Variant report

Variant	nsv524367
Chromosome Location	chr8:6790710-6829085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:6815704-6815918	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:6825706-6825903	K562	blood:	n/a	chr8:6825850-6825859 chr8:6825848-6825857 chr8:6825847-6825860 chr8:6825849-6825858 chr8:6825843-6825864 chr8:6825849-6825858
3	BHLHE40	chr8:6815759-6815899	K562	blood:	n/a	chr8:6815801-6815817
4	BRCA1	chr8:6815742-6815942	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:6805017-6805075	HepG2	liver:	n/a	chr8:6805026-6805037
6	CEBPB	chr8:6804991-6805097	A549	lung:	n/a	chr8:6805026-6805037
7	CEBPB	chr8:6805035-6805075	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr8:6812935-6812952	HepG2	liver:	n/a	n/a
9	CHD2	chr8:6815705-6815992	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr8:6815699-6815839	SK-N-SH_RA	brain:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
11	CTCF	chr8:6815654-6815927	SK-N-SH_RA	brain:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
12	CTCF	chr8:6815660-6815810	HCT-116	colon:	n/a	chr8:6815785-6815798
13	CTCF	chr8:6815660-6815810	AG04449	skin:	n/a	chr8:6815785-6815798
14	CTCF	chr8:6815510-6815966	GM12891	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
15	CTCF	chr8:6811137-6811340	K562	blood:	n/a	n/a
16	CTCF	chr8:6807095-6807396	H1-hESC	embryonic stem cell:	n/a	chr8:6807254-6807270 chr8:6807258-6807268 chr8:6807253-6807271 chr8:6807255-6807276
17	CTCF	chr8:6807120-6807270	SAEC	small airway:	n/a	chr8:6807254-6807270 chr8:6807258-6807268
18	CTCF	chr8:6792420-6792570	NHEK	skin:	n/a	chr8:6792493-6792514 chr8:6792491-6792509 chr8:6792492-6792508
19	CTCF	chr8:6815660-6815810	HMEC	breast:	n/a	chr8:6815785-6815798
20	CTCF	chr8:6792460-6792610	NHEK	skin:	n/a	chr8:6792493-6792514 chr8:6792491-6792509 chr8:6792492-6792508
21	CTCF	chr8:6815740-6815890	HMF	breast:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
22	CTCF	chr8:6827996-6828116	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr8:6815680-6815830	GM12872	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
24	CTCF	chr8:6815680-6815830	HCM	heart:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
25	CTCF	chr8:6815661-6815905	GM20000	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
26	CTCF	chr8:6792345-6792619	H1-hESC	embryonic stem cell:	n/a	chr8:6792493-6792514 chr8:6792491-6792509 chr8:6792492-6792508
27	CTCF	chr8:6815660-6815810	AG10803	skin:	n/a	chr8:6815785-6815798
28	CTCF	chr8:6815542-6816041	H1-hESC	embryonic stem cell:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
29	CTCF	chr8:6815760-6815910	BJ	skin:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
30	CTCF	chr8:6792348-6792661	K562	blood:	n/a	chr8:6792493-6792514 chr8:6792491-6792509 chr8:6792492-6792508
31	CTCF	chr8:6815700-6815850	GM12871	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
32	CTCF	chr8:6807222-6807310	LNCaP	prostate:	n/a	chr8:6807254-6807270 chr8:6807258-6807268 chr8:6807253-6807271 chr8:6807255-6807276
33	CTCF	chr8:6815660-6815810	GM12873	blood:	n/a	chr8:6815785-6815798
34	CTCF	chr8:6792400-6792550	GM12875	blood:	n/a	chr8:6792493-6792514 chr8:6792491-6792509 chr8:6792492-6792508
35	CTCF	chr8:6815700-6815850	HepG2	liver:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
36	CTCF	chr8:6792400-6792550	NB4	blood:	n/a	chr8:6792493-6792514 chr8:6792491-6792509 chr8:6792492-6792508
37	CTCF	chr8:6815635-6815939	MCF-7	breast:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
38	CTCF	chr8:6815740-6815890	HRE	kidney:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
39	CTCF	chr8:6807154-6807363	A549	lung:	n/a	chr8:6807254-6807270 chr8:6807258-6807268 chr8:6807253-6807271 chr8:6807255-6807276
40	CTCF	chr8:6827929-6828105	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:6807180-6807330	K562	blood:	n/a	chr8:6807254-6807270 chr8:6807258-6807268 chr8:6807253-6807271 chr8:6807255-6807276
