Variant report

Variant	nsv830326
Chromosome Location	chr1:79573379-79735667
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	ATF2	chr1:79728345-79728782	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:79658867-79659458	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:79658878-79659483	H1-hESC	embryonic stem cell:	n/a	chr1:79659052-79659066
4	BATF	chr1:79658862-79659246	GM12878	blood:	n/a	chr1:79659055-79659066
5	BATF	chr1:79658879-79659230	GM12878	blood:	n/a	chr1:79659055-79659066
6	BCL11A	chr1:79728386-79728591	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr1:79659126-79659356	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr1:79603898-79604245	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr1:79604022-79604167	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr1:79655568-79655570	GM12878	blood:	n/a	n/a
11	BRCA1	chr1:79617796-79617801	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr1:79658842-79659475	HCT-116	colon:	n/a	n/a
13	CEBPB	chr1:79718345-79718580	ECC-1	luminal epithelium:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
14	CEBPB	chr1:79665659-79665859	HepG2	liver:	n/a	chr1:79665731-79665742
15	CEBPB	chr1:79718311-79718646	HepG2	liver:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
16	CEBPB	chr1:79712529-79712866	IMR90	lung:	n/a	chr1:79712561-79712573
17	CEBPB	chr1:79594497-79595010	IMR90	lung:	n/a	chr1:79594917-79594928 chr1:79594917-79594928 chr1:79594917-79594930
18	CEBPB	chr1:79697149-79697373	HepG2	liver:	n/a	chr1:79697291-79697302
19	CEBPB	chr1:79659067-79659488	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:79658949-79659505	HCT-116	colon:	n/a	n/a
21	CEBPB	chr1:79587509-79587865	IMR90	lung:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
22	CEBPB	chr1:79697132-79697442	Hela-S3	cervix:	n/a	chr1:79697291-79697302
23	CEBPB	chr1:79659159-79659562	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:79697141-79697455	IMR90	lung:	n/a	chr1:79697291-79697302
25	CEBPB	chr1:79718318-79718634	A549	lung:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
26	CEBPB	chr1:79636675-79636862	HepG2	liver:	n/a	chr1:79636792-79636803
27	CEBPB	chr1:79654455-79654634	A549	lung:	n/a	n/a
28	CEBPB	chr1:79654054-79654728	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:79670718-79671120	Hela-S3	cervix:	n/a	chr1:79670933-79670944
30	CEBPB	chr1:79658909-79659649	HCT-116	colon:	n/a	n/a
31	CEBPB	chr1:79718247-79718614	A549	lung:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
32	CEBPB	chr1:79718310-79718665	H1-hESC	embryonic stem cell:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
33	CEBPB	chr1:79583039-79583331	IMR90	lung:	n/a	chr1:79583176-79583189
34	CEBPB	chr1:79712635-79712835	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:79620055-79620223	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:79718317-79718668	IMR90	lung:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
37	CEBPB	chr1:79603920-79604175	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr1:79712587-79712840	K562	blood:	n/a	n/a
39	CEBPB	chr1:79658668-79659683	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr1:79712595-79712823	A549	lung:	n/a	n/a
41	CEBPB	chr1:79697150-79697358	A549	lung:	n/a	chr1:79697291-79697302
42	CEBPB	chr1:79587527-79587826	HepG2	liver:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
43	CEBPB	chr1:79698273-79698970	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr1:79664513-79664900	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:79664528-79664874	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:79587579-79587715	H1-hESC	embryonic stem cell:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
47	CEBPB	chr1:79718304-79718629	ECC-1	luminal epithelium:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
48	CEBPB	chr1:79722314-79722606	HepG2	liver:	n/a	chr1:79722463-79722474
49	CEBPB	chr1:79626800-79627098	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr1:79712608-79712818	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79627622-79627672	AG09309	skin:	n/a
2	chr1:79627622-79627672	AG10803	skin:	n/a
3	chr1:79726633-79726683	NHDF-neo	bronchial:	n/a
4	chr1:79658903-79658953	HIPEpiC	eye:	n/a
5	chr1:79627622-79627672	HL-60	blood:	n/a
6	chr1:79726633-79726683	PANC-1	pancreas:	n/a
7	chr1:79594960-79595010	ProgFib	skin:	n/a
8	chr1:79653656-79653706	HNPCEpiC	eye:	n/a
9	chr1:79728608-79728658	SK-N-SH_RA	brain:	n/a
10	chr1:79653656-79653706	GM06990	blood:	n/a
11	chr1:79658903-79658953	NHDF-neo	bronchial:	n/a
12	chr1:79594960-79595010	MCF10A-Er-Src	breast:	n/a
13	chr1:79728608-79728658	RPTEC	kidney:	n/a
14	chr1:79653656-79653706	MCF-7	breast:	n/a
15	chr1:79726633-79726683	HCPEpiC	choroid plexus:	n/a
16	chr1:79627622-79627672	HCM	heart:	n/a
17	chr1:79653656-79653706	Hepatocyte	liver:	n/a
18	chr1:79658903-79658953	HCT-116	colon:	n/a
19	chr1:79658903-79658953	H1-hESC	embryonic stem cell:	embryo
