Variant report

Variant	nsv462550
Chromosome Location	chr1:95136071-95154279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:104)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:104 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:95154094-95154593	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:95154249-95154715	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:95143325-95143609	K562	blood:	n/a	n/a
4	BHLHE40	chr1:95143320-95143564	K562	blood:	n/a	n/a
5	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
6	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
9	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
10	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
12	CHD2	chr1:95154200-95154634	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr1:95154170-95154639	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
16	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
18	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
19	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
20	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
21	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
22	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
23	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	n/a	chr1:95150025-95150033
24	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
25	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F6	chr1:95149871-95150217	H1-hESC	embryonic stem cell:	n/a	n/a
27	EP300	chr1:95154046-95154617	H1-hESC	embryonic stem cell:	n/a	n/a
28	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
29	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
30	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
31	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
32	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
33	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
34	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
35	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
36	JUND	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
37	MAFF	chr1:95142755-95142907	K562	blood:	n/a	chr1:95142838-95142856
38	MAFF	chr1:95144917-95145234	HepG2	liver:	n/a	chr1:95145086-95145104
39	MAFF	chr1:95142674-95143010	HepG2	liver:	n/a	chr1:95142838-95142856
40	MAFF	chr1:95145041-95145241	K562	blood:	n/a	chr1:95145086-95145104
41	MAFK	chr1:95140858-95141414	IMR90	lung:	n/a	chr1:95141091-95141101
42	MAFK	chr1:95144909-95145272	Hela-S3	cervix:	n/a	chr1:95145087-95145102
43	MAFK	chr1:95138428-95138871	IMR90	lung:	n/a	n/a
44	MAFK	chr1:95144922-95145260	HepG2	liver:	n/a	chr1:95145087-95145102
45	MAFK	chr1:95144908-95145278	IMR90	lung:	n/a	chr1:95145087-95145102
46	MAFK	chr1:95144920-95145228	K562	blood:	n/a	chr1:95145087-95145102
47	MAFK	chr1:95144916-95145266	HepG2	liver:	n/a	chr1:95145087-95145102
48	MAFK	chr1:95142662-95143011	IMR90	lung:	n/a	chr1:95142839-95142854
49	MAFK	chr1:95142669-95143020	HepG2	liver:	n/a	chr1:95142839-95142854
50	MAFK	chr1:95142671-95143004	HepG2	liver:	n/a	chr1:95142839-95142854

