Variant report

Variant	nsv546667
Chromosome Location	chr1:80926312-81042755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

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	BCL11A	chr1:80975728-80975960	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr1:80996803-80997369	HCT-116	colon:	n/a	n/a
5	CBX3	chr1:81000531-81001133	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:80991142-80991478	IMR90	lung:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
7	CEBPB	chr1:80991202-80991443	HepG2	liver:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
8	CEBPB	chr1:81006300-81006629	A549	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
9	CEBPB	chr1:81006278-81006649	IMR90	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
10	CEBPB	chr1:81000600-81001165	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:81004063-81004214	A549	lung:	n/a	chr1:81004073-81004086 chr1:81004075-81004086 chr1:81004073-81004086 chr1:81004073-81004086
12	CEBPB	chr1:81000182-81001093	HCT-116	colon:	n/a	n/a
13	CEBPB	chr1:80991969-80992035	HepG2	liver:	n/a	chr1:80992011-80992022 chr1:80992011-80992024
14	CEBPB	chr1:80989668-80989956	A549	lung:	n/a	n/a
15	CEBPB	chr1:80927341-80927564	A549	lung:	n/a	chr1:80927464-80927477
16	CEBPB	chr1:80989649-80990016	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:81006302-81006643	HepG2	liver:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
18	CEBPB	chr1:81006283-81006695	Hela-S3	cervix:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
19	CEBPB	chr1:81009753-81009933	HepG2	liver:	n/a	chr1:81009799-81009812 chr1:81009799-81009810
20	CEBPB	chr1:80936700-80937019	HepG2	liver:	n/a	chr1:80936873-80936882 chr1:80936873-80936884 chr1:80936871-80936884 chr1:80936871-80936882 chr1:80936871-80936884 chr1:80936871-80936884
21	CHD1	chr1:80998537-80998660	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr1:80975773-80976006	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:80998820-80998970	HRE	kidney:	n/a	chr1:80998881-80998888
24	CTCF	chr1:81020220-81020370	AG09319	gingival:	n/a	n/a
25	CTCF	chr1:80951760-80951910	AG10803	skin:	n/a	n/a
26	CTCF	chr1:81000680-81000830	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr1:81000789-81000814	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:81000724-81000893	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr1:81000765-81000851	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:81000746-81000849	Gliobla	brain:	n/a	n/a
31	CTCF	chr1:81000698-81000888	GM12878	blood:	n/a	n/a
32	CTCF	chr1:81000720-81000870	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr1:81000760-81000910	HEK293	kidney:	n/a	n/a
34	CTCF	chr1:80998880-80999030	RPTEC	kidney:	n/a	chr1:80998881-80998888
35	CTCF	chr1:80953200-80953350	GM12868	blood:	n/a	n/a
36	CTCF	chr1:81001636-81001652	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:80962340-80962490	HCPEpiC	choroid plexus:	n/a	n/a
38	E2F4	chr1:81021556-81021890	MCF10A-Er-Src	breast:	n/a	n/a
39	EBF1	chr1:81025827-81026001	GM12878	blood:	n/a	chr1:81025887-81025898 chr1:81025867-81025878
40	EP300	chr1:80975532-80975535	K562	blood:	n/a	n/a
41	EP300	chr1:80996904-80997290	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr1:80975614-80976036	H1-hESC	embryonic stem cell:	n/a	n/a
43	EP300	chr1:80927045-80927335	T-47D	breast:	n/a	n/a
44	EP300	chr1:81004195-81004219	GM12878	blood:	n/a	n/a
