Variant report

Variant	nsv871285
Chromosome Location	chr1:80996970-81071433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:62)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:81022589-81022754	K562	blood:	n/a	n/a
2	BACH1	chr1:80998868-80999129	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr1:81000531-81001133	HCT-116	colon:	n/a	n/a
4	CBX3	chr1:80996803-80997369	HCT-116	colon:	n/a	n/a
5	CEBPB	chr1:81004063-81004214	A549	lung:	n/a	chr1:81004073-81004086 chr1:81004075-81004086 chr1:81004073-81004086 chr1:81004073-81004086
6	CEBPB	chr1:81059670-81060151	MCF-7	breast:	n/a	n/a
7	CEBPB	chr1:81059738-81060035	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:81009753-81009933	HepG2	liver:	n/a	chr1:81009799-81009812 chr1:81009799-81009810
9	CEBPB	chr1:81006300-81006629	A549	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
10	CEBPB	chr1:81006278-81006649	IMR90	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
11	CEBPB	chr1:81059645-81060123	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr1:81006283-81006695	Hela-S3	cervix:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
13	CEBPB	chr1:81059740-81060029	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr1:81000182-81001093	HCT-116	colon:	n/a	n/a
15	CEBPB	chr1:81000600-81001165	HCT-116	colon:	n/a	n/a
16	CEBPB	chr1:81006302-81006643	HepG2	liver:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
17	CHD1	chr1:80998537-80998660	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr1:81000789-81000814	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:80998880-80999030	RPTEC	kidney:	n/a	chr1:80998881-80998888
20	CTCF	chr1:81058180-81058330	AG09309	skin:	n/a	n/a
21	CTCF	chr1:81049281-81049353	Fibrobl	skin:	n/a	n/a
22	CTCF	chr1:81000724-81000893	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr1:81000765-81000851	MCF-7	breast:	n/a	n/a
24	CTCF	chr1:81000680-81000830	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr1:81000746-81000849	Gliobla	brain:	n/a	n/a
26	CTCF	chr1:81000760-81000910	HEK293	kidney:	n/a	n/a
27	CTCF	chr1:81000720-81000870	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr1:81000698-81000888	GM12878	blood:	n/a	n/a
29	CTCF	chr1:81059391-81059433	LNCaP	prostate:	n/a	n/a
30	CTCF	chr1:80998820-80998970	HRE	kidney:	n/a	chr1:80998881-80998888
31	CTCF	chr1:81001636-81001652	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr1:81020220-81020370	AG09319	gingival:	n/a	n/a
33	E2F4	chr1:81051688-81051984	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr1:81021556-81021890	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr1:81025827-81026001	GM12878	blood:	n/a	chr1:81025887-81025898 chr1:81025867-81025878
36	EP300	chr1:81059600-81060142	MCF-7	breast:	n/a	n/a
37	EP300	chr1:81059533-81060129	ECC-1	luminal epithelium:	n/a	n/a
38	EP300	chr1:81059696-81060016	T-47D	breast:	n/a	n/a
39	EP300	chr1:80996904-80997290	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr1:81004195-81004219	GM12878	blood:	n/a	n/a
41	EP300	chr1:81059702-81060113	T-47D	breast:	n/a	n/a
42	EP300	chr1:81059587-81060163	ECC-1	luminal epithelium:	n/a	n/a
43	EP300	chr1:80996848-80997428	SK-N-SH_RA	brain:	n/a	n/a
44	FAM48A	chr1:81015128-81015211	GM12878	blood:	n/a	n/a
45	FAM48A	chr1:81069989-81070138	GM12878	blood:	n/a	n/a
46	FAM48A	chr1:81024665-81024835	GM12878	blood:	n/a	n/a
47	FOS	chr1:81000236-81000453	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:81006323-81006657	MCF10A-Er-Src	breast:	n/a	chr1:81006491-81006501 chr1:81006492-81006500
49	FOS	chr1:81000650-81001004	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:81007986-81008262	MCF10A-Er-Src	breast:	n/a	chr1:81008039-81008048 chr1:81008131-81008140