20	chr1:79658903-79658953	PANC-1	pancreas:	n/a
21	chr1:79658903-79658953	HRPEpiC	eye:	n/a
22	chr1:79658903-79658953	MCF-7	breast:	n/a
23	chr1:79653656-79653706	ECC-1	luminal epithelium:	n/a
24	chr1:79726633-79726683	A549	lung:	n/a
25	chr1:79658903-79658953	Hepatocyte	liver:	n/a
26	chr1:79728608-79728658	BJ	skin:	n/a
27	chr1:79653656-79653706	NB4	blood:	n/a
28	chr1:79658903-79658953	HEEpiC	esophagus:	n/a
29	chr1:79627622-79627672	HCF	heart:	n/a
30	chr1:79728608-79728658	HEK293	kidney:	embryo
31	chr1:79658903-79658953	SK-N-MC	brain:	n/a
32	chr1:79653656-79653706	ovcar-3	ovarian:	n/a
33	chr1:79594960-79595010	HCT-116	colon:	n/a
34	chr1:79594960-79595010	AG09309	skin:	n/a
35	chr1:79728608-79728658	HL-60	blood:	n/a
36	chr1:79627622-79627672	SK-N-SH	brain:	n/a
37	chr1:79627622-79627672	HRPEpiC	eye:	n/a
38	chr1:79726633-79726683	AG04450	lung:	fetal
39	chr1:79726633-79726683	HNPCEpiC	eye:	n/a
40	chr1:79726633-79726683	ovcar-3	ovarian:	n/a
41	chr1:79726633-79726683	HAEpiC	amniotic membrane:	n/a
42	chr1:79594960-79595010	HEK293	kidney:	embryo
43	chr1:79726633-79726683	PFSK-1	brain:	n/a
44	chr1:79627622-79627672	HCPEpiC	choroid plexus:	n/a
45	chr1:79627622-79627672	MCF10A-Er-Src	breast:	n/a
46	chr1:79728608-79728658	Hela-S3	cervix:	n/a
47	chr1:79653656-79653706	HepG2	liver:	n/a
48	chr1:79653656-79653706	NT2-D1	testis:	n/a
49	chr1:79658903-79658953	U87	brain:	n/a
50	chr1:79726633-79726683	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:79616451..79619205-chr1:79639296..79641396,2	MCF-7	breast:
2	chr1:79728080..79730865-chr1:79731789..79734341,2	K562	blood:
3	chr1:79728080..79730865-chr1:79731789..79734341,2	K562	blood:
4	chr1:79725343..79726033-chr1:79818640..79819391,2	MCF-7	breast:
5	chr1:79154179..79155005-chr1:79663219..79663974,2	MCF-7	breast:
6	chr1:79717844..79719500-chr13:74206627..74209123,2	MCF-7	breast:
7	chr1:79304951..79305958-chr1:79662942..79663752,3	MCF-7	breast:
8	chr1:79702123..79704938-chr10:125479865..125482682,2	MCF-7	breast:
9	chr1:79616451..79619205-chr1:79639296..79641396,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000266388	TF binding region
ENSG00000266388	CpG island

Extended variants
information (count: 4725 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:4725 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529705805	chr1:79573415-79573416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549607153	chr1:79573457-79573458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190855830	chr1:79573462-79573463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10159209	chr1:79573541-79573542	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs183412205	chr1:79573555-79573556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4414001	chr1:79573586-79573587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs76889048	chr1:79573600-79573601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79866868	chr1:79573601-79573602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1487541	chr1:79573607-79573608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs538270072	chr1:79573608-79573609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533590915	chr1:79573639-79573640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557027477	chr1:79573642-79573643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575703315	chr1:79573644-79573645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376620996	chr1:79573646-79573647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542680320	chr1:79573676-79573677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554366218	chr1:79573697-79573698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529821336	chr1:79573708-79573709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186756954	chr1:79573733-79573734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200216621	chr1:79573758-79573759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149850661	chr1:79573803-79573804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532299007	chr1:79573804-79573805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544197332	chr1:79573817-79573818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562302272	chr1:79573828-79573829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552431634	chr1:79573853-79573854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549770133	chr1:79573861-79573862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72935509	chr1:79573862-79573863	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs191607264	chr1:79573875-79573876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386632705	chr1:79573899-79573900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74096016	chr1:79573901-79573902	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs368933768	chr1:79573915-79573916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534504217	