Variant report

Variant	nsv520069
Chromosome Location	chr15:76602212-76609181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:739)
CpG islands
(count:671)
Chromatin interactive
region (count:41)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76603464-76604159	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76605160-76605530	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76606202-76606440	K562	blood:	n/a	n/a
4	ATF2	chr15:76603628-76604065	GM12878	blood:	n/a	n/a
5	ATF2	chr15:76603538-76604212	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:76603579-76604246	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:76603464-76604290	GM12878	blood:	n/a	n/a
8	ATF3	chr15:76605038-76605685	A549	lung:	n/a	n/a
9	ATF3	chr15:76605256-76605435	HepG2	liver:	n/a	n/a
10	ATF3	chr15:76603499-76604201	A549	lung:	n/a	chr15:76603638-76603646
11	ATF3	chr15:76604945-76605665	A549	lung:	n/a	n/a
12	BACH1	chr15:76606095-76606327	K562	blood:	n/a	n/a
13	BATF	chr15:76603880-76604158	GM12878	blood:	n/a	n/a
14	BCL3	chr15:76603481-76604319	A549	lung:	n/a	n/a
15	BCL3	chr15:76603348-76604339	A549	lung:	n/a	n/a
16	BCL3	chr15:76604707-76606149	A549	lung:	n/a	n/a
17	BCL3	chr15:76604842-76605682	A549	lung:	n/a	n/a
18	BCLAF1	chr15:76603519-76604134	GM12878	blood:	n/a	n/a
19	BHLHE40	chr15:76603383-76604173	K562	blood:	n/a	n/a
20	BHLHE40	chr15:76603382-76604244	HepG2	liver:	n/a	n/a
21	BHLHE40	chr15:76603591-76604123	GM12878	blood:	n/a	n/a
22	BRCA1	chr15:76603391-76604162	GM12878	blood:	n/a	chr15:76603811-76603820
23	BRCA1	chr15:76602921-76604220	Hela-S3	cervix:	n/a	chr15:76602933-76602940 chr15:76603811-76603820
24	BRCA1	chr15:76603342-76604059	HepG2	liver:	n/a	chr15:76603811-76603820
25	BRCA1	chr15:76605034-76605511	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr15:76603556-76604223	H1-hESC	embryonic stem cell:	n/a	chr15:76603811-76603820
27	CBX3	chr15:76603433-76604339	K562	blood:	n/a	n/a
28	CBX3	chr15:76606060-76606463	K562	blood:	n/a	n/a
29	CCNT2	chr15:76603201-76604131	K562	blood:	n/a	n/a
30	CEBPB	chr15:76604708-76606479	A549	lung:	n/a	n/a
31	CEBPB	chr15:76603303-76603306	K562	blood:	n/a	n/a
32	CEBPB	chr15:76605076-76605953	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr15:76605146-76605610	A549	lung:	n/a	n/a
34	CEBPB	chr15:76603297-76604273	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr15:76605171-76605554	MCF-7	breast:	n/a	n/a
36	CEBPB	chr15:76605224-76605525	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:76605150-76605993	A549	lung:	n/a	n/a
38	CEBPD	chr15:76603458-76604170	HepG2	liver:	n/a	n/a
39	CEBPD	chr15:76603500-76604103	K562	blood:	n/a	n/a
40	CEBPD	chr15:76603511-76604132	K562	blood:	n/a	n/a
41	CHD1	chr15:76603509-76603734	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr15:76602790-76604267	GM12878	blood:	n/a	n/a
43	CHD2	chr15:76605057-76605607	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr15:76602898-76604242	GM12878	blood:	n/a	n/a
45	CHD2	chr15:76602829-76604253	K562	blood:	n/a	n/a
46	CHD2	chr15:76606057-76606357	K562	blood:	n/a	n/a
47	CHD2	chr15:76602919-76604189	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr15:76603450-76604220	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr15:76606029-76606397	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr15:76603237-76604143	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76606532-76606582	HCT-116	colon:	n/a
2	chr15:76604113-76604163	HCM	heart:	n/a
3	chr15:76603987-76604037	ECC-1	luminal epithelium:	n/a
4	chr15:76603736-76603786	GM06990	blood:	n/a
5	chr15:76603987-76604037	BE2_C	brain:	n/a
6	chr15:76604113-76604163	IMR90	lung:	fetal
7	chr15:76606532-76606582	CMK	blood:	n/a
8	chr15:76604340-76604390	Hepatocyte	liver:	n/a
9	chr15:76604113-76604163	HEEpiC	esophagus:	n/a
10	chr15:76604113-76604163	HRPEpiC	eye:	n/a
11	chr15:76604101-76604151	GM12891	blood:	n/a
12	chr15:76603276-76603326	HRCEpiC	kidney:	n/a
13	chr15:76603992-76604042	BE2_C	brain:	n/a
14	chr15:76603276-76603326	AG09309	skin:	n/a
15	chr15:76604340-76604390	SKMC	muscle:	n/a
16	chr15:76603992-76604042	HAEpiC	amniotic membrane:	n/a
17	chr15:76603787-76603837	GM12891	blood:	n/a
18	chr15:76604340-76604390	HepG2	liver:	n/a
19	chr15:76604340-76604390	SK-N-MC	brain:	n/a
20	chr15:76603992-76604042	SAEC	small airway:	n/a
21	chr15:76603992-76604042	Jurkat	blood:	n/a
22	chr15:76603736-76603786	GM19239	blood:	n/a
23	chr15:76603985-76604035	HepG2	liver:	n/a
24	chr15:76603787-76603837	GM12892	blood:	n/a
