Variant report

Variant	nsv609697
Chromosome Location	chr8:2520024-2653455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1097)
CpG islands
(count:1222)
Chromatin interactive
region (count:150)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2628561-2628762	K562	blood:	n/a	n/a
2	ARID3A	chr8:2571430-2571701	K562	blood:	n/a	n/a
3	ARID3A	chr8:2569699-2570363	K562	blood:	n/a	n/a
4	ARID3A	chr8:2645493-2646139	K562	blood:	n/a	n/a
5	ARID3A	chr8:2632277-2632294	K562	blood:	n/a	n/a
6	ARID3A	chr8:2586788-2587042	K562	blood:	n/a	n/a
7	ARID3A	chr8:2588688-2589234	K562	blood:	n/a	n/a
8	ARID3A	chr8:2592824-2593695	K562	blood:	n/a	chr8:2593039-2593055
9	ARID3A	chr8:2583362-2583786	K562	blood:	n/a	n/a
10	ARID3A	chr8:2640546-2640565	K562	blood:	n/a	n/a
11	ARID3A	chr8:2591085-2592231	K562	blood:	n/a	n/a
12	ARID3A	chr8:2640879-2641488	K562	blood:	n/a	n/a
13	ARID3A	chr8:2582455-2583099	K562	blood:	n/a	n/a
14	ATF1	chr8:2588667-2588920	K562	blood:	n/a	n/a
15	ATF1	chr8:2645670-2646221	K562	blood:	n/a	n/a
16	ATF1	chr8:2641154-2641440	K562	blood:	n/a	n/a
17	ATF1	chr8:2591024-2591651	K562	blood:	n/a	n/a
18	ATF1	chr8:2581374-2581475	K562	blood:	n/a	n/a
19	ATF2	chr8:2575121-2575588	GM12878	blood:	n/a	n/a
20	ATF2	chr8:2556809-2557171	GM12878	blood:	n/a	n/a
21	ATF2	chr8:2575097-2575545	GM12878	blood:	n/a	n/a
22	ATF2	chr8:2556735-2557319	GM12878	blood:	n/a	n/a
23	ATF3	chr8:2591062-2591346	K562	blood:	n/a	n/a
24	BACH1	chr8:2628552-2628844	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:2558085-2558096	K562	blood:	n/a	n/a
26	BACH1	chr8:2628652-2628871	K562	blood:	n/a	n/a
27	BATF	chr8:2577057-2577495	GM12878	blood:	n/a	chr8:2577308-2577319
28	BATF	chr8:2575236-2575412	GM12878	blood:	n/a	chr8:2575395-2575403
29	BATF	chr8:2556758-2557340	GM12878	blood:	n/a	n/a
30	BATF	chr8:2575165-2575442	GM12878	blood:	n/a	chr8:2575395-2575403
31	BATF	chr8:2577159-2577434	GM12878	blood:	n/a	chr8:2577308-2577319
32	BATF	chr8:2556819-2557194	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:2577041-2577262	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:2576992-2577351	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:2556744-2557182	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:2575139-2575457	GM12878	blood:	n/a	n/a
37	BCL3	chr8:2575150-2575417	GM12878	blood:	n/a	n/a
38	BCL3	chr8:2556799-2557285	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:2556824-2557149	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:2591118-2591666	K562	blood:	n/a	n/a
41	BHLHE40	chr8:2569644-2569660	GM12878	blood:	n/a	n/a
42	BHLHE40	chr8:2628562-2628861	K562	blood:	n/a	n/a
43	BHLHE40	chr8:2585550-2585876	K562	blood:	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	chr8:2590944-2591676	K562	blood:	n/a	n/a
47	BHLHE40	chr8:2589918-2590649	K562	blood:	n/a	n/a
48	BHLHE40	chr8:2556762-2557433	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:2588692-2588697	K562	blood:	n/a	n/a
50	BHLHE40	chr8:2645764-2646221	K562	blood:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2549270-2549320	ECC-1	luminal epithelium:	n/a
2	chr8:2628628-2628678	MCF10A-Er-Src	breast:	n/a
3	chr8:2549270-2549320	ECC-1	luminal epithelium:	n/a
4	chr8:2628628-2628678	MCF10A-Er-Src	breast:	n/a
5	chr8:2538305-2538355	HCT-116	colon:	n/a
6	chr8:2545988-2546038	K562	blood:	n/a
7	chr8:2609691-2609741	Caco-2	colon:	n/a
8	chr8:2609661-2609711	Caco-2	colon:	n/a
9	chr8:2585666-2585716	Hela-S3	cervix:	n/a
10	chr8:2585235-2585285	AG09309	skin:	n/a
11	chr8:2538305-2538355	NT2-D1	testis:	n/a
12	chr8:2585666-2585716	GM06990	blood:	n/a