chr1:79573925-79573926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371341163	chr1:79573927-79573928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571913260	chr1:79573938-79573939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538924457	chr1:79573950-79573951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117813648	chr1:79573967-79573968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549292328	chr1:79573994-79573995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536227045	chr1:79574000-79574001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1906280	chr1:79574011-79574012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554006622	chr1:79574012-79574013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139499947	chr1:79574045-79574046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144216851	chr1:79574125-79574126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371157703	chr1:79574140-79574141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200914164	chr1:79574227-79574228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577075586	chr1:79574246-79574247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537098451	chr1:79574258-79574259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557056477	chr1:79574278-79574279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562524902	chr1:79574347-79574348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574377668	chr1:79574371-79574372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541829819	chr1:79574374-79574375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560337314	chr1:79574404-79574405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79571200-79594600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:79572200-79590200	Weak transcription	HUVEC	blood vessel
3	chr1:79579600-79579800	Enhancers	Osteobl	bone
4	chr1:79589000-79601000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:79590200-79591000	Enhancers	HUVEC	blood vessel
6	chr1:79591000-79594400	Weak transcription	HUVEC	blood vessel
7	chr1:79593400-79593800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:79593800-79594800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:79594000-79594400	Enhancers	Hela-S3	cervix
10	chr1:79594200-79594400	Enhancers	A549	lung
11	chr1:79594200-79595000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:79594200-79595200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:79594200-79595200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr1:79594200-79595200	Enhancers	NHDF-Ad	bronchial
15	chr1:79594400-79594800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:79594400-79594800	Enhancers	HUVEC	blood vessel
17	chr1:79594400-79595000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:79594400-79595000	Flanking Active TSS	A549	lung
19	chr1:79594400-79595200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:79594400-79595200	Enhancers	Osteobl	bone
21	chr1:79594600-79595200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:79595000-79595200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:79595000-79604000	Weak transcription	A549	lung
24	chr1:79595200-79598400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:79604000-79604600	Active TSS	A549	lung
26	chr1:79604200-79605000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:79604600-79604800	Flanking Active TSS	A549	lung
28	chr1:79604600-79605400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
29	chr1:79604800-79605000	Enhancers	A549	lung
30	chr1:79614000-79614400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr1:79614400-79615600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:79614600-79615400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:79615200-79615800	Enhancers	Fetal Stomach	stomach
34	chr1:79615600-79616200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr1:79615800-79616800	Weak transcription	Fetal Stomach	stomach
36	chr1:79616000-79617000	Enhancers	Fetal Lung	lung
37	chr1:79616200-79617200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:79616400-79617600	Enhancers	HUVEC	blood vessel
39	chr1:79616600-79617000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:79616800-79617600	Enhancers	Fetal Stomach	stomach
41	chr1:79617000-79618800	Weak transcription	Fetal Lung	lung
42	chr1:79617400-79617600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr1:79618800-79619800	Enhancers	Fetal Lung	lung
44	chr1:79619600-79619800	Enhancers	Adipose Nuclei	Adipose
45	chr1:79619600-79619800	Enhancers	Gastric	stomach
46	chr1:79619600-79619800	Enhancers	Left Ventricle	heart
47	chr1:79621200-79621800	Enhancers	Fetal Heart	heart
48	chr1:79621400-79621800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:79621600-79622000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:79621800-79626800	Weak transcription	Fetal Heart	heart

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