Variant report

Variant	nsv1043284
Chromosome Location	chr15:77740632-77884026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2477)
CpG islands
(count:1407)
Chromatin interactive
region (count:210)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2477 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77757023-77757034	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:77861390-77861782	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:77835703-77836012	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:77827054-77827116	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:77754440-77754598	K562	blood:	n/a	n/a
6	ARID3A	chr15:77789170-77789590	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:77811989-77812189	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:77836243-77836280	K562	blood:	n/a	n/a
9	ARID3A	chr15:77789173-77789486	K562	blood:	n/a	n/a
10	ATF1	chr15:77838359-77838720	K562	blood:	n/a	n/a
11	ATF1	chr15:77785371-77786134	K562	blood:	n/a	n/a
12	ATF1	chr15:77794789-77795090	K562	blood:	n/a	n/a
13	ATF2	chr15:77785598-77786151	GM12878	blood:	n/a	n/a
14	ATF2	chr15:77788913-77789730	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr15:77830137-77830819	GM12878	blood:	n/a	n/a
16	ATF2	chr15:77802344-77802992	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr15:77802430-77802984	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr15:77835606-77836142	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr15:77835603-77836035	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr15:77785593-77786196	GM12878	blood:	n/a	n/a
21	ATF2	chr15:77788960-77789525	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr15:77838443-77838682	K562	blood:	n/a	n/a
23	ATF3	chr15:77835926-77836209	K562	blood:	n/a	n/a
24	ATF3	chr15:77838356-77838704	K562	blood:	n/a	n/a
25	ATF3	chr15:77835582-77836093	A549	lung:	n/a	n/a
26	ATF3	chr15:77835760-77835918	K562	blood:	n/a	n/a
27	ATF3	chr15:77835597-77836248	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr15:77835722-77836033	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr15:77789165-77789518	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr15:77788915-77789105	K562	blood:	n/a	n/a
31	BATF	chr15:77765770-77765985	GM12878	blood:	n/a	chr15:77765877-77765887 chr15:77765876-77765887
32	BATF	chr15:77785709-77786080	GM12878	blood:	n/a	n/a
33	BCL3	chr15:77789012-77789617	A549	lung:	n/a	n/a
34	BCL3	chr15:77813539-77813796	GM12878	blood:	n/a	n/a
35	BCL3	chr15:77845554-77846010	GM12878	blood:	n/a	chr15:77845994-77846007
36	BCL3	chr15:77838196-77839048	A549	lung:	n/a	n/a
37	BCLAF1	chr15:77830150-77830782	GM12878	blood:	n/a	chr15:77830612-77830621 chr15:77830465-77830474
38	BCLAF1	chr15:77789755-77790220	GM12878	blood:	n/a	chr15:77790123-77790132
39	BCLAF1	chr15:77835579-77836098	GM12878	blood:	n/a	chr15:77836078-77836086 chr15:77835737-77835746
40	BHLHE40	chr15:77835680-77836182	GM12878	blood:	n/a	chr15:77835790-77835806
41	BHLHE40	chr15:77849561-77849608	K562	blood:	n/a	n/a
42	BHLHE40	chr15:77838362-77838711	K562	blood:	n/a	n/a
43	BHLHE40	chr15:77835676-77836214	K562	blood:	n/a	chr15:77835790-77835806
44	BHLHE40	chr15:77869841-77869966	K562	blood:	n/a	n/a
45	BHLHE40	chr15:77789129-77789511	GM12878	blood:	n/a	n/a
46	BHLHE40	chr15:77849986-77850257	K562	blood:	n/a	n/a
47	BHLHE40	chr15:77876682-77876905	K562	blood:	n/a	n/a
48	BHLHE40	chr15:77830156-77830915	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:77789079-77789451	K562	blood:	n/a	n/a
50	BRCA1	chr15:77835656-77836103	Hela-S3	cervix:	n/a	n/a

