Variant report

Variant	esv12694
Chromosome Location	chr1:95134798-95156000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:121)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:121 , 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	ATF2	chr1:95154094-95154593	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:95154249-95154715	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr1:95143325-95143609	K562	blood:	n/a	n/a
5	BHLHE40	chr1:95143320-95143564	K562	blood:	n/a	n/a
6	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
8	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
9	CEBPB	chr1:95155506-95155922	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
11	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
13	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr1:95154200-95154634	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr1:95154170-95154639	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
17	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
18	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:95154620-95154770	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
21	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
22	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
23	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
24	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
25	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
26	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	n/a	chr1:95150025-95150033
28	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F6	chr1:95149871-95150217	H1-hESC	embryonic stem cell:	n/a	n/a
30	EP300	chr1:95154046-95154617	H1-hESC	embryonic stem cell:	n/a	n/a
31	EP300	chr1:95134844-95134975	K562	blood:	n/a	n/a
32	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
33	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
36	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
37	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
38	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
39	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
42	GTF2F1	chr1:95154288-95154524	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
44	JUND	chr1:95154310-95154479	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUND	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
46	MAFF	chr1:95144917-95145234	HepG2	liver:	n/a	chr1:95145086-95145104
47	MAFF	chr1:95142755-95142907	K562	blood:	n/a	chr1:95142838-95142856
48	MAFF	chr1:95145041-95145241	K562	blood:	n/a	chr1:95145086-95145104
49	MAFF	chr1:95142674-95143010	HepG2	liver:	n/a	chr1:95142838-95142856
50	MAFF	chr1:95134814-95135118	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95149580-95149630	T-47D	breast:	n/a
2	chr1:95149580-95149630	GM12892	blood:	n/a
3	chr1:95149580-95149630	HCPEpiC	choroid plexus:	n/a
4	chr1:95141800-95141850	SAEC	small airway:	n/a
5	chr1:95155557-95155607	RPTEC	kidney:	n/a
6	chr1:95141800-95141850	SKMC	muscle:	n/a
7	chr1:95141800-95141850	Hepatocyte	liver:	n/a
8	chr1:95149580-95149630	K562	blood:	n/a
9	chr1:95149580-95149630	Jurkat	blood:	n/a
10	chr1:95155557-95155607	HCPEpiC	choroid plexus:	n/a
11	chr1:95141800-95141850	GM12892	blood:	n/a
12	chr1:95149580-95149630	AG04450	lung:	fetal
13	chr1:95155557-95155607	ProgFib	skin:	n/a
14	chr1:95149580-95149630	BJ	skin:	n/a
15	chr1:95141800-95141850	Caco-2	colon:	n/a
16	chr1:95149580-95149630	NT2-D1	testis:	n/a
17	chr1:95149580-95149630	AG10803	skin:	n/a
18	chr1:95155557-95155607	Hepatocyte	liver:	n/a
19	chr1:95149580-95149630	AoSMC	blood vessel:	n/a
20	chr1:95141800-95141850	AG04450	lung:	fetal
21	chr1:95149580-95149630	HRPEpiC	eye:	n/a
22	chr1:95155557-95155607	HMEC	breast:	n/a
23	chr1:95141800-95141850	ProgFib	skin:	n/a
24	chr1:95141800-95141850	HMEC	breast:	n/a
25	chr1:95149580-95149630	Hepatocyte	liver:	n/a
26	chr1:95141800-95141850	AG10803	skin:	n/a
27	chr1:95155557-95155607	GM06990	blood:	n/a
28	chr1:95149580-95149630	NB4	blood:	n/a
29	chr1:95149580-95149630	SK-N-SH	brain:	n/a
30	chr1:95141800-95141850	GM19239	blood:	n/a
31	chr1:95155557-95155607	HCF	heart:	n/a
32	chr1:95141800-95141850	HUVEC	blood vessel:	n/a
33	chr1:95155557-95155607	AG09319	gingival:	n/a
34	chr1:95141800-95141850	A549	lung:	n/a
35	chr1:95149580-95149630	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:95149580-95149630	GM12878	blood:	n/a
37	chr1:95155557-95155607	BJ	skin:	n/a
38	chr1:95141800-95141850	MCF-7	breast:	n/a
39	chr1:95155557-95155607	Jurkat	blood:	n/a
40	chr1:95149580-95149630	U87	brain:	n/a
41	chr1:95149580-95149630	HAEpiC	amniotic membrane:	n/a
42	chr1:95141800-95141850	HAEpiC	amniotic membrane:	n/a
43	chr1:95141800-95141850	K562	blood:	n/a
44	chr1:95155557-95155607	HRPEpiC	eye:	n/a
45	chr1:95149580-95149630	Hela-S3	cervix:	n/a
46	chr1:95155557-95155607	T-47D	breast:	n/a
47	chr1:95155557-95155607	PANC-1	pancreas:	n/a
48	chr1:95141800-95141850	GM12891	blood:	n/a
49	chr1:95141800-95141850	NH-A	brain:	n/a
50	chr1:95155557-95155607	AG04449	skin:	fetal

