Variant report

Variant	nsv546666
Chromosome Location	chr1:80909417-81052058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 50 per page) page: 1 2 3 4 5 6

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	chr1:81000531-81001133	HCT-116	colon:	n/a	n/a
6	CBX3	chr1:80996803-80997369	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:80912210-80912676	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:80923285-80923514	A549	lung:	n/a	chr1:80923417-80923428 chr1:80923417-80923430
9	CEBPB	chr1:81004063-81004214	A549	lung:	n/a	chr1:81004073-81004086 chr1:81004075-81004086 chr1:81004073-81004086 chr1:81004073-81004086
10	CEBPB	chr1:80912499-80912558	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:80912368-80912659	A549	lung:	n/a	n/a
12	CEBPB	chr1:80913237-80913619	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:81000182-81001093	HCT-116	colon:	n/a	n/a
14	CEBPB	chr1:81006278-81006649	IMR90	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
15	CEBPB	chr1:80991202-80991443	HepG2	liver:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
16	CEBPB	chr1:80923262-80923547	Hela-S3	cervix:	n/a	chr1:80923417-80923428 chr1:80923417-80923430
17	CEBPB	chr1:80910551-80911194	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:80989649-80990016	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:81000600-81001165	HCT-116	colon:	n/a	n/a
20	CEBPB	chr1:81006283-81006695	Hela-S3	cervix:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
21	CEBPB	chr1:81006302-81006643	HepG2	liver:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
22	CEBPB	chr1:81009753-81009933	HepG2	liver:	n/a	chr1:81009799-81009812 chr1:81009799-81009810
23	CEBPB	chr1:80910689-80911261	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:80989668-80989956	A549	lung:	n/a	n/a
25	CEBPB	chr1:80912346-80912654	IMR90	lung:	n/a	n/a
26	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
27	CEBPB	chr1:80910816-80911185	HCT-116	colon:	n/a	n/a
28	CEBPB	chr1:80991142-80991478	IMR90	lung:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
29	CEBPB	chr1:80923207-80923467	H1-hESC	embryonic stem cell:	n/a	chr1:80923417-80923428 chr1:80923417-80923430
30	CEBPB	chr1:81006300-81006629	A549	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
31	CEBPB	chr1:80927341-80927564	A549	lung:	n/a	chr1:80927464-80927477
32	CEBPB	chr1:80991969-80992035	HepG2	liver:	n/a	chr1:80992011-80992022 chr1:80992011-80992024
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	chr1:80962340-80962490	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr1:81000724-81000893	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr1:81000746-81000849	Gliobla	brain:	n/a	n/a
38	CTCF	chr1:81020220-81020370	AG09319	gingival:	n/a	n/a
39	CTCF	chr1:81000765-81000851	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:80998820-80998970	HRE	kidney:	n/a	chr1:80998881-80998888
41	CTCF	chr1:81001636-81001652	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr1:81049281-81049353	Fibrobl	skin:	n/a	n/a
43	CTCF	chr1:81000698-81000888	GM12878	blood:	n/a	n/a
44	CTCF	chr1:81000760-81000910	HEK293	kidney:	n/a	n/a
45	CTCF	chr1:81000680-81000830	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr1:80925696-80925751	GM20000	blood:	n/a	n/a
47	CTCF	chr1:80914700-80914850	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr1:80953200-80953350	GM12868	blood:	n/a	n/a