45	EP300	chr1:80996848-80997428	SK-N-SH_RA	brain:	n/a	n/a
46	FAM48A	chr1:81015128-81015211	GM12878	blood:	n/a	n/a
47	FAM48A	chr1:81024665-81024835	GM12878	blood:	n/a	n/a
48	FOS	chr1:81000687-81001000	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:80945014-80945348	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:80945028-80945316	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:81001617-81001667	BE2_C	brain:	n/a
2	chr1:81001617-81001667	AG09309	skin:	n/a
3	chr1:81001617-81001667	HUVEC	blood vessel:	n/a
4	chr1:80961906-80961956	ovcar-3	ovarian:	n/a
5	chr1:81001617-81001667	AG04449	skin:	fetal
6	chr1:80961906-80961956	U87	brain:	n/a
7	chr1:80961776-80961826	AG09319	gingival:	n/a
8	chr1:80961769-80961819	GM19239	blood:	n/a
9	chr1:80961906-80961956	HRCEpiC	kidney:	n/a
10	chr1:81001617-81001667	NHBE	bronchial:	n/a
11	chr1:80961906-80961956	MCF10A-Er-Src	breast:	n/a
12	chr1:80961906-80961956	SKMC	muscle:	n/a
13	chr1:80961906-80961956	HCM	heart:	n/a
14	chr1:81001617-81001667	ovcar-3	ovarian:	n/a
15	chr1:81001617-81001667	HCT-116	colon:	n/a
16	chr1:80961769-80961819	T-47D	breast:	n/a
17	chr1:80961906-80961956	ECC-1	luminal epithelium:	n/a
18	chr1:81001617-81001667	CMK	blood:	n/a
19	chr1:80961906-80961956	SK-N-SH_RA	brain:	n/a
20	chr1:81001617-81001667	HL-60	blood:	n/a
21	chr1:80961776-80961826	HRCEpiC	kidney:	n/a
22	chr1:80961769-80961819	SKMC	muscle:	n/a
23	chr1:80961769-80961819	HRPEpiC	eye:	n/a
24	chr1:81001617-81001667	NHDF-neo	bronchial:	n/a
25	chr1:80961776-80961826	K562	blood:	n/a
26	chr1:80961906-80961956	HEEpiC	esophagus:	n/a
27	chr1:81001617-81001667	SAEC	small airway:	n/a
28	chr1:80961906-80961956	LNCaP	prostate:	n/a
29	chr1:80961906-80961956	HAEpiC	amniotic membrane:	n/a
30	chr1:80961906-80961956	BJ	skin:	n/a
31	chr1:81001617-81001667	PFSK-1	brain:	n/a
32	chr1:80961769-80961819	HL-60	blood:	n/a
33	chr1:80961906-80961956	PrEC	prostate:	n/a
34	chr1:80961769-80961819	HEK293	kidney:	embryo
35	chr1:80961776-80961826	HepG2	liver:	n/a
36	chr1:80961906-80961956	HNPCEpiC	eye:	n/a
37	chr1:80961769-80961819	GM12892	blood:	n/a
38	chr1:80961906-80961956	GM12878	blood:	n/a
39	chr1:80961906-80961956	GM06990	blood:	n/a
40	chr1:80961906-80961956	HUVEC	blood vessel:	n/a
41	chr1:80961906-80961956	GM12891	blood:	n/a
42	chr1:80961776-80961826	PFSK-1	brain:	n/a
43	chr1:80961769-80961819	HEEpiC	esophagus:	n/a
44	chr1:80961769-80961819	PFSK-1	brain:	n/a
45	chr1:80961906-80961956	HRE	kidney:	n/a
46	chr1:81001617-81001667	GM19239	blood:	n/a
47	chr1:80961769-80961819	HNPCEpiC	eye:	n/a
48	chr1:80961769-80961819	AG04450	lung:	fetal
49	chr1:81001617-81001667	Hepatocyte	liver:	n/a
50	chr1:81001617-81001667	PrEC	prostate:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:80928602..80929152-chr11:66112041..66112777,2	HCT-116	colon:
2	chr1:81001450..81003092-chr6:32940222..32942950,2	MCF-7	breast:
3	chr1:80968594..80969285-chr1:159113721..159114329,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPHN2-1	chr1:81001424-81001627	NONHSAT004117
2	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
3	lnc-LPHN2-1	chr1:81006273-81006321	NONHSAT004118
4	lnc-LPHN2-1	chr1:81001445-81001627	XLOC_000268
5	lnc-ELTD1-8	chr1:81000663-81000937	XLOC_000883
6	lnc-LPHN2-1	chr1:81001439-81001627	NONHSAT004118
7	lnc-ELTD1-14	chr1:80929986-80930403	NONHSAT004115
8	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
9	lnc-LPHN2-1	chr1:81006274-81006321	XLOC_000268