42	CTCF	chr8:6792460-6792610	GM12869	blood:	n/a	chr8:6792493-6792514 chr8:6792491-6792509 chr8:6792492-6792508
43	CTCF	chr8:6815660-6815810	GM06990	blood:	n/a	chr8:6815785-6815798
44	CTCF	chr8:6811180-6811330	GM12874	blood:	n/a	n/a
45	CTCF	chr8:6811100-6811250	GM12865	blood:	n/a	n/a
46	CTCF	chr8:6807104-6807366	GM19238	blood:	n/a	chr8:6807254-6807270 chr8:6807258-6807268 chr8:6807253-6807271 chr8:6807255-6807276
47	CTCF	chr8:6807129-6807344	Fibrobl	skin:	n/a	chr8:6807254-6807270 chr8:6807258-6807268 chr8:6807253-6807271 chr8:6807255-6807276
48	CTCF	chr8:6811120-6811270	NB4	blood:	n/a	n/a
49	CTCF	chr8:6815700-6815850	RPTEC	kidney:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
50	CTCF	chr8:6807174-6807349	HepG2	liver:	n/a	chr8:6807254-6807270 chr8:6807258-6807268 chr8:6807253-6807271 chr8:6807255-6807276

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6793506-6793556	ECC-1	luminal epithelium:	n/a
2	chr8:6795162-6795212	HL-60	blood:	n/a
3	chr8:6793506-6793556	ECC-1	luminal epithelium:	n/a
4	chr8:6795162-6795212	HL-60	blood:	n/a
5	chr8:6796902-6796952	HUVEC	blood vessel:	n/a
6	chr8:6827800-6827850	ProgFib	skin:	n/a
7	chr8:6795162-6795212	GM12892	blood:	n/a
8	chr8:6796176-6796226	Hepatocyte	liver:	n/a
9	chr8:6827800-6827850	AG10803	skin:	n/a
10	chr8:6828103-6828153	HRCEpiC	kidney:	n/a
11	chr8:6826392-6826442	GM12892	blood:	n/a
12	chr8:6826392-6826442	HPAEpiC	pulmonary alveolar:	n/a
13	chr8:6796176-6796226	HCF	heart:	n/a
14	chr8:6795980-6796030	H1-hESC	embryonic stem cell:	embryo
15	chr8:6828103-6828153	K562	blood:	n/a
16	chr8:6796176-6796226	K562	blood:	n/a
17	chr8:6796176-6796226	SKMC	muscle:	n/a
18	chr8:6795980-6796030	SKMC	muscle:	n/a
19	chr8:6826392-6826442	CMK	blood:	n/a
20	chr8:6796176-6796226	GM12878	blood:	n/a
21	chr8:6827800-6827850	IMR90	lung:	fetal
22	chr8:6796902-6796952	HL-60	blood:	n/a
23	chr8:6796176-6796226	GM12891	blood:	n/a
24	chr8:6828103-6828153	SK-N-SH	brain:	n/a
25	chr8:6826392-6826442	SK-N-SH	brain:	n/a
26	chr8:6826392-6826442	HepG2	liver:	n/a
27	chr8:6795980-6796030	AoSMC	blood vessel:	n/a
28	chr8:6796902-6796952	PANC-1	pancreas:	n/a
29	chr8:6795162-6795212	HepG2	liver:	n/a
30	chr8:6794872-6794922	SKMC	muscle:	n/a
31	chr8:6827800-6827850	H1-hESC	embryonic stem cell:	embryo
32	chr8:6796176-6796226	T-47D	breast:	n/a
33	chr8:6827800-6827850	MCF-7	breast:	n/a
34	chr8:6795980-6796030	BJ	skin:	n/a
35	chr8:6793506-6793556	HAEpiC	amniotic membrane:	n/a
36	chr8:6828103-6828153	HRE	kidney:	n/a
37	chr8:6796902-6796952	HEK293	kidney:	embryo
38	chr8:6795980-6796030	RPTEC	kidney:	n/a
39	chr8:6827814-6827864	HAEpiC	amniotic membrane:	n/a
40	chr8:6794872-6794922	HRE	kidney:	n/a
41	chr8:6796902-6796952	H1-hESC	embryonic stem cell:	embryo
42	chr8:6827814-6827864	SK-N-SH_RA	brain:	n/a
43	chr8:6827800-6827850	HL-60	blood:	n/a
44	chr8:6828103-6828153	HCT-116	colon:	n/a
45	chr8:6828103-6828153	BJ	skin:	n/a
46	chr8:6796902-6796952	HCF	heart:	n/a
47	chr8:6828103-6828153	H1-hESC	embryonic stem cell:	embryo
48	chr8:6794872-6794922	NH-A	brain:	n/a
49	chr8:6827800-6827850	SKMC	muscle:	n/a
50	chr8:6793506-6793556	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:6698096..6698895-chr8:6806928..6807708,2	K562	blood:
2	chr8:6813895..6816114-chr8:6818168..6820677,2	MCF-7	breast:
3	chr8:6775337..6778035-chr8:6790742..6792474,2	K562	blood:
4	chr8:6796114..6798602-chr8:6803030..6805863,2	K562	blood:
5	chr8:6810171..6811870-chr8:6814020..6816721,2	K562	blood:
6	chr8:6810171..6811870-chr8:6814020..6816721,2	K562	blood:
7	chr8:6796114..6798602-chr8:6803030..6805863,2	K562	blood:
8	chr8:6813895..6816114-chr8:6818168..6820677,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFA4-1	chr8:6808248-6808360	NONHSAT124800
2	lnc-DEFA1-1	chr8:6825663-6825775	NONHSAT124803
3	lnc-DEFA1-1	chr8:6826461-6826635	NONHSAT124803
4	lnc-DEFA1-1	chr8:6826452-6826635	NONHSAT124802
5	lnc-DEFA1-2	chr8:6817512-6817683	NONHSAT124801
6	lnc-DEFA1-2	chr8:6816811-6816923	NONHSAT124801
7	lnc-DEFA1-1	chr8:6825663-6825769	NONHSAT124802
