Variant report

Variant	nsv548551
Chromosome Location	chr1:190433413-190496007
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	ATF1	chr1:190468018-190468035	K562	blood:	n/a	n/a
2	BACH1	chr1:190444539-190444919	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:190486481-190486484	K562	blood:	n/a	n/a
4	BRCA1	chr1:190448178-190448180	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:190482609-190482928	K562	blood:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
6	CEBPB	chr1:190447237-190447354	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr1:190448377-190448519	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:190482603-190482902	Hela-S3	cervix:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
9	CEBPB	chr1:190482561-190482944	IMR90	lung:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
10	CEBPB	chr1:190444585-190445212	IMR90	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
11	CEBPB	chr1:190482588-190482907	A549	lung:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
12	CEBPB	chr1:190444708-190445343	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
13	CEBPB	chr1:190463528-190463986	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:190444814-190445176	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
15	CEBPB	chr1:190482496-190482946	HepG2	liver:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
16	CEBPB	chr1:190444631-190445184	H1-hESC	embryonic stem cell:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
17	CEBPB	chr1:190444837-190445233	MCF-7	breast:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
18	CEBPB	chr1:190482634-190482949	H1-hESC	embryonic stem cell:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
19	CEBPB	chr1:190444847-190445175	K562	blood:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
20	CEBPB	chr1:190444781-190445213	MCF-7	breast:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
21	CEBPB	chr1:190444799-190445222	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
22	CEBPB	chr1:190444800-190445186	HepG2	liver:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
23	CHD1	chr1:190444232-190444267	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr1:190448119-190448317	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr1:190447111-190447248	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr1:190448095-190448332	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:190447252-190447284	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr1:190444200-190444215	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr1:190447174-190448394	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:190448840-190448990	BE2_C	brain:	n/a	n/a
31	CTCF	chr1:190447380-190447530	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr1:190447522-190447524	Gliobla	brain:	n/a	n/a
33	CTCF	chr1:190447340-190447490	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr1:190460620-190460770	HCT-116	colon:	n/a	n/a
35	CTCF	chr1:190447380-190447530	HPF	lung:	n/a	n/a
36	CTCF	chr1:190447320-190447470	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr1:190447280-190447430	HAc	cerebellar:	n/a	n/a
38	CTCF	chr1:190447393-190447440	GM12891	blood:	n/a	n/a
39	CTCF	chr1:190447200-190447350	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:190460637-190460740	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr1:190447360-190447510	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr1:190447312-190447506	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:190448845-190448930	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:190447360-190447510	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr1:190448800-190448950	HCT-116	colon:	n/a	n/a
46	CTCF	chr1:190447280-190447430	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr1:190447340-190447490	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr1:190447460-190447610	AG04450	lung:	n/a	n/a
49	CTCF	chr1:190447360-190447510	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr1:190460400-190460550	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:190447421-190447471	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:190446829-190446879	HEK293	kidney:	embryo
3	chr1:190447421-190447471	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:190446829-190446879	HEK293	kidney:	embryo
