Variant report

Variant	nsv1533
Chromosome Location	chr1:77990504-78036279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:829)
CpG islands
(count:427)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:78004634-78005001	HepG2	liver:	n/a	n/a
2	ATF1	chr1:78013850-78014011	K562	blood:	n/a	n/a
3	ATF2	chr1:78006894-78007236	GM12878	blood:	n/a	n/a
4	ATF3	chr1:77999393-77999814	A549	lung:	n/a	n/a
5	BATF	chr1:78006267-78006512	GM12878	blood:	n/a	n/a
6	BATF	chr1:78006223-78006447	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:78006176-78006430	GM12878	blood:	n/a	chr1:78006375-78006384
8	BCL11A	chr1:78004628-78004881	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:77999392-77999890	K562	blood:	n/a	n/a
10	BHLHE40	chr1:78021009-78021209	K562	blood:	n/a	n/a
11	BHLHE40	chr1:78006167-78006554	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:78004801-78004899	A549	lung:	n/a	n/a
13	BHLHE40	chr1:77999414-77999745	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:78019351-78019629	K562	blood:	n/a	n/a
15	BRCA1	chr1:78006157-78006503	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:78002310-78003153	HCT-116	colon:	n/a	n/a
17	CEBPB	chr1:77999371-77999950	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:78009528-78009878	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:78024739-78024962	Hela-S3	cervix:	n/a	chr1:78024879-78024890
20	CEBPB	chr1:78004498-78005306	A549	lung:	n/a	n/a
21	CEBPB	chr1:78006039-78006630	A549	lung:	n/a	n/a
22	CEBPB	chr1:78004548-78005230	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:77999552-78000023	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:78009530-78009862	A549	lung:	n/a	n/a
25	CEBPB	chr1:78002382-78003041	A549	lung:	n/a	n/a
26	CEBPB	chr1:78024721-78024988	A549	lung:	n/a	chr1:78024879-78024890
27	CEBPB	chr1:78008797-78009013	IMR90	lung:	n/a	chr1:78008921-78008932
28	CEBPB	chr1:77991910-77991945	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:78004667-78005222	A549	lung:	n/a	n/a
30	CEBPB	chr1:78002415-78003017	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:78002475-78002971	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:78006414-78006665	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr1:78006556-78006786	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:78024731-78025017	IMR90	lung:	n/a	chr1:78024879-78024890
35	CEBPB	chr1:78004592-78006983	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:78002272-78002990	HCT-116	colon:	n/a	n/a
37	CEBPB	chr1:78005674-78006766	A549	lung:	n/a	n/a
38	CEBPB	chr1:78024711-78025062	HepG2	liver:	n/a	chr1:78024879-78024890
39	CHD1	chr1:78004716-78004773	GM12878	blood:	n/a	n/a
40	CHD2	chr1:78006123-78006503	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr1:78002529-78002908	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr1:78005361-78005912	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr1:78005393-78005819	A549	lung:	n/a	n/a
44	CTCF	chr1:77999480-77999630	HCT-116	colon:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575
45	CTCF	chr1:78002960-78003110	HMF	breast:	n/a	n/a
46	CTCF	chr1:77999480-77999630	HBMEC	blood vessel:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575
47	CTCF	chr1:77999241-77999330	GM19240	blood:	n/a	n/a
48	CTCF	chr1:77999500-77999650	HRPEpiC	eye:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575
49	CTCF	chr1:77999460-77999610	GM12878	blood:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575
50	CTCF	chr1:77999500-77999650	GM12872	blood:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78024449-78024499	HCF	heart:	n/a
2	chr1:77997502-77997552	GM12878	blood:	n/a
3	chr1:77997502-77997552	HCF	heart:	n/a
