Variant report

Variant	nsv528991
Chromosome Location	chr1:92191534-92198162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:396)
CpG islands
(count:124)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92191604-92191892	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92197761-92198425	K562	blood:	n/a	n/a
3	ARID3A	chr1:92196941-92197327	K562	blood:	n/a	chr1:92197183-92197199
4	ATF1	chr1:92197884-92198458	K562	blood:	n/a	n/a
5	ATF1	chr1:92196313-92196636	K562	blood:	n/a	n/a
6	ATF3	chr1:92198028-92198372	K562	blood:	n/a	n/a
7	ATF3	chr1:92196237-92196599	K562	blood:	n/a	n/a
8	ATF3	chr1:92197931-92198501	K562	blood:	n/a	n/a
9	BACH1	chr1:92197491-92198200	K562	blood:	n/a	n/a
10	BCL3	chr1:92197333-92197701	GM12878	blood:	n/a	chr1:92197586-92197595
11	BCL3	chr1:92197434-92197789	A549	lung:	n/a	chr1:92197586-92197595
12	BCL3	chr1:92197385-92197844	A549	lung:	n/a	chr1:92197586-92197595
13	BHLHE40	chr1:92195148-92195280	K562	blood:	n/a	n/a
14	BHLHE40	chr1:92196306-92198601	K562	blood:	n/a	n/a
15	CBX3	chr1:92197685-92198551	K562	blood:	n/a	n/a
16	CBX3	chr1:92197993-92198468	K562	blood:	n/a	n/a
17	CBX3	chr1:92196661-92197390	K562	blood:	n/a	n/a
18	CCNT2	chr1:92197667-92198452	K562	blood:	n/a	n/a
19	CCNT2	chr1:92193228-92193638	K562	blood:	n/a	n/a
20	CEBPB	chr1:92196384-92196617	K562	blood:	n/a	n/a
21	CEBPB	chr1:92191429-92191940	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:92196229-92196716	K562	blood:	n/a	n/a
23	CEBPB	chr1:92196284-92196984	IMR90	lung:	n/a	chr1:92196831-92196844
24	CEBPB	chr1:92197997-92198417	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:92196321-92196644	A549	lung:	n/a	n/a
26	CEBPB	chr1:92196296-92197209	K562	blood:	n/a	chr1:92196831-92196844
27	CEBPB	chr1:92197909-92198441	K562	blood:	n/a	n/a
28	CEBPB	chr1:92196245-92196873	Hela-S3	cervix:	n/a	chr1:92196831-92196844
29	CEBPB	chr1:92196394-92196592	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:92197876-92198358	K562	blood:	n/a	n/a
31	CEBPB	chr1:92196235-92196716	A549	lung:	n/a	n/a
32	CEBPD	chr1:92197853-92198443	K562	blood:	n/a	n/a
33	CHD2	chr1:92197960-92198520	K562	blood:	n/a	n/a
34	CHD2	chr1:92197994-92198496	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr1:92196763-92197187	K562	blood:	n/a	n/a
36	CHD2	chr1:92196407-92196674	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr1:92197662-92198499	K562	blood:	n/a	n/a
38	CTCF	chr1:92194624-92194703	Fibrobl	skin:	n/a	n/a
39	CTCF	chr1:92195681-92195755	K562	blood:	n/a	n/a
40	CTCF	chr1:92193748-92193835	K562	blood:	n/a	n/a
41	CTCF	chr1:92191440-92191590	AG04450	lung:	n/a	n/a
42	CUX1	chr1:92196507-92196528	K562	blood:	n/a	n/a
43	CUX1	chr1:92197711-92198449	K562	blood:	n/a	n/a
44	CUX1	chr1:92197827-92197915	GM12878	blood:	n/a	n/a
45	CUX1	chr1:92196918-92197110	K562	blood:	n/a	n/a
46	E2F4	chr1:92197426-92197643	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:92196316-92196712	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F6	chr1:92198030-92198437	K562	blood:	n/a	n/a
49	E2F6	chr1:92197812-92198499	K562	blood:	n/a	n/a
50	E2F6	chr1:92196386-92196601	K562	blood:	n/a	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92191625-92191675	SAEC	small airway:	n/a
2	chr1:92191625-92191675	NHDF-neo	bronchial:	n/a
3	chr1:92191625-92191675	SAEC	small airway:	n/a
4	chr1:92191625-92191675	NHDF-neo	bronchial:	n/a
5	chr1:92197531-92197581	HIPEpiC	eye:	n/a
