Variant report

Variant	nsv871279
Chromosome Location	chr1:95028981-95083836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:669)
CpG islands
(count:428)
Chromatin interactive
region (count:26)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:95045656-95045854	HepG2	liver:	n/a	n/a
2	BACH1	chr1:95068522-95068525	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:95046483-95046614	K562	blood:	n/a	n/a
4	BACH1	chr1:95045344-95045736	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr1:95063292-95063639	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:95064269-95064582	K562	blood:	n/a	n/a
7	BRCA1	chr1:95046209-95046570	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr1:95071745-95071785	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:95045221-95045801	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr1:95038362-95038802	HCT-116	colon:	n/a	n/a
11	CBX3	chr1:95033783-95034080	K562	blood:	n/a	n/a
12	CBX3	chr1:95038385-95038614	K562	blood:	n/a	n/a
13	CBX3	chr1:95038307-95038792	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:95082607-95083565	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:95038360-95038684	K562	blood:	n/a	n/a
16	CBX3	chr1:95033759-95034127	K562	blood:	n/a	n/a
17	CEBPB	chr1:95061343-95061661	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:95073784-95074058	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:95045398-95045901	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:95044520-95044760	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:95063164-95063687	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr1:95065095-95065304	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:95047899-95048402	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:95063258-95063707	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:95078300-95078549	K562	blood:	n/a	n/a
26	CEBPB	chr1:95044467-95044783	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:95034556-95034578	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:95065084-95065371	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:95078289-95078574	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:95063366-95063603	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:95073106-95073116	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:95061275-95061688	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:95067975-95068859	IMR90	lung:	n/a	chr1:95068159-95068170
34	CEBPB	chr1:95078287-95078468	HepG2	liver:	n/a	n/a
35	CHD2	chr1:95046050-95046127	HepG2	liver:	n/a	n/a
36	CHD2	chr1:95063283-95063615	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr1:95045373-95046021	Hela-S3	cervix:	n/a	n/a
38	CREB1	chr1:95079635-95080202	K562	blood:	n/a	chr1:95079917-95079930 chr1:95079873-95079886
39	CTCF	chr1:95061900-95062050	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr1:95061900-95062050	SAEC	small airway:	n/a	n/a
41	CTCF	chr1:95061200-95061350	HEEpiC	esophagus:	n/a	chr1:95061252-95061265
42	CTCF	chr1:95064960-95065384	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:95077260-95077410	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr1:95065120-95065270	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:95045720-95045870	HepG2	liver:	n/a	n/a
46	CTCF	chr1:95061976-95062002	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:95065200-95065350	WI-38	lung:	n/a	n/a
48	CTCF	chr1:95072417-95072503	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr1:95065178-95065240	GM19239	blood:	n/a	n/a
50	CTCF	chr1:95065020-95065170	HCM	heart:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95045763-95045813	SKMC	muscle:	n/a
2	chr1:95045763-95045813	SKMC	muscle:	n/a
3	chr1:95080047-95080097	PFSK-1	brain:	n/a
4	chr1:95082321-95082371	NB4	blood:	n/a
5	chr1:95056619-95056669	RPTEC	kidney:	n/a
6	chr1:95074231-95074281	NT2-D1	testis:	n/a
7	chr1:95082321-95082371	ovcar-3	ovarian:	n/a
8	chr1:95080047-95080097	NT2-D1	testis:	n/a
9	chr1:95061616-95061666	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:95068029-95068079	GM12892	blood:	n/a
11	chr1:95056619-95056669	PFSK-1	brain:	n/a
