Variant report

Variant	nsv1041239
Chromosome Location	chr15:56888945-56959028
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:158)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:56900264-56900669	GM12878	blood:	n/a	n/a
2	ATF2	chr15:56900197-56900791	GM12878	blood:	n/a	n/a
3	BACH1	chr15:56908848-56908851	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr15:56900317-56900711	GM12878	blood:	n/a	n/a
5	BCLAF1	chr15:56900222-56900787	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:56900236-56900673	GM12878	blood:	n/a	n/a
7	BHLHE40	chr15:56946995-56947086	K562	blood:	n/a	n/a
8	CEBPB	chr15:56946053-56946341	HepG2	liver:	n/a	n/a
9	CEBPB	chr15:56916596-56916623	HepG2	liver:	n/a	n/a
10	CEBPB	chr15:56932384-56932708	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr15:56933840-56933990	HRE	kidney:	n/a	n/a
12	CTCF	chr15:56921144-56921370	K562	blood:	n/a	n/a
13	CTCF	chr15:56908788-56908841	LNCaP	prostate:	n/a	n/a
14	CTCF	chr15:56921197-56921383	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr15:56921220-56921345	K562	blood:	n/a	n/a
16	CTCF	chr15:56908697-56908947	GM12878	blood:	n/a	n/a
17	CTCF	chr15:56909072-56909139	MCF-7	breast:	n/a	n/a
18	CTCF	chr15:56908775-56908837	GM10248	blood:	n/a	n/a
19	CTCF	chr15:56921248-56921333	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr15:56921140-56921408	GM12878	blood:	n/a	n/a
21	CTCF	chr15:56909048-56909119	MCF-7	breast:	n/a	n/a
22	CTCF	chr15:56908600-56908750	AG09319	gingival:	n/a	n/a
23	CTCF	chr15:56935384-56935436	LNCaP	prostate:	n/a	n/a
24	CUX1	chr15:56935576-56935616	GM12878	blood:	n/a	n/a
25	CUX1	chr15:56892760-56892896	K562	blood:	n/a	n/a
26	CUX1	chr15:56924071-56924103	K562	blood:	n/a	n/a
27	E2F4	chr15:56891359-56891411	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr15:56907822-56907848	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr15:56908296-56908404	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr15:56900345-56900635	GM12878	blood:	n/a	n/a
31	EBF1	chr15:56900285-56900632	GM12878	blood:	n/a	n/a
32	EGR1	chr15:56946892-56947122	K562	blood:	n/a	n/a
33	EGR1	chr15:56946915-56947096	K562	blood:	n/a	n/a
34	EP300	chr15:56891389-56891443	Hela-S3	cervix:	n/a	n/a
35	EP300	chr15:56900353-56900810	GM12878	blood:	n/a	n/a
36	EP300	chr15:56891200-56891475	SK-N-SH_RA	brain:	n/a	n/a
37	FAM48A	chr15:56894862-56894955	GM12878	blood:	n/a	n/a
38	FOS	chr15:56891249-56891648	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr15:56893089-56893151	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr15:56933258-56933480	MCF10A-Er-Src	breast:	n/a	chr15:56933317-56933326 chr15:56933316-56933327 chr15:56933321-56933328
41	FOS	chr15:56891237-56891703	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr15:56891244-56891883	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr15:56891237-56891625	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr15:56891306-56891643	HUVEC	blood vessel:	n/a	n/a
45	FOSL1	chr15:56891268-56891829	HCT-116	colon:	n/a	n/a
46	FOSL1	chr15:56891287-56891710	HCT-116	colon:	n/a	n/a
47	FOSL2	chr15:56891197-56891712	SK-N-SH	brain:	n/a	n/a
48	FOXA1	chr15:56950904-56951325	HepG2	liver:	n/a	n/a
49	FOXA1	chr15:56945948-56946441	HepG2	liver:	n/a	n/a
50	FOXA1	chr15:56946065-56946331	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56923479-56923529	GM12891	blood:	n/a
2	chr15:56923479-56923529	Caco-2	colon:	n/a
3	chr15:56923479-56923529	HEK293	kidney:	embryo
4	chr15:56923479-56923529	BJ	skin:	n/a
5	chr15:56923479-56923529	H1-hESC	embryonic stem cell:	embryo
6	chr15:56923479-56923529	LNCaP	prostate:	n/a
7	chr15:56923479-56923529	AG09309	skin:	n/a
8	chr15:56923479-56923529	NT2-D1	testis:	n/a
9	chr15:56923479-56923529	MCF10A-Er-Src	breast:	n/a
10	chr15:56923479-56923529	K562	blood:	n/a
11	chr15:56923479-56923529	NHBE	bronchial:	n/a
12	chr15:56923479-56923529	AoSMC	blood vessel:	n/a
13	chr15:56923479-56923529	T-47D	breast:	n/a
14	chr15:56923479-56923529	HRCEpiC	kidney:	n/a
15	chr15:56923479-56923529	IMR90	lung:	fetal