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95149580-95149630	SK-N-MC	brain:	n/a
2	chr1:95141800-95141850	HRPEpiC	eye:	n/a
3	chr1:95149580-95149630	HCM	heart:	n/a
4	chr1:95149580-95149630	HL-60	blood:	n/a
5	chr1:95149580-95149630	ProgFib	skin:	n/a
6	chr1:95141800-95141850	HCT-116	colon:	n/a
7	chr1:95141800-95141850	Jurkat	blood:	n/a
8	chr1:95149580-95149630	AG04449	skin:	fetal
9	chr1:95141800-95141850	HAEpiC	amniotic membrane:	n/a
10	chr1:95149580-95149630	ECC-1	luminal epithelium:	n/a
11	chr1:95149580-95149630	HNPCEpiC	eye:	n/a
12	chr1:95141800-95141850	SK-N-SH_RA	brain:	n/a
13	chr1:95141800-95141850	A549	lung:	n/a
14	chr1:95149580-95149630	GM06990	blood:	n/a
15	chr1:95149580-95149630	PrEC	prostate:	n/a
16	chr1:95141800-95141850	HEK293	kidney:	embryo
17	chr1:95141800-95141850	PANC-1	pancreas:	n/a
18	chr1:95149580-95149630	SK-N-SH	brain:	n/a
19	chr1:95141800-95141850	IMR90	lung:	fetal
20	chr1:95141800-95141850	H1-hESC	embryonic stem cell:	embryo
21	chr1:95141800-95141850	HMEC	breast:	n/a
22	chr1:95141800-95141850	SK-N-SH	brain:	n/a
23	chr1:95149580-95149630	H1-hESC	embryonic stem cell:	embryo
24	chr1:95149580-95149630	NH-A	brain:	n/a
25	chr1:95141800-95141850	NHDF-neo	bronchial:	n/a
26	chr1:95149580-95149630	HIPEpiC	eye:	n/a
27	chr1:95149580-95149630	PFSK-1	brain:	n/a
28	chr1:95149580-95149630	LNCaP	prostate:	n/a
29	chr1:95141800-95141850	K562	blood:	n/a
30	chr1:95149580-95149630	GM12891	blood:	n/a
31	chr1:95141800-95141850	HRCEpiC	kidney:	n/a
32	chr1:95149580-95149630	HAEpiC	amniotic membrane:	n/a
33	chr1:95149580-95149630	SKMC	muscle:	n/a
34	chr1:95149580-95149630	HCF	heart:	n/a
35	chr1:95141800-95141850	T-47D	breast:	n/a
36	chr1:95141800-95141850	AG09309	skin:	n/a
37	chr1:95149580-95149630	BE2_C	brain:	n/a
38	chr1:95149580-95149630	NHDF-neo	bronchial:	n/a
39	chr1:95141800-95141850	BE2_C	brain:	n/a
40	chr1:95141800-95141850	HCPEpiC	choroid plexus:	n/a
41	chr1:95149580-95149630	GM19239	blood:	n/a
42	chr1:95149580-95149630	PANC-1	pancreas:	n/a
43	chr1:95149580-95149630	HUVEC	blood vessel:	n/a
44	chr1:95149580-95149630	HepG2	liver:	n/a
45	chr1:95149580-95149630	GM12892	blood:	n/a
46	chr1:95149580-95149630	MCF10A-Er-Src	breast:	n/a
47	chr1:95141800-95141850	HUVEC	blood vessel:	n/a
48	chr1:95149580-95149630	MCF-7	breast:	n/a
49	chr1:95149580-95149630	HCPEpiC	choroid plexus:	n/a
50	chr1:95149580-95149630	AG09309	skin:	n/a

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

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

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A3-2	chr1:95143531-95144178	NONHSAT004611
2	lnc-F3-2	chr1:95144981-95145163	NONHSAT004607
3	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
4	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
5	lnc-SLC44A3-2	chr1:95149016-95149176	XLOC_000303
6	lnc-F3-2	chr1:95144981-95145163	NONHSAT004613
7	lnc-CNN3-3	chr1:95138685-95138827	ENSG00000224081.2
8	lnc-CNN3-3	chr1:95138453-95138827	ENSG00000224081.2
9	lnc-F3-2	chr1:95145136-95145163	ENSG00000224081.3
10	lnc-SLC44A3-2	chr1:95153449-95153875	XLOC_000303
11	lnc-F3-2	chr1:95138492-95138827	NONHSAT004609
12	lnc-F3-2	chr1:95144981-95145163	NONHSAT004609
13	lnc-F3-2	chr1:95144981-95145163	NONHSAT004608
14	lnc-SLC44A3-2	chr1:95148857-95149176	XLOC_000303
15	lnc-SLC44A3-2	chr1:95153449-95153875	XLOC_000303
16	lnc-SLC44A3-2	chr1:95144981-95145163	NONHSAT004611
17	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
18	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
19	lnc-F3-2	chr1:95138492-95138827	NONHSAT004608
20	lnc-SLC44A3-2	chr1:95143554-95143579	XLOC_000303
21	lnc-SLC44A3-2	chr1:95149856-95150619	XLOC_000303
22	lnc-SLC44A3-2	chr1:95153449-95155440	XLOC_000303
23	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2

