Variant report

Variant	nsv517330
Chromosome Location	chr1:95128546-95153262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:184)
Chromatin interactive
region (count:10)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:120 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:95134884-95134905	K562	blood:	n/a	n/a
2	ATF3	chr1:95143325-95143609	K562	blood:	n/a	n/a
3	BHLHE40	chr1:95143320-95143564	K562	blood:	n/a	n/a
4	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
5	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
6	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
9	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:95132331-95132574	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	n/a	chr1:95150025-95150033
13	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
14	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
15	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
16	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
19	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
20	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
22	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
23	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
24	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F6	chr1:95149871-95150217	H1-hESC	embryonic stem cell:	n/a	n/a
26	EP300	chr1:95130100-95130300	Hela-S3	cervix:	n/a	n/a
27	EP300	chr1:95134844-95134975	K562	blood:	n/a	n/a
28	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
29	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
30	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
31	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
32	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
33	FOXA1	chr1:95131200-95131489	HepG2	liver:	n/a	chr1:95131350-95131365
34	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
35	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
36	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
37	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
38	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
39	HDAC2	chr1:95132354-95132585	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
41	JUND	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
42	MAFF	chr1:95134814-95135118	K562	blood:	n/a	n/a
43	MAFF	chr1:95142674-95143010	HepG2	liver:	n/a	chr1:95142838-95142856
44	MAFF	chr1:95144917-95145234	HepG2	liver:	n/a	chr1:95145086-95145104
45	MAFF	chr1:95145041-95145241	K562	blood:	n/a	chr1:95145086-95145104
46	MAFF	chr1:95142755-95142907	K562	blood:	n/a	chr1:95142838-95142856
47	MAFK	chr1:95142749-95143012	Hela-S3	cervix:	n/a	chr1:95142839-95142854
48	MAFK	chr1:95144908-95145278	IMR90	lung:	n/a	chr1:95145087-95145102
49	MAFK	chr1:95134884-95135098	K562	blood:	n/a	n/a
50	MAFK	chr1:95129226-95129431	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95133907-95133957	HEEpiC	esophagus:	n/a
2	chr1:95133907-95133957	HEEpiC	esophagus:	n/a
3	chr1:95149580-95149630	PrEC	prostate:	n/a
4	chr1:95133907-95133957	HMEC	breast:	n/a
5	chr1:95133907-95133957	MCF-7	breast:	n/a
6	chr1:95149580-95149630	LNCaP	prostate:	n/a
7	chr1:95133907-95133957	CMK	blood:	n/a
8	chr1:95141800-95141850	BJ	skin:	n/a
9	chr1:95133907-95133957	NHDF-neo	bronchial:	n/a
10	chr1:95133907-95133957	HNPCEpiC	eye:	n/a
11	chr1:95141800-95141850	IMR90	lung:	fetal
12	chr1:95141800-95141850	A549	lung:	n/a
13	chr1:95149580-95149630	Hela-S3	cervix:	n/a
14	chr1:95133907-95133957	GM12878	blood:	n/a
15	chr1:95133907-95133957	H1-hESC	embryonic stem cell:	embryo
16	chr1:95141800-95141850	SAEC	small airway:	n/a
17	chr1:95149580-95149630	HRPEpiC	eye:	n/a
18	chr1:95133907-95133957	SK-N-SH_RA	brain:	n/a
19	chr1:95133907-95133957	SK-N-SH	brain:	n/a
20	chr1:95141800-95141850	K562	blood:	n/a
21	chr1:95133907-95133957	GM12891	blood:	n/a
22	chr1:95133907-95133957	HRE	kidney:	n/a
23	chr1:95149580-95149630	GM19239	blood:	n/a
24	chr1:95141800-95141850	MCF10A-Er-Src	breast:	n/a
25	chr1:95133907-95133957	A549	lung:	n/a
26	chr1:95149580-95149630	NH-A	brain:	n/a
27	chr1:95141800-95141850	MCF-7	breast:	n/a
28	chr1:95149580-95149630	HL-60	blood:	n/a
29	chr1:95141800-95141850	Hepatocyte	liver:	n/a
30	chr1:95149580-95149630	HCF	heart:	n/a
31	chr1:95133907-95133957	MCF10A-Er-Src	breast:	n/a
32	chr1:95149580-95149630	GM12891	blood:	n/a
33	chr1:95141800-95141850	CMK	blood:	n/a
34	chr1:95133907-95133957	Hela-S3	cervix:	n/a
35	chr1:95141800-95141850	HCF	heart:	n/a
36	chr1:95149580-95149630	AG10803	skin:	n/a
37	chr1:95141800-95141850	HRPEpiC	eye:	n/a
38	chr1:95149580-95149630	BJ	skin:	n/a
39	chr1:95133907-95133957	U87	brain:	n/a
40	chr1:95149580-95149630	AG09319	gingival:	n/a
41	chr1:95149580-95149630	A549	lung:	n/a
42	chr1:95133907-95133957	ECC-1	luminal epithelium:	n/a
43	chr1:95141800-95141850	NHDF-neo	bronchial:	n/a
44	chr1:95141800-95141850	LNCaP	prostate:	n/a
45	chr1:95149580-95149630	AG04450	lung:	fetal
46	chr1:95141800-95141850	T-47D	breast:	n/a
47	chr1:95149580-95149630	PFSK-1	brain:	n/a
48	chr1:95133907-95133957	HRPEpiC	eye:	n/a
49	chr1:95149580-95149630	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:95133907-95133957	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:
2	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
3	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
4	chr1:95116283..95118037-chr1:95153158..95155389,2	K562	blood:
5	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
6	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
7	chr1:95130856..95133124-chr1:95137358..95139966,2	K562	blood:
8	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:
9	chr1:95147936..95149911-chr1:95157813..95160581,2	K562	blood:
10	chr1:95145448..95146125-chr1:113615023..113615898,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNN3-3	chr1:95138453-95138827	ENSG00000224081.2
2	lnc-SLC44A3-2	chr1:95149856-95150619	XLOC_000303
3	lnc-CNN3-3	chr1:95138685-95138827	ENSG00000224081.2
4	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
5	lnc-F3-2	chr1:95138492-95138827	NONHSAT004608
6	lnc-F3-2	chr1:95144981-95145163	NONHSAT004609
7	lnc-SLC44A3-2	chr1:95149016-95149176	XLOC_000303
8	lnc-F3-2	chr1:95144981-95145163	NONHSAT004607
9	lnc-SLC44A3-2	chr1:95148857-95149176	XLOC_000303
10	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
11	lnc-F3-2	chr1:95138492-95138827	NONHSAT004609
12	lnc-SLC44A3-2	chr1:95143554-95143579	XLOC_000303
13	lnc-SLC44A3-2	chr1:95143531-95144178	NONHSAT004611
14	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
15	lnc-SLC44A3-2	chr1:95144981-95145163	NONHSAT004611
16	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
17	lnc-F3-2	chr1:95145136-95145163	ENSG00000224081.3
18	lnc-F3-2	chr1:95144981-95145163	NONHSAT004613
19	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
20	lnc-F3-2	chr1:95144981-95145163	NONHSAT004608

No data

Variant related genes	Relation type
LINC01057	TF binding region
PGBD4P7	TF binding region
LINC01057	CpG island
PGBD4P7	CpG island
ENSG00000232857	chromatin interactions
ENSG00000238198	chromatin interactions
ENSG00000244433	chromatin interactions
ENSG00000198799	chromatin interactions
SPTLC1	miRNA target sites
FUBP1	miRNA target sites

Extended variants
information (count: 895 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4847328	chr1:95128546-95128547	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533497393	chr1:95128627-95128628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533046733	chr1:95128636-95128637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546985610	chr1:95128689-95128690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566784489	chr1:95128720-95128721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529274245	chr1:95128780-95128781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183659769	chr1:95128789-95128790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147817313	chr1:95128798-95128799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4847329	chr1:95128806-95128807	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs558343423	chr1:95128848-95128849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4847330	chr1:95128861-95128862	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs377195905	chr1:95128894-95128895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115867836	chr1:95128914-95128915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529495798	chr1:95128926-95128927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4847331	chr1:95128927-95128928	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs143570253	chr1:95128957-95128958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535071646	chr1:95128958-95128959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1098615	chr1:95128960-95128961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs555979703	chr1:95128965-95128966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1098616	chr1:95128970-95128971	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs544007977	chr1:95128971-95128972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538452074	chr1:95128986-95128987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200549200	chr1:95128988-95128989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551130738	chr1:95129006-95129007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540194455	chr1:95129026-95129027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560387764	chr1:95129028-95129029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529354492	chr1:95129029-95129030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549352392	chr1:95129038-95129039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562980067	chr1:95129067-95129068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531806176	chr1:95129068-95129069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552025496	chr1:95129069-95129070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571775236	chr1:95129070-95129071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs58981969	chr1:95129096-95129097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558130529	chr1:95129103-95129104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567944114	chr1:95129124-95129125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140737067	