5	chr1:190444761-190444811	NHBE	bronchial:	n/a
6	chr1:190446756-190446806	AG09319	gingival:	n/a
7	chr1:190447290-190447340	HAEpiC	amniotic membrane:	n/a
8	chr1:190447603-190447653	Hela-S3	cervix:	n/a
9	chr1:190444825-190444875	IMR90	lung:	fetal
10	chr1:190446756-190446806	ECC-1	luminal epithelium:	n/a
11	chr1:190447290-190447340	SK-N-SH_RA	brain:	n/a
12	chr1:190447603-190447653	SK-N-MC	brain:	n/a
13	chr1:190445197-190445247	Hepatocyte	liver:	n/a
14	chr1:190447421-190447471	AG04450	lung:	fetal
15	chr1:190447421-190447471	AG10803	skin:	n/a
16	chr1:190446829-190446879	SK-N-SH	brain:	n/a
17	chr1:190447232-190447282	HAEpiC	amniotic membrane:	n/a
18	chr1:190447640-190447690	GM19239	blood:	n/a
19	chr1:190444387-190444437	LNCaP	prostate:	n/a
20	chr1:190444387-190444437	HNPCEpiC	eye:	n/a
21	chr1:190447290-190447340	SK-N-MC	brain:	n/a
22	chr1:190447603-190447653	A549	lung:	n/a
23	chr1:190447603-190447653	HAEpiC	amniotic membrane:	n/a
24	chr1:190446829-190446879	AG09309	skin:	n/a
25	chr1:190446756-190446806	HCF	heart:	n/a
26	chr1:190444825-190444875	PrEC	prostate:	n/a
27	chr1:190447421-190447471	NT2-D1	testis:	n/a
28	chr1:190444776-190444826	SK-N-MC	brain:	n/a
29	chr1:190444387-190444437	HCF	heart:	n/a
30	chr1:190446756-190446806	ProgFib	skin:	n/a
31	chr1:190447290-190447340	GM12892	blood:	n/a
32	chr1:190446756-190446806	SK-N-SH	brain:	n/a
33	chr1:190445197-190445247	LNCaP	prostate:	n/a
34	chr1:190447232-190447282	Hepatocyte	liver:	n/a
35	chr1:190447603-190447653	GM12892	blood:	n/a
36	chr1:190444761-190444811	MCF10A-Er-Src	breast:	n/a
37	chr1:190447640-190447690	SK-N-SH_RA	brain:	n/a
38	chr1:190447290-190447340	K562	blood:	n/a
39	chr1:190447421-190447471	NB4	blood:	n/a
40	chr1:190444387-190444437	PFSK-1	brain:	n/a
41	chr1:190447640-190447690	H1-hESC	embryonic stem cell:	embryo
42	chr1:190445197-190445247	HRE	kidney:	n/a
43	chr1:190447290-190447340	GM06990	blood:	n/a
44	chr1:190444776-190444826	AG04449	skin:	fetal
45	chr1:190447603-190447653	AG09319	gingival:	n/a
46	chr1:190446756-190446806	MCF10A-Er-Src	breast:	n/a
47	chr1:190445197-190445247	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:190447640-190447690	NHDF-neo	bronchial:	n/a
49	chr1:190447421-190447471	LNCaP	prostate:	n/a
50	chr1:190448126-190448176	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:190405958..190408213-chr1:190432999..190435234,2	K562	blood:
2	chr1:190456328..190457105-chr20:42218949..42219566,2	Hela-S3	cervix:
3	chr1:190438085..190440650-chr1:190553313..190555425,2	K562	blood:
4	chr1:190476606..190478933-chr1:190479727..190481548,2	MCF-7	breast:
5	chr1:190481525..190484334-chr1:190501308..190503770,2	K562	blood:
6	chr1:190476606..190478933-chr1:190479727..190481548,2	MCF-7	breast:
7	chr1:190443878..190446178-chr1:190461343..190463264,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-5	chr1:190449475-190450669	XLOC_000505
2	lnc-RGS18-5	chr1:190448171-190448271	XLOC_000505
3	lnc-RGS18-5	chr1:190445011-190445157	NONHSAT008495
4	lnc-RGS18-5	chr1:190448136-190448270	XLOC_000505
5	lnc-RGS18-5	chr1:190449509-190449554	ENSG00000241505
6	lnc-RGS18-5	chr1:190444703-190444884	NONHSAT008495
7	lnc-RGS18-5	chr1:190449475-190449779	NONHSAT008496
8	lnc-RGS18-5	chr1:190449475-190450669	XLOC_000505
9	lnc-RGS18-5	chr1:190449475-190449865	XLOC_000505
10	lnc-RGS18-5	chr1:190447681-190447761	XLOC_000505
11	lnc-RGS18-5	chr1:190447329-190447761	NONHSAT008498
12	lnc-RGS18-5	chr1:190449475-190450667	XLOC_000505
13	lnc-RGS18-5	chr1:190448171-190448270	XLOC_000505
14	lnc-RGS18-5	chr1:190462968-190463251	XLOC_000505
15	lnc-RGS18-5	chr1:190449475-190449865	XLOC_000505
16	lnc-RGS18-5	chr1:190449475-190449704	XLOC_000505
17	lnc-RGS18-5	chr1:190449475-190450523	XLOC_000505
18	lnc-RGS18-5	chr1:190444999-190445131	NONHSAT008496
19	lnc-RGS18-5	chr1:190446965-190447761	NONHSAT008497
20	lnc-RGS18-5	chr1:190447356-190447622	XLOC_000505
21	lnc-RGS18-5	chr1:190447390-190447622	XLOC_000505
22	lnc-RGS18-5	chr1:190447611-190447761	XLOC_000505
23	lnc-RGS18-5	chr1:190447593-190447761	XLOC_000505
24	lnc-RGS18-5	chr1:190448212-190448255	NONHSAT008497
25	lnc-RGS18-5	chr1:190447753-190447761	XLOC_000505
26	lnc-RGS18-5	chr1:190447888-190448066	NONHSAT008498
27	lnc-RGS18-5	chr1:190462968-190463427	ENSG00000241505