4	chr1:78001627-78001677	MCF-7	breast:	n/a
5	chr1:77999560-77999610	A549	lung:	n/a
6	chr1:78005352-78005402	SAEC	small airway:	n/a
7	chr1:78024449-78024499	GM06990	blood:	n/a
8	chr1:78011748-78011798	CMK	blood:	n/a
9	chr1:77999560-77999610	SKMC	muscle:	n/a
10	chr1:78024449-78024499	HL-60	blood:	n/a
11	chr1:77999560-77999610	H1-hESC	embryonic stem cell:	embryo
12	chr1:77999560-77999610	SK-N-SH_RA	brain:	n/a
13	chr1:77999560-77999610	ovcar-3	ovarian:	n/a
14	chr1:78001627-78001677	ProgFib	skin:	n/a
15	chr1:77999560-77999610	HNPCEpiC	eye:	n/a
16	chr1:78005352-78005402	HMEC	breast:	n/a
17	chr1:78005352-78005402	A549	lung:	n/a
18	chr1:77997502-77997552	CMK	blood:	n/a
19	chr1:78001627-78001677	A549	lung:	n/a
20	chr1:78005352-78005402	AG04450	lung:	fetal
21	chr1:77997502-77997552	AG04450	lung:	fetal
22	chr1:78005352-78005402	HCPEpiC	choroid plexus:	n/a
23	chr1:78001627-78001677	HCPEpiC	choroid plexus:	n/a
24	chr1:78011748-78011798	HCM	heart:	n/a
25	chr1:78001627-78001677	Jurkat	blood:	n/a
26	chr1:78005352-78005402	CMK	blood:	n/a
27	chr1:78005352-78005402	MCF10A-Er-Src	breast:	n/a
28	chr1:78011748-78011798	HEEpiC	esophagus:	n/a
29	chr1:78011748-78011798	AG09319	gingival:	n/a
30	chr1:78031187-78031237	HCT-116	colon:	n/a
31	chr1:78005352-78005402	Hela-S3	cervix:	n/a
32	chr1:78031187-78031237	AoSMC	blood vessel:	n/a
33	chr1:78031187-78031237	HepG2	liver:	n/a
34	chr1:78011748-78011798	HAEpiC	amniotic membrane:	n/a
35	chr1:77999560-77999610	RPTEC	kidney:	n/a
36	chr1:77999560-77999610	AG04450	lung:	fetal
37	chr1:78005352-78005402	NT2-D1	testis:	n/a
38	chr1:78005352-78005402	HL-60	blood:	n/a
39	chr1:77997502-77997552	AoSMC	blood vessel:	n/a
40	chr1:78001627-78001677	HL-60	blood:	n/a
41	chr1:78011748-78011798	NHBE	bronchial:	n/a
42	chr1:77999560-77999610	ECC-1	luminal epithelium:	n/a
43	chr1:78001627-78001677	AG09309	skin:	n/a
44	chr1:77999560-77999610	K562	blood:	n/a
45	chr1:78011748-78011798	A549	lung:	n/a
46	chr1:78005352-78005402	HUVEC	blood vessel:	n/a
47	chr1:78005352-78005402	H1-hESC	embryonic stem cell:	embryo
48	chr1:77999560-77999610	NHBE	bronchial:	n/a
49	chr1:78024449-78024499	CMK	blood:	n/a
50	chr1:78001627-78001677	HIPEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:78032016..78034356-chr1:78044391..78045977,2	K562	blood:
2	chr1:78013815..78015446-chr1:78033681..78035927,2	K562	blood:
3	chr1:77991832..77994057-chr1:78008305..78010332,2	MCF-7	breast:
4	chr1:78013815..78015446-chr1:78033681..78035927,2	K562	blood:
5	chr1:76619553..76620451-chr1:77999109..77999974,2	K562	blood:
6	chr1:77999652..78002822-chr1:78004325..78005902,3	K562	blood:
7	chr1:78028621..78030730-chr1:78147170..78149794,2	K562	blood:
8	chr1:78012030..78014042-chr1:78469948..78471688,2	K562	blood:
9	chr1:78020809..78023858-chr1:78146827..78149846,3	K562	blood:
10	chr1:78011348..78013511-chr1:78016318..78019247,2	K562	blood:
11	chr1:77996828..77998774-chr1:78147470..78149282,2	K562	blood:
12	chr1:78011874..78013427-chr1:78147037..78148549,2	K562	blood:
13	chr1:77991832..77994057-chr1:78008305..78010332,2	MCF-7	breast:
14	chr1:78000743..78003478-chr1:78147875..78150307,2	MCF-7	breast:
15	chr1:77999652..78002822-chr1:78004325..78005902,3	K562	blood:
16	chr1:78030983..78033542-chr1:78034721..78037146,2	K562	blood:
17	chr1:78028174..78030730-chr1:78147170..78149794,3	K562	blood:
18	chr1:78030983..78033542-chr1:78034721..78037146,2	K562	blood:
19	chr1:78017249..78019893-chr17:59489545..59491319,2	MCF-7	breast:
20	chr1:78011348..78013511-chr1:78016318..78019247,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM73A-2	chr1:78006181-78006374	NONHSAT004030
2	lnc-FAM73A-2	chr1:78024287-78024416	NONHSAT004030

