Variant report

Variant	nsv546665
Chromosome Location	chr1:80888808-81042755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:306)
Chromatin interactive
region (count:7)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

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	BRCA1	chr1:80910757-80911113	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr1:80996803-80997369	HCT-116	colon:	n/a	n/a
6	CBX3	chr1:81000531-81001133	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:80923207-80923467	H1-hESC	embryonic stem cell:	n/a	chr1:80923417-80923428 chr1:80923417-80923430
8	CEBPB	chr1:80910816-80911185	HCT-116	colon:	n/a	n/a
9	CEBPB	chr1:80989668-80989956	A549	lung:	n/a	n/a
10	CEBPB	chr1:81006302-81006643	HepG2	liver:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
11	CEBPB	chr1:80991202-80991443	HepG2	liver:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
12	CEBPB	chr1:80991142-80991478	IMR90	lung:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
13	CEBPB	chr1:80912499-80912558	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:81000600-81001165	HCT-116	colon:	n/a	n/a
15	CEBPB	chr1:81006300-81006629	A549	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
16	CEBPB	chr1:81006283-81006695	Hela-S3	cervix:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
17	CEBPB	chr1:80910551-80911194	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:80923285-80923514	A549	lung:	n/a	chr1:80923417-80923428 chr1:80923417-80923430
19	CEBPB	chr1:80912368-80912659	A549	lung:	n/a	n/a
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	CEBPB	chr1:80912210-80912676	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:81004063-81004214	A549	lung:	n/a	chr1:81004073-81004086 chr1:81004075-81004086 chr1:81004073-81004086 chr1:81004073-81004086
23	CEBPB	chr1:80989649-80990016	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:80912346-80912654	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:80923262-80923547	Hela-S3	cervix:	n/a	chr1:80923417-80923428 chr1:80923417-80923430
26	CEBPB	chr1:80913237-80913619	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:81009753-81009933	HepG2	liver:	n/a	chr1:81009799-81009812 chr1:81009799-81009810
28	CEBPB	chr1:80927341-80927564	A549	lung:	n/a	chr1:80927464-80927477
29	CEBPB	chr1:81000182-81001093	HCT-116	colon:	n/a	n/a
30	CEBPB	chr1:80991969-80992035	HepG2	liver:	n/a	chr1:80992011-80992022 chr1:80992011-80992024
31	CEBPB	chr1:81006278-81006649	IMR90	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
32	CEBPB	chr1:80910689-80911261	HCT-116	colon:	n/a	n/a
33	CHD1	chr1:80998537-80998660	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr1:80975773-80976006	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr1:81000680-81000830	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr1:81001636-81001652	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:80907480-80907630	HMEC	breast:	n/a	n/a
38	CTCF	chr1:80907480-80907630	GM12873	blood:	n/a	n/a
39	CTCF	chr1:80907460-80907610	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:80907480-80907630	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr1:81000765-81000851	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:80907482-80907644	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:80907479-80907584	HepG2	liver:	n/a	n/a
44	CTCF	chr1:80907460-80907610	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr1:81000724-81000893	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr1:80907468-80907577	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr1:80907487-80907613	ProgFib	skin:	n/a	n/a
