Variant report

Variant	esv1806743
Chromosome Location	chr3:159723529-159744022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:159734744-159735049	HepG2	liver:	n/a	n/a
2	ATF2	chr3:159729767-159730313	GM12878	blood:	n/a	n/a
3	ATF2	chr3:159729781-159730314	GM12878	blood:	n/a	n/a
4	BACH1	chr3:159729272-159729283	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:159729912-159730123	GM12878	blood:	n/a	n/a
6	BATF	chr3:159728368-159728655	GM12878	blood:	n/a	n/a
7	BATF	chr3:159728310-159728734	GM12878	blood:	n/a	n/a
8	BATF	chr3:159729908-159730310	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:159728419-159728675	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:159729843-159730281	GM12878	blood:	n/a	chr3:159730049-159730058
11	BCL11A	chr3:159729912-159730274	GM12878	blood:	n/a	chr3:159730049-159730058
12	BCL3	chr3:159729862-159730261	GM12878	blood:	n/a	chr3:159730049-159730058
13	BCLAF1	chr3:159729793-159730278	GM12878	blood:	n/a	chr3:159730049-159730058
14	BCLAF1	chr3:159728278-159728792	GM12878	blood:	n/a	chr3:159728695-159728704
15	BCLAF1	chr3:159728358-159728748	GM12878	blood:	n/a	chr3:159728695-159728704
16	BCLAF1	chr3:159729804-159730250	GM12878	blood:	n/a	chr3:159730049-159730058
17	BHLHE40	chr3:159729679-159730746	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:159724346-159724675	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:159728368-159728759	GM12878	blood:	n/a	n/a
20	BRCA1	chr3:159730220-159730379	GM12878	blood:	n/a	n/a
21	CEBPB	chr3:159726803-159727056	IMR90	lung:	n/a	chr3:159726904-159726915
22	CEBPB	chr3:159726769-159727029	H1-hESC	embryonic stem cell:	n/a	chr3:159726904-159726915
23	CEBPB	chr3:159726785-159727080	A549	lung:	n/a	chr3:159726904-159726915
24	CEBPB	chr3:159726765-159727049	K562	blood:	n/a	chr3:159726904-159726915
25	CEBPB	chr3:159726749-159727092	Hela-S3	cervix:	n/a	chr3:159726904-159726915
26	CEBPB	chr3:159726791-159727096	MCF-7	breast:	n/a	chr3:159726904-159726915
27	CEBPB	chr3:159726798-159726961	K562	blood:	n/a	chr3:159726904-159726915
28	CEBPB	chr3:159726762-159727076	HepG2	liver:	n/a	chr3:159726904-159726915
29	CEBPB	chr3:159726785-159726999	K562	blood:	n/a	chr3:159726904-159726915
30	CEBPB	chr3:159734746-159735090	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:159734616-159735150	MCF-7	breast:	n/a	n/a
32	CHD1	chr3:159729890-159730483	GM12878	blood:	n/a	n/a
33	CHD2	chr3:159734813-159735060	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr3:159737723-159737923	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr3:159729901-159730629	GM12878	blood:	n/a	n/a
36	CTCF	chr3:159726840-159726990	GM12874	blood:	n/a	n/a
37	CTCF	chr3:159724237-159724755	T-47D	breast:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
38	CTCF	chr3:159724363-159724651	Gliobla	brain:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
39	CTCF	chr3:159724420-159724570	GM12875	blood:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
40	CTCF	chr3:159724384-159724626	Fibrobl	skin:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
41	CTCF	chr3:159726919-159726991	GM12878	blood:	n/a	n/a
42	CTCF	chr3:159724460-159724610	GM12875	blood:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
43	CTCF	chr3:159724380-159724627	NHEK	skin:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
44	CTCF	chr3:159724379-159724634	A549	lung:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
45	CTCF	chr3:159724440-159724590	AG09309	skin:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
46	CTCF	chr3:159724760-159724910	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr3:159724440-159724590	GM12865	blood:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
48	CTCF	chr3:159724395-159724634	ProgFib	skin:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
49	CTCF	chr3:159724337-159724620	A549	lung:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520
50	CTCF	chr3:159724480-159724630	GM12873	blood:	n/a	chr3:159724507-159724525 chr3:159724502-159724523 chr3:159724508-159724524 chr3:159724512-159724520

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:159733028-159733078	HCT-116	colon:	n/a
2	chr3:159733028-159733078	Jurkat	blood:	n/a
3	chr3:159733028-159733078	K562	blood:	n/a