25	chr15:76606532-76606582	HepG2	liver:	n/a
26	chr15:76603657-76603707	AG10803	skin:	n/a
27	chr15:76603787-76603837	AG10803	skin:	n/a
28	chr15:76603736-76603786	BE2_C	brain:	n/a
29	chr15:76603992-76604042	AG09309	skin:	n/a
30	chr15:76603657-76603707	IMR90	lung:	fetal
31	chr15:76604101-76604151	CMK	blood:	n/a
32	chr15:76603787-76603837	NHBE	bronchial:	n/a
33	chr15:76603276-76603326	H1-hESC	embryonic stem cell:	embryo
34	chr15:76603736-76603786	HRPEpiC	eye:	n/a
35	chr15:76603276-76603326	HCT-116	colon:	n/a
36	chr15:76603985-76604035	HAEpiC	amniotic membrane:	n/a
37	chr15:76606532-76606582	GM19239	blood:	n/a
38	chr15:76604101-76604151	SK-N-MC	brain:	n/a
39	chr15:76604113-76604163	PFSK-1	brain:	n/a
40	chr15:76603985-76604035	HCF	heart:	n/a
41	chr15:76604101-76604151	HCM	heart:	n/a
42	chr15:76603787-76603837	HIPEpiC	eye:	n/a
43	chr15:76603987-76604037	MCF10A-Er-Src	breast:	n/a
44	chr15:76606532-76606582	HCF	heart:	n/a
45	chr15:76603276-76603326	HNPCEpiC	eye:	n/a
46	chr15:76604113-76604163	GM12878	blood:	n/a
47	chr15:76603987-76604037	SAEC	small airway:	n/a
48	chr15:76604340-76604390	HUVEC	blood vessel:	n/a
49	chr15:76603987-76604037	HCF	heart:	n/a
50	chr15:76604113-76604163	SK-N-SH	brain:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76585004..76587553-chr15:76607563..76610231,2	MCF-7	breast:
2	chr15:76584959..76587924-chr15:76602984..76605259,2	K562	blood:
3	chr15:76603407..76604071-chr16:2204657..2205287,2	Hela-S3	cervix:
4	chr15:76602919..76604847-chr15:77361875..77364736,2	K562	blood:
5	chr15:76605423..76608075-chr15:76608528..76612438,4	MCF-7	breast:
6	chr15:76603390..76603920-chr7:104653783..104654640,2	Hela-S3	cervix:
7	chr15:76608689..76611193-chr15:76611835..76613495,2	MCF-7	breast:
8	chr15:76584135..76596152-chr15:76600630..76606670,15	MCF-7	breast:
9	chr15:76604802..76606411-chr15:76677326..76680311,2	MCF-7	breast:
10	chr15:76603349..76604082-chr5:31532161..31532828,2	Hela-S3	cervix:
11	chr15:76603682..76604209-chr22:19419697..19420202,2	HCT-116	colon:
12	chr15:76608047..76610382-chr15:76618699..76620905,3	K562	blood:
13	chr15:76586485..76588241-chr15:76606261..76609045,2	K562	blood:
14	chr15:76603148..76604121-chr2:97001077..97001691,2	Hela-S3	cervix:
15	chr15:76603254..76604196-chr17:34900638..34901493,2	Hela-S3	cervix:
16	chr15:76603879..76604550-chr2:9695486..9696482,2	NB4	blood:
17	chr15:76601310..76610583-chr15:76618699..76634643,40	K562	blood:
18	chr11:46867369..46868150-chr15:76603245..76603939,2	Hela-S3	cervix:
19	chr15:76573073..76575469-chr15:76605288..76607304,2	MCF-7	breast:
20	chr15:76577457..76578224-chr15:76604901..76605413,2	MCF-7	breast:
21	chr15:76603268..76604108-chr17:41465695..41466359,2	Hela-S3	cervix:
22	chr15:76589441..76591088-chr15:76601198..76602843,2	K562	blood:
23	chr15:76605423..76608075-chr15:76608528..76612438,4	MCF-7	breast:
24	chr15:76600511..76607655-chr15:76613791..76629933,32	MCF-7	breast:
25	chr15:76602967..76603663-chr17:61850570..61851532,2	Hela-S3	cervix:
26	chr1:32403461..32404101-chr15:76603301..76604035,2	Hela-S3	cervix:
27	chr15:76605907..76608754-chr15:76611748..76613276,2	K562	blood:
28	chr15:76606947..76607819-chr15:76622249..76623219,2	MCF-7	breast:
29	chr15:76601574..76614388-chr15:76623703..76634730,38	K562	blood:
30	chr15:76582923..76594852-chr15:76601949..76606997,18	MCF-7	breast:
31	chr15:76579019..76580557-chr15:76600815..76603366,2	K562	blood:
32	chr15:76517181..76519721-chr15:76602211..76604425,2	K562	blood:
33	chr15:76602419..76607116-chr15:76626572..76631104,6	MCF-7	breast:
34	chr15:76603369..76604011-chr4:79859804..79860621,2	Hela-S3	cervix:
35	chr15:76603454..76604019-chr16:67969707..67970408,2	Hela-S3	cervix:
36	chr15:76603595..76604138-chr2:54342354..54343006,2	HCT-116	colon:
37	chr15:76601284..76605220-chr15:76605803..76613495,17	K562	blood:
38	chr15:76603305..76604106-chr2:100105951..100106601,2	Hela-S3	cervix:
39	chr15:76586585..76588473-chr15:76607510..76609209,2	MCF-7	breast:
40	chr15:76573739..76576523-chr15:76603684..76605605,3	K562	blood:
41	chr15:76577736..76580355-chr15:76602966..76605157,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ISL2-2	chr15:76606632-76606697	NONHSAT047399
2	lnc-ISL2-2	chr15:76605419-76605558	NONHSAT047399

No data

Variant related genes	Relation type
ETFA	TF binding region
ETFA	CpG island
ENSG00000159556	chromatin interactions
ENSG00000184007	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000247675	chromatin interactions
