Variant report

Variant	nsv887845
Chromosome Location	chr7:25220519-25276424
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	CBX3	chr7:25249318-25249814	HCT-116	colon:	n/a	n/a
2	CBX3	chr7:25235781-25236033	K562	blood:	n/a	n/a
3	CBX3	chr7:25227560-25227934	K562	blood:	n/a	n/a
4	CBX3	chr7:25219876-25220555	K562	blood:	n/a	n/a
5	CEBPB	chr7:25256519-25256729	MCF-7	breast:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
6	CEBPB	chr7:25256438-25256747	K562	blood:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
7	CEBPB	chr7:25256490-25256742	IMR90	lung:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
8	CEBPB	chr7:25256448-25256731	HepG2	liver:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
9	CEBPB	chr7:25256422-25256762	Hela-S3	cervix:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
10	CEBPB	chr7:25256310-25256848	A549	lung:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
11	CEBPB	chr7:25256325-25256722	HCT-116	colon:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
12	CEBPB	chr7:25232508-25232672	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:25256454-25256742	H1-hESC	embryonic stem cell:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
14	CEBPB	chr7:25256462-25256763	K562	blood:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
15	CEBPB	chr7:25256446-25256813	MCF-7	breast:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
16	CEBPB	chr7:25256456-25256742	A549	lung:	n/a	chr7:25256596-25256607 chr7:25256595-25256606 chr7:25256595-25256608 chr7:25256595-25256608 chr7:25256595-25256606
17	CHD2	chr7:25219821-25220914	HepG2	liver:	n/a	n/a
18	CHD2	chr7:25219883-25220935	K562	blood:	n/a	n/a
19	CHD2	chr7:25220653-25220854	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr7:25220440-25220590	GM12864	blood:	n/a	n/a
21	CTCF	chr7:25227800-25227950	K562	blood:	n/a	n/a
22	CTCF	chr7:25256100-25256250	NHLF	lung:	n/a	n/a
23	CTCF	chr7:25220680-25220830	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr7:25255380-25255530	GM12875	blood:	n/a	n/a
25	CTCF	chr7:25220720-25220870	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr7:25255680-25255830	GM12874	blood:	n/a	n/a
27	CTCF	chr7:25227843-25227894	GM12878	blood:	n/a	n/a
28	CTCF	chr7:25256491-25256701	LNCaP	prostate:	n/a	chr7:25256574-25256587 chr7:25256577-25256585 chr7:25256573-25256589 chr7:25256567-25256588 chr7:25256572-25256590
29	CTCF	chr7:25227700-25228000	K562	blood:	n/a	n/a
30	CTCF	chr7:25220740-25220890	AG09309	skin:	n/a	n/a
31	CTCF	chr7:25255440-25255590	NHEK	skin:	n/a	n/a
32	CTCF	chr7:25220420-25220570	WI-38	lung:	n/a	n/a
33	CTCF	chr7:25256520-25256670	RPTEC	kidney:	n/a	chr7:25256574-25256587 chr7:25256577-25256585 chr7:25256573-25256589 chr7:25256567-25256588 chr7:25256572-25256590
34	CTCF	chr7:25256340-25256490	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr7:25220720-25220870	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr7:25220740-25220890	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr7:25256380-25256530	NHLF	lung:	n/a	n/a
38	CTCF	chr7:25220760-25220910	HEK293	kidney:	n/a	n/a
39	CTCF	chr7:25220740-25220890	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr7:25227800-25227950	GM12873	blood:	n/a	n/a
41	CTCF	chr7:25256534-25256662	HepG2	liver:	n/a	chr7:25256574-25256587 chr7:25256577-25256585 chr7:25256573-25256589 chr7:25256567-25256588 chr7:25256572-25256590
42	CTCF	chr7:25256540-25256690	NHDF-neo	bronchial:	n/a	chr7:25256574-25256587 chr7:25256577-25256585 chr7:25256573-25256589 chr7:25256567-25256588 chr7:25256572-25256590
43	CTCF	chr7:25220740-25220890	AG09319	gingival:	n/a	n/a
44	CTCF	chr7:25256466-25256729	Pancreas_OC	pancreas:	n/a	chr7:25256574-25256587 chr7:25256577-25256585 chr7:25256573-25256589 chr7:25256567-25256588 chr7:25256572-25256590
45	CTCF	chr7:25255380-25255530	GM12864	blood:	n/a	n/a
46	CTCF	chr7:25256160-25256310	A549	lung:	n/a	n/a
47	CTCF	chr7:25256540-25256690	HMF	breast:	n/a	chr7:25256574-25256587 chr7:25256577-25256585 chr7:25256573-25256589 chr7:25256567-25256588 chr7:25256572-25256590
48	CTCF	chr7:25220840-25220990	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:25256520-25256670	AG09309	skin:	n/a	chr7:25256574-25256587 chr7:25256577-25256585 chr7:25256573-25256589 chr7:25256567-25256588 chr7:25256572-25256590
