Variant report

Variant	nsv608342
Chromosome Location	chr7:124549573-124600505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:696)
CpG islands
(count:732)
Chromatin interactive
region (count:26)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:124569744-124570422	K562	blood:	n/a	n/a
2	ARID3A	chr7:124569498-124570414	HepG2	liver:	n/a	n/a
3	ATF1	chr7:124581503-124581757	K562	blood:	n/a	n/a
4	ATF1	chr7:124569485-124570398	K562	blood:	n/a	n/a
5	ATF1	chr7:124570984-124571240	K562	blood:	n/a	n/a
6	ATF2	chr7:124558506-124559165	GM12878	blood:	n/a	n/a
7	ATF2	chr7:124569305-124570360	GM12878	blood:	n/a	chr7:124569893-124569904
8	ATF2	chr7:124569664-124570198	H1-hESC	embryonic stem cell:	n/a	chr7:124569893-124569904
9	ATF2	chr7:124569670-124570211	H1-hESC	embryonic stem cell:	n/a	chr7:124569893-124569904
10	ATF2	chr7:124558530-124559112	GM12878	blood:	n/a	n/a
11	ATF2	chr7:124569554-124570221	GM12878	blood:	n/a	chr7:124569893-124569904
12	ATF3	chr7:124569768-124570050	HepG2	liver:	n/a	chr7:124569883-124569903 chr7:124569892-124569902 chr7:124569891-124569906 chr7:124569893-124569904 chr7:124569894-124569905 chr7:124569891-124569904 chr7:124569894-124569902 chr7:124569895-124569902 chr7:124569895-124569903
13	ATF3	chr7:124569622-124570250	K562	blood:	n/a	chr7:124569883-124569903 chr7:124569892-124569902 chr7:124569891-124569906 chr7:124569893-124569904 chr7:124569894-124569905 chr7:124569891-124569904 chr7:124569894-124569902 chr7:124569895-124569902 chr7:124569895-124569903
14	ATF3	chr7:124569717-124570123	K562	blood:	n/a	chr7:124569883-124569903 chr7:124569892-124569902 chr7:124569891-124569906 chr7:124569893-124569904 chr7:124569894-124569905 chr7:124569891-124569904 chr7:124569894-124569902 chr7:124569895-124569902 chr7:124569895-124569903
15	ATF3	chr7:124569583-124570303	A549	lung:	n/a	chr7:124569883-124569903 chr7:124569892-124569902 chr7:124569891-124569906 chr7:124569893-124569904 chr7:124569894-124569905 chr7:124569891-124569904 chr7:124569894-124569902 chr7:124569895-124569902 chr7:124569895-124569903
16	BACH1	chr7:124569663-124570188	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:124569540-124569970	K562	blood:	n/a	n/a
18	BATF	chr7:124558745-124559050	GM12878	blood:	n/a	n/a
19	BATF	chr7:124558692-124559112	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:124558754-124559082	GM12878	blood:	n/a	n/a
21	BCLAF1	chr7:124569863-124570442	K562	blood:	n/a	chr7:124570126-124570135
22	BCLAF1	chr7:124569511-124570294	GM12878	blood:	n/a	chr7:124570126-124570135
23	BHLHE40	chr7:124569400-124570154	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:124554502-124554557	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:124569453-124570339	K562	blood:	n/a	n/a
26	BRCA1	chr7:124569623-124570229	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr7:124569820-124570110	HepG2	liver:	n/a	n/a
28	BRCA1	chr7:124569630-124570391	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr7:124581318-124581885	K562	blood:	n/a	n/a
30	CBX3	chr7:124569488-124570445	HCT-116	colon:	n/a	n/a
31	CBX3	chr7:124598035-124598565	K562	blood:	n/a	n/a
32	CBX3	chr7:124569430-124570486	K562	blood:	n/a	n/a
33	CBX3	chr7:124598035-124598354	K562	blood:	n/a	n/a
34	CBX3	chr7:124569517-124570429	K562	blood:	n/a	n/a
35	CBX3	chr7:124569459-124570397	HCT-116	colon:	n/a	n/a
36	CCNT2	chr7:124569447-124570291	K562	blood:	n/a	n/a
37	CEBPB	chr7:124569721-124570262	A549	lung:	n/a	n/a
38	CEBPB	chr7:124569402-124570224	K562	blood:	n/a	n/a
39	CEBPB	chr7:124567942-124568156	K562	blood:	n/a	n/a
40	CEBPB	chr7:124569830-124570039	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:124569565-124570297	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:124569430-124570216	K562	blood:	n/a	n/a
43	CEBPB	chr7:124569823-124570214	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:124569727-124570127	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr7:124569712-124570187	IMR90	lung:	n/a	n/a
46	CEBPB	chr7:124569634-124570192	A549	lung:	n/a	n/a
47	CEBPB	chr7:124569677-124570240	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:124569662-124570214	MCF-7	breast:	n/a	n/a
49	CEBPB	chr7:124569693-124570134	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPD	chr7:124569808-124570297	HepG2	liver:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124574073-124574123	HCT-116	colon:	n/a
2	chr7:124570359-124570409	HRE	kidney:	n/a
3	chr7:124565947-124565997	PFSK-1	brain:	n/a
4	chr7:124570359-124570409	HL-60	blood:	n/a
5	chr7:124570359-124570409	NHDF-neo	bronchial:	n/a
6	chr7:124570130-124570180	HCT-116	colon:	n/a