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77749559-77749609	AoSMC	blood vessel:	n/a
2	chr15:77800637-77800687	HUVEC	blood vessel:	n/a
3	chr15:77789307-77789357	Hela-S3	cervix:	n/a
4	chr15:77835708-77835758	K562	blood:	n/a
5	chr15:77749559-77749609	AoSMC	blood vessel:	n/a
6	chr15:77800637-77800687	HUVEC	blood vessel:	n/a
7	chr15:77789307-77789357	Hela-S3	cervix:	n/a
8	chr15:77835708-77835758	K562	blood:	n/a
9	chr15:77857909-77857959	HMEC	breast:	n/a
10	chr15:77876657-77876707	MCF-7	breast:	n/a
11	chr15:77819839-77819889	HNPCEpiC	eye:	n/a
12	chr15:77789307-77789357	Caco-2	colon:	n/a
13	chr15:77835749-77835799	H1-hESC	embryonic stem cell:	embryo
14	chr15:77760532-77760582	NB4	blood:	n/a
15	chr15:77811681-77811731	GM19239	blood:	n/a
16	chr15:77800637-77800687	HEEpiC	esophagus:	n/a
17	chr15:77852711-77852761	MCF-7	breast:	n/a
18	chr15:77830579-77830629	HIPEpiC	eye:	n/a
19	chr15:77748245-77748295	PANC-1	pancreas:	n/a
20	chr15:77811681-77811731	NHDF-neo	bronchial:	n/a
21	chr15:77760532-77760582	Hepatocyte	liver:	n/a
22	chr15:77775623-77775673	AG09319	gingival:	n/a
23	chr15:77835568-77835618	K562	blood:	n/a
24	chr15:77835568-77835618	HCM	heart:	n/a
25	chr15:77760532-77760582	HL-60	blood:	n/a
26	chr15:77760532-77760582	NT2-D1	testis:	n/a
27	chr15:77811681-77811731	AG09309	skin:	n/a
28	chr15:77876657-77876707	HRE	kidney:	n/a
29	chr15:77861673-77861723	PFSK-1	brain:	n/a
30	chr15:77760532-77760582	PFSK-1	brain:	n/a
31	chr15:77852711-77852761	PrEC	prostate:	n/a
32	chr15:77862098-77862148	HEEpiC	esophagus:	n/a
33	chr15:77852897-77852947	GM12892	blood:	n/a
34	chr15:77852897-77852947	HIPEpiC	eye:	n/a
35	chr15:77749559-77749609	HMEC	breast:	n/a
36	chr15:77748245-77748295	HIPEpiC	eye:	n/a
37	chr15:77858130-77858180	Caco-2	colon:	n/a
38	chr15:77811681-77811731	HCF	heart:	n/a
39	chr15:77857909-77857959	HPAEpiC	pulmonary alveolar:	n/a
40	chr15:77852711-77852761	ProgFib	skin:	n/a
41	chr15:77862098-77862148	IMR90	lung:	fetal
42	chr15:77789307-77789357	PANC-1	pancreas:	n/a
43	chr15:77857997-77858047	PANC-1	pancreas:	n/a
44	chr15:77841106-77841156	SKMC	muscle:	n/a
45	chr15:77861673-77861723	T-47D	breast:	n/a
46	chr15:77789307-77789357	AG09319	gingival:	n/a
47	chr15:77852711-77852761	NB4	blood:	n/a
48	chr15:77800637-77800687	GM06990	blood:	n/a
49	chr15:77835568-77835618	HRPEpiC	eye:	n/a
50	chr15:77862098-77862148	ProgFib	skin:	n/a