6	chr1:92191625-92191675	HIPEpiC	eye:	n/a
7	chr1:92197531-92197581	HUVEC	blood vessel:	n/a
8	chr1:92197531-92197581	ECC-1	luminal epithelium:	n/a
9	chr1:92191625-92191675	LNCaP	prostate:	n/a
10	chr1:92197531-92197581	Hepatocyte	liver:	n/a
11	chr1:92197531-92197581	GM12878	blood:	n/a
12	chr1:92191625-92191675	CMK	blood:	n/a
13	chr1:92191625-92191675	AG10803	skin:	n/a
14	chr1:92197531-92197581	HEK293	kidney:	embryo
15	chr1:92191625-92191675	GM12878	blood:	n/a
16	chr1:92191625-92191675	AG04450	lung:	fetal
17	chr1:92191625-92191675	IMR90	lung:	fetal
18	chr1:92191625-92191675	Jurkat	blood:	n/a
19	chr1:92191625-92191675	SK-N-MC	brain:	n/a
20	chr1:92197531-92197581	AG09319	gingival:	n/a
21	chr1:92191625-92191675	NHBE	bronchial:	n/a
22	chr1:92197531-92197581	HepG2	liver:	n/a
23	chr1:92197531-92197581	SK-N-MC	brain:	n/a
24	chr1:92197531-92197581	HAEpiC	amniotic membrane:	n/a
25	chr1:92197531-92197581	Hela-S3	cervix:	n/a
26	chr1:92191625-92191675	PFSK-1	brain:	n/a
27	chr1:92197531-92197581	HRCEpiC	kidney:	n/a
28	chr1:92197531-92197581	HCPEpiC	choroid plexus:	n/a
29	chr1:92197531-92197581	ProgFib	skin:	n/a
30	chr1:92197531-92197581	NHDF-neo	bronchial:	n/a
31	chr1:92191625-92191675	PrEC	prostate:	n/a
32	chr1:92191625-92191675	U87	brain:	n/a
33	chr1:92197531-92197581	BE2_C	brain:	n/a
34	chr1:92191625-92191675	HUVEC	blood vessel:	n/a
35	chr1:92191625-92191675	MCF10A-Er-Src	breast:	n/a
36	chr1:92197531-92197581	HMEC	breast:	n/a
37	chr1:92191625-92191675	GM12892	blood:	n/a
38	chr1:92197531-92197581	HCM	heart:	n/a
39	chr1:92191625-92191675	NB4	blood:	n/a
40	chr1:92197531-92197581	RPTEC	kidney:	n/a
41	chr1:92197531-92197581	SK-N-SH	brain:	n/a
42	chr1:92191625-92191675	GM12891	blood:	n/a
43	chr1:92191625-92191675	RPTEC	kidney:	n/a
44	chr1:92191625-92191675	SK-N-SH_RA	brain:	n/a
45	chr1:92197531-92197581	GM12891	blood:	n/a
46	chr1:92197531-92197581	MCF-7	breast:	n/a
47	chr1:92197531-92197581	LNCaP	prostate:	n/a
48	chr1:92191625-92191675	A549	lung:	n/a
49	chr1:92197531-92197581	MCF10A-Er-Src	breast:	n/a
50	chr1:92197531-92197581	GM06990	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:92196121..92198991-chr1:92207192..92209304,2	MCF-7	breast:
2	chr1:92192178..92194320-chr1:92196821..92198679,2	K562	blood:
3	chr1:92198152..92200213-chr1:92201193..92206399,7	K562	blood:
4	chr1:92184011..92187610-chr1:92188347..92192369,4	K562	blood:
5	chr1:92197202..92203288-chr1:92206365..92210533,5	K562	blood:
6	chr1:92196725..92200248-chr1:92206849..92210560,4	K562	blood:
7	chr1:92189258..92193188-chr1:92194522..92196591,3	K562	blood:
8	chr1:92197642..92200532-chr1:92350997..92352784,2	K562	blood:
9	chr1:92182554..92184890-chr1:92189322..92192184,2	K562	blood:
10	chr1:92189258..92193188-chr1:92194522..92196591,3	K562	blood:
11	chr1:92195746..92200158-chr1:92212228..92214643,4	K562	blood:
12	chr1:92196960..92199922-chr1:92201744..92205146,4	K562	blood:
13	chr1:92194536..92198402-chr1:92243329..92245903,3	K562	blood:
14	chr1:92170602..92173339-chr1:92193646..92196655,3	K562	blood:
15	chr1:92196718..92198594-chr1:92235219..92237131,2	K562	blood:
16	chr1:92177009..92179682-chr1:92195748..92197642,2	K562	blood:
17	chr1:92162441..92164446-chr1:92195933..92198118,2	K562	blood:
18	chr1:92181357..92183863-chr1:92196120..92197770,2	K562	blood:
19	chr1:92186351..92189237-chr1:92195630..92198229,2	K562	blood:

