17782256	K562	blood:	n/a	n/a
35	CCNT2	chr11:17738413-17738634	K562	blood:	n/a	n/a
36	CEBPB	chr11:17791598-17791899	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:17752665-17752866	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:17772452-17772532	H1-hESC	embryonic stem cell:	n/a	chr11:17772511-17772522
39	CEBPB	chr11:17772348-17772662	HepG2	liver:	n/a	chr11:17772511-17772522
40	CEBPB	chr11:17772512-17772518	K562	blood:	n/a	n/a
41	CEBPB	chr11:17772343-17772697	HepG2	liver:	n/a	chr11:17772511-17772522
42	CEBPB	chr11:17772354-17772618	HepG2	liver:	n/a	chr11:17772511-17772522
43	CEBPB	chr11:17725586-17725830	K562	blood:	n/a	n/a
44	CEBPB	chr11:17725560-17725583	A549	lung:	n/a	n/a
45	CEBPB	chr11:17741695-17741950	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr11:17772409-17772648	HepG2	liver:	n/a	chr11:17772511-17772522
47	CEBPB	chr11:17782011-17782346	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr11:17752652-17752914	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr11:17779238-17779303	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:17776105-17776129	HepG2	liver:	n/a	n/a

(count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17742135-17742185	HAEpiC	amniotic membrane:	n/a
2	chr11:17765568-17765618	Caco-2	colon:	n/a
3	chr11:17742741-17742791	HCPEpiC	choroid plexus:	n/a
4	chr11:17757415-17757465	NH-A	brain:	n/a
5	chr11:17765568-17765618	Hepatocyte	liver:	n/a
6	chr11:17742135-17742185	HAEpiC	amniotic membrane:	n/a
7	chr11:17765568-17765618	Caco-2	colon:	n/a
8	chr11:17742741-17742791	HCPEpiC	choroid plexus:	n/a
9	chr11:17757415-17757465	NH-A	brain:	n/a
10	chr11:17765568-17765618	Hepatocyte	liver:	n/a
11	chr11:17741687-17741737	AG09309	skin:	n/a
12	chr11:17741925-17741975	SAEC	small airway:	n/a
13	chr11:17765568-17765618	BE2_C	brain:	n/a
14	chr11:17740977-17741027	HEK293	kidney:	embryo
15	chr11:17757342-17757392	SKMC	muscle:	n/a
16	chr11:17747289-17747339	T-47D	breast:	n/a
17	chr11:17756761-17756811	GM12891	blood:	n/a
18	chr11:17791761-17791811	MCF10A-Er-Src	breast:	n/a
19	chr11:17756986-17757036	AG09319	gingival:	n/a
20	chr11:17760574-17760624	Hepatocyte	liver:	n/a
21	chr11:17765568-17765618	K562	blood:	n/a
22	chr11:17760602-17760652	T-47D	breast:	n/a
23	chr11:17755937-17755987	SAEC	small airway:	n/a
24	chr11:17741687-17741737	RPTEC	kidney:	n/a
25	chr11:17717574-17717624	U87	brain:	n/a
26	chr11:17760956-17761006	HRCEpiC	kidney:	n/a
27	chr11:17756761-17756811	HCM	heart:	n/a
28	chr11:17717280-17717330	GM19239	blood:	n/a
29	chr11:17717588-17717638	HUVEC	blood vessel:	n/a
30	chr11:17756479-17756529	H1-hESC	embryonic stem cell:	embryo
31	chr11:17765568-17765618	PFSK-1	brain:	n/a
32	chr11:17761718-17761768	MCF-7	breast:	n/a
33	chr11:17743761-17743811	ECC-1	luminal epithelium:	n/a
34	chr11:17743610-17743660	U87	brain:	n/a
35	chr11:17742502-17742552	NH-A	brain:	n/a
36	chr11:17747289-17747339	NHDF-neo	bronchial:	n/a
37	chr11:17761718-17761768	AoSMC	blood vessel:	n/a
38	chr11:17760574-17760624	SK-N-MC	brain:	n/a
39	chr11:17760602-17760652	AG09309	skin:	n/a
40	chr11:17790285-17790335	HRCEpiC	kidney:	n/a
41	chr11:17752634-17752684	HCM	heart:	n/a
42	chr11:17740967-17741017	HepG2	liver:	n/a
43	chr11:17717818-17717868	NT2-D1	testis:	n/a
44	chr11:17738031-17738081	H1-hESC	embryonic stem cell:	embryo
45	chr11:17742759-17742809	GM12892	blood:	n/a
46	chr11:17713884-17713934	ovcar-3	ovarian:	n/a
47	chr11:17760602-17760652	AG09319	gingival:	n/a
48	chr11:17743946-17743996	SK-N-SH_RA	brain:	n/a
49	chr11:17757342-17757392	HCPEpiC	choroid plexus:	n/a
50	chr11:17760956-17761006	AG09309	skin:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:17769238..17771607-chr11:17779598..17782123,2	K562	blood:
2	chr11:17789104..17793559-chr11:17796092..17800270,5	MCF-7	breast:
3	chr11:17788319..17789007-chr11:17994351..17995171,2	MCF-7	breast:
4	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
5	chr11:17791247..17794224-chr11:17800123..17802336,2	MCF-7	breast:
6	chr11:17790395..17791963-chr11:17795616..17797848,2	K562	blood:
7	chr11:17782032..17782544-chr11:17801368..17801871,2	MCF-7	breast:
8	chr11:17791157..17792211-chr11:17946174..17946920,6	MCF-7	breast:
9	chr11:17783615..17784490-chr11:17868027..17868802,2	MCF-7	breast:
10	chr11:17588922..17590478-chr11:17766034..17768818,2	K562	blood:
11	chr11:17622618..17623441-chr11:17752027..17752742,2	K562	blood:
12	chr11:17735220..17735764-chr11:17743713..17744525,2	MCF-7	breast:
13	chr11:17783850..17786298-chr11:17789626..17792965,4	K562	blood:
14	chr11:17426978..17427915-chr11:17791365..17792205,5	MCF-7	breast:
15	chr11:17620244..17621142-chr11:17752157..17753016,5	MCF-7	breast:
16	chr11:17783515..17784102-chr11:17848668..17849177,2	MCF-7	breast:
17	chr11:17781675..17782374-chr11:17994338..17995285,3	MCF-7	breast:
18	chr11:17781047..17783603-chr11:17891179..17893367,2	K562	blood:
19	chr11:17752292..17753246-chr11:17999986..18000903,4	K562	blood:
20	chr11:17781589..17782577-chr11:17885405..17886255,2	K562	blood:
21	chr11:17768263..17770539-chr11:17771638..17773890,2	MCF-7	breast:
22	chr11:17705084..17707821-chr11:17711837..17714694,2	K562	blood:
23	chr11:17426978..17427915-chr11:17791365..17792221,7	MCF-7	breast:
24	chr11:17791549..17792453-chr11:17833752..17834540,3	MCF-7	breast:
25	chr11:17764908..17766462-chr11:17767114..17769351,2	K562	blood:
26	chr11:17781658..17782593-chr11:18000009..18000810,4	MCF-7	breast:
27	chr11:17619891..17621109-chr11:17743288..17744431,5	MCF-7	breast:
28	chr11:17755705..17757483-chr11:17762543..17764877,2	K562	blood:
29	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
30	chr11:17620168..17621149-chr11:17752060..17752755,3	K562	blood:
31	chr11:17752210..17753037-chr11:17762564..17763159,2	K562	blood:
32	chr11:17751921..17752763-chr19:36040271..36040795,2	MCF-7	breast:
33	chr11:17769238..17771607-chr11:17779598..17782123,2	K562	blood:
34	chr11:17781854..17784746-chr11:17785272..17786871,2	MCF-7	breast:
35	chr11:17726249..17728928-chr11:17732573..17735083,2	MCF-7	breast:
36	chr11:17710440..17715421-chr11:17715832..17719362,5	K562	blood:
37	chr11:17722486..17724717-chr11:17727954..17730842,2	K562	blood:
38	chr11:17783850..17786298-chr11:17789626..17792965,4	K562	blood:
39	chr11:17620217..17621179-chr11:17742829..17744247,6	MCF-7	breast:
40	chr11:17781823..17782570-chr11:18001193..18001905,2	MCF-7	breast:
41	chr11:17781608..17782534-chr11:17926929..17928261,6	MCF-7	breast:
42	chr11:17783547..17784473-chr11:18000133..18001470,5	MCF-7	breast:
43	chr11:17622892..17623600-chr11:17752018..17752807,2	MCF-7	breast:
44	chr11:17768773..17771131-chr11:17771902..17774873,3	K562	blood:
45	chr11:17752308..17752866-chr11:17774705..17775593,2	MCF-7	breast:
46	chr11:17768263..17770539-chr11:17771638..17773890,2	MCF-7	breast:
47	chr11:17622422..17624117-chr11:17750393..17752396,2	MCF-7	breast:
48	chr11:17752076..17753447-chr11:17867688..17868717,4	MCF-7	breast:
49	chr11:17733888..17735691-chr11:17739053..17741610,3	K562	blood:
50	chr11:17783974..17784521-chr11:17848366..17848887,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOD1-1	chr11:17716844-17716913	ENSG00000254586
2	lnc-SERGEF-2	chr11:17718366-17718523	XLOC_009385
3	lnc-SERGEF-2	chr11:17717579-17717919	XLOC_009385
4	lnc-SERGEF-2	chr11:17718366-17719033	XLOC_009385
5	lnc-MYOD1-1	chr11:17716569-17716597	ENSG00000254586
6	lnc-MYOD1-1	chr11:17716600-17716913	ENSG00000254586
7	lnc-MYOD1-1	chr11:17718516-17718844	ENSG00000254586
8	lnc-SERGEF-2	chr11:17716827-17717311	XLOC_009385
9	lnc-SERGEF-2	chr11:17716814-17717247	ENSG00000255335.1
10	lnc-SERGEF-2	chr11:17716818-17717247	XLOC_009385
11	lnc-SERGEF-2	chr11:17718366-17718487	ENSG00000255335.1
12	lnc-MYOD1-1	chr11:17718516-17719018	ENSG00000254586
13	lnc-SERGEF-2	chr11:17718366-17718751	NONHSAT018243
14	lnc-SERGEF-2	chr11:17718427-17718751	NONHSAT018242
15	lnc-SERGEF-2	chr11:17716823-17717247	NONHSAT018243
16	lnc-SERGEF-2	chr11:17716823-17717247	NONHSAT018242
17	lnc-SERGEF-2	chr11:17716827-17717247	XLOC_009385

No data

Variant related genes	Relation type
KCNC1	TF binding region
ENSG00000254586	TF binding region
ENSG00000255335	TF binding region
MYOD1	TF binding region
KCNC1	CpG island
ENSG00000254586	CpG island
ENSG00000255335	CpG island
MYOD1	CpG island
ENSG00000129159	chromatin interactions