ENSG00000140391	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000271855	chromatin interactions
ENSG00000005955	chromatin interactions
ENSG00000261884	chromatin interactions
ENSG00000135945	chromatin interactions
ENSG00000140386	chromatin interactions
ENSG00000205220	chromatin interactions
ENSG00000082213	chromatin interactions
ENSG00000198231	chromatin interactions
ENSG00000113360	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000151694	chromatin interactions
ENSG00000185608	chromatin interactions
ENSG00000259514	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000163291	chromatin interactions
ENSG00000121152	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000108588	chromatin interactions
ENSG00000175216	chromatin interactions

Extended variants
information (count: 252 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2404972	chr15:76602212-76602213	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575563523	chr15:76602269-76602270	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs577623473	chr15:76602275-76602276	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs4453439	chr15:76602287-76602288	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs186537305	chr15:76602338-76602339	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs558958295	chr15:76602339-76602340	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs2404971	chr15:76602346-76602347	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369826410	chr15:76602371-76602372	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs2469213	chr15:76602406-76602407	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs372841630	chr15:76602408-76602409	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs71143312	chr15:76602437-76602438	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs191122016	chr15:76602479-76602480	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs574927117	chr15:76602480-76602481	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs11631935	chr15:76602490-76602491	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563640424	chr15:76602502-76602503	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs4359400	chr15:76602538-76602539	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs566995290	chr15:76602563-76602564	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs200680902	chr15:76602577-76602578	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs562338304	chr15:76602593-76602594	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs531704327	chr15:76602594-76602595	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs182867344	chr15:76602609-76602610	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs150922545	chr15:76602614-76602615	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs200222031	chr15:76602620-76602621	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs11631913	chr15:76602624-76602625	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369806215	chr15:76602669-76602670	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs188696706	chr15:76602678-76602679	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs2469576	chr15:76602707-76602708	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs34111559	chr15:76602710-76602711	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs201272249	chr15:76602711-76602712	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs386383520	chr15:76602732-76602733	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs61682617	chr15:76602733-76602734	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs144035645	chr15:76602806-76602807	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs192680717	chr15:76602830-76602831	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs145956327	chr15:76602911-76602912	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs12439484	chr15:76602937-76602938	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs569192440	chr15:76602953-76602954	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs561891615	chr15:76602965-76602966	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs183461950	chr15:76602970-76602971	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs559023010	chr15:76603018-76603019	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs577296159	chr15:76603066-76603067	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs575287252	chr15:76603096-76603097	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs74026428	chr15:76603127-76603128	