8	lnc-DEFA4-1	chr8:6808950-6809121	NONHSAT124800

Variant related genes	Relation type
DEFA9P	TF binding region
DEFA8P	TF binding region
DEFA10P	TF binding region
DEFA4	TF binding region
DEFA9P	CpG island
DEFA8P	CpG island
DEFA10P	CpG island
DEFA4	CpG island

Extended variants
information (count: 2463 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:2463 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13251447	chr8:6790710-6790711	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559852244	chr8:6790714-6790715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573386790	chr8:6790718-6790719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541182357	chr8:6790735-6790736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564272440	chr8:6790745-6790746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533195593	chr8:6790762-6790763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557694713	chr8:6790774-6790775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2741682	chr8:6790809-6790810	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2702862	chr8:6790812-6790813	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs375600781	chr8:6790830-6790831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72494230	chr8:6790836-6790837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184263076	chr8:6790853-6790854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111954836	chr8:6790860-6790861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117010291	chr8:6790872-6790873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199922416	chr8:6790875-6790876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565388978	chr8:6790915-6790916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534408985	chr8:6790957-6790958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs59334047	chr8:6791023-6791024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192887473	chr8:6791031-6791032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564110729	chr8:6791121-6791122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57619115	chr8:6791122-6791123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201902122	chr8:6791189-6791190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199883045	chr8:6791190-6791191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112811467	chr8:6791193-6791194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563757325	chr8:6791208-6791209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73521750	chr8:6791220-6791221	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185321758	chr8:6791222-6791223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148063830	chr8:6791240-6791241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574292581	chr8:6791258-6791259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190218162	chr8:6791260-6791261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546021266	chr8:6791295-6791296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375233511	chr8:6791305-6791306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141719685	chr8:6791316-6791317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150562638	chr8:6791358-6791359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192498114	chr8:6791361-6791362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559791507	chr8:6791472-6791473	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs373382135	chr8:6791491-6791492	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs138699539	chr8:6791537-6791538	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs2702863	chr8:6791559-6791560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs2702864	chr8:6791576-6791577	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562381936	chr8:6791577-6791578	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs13262140	chr8:6791601-6791602	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs548911692	chr8:6791602-6791603	