(count:210 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr15:77835732..77836546-chr15:78113747..78114395,2	MCF-7	breast:
2	chr15:77734206..77736297-chr15:77744808..77747218,2	K562	blood:
3	chr15:77883341..77886336-chr15:77886431..77889031,3	MCF-7	breast:
4	chr15:77793037..77794591-chr15:77835207..77836439,4	MCF-7	breast:
5	chr15:77478458..77479486-chr15:77835010..77836461,5	MCF-7	breast:
6	chr15:77848566..77850112-chr15:77856631..77859198,2	K562	blood:
7	chr15:77745907..77748744-chr15:77783742..77785823,2	K562	blood:
8	chr15:77822210..77823977-chr15:77824433..77827126,2	MCF-7	breast:
9	chr15:77789332..77790391-chr15:77834947..77835831,3	MCF-7	breast:
10	chr15:77741931..77744582-chr15:77746845..77748481,2	K562	blood:
11	chr15:77824813..77828626-chr15:77832957..77835709,3	K562	blood:
12	chr15:77856989..77859495-chr15:77861940..77865382,3	K562	blood:
13	chr15:77789053..77790918-chr15:77831495..77833590,2	MCF-7	breast:
14	chr15:77795420..77798597-chr15:77834386..77837370,5	MCF-7	breast:
15	chr15:77795040..77797177-chr15:77834449..77837320,2	MCF-7	breast:
16	chr15:77879443..77881773-chr15:77883698..77885210,2	K562	blood:
17	chr15:77851228..77852752-chr15:77859516..77862066,2	K562	blood:
18	chr15:77789312..77792548-chr15:77795862..77798378,3	K562	blood:
19	chr15:77789449..77791631-chr15:77818206..77819857,2	MCF-7	breast:
20	chr15:77712321..77714990-chr15:77817270..77818791,2	MCF-7	breast:
21	chr15:77710223..77714353-chr15:77793653..77797346,4	MCF-7	breast:
22	chr15:77835384..77837203-chr15:77911255..77913813,2	MCF-7	breast:
23	chr15:77789092..77789858-chr15:77810951..77811581,2	MCF-7	breast:
24	chr15:77822048..77824496-chr15:77832446..77834927,2	K562	blood:
25	chr15:77839042..77839906-chr15:77876314..77877043,2	MCF-7	breast:
26	chr15:77789311..77789873-chr15:77836001..77836547,2	K562	blood:
27	chr15:77788121..77789886-chr15:77835389..77836306,7	MCF-7	breast:
28	chr15:77797715..77799505-chr15:77800913..77803118,3	MCF-7	breast:
29	chr15:77840852..77845440-chr15:77846808..77850692,5	K562	blood:
30	chr15:77839369..77839946-chr15:77923059..77923563,2	MCF-7	breast:
31	chr15:77412894..77414915-chr15:77833378..77835255,2	K562	blood:
32	chr15:77411217..77412383-chr15:77835511..77836330,5	MCF-7	breast:
33	chr15:77819703..77822055-chr15:77824303..77826129,2	MCF-7	breast:
34	chr15:77811694..77814314-chr15:77820121..77822806,2	K562	blood:
35	chr15:77800020..77805731-chr15:77808908..77813033,5	MCF-7	breast:
36	chr15:77835652..77836578-chr15:77876310..77876975,3	MCF-7	breast:
37	chr15:77797488..77799735-chr15:77817665..77820663,3	MCF-7	breast:
38	chr15:77838960..77839788-chr15:77925715..77926415,4	MCF-7	breast:
39	chr15:77810042..77814304-chr15:77818656..77821099,4	MCF-7	breast:
40	chr15:77793530..77795240-chr15:77834025..77836291,2	MCF-7	breast:
41	chr15:77779791..77781674-chr15:77785358..77787306,2	K562	blood:
42	chr15:77866782..77869407-chr15:77890484..77892735,2	MCF-7	breast:
43	chr15:77810042..77814304-chr15:77818656..77821099,4	MCF-7	breast:
44	chr15:77835406..77836055-chr15:77951749..77952721,2	K562	blood:
45	chr15:77803142..77806483-chr15:77808853..77811512,3	K562	blood:
46	chr15:77764294..77766424-chr15:77768357..77770654,2	K562	blood:
47	chr15:77862030..77863568-chr15:77895689..77897664,2	MCF-7	breast:
48	chr15:77864365..77867025-chr15:77869640..77872108,2	MCF-7	breast:
49	chr15:77779791..77781674-chr15:77785358..77787306,2	K562	blood:
50	chr15:77824813..77828626-chr15:77832957..77835709,3	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMG20A-2	chr15:77864593-77864787	ENSG00000259420.1
2	lnc-HMG20A-2	chr15:77864593-77864787	ENSG00000259420.1
3	lnc-PEAK1.1-2	chr15:77776140-77776947	ENSG00000244881
4	lnc-HMG20A-6	chr15:77774392-77777949	NONHSAT047442
5	lnc-HMG20A-1	chr15:77817882-77818687	ENSG00000259362.2
6	lnc-HMG20A-2	chr15:77861312-77861518	ENSG00000259420.1
7	lnc-HMG20A-2	chr15:77864907-77865206	ENSG00000259420.1
8	lnc-HMG20A-2	chr15:77864907-77865081	ENSG00000259420.1
9	lnc-HMG20A-1	chr15:77823445-77826452	ENSG00000259362.2
10	lnc-HMG20A-2	chr15:77861312-77861518	ENSG00000259420.1
11	lnc-PEAK1.1-5	chr15:77777399-77777941	NONHSAT047445

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HMG20A	hsa-miR-30c-5p	chr15:77776464-77776486

Variant related genes	Relation type
ENSG00000259362	TF binding region
HMG20A	TF binding region
ENSG00000259420	TF binding region
ENSG00000259362	CpG island
HMG20A	CpG island
ENSG00000259420	CpG island
ENSG00000184163	chromatin interactions
ENSG00000140382	chromatin interactions
ENSG00000259362	chromatin interactions
ENSG00000070413	chromatin interactions
ENSG00000180900	chromatin interactions
ENSG00000173517	chromatin interactions
ENSG00000259281	chromatin interactions
ENSG00000169783	chromatin interactions
ENSG00000259420	chromatin interactions
ENSG00000140368	chromatin interactions
ENSG00000223461	chromatin interactions