4	chr3:159733028-159733078	PFSK-1	brain:	n/a
5	chr3:159733028-159733078	U87	brain:	n/a
6	chr3:159733028-159733078	BE2_C	brain:	n/a
7	chr3:159733028-159733078	HMEC	breast:	n/a
8	chr3:159733028-159733078	AoSMC	blood vessel:	n/a
9	chr3:159733028-159733078	HRE	kidney:	n/a
10	chr3:159733028-159733078	LNCaP	prostate:	n/a
11	chr3:159733028-159733078	AG04450	lung:	fetal
12	chr3:159733028-159733078	PANC-1	pancreas:	n/a
13	chr3:159733028-159733078	CMK	blood:	n/a
14	chr3:159733028-159733078	AG04449	skin:	fetal
15	chr3:159733028-159733078	MCF10A-Er-Src	breast:	n/a
16	chr3:159733028-159733078	MCF-7	breast:	n/a
17	chr3:159733028-159733078	SK-N-SH	brain:	n/a
18	chr3:159733028-159733078	HEK293	kidney:	embryo
19	chr3:159733028-159733078	NT2-D1	testis:	n/a
20	chr3:159733028-159733078	PrEC	prostate:	n/a
21	chr3:159733028-159733078	A549	lung:	n/a
22	chr3:159733028-159733078	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:159733028-159733078	NHDF-neo	bronchial:	n/a
24	chr3:159733028-159733078	NB4	blood:	n/a
25	chr3:159733028-159733078	HepG2	liver:	n/a
26	chr3:159733028-159733078	Hela-S3	cervix:	n/a
27	chr3:159733028-159733078	Caco-2	colon:	n/a
28	chr3:159733028-159733078	AG09319	gingival:	n/a
29	chr3:159733028-159733078	H1-hESC	embryonic stem cell:	embryo
30	chr3:159733028-159733078	HCPEpiC	choroid plexus:	n/a
31	chr3:159733028-159733078	GM12878	blood:	n/a
32	chr3:159733028-159733078	HNPCEpiC	eye:	n/a
33	chr3:159733028-159733078	GM19239	blood:	n/a
34	chr3:159733028-159733078	AG10803	skin:	n/a
35	chr3:159733028-159733078	BJ	skin:	n/a
36	chr3:159733028-159733078	HRPEpiC	eye:	n/a
37	chr3:159733028-159733078	SK-N-SH_RA	brain:	n/a
38	chr3:159733028-159733078	HRCEpiC	kidney:	n/a
39	chr3:159733028-159733078	NHBE	bronchial:	n/a
40	chr3:159733028-159733078	GM12892	blood:	n/a
41	chr3:159733028-159733078	NH-A	brain:	n/a
42	chr3:159733028-159733078	ECC-1	luminal epithelium:	n/a
43	chr3:159733028-159733078	T-47D	breast:	n/a
44	chr3:159733028-159733078	IMR90	lung:	fetal
45	chr3:159733028-159733078	AG09309	skin:	n/a
46	chr3:159733028-159733078	HAEpiC	amniotic membrane:	n/a
47	chr3:159733028-159733078	ovcar-3	ovarian:	n/a
48	chr3:159733028-159733078	HIPEpiC	eye:	n/a
49	chr3:159733028-159733078	RPTEC	kidney:	n/a
50	chr3:159733028-159733078	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:159647093..159647612-chr3:159724029..159724614,3	MCF-7	breast:
2	chr3:159546031..159546605-chr3:159724021..159724764,2	MCF-7	breast:
3	chr3:159743386..159744098-chr6:75327633..75328501,2	MCF-7	breast:
4	chr17:56967806..56968586-chr3:159738097..159738880,2	MCF-7	breast:
5	chr3:159733046..159734657-chr3:159735907..159738119,2	K562	blood:
6	chr3:159647281..159647881-chr3:159724273..159724824,2	MCF-7	breast:
7	chr3:159602722..159603235-chr3:159724067..159724970,2	MCF-7	breast:
8	chr3:159602350..159603648-chr3:159724014..159724862,4	MCF-7	breast:
9	chr3:159535836..159536605-chr3:159726358..159726912,2	MCF-7	breast:
10	chr3:159739668..159742959-chr3:159743211..159746773,4	MCF-7	breast:
11	chr3:159479933..159482326-chr3:159723100..159725647,2	MCF-7	breast:
12	chr3:159602300..159603246-chr3:159724184..159724957,3	K562	blood:
13	chr3:159545989..159547250-chr3:159724070..159724936,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-432B6.3.1-1	chr3:159733483-159733648	NONHSAT092972
2	lnc-RP11-432B6.3.1-1	chr3:159729253-159729338	ENSG00000244040
3	lnc-RP11-432B6.3.1-1	chr3:159743257-159743321	NR_108088
4	lnc-RP11-432B6.3.1-1	chr3:159726899-159727044	ENSG00000244040
5	lnc-RP11-432B6.3.1-1	chr3:159729452-159729897	ENSG00000244040
6	lnc-RP11-432B6.3.1-1	chr3:159726899-159727044	NR_108088
7	lnc-RP11-432B6.3.1-1	chr3:159726899-159727044	ENSG00000244040
8	lnc-CTD-2049J23.3.1-1	chr3:159738436-159738531	NR_104132
9	lnc-RP11-432B6.3.1-1	chr3:159733483-159733648	ENSG00000244040
10	lnc-CTD-2049J23.3.1-2	chr3:159728598-159728808	ucExp_134_+
11	lnc-RP11-432B6.3.1-1	chr3:159743257-159743321	ENSG00000244040
12	lnc-RP11-432B6.3.1-4	chr3:159728598-159728808	ucExp_134_-
13	lnc-RP11-432B6.3.1-1	chr3:159725569-159725662	NR_108088
14	lnc-RP11-432B6.3.1-1	chr3:159725569-159725662	ENSG00000244040

Variant related genes	Relation type
IL12A-AS1	TF binding region