16	chr15:56923479-56923529	ECC-1	luminal epithelium:	n/a
17	chr15:56923479-56923529	HepG2	liver:	n/a
18	chr15:56923479-56923529	PrEC	prostate:	n/a
19	chr15:56923479-56923529	Hepatocyte	liver:	n/a
20	chr15:56923479-56923529	HEEpiC	esophagus:	n/a
21	chr15:56923479-56923529	HRPEpiC	eye:	n/a
22	chr15:56923479-56923529	HL-60	blood:	n/a
23	chr15:56923479-56923529	CMK	blood:	n/a
24	chr15:56923479-56923529	GM06990	blood:	n/a
25	chr15:56923479-56923529	PFSK-1	brain:	n/a
26	chr15:56923479-56923529	HNPCEpiC	eye:	n/a
27	chr15:56923479-56923529	HCF	heart:	n/a
28	chr15:56923479-56923529	MCF-7	breast:	n/a
29	chr15:56923479-56923529	AG04449	skin:	fetal
30	chr15:56923479-56923529	AG09319	gingival:	n/a
31	chr15:56923479-56923529	HIPEpiC	eye:	n/a
32	chr15:56923479-56923529	SK-N-SH_RA	brain:	n/a
33	chr15:56923479-56923529	BE2_C	brain:	n/a
34	chr15:56923479-56923529	GM12892	blood:	n/a
35	chr15:56923479-56923529	HAEpiC	amniotic membrane:	n/a
36	chr15:56923479-56923529	RPTEC	kidney:	n/a
37	chr15:56923479-56923529	Jurkat	blood:	n/a
38	chr15:56923479-56923529	SK-N-SH	brain:	n/a
39	chr15:56923479-56923529	GM12878	blood:	n/a
40	chr15:56923479-56923529	AG04450	lung:	fetal
41	chr15:56923479-56923529	AG10803	skin:	n/a
42	chr15:56923479-56923529	NB4	blood:	n/a
43	chr15:56923479-56923529	SKMC	muscle:	n/a
44	chr15:56923479-56923529	SAEC	small airway:	n/a
45	chr15:56923479-56923529	A549	lung:	n/a
46	chr15:56923479-56923529	NHDF-neo	bronchial:	n/a
47	chr15:56923479-56923529	NH-A	brain:	n/a
48	chr15:56923479-56923529	HCM	heart:	n/a
49	chr15:56923479-56923529	HRE	kidney:	n/a
50	chr15:56923479-56923529	PANC-1	pancreas:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:56941469..56943410-chr15:56946852..56948408,2	MCF-7	breast:
2	chr15:56954012..56957476-chr15:56973562..56976021,3	MCF-7	breast:
3	chr15:56952424..56953252-chr8:43092410..43092931,2	MCF-7	breast:
4	chr15:56957841..56960348-chr15:57024412..57027356,2	MCF-7	breast:
5	chr15:56917635..56921427-chr15:56927858..56931559,3	K562	blood:
6	chr15:56932749..56935204-chr15:56940606..56943085,2	MCF-7	breast:
7	chr15:56951029..56951802-chr19:41309134..41309780,2	NB4	blood:
8	chr15:56947710..56949371-chr15:56958566..56961070,2	K562	blood:
9	chr15:56911097..56913730-chr15:56923254..56925300,2	K562	blood:
10	chr15:56947710..56949371-chr15:56958566..56961070,2	K562	blood:
11	chr15:56911097..56913730-chr15:56923254..56925300,2	K562	blood:
12	chr15:56932749..56935204-chr15:56940606..56943085,2	MCF-7	breast:
13	chr15:56946938..56949698-chr15:56952748..56954656,3	MCF-7	breast:
14	chr15:56941469..56943410-chr15:56946852..56948408,2	MCF-7	breast:
15	chr15:56932815..56934902-chr15:56936012..56938513,4	K562	blood:
16	chr15:56946938..56949698-chr15:56952748..56954656,3	MCF-7	breast:
17	chr15:56930177..56932664-chr15:57118499..57120960,2	K562	blood:
18	chr15:56933111..56934804-chr15:56936509..56938281,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MNS1-5	chr15:56935150-56935195	NONHSAT044026
2	lnc-MNS1-5	chr15:56924041-56924320	NONHSAT044026
3	lnc-ZNF280D-1	chr15:56896038-56896069	ENSG00000260392.1
4	lnc-TEX9-3	chr15:56938928-56939226	expReg_chr15_3592_+
5	lnc-TEX9-4	chr15:56940274-56941388	ucscGeneNc_uc002afm_2
6	lnc-ZNF280D-1	chr15:56897574-56897681	ENSG00000260392.1
7	lnc-MNS1-5	chr15:56927373-56927448	NONHSAT044027
8	lnc-ZNF280D-1	chr15:56921713-56921790	ENSG00000260392.1
9	lnc-ZNF280D-1	chr15:56921002-56921089	ENSG00000260392.1
10	lnc-MNS1-5	chr15:56927393-56927448	NONHSAT044026
11	lnc-MNS1-5	chr15:56937333-56937537	NONHSAT044026
12	lnc-MNS1-5	chr15:56935150-56935342	NONHSAT044027
13	lnc-ZNF280D-1	chr15:56921584-56921598	ENSG00000260392.1
14	lnc-ZNF280D-1	chr15:56921002-56921089	ENSG00000260392.1
15	lnc-ZNF280D-1	chr15:56921713-56921763	ENSG00000260392.1

No data

Variant related genes	Relation type
ZNF280D	TF binding region
ENSG00000260392	TF binding region
ZNF280D	CpG island
ENSG00000260392	CpG island
ENSG00000137871	chromatin interactions

Extended variants