49	CTCF	chr1:81000789-81000814	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:80951760-80951910	AG10803	skin:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:80961906-80961956	HMEC	breast:	n/a
2	chr1:80961906-80961956	SK-N-MC	brain:	n/a
3	chr1:80923103-80923153	SAEC	small airway:	n/a
4	chr1:80961906-80961956	LNCaP	prostate:	n/a
5	chr1:80923103-80923153	GM12878	blood:	n/a
6	chr1:80961769-80961819	HCT-116	colon:	n/a
7	chr1:80961776-80961826	SK-N-SH_RA	brain:	n/a
8	chr1:81001617-81001667	HEEpiC	esophagus:	n/a
9	chr1:80961769-80961819	HNPCEpiC	eye:	n/a
10	chr1:80923103-80923153	AG09309	skin:	n/a
11	chr1:81001617-81001667	BJ	skin:	n/a
12	chr1:80961776-80961826	HMEC	breast:	n/a
13	chr1:80961769-80961819	AoSMC	blood vessel:	n/a
14	chr1:80961906-80961956	GM12878	blood:	n/a
15	chr1:80923103-80923153	SK-N-SH	brain:	n/a
16	chr1:80961776-80961826	HRCEpiC	kidney:	n/a
17	chr1:80961776-80961826	ovcar-3	ovarian:	n/a
18	chr1:80961906-80961956	AG10803	skin:	n/a
19	chr1:80923103-80923153	HMEC	breast:	n/a
20	chr1:80961776-80961826	ProgFib	skin:	n/a
21	chr1:80961776-80961826	CMK	blood:	n/a
22	chr1:81001617-81001667	PrEC	prostate:	n/a
23	chr1:80923103-80923153	GM19239	blood:	n/a
24	chr1:80961769-80961819	GM12892	blood:	n/a
25	chr1:80961776-80961826	SK-N-SH	brain:	n/a
26	chr1:80961769-80961819	CMK	blood:	n/a
27	chr1:80961769-80961819	HRCEpiC	kidney:	n/a
28	chr1:80923103-80923153	AG10803	skin:	n/a
29	chr1:80961906-80961956	RPTEC	kidney:	n/a
30	chr1:81001617-81001667	HEK293	kidney:	embryo
31	chr1:80961769-80961819	HIPEpiC	eye:	n/a
32	chr1:80923103-80923153	HepG2	liver:	n/a
33	chr1:80923103-80923153	HCPEpiC	choroid plexus:	n/a
34	chr1:80961769-80961819	HL-60	blood:	n/a
35	chr1:80961769-80961819	AG04450	lung:	fetal
36	chr1:80961906-80961956	AG09319	gingival:	n/a
37	chr1:80961906-80961956	HRE	kidney:	n/a
38	chr1:80923103-80923153	HCT-116	colon:	n/a
39	chr1:80961776-80961826	HCM	heart:	n/a
40	chr1:80961769-80961819	GM06990	blood:	n/a
41	chr1:80961769-80961819	PrEC	prostate:	n/a
42	chr1:80923103-80923153	SK-N-SH_RA	brain:	n/a
43	chr1:80961776-80961826	NB4	blood:	n/a
44	chr1:80961776-80961826	RPTEC	kidney:	n/a
45	chr1:81001617-81001667	Caco-2	colon:	n/a
46	chr1:80961906-80961956	AG04450	lung:	fetal
47	chr1:80961776-80961826	AG04449	skin:	fetal
48	chr1:80961776-80961826	HRE	kidney:	n/a
49	chr1:80961906-80961956	GM12891	blood:	n/a
50	chr1:80961906-80961956	NT2-D1	testis:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:80968594..80969285-chr1:159113721..159114329,2	MCF-7	breast:
2	chr1:80911280..80913153-chr1:81098711..81100773,2	MCF-7	breast:
3	chr1:81001450..81003092-chr6:32940222..32942950,2	MCF-7	breast:
4	chr1:80928602..80929152-chr11:66112041..66112777,2	HCT-116	colon:
5	chr1:80908006..80910063-chr1:80913147..80915791,2	K562	blood:
6	chr1:80908006..80910063-chr1:80913147..80915791,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-14	chr1:80929986-80930403	NONHSAT004115
2	lnc-ELTD1-8	chr1:81049975-81050048	XLOC_000883
3	lnc-ELTD1-8	chr1:81000663-81000937	XLOC_000883
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	chr1:81001440-81001627	XLOC_000268
8	lnc-LPHN2-1	chr1:81006274-81006321	XLOC_000268
9	lnc-LPHN2-1	chr1:81001445-81001627	XLOC_000268
10	lnc-LPHN2-1	chr1:81001439-81001627	NONHSAT004118

