Variant report

Variant	nsv818267
Chromosome Location	chr1:95131929-95153262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:184)
Chromatin interactive
region (count:10)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 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	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
5	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
6	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
7	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:95132331-95132574	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
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	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
17	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
18	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
19	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
20	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
21	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	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	chr1:95134844-95134975	K562	blood:	n/a	n/a
27	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
28	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
29	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
30	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
31	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
32	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
33	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
34	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
35	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
36	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
37	HDAC2	chr1:95132354-95132585	H1-hESC	embryonic stem cell:	n/a	n/a
38	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
39	JUND	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
40	MAFF	chr1:95142755-95142907	K562	blood:	n/a	chr1:95142838-95142856
41	MAFF	chr1:95142674-95143010	HepG2	liver:	n/a	chr1:95142838-95142856
42	MAFF	chr1:95145041-95145241	K562	blood:	n/a	chr1:95145086-95145104
43	MAFF	chr1:95144917-95145234	HepG2	liver:	n/a	chr1:95145086-95145104
44	MAFF	chr1:95134814-95135118	K562	blood:	n/a	n/a
45	MAFK	chr1:95142671-95143004	HepG2	liver:	n/a	chr1:95142839-95142854
46	MAFK	chr1:95138428-95138871	IMR90	lung:	n/a	n/a
47	MAFK	chr1:95142669-95143020	HepG2	liver:	n/a	chr1:95142839-95142854
48	MAFK	chr1:95132369-95132608	H1-hESC	embryonic stem cell:	n/a	n/a
49	MAFK	chr1:95144909-95145272	Hela-S3	cervix:	n/a	chr1:95145087-95145102
50	MAFK	chr1:95134896-95135138	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95149580-95149630	SAEC	small airway:	n/a
2	chr1:95149580-95149630	SAEC	small airway:	n/a
3	chr1:95133907-95133957	NHDF-neo	bronchial:	n/a
4	chr1:95133907-95133957	NB4	blood:	n/a
5	chr1:95149580-95149630	SK-N-MC	brain:	n/a
6	chr1:95149580-95149630	AG04449	skin:	fetal
7	chr1:95141800-95141850	HRCEpiC	kidney:	n/a
8	chr1:95133907-95133957	LNCaP	prostate:	n/a
9	chr1:95141800-95141850	NH-A	brain:	n/a
10	chr1:95133907-95133957	HCT-116	colon:	n/a
11	chr1:95141800-95141850	Hepatocyte	liver:	n/a
12	chr1:95149580-95149630	GM12878	blood:	n/a
13	chr1:95133907-95133957	IMR90	lung:	fetal
14	chr1:95133907-95133957	PANC-1	pancreas:	n/a
15	chr1:95133907-95133957	H1-hESC	embryonic stem cell:	embryo
16	chr1:95141800-95141850	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:95133907-95133957	NHBE	bronchial:	n/a
18	chr1:95141800-95141850	MCF10A-Er-Src	breast:	n/a
19	chr1:95133907-95133957	A549	lung:	n/a
20	chr1:95149580-95149630	HNPCEpiC	eye:	n/a
21	chr1:95133907-95133957	AG09309	skin:	n/a
22	chr1:95133907-95133957	AG04449	skin:	fetal
23	chr1:95133907-95133957	SK-N-SH	brain:	n/a
24	chr1:95149580-95149630	HUVEC	blood vessel:	n/a
25	chr1:95149580-95149630	HepG2	liver:	n/a
26	chr1:95149580-95149630	HRCEpiC	kidney:	n/a
27	chr1:95149580-95149630	IMR90	lung:	fetal
28	chr1:95141800-95141850	GM12892	blood:	n/a
29	chr1:95141800-95141850	AG09309	skin:	n/a
30	chr1:95141800-95141850	HNPCEpiC	eye:	n/a
31	chr1:95149580-95149630	NHBE	bronchial:	n/a
32	chr1:95149580-95149630	BE2_C	brain:	n/a
33	chr1:95133907-95133957	HUVEC	blood vessel:	n/a
34	chr1:95133907-95133957	HCPEpiC	choroid plexus:	n/a
35	chr1:95133907-95133957	NT2-D1	testis:	n/a
36	chr1:95149580-95149630	AG09309	skin:	n/a
37	chr1:95133907-95133957	HRPEpiC	eye:	n/a
38	chr1:95141800-95141850	Jurkat	blood:	n/a
39	chr1:95133907-95133957	HRCEpiC	kidney:	n/a
40	chr1:95141800-95141850	CMK	blood:	n/a
41	chr1:95149580-95149630	HRE	kidney:	n/a
42	chr1:95141800-95141850	SK-N-SH	brain:	n/a
43	chr1:95141800-95141850	GM12878	blood:	n/a
44	chr1:95133907-95133957	NH-A	brain:	n/a
45	chr1:95149580-95149630	Hepatocyte	liver:	n/a
46	chr1:95133907-95133957	GM12892	blood:	n/a
47	chr1:95141800-95141850	NHDF-neo	bronchial:	n/a
48	chr1:95149580-95149630	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:95133907-95133957	BE2_C	brain:	n/a
50	chr1:95133907-95133957	GM12878	blood:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 783 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10127519	chr1:95131929-95131930	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs180765967	chr1:95131947-95131948	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542629099	chr1:95131957-95131958	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148005278	chr1:95131976-95131977	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs4847333	chr1:95132116-95132117	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536451843	chr1:95132120-95132121	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549959532	chr1:95132141-95132142	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569864242	chr1:95132191-95132192	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538894445	chr1:95132247-95132248	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558560296	chr1:95132337-95132338	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141687823	chr1:95132338-95132339	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534707570	chr1:95132340-95132341	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs4847211	chr1:95132411-95132412	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs4847334	chr1:95132450-95132451	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs543625754	chr1:95132485-95132486	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs55966239	chr1:95132518-95132519	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577345151	chr1:95132528-95132529	