information (count: 2524 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2524 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372884006	chr15:56888948-56888949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79449834	chr15:56888995-56888996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147076223	chr15:56889030-56889031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577910864	chr15:56889032-56889033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540576479	chr15:56889091-56889092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554678187	chr15:56889132-56889133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576185303	chr15:56889134-56889135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560465858	chr15:56889158-56889159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573954419	chr15:56889279-56889280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377276999	chr15:56889290-56889291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542256417	chr15:56889304-56889305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562096660	chr15:56889310-56889311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2128175	chr15:56889321-56889322	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs551050590	chr15:56889400-56889401	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs138484295	chr15:56889422-56889423	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs374174354	chr15:56889485-56889486	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs372548100	chr15:56889570-56889571	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs80189038	chr15:56889578-56889579	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs79665443	chr15:56889579-56889580	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs546745342	chr15:56889586-56889587	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs566847944	chr15:56889587-56889588	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs535715675	chr15:56889602-56889603	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs149216194	chr15:56889609-56889610	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs568816102	chr15:56889637-56889638	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs28409651	chr15:56889663-56889664	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs557827392	chr15:56889679-56889680	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs577763191	chr15:56889705-56889706	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs547524889	chr15:56889749-56889750	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs533997133	chr15:56889783-56889784	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs553972784	chr15:56889786-56889787	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs74016538	chr15:56889791-56889792	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs561048820	chr15:56889796-56889797	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs529965838	chr15:56889806-56889807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555523554	chr15:56889810-56889811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575585259	chr15:56889829-56889830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60541074	chr15:56889884-56889885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2128174	chr15:56889952-56889953	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs564609270	chr15:56889965-56889966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569760937	chr15:56889992-56889993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538637690	chr15:56890008-56890009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200535754	chr15:56890021-56890022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372841674	chr15:56890047-56890048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141648949	chr15:56890080-56890081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560299582	chr15:56890093-56890094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529573294	chr15:56890104-56890105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs67546549	chr15:56890105-56890106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201218036	chr15:56890106-56890107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112911254	chr15:56890107-56890108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs57650049	chr15:56890122-56890123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549650428	chr15:56890131-56890132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Colorectal cancer	16774939	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
