Variant report

Variant	nsv889875
Chromosome Location	chr8:2558468-2739988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1313)
CpG islands
(count:915)
Chromatin interactive
region (count:158)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1313 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2640879-2641488	K562	blood:	n/a	n/a
2	ARID3A	chr8:2586788-2587042	K562	blood:	n/a	n/a
3	ARID3A	chr8:2569699-2570363	K562	blood:	n/a	n/a
4	ARID3A	chr8:2583362-2583786	K562	blood:	n/a	n/a
5	ARID3A	chr8:2592824-2593695	K562	blood:	n/a	chr8:2593039-2593055
6	ARID3A	chr8:2736432-2736497	K562	blood:	n/a	n/a
7	ARID3A	chr8:2640546-2640565	K562	blood:	n/a	n/a
8	ARID3A	chr8:2588688-2589234	K562	blood:	n/a	n/a
9	ARID3A	chr8:2632277-2632294	K562	blood:	n/a	n/a
10	ARID3A	chr8:2571430-2571701	K562	blood:	n/a	n/a
11	ARID3A	chr8:2628561-2628762	K562	blood:	n/a	n/a
12	ARID3A	chr8:2582455-2583099	K562	blood:	n/a	n/a
13	ARID3A	chr8:2591085-2592231	K562	blood:	n/a	n/a
14	ARID3A	chr8:2645493-2646139	K562	blood:	n/a	n/a
15	ATF1	chr8:2591024-2591651	K562	blood:	n/a	n/a
16	ATF1	chr8:2581374-2581475	K562	blood:	n/a	n/a
17	ATF1	chr8:2645670-2646221	K562	blood:	n/a	n/a
18	ATF1	chr8:2641154-2641440	K562	blood:	n/a	n/a
19	ATF1	chr8:2588667-2588920	K562	blood:	n/a	n/a
20	ATF2	chr8:2575121-2575588	GM12878	blood:	n/a	n/a
21	ATF2	chr8:2575097-2575545	GM12878	blood:	n/a	n/a
22	ATF3	chr8:2591062-2591346	K562	blood:	n/a	n/a
23	BACH1	chr8:2628652-2628871	K562	blood:	n/a	n/a
24	BACH1	chr8:2628552-2628844	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:2710537-2710713	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr8:2575165-2575442	GM12878	blood:	n/a	chr8:2575395-2575403
27	BATF	chr8:2575236-2575412	GM12878	blood:	n/a	chr8:2575395-2575403
28	BATF	chr8:2577057-2577495	GM12878	blood:	n/a	chr8:2577308-2577319
29	BATF	chr8:2577159-2577434	GM12878	blood:	n/a	chr8:2577308-2577319
30	BCL11A	chr8:2577041-2577262	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:2576992-2577351	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:2575139-2575457	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:2690564-2690825	GM12878	blood:	n/a	chr8:2690626-2690635
34	BCL3	chr8:2575150-2575417	GM12878	blood:	n/a	n/a
35	BCLAF1	chr8:2672014-2672364	GM12878	blood:	n/a	n/a
36	BCLAF1	chr8:2591118-2591666	K562	blood:	n/a	n/a
37	BHLHE40	chr8:2628562-2628861	K562	blood:	n/a	n/a
38	BHLHE40	chr8:2589918-2590649	K562	blood:	n/a	n/a
39	BHLHE40	chr8:2588692-2588697	K562	blood:	n/a	n/a
40	BHLHE40	chr8:2645764-2646221	K562	blood:	n/a	n/a
41	BHLHE40	chr8:2569644-2569660	GM12878	blood:	n/a	n/a
42	BHLHE40	chr8:2585550-2585876	K562	blood:	n/a	n/a
43	BHLHE40	chr8:2671943-2671964	HepG2	liver:	n/a	n/a
44	BHLHE40	chr8:2584393-2584840	K562	blood:	n/a	n/a
45	BHLHE40	chr8:2586753-2587008	K562	blood:	n/a	n/a
46	BHLHE40	chr8:2690697-2690730	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:2590944-2591676	K562	blood:	n/a	n/a
48	BRCA1	chr8:2652847-2652944	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr8:2569298-2569688	K562	blood:	n/a	n/a
50	CBX3	chr8:2597494-2597918	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2591207-2591257	SK-N-SH_RA	brain:	n/a
2	chr8:2670187-2670237	PFSK-1	brain:	n/a
3	chr8:2591411-2591461	Hela-S3	cervix:	n/a
4	chr8:2585666-2585716	HRPEpiC	eye:	n/a
5	chr8:2585976-2586026	HCF	heart:	n/a
6	chr8:2585666-2585716	SK-N-SH_RA	brain:	n/a
7	chr8:2585976-2586026	Hela-S3	cervix:	n/a
8	chr8:2591265-2591315	SK-N-SH_RA	brain:	n/a
9	chr8:2591265-2591315	RPTEC	kidney:	n/a
10	chr8:2609691-2609741	PrEC	prostate:	n/a
11	chr8:2669421-2669471	HEEpiC	esophagus:	n/a
