Variant report

Variant	nsv1004669
Chromosome Location	chr1:76301198-76409451
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	chr1:76320748-76320934	K562	blood:	n/a	n/a
2	ARID3A	chr1:76320652-76320915	HepG2	liver:	n/a	n/a
3	ATF1	chr1:76320739-76320991	K562	blood:	n/a	n/a
4	ATF1	chr1:76337837-76338185	K562	blood:	n/a	n/a
5	BATF	chr1:76402769-76403052	GM12878	blood:	n/a	n/a
6	BCL3	chr1:76402779-76403076	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:76408798-76409160	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:76408753-76409142	K562	blood:	n/a	n/a
9	BHLHE40	chr1:76320708-76320981	K562	blood:	n/a	n/a
10	CEBPB	chr1:76397180-76397391	HepG2	liver:	n/a	chr1:76397281-76397292
11	CEBPB	chr1:76340847-76341003	K562	blood:	n/a	chr1:76340931-76340942
12	CEBPB	chr1:76343758-76343986	K562	blood:	n/a	chr1:76343874-76343885
13	CEBPB	chr1:76401284-76401590	K562	blood:	n/a	chr1:76401435-76401448 chr1:76401435-76401446 chr1:76401437-76401448 chr1:76401435-76401448
14	CEBPB	chr1:76321244-76321816	IMR90	lung:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
15	CEBPB	chr1:76340798-76341108	HepG2	liver:	n/a	chr1:76340931-76340942
16	CEBPB	chr1:76401333-76401597	HepG2	liver:	n/a	chr1:76401435-76401448 chr1:76401435-76401446 chr1:76401437-76401448 chr1:76401435-76401448
17	CEBPB	chr1:76320619-76321020	K562	blood:	n/a	chr1:76320818-76320829
18	CEBPB	chr1:76321321-76321799	HepG2	liver:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
19	CEBPB	chr1:76317452-76317652	K562	blood:	n/a	n/a
20	CEBPB	chr1:76340779-76341116	IMR90	lung:	n/a	chr1:76340931-76340942
21	CEBPB	chr1:76320689-76320951	HepG2	liver:	n/a	chr1:76320818-76320829
22	CEBPB	chr1:76320701-76321133	HCT-116	colon:	n/a	chr1:76320818-76320829
23	CEBPB	chr1:76320633-76321019	HepG2	liver:	n/a	chr1:76320818-76320829
24	CEBPB	chr1:76357194-76357223	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr1:76320629-76321043	MCF-7	breast:	n/a	chr1:76320818-76320829
26	CEBPB	chr1:76403902-76404167	HepG2	liver:	n/a	chr1:76404006-76404017
27	CEBPB	chr1:76320673-76320990	HepG2	liver:	n/a	chr1:76320818-76320829
28	CEBPB	chr1:76320631-76321012	HepG2	liver:	n/a	chr1:76320818-76320829
29	CEBPB	chr1:76403984-76404024	A549	lung:	n/a	chr1:76404006-76404017
30	CEBPB	chr1:76403927-76404126	K562	blood:	n/a	chr1:76404006-76404017
31	CEBPB	chr1:76405201-76405367	K562	blood:	n/a	n/a
32	CEBPB	chr1:76321572-76321747	H1-hESC	embryonic stem cell:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
33	CEBPB	chr1:76302322-76302430	HepG2	liver:	n/a	chr1:76302408-76302419
34	CEBPB	chr1:76320619-76321015	K562	blood:	n/a	chr1:76320818-76320829
35	CEBPB	chr1:76403891-76404185	IMR90	lung:	n/a	chr1:76404006-76404017
36	CEBPB	chr1:76320641-76321823	Hela-S3	cervix:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76320818-76320829 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
37	CEBPB	chr1:76321460-76321852	K562	blood:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
38	CEBPB	chr1:76340832-76341109	A549	lung:	n/a	chr1:76340931-76340942
39	CEBPB	chr1:76320731-76320940	K562	blood:	n/a	chr1:76320818-76320829
40	CEBPB	chr1:76343805-76344014	HepG2	liver:	n/a	chr1:76343874-76343885
41	CEBPB	chr1:76321326-76321765	A549	lung:	n/a	chr1:76321647-76321660 chr1:76321648-76321659 chr1:76321647-76321660 chr1:76321647-76321658 chr1:76321647-76321660
42	CEBPB	chr1:76320533-76321186	HCT-116	colon:	n/a	chr1:76320818-76320829
43	CEBPB	chr1:76302317-76302563	IMR90	lung:	n/a	chr1:76302408-76302419
44	CEBPB	chr1:76320629-76321005	IMR90	lung:	n/a	chr1:76320818-76320829
45	CEBPD	chr1:76320743-76320886	HepG2	liver:	n/a	n/a
46	CEBPD	chr1:76320651-76320976	K562	blood:	n/a	n/a
47	CEBPD	chr1:76320695-76320891	HepG2	liver:	n/a	n/a
48	CEBPD	chr1:76320728-76321019	K562	blood:	n/a	n/a
49	CTCF	chr1:76398619-76398658	GM20000	blood:	n/a	n/a
50	CTCF	chr1:76308320-76308470	GM12867	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76396165-76396215	Hela-S3	cervix:	n/a
2	chr1:76396165-76396215	ovcar-3	ovarian:	n/a
3	chr1:76397847-76397897	AG10803	skin:	n/a
4	chr1:76396165-76396215	K562	blood:	n/a
5	chr1:76396165-76396215	NB4	blood:	n/a
6	chr1:76396165-76396215	CMK	blood:	n/a
7	chr1:76397847-76397897	IMR90	lung:	fetal
8	chr1:76396165-76396215	HEEpiC	esophagus:	n/a
9	chr1:76397847-76397897	NHBE	bronchial:	n/a
10	chr1:76397847-76397897	A549	lung:	n/a
11	chr1:76397847-76397897	Hepatocyte	liver:	n/a
12	chr1:76397847-76397897	NT2-D1	testis:	n/a
13	chr1:76396165-76396215	AoSMC	blood vessel:	n/a
14	chr1:76396165-76396215	SKMC	muscle:	n/a
15	chr1:76396165-76396215	H1-hESC	embryonic stem cell:	embryo
16	chr1:76396165-76396215	HCF	heart:	n/a
17	chr1:76397847-76397897	GM12891	blood:	n/a
18	chr1:76396165-76396215	GM06990	blood:	n/a
19	chr1:76396165-76396215	NHDF-neo	bronchial:	n/a
20	chr1:76396165-76396215	SAEC	small airway:	n/a
21	chr1:76396165-76396215	SK-N-SH	brain:	n/a
22	chr1:76396165-76396215	MCF-7	breast:	n/a
23	chr1:76397847-76397897	ovcar-3	ovarian:	n/a
24	chr1:76396165-76396215	RPTEC	kidney:	n/a
25	chr1:76396165-76396215	AG09319	gingival:	n/a
26	chr1:76396165-76396215	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:76397847-76397897	SK-N-MC	brain:	n/a
28	chr1:76397847-76397897	PFSK-1	brain:	n/a