No data

Variant related genes	Relation type
TGFBR3	TF binding region
TGFBR3	CpG island
ENSG00000069702	chromatin interactions

Extended variants
information (count: 254 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:254 , 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	rs12722864	chr1:92191534-92191535	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374336316	chr1:92191537-92191538	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs548808302	chr1:92191668-92191669	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs567213154	chr1:92191711-92191712	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs17882019	chr1:92191721-92191722	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs17884981	chr1:92191776-92191777	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs371312976	chr1:92191777-92191778	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs17882489	chr1:92191782-92191783	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs538428881	chr1:92191794-92191795	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs17131541	chr1:92191809-92191810	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs566845720	chr1:92191821-92191822	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567362545	chr1:92191825-92191826	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534250745	chr1:92191858-92191859	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185157874	chr1:92191873-92191874	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188828082	chr1:92191945-92191946	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17886361	chr1:92191994-92191995	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151005742	chr1:92191995-92191996	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs578260268	chr1:92192000-92192001	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545615446	chr1:92192085-92192086	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560623636	chr1:92192097-92192098	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201248609	chr1:92192098-92192099	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374295688	chr1:92192104-92192105	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535836603	chr1:92192116-92192117	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527890982	chr1:92192186-92192187	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142922843	chr1:92192195-92192196	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139267712	chr1:92192203-92192204	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs114402241	chr1:92192227-92192228	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs531317421	chr1:92192238-92192239	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs570193070	chr1:92192348-92192349	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs561503000	chr1:92192373-92192374	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs61778536	chr1:92192376-92192377	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs10874909	chr1:92192383-92192384	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs149982990	chr1:92192411-92192412	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563135728	chr1:92192469-92192470	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532316041	chr1:92192509-92192510	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573647030	chr1:92192532-92192533	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11165350	chr1:92192600-92192601	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11165351	chr1:92192626-92192627	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192394129	chr1:92192670-92192671	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7532589	chr1:92192679-92192680	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558785440	chr1:92192730-92192731	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12057252	chr1:92192746-92192747	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555802208	chr1:92192829-92192830	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567682952	chr1:92192869-92192870	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146589622	chr1:92192944-92192945	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17880750	chr1:92193024-92193025	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs578072463	chr1:92193031-92193032	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs61748117	chr1:92193037-92193038	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6678980	chr1:92193054-92193055	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs141277080	chr1:92193074-92193075	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92153000-92197000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:92164000-92195000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr1:92165800-92196800	Weak transcription	Small Intestine	intestine
4	chr1:92171000-92196800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr1:92171200-92196800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:92172800-92197000	Weak transcription	Colonic Mucosa	Colon
7	chr1:92173200-92202400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr1:92173600-92197800	Weak transcription	Brain Angular Gyrus	brain
9	chr1:92179000-92191600	Strong transcription	Placenta	Placenta
10	chr1:92179400-92192600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:92179400-92195200	Weak transcription	GM12878-XiMat	blood
12	chr1:92180800-92194400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:92182000-92194400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:92184000-92195000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr1:92184800-92195600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:92185200-92196600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:92185400-92191600	Weak transcription	Brain Anterior Caudate	brain
18	chr1:92185400-92196400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:92185400-92196600	Weak transcription	A549	lung
20	chr1:92185600-92193400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr1:92185600-92196800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:92185800-92191600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:92185800-92192800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr1:92185800-92194400	Weak transcription	Fetal Intestine Large	intestine
25	chr1:92185800-92194600	Weak transcription	Lung	lung
26	chr1:92185800-92195200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr1:92185800-92196800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:92185800-92196800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr1:92185800-92196800	Weak transcription	Pancreas	Pancrea
30	chr1:92185800-92197600	Weak transcription	Fetal Intestine Small	intestine
31	chr1:92186000-92194600	Weak transcription	Spleen	Spleen
32	chr1:92186000-92195200	Weak transcription	Esophagus	oesophagus
33	chr1:92186000-92196800	Weak transcription	Gastric	stomach
34	chr1:92186200-92195400	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr1:92186400-92196400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:92187000-92195600	Weak transcription	Hela-S3	cervix
37	chr1:92187200-92192600	Weak transcription	Liver	Liver
38	chr1:92187200-92195000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:92187200-92196400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr1:92187200-92197000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:92187400-92192800	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr1:92187600-92191800	Weak transcription	Fetal Muscle Trunk	muscle
43	chr1:92188200-92192200	Enhancers	Psoas Muscle	Psoas
44	chr1:92189200-92192000	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr1:92189200-92193000	Enhancers	Colon Smooth Muscle	Colon
46	chr1:92189200-92194000	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr1:92189200-92202200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:92189600-92192600	Enhancers	Fetal Heart	heart
49	chr1:92189800-92192400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:92189800-92192800	Enhancers	Right Atrium	heart

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