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:81001617-81001667	PANC-1	pancreas:	n/a
2	chr1:81001617-81001667	PANC-1	pancreas:	n/a
3	chr1:81001617-81001667	GM06990	blood:	n/a
4	chr1:81001617-81001667	SAEC	small airway:	n/a
5	chr1:81001617-81001667	GM12891	blood:	n/a
6	chr1:81001617-81001667	BJ	skin:	n/a
7	chr1:81001617-81001667	HNPCEpiC	eye:	n/a
8	chr1:81001617-81001667	GM19239	blood:	n/a
9	chr1:81001617-81001667	HIPEpiC	eye:	n/a
10	chr1:81001617-81001667	HUVEC	blood vessel:	n/a
11	chr1:81001617-81001667	NHDF-neo	bronchial:	n/a
12	chr1:81001617-81001667	AG04450	lung:	fetal
13	chr1:81001617-81001667	HCT-116	colon:	n/a
14	chr1:81001617-81001667	H1-hESC	embryonic stem cell:	embryo
15	chr1:81001617-81001667	NHBE	bronchial:	n/a
16	chr1:81001617-81001667	HEK293	kidney:	embryo
17	chr1:81001617-81001667	Hela-S3	cervix:	n/a
18	chr1:81001617-81001667	AG04449	skin:	fetal
19	chr1:81001617-81001667	BE2_C	brain:	n/a
20	chr1:81001617-81001667	HAEpiC	amniotic membrane:	n/a
21	chr1:81001617-81001667	T-47D	breast:	n/a
22	chr1:81001617-81001667	PFSK-1	brain:	n/a
23	chr1:81001617-81001667	PrEC	prostate:	n/a
24	chr1:81001617-81001667	HepG2	liver:	n/a
25	chr1:81001617-81001667	ProgFib	skin:	n/a
26	chr1:81001617-81001667	SK-N-SH	brain:	n/a
27	chr1:81001617-81001667	MCF-7	breast:	n/a
28	chr1:81001617-81001667	GM12892	blood:	n/a
29	chr1:81001617-81001667	RPTEC	kidney:	n/a
30	chr1:81001617-81001667	HRPEpiC	eye:	n/a
31	chr1:81001617-81001667	CMK	blood:	n/a
32	chr1:81001617-81001667	HRCEpiC	kidney:	n/a
33	chr1:81001617-81001667	Jurkat	blood:	n/a
34	chr1:81001617-81001667	SK-N-SH_RA	brain:	n/a
35	chr1:81001617-81001667	SK-N-MC	brain:	n/a
36	chr1:81001617-81001667	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:81001617-81001667	Caco-2	colon:	n/a
38	chr1:81001617-81001667	NB4	blood:	n/a
39	chr1:81001617-81001667	HCF	heart:	n/a
40	chr1:81001617-81001667	A549	lung:	n/a
41	chr1:81001617-81001667	HCM	heart:	n/a
42	chr1:81001617-81001667	NH-A	brain:	n/a
43	chr1:81001617-81001667	HL-60	blood:	n/a
44	chr1:81001617-81001667	GM12878	blood:	n/a
45	chr1:81001617-81001667	AG09319	gingival:	n/a
46	chr1:81001617-81001667	AG09309	skin:	n/a
47	chr1:81001617-81001667	ovcar-3	ovarian:	n/a
48	chr1:81001617-81001667	HCPEpiC	choroid plexus:	n/a
49	chr1:81001617-81001667	IMR90	lung:	fetal
50	chr1:81001617-81001667	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:81070565..81072592-chr1:81090453..81092983,2	MCF-7	breast:
2	chr1:81001450..81003092-chr6:32940222..32942950,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPHN2-1	chr1:81001439-81001627	NONHSAT004118
2	lnc-LPHN2-1	chr1:81006274-81006321	XLOC_000268
3	lnc-LPHN2-1	chr1:81001445-81001627	XLOC_000268
4	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
5	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
6	lnc-LPHN2-1	chr1:81006273-81006321	NONHSAT004118
7	lnc-ELTD1-8	chr1:81049975-81050048	XLOC_000883
8	lnc-LPHN2-1	chr1:81001424-81001627	NONHSAT004117
9	lnc-ELTD1-8	chr1:81000663-81000937	XLOC_000883

No data

Variant related genes	Relation type
ENSG00000234184	TF binding region
ENSG00000224326	TF binding region
ENSG00000234184	CpG island
ENSG00000224326	CpG island
ENSG00000204256	chromatin interactions
ENSG00000263756	chromatin interactions
NUFIP2	miRNA target sites