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs56372945	chr15:76603164-76603165	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs57217518	chr15:76603169-76603170	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs563504508	chr15:76603171-76603172	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs149711306	chr15:76603175-76603176	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs546065708	chr15:76603176-76603177	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs563772774	chr15:76603177-76603178	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs533326222	chr15:76603179-76603180	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs370945290	chr15:76603239-76603240	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 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
small cell lung cancer	20016488	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
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76558000-76603000	Weak transcription	Aorta	Aorta
2	chr15:76576200-76602800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:76584600-76602400	Weak transcription	Primary B cells from cord blood	blood
4	chr15:76585200-76602400	Weak transcription	Primary T cells from cord blood	blood
5	chr15:76586200-76602400	Weak transcription	NH-A	brain
6	chr15:76586400-76602400	Weak transcription	Brain Hippocampus Middle	brain
7	chr15:76592600-76602400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr15:76593400-76602400	Weak transcription	Lung	lung
9	chr15:76593400-76602600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr15:76597000-76602600	Weak transcription	Fetal Intestine Small	intestine
11	chr15:76599400-76602800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr15:76599800-76602400	Weak transcription	Fetal Brain Female	brain
13	chr15:76600800-76602800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr15:76601000-76602800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr15:76601200-76602600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr15:76601200-76602800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr15:76601400-76602400	Enhancers	Right Atrium	heart
18	chr15:76601400-76602800	Enhancers	Placenta	Placenta
19	chr15:76601600-76603000	Weak transcription	Gastric	stomach
20	chr15:76601800-76602400	Active TSS	GM12878-XiMat	blood
21	chr15:76601800-76602400	Enhancers	HUVEC	blood vessel
22	chr15:76601800-76602400	Enhancers	NHDF-Ad	bronchial
23	chr15:76601800-76602600	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr15:76601800-76602800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr15:76601800-76602800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr15:76601800-76602800	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr15:76601800-76602800	Flanking Active TSS	HepG2	liver
28	chr15:76601800-76603000	Flanking Active TSS	Hela-S3	cervix
29	chr15:76602000-76602400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr15:76602000-76602400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr15:76602000-76602400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr15:76602000-76602400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr15:76602000-76602400	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr15:76602000-76602400	Enhancers	Fetal Intestine Large	intestine
35	chr15:76602000-76602400	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr15:76602000-76602400	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr15:76602000-76602400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr15:76602000-76602400	Enhancers	HSMM	muscle
39	chr15:76602000-76602400	Enhancers	Osteobl	bone
40	chr15:76602000-76602600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr15:76602000-76602600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:76602000-76602600	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr15:76602000-76602600	Enhancers	Fetal Brain Male	brain
44	chr15:76602000-76602600	Enhancers	Fetal Lung	lung
45	chr15:76602000-76602600	Enhancers	Right Ventricle	heart
46	chr15:76602000-76602600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr15:76602000-76602800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr15:76602000-76602800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr15:76602000-76602800	Enhancers	Primary B cells from peripheral blood	blood
50	chr15:76602000-76602800	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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