29	chr1:76396165-76396215	T-47D	breast:	n/a
30	chr1:76397847-76397897	HRCEpiC	kidney:	n/a
31	chr1:76397847-76397897	NB4	blood:	n/a
32	chr1:76397847-76397897	HIPEpiC	eye:	n/a
33	chr1:76396165-76396215	GM12891	blood:	n/a
34	chr1:76397847-76397897	HL-60	blood:	n/a
35	chr1:76396165-76396215	GM12892	blood:	n/a
36	chr1:76397847-76397897	HUVEC	blood vessel:	n/a
37	chr1:76397847-76397897	SAEC	small airway:	n/a
38	chr1:76397847-76397897	Caco-2	colon:	n/a
39	chr1:76396165-76396215	PrEC	prostate:	n/a
40	chr1:76397847-76397897	ECC-1	luminal epithelium:	n/a
41	chr1:76396165-76396215	HAEpiC	amniotic membrane:	n/a
42	chr1:76396165-76396215	AG09309	skin:	n/a
43	chr1:76397847-76397897	GM12878	blood:	n/a
44	chr1:76396165-76396215	HCM	heart:	n/a
45	chr1:76396165-76396215	BE2_C	brain:	n/a
46	chr1:76397847-76397897	HEEpiC	esophagus:	n/a
47	chr1:76396165-76396215	NH-A	brain:	n/a
48	chr1:76397847-76397897	T-47D	breast:	n/a
49	chr1:76397847-76397897	RPTEC	kidney:	n/a
50	chr1:76397847-76397897	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:76260266..76263027-chr1:76396916..76399571,2	K562	blood:
2	chr1:76373718..76374271-chr1:76796370..76797302,2	MCF-7	breast:
3	chr1:76392792..76394366-chr1:76397859..76400177,2	K562	blood:
4	chr1:76383436..76384363-chr16:27389146..27390073,2	MCF-7	breast:
5	chr1:76349813..76351661-chr1:76356485..76359051,2	K562	blood:
6	chr1:76332563..76334955-chr1:76337624..76339658,2	K562	blood:
7	chr1:76380506..76383484-chr1:76388793..76390855,2	K562	blood:
8	chr1:76332563..76334955-chr1:76337624..76339658,2	K562	blood:
9	chr1:76374124..76374771-chr1:76619576..76620091,2	MCF-7	breast:
10	chr1:76262942..76264627-chr1:76319779..76321493,2	K562	blood:
11	chr1:76333672..76334172-chr20:20341161..20341713,2	MCF-7	breast:
12	chr1:76327097..76328864-chr1:76332786..76334905,2	K562	blood:
13	chr1:76349813..76351661-chr1:76356485..76359051,2	K562	blood:
14	chr1:76256252..76258786-chr1:76340738..76342721,2	K562	blood:
15	chr1:76327097..76328864-chr1:76332786..76334905,2	K562	blood:
16	chr1:76380506..76383484-chr1:76388793..76390855,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABGGTB-2	chr1:76304311-76304501	NONHSAT004005
2	lnc-RABGGTB-2	chr1:76304311-76304643	l_74_chr1:76279982-76304643_kidney
3	lnc-MSH4-1	chr1:76400119-76400171	NONHSAT004007
4	lnc-MSH4-1	chr1:76398207-76398355	NONHSAT004007

Variant related genes	Relation type
ENSG00000266832	TF binding region
ASB17	TF binding region
ENSG00000266832	CpG island
ASB17	CpG island
ENSG00000057468	chromatin interactions
ENSG00000154007	chromatin interactions
ENSG00000137955	chromatin interactions

Extended variants
information (count: 1628 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1466817	chr1:76301198-76301199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191278483	chr1:76301199-76301200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558947741	chr1:76301298-76301299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546311659	chr1:76301327-76301328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184987230	chr1:76301330-76301331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538783902	chr1:76301352-76301353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377632992	chr1:76301367-76301368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148635339	chr1:76301370-76301371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371396901	chr1:76301380-76301381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557093862	chr1:76301387-76301388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575367516	chr1:76301399-76301400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536850153	chr1:76301403-76301404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188002902	chr1:76301413-76301414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573495771	chr1:76301425-76301426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151130685	chr1:76301439-76301440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558731368	chr1:76301483-76301484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577172998	chr1:76301518-76301519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544160524	chr1:76301564-76301565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570832537	chr1:76301589-76301590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562658024	chr1:76301602-76301603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530106784	chr1:76301604-76301605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147002876	chr1:76301615-76301616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577525448	chr1:76301624-76301625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17648749	chr1:76301628-76301629	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs12076093	chr1:76301656-76301657	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546869136	chr1:76301707-76301708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147635843	chr1:76301713-76301714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531967396	chr1:76301759-76301760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550557951	chr1:76301783-76301784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139533650	