12	chr8:2669372-2669422	GM06990	blood:	n/a
13	chr8:2609661-2609711	K562	blood:	n/a
14	chr8:2609661-2609711	SK-N-SH	brain:	n/a
15	chr8:2586911-2586961	SAEC	small airway:	n/a
16	chr8:2609661-2609711	HCPEpiC	choroid plexus:	n/a
17	chr8:2586911-2586961	U87	brain:	n/a
18	chr8:2669421-2669471	LNCaP	prostate:	n/a
19	chr8:2591265-2591315	HRPEpiC	eye:	n/a
20	chr8:2670187-2670237	NT2-D1	testis:	n/a
21	chr8:2591265-2591315	Hela-S3	cervix:	n/a
22	chr8:2609691-2609741	AG10803	skin:	n/a
23	chr8:2591265-2591315	HCPEpiC	choroid plexus:	n/a
24	chr8:2609691-2609741	GM12892	blood:	n/a
25	chr8:2628628-2628678	SKMC	muscle:	n/a
26	chr8:2591411-2591461	NHBE	bronchial:	n/a
27	chr8:2585976-2586026	BJ	skin:	n/a
28	chr8:2609691-2609741	MCF-7	breast:	n/a
29	chr8:2586225-2586275	HRE	kidney:	n/a
30	chr8:2669372-2669422	LNCaP	prostate:	n/a
31	chr8:2669421-2669471	HAEpiC	amniotic membrane:	n/a
32	chr8:2628628-2628678	GM06990	blood:	n/a
33	chr8:2609661-2609711	HUVEC	blood vessel:	n/a
34	chr8:2585235-2585285	SK-N-SH	brain:	n/a
35	chr8:2585976-2586026	HEEpiC	esophagus:	n/a
36	chr8:2585976-2586026	HIPEpiC	eye:	n/a
37	chr8:2591411-2591461	Caco-2	colon:	n/a
38	chr8:2670187-2670237	H1-hESC	embryonic stem cell:	embryo
39	chr8:2669372-2669422	HIPEpiC	eye:	n/a
40	chr8:2591265-2591315	LNCaP	prostate:	n/a
41	chr8:2591411-2591461	BE2_C	brain:	n/a
42	chr8:2670359-2670409	HRCEpiC	kidney:	n/a
43	chr8:2585235-2585285	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:2591411-2591461	AoSMC	blood vessel:	n/a
45	chr8:2586225-2586275	HRCEpiC	kidney:	n/a
46	chr8:2670187-2670237	CMK	blood:	n/a
47	chr8:2670187-2670237	AG09309	skin:	n/a
48	chr8:2591411-2591461	NB4	blood:	n/a
49	chr8:2586911-2586961	HMEC	breast:	n/a
50	chr8:2609661-2609711	IMR90	lung:	fetal

(count:158 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:2568252..2570741-chr8:2670037..2672346,3	K562	blood:
2	chr8:2631918..2634126-chr8:2639188..2641827,3	K562	blood:
3	chr8:2564777..2566535-chr8:2633073..2636041,2	K562	blood:
4	chr8:2598798..2600959-chr8:2603763..2608405,4	K562	blood:
5	chr8:2630755..2632834-chr8:2650652..2652206,2	K562	blood:
6	chr8:2585736..2588066-chr8:2601157..2603810,2	K562	blood:
7	chr8:2426482..2427246-chr8:2671820..2672460,2	MCF-7	breast:
8	chr8:2607594..2609173-chr8:2610051..2612762,2	K562	blood:
9	chr8:2593399..2598428-chr8:2599653..2604121,4	K562	blood:
10	chr8:2620268..2621855-chr8:2623779..2625844,2	K562	blood:
11	chr8:2624634..2626171-chr8:2626385..2627921,2	K562	blood:
12	chr8:2564777..2566535-chr8:2633073..2636041,2	K562	blood:
13	chr8:2671763..2673486-chr8:2679211..2682060,2	K562	blood:
14	chr8:2599818..2601466-chr8:2615794..2618126,2	K562	blood:
15	chr8:2555193..2558064-chr8:2558370..2560198,2	K562	blood:
16	chr8:2593273..2595821-chr8:2597138..2598928,2	K562	blood:
17	chr8:2613070..2615435-chr8:2618441..2620746,3	K562	blood:
18	chr8:2591672..2593360-chr8:2600937..2603510,2	K562	blood:
19	chr8:2675575..2676101-chr8:3394089..3394683,2	MCF-7	breast:
20	chr8:2631963..2633946-chr8:2635441..2638844,4	K562	blood:
21	chr8:2620268..2621855-chr8:2623779..2625844,2	K562	blood:
22	chr8:2636014..2638648-chr8:2639734..2641610,2	K562	blood:
23	chr8:2599818..2601466-chr8:2615794..2618126,2	K562	blood:
24	chr8:2582217..2585126-chr8:2645115..2648033,3	K562	blood:
25	chr8:2660909..2663235-chr8:2664296..2666445,2	K562	blood:
26	chr8:2617946..2621855-chr8:2622304..2626900,6	K562	blood:
27	chr8:2631963..2633946-chr8:2635441..2638844,4	K562	blood:
28	chr8:2562242..2563775-chr8:2567486..2569900,2	K562	blood:
29	chr8:2597895..2600148-chr8:2611111..2612738,2	K562	blood:
30	chr8:2563425..2566170-chr8:2680096..2682261,2	K562	blood:
31	chr8:2588918..2591630-chr8:2632391..2633990,2	K562	blood:
32	chr8:2499248..2502177-chr8:2672093..2674140,2	K562	blood:
33	chr8:2584493..2586709-chr8:2648044..2650794,2	K562	blood:
34	chr8:2590579..2593269-chr8:2597345..2599839,2	K562	blood:
35	chr8:2578255..2580228-chr8:2646659..2649405,2	K562	blood:
36	chr8:2552954..2555727-chr8:2581547..2584514,2	K562	blood:
37	chr8:2622298..2624399-chr8:2625541..2627206,2	K562	blood:
38	chr8:2591282..2593372-chr8:2644947..2647194,2	K562	blood:
39	chr8:2596453..2598067-chr8:2617789..2620635,2	K562	blood:
40	chr8:2588732..2590770-chr8:2607526..2610029,2	K562	blood:
41	chr8:2591282..2593372-chr8:2644947..2647194,2	K562	blood:
42	chr8:2617946..2621855-chr8:2622304..2626900,6	K562	blood:
43	chr8:2586489..2588767-chr8:2645742..2647467,2	K562	blood:
44	chr8:2569834..2572343-chr8:2683951..2686234,2	K562	blood:
45	chr8:2596453..2598067-chr8:2617789..2620635,2	K562	blood:
46	chr8:2676109..2678160-chr8:2681617..2684101,2	K562	blood:
47	chr8:2582217..2584470-chr8:2644052..2646887,2	K562	blood:
48	chr8:2606417..2608305-chr8:6263383..6265567,2	K562	blood:
49	chr8:2587156..2590098-chr8:2597980..2600237,2	K562	blood:
50	chr8:2733961..2735891-chr8:2736089..2737715,2	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOM2-4	chr8:2679916-2680004	ENSG00000253853
2	lnc-MYOM2-4	chr8:2584690-2585033	XLOC_006690
3	lnc-MYOM2-4	chr8:2662104-2662202	XLOC_006690
4	lnc-CSMD1-1	chr8:2579024-2579126	ENSG00000254319
5	lnc-MYOM2-11	chr8:2670856-2671431	NONHSAT124737
6	lnc-MYOM2-4	chr8:2676789-2676941	ENSG00000253853
7	lnc-MYOM2-4	chr8:2584858-2585033	ENSG00000253853
8	lnc-CSMD1-1	chr8:2585870-2585991	ENSG00000254319
9	lnc-CSMD1-1	chr8:2585870-2585959	ENSG00000254319
10	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
11	lnc-CSMD1-1	chr8:2558974-2559395	ENSG00000254319
12	lnc-MYOM2-4	chr8:2665889-2665956	ENSG00000253853
13	lnc-MYOM2-4	chr8:2662104-2662227	ENSG00000253853
14	lnc-CSMD1-1	chr8:2585870-2585957	ENSG00000254319
15	lnc-MYOM2-12	chr8:2692294-2692594	NONHSAT124738
16	lnc-MYOM2-12	chr8:2694306-2694604	NONHSAT124738
17	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
18	lnc-CSMD1-12	chr8:2573277-2573364	ucscGeneNc_uc003wqb_1
19	lnc-CSMD1-1	chr8:2562746-2562817	XLOC_006980
20	lnc-CSMD1-1	chr8:2585870-2585959	ENSG00000254319
21	lnc-CSMD1-1	chr8:2562746-2562851	XLOC_006980
22	lnc-CSMD1-1	chr8:2562746-2562808	XLOC_006980
23	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
24	lnc-MYOM2-12	chr8:2691861-2692100	NONHSAT124738
25	lnc-CSMD1-1	chr8:2585870-2585957	XLOC_006980

No data

Variant related genes	Relation type
ENSG00000253853	TF binding region
ENSG00000254319	TF binding region
ENSG00000253853	CpG island
ENSG00000254319	CpG island
ENSG00000249694	chromatin interactions
ENSG00000254319	chromatin interactions
ENSG00000253853	chromatin interactions
ENSG00000246089	chromatin interactions
ENSG00000147316	chromatin interactions
TXNDC16	miRNA target sites
SFRS2IP	miRNA target sites

Extended variants
information (count: 9467 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:9467 , 50 per page) page: 1 2 3 4 5 6 7 ... 190