7	chr7:124565947-124565997	AG10803	skin:	n/a
8	chr7:124570130-124570180	HEEpiC	esophagus:	n/a
9	chr7:124574073-124574123	GM06990	blood:	n/a
10	chr7:124570130-124570180	GM12891	blood:	n/a
11	chr7:124570181-124570231	HL-60	blood:	n/a
12	chr7:124570053-124570103	ProgFib	skin:	n/a
13	chr7:124565947-124565997	HCT-116	colon:	n/a
14	chr7:124574073-124574123	BE2_C	brain:	n/a
15	chr7:124570130-124570180	Hela-S3	cervix:	n/a
16	chr7:124571219-124571269	HEEpiC	esophagus:	n/a
17	chr7:124565947-124565997	GM19239	blood:	n/a
18	chr7:124570359-124570409	NT2-D1	testis:	n/a
19	chr7:124570081-124570131	PFSK-1	brain:	n/a
20	chr7:124569883-124569933	HCM	heart:	n/a
21	chr7:124570081-124570131	HRPEpiC	eye:	n/a
22	chr7:124570047-124570097	CMK	blood:	n/a
23	chr7:124570181-124570231	HEEpiC	esophagus:	n/a
24	chr7:124574073-124574123	RPTEC	kidney:	n/a
25	chr7:124571219-124571269	IMR90	lung:	fetal
26	chr7:124570047-124570097	AG10803	skin:	n/a
27	chr7:124570081-124570131	SKMC	muscle:	n/a
28	chr7:124570181-124570231	GM12878	blood:	n/a
29	chr7:124569883-124569933	A549	lung:	n/a
30	chr7:124570081-124570131	HEK293	kidney:	embryo
31	chr7:124570130-124570180	HIPEpiC	eye:	n/a
32	chr7:124570059-124570109	AG09309	skin:	n/a
33	chr7:124569883-124569933	T-47D	breast:	n/a
34	chr7:124571219-124571269	CMK	blood:	n/a
35	chr7:124569883-124569933	HNPCEpiC	eye:	n/a
36	chr7:124570181-124570231	NB4	blood:	n/a
37	chr7:124570053-124570103	GM12891	blood:	n/a
38	chr7:124569883-124569933	PrEC	prostate:	n/a
39	chr7:124570047-124570097	IMR90	lung:	fetal
40	chr7:124570181-124570231	SAEC	small airway:	n/a
41	chr7:124569883-124569933	PFSK-1	brain:	n/a
42	chr7:124570053-124570103	Jurkat	blood:	n/a
43	chr7:124569883-124569933	ECC-1	luminal epithelium:	n/a
44	chr7:124565947-124565997	NB4	blood:	n/a
45	chr7:124571219-124571269	H1-hESC	embryonic stem cell:	embryo
46	chr7:124571219-124571269	PrEC	prostate:	n/a
47	chr7:124570053-124570103	SK-N-SH_RA	brain:	n/a
48	chr7:124565947-124565997	HIPEpiC	eye:	n/a
49	chr7:124569713-124569763	SKMC	muscle:	n/a
50	chr7:124569883-124569933	GM12891	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124549176..124550827-chr7:124558825..124561252,2	K562	blood:
2	chr1:109203393..109204157-chr7:124570156..124570737,2	NB4	blood:
3	chr7:124549176..124550827-chr7:124558825..124561252,2	K562	blood:
4	chr6:7312619..7313448-chr7:124569849..124570638,2	Hela-S3	cervix:
5	chr7:124559701..124562289-chr7:124568548..124571040,2	K562	blood:
6	chr7:124550905..124554322-chr7:124566903..124570128,4	K562	blood:
7	chr7:124559307..124561381-chr7:124633111..124635066,2	MCF-7	breast:
8	chr7:124520545..124522828-chr7:124555215..124557862,2	K562	blood:
9	chr7:124524737..124527454-chr7:124559196..124561248,2	K562	blood:
10	chr7:124537777..124539651-chr7:124561497..124564089,2	K562	blood:
11	chr7:124568199..124570049-chr7:127030538..127032262,2	K562	blood:
12	chr7:124557098..124558767-chr7:124568438..124571328,3	K562	blood:
13	chr7:124551396..124553692-chr7:124554817..124557525,2	K562	blood:
14	chr7:124570081..124571601-chr7:127030637..127032791,2	K562	blood:
15	chr7:124558834..124561175-chr7:124980135..124981921,2	K562	blood:
16	chr7:124584280..124585909-chr7:124591798..124594072,2	K562	blood:
17	chr7:124570010..124572071-chr7:124632097..124634842,3	MCF-7	breast:
18	chr7:124521370..124523136-chr7:124567552..124569550,2	K562	blood:
19	chr7:124584280..124585909-chr7:124591798..124594072,2	K562	blood:
20	chr7:124570250..124573246-chr7:124575640..124577419,2	K562	blood:
21	chr7:124534351..124537236-chr7:124567413..124569702,2	K562	blood:
22	chr7:124570250..124573246-chr7:124575640..124577419,2	K562	blood:
23	chr7:124535840..124537776-chr7:124559363..124562041,2	K562	blood:
24	chr7:124551396..124553692-chr7:124554817..124557525,2	K562	blood:
25	chr7:124560803..124563318-chr7:124567698..124570085,3	K562	blood:
26	chr7:124546480..124548936-chr7:124561383..124564382,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-4	chr7:124565824-124565949	l_3475_chr7:124565823-124571862_testes
2	lnc-GPR37-2	chr7:124569512-124569856	NONHSAT123087
3	lnc-SPAM1-4	chr7:124569969-124570070	ENSG00000224897
4	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
5	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
6	lnc-GPR37-2	chr7:124568869-124569053	NONHSAT123087
7	lnc-SPAM1-4	chr7:124569975-124570070	ENSG00000224897
8	lnc-SPAM1-4	chr7:124569927-124570070	ENSG00000224897
9	lnc-GPR37-2	chr7:124569613-124569840	NONHSAT123088
10	lnc-GPR37-2	chr7:124568975-124569053	NONHSAT123088
11	lnc-SPAM1-4	chr7:124569952-124570070	ENSG00000224897