13	chr8:2549296-2549346	SKMC	muscle:	n/a
14	chr8:2549296-2549346	CMK	blood:	n/a
15	chr8:2585976-2586026	GM12891	blood:	n/a
16	chr8:2585235-2585285	HRPEpiC	eye:	n/a
17	chr8:2538355-2538405	HIPEpiC	eye:	n/a
18	chr8:2549080-2549130	HepG2	liver:	n/a
19	chr8:2585666-2585716	SK-N-SH	brain:	n/a
20	chr8:2591207-2591257	HAEpiC	amniotic membrane:	n/a
21	chr8:2549296-2549346	AG09309	skin:	n/a
22	chr8:2628628-2628678	PFSK-1	brain:	n/a
23	chr8:2586225-2586275	GM06990	blood:	n/a
24	chr8:2585235-2585285	PrEC	prostate:	n/a
25	chr8:2591265-2591315	SAEC	small airway:	n/a
26	chr8:2585666-2585716	HAEpiC	amniotic membrane:	n/a
27	chr8:2628628-2628678	HNPCEpiC	eye:	n/a
28	chr8:2609661-2609711	MCF-7	breast:	n/a
29	chr8:2549270-2549320	U87	brain:	n/a
30	chr8:2628628-2628678	NT2-D1	testis:	n/a
31	chr8:2586911-2586961	IMR90	lung:	fetal
32	chr8:2609691-2609741	HIPEpiC	eye:	n/a
33	chr8:2549244-2549294	AG04449	skin:	fetal
34	chr8:2585666-2585716	NH-A	brain:	n/a
35	chr8:2548901-2548951	A549	lung:	n/a
36	chr8:2549080-2549130	GM19239	blood:	n/a
37	chr8:2538249-2538299	HL-60	blood:	n/a
38	chr8:2538305-2538355	HNPCEpiC	eye:	n/a
39	chr8:2538355-2538405	A549	lung:	n/a
40	chr8:2591265-2591315	SK-N-MC	brain:	n/a
41	chr8:2545988-2546038	ECC-1	luminal epithelium:	n/a
42	chr8:2548901-2548951	HEEpiC	esophagus:	n/a
43	chr8:2586225-2586275	SK-N-SH_RA	brain:	n/a
44	chr8:2549080-2549130	GM06990	blood:	n/a
45	chr8:2609691-2609741	BE2_C	brain:	n/a
46	chr8:2538305-2538355	A549	lung:	n/a
47	chr8:2538305-2538355	PrEC	prostate:	n/a
48	chr8:2549244-2549294	PANC-1	pancreas:	n/a
49	chr8:2586911-2586961	BJ	skin:	n/a
50	chr8:2549296-2549346	IMR90	lung:	fetal

(count:150 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:2631963..2633946-chr8:2635441..2638844,4	K562	blood:
2	chr8:2578568..2580077-chr8:2629449..2631121,2	K562	blood:
3	chr8:2591672..2593360-chr8:2600937..2603510,2	K562	blood:
4	chr8:2522746..2525296-chr8:2550223..2552690,2	K562	blood:
5	chr8:2582217..2584470-chr8:2644052..2646887,2	K562	blood:
6	chr8:2594821..2596661-chr8:2659400..2661815,2	K562	blood:
7	chr8:2590579..2593269-chr8:2597345..2599839,2	K562	blood:
8	chr8:2594321..2595985-chr8:2596545..2598928,2	K562	blood:
9	chr8:2631918..2634126-chr8:2639188..2641827,3	K562	blood:
10	chr8:2588672..2591604-chr8:2606736..2608704,2	K562	blood:
11	chr8:2522746..2525296-chr8:2550223..2552690,2	K562	blood:
12	chr8:2544394..2547275-chr8:2569215..2571257,2	K562	blood:
13	chr8:2607558..2609833-chr8:2620267..2622243,2	K562	blood:
14	chr8:2590579..2593269-chr8:2597345..2599839,2	K562	blood:
15	chr8:2527298..2531531-chr8:2571196..2574583,3	K562	blood:
16	chr8:2599818..2601466-chr8:2615794..2618126,2	K562	blood:
17	chr8:2607594..2609173-chr8:2610051..2612762,2	K562	blood:
18	chr8:2606417..2608305-chr8:6263383..6265567,2	K562	blood:
19	chr8:2599818..2601466-chr8:2615794..2618126,2	K562	blood:
20	chr8:2588399..2590579-chr8:2619953..2621933,2	K562	blood:
21	chr8:2547306..2548966-chr8:2550083..2551801,2	K562	blood:
22	chr8:2582217..2585126-chr8:2645115..2648033,3	K562	blood:
23	chr8:2564777..2566535-chr8:2633073..2636041,2	K562	blood:
24	chr8:2592045..2593873-chr8:2639139..2641093,2	K562	blood:
25	chr8:2626526..2629237-chr8:2643013..2645044,2	K562	blood:
26	chr8:2523638..2525296-chr8:2550223..2552955,2	K562	blood:
27	chr8:2607225..2609833-chr8:2620743..2622482,2	K562	blood:
28	chr8:2527298..2531531-chr8:2571196..2574583,3	K562	blood:
29	chr8:2574708..2577541-chr8:2645508..2647339,2	K562	blood:
30	chr8:2578568..2580077-chr8:2629449..2631121,2	K562	blood:
31	chr8:2522780..2524643-chr8:2526596..2529136,3	K562	blood:
32	chr8:2624634..2626171-chr8:2626385..2627921,2	K562	blood:
33	chr8:2646083..2648399-chr8:2651265..2652785,2	K562	blood:
34	chr8:2607225..2609833-chr8:2620743..2622482,2	K562	blood:
35	chr8:2578255..2580228-chr8:2646659..2649405,2	K562	blood:
36	chr8:2582656..2585104-chr8:2624688..2627704,3	K562	blood:
37	chr8:2581583..2583717-chr8:2629779..2632659,2	K562	blood:
38	chr8:2585736..2588066-chr8:2601157..2603810,2	K562	blood:
39	chr8:2631963..2633946-chr8:2635441..2638844,4	K562	blood:
40	chr8:2584493..2586709-chr8:2648044..2650794,2	K562	blood:
41	chr8:2568252..2570741-chr8:2670037..2672346,3	K562	blood:
42	chr8:2640358..2642193-chr8:2645128..2647083,3	K562	blood:
43	chr8:2620299..2623099-chr8:2627454..2628985,2	K562	blood:
44	chr8:2596453..2598067-chr8:2617789..2620635,2	K562	blood:
45	chr8:2597895..2600148-chr8:2611111..2612738,2	K562	blood:
46	chr8:2588918..2591630-chr8:2632391..2633990,2	K562	blood:
47	chr8:2597895..2600148-chr8:2611111..2612738,2	K562	blood:
48	chr8:2522780..2524643-chr8:2526596..2529136,3	K562	blood:
49	chr8:2631918..2634126-chr8:2639188..2641827,3	K562	blood:
50	chr8:2586489..2588767-chr8:2645742..2647467,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
2	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
3	lnc-MYOM2-10	chr8:2533633-2534528	NONHSAT124732
4	lnc-CSMD1-1	chr8:2527314-2527521	ENSG00000254319
5	lnc-CSMD1-1	chr8:2527341-2527521	ENSG00000254319
6	lnc-CSMD1-1	chr8:2585870-2585957	XLOC_006980
7	lnc-CSMD1-1	chr8:2585870-2585959	ENSG00000254319
8	lnc-CSMD1-1	chr8:2562746-2562808	XLOC_006980
9	lnc-CSMD1-1	chr8:2527293-2527521	ENSG00000254319
10	lnc-CSMD1-12	chr8:2541463-2541879	ucscGeneNc_uc003wqb_1
11	lnc-CSMD1-1	chr8:2532111-2532353	XLOC_006980
12	lnc-CSMD1-1	chr8:2523591-2523700	ENSG00000254319
13	lnc-MYOM2-4	chr8:2584690-2585033	XLOC_006690
14	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
15	lnc-CSMD1-1	chr8:2585870-2585959	ENSG00000254319
16	lnc-CSMD1-1	chr8:2554056-2554472	XLOC_006980
17	lnc-CSMD1-1	chr8:2585870-2585957	ENSG00000254319
18	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
19	lnc-CSMD1-1	chr8:2562746-2562817	XLOC_006980
20	lnc-CSMD1-1	chr8:2585870-2585991	ENSG00000254319
21	lnc-CSMD1-1	chr8:2562746-2562851	XLOC_006980
22	lnc-CSMD1-1	chr8:2579024-2579126	ENSG00000254319
23	lnc-MYOM2-4	chr8:2584858-2585033	ENSG00000253853
24	lnc-CSMD1-1	chr8:2536358-2536440	ENSG00000254319
25	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
26	lnc-CSMD1-1	chr8:2558974-2559395	ENSG00000254319
27	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
28	lnc-CSMD1-12	chr8:2573277-2573364	ucscGeneNc_uc003wqb_1
29	lnc-CSMD1-1	chr8:2554297-2554472	XLOC_006980
30	lnc-CSMD1-12	chr8:2550153-2550224	ucscGeneNc_uc003wqb_1

No data

Variant related genes	Relation type
ENSG00000253853	TF binding region
ENSG00000254319	TF binding region
ENSG00000253853	CpG island
ENSG00000254319	CpG island
ENSG00000253853	chromatin interactions
ENSG00000147316	chromatin interactions
ENSG00000254319	chromatin interactions
ENSG00000246089	chromatin interactions
BCL11A	miRNA target sites
TXNDC16	miRNA target sites
SFRS2IP	miRNA target sites

Extended variants