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4367579	chr8:2558468-2558469	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559641392	chr8:2558472-2558473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528791370	chr8:2558473-2558474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548565199	chr8:2558489-2558490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568462005	chr8:2558509-2558510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368138488	chr8:2558535-2558536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564444498	chr8:2558537-2558538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181394781	chr8:2558538-2558539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537468427	chr8:2558539-2558540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60265850	chr8:2558546-2558547	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs35579837	chr8:2558555-2558556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76241604	chr8:2558567-2558568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs71215599	chr8:2558569-2558570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571005547	chr8:2558580-2558581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539895494	chr8:2558585-2558586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540586660	chr8:2558603-2558604	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185683251	chr8:2558604-2558605	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34241368	chr8:2558640-2558641	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560495742	chr8:2558675-2558676	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190734997	chr8:2558688-2558689	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183362287	chr8:2558710-2558711	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543844310	chr8:2558729-2558730	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529391398	chr8:2558730-2558731	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577319906	chr8:2558745-2558746	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186836185	chr8:2558750-2558751	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562939787	chr8:2558765-2558766	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550974072	chr8:2558783-2558784	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559912275	chr8:2558820-2558821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150452635	chr8:2558830-2558831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140523293	chr8:2558836-2558837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571878318	chr8:2558842-2558843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs398112105	chr8:2558843-2558844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144963484	chr8:2558851-2558852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562278219	chr8:2558858-2558859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149052362	chr8:2558898-2558899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571864392	chr8:2558958-2558959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550998954	chr8:2558966-2558967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143036407	chr8:2558972-2558973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533480997	chr8:2558979-2558980	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs546156412	chr8:2558992-2558993	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs370205160	chr8:2558993-2558994	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs4366100	chr8:2559033-2559034	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535153028	chr8:2559036-2559037	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs374316311	chr8:2559080-2559081	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs566937316	chr8:2559093-2559094	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs192030693	chr8:2559109-2559110	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs555483244	chr8:2559114-2559115	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs555530248	chr8:2559129-2559130	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs183865581	chr8:2559131-2559132	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs537697743	chr8:2559167-2559168	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