Extended variants
information (count: 1310 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1310 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs356298	chr1:80996970-80996971	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186206281	chr1:80997016-80997017	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs546621146	chr1:80997022-80997023	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs372253774	chr1:80997090-80997091	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs191350507	chr1:80997107-80997108	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs116302087	chr1:80997116-80997117	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs60224894	chr1:80997134-80997135	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs75745337	chr1:80997148-80997149	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs547677651	chr1:80997164-80997165	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs117313206	chr1:80997172-80997173	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs555193990	chr1:80997203-80997204	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551401388	chr1:80997214-80997215	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141964618	chr1:80997217-80997218	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12136919	chr1:80997222-80997223	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs66657776	chr1:80997223-80997224	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs76301612	chr1:80997225-80997226	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs571243467	chr1:80997254-80997255	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs72937337	chr1:80997257-80997258	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs530623958	chr1:80997280-80997281	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs550399021	chr1:80997331-80997332	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs537182950	chr1:80997343-80997344	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs199652675	chr1:80997365-80997366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs373395586	chr1:80997384-80997385	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs550083152	chr1:80997402-80997403	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs570154170	chr1:80997434-80997435	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs566541247	chr1:80997488-80997489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569883670	chr1:80997505-80997506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139252080	chr1:80997547-80997548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149597745	chr1:80997564-80997565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569293833	chr1:80997586-80997587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17104942	chr1:80997644-80997645	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs182992034	chr1:80997645-80997646	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs535664593	chr1:80997648-80997649	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs144268569	chr1:80997662-80997663	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs538716090	chr1:80997663-80997664	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs187363729	chr1:80997691-80997692	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs572798203	chr1:80997710-80997711	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs148461517	chr1:80997736-80997737	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs12070796	chr1:80997745-80997746	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572323808	chr1:80997802-80997803	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs374090136	chr1:80997809-80997810	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs535342638	chr1:80997819-80997820	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs575275919	chr1:80997869-80997870	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs533757458	chr1:80997888-80997889	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs560770613	chr1:80997907-80997908	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs191057084	chr1:80997947-80997948	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs546498385	chr1:80997953-80997954	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs560235300	chr1:80997974-80997975	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs114960834	chr1:80998007-80998008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369381069	chr1:80998037-80998038	Weak transcription Enhancers	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
Multiple myeloma	17550852	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80996400-80997600	Enhancers	Primary T cells from cord blood	blood
2	chr1:80996800-80997200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:80996800-80997200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:80997000-80997200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr1:80997000-80997200	Enhancers	Fetal Kidney	kidney
6	chr1:80997000-80997400	Enhancers	Dnd41	blood
7	chr1:80997000-80999400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr1:80997200-80997400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:80997200-80997400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:80997200-80998000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr1:80997200-80998600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:80997200-80998600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:80997200-80998600	Weak transcription	Fetal Kidney	kidney
14	chr1:80997400-81000600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:80997600-80997800	Enhancers	Ovary	ovary
16	chr1:80997600-80998000	Bivalent Enhancer	Primary T cells from cord blood	blood
17	chr1:80998000-80998200	Enhancers	Colon Smooth Muscle	Colon
18	chr1:80998000-80998400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:80998000-81001800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:80998200-80998800	Weak transcription	Colon Smooth Muscle	Colon
21	chr1:80998400-80999200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr1:80998400-80999400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:80998400-80999400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:80998400-80999400	Enhancers	Brain Germinal Matrix	brain
25	chr1:80998400-81000200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:80998400-81001000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr1:80998600-80998800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr1:80998600-80998800	Active TSS	A549	lung
29	chr1:80998600-80999400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:80998600-80999400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr1:80998600-81000000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr1:80998600-81000000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:80998600-81000000	Enhancers	Fetal Kidney	kidney
34	chr1:80998600-81000800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr1:80998600-81000800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:80998600-81001600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:80998600-81003400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:80998600-81003600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr1:80998600-81003600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr1:80998800-80999000	Flanking Active TSS	A549	lung
41	chr1:80998800-80999400	Enhancers	Brain Hippocampus Middle	brain
42	chr1:80998800-80999400	Enhancers	HMEC	breast
43	chr1:80998800-80999800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr1:80998800-81000000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr1:80998800-81000000	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr1:80998800-81000800	Enhancers	Colon Smooth Muscle	Colon
47	chr1:80999000-80999200	Active TSS	A549	lung
48	chr1:80999000-81000000	Enhancers	Fetal Brain Female	brain
49	chr1:80999200-80999400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr1:80999200-80999400	Enhancers	Brain Cingulate Gyrus	brain

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