ENSG00000255335	chromatin interactions
ENSG00000254586	chromatin interactions
ENSG00000129152	chromatin interactions
ZNF644	miRNA target sites

Extended variants
information (count: 3025 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3025 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2878806	chr11:17713507-17713508	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545746818	chr11:17713570-17713571	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs184747356	chr11:17713579-17713580	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531587171	chr11:17713634-17713635	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs117281367	chr11:17713673-17713674	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs540531105	chr11:17713717-17713718	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs530249597	chr11:17713778-17713779	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs116183572	chr11:17713797-17713798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs28609365	chr11:17713813-17713814	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs533962584	chr11:17713818-17713819	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs141698440	chr11:17713841-17713842	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571069056	chr11:17713849-17713850	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143644267	chr11:17713850-17713851	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538206572	chr11:17713885-17713886	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs78127315	chr11:17713890-17713891	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs28683112	chr11:17713916-17713917	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553598451	chr11:17713921-17713922	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs189298845	chr11:17713976-17713977	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs545481927	chr11:17714064-17714065	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs76101852	chr11:17714109-17714110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531686264	chr11:17714129-17714130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543720505	chr11:17714157-17714158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs561900371	chr11:17714181-17714182	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs192294773	chr11:17714183-17714184	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547540274	chr11:17714193-17714194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566855321	chr11:17714260-17714261	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs527745791	chr11:17714284-17714285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs542031920	chr11:17714301-17714302	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs3858500	chr11:17714317-17714318	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs570508756	chr11:17714318-17714319	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs538173636	chr11:17714338-17714339	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs556424539	chr11:17714358-17714359	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs536319238	chr11:17714440-17714441	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs568379358	chr11:17714502-17714503	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140945221	chr11:17714514-17714515	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550032432	chr11:17714528-17714529	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554292909	chr11:17714566-17714567	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369634294	chr11:17714584-17714585	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs572054667	chr11:17714610-17714611	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs185198558	chr11:17714615-17714616	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs557498872	chr11:17714664-17714665	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189729915	chr11:17714714-17714715	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs150264158	chr11:17714716-17714717	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs561051531	chr11:17714717-17714718	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2878807	