No data

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

Extended variants
information (count: 692 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11165207	chr1:95136071-95136072	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11165208	chr1:95136076-95136077	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs185376354	chr1:95136077-95136078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374903702	chr1:95136086-95136087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188496772	chr1:95136122-95136123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148374338	chr1:95136138-95136139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78456884	chr1:95136160-95136161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543733538	chr1:95136271-95136272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7539572	chr1:95136335-95136336	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs841342	chr1:95136342-95136343	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs540655392	chr1:95136359-95136360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12132193	chr1:95136361-95136362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140649524	chr1:95136430-95136431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181304424	chr1:95136491-95136492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576740038	chr1:95136570-95136571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562997414	chr1:95136600-95136601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34637676	chr1:95136648-95136649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79427984	chr1:95136696-95136697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376746998	chr1:95136698-95136699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551909997	chr1:95136701-95136702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571860772	chr1:95136720-95136721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183744022	chr1:95136745-95136746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369925363	chr1:95136750-95136751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559353927	chr1:95136795-95136796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188468006	chr1:95136824-95136825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182295111	chr1:95136829-95136830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566163189	chr1:95136833-95136834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547578028	chr1:95136860-95136861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561182444	chr1:95136900-95136901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535071697	chr1:95136941-95136942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112435667	chr1:95136958-95136959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555087923	chr1:95136970-95136971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187332978	chr1:95137019-95137020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150443282	chr1:95137025-95137026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373394619	chr1:95137035-95137036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530309973	chr1:95137053-95137054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556870697	chr1:95137105-95137106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143578066	chr1:95137107-95137108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577744506	chr1:95137109-95137110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540568402	chr1:95137188-95137189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192347138	chr1:95137234-95137235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377740687	chr1:95137265-95137266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567679359	chr1:95137312-95137313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550423203	chr1:95137381-95137382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570267088	chr1:95137456-95137457	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181535751	chr1:95137458-95137459	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112147730	chr1:95137459-95137460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77098789	chr1:95137532-95137533	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545294587	chr1:95137607-95137608	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565502596	chr1:95137651-95137652	Weak transcription Enhancers Strong transcription	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:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95126800-95137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:95126800-95141600	Weak transcription	Pancreas	Pancrea
3	chr1:95126800-95164200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:95128400-95154600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:95133400-95141200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:95133600-95141600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr1:95133800-95136200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:95133800-95136200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:95133800-95137400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:95134000-95142800	Weak transcription	Small Intestine	intestine
11	chr1:95134400-95137400	Weak transcription	Fetal Intestine Small	intestine
12	chr1:95134400-95141600	Weak transcription	Gastric	stomach
13	chr1:95134800-95139800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr1:95135000-95136200	Weak transcription	HepG2	liver
15	chr1:95135000-95136800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:95135000-95154400	Weak transcription	NHLF	lung
17	chr1:95135200-95137400	Weak transcription	Fetal Intestine Large	intestine
18	chr1:95135200-95137400	Weak transcription	NH-A	brain
19	chr1:95135200-95144200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:95135400-95141000	Weak transcription	Stomach Mucosa	stomach
21	chr1:95135400-95143000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr1:95135400-95150400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:95135600-95141000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr1:95136000-95136200	Enhancers	Hela-S3	cervix
25	chr1:95136000-95136800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr1:95136000-95136800	Enhancers	NHDF-Ad	bronchial
27	chr1:95136000-95139000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:95136200-95142200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:95136400-95136600	Enhancers	HepG2	liver
30	chr1:95136800-95137200	Weak transcription	NHDF-Ad	bronchial
31	chr1:95136800-95141800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:95137200-95139000	Enhancers	NHDF-Ad	bronchial
33	chr1:95137200-95139800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:95137400-95137800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr1:95137400-95138800	Strong transcription	Fetal Intestine Large	intestine
36	chr1:95137400-95139000	Enhancers	NH-A	brain
37	chr1:95137400-95139600	Strong transcription	Fetal Intestine Small	intestine
38	chr1:95137600-95141600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr1:95137800-95138200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr1:95137800-95138400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:95138200-95148800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr1:95138400-95141200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:95138400-95141800	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr1:95138800-95141200	Weak transcription	Fetal Intestine Large	intestine
45	chr1:95139000-95140400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:95139400-95141400	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr1:95139600-95140400	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr1:95139600-95140600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr1:95139600-95141000	Weak transcription	Fetal Intestine Small	intestine
50	chr1:95139800-95140200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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