No data

Variant related genes	Relation type
ENSG00000234184	TF binding region
ENSG00000227062	TF binding region
ENSG00000234108	TF binding region
ENSG00000234184	CpG island
ENSG00000227062	CpG island
ENSG00000234108	CpG island
ENSG00000204256	chromatin interactions
ENSG00000174744	chromatin interactions
ENSG00000263756	chromatin interactions
NUFIP2	miRNA target sites

Extended variants
information (count: 1557 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1557 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201411974	chr1:80928732-80928733	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs184139031	chr1:80928736-80928737	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143816422	chr1:80928753-80928754	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148094364	chr1:80928756-80928757	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs74773764	chr1:80928782-80928783	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543916683	chr1:80928799-80928800	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs188694595	chr1:80928876-80928877	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141831847	chr1:80928910-80928911	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552691707	chr1:80928940-80928941	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs544411349	chr1:80929004-80929005	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544828692	chr1:80929017-80929018	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565112145	chr1:80929040-80929041	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147276033	chr1:80929050-80929051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540873613	chr1:80929110-80929111	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs115735407	chr1:80929120-80929121	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139569042	chr1:80930003-80930004	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs149753523	chr1:80930031-80930032	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs79932004	chr1:80930058-80930059	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs117734373	chr1:80930089-80930090	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs75606785	chr1:80930147-80930148	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs76859691	chr1:80930148-80930149	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs527999736	chr1:80930179-80930180	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs115920966	chr1:80930204-80930205	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs145611541	chr1:80930216-80930217	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs548127169	chr1:80930220-80930221	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs148407076	chr1:80930237-80930238	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs17104872	chr1:80930270-80930271	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs568950629	chr1:80930331-80930332	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs567946778	chr1:80930337-80930338	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs75964668	chr1:80930371-80930372	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs558583090	chr1:80930392-80930393	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs568287932	chr1:80931056-80931057	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs560719234	chr1:80931096-80931097	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs534075654	chr1:80931124-80931125	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs188128248	chr1:80931131-80931132	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs17104873	chr1:80931197-80931198	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs74099210	chr1:80931256-80931257	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs144663707	chr1:80931267-80931268	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs531410684	chr1:80931757-80931758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs548348530	chr1:80931779-80931780	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs147867023	chr1:80931847-80931848	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs199613175	chr1:80931886-80931887	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568249564	chr1:80931913-80931914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs533946212	chr1:80931938-80931939	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs547276418	chr1:80931955-80931956	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs570696105	chr1:80932000-80932001	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs10735761	chr1:80932058-80932059	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs527723582	chr1:80932059-80932060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs181241389	chr1:80932101-80932102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs140539314	chr1:80932183-80932184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80938800-80939600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:80939600-80940200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:80951200-80951800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:80961600-80961800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:80961600-80961800	ZNF genes & repeats	Pancreas	Pancrea
6	chr1:80963600-80964600	Enhancers	Fetal Lung	lung
7	chr1:80964200-80964600	Enhancers	Adipose Nuclei	Adipose
8	chr1:80964200-80964600	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr1:80964200-80964600	Enhancers	Fetal Brain Female	brain
10	chr1:80964200-80964800	Enhancers	Fetal Heart	heart
11	chr1:80964200-80965000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:80964400-80964600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:80970800-80971000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:80971200-80972000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:80971600-80971800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:80971600-80972600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:80971800-80972200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr1:80971800-80972200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr1:80971800-80972200	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr1:80971800-80972400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:80971800-80972400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr1:80971800-80972600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:80972000-80972200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:80972000-80972200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:80972000-80972400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr1:80972200-80972600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr1:80972200-80975600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr1:80972400-80975400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:80972400-80975600	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr1:80975400-80975800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:80975400-80975800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:80975400-80975800	Enhancers	HSMMtube	muscle
33	chr1:80975400-80976000	Enhancers	H9 Cell Line	embryonic stem cell
34	chr1:80975600-80975800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr1:80975600-80975800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr1:80975600-80975800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:80975600-80976200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr1:80975600-80976200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:80987400-80988000	Enhancers	Adipose Nuclei	Adipose
40	chr1:80989800-80990000	Enhancers	Adipose Nuclei	Adipose
41	chr1:80989800-80990400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:80996400-80997600	Enhancers	Primary T cells from cord blood	blood
43	chr1:80996800-80997200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:80996800-80997200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:80997000-80997200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr1:80997000-80997200	Enhancers	Fetal Kidney	kidney
47	chr1:80997000-80997400	Enhancers	Dnd41	blood
48	chr1:80997000-80999400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr1:80997200-80997400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:80997200-80997400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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