12	chr1:95082321-95082371	IMR90	lung:	fetal
13	chr1:95074231-95074281	AG09319	gingival:	n/a
14	chr1:95074231-95074281	H1-hESC	embryonic stem cell:	embryo
15	chr1:95045763-95045813	PFSK-1	brain:	n/a
16	chr1:95068029-95068079	T-47D	breast:	n/a
17	chr1:95068029-95068079	SAEC	small airway:	n/a
18	chr1:95061616-95061666	HCT-116	colon:	n/a
19	chr1:95061616-95061666	U87	brain:	n/a
20	chr1:95082321-95082371	LNCaP	prostate:	n/a
21	chr1:95068029-95068079	A549	lung:	n/a
22	chr1:95068029-95068079	SK-N-MC	brain:	n/a
23	chr1:95045763-95045813	NHBE	bronchial:	n/a
24	chr1:95061616-95061666	PrEC	prostate:	n/a
25	chr1:95080047-95080097	ovcar-3	ovarian:	n/a
26	chr1:95074231-95074281	Hela-S3	cervix:	n/a
27	chr1:95045763-95045813	AG09309	skin:	n/a
28	chr1:95082321-95082371	BE2_C	brain:	n/a
29	chr1:95080047-95080097	LNCaP	prostate:	n/a
30	chr1:95074231-95074281	NH-A	brain:	n/a
31	chr1:95056619-95056669	HIPEpiC	eye:	n/a
32	chr1:95074231-95074281	AoSMC	blood vessel:	n/a
33	chr1:95045763-95045813	GM12891	blood:	n/a
34	chr1:95074231-95074281	HEK293	kidney:	embryo
35	chr1:95061616-95061666	MCF10A-Er-Src	breast:	n/a
36	chr1:95045763-95045813	H1-hESC	embryonic stem cell:	embryo
37	chr1:95056619-95056669	PrEC	prostate:	n/a
38	chr1:95056619-95056669	HRE	kidney:	n/a
39	chr1:95082321-95082371	HUVEC	blood vessel:	n/a
40	chr1:95074231-95074281	HEEpiC	esophagus:	n/a
41	chr1:95045763-95045813	HAEpiC	amniotic membrane:	n/a
42	chr1:95068029-95068079	ECC-1	luminal epithelium:	n/a
43	chr1:95082321-95082371	SK-N-MC	brain:	n/a
44	chr1:95082321-95082371	AG04450	lung:	fetal
45	chr1:95056619-95056669	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:95045763-95045813	ECC-1	luminal epithelium:	n/a
47	chr1:95068029-95068079	GM12878	blood:	n/a
48	chr1:95080047-95080097	PrEC	prostate:	n/a
49	chr1:95082321-95082371	MCF-7	breast:	n/a
50	chr1:95045763-95045813	T-47D	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:95043796..95046993-chr1:95048870..95051582,3	K562	blood:
2	chr1:95075515..95077960-chr1:95084097..95086216,2	K562	blood:
3	chr1:95044875..95047288-chr1:95048137..95050937,2	MCF-7	breast:
4	chr1:95054539..95057690-chr1:95058025..95060713,3	K562	blood:
5	chr1:95044965..95045519-chr1:95065172..95065776,2	MCF-7	breast:
6	chr1:95043796..95046691-chr1:95048870..95051582,2	K562	blood:
7	chr1:95068045..95070486-chr1:95071108..95072675,2	K562	blood:
8	chr1:95006436..95008771-chr1:95043871..95046807,3	MCF-7	breast:
9	chr1:95064700..95065302-chr1:95267166..95268188,3	MCF-7	breast:
10	chr1:95002334..95004389-chr1:95062847..95065293,3	MCF-7	breast:
11	chr1:95044965..95045519-chr1:95065172..95065776,2	MCF-7	breast:
12	chr1:95080479..95082832-chr1:95086788..95088378,2	K562	blood:
13	chr1:95067748..95070486-chr1:95070993..95073979,4	K562	blood:
14	chr1:94992707..94993493-chr1:95064769..95065395,2	MCF-7	breast:
15	chr1:94997172..94998108-chr1:95064305..95065624,5	MCF-7	breast:
16	chr1:95083696..95086099-chr1:95111956..95113779,2	MCF-7	breast:
17	chr1:95044875..95047288-chr1:95048137..95050937,2	MCF-7	breast:
18	chr1:94987992..94988549-chr1:95064767..95065433,2	MCF-7	breast:
19	chr1:95043796..95046993-chr1:95048870..95051582,3	K562	blood:
20	chr1:95007807..95010747-chr1:95056056..95057592,2	MCF-7	breast:
21	chr1:95054539..95057690-chr1:95058025..95060713,3	K562	blood:
22	chr1:95005520..95008552-chr1:95083214..95086682,3	MCF-7	breast:
23	chr1:95067748..95070486-chr1:95070993..95073979,4	K562	blood:
24	chr1:95043796..95046691-chr1:95048870..95051582,2	K562	blood:
25	chr1:95079718..95082412-chr1:95085713..95087293,2	MCF-7	breast:
26	chr1:95068045..95070486-chr1:95071108..95072675,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-1	chr1:95056890-95057853	XLOC_000921
2	lnc-F3-1	chr1:95051112-95052318	XLOC_000921
3	lnc-F3-2	chr1:95082302-95082627	XLOC_000922
4	lnc-F3-2	chr1:95081953-95082627	XLOC_000922
5	lnc-F3-3	chr1:95058100-95058233	l_89_chr1:94917575-94970548_76bGuttman_hLF
6	lnc-F3-2	chr1:95082006-95082627	NONHSAT004599
7	lnc-F3-2	chr1:95081924-95082321	NONHSAT004597
8	lnc-F3-3	chr1:95031090-95031132	l_89_chr1:94917575-94970548_76bGuttman_hLF