Extended variants
information (count: 5383 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:5383 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554537853	chr15:77740685-77740686	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140330526	chr15:77740745-77740746	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548064946	chr15:77740769-77740770	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35946137	chr15:77740771-77740772	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12917211	chr15:77740808-77740809	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs558641121	chr15:77740816-77740817	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576934229	chr15:77740861-77740862	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187944332	chr15:77740866-77740867	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368223090	chr15:77740904-77740905	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs12917359	chr15:77740921-77740922	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs529999062	chr15:77741030-77741031	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs58442334	chr15:77741040-77741041	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554754870	chr15:77741041-77741042	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144176446	chr15:77741047-77741048	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs193244307	chr15:77741061-77741062	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs75464222	chr15:77741105-77741106	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183554706	chr15:77741149-77741150	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139233003	chr15:77741150-77741151	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552276889	chr15:77741152-77741153	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188547036	chr15:77741153-77741154	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs528210467	chr15:77741200-77741201	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147809983	chr15:77741226-77741227	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192734152	chr15:77741242-77741243	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139547231	chr15:77741300-77741301	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs554850215	chr15:77741310-77741311	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113064652	chr15:77741313-77741314	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs62007313	chr15:77741323-77741324	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs116352279	chr15:77741360-77741361	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184000918	chr15:77741403-77741404	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113191276	chr15:77741414-77741415	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188290464	chr15:77741420-77741421	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577252419	chr15:77741450-77741451	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs578058099	chr15:77741501-77741502	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111779777	chr15:77741512-77741513	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs145244431	chr15:77741521-77741522	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558797014	chr15:77741527-77741528	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs574555725	chr15:77741591-77741592	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs115445378	chr15:77741592-77741593	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs150971494	chr15:77741598-77741599	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7179544	chr15:77741605-77741606	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191598941	chr15:77741639-77741640	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1565756	chr15:77741640-77741641	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546379040	chr15:77741655-77741656	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559854943	chr15:77741738-77741739	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530245011	chr15:77741899-77741900	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs150176095	chr15:77741900-77741901	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs569992397	chr15:77741948-77741949	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537381017	chr15:77741957-77741958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs145607411	chr15:77741964-77741965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs183739668	chr15:77741992-77741993	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4661 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77714000-77748600	Weak transcription	Placenta	Placenta
2	chr15:77714400-77741600	Weak transcription	Fetal Thymus	thymus
3	chr15:77716400-77741400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr15:77716800-77742600	Weak transcription	Hela-S3	cervix
5	chr15:77717000-77754400	Weak transcription	K562	blood
6	chr15:77720200-77743000	Weak transcription	Primary B cells from cord blood	blood
7	chr15:77727200-77741200	Weak transcription	Fetal Stomach	stomach
8	chr15:77727400-77747800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr15:77728200-77746200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr15:77729400-77747200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr15:77729600-77748000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr15:77729600-77749200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr15:77729800-77747200	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr15:77730400-77748600	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr15:77730600-77758800	Weak transcription	Lung	lung
16	chr15:77733200-77744600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr15:77733200-77748000	Weak transcription	HMEC	breast
18	chr15:77733200-77749200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr15:77733200-77750200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:77733400-77741600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr15:77733400-77746800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr15:77733400-77747000	Weak transcription	NH-A	brain
23	chr15:77733400-77747000	Weak transcription	NHDF-Ad	bronchial
24	chr15:77733600-77741600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr15:77733600-77742000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:77733600-77742000	Weak transcription	HSMM	muscle
27	chr15:77734000-77745000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr15:77734600-77746400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr15:77735200-77741600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:77735200-77742200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr15:77735200-77742800	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr15:77735200-77743200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr15:77736400-77741000	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr15:77736400-77748800	Weak transcription	Pancreas	Pancrea
35	chr15:77736600-77741800	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr15:77736800-77749400	Weak transcription	Gastric	stomach
37	chr15:77736800-77750800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr15:77737000-77747800	Weak transcription	Fetal Kidney	kidney
39	chr15:77737200-77747000	Weak transcription	HUVEC	blood vessel
40	chr15:77737200-77749400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr15:77737400-77741600	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr15:77737800-77748000	Weak transcription	Left Ventricle	heart
43	chr15:77737800-77749200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr15:77738200-77749400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr15:77738400-77743200	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr15:77738400-77747200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr15:77738400-77748000	Weak transcription	Psoas Muscle	Psoas
48	chr15:77738400-77749200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr15:77738400-77749400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr15:77738600-77747800	Weak transcription	Fetal Heart	heart

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