50	CTCF	chr7:25220787-25220890	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:25268894-25268944	HRPEpiC	eye:	n/a
2	chr7:25268894-25268944	SK-N-SH_RA	brain:	n/a
3	chr7:25272454-25272504	PANC-1	pancreas:	n/a
4	chr7:25268974-25269024	BJ	skin:	n/a
5	chr7:25268974-25269024	AG09309	skin:	n/a
6	chr7:25264629-25264679	HMEC	breast:	n/a
7	chr7:25268894-25268944	ProgFib	skin:	n/a
8	chr7:25272454-25272504	MCF-7	breast:	n/a
9	chr7:25268974-25269024	HL-60	blood:	n/a
10	chr7:25222516-25222566	SK-N-SH	brain:	n/a
11	chr7:25222516-25222566	AoSMC	blood vessel:	n/a
12	chr7:25222516-25222566	Hela-S3	cervix:	n/a
13	chr7:25272454-25272504	GM12878	blood:	n/a
14	chr7:25264629-25264679	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:25264629-25264679	SAEC	small airway:	n/a
16	chr7:25222516-25222566	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:25268518-25268568	RPTEC	kidney:	n/a
18	chr7:25272454-25272504	NHDF-neo	bronchial:	n/a
19	chr7:25268894-25268944	AG10803	skin:	n/a
20	chr7:25268518-25268568	K562	blood:	n/a
21	chr7:25268894-25268944	BJ	skin:	n/a
22	chr7:25264629-25264679	AG09309	skin:	n/a
23	chr7:25222516-25222566	HMEC	breast:	n/a
24	chr7:25268974-25269024	AG09319	gingival:	n/a
25	chr7:25272454-25272504	HNPCEpiC	eye:	n/a
26	chr7:25268974-25269024	LNCaP	prostate:	n/a
27	chr7:25268974-25269024	PANC-1	pancreas:	n/a
28	chr7:25264629-25264679	NB4	blood:	n/a
29	chr7:25268518-25268568	HRPEpiC	eye:	n/a
30	chr7:25268894-25268944	SK-N-SH	brain:	n/a
31	chr7:25272454-25272504	LNCaP	prostate:	n/a
32	chr7:25268894-25268944	SAEC	small airway:	n/a
33	chr7:25268518-25268568	AG04449	skin:	fetal
34	chr7:25268894-25268944	GM12891	blood:	n/a
35	chr7:25268974-25269024	GM12892	blood:	n/a
36	chr7:25268974-25269024	ProgFib	skin:	n/a
37	chr7:25272454-25272504	HepG2	liver:	n/a
38	chr7:25268894-25268944	U87	brain:	n/a
39	chr7:25264629-25264679	HAEpiC	amniotic membrane:	n/a
40	chr7:25272454-25272504	AG10803	skin:	n/a
41	chr7:25268518-25268568	NH-A	brain:	n/a
42	chr7:25268518-25268568	HRCEpiC	kidney:	n/a
43	chr7:25268974-25269024	AG04450	lung:	fetal
44	chr7:25222516-25222566	HCF	heart:	n/a
45	chr7:25272454-25272504	HCPEpiC	choroid plexus:	n/a
46	chr7:25264629-25264679	HIPEpiC	eye:	n/a
47	chr7:25268518-25268568	Hela-S3	cervix:	n/a
48	chr7:25268518-25268568	Hepatocyte	liver:	n/a
49	chr7:25272454-25272504	PFSK-1	brain:	n/a
50	chr7:25268974-25269024	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:25254943..25257850-chr7:25260615..25262250,2	K562	blood:
2	chr7:25276382..25277977-chr7:25280385..25282030,2	K562	blood:
3	chr7:25219514..25220543-chr7:25255978..25256993,5	K562	blood:
4	chr7:25218102..25221598-chr7:25223987..25227915,4	K562	blood:
5	chr7:25235543..25237951-chr7:25240550..25242102,2	K562	blood:
6	chr7:25219298..25221104-chr7:25254526..25257148,2	K562	blood:
7	chr7:25219298..25221174-chr7:25254526..25256590,2	K562	blood:
8	chr7:25199215..25199746-chr7:25256226..25256869,2	MCF-7	breast:
9	chr4:4249562..4250321-chr7:25228586..25229086,2	Hela-S3	cervix:
10	chr7:25155898..25158442-chr7:25226325..25227872,2	MCF-7	breast:
11	chr7:25163234..25166939-chr7:25217425..25221477,8	K562	blood:
12	chr7:25218102..25221598-chr7:25223987..25227915,4	K562	blood:
13	chr7:25163373..25164943-chr7:25257824..25260603,2	MCF-7	breast:
14	chr7:25235543..25237951-chr7:25240550..25242102,2	K562	blood:
15	chr7:25256547..25257067-chr7:25608230..25609163,2	K562	blood:
16	chr7:25217763..25221342-chr7:25223056..25226500,4	K562	blood:
17	chr7:25162177..25164898-chr7:25242251..25244708,2	MCF-7	breast:
18	chr7:25254943..25257850-chr7:25260615..25262250,2	K562	blood:
19	chr7:25262070..25264752-chr7:25275040..25277234,2	K562	blood:
20	chr7:25162308..25164460-chr7:25245338..25246986,2	K562	blood:
21	chr7:25262070..25264752-chr7:25275040..25277234,2	K562	blood:
22	chr7:25163338..25164946-chr7:25254340..25256031,3	MCF-7	breast:
23	chr7:25163425..25166435-chr7:25223667..25226551,3	K562	blood:
24	chr7:25164198..25165934-chr7:25256419..25258186,2	K562	blood:
25	chr7:25164671..25166256-chr7:25271573..25273792,2	K562	blood:
26	chr7:25156146..25157913-chr7:25258604..25261046,2	K562	blood:
27	chr7:25217763..25221342-chr7:25223056..25226500,4	K562	blood:
28	chr7:25162226..25166939-chr7:25217425..25223469,13	K562	blood:

Variant related genes	Relation type