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

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

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

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

No data

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

Extended variants
information (count: 819 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543423005	chr1:95134805-95134806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556657102	chr1:95134807-95134808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576752353	chr1:95134808-95134809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145004507	chr1:95134820-95134821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148942326	chr1:95134883-95134884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6668794	chr1:95134903-95134904	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541578013	chr1:95134907-95134908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144316632	chr1:95134939-95134940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530680857	chr1:95134997-95134998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186804732	chr1:95135007-95135008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543903607	chr1:95135061-95135062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs57146533	chr1:95135091-95135092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34702033	chr1:95135135-95135136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146536390	chr1:95135164-95135165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11165205	chr1:95135185-95135186	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546816554	chr1:95135186-95135187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566927683	chr1:95135246-95135247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192491952	chr1:95135258-95135259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549566300	chr1:95135346-95135347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11165206	chr1:95135395-95135396	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs570062314	chr1:95135396-95135397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141202488	chr1:95135405-95135406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558414698	chr1:95135462-95135463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576804991	chr1:95135487-95135488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539416234	chr1:95135492-95135493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552653119	chr1:95135556-95135557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374172328	chr1:95135663-95135664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541637319	chr1:95135681-95135682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185675518	chr1:95135724-95135725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372314669	chr1:95135766-95135767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77929546	chr1:95135827-95135828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544211377	chr1:95135848-95135849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564393855	chr1:95135852-95135853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533178750	chr1:95135877-95135878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12409691	chr1:95135880-95135881	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs560586609	chr1:95135883-95135884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529381113	chr1:95135884-95135885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549478105	chr1:95135888-95135889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569507740	chr1:95135925-95135926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188601019	chr1:95135957-95135958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145015928	chr1:95135966-95135967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192835400	chr1:95135987-95135988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539069883	chr1:95135995-95135996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377716764	chr1:95136020-95136021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11165207	chr1:95136071-95136072	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs11165208	chr1:95136076-95136077	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs185376354	chr1:95136077-95136078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374903702	chr1:95136086-95136087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188496772	chr1:95136122-95136123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148374338	chr1:95136138-95136139	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:287 , 50 per page) page: 1 2 3 4 5 6

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	chr1:95131400-95135200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr1:95131400-95135400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr1:95131800-95135600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:95132400-95135000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:95133000-95134800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr1:95133200-95135000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:95133400-95134800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr1:95133400-95134800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:95133400-95135400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr1:95133400-95135600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr1:95133400-95136000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:95133400-95141200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr1:95133600-95141600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr1:95133800-95136200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:95133800-95136200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:95133800-95137400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:95134000-95135200	Enhancers	Hela-S3	cervix
22	chr1:95134000-95142800	Weak transcription	Small Intestine	intestine
23	chr1:95134200-95134800	Enhancers	Primary hematopoietic stem cells	blood
24	chr1:95134200-95135200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:95134200-95135200	Enhancers	NH-A	brain
26	chr1:95134200-95135400	Enhancers	Stomach Mucosa	stomach
27	chr1:95134200-95135800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:95134400-95135000	Enhancers	HepG2	liver
29	chr1:95134400-95135200	Enhancers	Fetal Intestine Large	intestine
30	chr1:95134400-95135600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:95134400-95136000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:95134400-95137400	Weak transcription	Fetal Intestine Small	intestine
33	chr1:95134400-95141600	Weak transcription	Gastric	stomach
34	chr1:95134600-95135000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:95134600-95135000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:95134600-95135200	Enhancers	NHEK	skin
37	chr1:95134600-95135600	Enhancers	Placenta Amnion	Placenta Amnion
38	chr1:95134800-95135000	Enhancers	NHLF	lung
39	chr1:95134800-95135200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:95134800-95135400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:95134800-95135400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:95134800-95135400	Enhancers	HSMM	muscle
43	chr1:95134800-95135600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr1:95134800-95139800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr1:95135000-95136000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:95135000-95136200	Weak transcription	HepG2	liver
47	chr1:95135000-95136800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr1:95135000-95154400	Weak transcription	NHLF	lung
49	chr1:95135200-95136000	Weak transcription	Hela-S3	cervix
50	chr1:95135200-95137400	Weak transcription	Fetal Intestine Large	intestine

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