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs117842967	chr8:6791605-6791606	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs528106330	chr8:6791625-6791626	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs551037341	chr8:6791645-6791646	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs368374502	chr8:6791646-6791647	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs80157953	chr8:6791649-6791650	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs537213000	chr8:6791676-6791677	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551165197	chr8:6791691-6791692	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Autism	21865298	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6785800-6798800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr8:6789200-6791800	Weak transcription	Fetal Thymus	thymus
3	chr8:6789400-6791600	Weak transcription	Thymus	Thymus
4	chr8:6790600-6791400	Enhancers	Dnd41	blood
5	chr8:6791400-6793000	Flanking Active TSS	Dnd41	blood
6	chr8:6791600-6792800	Enhancers	Thymus	Thymus
7	chr8:6791800-6792000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
8	chr8:6791800-6793200	Enhancers	Fetal Thymus	thymus
9	chr8:6792000-6792200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
10	chr8:6792200-6792800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
11	chr8:6792200-6792800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:6792400-6793800	Enhancers	Fetal Brain Male	brain
13	chr8:6793000-6798000	Enhancers	Dnd41	blood
14	chr8:6793200-6793600	Weak transcription	Fetal Thymus	thymus
15	chr8:6793600-6793800	Enhancers	Fetal Thymus	thymus
16	chr8:6793800-6800200	Weak transcription	Fetal Thymus	thymus
17	chr8:6794400-6794600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:6794600-6829200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:6795600-6796200	Enhancers	GM12878-XiMat	blood
20	chr8:6796200-6796400	Enhancers	Primary B cells from cord blood	blood
21	chr8:6796200-6797200	Weak transcription	GM12878-XiMat	blood
22	chr8:6796400-6796600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
23	chr8:6796400-6797400	Weak transcription	Primary B cells from cord blood	blood
24	chr8:6796600-6797600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
25	chr8:6796600-6797800	Enhancers	Primary hematopoietic stem cells	blood
26	chr8:6796600-6797800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:6796600-6797800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:6796600-6797800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
29	chr8:6796800-6797000	Enhancers	Spleen	Spleen
30	chr8:6796800-6798000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
31	chr8:6797200-6797400	Enhancers	GM12878-XiMat	blood
32	chr8:6797400-6797800	Enhancers	Primary B cells from cord blood	blood
33	chr8:6798000-6799600	Weak transcription	Dnd41	blood
34	chr8:6799600-6802800	Enhancers	Dnd41	blood
35	chr8:6799800-6800400	Enhancers	HMEC	breast
36	chr8:6800000-6800200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
37	chr8:6800200-6803200	Enhancers	Fetal Thymus	thymus
38	chr8:6800200-6804000	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr8:6800800-6801400	Weak transcription	Spleen	Spleen
40	chr8:6800800-6802800	Enhancers	Thymus	Thymus
41	chr8:6801000-6801400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
42	chr8:6801000-6801800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
43	chr8:6801000-6802400	Enhancers	GM12878-XiMat	blood
44	chr8:6801400-6801600	Enhancers	Spleen	Spleen
45	chr8:6801600-6808800	Weak transcription	Spleen	Spleen
46	chr8:6802000-6802400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr8:6802800-6805000	Weak transcription	Dnd41	blood
48	chr8:6802800-6806400	Weak transcription	Thymus	Thymus
49	chr8:6803200-6806400	Weak transcription	Fetal Thymus	thymus
50	chr8:6804000-6804400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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