chr1:95129202-95129203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs59566212	chr1:95129222-95129223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373332395	chr1:95129260-95129261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554899538	chr1:95129339-95129340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60897247	chr1:95129365-95129366	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189209125	chr1:95129368-95129369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs34573410	chr1:95129531-95129532	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs557821254	chr1:95129546-95129547	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs540215343	chr1:95129554-95129555	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs6680518	chr1:95129556-95129557	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs11165193	chr1:95129585-95129586	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs192546678	chr1:95129594-95129595	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs536008631	chr1:95129626-95129627	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543059946	chr1:95129641-95129642	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185258220	chr1:95129642-95129643	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
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
Medulloblastoma	21979893	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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95124200-95131800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:95125000-95133200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:95125800-95128800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:95125800-95128800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:95126000-95128600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:95126000-95128800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:95126000-95128800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:95126800-95133000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:95126800-95137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:95126800-95141600	Weak transcription	Pancreas	Pancrea
11	chr1:95126800-95164200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:95127000-95130000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:95127400-95128800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr1:95127400-95129400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr1:95127400-95130000	Weak transcription	Fetal Heart	heart
16	chr1:95127400-95130000	Weak transcription	Stomach Mucosa	stomach
17	chr1:95127600-95128600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr1:95127600-95128800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr1:95127600-95128800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr1:95127600-95133200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr1:95127600-95133400	Weak transcription	Fetal Intestine Small	intestine
22	chr1:95127600-95134600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:95127800-95128800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr1:95128400-95129600	Weak transcription	Hela-S3	cervix
25	chr1:95128400-95131800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:95128400-95134200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr1:95128400-95134400	Weak transcription	Fetal Intestine Large	intestine
28	chr1:95128400-95154600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:95128800-95129400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr1:95128800-95129600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr1:95128800-95130000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:95128800-95130000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:95128800-95130400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:95128800-95131800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr1:95128800-95134200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:95129400-95131000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr1:95129600-95130600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr1:95129600-95130600	Enhancers	Rectal Smooth Muscle	rectum
39	chr1:95130000-95130400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:95130000-95130400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:95130000-95130400	Enhancers	Fetal Heart	heart
42	chr1:95130000-95130400	Enhancers	Stomach Mucosa	stomach
43	chr1:95130000-95131000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
44	chr1:95130400-95130600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr1:95130400-95133200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:95130400-95133200	Weak transcription	Stomach Mucosa	stomach
47	chr1:95130600-95131400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr1:95130600-95131800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr1:95131000-95131400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr1:95131000-95131800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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