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Glioblastoma multiforme	21510904	CNVD
Pancreatic cancer	17952125	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56881800-56891600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr15:56884200-56892000	Weak transcription	Thymus	Thymus
3	chr15:56884400-56889400	Weak transcription	Fetal Thymus	thymus
4	chr15:56889400-56889800	ZNF genes & repeats	Fetal Thymus	thymus
5	chr15:56889600-56890000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr15:56889800-56893200	Weak transcription	Fetal Thymus	thymus
7	chr15:56890800-56892200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr15:56891400-56892200	Enhancers	Osteobl	bone
9	chr15:56891600-56891800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr15:56891600-56892000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr15:56891600-56892400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr15:56891600-56892600	Enhancers	HSMM	muscle
13	chr15:56891600-56892600	Enhancers	NHLF	lung
14	chr15:56892200-56892400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr15:56893200-56893600	ZNF genes & repeats	Fetal Thymus	thymus
16	chr15:56893600-56894200	Weak transcription	Fetal Thymus	thymus
17	chr15:56894200-56894800	Strong transcription	Fetal Thymus	thymus
18	chr15:56894800-56895200	Weak transcription	Fetal Thymus	thymus
19	chr15:56895200-56895800	Strong transcription	Fetal Thymus	thymus
20	chr15:56895800-56897800	Weak transcription	Fetal Thymus	thymus
21	chr15:56896400-56900200	Weak transcription	HSMMtube	muscle
22	chr15:56897800-56898800	ZNF genes & repeats	Fetal Thymus	thymus
23	chr15:56898400-56898600	Enhancers	Primary B cells from peripheral blood	blood
24	chr15:56898400-56900200	Enhancers	Dnd41	blood
25	chr15:56898400-56902200	Enhancers	Primary B cells from cord blood	blood
26	chr15:56898600-56899800	Weak transcription	Primary B cells from peripheral blood	blood
27	chr15:56898800-56899600	Weak transcription	Fetal Thymus	thymus
28	chr15:56899200-56899600	Enhancers	GM12878-XiMat	blood
29	chr15:56899600-56901400	Flanking Active TSS	GM12878-XiMat	blood
30	chr15:56899600-56902000	Enhancers	Fetal Thymus	thymus
31	chr15:56899800-56901800	Enhancers	Primary B cells from peripheral blood	blood
32	chr15:56899800-56901800	Enhancers	Thymus	Thymus
33	chr15:56900000-56900600	Enhancers	HSMM	muscle
34	chr15:56900200-56900400	Flanking Active TSS	Dnd41	blood
35	chr15:56900200-56901600	Enhancers	HSMMtube	muscle
36	chr15:56900400-56900600	Enhancers	Dnd41	blood
37	chr15:56900600-56900800	Flanking Active TSS	Dnd41	blood
38	chr15:56900800-56902600	Enhancers	Dnd41	blood
39	chr15:56901200-56901400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:56901400-56901800	Enhancers	GM12878-XiMat	blood
41	chr15:56901600-56901800	Weak transcription	HSMMtube	muscle
42	chr15:56901800-56905800	Weak transcription	Thymus	Thymus
43	chr15:56902000-56902400	Weak transcription	Fetal Thymus	thymus
44	chr15:56902400-56902600	Enhancers	Fetal Thymus	thymus
45	chr15:56902600-56903800	Weak transcription	Fetal Thymus	thymus
46	chr15:56902600-56904600	Weak transcription	Dnd41	blood
47	chr15:56902800-56945400	Weak transcription	Right Ventricle	heart
48	chr15:56903800-56907800	Enhancers	Fetal Thymus	thymus
49	chr15:56904600-56905800	Enhancers	Dnd41	blood
50	chr15:56905600-56923600	Weak transcription	Left Ventricle	heart

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