information (count: 6649 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:6649 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113881300	chr8:2522012-2522013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34694098	chr8:2522026-2522027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs542766135	chr8:2522028-2522029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs36065189	chr8:2522039-2522040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs184149966	chr8:2522042-2522043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117603617	chr8:2522043-2522044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188450393	chr8:2522064-2522065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539490240	chr8:2522089-2522090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4620309	chr8:2522115-2522116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572707868	chr8:2522122-2522123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541642614	chr8:2522184-2522185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555345200	chr8:2522211-2522212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62488414	chr8:2522256-2522257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs543456181	chr8:2522266-2522267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10780165	chr8:2522277-2522278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577284163	chr8:2522296-2522297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73488663	chr8:2522307-2522308	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559398299	chr8:2522356-2522357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562941971	chr8:2522359-2522360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200233564	chr8:2522361-2522362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528316069	chr8:2522363-2522364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547973157	chr8:2522391-2522392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560445594	chr8:2522415-2522416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529216478	chr8:2522442-2522443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559525115	chr8:2522459-2522460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530668659	chr8:2522468-2522469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550324436	chr8:2522488-2522489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181640348	chr8:2522541-2522542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539045225	chr8:2522552-2522553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113966359	chr8:2522555-2522556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528751807	chr8:2522564-2522565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377669864	chr8:2522571-2522572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144758351	chr8:2522572-2522573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200937746	chr8:2522574-2522575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201326043	chr8:2522582-2522583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs66786658	chr8:2522583-2522584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535244635	chr8:2522590-2522591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555154886	chr8:2522606-2522607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575233530	chr8:2522608-2522609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146167773	chr8:2522639-2522640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557356357	chr8:2522657-2522658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577195067	chr8:2522676-2522677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545873974	chr8:2522704-2522705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200007115	chr8:2522710-2522711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559461485	chr8:2522725-2522726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567134556	chr8:2522728-2522729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541625239	