12	lnc-SPAM1-4	chr7:124580334-124580439	NONHSAT123092
13	lnc-GPR37-2	chr7:124555628-124555700	NONHSAT123087
14	lnc-SPAM1-4	chr7:124570005-124572498	l_3475_chr7:124565823-124571862_testes
15	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
16	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
17	lnc-SPAM1-4	chr7:124569973-124570070	NONHSAT123092

No data

Variant related genes	Relation type
POT1-AS1	TF binding region
POT1	TF binding region
POT1-AS1	CpG island
POT1	CpG island
ENSG00000124783	chromatin interactions
ENSG00000224897	chromatin interactions
ENSG00000162639	chromatin interactions
ENSG00000048405	chromatin interactions
ENSG00000128513	chromatin interactions
BAHCC1	miRNA target sites
ODAM	miRNA target sites
UCK1	miRNA target sites
ZNHIT1	miRNA target sites
IL1RAP	miRNA target sites
CCDC6	miRNA target sites
FIGN	miRNA target sites
AXL	miRNA target sites

Extended variants
information (count: 1654 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1654 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10271646	chr7:124549573-124549574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs201795950	chr7:124549589-124549590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188901603	chr7:124549594-124549595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10256055	chr7:124549649-124549650	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186503974	chr7:124549731-124549732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541461428	chr7:124549769-124549770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532656814	chr7:124549806-124549807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564503164	chr7:124549843-124549844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533241924	chr7:124549861-124549862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543394852	chr7:124549872-124549873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369750577	chr7:124549886-124549887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563496426	chr7:124549919-124549920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6968693	chr7:124549976-124549977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs548628274	chr7:124549983-124549984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559813406	chr7:124550004-124550005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139743070	chr7:124550017-124550018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6968863	chr7:124550106-124550107	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs12706627	chr7:124550133-124550134	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs571194586	chr7:124550138-124550139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570362147	chr7:124550148-124550149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368293019	chr7:124550152-124550153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35602069	chr7:124550159-124550160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540120425	chr7:124550168-124550169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550208394	chr7:124550175-124550176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577834400	chr7:124550194-124550195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144668121	chr7:124550396-124550397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191333710	chr7:124550435-124550436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555873258	chr7:124550478-124550479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572552321	chr7:124550480-124550481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs66665074	chr7:124550526-124550527	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs558176378	chr7:124550541-124550542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528082661	chr7:124550567-124550568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577996062	chr7:124550662-124550663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543656721	chr7:124550666-124550667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11972411	chr7:124550688-124550689	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs573746173	chr7:124550689-124550690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182755999	chr7:124550698-124550699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73223583	chr7:124550719-124550720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559156616	chr7:124550723-124550724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528162132	chr7:124550748-124550749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551106884	