chr11:17714733-17714734	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs573936609	chr11:17714779-17714780	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs540878742	chr11:17714818-17714819	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs115379106	chr11:17714935-17714936	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs139020597	chr11:17714952-17714953	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs6416178	chr11:17715003-17715004	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17711200-17714400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr11:17712600-17714000	Enhancers	HSMM	muscle
3	chr11:17712800-17714400	Enhancers	Fetal Muscle Leg	muscle
4	chr11:17712800-17716000	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr11:17713200-17713600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr11:17713200-17718000	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr11:17713200-17721800	Enhancers	Psoas Muscle	Psoas
8	chr11:17713400-17717200	Enhancers	HSMMtube	muscle
9	chr11:17714000-17715200	Weak transcription	HSMM	muscle
10	chr11:17714400-17714600	Enhancers	Fetal Muscle Trunk	muscle
11	chr11:17714400-17714800	Bivalent Enhancer	Fetal Heart	heart
12	chr11:17714400-17714800	Bivalent Enhancer	Left Ventricle	heart
13	chr11:17714400-17717000	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr11:17714600-17714800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr11:17715000-17715400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr11:17715200-17715400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr11:17715200-17715400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:17715200-17722000	Enhancers	HSMM	muscle
19	chr11:17716000-17716400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
20	chr11:17716000-17716600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr11:17716400-17716800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr11:17716400-17718400	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr11:17716600-17717400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
24	chr11:17716800-17718200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr11:17717000-17717200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr11:17717000-17717200	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr11:17717000-17717200	Bivalent Enhancer	Right Ventricle	heart
28	chr11:17717000-17717400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:17717000-17717400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
30	chr11:17717000-17718000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
31	chr11:17717000-17718000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
32	chr11:17717000-17718000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr11:17717200-17717400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:17717200-17717400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
35	chr11:17717200-17717400	Bivalent Enhancer	Fetal Stomach	stomach
36	chr11:17717200-17717600	Bivalent Enhancer	Brain Hippocampus Middle	brain
37	chr11:17717200-17717600	Bivalent/Poised TSS	Right Ventricle	heart
38	chr11:17717200-17717600	Weak transcription	HSMMtube	muscle
39	chr11:17717200-17717800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:17717200-17717800	Bivalent Enhancer	Fetal Heart	heart
41	chr11:17717200-17718000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
42	chr11:17717200-17718000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
43	chr11:17717200-17718000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr11:17717200-17718000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr11:17717200-17718000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:17717200-17718200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
47	chr11:17717400-17717600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
48	chr11:17717400-17717600	Active TSS	Right Atrium	heart
49	chr11:17717400-17717800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:17717400-17717800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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