28	lnc-RGS18-5	chr1:190448171-190448270	XLOC_000505
29	lnc-RGS18-5	chr1:190448212-190448270	XLOC_000505
30	lnc-RGS18-5	chr1:190447939-190447943	XLOC_000505

Variant related genes	Relation type
ENSG00000237457	TF binding region
ENSG00000241505	TF binding region
BRINP3	TF binding region
ENSG00000237457	CpG island
ENSG00000241505	CpG island
BRINP3	CpG island
ENSG00000162670	chromatin interactions
NRAS	miRNA target sites
PDLIM5	miRNA target sites
FECH	miRNA target sites
PRNP	miRNA target sites

Extended variants
information (count: 1057 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1697590	chr1:190433413-190433414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182895243	chr1:190433436-190433437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557286351	chr1:190433480-190433481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187525937	chr1:190433568-190433569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544963899	chr1:190433611-190433612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542759168	chr1:190433622-190433623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115244145	chr1:190433653-190433654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528517463	chr1:190433654-190433655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192051890	chr1:190433669-190433670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564070001	chr1:190433696-190433697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578144204	chr1:190433748-190433749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533081785	chr1:190433770-190433771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551757947	chr1:190433781-190433782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114388739	chr1:190433824-190433825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185682176	chr1:190433831-190433832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548843070	chr1:190433841-190433842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368866064	chr1:190433854-190433855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565749936	chr1:190433910-190433911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188961700	chr1:190433930-190433931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369110460	chr1:190433933-190433934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142991616	chr1:190433962-190433963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192395219	chr1:190433973-190433974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374372403	chr1:190433982-190433983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184297955	chr1:190434006-190434007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557586839	chr1:190434058-190434059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574200012	chr1:190434083-190434084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536843457	chr1:190434101-190434102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560903798	chr1:190434189-190434190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553228170	chr1:190434267-190434268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188723411	chr1:190434273-190434274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545073052	chr1:190434275-190434276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564955321	chr1:190434287-190434288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575193755	chr1:190434301-190434302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12121826	chr1:190434304-190434305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181107216	chr1:190434312-190434313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550505933	chr1:190434313-190434314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563587848	chr1:190434353-190434354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7413967	chr1:190434411-190434412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150689937	chr1:190434414-190434415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184163036	chr1:190434507-190434508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189241280	chr1:190434525-190434526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528209906	chr1:190434560-190434561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551453506	