48	CTCF	chr1:80951760-80951910	AG10803	skin:	n/a	n/a
49	CTCF	chr1:80907440-80907590	BE2_C	brain:	n/a	n/a
50	CTCF	chr1:80907480-80907630	HMF	breast:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:80961906-80961956	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:80961906-80961956	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:80961769-80961819	RPTEC	kidney:	n/a
4	chr1:80961776-80961826	Jurkat	blood:	n/a
5	chr1:80961906-80961956	HCPEpiC	choroid plexus:	n/a
6	chr1:80961906-80961956	NHDF-neo	bronchial:	n/a
7	chr1:80961769-80961819	AG09309	skin:	n/a
8	chr1:80961906-80961956	NH-A	brain:	n/a
9	chr1:80961776-80961826	HCT-116	colon:	n/a
10	chr1:80961776-80961826	HCF	heart:	n/a
11	chr1:81001617-81001667	MCF10A-Er-Src	breast:	n/a
12	chr1:80923103-80923153	HMEC	breast:	n/a
13	chr1:81001617-81001667	HRPEpiC	eye:	n/a
14	chr1:81001617-81001667	MCF-7	breast:	n/a
15	chr1:81001617-81001667	Caco-2	colon:	n/a
16	chr1:80923103-80923153	MCF10A-Er-Src	breast:	n/a
17	chr1:80961906-80961956	K562	blood:	n/a
18	chr1:80961769-80961819	LNCaP	prostate:	n/a
19	chr1:80961769-80961819	BJ	skin:	n/a
20	chr1:80961776-80961826	AG09309	skin:	n/a
21	chr1:80961769-80961819	HCPEpiC	choroid plexus:	n/a
22	chr1:81001617-81001667	Jurkat	blood:	n/a
23	chr1:81001617-81001667	BJ	skin:	n/a
24	chr1:80961906-80961956	HIPEpiC	eye:	n/a
25	chr1:80961769-80961819	NH-A	brain:	n/a
26	chr1:80961769-80961819	AG09319	gingival:	n/a
27	chr1:81001617-81001667	AG09319	gingival:	n/a
28	chr1:80961776-80961826	H1-hESC	embryonic stem cell:	embryo
29	chr1:80961769-80961819	CMK	blood:	n/a
30	chr1:80961776-80961826	NHBE	bronchial:	n/a
31	chr1:81001617-81001667	HEEpiC	esophagus:	n/a
32	chr1:80961906-80961956	GM19239	blood:	n/a
33	chr1:80961769-80961819	PrEC	prostate:	n/a
34	chr1:80961906-80961956	HRCEpiC	kidney:	n/a
35	chr1:80961769-80961819	SAEC	small airway:	n/a
36	chr1:80961776-80961826	HRPEpiC	eye:	n/a
37	chr1:80923103-80923153	BJ	skin:	n/a
38	chr1:81001617-81001667	ovcar-3	ovarian:	n/a
39	chr1:80961776-80961826	HEEpiC	esophagus:	n/a
40	chr1:80961769-80961819	HCT-116	colon:	n/a
41	chr1:80961769-80961819	HAEpiC	amniotic membrane:	n/a
42	chr1:81001617-81001667	SK-N-SH_RA	brain:	n/a
43	chr1:80961769-80961819	SKMC	muscle:	n/a
44	chr1:80961776-80961826	SK-N-SH_RA	brain:	n/a
45	chr1:80961776-80961826	GM12878	blood:	n/a
46	chr1:80961769-80961819	MCF-7	breast:	n/a
47	chr1:80961906-80961956	MCF10A-Er-Src	breast:	n/a
48	chr1:80961776-80961826	AG04449	skin:	fetal
49	chr1:80961906-80961956	BJ	skin:	n/a
50	chr1:80961776-80961826	BJ	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:81001450..81003092-chr6:32940222..32942950,2	MCF-7	breast:
2	chr1:80911280..80913153-chr1:81098711..81100773,2	MCF-7	breast:
3	chr1:80928602..80929152-chr11:66112041..66112777,2	HCT-116	colon:
4	chr1:80879820..80881703-chr1:80888899..80891310,2	MCF-7	breast:
5	chr1:80908006..80910063-chr1:80913147..80915791,2	K562	blood:
6	chr1:80908006..80910063-chr1:80913147..80915791,2	K562	blood:
7	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	chr1:81001440-81001627	XLOC_000268
2	lnc-LPHN2-1	chr1:81006274-81006321	XLOC_000268
3	lnc-ELTD1-14	chr1:80929986-80930403	NONHSAT004115
4	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
5	lnc-LPHN2-1	chr1:81006273-81006321	NONHSAT004118
6	lnc-LPHN2-1	chr1:81001424-81001627	NONHSAT004117
7	lnc-LPHN2-1	chr1:81001439-81001627	NONHSAT004118
8	lnc-ELTD1-8	chr1:81000663-81000937	XLOC_000883
9	lnc-LPHN2-1	chr1:81001445-81001627	XLOC_000268