No data

Variant related genes	Relation type
ENSG00000234184	TF binding region
ENSG00000227062	TF binding region
HNRNPA1P64	TF binding region
ENSG00000234108	TF binding region
ENSG00000224326	TF binding region
ENSG00000234184	CpG island
ENSG00000227062	CpG island
HNRNPA1P64	CpG island
ENSG00000234108	CpG island
ENSG00000224326	CpG island
ENSG00000263756	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000174744	chromatin interactions
NUFIP2	miRNA target sites

Extended variants
information (count: 1840 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1840 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6424705	chr1:80909417-80909418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182555272	chr1:80909427-80909428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185278344	chr1:80909434-80909435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142493521	chr1:80909435-80909436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557712939	chr1:80909454-80909455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535476875	chr1:80909466-80909467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549097022	chr1:80909480-80909481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190584734	chr1:80909490-80909491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565678129	chr1:80909491-80909492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534726622	chr1:80909492-80909493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557621259	chr1:80909527-80909528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577791817	chr1:80909567-80909568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74531198	chr1:80909618-80909619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539269233	chr1:80909642-80909643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12023521	chr1:80909643-80909644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573679501	chr1:80909645-80909646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75584480	chr1:80909651-80909652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182752175	chr1:80909663-80909664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553037466	chr1:80909681-80909682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573215046	chr1:80909688-80909689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77045450	chr1:80909692-80909693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200660703	chr1:80909717-80909718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141744617	chr1:80909795-80909796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79313505	chr1:80909842-80909843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531150095	chr1:80909955-80909956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188588575	chr1:80909967-80909968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577709981	chr1:80909975-80909976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11799664	chr1:80909978-80909979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs193125721	chr1:80910042-80910043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199751759	chr1:80910048-80910049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150964143	chr1:80910059-80910060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11802992	chr1:80910120-80910121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs573323745	chr1:80910127-80910128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139492174	chr1:80910128-80910129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11799688	chr1:80910134-80910135	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536877031	chr1:80910193-80910194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191248524	chr1:80910194-80910195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149828157	chr1:80910213-80910214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147941204	chr1:80910218-80910219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184264941	chr1:80910219-80910220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141748126	chr1:80910260-80910261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545137180	chr1:80910323-80910324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367822959	chr1:80910331-80910332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575727278	chr1:80910476-80910477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544860822	chr1:80910504-80910505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78996532	chr1:80910508-80910509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530372271	chr1:80910512-80910513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540951199	chr1:80910551-80910552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191727307	chr1:80910581-80910582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184645816	chr1:80910589-80910590	Weak transcription Enhancers	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:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80903200-80911000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:80910200-80910600	Enhancers	HSMMtube	muscle
3	chr1:80910400-80910800	Enhancers	Hela-S3	cervix
4	chr1:80910600-80911200	Enhancers	HMEC	breast
5	chr1:80911000-80911200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:80911200-80912400	Weak transcription	HMEC	breast
7	chr1:80911200-80912800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:80912400-80912600	Enhancers	HMEC	breast
9	chr1:80912800-80913000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:80916800-80917200	Enhancers	Esophagus	oesophagus
11	chr1:80921400-80921600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr1:80922400-80923600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr1:80922400-80923800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:80922400-80923800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr1:80922400-80924000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr1:80922600-80922800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:80922600-80923800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:80922600-80924000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:80923200-80923600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:80923200-80923800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr1:80923200-80923800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr1:80923400-80923600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:80923400-80923800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:80923400-80923800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr1:80938800-80939600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:80939600-80940200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:80951200-80951800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:80961600-80961800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:80961600-80961800	ZNF genes & repeats	Pancreas	Pancrea
30	chr1:80963600-80964600	Enhancers	Fetal Lung	lung
31	chr1:80964200-80964600	Enhancers	Adipose Nuclei	Adipose
32	chr1:80964200-80964600	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr1:80964200-80964600	Enhancers	Fetal Brain Female	brain
34	chr1:80964200-80964800	Enhancers	Fetal Heart	heart
35	chr1:80964200-80965000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:80964400-80964600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr1:80970800-80971000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr1:80971200-80972000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr1:80971600-80971800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:80971600-80972600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:80971800-80972200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr1:80971800-80972200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr1:80971800-80972200	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr1:80971800-80972400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr1:80971800-80972400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr1:80971800-80972600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:80972000-80972200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr1:80972000-80972200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:80972000-80972400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:80972200-80972600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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