No data

Variant related genes	Relation type
ENSG00000223675	TF binding region
ENSG00000223675	CpG island
ENSG00000117525	chromatin interactions

Extended variants
information (count: 2416 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2416 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs957334	chr1:95028981-95028982	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34365422	chr1:95028989-95028990	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs548281646	chr1:95028995-95028996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369596500	chr1:95029078-95029079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568263987	chr1:95029097-95029098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548119314	chr1:95029140-95029141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531017282	chr1:95029196-95029197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142412776	chr1:95029198-95029199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150885394	chr1:95029202-95029203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567505606	chr1:95029271-95029272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191491243	chr1:95029277-95029278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141632950	chr1:95029341-95029342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs61452750	chr1:95029349-95029350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375503099	chr1:95029358-95029359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2798942	chr1:95029388-95029389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78237975	chr1:95029417-95029418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574620108	chr1:95029443-95029444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183553204	chr1:95029466-95029467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139090510	chr1:95029570-95029571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1146509	chr1:95029581-95029582	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
21	rs546157044	chr1:95029588-95029589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545790529	chr1:95029604-95029605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1146508	chr1:95029621-95029622	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs187427860	chr1:95029629-95029630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541863372	chr1:95029706-95029707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191520825	chr1:95029752-95029753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552077013	chr1:95029785-95029786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372619223	chr1:95029832-95029833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183998394	chr1:95029870-95029871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1146507	chr1:95029895-95029896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149915387	chr1:95029900-95029901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533521819	chr1:95029930-95029931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147551526	chr1:95030018-95030019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567210641	chr1:95030121-95030122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534566823	chr1:95030123-95030124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554855094	chr1:95030131-95030132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536139511	chr1:95030148-95030149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141959673	chr1:95030194-95030195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112134270	chr1:95030203-95030204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369551785	chr1:95030218-95030219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568021884	chr1:95030255-95030256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536762762	chr1:95030262-95030263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144483928	chr1:95030263-95030264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574448716	chr1:95030309-95030310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576971410	chr1:95030319-95030320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539668778	chr1:95030368-95030369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552742505	chr1:95030380-95030381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147853946	chr1:95030388-95030389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186642410	chr1:95030399-95030400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192802087	chr1:95030404-95030405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95027000-95029000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:95028000-95029000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:95028000-95029000	Enhancers	Stomach Mucosa	stomach
4	chr1:95028000-95029000	Enhancers	HSMMtube	muscle
5	chr1:95028000-95029200	Enhancers	Fetal Intestine Large	intestine
6	chr1:95028200-95029000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:95028200-95029000	Enhancers	Colonic Mucosa	Colon
8	chr1:95028200-95029000	Enhancers	Duodenum Mucosa	Duodenum
9	chr1:95028200-95029000	Enhancers	Fetal Intestine Small	intestine
10	chr1:95028200-95029000	Enhancers	Placenta	Placenta
11	chr1:95028200-95029000	Enhancers	Placenta Amnion	Placenta Amnion
12	chr1:95028200-95029200	Enhancers	Hela-S3	cervix
13	chr1:95028400-95031400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:95028600-95029200	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr1:95028600-95032000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:95028600-95043400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:95028800-95029000	Enhancers	A549	lung
18	chr1:95028800-95029000	Enhancers	HepG2	liver
19	chr1:95028800-95029200	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr1:95029000-95034400	Weak transcription	HSMMtube	muscle
21	chr1:95031400-95031800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:95031800-95032400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr1:95031800-95032800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:95031800-95032800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:95032000-95032200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:95032200-95032600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:95032600-95033400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr1:95032800-95033000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:95033000-95033200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:95033200-95033800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:95033800-95035400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:95034400-95035000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:95034400-95035000	Enhancers	HSMMtube	muscle
34	chr1:95034800-95036600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:95035400-95036400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:95036400-95038600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:95036600-95036800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:95036600-95036800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:95036800-95037000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:95036800-95045200	Weak transcription	Stomach Mucosa	stomach
41	chr1:95038200-95038600	ZNF genes & repeats	Right Ventricle	heart
42	chr1:95038600-95038800	Weak transcription	Right Ventricle	heart
43	chr1:95038600-95046200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:95043400-95044000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:95043800-95044000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr1:95044000-95044200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:95044000-95044800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr1:95044200-95044600	Enhancers	Hela-S3	cervix
49	chr1:95044200-95046600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:95044200-95047000	Enhancers	NHEK	skin

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