chr1:76301857-76301858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142204508	chr1:76301873-76301874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192468929	chr1:76301888-76301889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536339967	chr1:76301893-76301894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145938045	chr1:76301900-76301901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529357267	chr1:76301920-76301921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567053869	chr1:76301937-76301938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369484756	chr1:76301972-76301973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371408309	chr1:76301987-76301988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386367372	chr1:76301988-76301989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386367373	chr1:76302000-76302001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71071968	chr1:76302001-76302002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534088428	chr1:76302094-76302095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551782104	chr1:76302143-76302144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565432209	chr1:76302146-76302147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559213318	chr1:76302214-76302215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72979226	chr1:76302222-76302223	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs10873738	chr1:76302233-76302234	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574625803	chr1:76302275-76302276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184687700	chr1:76302293-76302294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138856458	chr1:76302335-76302336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76295800-76307800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr1:76300800-76304600	Weak transcription	Psoas Muscle	Psoas
3	chr1:76301600-76303000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:76301600-76304600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:76301800-76303000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:76302000-76303200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:76302200-76302800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:76303200-76303600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr1:76303600-76304000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr1:76304600-76306600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:76306600-76307200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:76306600-76308200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:76307000-76307600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:76307000-76308800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:76319600-76327400	Weak transcription	Aorta	Aorta
16	chr1:76319800-76320200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:76320000-76320400	Enhancers	Hela-S3	cervix
18	chr1:76320000-76320400	Enhancers	HMEC	breast
19	chr1:76320000-76320800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:76320000-76321400	Enhancers	HepG2	liver
21	chr1:76320000-76321400	Enhancers	K562	blood
22	chr1:76320200-76320400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:76320400-76321000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:76321000-76321400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:76327200-76327400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr1:76327200-76327800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:76327400-76327800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr1:76327400-76327800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:76327400-76328000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr1:76327400-76328000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:76327400-76328000	Strong transcription	Aorta	Aorta
32	chr1:76327600-76327800	Enhancers	HepG2	liver
33	chr1:76327600-76328000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr1:76327800-76328000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr1:76328000-76338400	Weak transcription	Aorta	Aorta
36	chr1:76335200-76335400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:76336000-76338400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr1:76338400-76338800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr1:76338600-76338800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr1:76338600-76339000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr1:76352600-76353000	Active TSS	A549	lung
42	chr1:76353000-76353200	Enhancers	A549	lung
43	chr1:76366400-76368000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:76366800-76367800	Enhancers	Fetal Heart	heart
45	chr1:76374600-76374800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:76374600-76375000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr1:76374600-76375000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr1:76374600-76375000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:76374600-76375000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:76374600-76375000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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