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185327746	chr1:95132541-95132542	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs527577708	chr1:95132560-95132561	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559785750	chr1:95132562-95132563	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147128286	chr1:95132668-95132669	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs190867251	chr1:95132696-95132697	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370321606	chr1:95132726-95132727	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560973049	chr1:95132762-95132763	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529778673	chr1:95132869-95132870	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs841350	chr1:95132874-95132875	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184056081	chr1:95132928-95132929	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541363165	chr1:95132960-95132961	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538448417	chr1:95132973-95132974	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552493780	chr1:95132997-95132998	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186954597	chr1:95133059-95133060	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534709161	chr1:95133083-95133084	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191693351	chr1:95133153-95133154	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs554509168	chr1:95133182-95133183	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs11809131	chr1:95133244-95133245	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs140320448	chr1:95133273-95133274	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs574426202	chr1:95133322-95133323	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs557159502	chr1:95133337-95133338	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs543302052	chr1:95133339-95133340	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs183193875	chr1:95133397-95133398	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs529676623	chr1:95133442-95133443	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs371715591	chr1:95133451-95133452	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs141661256	chr1:95133474-95133475	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs374907307	chr1:95133475-95133476	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs34075888	chr1:95133476-95133477	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs35592077	chr1:95133509-95133510	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs112625399	chr1:95133510-95133511	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs397720749	chr1:95133511-95133512	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs386633576	chr1:95133553-95133554	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs11165199	chr1:95133572-95133573	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95125000-95133200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:95126800-95133000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:95126800-95137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:95126800-95141600	Weak transcription	Pancreas	Pancrea
5	chr1:95126800-95164200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:95127600-95133200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr1:95127600-95133400	Weak transcription	Fetal Intestine Small	intestine
8	chr1:95127600-95134600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr1:95128400-95134200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr1:95128400-95134400	Weak transcription	Fetal Intestine Large	intestine
11	chr1:95128400-95154600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:95128800-95134200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:95130400-95133200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:95130400-95133200	Weak transcription	Stomach Mucosa	stomach
15	chr1:95131400-95132000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr1:95131400-95132800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr1:95131400-95135200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:95131400-95135400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:95131600-95132000	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr1:95131600-95132600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:95131800-95132000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr1:95131800-95132000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr1:95131800-95132000	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr1:95131800-95133200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:95131800-95133400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr1:95131800-95133400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr1:95131800-95133400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:95131800-95135600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:95132000-95132200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:95132000-95132200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr1:95132000-95133400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr1:95132200-95132400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr1:95132200-95132400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr1:95132400-95133400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:95132400-95135000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr1:95132600-95134400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:95132800-95133000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr1:95132800-95133400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:95132800-95134000	Enhancers	Small Intestine	intestine
40	chr1:95133000-95133200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr1:95133000-95134000	Weak transcription	Hela-S3	cervix
42	chr1:95133000-95134600	Enhancers	H9 Cell Line	embryonic stem cell
43	chr1:95133000-95134800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr1:95133200-95133400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr1:95133200-95133400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:95133200-95133600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr1:95133200-95133600	Enhancers	Duodenum Mucosa	Duodenum
48	chr1:95133200-95133600	Enhancers	Lung	lung
49	chr1:95133200-95133800	Enhancers	Stomach Mucosa	stomach
50	chr1:95133200-95134400	Enhancers	Gastric	stomach

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