LINC01100	TF binding region
IL12A-AS1	CpG island
LINC01100	CpG island
ENSG00000250588	chromatin interactions
ENSG00000244040	chromatin interactions
ENSG00000242107	chromatin interactions
EZH2	miRNA target sites
RNF160	miRNA target sites
G3BP1	miRNA target sites
FHIT	miRNA target sites

Extended variants
information (count: 1020 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9812995	chr3:159723529-159723530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549096390	chr3:159723534-159723535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140515180	chr3:159723539-159723540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531249582	chr3:159723617-159723618	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550851230	chr3:159723665-159723666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181872068	chr3:159723702-159723703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539767398	chr3:159723726-159723727	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558036552	chr3:159723727-159723728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186543993	chr3:159723776-159723777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530961099	chr3:159723787-159723788	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs9830969	chr3:159723788-159723789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs189880781	chr3:159723805-159723806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112591072	chr3:159723813-159723814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573944200	chr3:159723887-159723888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs4679867	chr3:159723903-159723904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs534685394	chr3:159723921-159723922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs9872678	chr3:159723926-159723927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs577977444	chr3:159723942-159723943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545337562	chr3:159723950-159723951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181146865	chr3:159723972-159723973	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs9873090	chr3:159723988-159723989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs150422594	chr3:159724000-159724001	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148136078	chr3:159724044-159724045	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs199528177	chr3:159724047-159724048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113398335	chr3:159724048-159724049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549016421	chr3:159724052-159724053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs398062967	chr3:159724063-159724064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561077740	chr3:159724067-159724068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575493004	chr3:159724075-159724076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560427835	chr3:159724142-159724143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs4679868	chr3:159724154-159724155	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs377246080	chr3:159724203-159724204	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185160961	chr3:159724228-159724229	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138264915	chr3:159724240-159724241	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554324933	chr3:159724245-159724246	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552082491	chr3:159724259-159724260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs9835467	chr3:159724260-159724261	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs541097644	chr3:159724261-159724262	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189621253	chr3:159724262-159724263	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181982041	chr3:159724279-159724280	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567716692	chr3:159724305-159724306	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs538362910	chr3:159724371-159724372	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375506487	chr3:159724420-159724421	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556561360	chr3:159724452-159724453	