chr1:190434589-190434590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115380203	chr1:190434620-190434621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537041226	chr1:190434626-190434627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79192931	chr1:190434639-190434640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139942685	chr1:190434670-190434671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149772249	chr1:190434674-190434675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553555966	chr1:190434683-190434684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573068769	chr1:190434736-190434737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:190422000-190438400	Weak transcription	Fetal Intestine Large	intestine
2	chr1:190422800-190438800	Weak transcription	Fetal Intestine Small	intestine
3	chr1:190436200-190436600	Enhancers	Fetal Heart	heart
4	chr1:190438400-190439000	Active TSS	Fetal Intestine Large	intestine
5	chr1:190438800-190439400	Enhancers	Fetal Intestine Small	intestine
6	chr1:190439000-190440200	Weak transcription	Fetal Intestine Large	intestine
7	chr1:190439400-190441200	Weak transcription	Fetal Intestine Small	intestine
8	chr1:190440000-190440200	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr1:190440000-190448800	Active TSS	Duodenum Mucosa	Duodenum
10	chr1:190440200-190448800	Active TSS	Fetal Intestine Large	intestine
11	chr1:190440600-190441000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:190440800-190448600	Active TSS	Rectal Mucosa Donor 31	rectum
13	chr1:190440800-190448800	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr1:190441000-190445800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:190441200-190441800	Active TSS	Brain Germinal Matrix	brain
16	chr1:190441200-190443600	Active TSS	Brain Inferior Temporal Lobe	brain
17	chr1:190441200-190448600	Active TSS	Fetal Intestine Small	intestine
18	chr1:190441200-190448600	Active TSS	Right Atrium	heart
19	chr1:190441400-190444600	Active TSS	Brain Angular Gyrus	brain
20	chr1:190441400-190445600	Active TSS	Brain Anterior Caudate	brain
21	chr1:190441800-190442200	Active TSS	Fetal Lung	lung
22	chr1:190441800-190442600	Weak transcription	Brain Germinal Matrix	brain
23	chr1:190442200-190442400	Bivalent/Poised TSS	Fetal Lung	lung
24	chr1:190442600-190443800	Active TSS	Fetal Stomach	stomach
25	chr1:190442600-190445000	Active TSS	Cortex derived primary cultured neurospheres	brain
26	chr1:190442600-190445200	Active TSS	Brain Germinal Matrix	brain
27	chr1:190442800-190444200	Active TSS	Fetal Brain Female	brain
28	chr1:190443000-190443800	Active TSS	Brain Cingulate Gyrus	brain
29	chr1:190443000-190445600	Active TSS	Colonic Mucosa	Colon
30	chr1:190443000-190449600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr1:190443200-190443400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr1:190443200-190443400	Active TSS	Fetal Brain Male	brain
33	chr1:190443200-190445600	Bivalent/Poised TSS	Fetal Lung	lung
34	chr1:190443200-190445800	Active TSS	Fetal Heart	heart
35	chr1:190443400-190443600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
36	chr1:190443400-190443600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chr1:190443400-190443600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
38	chr1:190443400-190443600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
39	chr1:190443400-190443600	Active TSS	Small Intestine	intestine
40	chr1:190443400-190443600	Active TSS	Stomach Smooth Muscle	stomach
41	chr1:190443400-190443800	Bivalent/Poised TSS	Fetal Brain Male	brain
42	chr1:190443400-190443800	Flanking Bivalent TSS/Enh	A549	lung
43	chr1:190443400-190444000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
44	chr1:190443400-190444200	Active TSS	Brain Substantia Nigra	brain
45	chr1:190443400-190444600	Active TSS	Brain Hippocampus Middle	brain
46	chr1:190443400-190445400	Bivalent/Poised TSS	Fetal Kidney	kidney
47	chr1:190443400-190445800	Active TSS	Rectal Smooth Muscle	rectum
48	chr1:190443600-190443800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
49	chr1:190443600-190443800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
50	chr1:190443600-190443800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell

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