No data

Variant related genes	Relation type
HNRNPA1P64	TF binding region
ENSG00000234108	TF binding region
ENSG00000234184	TF binding region
ENSG00000227062	TF binding region
HNRNPA1P64	CpG island
ENSG00000234108	CpG island
ENSG00000234184	CpG island
ENSG00000227062	CpG island
ENSG00000263756	chromatin interactions
ENSG00000174744	chromatin interactions
ENSG00000204256	chromatin interactions
NUFIP2	miRNA target sites

Extended variants
information (count: 2159 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2159 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549518835	chr1:80891803-80891804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537022529	chr1:80891805-80891806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs386632809	chr1:80891810-80891811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114209824	chr1:80891826-80891827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs72933182	chr1:80891829-80891830	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536302245	chr1:80891921-80891922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74878420	chr1:80891959-80891960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572961963	chr1:80891987-80891988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148468908	chr1:80892063-80892064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201161831	chr1:80892066-80892067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544816897	chr1:80892146-80892147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371914703	chr1:80892148-80892149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558410777	chr1:80892153-80892154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575193351	chr1:80892155-80892156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545863189	chr1:80892193-80892194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11163013	chr1:80895401-80895402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs35043627	chr1:80895444-80895445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189194049	chr1:80895534-80895535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553090551	chr1:80895536-80895537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557252816	chr1:80895565-80895566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4650462	chr1:80895566-80895567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs552249897	chr1:80895593-80895594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541841364	chr1:80895600-80895601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561604063	chr1:80895605-80895606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572151586	chr1:80895624-80895625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76342836	chr1:80895628-80895629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564229188	chr1:80895635-80895636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533185566	chr1:80895672-80895673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564147129	chr1:80895679-80895680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550069278	chr1:80895723-80895724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200815631	chr1:80895739-80895740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377488866	chr1:80895740-80895741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563636977	chr1:80895742-80895743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35995524	chr1:80895758-80895759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs12120475	chr1:80895763-80895764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs148891094	chr1:80895812-80895813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142516432	chr1:80895818-80895819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150942065	chr1:80895822-80895823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571479791	chr1:80895829-80895830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140798458	chr1:80895849-80895850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557213794	chr1:80895902-80895903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12121256	chr1:80895946-80895947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535099368	chr1:80895953-80895954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112169151	chr1:80896052-80896053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77324845	chr1:80896090-80896091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528220003	chr1:80896092-80896093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541100613	chr1:80896121-80896122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564188333	chr1:80896147-80896148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577898709	chr1:80896164-80896165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181831691	chr1:80896195-80896196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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	18451855	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:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80891800-80892200	Enhancers	Fetal Muscle Leg	muscle
2	chr1:80895400-80898000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:80902600-80903400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:80903000-80903200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:80903000-80903400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr1:80903200-80911000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:80905200-80906200	Enhancers	Fetal Intestine Small	intestine
8	chr1:80905400-80905800	Enhancers	Spleen	Spleen
9	chr1:80905400-80906200	Enhancers	Fetal Intestine Large	intestine
10	chr1:80905400-80906600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:80906600-80907200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr1:80906600-80907200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr1:80910200-80910600	Enhancers	HSMMtube	muscle
14	chr1:80910400-80910800	Enhancers	Hela-S3	cervix
15	chr1:80910600-80911200	Enhancers	HMEC	breast
16	chr1:80911000-80911200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:80911200-80912400	Weak transcription	HMEC	breast
18	chr1:80911200-80912800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:80912400-80912600	Enhancers	HMEC	breast
20	chr1:80912800-80913000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:80916800-80917200	Enhancers	Esophagus	oesophagus
22	chr1:80921400-80921600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr1:80922400-80923600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr1:80922400-80923800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:80922400-80923800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:80922400-80924000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:80922600-80922800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:80922600-80923800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr1:80922600-80924000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:80923200-80923600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:80923200-80923800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr1:80923200-80923800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr1:80923400-80923600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:80923400-80923800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:80923400-80923800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr1:80938800-80939600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:80939600-80940200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:80951200-80951800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:80961600-80961800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:80961600-80961800	ZNF genes & repeats	Pancreas	Pancrea
41	chr1:80963600-80964600	Enhancers	Fetal Lung	lung
42	chr1:80964200-80964600	Enhancers	Adipose Nuclei	Adipose
43	chr1:80964200-80964600	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr1:80964200-80964600	Enhancers	Fetal Brain Female	brain
45	chr1:80964200-80964800	Enhancers	Fetal Heart	heart
46	chr1:80964200-80965000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:80964400-80964600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:80970800-80971000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:80971200-80972000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr1:80971600-80971800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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