chr7:124550778-124550779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184971491	chr7:124550783-124550784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4377886	chr7:124550812-124550813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189775673	chr7:124550818-124550819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4579448	chr7:124550883-124550884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550412727	chr7:124550944-124550945	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570271598	chr7:124550950-124550951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs201459986	chr7:124550952-124550953	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs372958948	chr7:124551083-124551084	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs549586478	chr7:124551129-124551130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myxofibrosarcoma	20639860	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124462200-124568200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr7:124466400-124562200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr7:124466600-124563400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr7:124484200-124554400	Weak transcription	HUVEC	blood vessel
5	chr7:124498200-124568800	Weak transcription	Brain Anterior Caudate	brain
6	chr7:124522800-124568400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr7:124527600-124562200	Weak transcription	A549	lung
8	chr7:124527600-124569000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr7:124527600-124569000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr7:124528000-124567400	Weak transcription	HepG2	liver
11	chr7:124529800-124553400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr7:124529800-124564400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr7:124530000-124569000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr7:124531400-124559800	Weak transcription	Ovary	ovary
15	chr7:124532000-124569000	Weak transcription	Duodenum Mucosa	Duodenum
16	chr7:124532600-124552400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:124532600-124562600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr7:124532600-124568400	Weak transcription	NHDF-Ad	bronchial
19	chr7:124532600-124568800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr7:124532600-124569000	Weak transcription	HSMM	muscle
21	chr7:124532800-124557000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:124532800-124559000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:124532800-124568400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr7:124532800-124569000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:124533200-124562800	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr7:124534000-124550000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:124534600-124558400	Weak transcription	Brain Hippocampus Middle	brain
28	chr7:124535000-124556800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:124535400-124551800	Weak transcription	K562	blood
30	chr7:124535600-124551800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:124535800-124552400	Weak transcription	Primary B cells from cord blood	blood
32	chr7:124535800-124563000	Weak transcription	Primary T cells from cord blood	blood
33	chr7:124537400-124553200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:124537800-124566000	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr7:124538000-124552800	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr7:124538000-124552800	Weak transcription	Liver	Liver
37	chr7:124538000-124553200	Weak transcription	Fetal Lung	lung
38	chr7:124538000-124554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:124538000-124555000	Weak transcription	Dnd41	blood
40	chr7:124538000-124569200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr7:124539400-124556800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:124541000-124553000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:124541000-124568600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr7:124541000-124569000	Weak transcription	Fetal Muscle Leg	muscle
45	chr7:124541200-124552800	Weak transcription	Left Ventricle	heart
46	chr7:124541400-124552400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:124541400-124552600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:124541400-124552600	Weak transcription	Adipose Nuclei	Adipose
49	chr7:124541400-124552800	Weak transcription	Fetal Thymus	thymus
50	chr7:124541400-124553200	Weak transcription	Primary monocytes fromperipheralblood	blood

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