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs578095444	chr3:159724490-159724491	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs632105	chr3:159724491-159724492	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554080094	chr3:159724503-159724504	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572135912	chr3:159724539-159724540	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs142754456	chr3:159724547-159724548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145570590	chr3:159724552-159724553	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Effusion lymphoma	18079361	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:159707200-159724200	Weak transcription	Psoas Muscle	Psoas
2	chr3:159709800-159723800	Weak transcription	Fetal Muscle Leg	muscle
3	chr3:159711600-159724200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr3:159712000-159729600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr3:159713000-159734800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:159719800-159724200	Weak transcription	Brain Anterior Caudate	brain
7	chr3:159720000-159724200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:159720000-159724200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:159720200-159723800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr3:159720200-159724200	Weak transcription	Brain Hippocampus Middle	brain
11	chr3:159720800-159724000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr3:159721000-159724200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:159721000-159730000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr3:159721400-159724200	Weak transcription	Osteobl	bone
15	chr3:159721800-159724200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr3:159721800-159724200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr3:159722000-159724000	Weak transcription	NHLF	lung
18	chr3:159722200-159723600	Weak transcription	NHDF-Ad	bronchial
19	chr3:159722800-159725000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:159722800-159725000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:159723400-159724800	Enhancers	GM12878-XiMat	blood
22	chr3:159723600-159724800	Enhancers	NHDF-Ad	bronchial
23	chr3:159723800-159724600	Enhancers	Fetal Muscle Leg	muscle
24	chr3:159723800-159724800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr3:159724000-159724400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:159724000-159724400	Enhancers	Stomach Smooth Muscle	stomach
27	chr3:159724000-159724400	Enhancers	A549	lung
28	chr3:159724000-159725000	Enhancers	NHLF	lung
29	chr3:159724200-159724400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr3:159724200-159724400	Enhancers	Brain Cingulate Gyrus	brain
31	chr3:159724200-159724400	Enhancers	Brain Hippocampus Middle	brain
32	chr3:159724200-159724400	Enhancers	Fetal Kidney	kidney
33	chr3:159724200-159724400	Enhancers	Psoas Muscle	Psoas
34	chr3:159724200-159724600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr3:159724200-159724600	Enhancers	Primary B cells from peripheral blood	blood
36	chr3:159724200-159724600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:159724200-159724600	Enhancers	Brain Anterior Caudate	brain
38	chr3:159724200-159724600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr3:159724200-159724600	Enhancers	Rectal Smooth Muscle	rectum
40	chr3:159724200-159724800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:159724200-159724800	Enhancers	Osteobl	bone
42	chr3:159724600-159726000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:159724600-159726600	Weak transcription	Primary B cells from peripheral blood	blood
44	chr3:159724800-159726800	Weak transcription	GM12878-XiMat	blood
45	chr3:159724800-159729800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr3:159724800-159729800	Weak transcription	Osteobl	bone
47	chr3:159725000-159728600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:159725000-159729000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:159726600-159731000	Enhancers	Primary B cells from peripheral blood	blood
50	chr3:159726800-159727000	Enhancers	GM12878-XiMat	blood

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