C7orf31	TF binding region
ENSG00000213798	TF binding region
NPVF	TF binding region
ENSG00000234406	TF binding region
C7orf31	CpG island
ENSG00000213798	CpG island
NPVF	CpG island
ENSG00000234406	CpG island
ENSG00000172115	chromatin interactions
ENSG00000132406	chromatin interactions
ENSG00000153790	chromatin interactions
ENSG00000234406	chromatin interactions

Extended variants
information (count: 1883 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1883 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10272529	chr7:25220519-25220520	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs199836140	chr7:25220533-25220534	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs528401329	chr7:25220534-25220535	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs542193290	chr7:25220539-25220540	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs181005939	chr7:25220550-25220551	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs561393809	chr7:25220551-25220552	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs530768766	chr7:25220601-25220602	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs550480056	chr7:25220650-25220651	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs186487016	chr7:25220706-25220707	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs532458956	chr7:25220709-25220710	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs148082781	chr7:25220712-25220713	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs189775018	chr7:25220722-25220723	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs181209958	chr7:25220734-25220735	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs375110756	chr7:25220753-25220754	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs554874798	chr7:25220814-25220815	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs552072883	chr7:25220816-25220817	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs568635715	chr7:25220825-25220826	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs375633473	chr7:25220849-25220850	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs557241461	chr7:25220882-25220883	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs559530450	chr7:25220919-25220920	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs574642138	chr7:25220944-25220945	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs576882723	chr7:25221018-25221019	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs545536676	chr7:25221026-25221027	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs77773520	chr7:25221055-25221056	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs572917895	chr7:25221072-25221073	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs143929023	chr7:25221082-25221083	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs574727171	chr7:25221160-25221161	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs531704167	chr7:25221179-25221180	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs2158246	chr7:25221192-25221193	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548507520	chr7:25221211-25221212	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs367891473	chr7:25221212-25221213	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs560456897	chr7:25221240-25221241	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs116308883	chr7:25221285-25221286	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs79037587	chr7:25221300-25221301	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs533147067	chr7:25221304-25221305	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs552292084	chr7:25221310-25221311	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs73691510	chr7:25221317-25221318	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs115160143	chr7:25221328-25221329	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs562549429	chr7:25221337-25221338	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs1859207	chr7:25221348-25221349	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs548534554	chr7:25221379-25221380	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs568754492	chr7:25221442-25221443	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs35711526	chr7:25221445-25221446	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs537308402	