No data

Variant related genes	Relation type
AK5	TF binding region
AK5	CpG island
ENSG00000273338	chromatin interactions
ENSG00000036549	chromatin interactions
ENSG00000162616	chromatin interactions

Extended variants
information (count: 1778 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35751413	chr1:77990504-77990505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs397860473	chr1:77990507-77990508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142566911	chr1:77990514-77990515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6680716	chr1:77990516-77990517	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs146014444	chr1:77990556-77990557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555913827	chr1:77990578-77990579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575962000	chr1:77990652-77990653	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148688479	chr1:77990675-77990676	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193245692	chr1:77990702-77990703	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59447555	chr1:77990799-77990800	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534924478	chr1:77990812-77990813	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552943806	chr1:77990836-77990837	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572492345	chr1:77990837-77990838	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532513280	chr1:77990874-77990875	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141380816	chr1:77990880-77990881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150713646	chr1:77990925-77990926	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576584139	chr1:77991024-77991025	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543704797	chr1:77991025-77991026	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4949805	chr1:77991029-77991030	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs4949806	chr1:77991037-77991038	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185694952	chr1:77991051-77991052	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189371165	chr1:77991059-77991060	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532800353	chr1:77991075-77991076	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550941389	chr1:77991094-77991095	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569462706	chr1:77991096-77991097	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541021558	chr1:77991100-77991101	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537144036	chr1:77991122-77991123	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115281275	chr1:77991129-77991130	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574950984	chr1:77991132-77991133	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75865325	chr1:77991168-77991169	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369509083	chr1:77991169-77991170	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145644474	chr1:77991202-77991203	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567362905	chr1:77991230-77991231	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74888882	chr1:77991253-77991254	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139052981	chr1:77991258-77991259	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539868777	chr1:77991287-77991288	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558180504	chr1:77991310-77991311	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2803137	chr1:77991312-77991313	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs149896511	chr1:77991316-77991317	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs180955043	chr1:77991336-77991337	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184757875	chr1:77991367-77991368	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541252152	chr1:77991368-77991369	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147590521	chr1:77991392-77991393	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533445256	chr1:77991423-77991424	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4949656	chr1:77991452-77991453	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544647404	chr1:77991459-77991460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562951797	chr1:77991463-77991464	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530376847	chr1:77991490-77991491	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4949657	chr1:77991508-77991509	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs567213530	chr1:77991513-77991514	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	16774939	CNVD

Chromatin state (count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77980800-77999400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:77981800-77998400	Weak transcription	Osteobl	bone
3	chr1:77981800-77999200	Weak transcription	NHLF	lung
4	chr1:77981800-77999400	Weak transcription	HSMMtube	muscle
5	chr1:77982000-77998200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:77982000-77998200	Weak transcription	Brain Angular Gyrus	brain
7	chr1:77982200-77998200	Weak transcription	Brain Anterior Caudate	brain
8	chr1:77983000-78009200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr1:77984600-77991200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr1:77984600-77996400	Strong transcription	NHDF-Ad	bronchial
11	chr1:77984800-77991600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr1:77984800-77991600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr1:77985000-77991200	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:77985200-77999400	Weak transcription	Brain Substantia Nigra	brain
15	chr1:77985400-77999800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:77987200-77991400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:77987200-77992000	Strong transcription	HSMM	muscle
18	chr1:77987600-77993200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:77988400-77999800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr1:77988600-77991000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr1:77988600-77991200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr1:77988600-77999400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr1:77988800-77992600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:77989000-77990600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:77989000-77998200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr1:77989200-77990800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:77989800-77991200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:77990000-77991800	Weak transcription	Primary T cells from cord blood	blood
29	chr1:77990000-77991800	Weak transcription	HUVEC	blood vessel
30	chr1:77990400-77998200	Weak transcription	Brain Hippocampus Middle	brain
31	chr1:77990600-77991400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:77990800-77992000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:77991000-77992200	Strong transcription	Muscle Satellite Cultured Cells	--
34	chr1:77991200-77991400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr1:77991200-77992000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr1:77991200-77992000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr1:77991200-77992200	Enhancers	Primary T cells fromperipheralblood	blood
38	chr1:77991200-77993200	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr1:77991400-77995600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:77991400-77996200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:77991400-77996400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:77991600-77992000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr1:77991600-77992000	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr1:77991600-77992000	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr1:77991600-77992000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr1:77991600-77992000	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr1:77991600-77992200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr1:77991800-77992000	Enhancers	HUVEC	blood vessel
49	chr1:77991800-77992200	Enhancers	Primary T cells from cord blood	blood
50	chr1:77991800-77992200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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