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
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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	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
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2548400-2565200	Weak transcription	Fetal Kidney	kidney
2	chr8:2555600-2558600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:2557800-2558800	Strong transcription	K562	blood
4	chr8:2558600-2560200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:2558600-2560400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:2558800-2569200	Weak transcription	K562	blood
7	chr8:2559200-2559800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:2559200-2559800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:2559400-2560000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:2565200-2565800	Enhancers	Fetal Kidney	kidney
11	chr8:2565800-2567200	Weak transcription	Fetal Kidney	kidney
12	chr8:2566600-2569400	Weak transcription	Right Atrium	heart
13	chr8:2567200-2567600	ZNF genes & repeats	Fetal Kidney	kidney
14	chr8:2567200-2582800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr8:2567400-2567600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:2567600-2568600	Weak transcription	Fetal Kidney	kidney
17	chr8:2568600-2568800	Enhancers	Fetal Kidney	kidney
18	chr8:2568800-2569400	Weak transcription	Fetal Kidney	kidney
19	chr8:2569200-2569400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:2569200-2569400	Weak transcription	Fetal Stomach	stomach
21	chr8:2569200-2570200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:2569200-2570600	Active TSS	K562	blood
23	chr8:2569400-2569600	Active TSS	Brain Angular Gyrus	brain
24	chr8:2569400-2569600	Enhancers	Fetal Brain Male	brain
25	chr8:2569400-2569600	Enhancers	Fetal Heart	heart
26	chr8:2569400-2569600	Flanking Active TSS	Fetal Kidney	kidney
27	chr8:2569400-2569800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:2569400-2569800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:2569400-2569800	Active TSS	Brain Hippocampus Middle	brain
30	chr8:2569400-2569800	Enhancers	Fetal Lung	lung
31	chr8:2569400-2569800	Enhancers	Fetal Stomach	stomach
32	chr8:2569400-2569800	Enhancers	Psoas Muscle	Psoas
33	chr8:2569400-2569800	Enhancers	Right Atrium	heart
34	chr8:2569400-2570000	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr8:2569400-2570000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr8:2569400-2570000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:2569400-2570000	Active TSS	Brain Anterior Caudate	brain
38	chr8:2569400-2570000	Active TSS	Brain Cingulate Gyrus	brain
39	chr8:2569400-2570000	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr8:2569400-2570000	Active TSS	Brain Substantia Nigra	brain
41	chr8:2569400-2570000	Active TSS	Colon Smooth Muscle	Colon
42	chr8:2569400-2570000	Active TSS	Fetal Brain Female	brain
43	chr8:2569400-2570000	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr8:2569400-2570000	Active TSS	NHEK	skin
45	chr8:2569400-2570200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:2569400-2570200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:2569400-2570200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:2569400-2570200	Active TSS	Duodenum Mucosa	Duodenum
49	chr8:2569400-2570200	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr8:2569400-2570200	Active TSS	Fetal Adrenal Gland	Adrenal Gland

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