chr7:25221480-25221481	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs185705301	chr7:25221488-25221489	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs571006966	chr7:25221515-25221516	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs540030300	chr7:25221528-25221529	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs553140375	chr7:25221530-25221531	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs201542582	chr7:25221550-25221551	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs139707763	chr7:25221556-25221557	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Lung cancer	16773561	CNVD
Schizophrenia	19546859	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25218800-25220600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:25218800-25220600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:25218800-25220600	Active TSS	Fetal Kidney	kidney
4	chr7:25218800-25220600	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr7:25218800-25220800	Active TSS	Rectal Smooth Muscle	rectum
6	chr7:25219000-25220600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:25219000-25220600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:25219000-25220600	Active TSS	Aorta	Aorta
9	chr7:25219200-25220600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:25219200-25220600	Active TSS	Fetal Brain Female	brain
11	chr7:25219400-25220600	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr7:25219400-25220600	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr7:25219400-25220600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
14	chr7:25219400-25220600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:25219400-25220600	Active TSS	A549	lung
16	chr7:25219400-25220600	Active TSS	NHEK	skin
17	chr7:25219400-25221000	Active TSS	Colon Smooth Muscle	Colon
18	chr7:25219600-25220600	Active TSS	Primary hematopoietic stem cells	blood
19	chr7:25219600-25220600	Active TSS	Cortex derived primary cultured neurospheres	brain
20	chr7:25219600-25220600	Active TSS	Fetal Lung	lung
21	chr7:25219800-25220600	Enhancers	Fetal Brain Male	brain
22	chr7:25220000-25220600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
23	chr7:25220000-25220600	Enhancers	Fetal Heart	heart
24	chr7:25220200-25220600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr7:25220200-25220600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr7:25220200-25220600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:25220200-25220600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr7:25220200-25220600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:25220200-25220600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
30	chr7:25220200-25220600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr7:25220200-25220600	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr7:25220200-25220600	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr7:25220200-25220600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
34	chr7:25220200-25220600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr7:25220200-25220600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr7:25220200-25220600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr7:25220200-25220600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:25220200-25220600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr7:25220200-25220600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
40	chr7:25220200-25220600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:25220200-25220600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:25220200-25220600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:25220200-25220600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:25220200-25220600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr7:25220200-25220600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:25220200-25220600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:25220200-25220600	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr7:25220200-25220600	Flanking Active TSS	Liver	Liver
49	chr7:25220200-25220600	Flanking Active TSS	Brain Angular Gyrus	brain
50	chr7:25220200-25220600	Flanking Active TSS	Brain Cingulate Gyrus	brain

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