chr8:2522743-2522744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10453151	chr8:2522769-2522770	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs530728562	chr8:2522807-2522808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550884836	chr8:2522821-2522822	Enhancers Weak transcription	n/a	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2522000-2527000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:2522800-2523000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:2524600-2526200	Weak transcription	Fetal Stomach	stomach
4	chr8:2525400-2525600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:2525800-2526000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:2526000-2526800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr8:2526200-2527400	Strong transcription	Fetal Stomach	stomach
8	chr8:2526600-2527400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:2526800-2527400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:2527000-2527600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:2527200-2527600	Enhancers	Esophagus	oesophagus
12	chr8:2527400-2527600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:2527400-2534800	Weak transcription	Fetal Stomach	stomach
14	chr8:2527600-2529200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:2530400-2531200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:2531200-2533800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:2531800-2532400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:2531800-2532600	Enhancers	Esophagus	oesophagus
19	chr8:2532400-2534000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:2532600-2533800	Weak transcription	Esophagus	oesophagus
21	chr8:2533800-2534400	Enhancers	Esophagus	oesophagus
22	chr8:2533800-2535200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr8:2533800-2535400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:2533800-2535400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:2533800-2535400	Enhancers	NHEK	skin
26	chr8:2533800-2535400	Enhancers	Osteobl	bone
27	chr8:2534000-2534400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:2534800-2535000	Enhancers	Fetal Stomach	stomach
29	chr8:2535000-2535600	Weak transcription	Fetal Stomach	stomach
30	chr8:2540000-2540400	Weak transcription	Gastric	stomach
31	chr8:2540400-2540600	Enhancers	Gastric	stomach
32	chr8:2544600-2544800	Weak transcription	Fetal Stomach	stomach
33	chr8:2544800-2545000	Enhancers	Fetal Stomach	stomach
34	chr8:2544800-2545400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:2545000-2545800	Weak transcription	Fetal Stomach	stomach
36	chr8:2545000-2546200	Enhancers	Fetal Heart	heart
37	chr8:2545000-2546200	Enhancers	Fetal Lung	lung
38	chr8:2545400-2545800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:2545600-2545800	Enhancers	Fetal Muscle Leg	muscle
40	chr8:2545600-2545800	Active TSS	Osteobl	bone
41	chr8:2545800-2546000	Flanking Active TSS	Fetal Muscle Leg	muscle
42	chr8:2545800-2546000	Enhancers	Fetal Stomach	stomach
43	chr8:2545800-2546200	Flanking Active TSS	Osteobl	bone
44	chr8:2545800-2546400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:2545800-2546400	Active TSS	Right Atrium	heart
46	chr8:2546000-2546200	Enhancers	Fetal Muscle Leg	muscle
47	chr8:2546000-2546200	Flanking Active TSS	Fetal Stomach	stomach
48	chr8:2546200-2546400	Active TSS	Fetal Muscle Leg	muscle
49	chr8:2546200-2546400	Enhancers	Osteobl	bone
50	chr8:2546200-2546800	Enhancers	Fetal Stomach	stomach

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