Variant report

Variant	nsv546853
Chromosome Location	chr1:95127463-95154279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 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	chr1:95132331-95132574	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
8	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
9	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
12	CEBPB	chr1:95126571-95127497	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
15	CHD2	chr1:95154200-95154634	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr1:95154170-95154639	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	n/a	chr1:95150025-95150033
19	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
21	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
22	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
24	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
25	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
26	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
27	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
28	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
29	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F6	chr1:95149871-95150217	H1-hESC	embryonic stem cell:	n/a	n/a
31	EP300	chr1:95154046-95154617	H1-hESC	embryonic stem cell:	n/a	n/a
32	EP300	chr1:95130100-95130300	Hela-S3	cervix:	n/a	n/a
33	EP300	chr1:95134844-95134975	K562	blood:	n/a	n/a
34	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
38	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
39	FOXA1	chr1:95131200-95131489	HepG2	liver:	n/a	chr1:95131350-95131365
40	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
41	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
42	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
43	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
45	HDAC2	chr1:95132354-95132585	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
47	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
48	MAFF	chr1:95142755-95142907	K562	blood:	n/a	chr1:95142838-95142856
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	chr1:95141800-95141850	HCT-116	colon:	n/a
2	chr1:95149580-95149630	HRPEpiC	eye:	n/a
3	chr1:95149580-95149630	HUVEC	blood vessel:	n/a
4	chr1:95149580-95149630	HCPEpiC	choroid plexus:	n/a
5	chr1:95149580-95149630	RPTEC	kidney:	n/a
6	chr1:95149580-95149630	HNPCEpiC	eye:	n/a
7	chr1:95149580-95149630	ovcar-3	ovarian:	n/a
8	chr1:95149580-95149630	HL-60	blood:	n/a
9	chr1:95149580-95149630	T-47D	breast:	n/a
10	chr1:95141800-95141850	Hela-S3	cervix:	n/a
11	chr1:95141800-95141850	HAEpiC	amniotic membrane:	n/a
12	chr1:95141800-95141850	HEEpiC	esophagus:	n/a
13	chr1:95149580-95149630	GM19239	blood:	n/a
14	chr1:95141800-95141850	HCM	heart:	n/a
15	chr1:95149580-95149630	BE2_C	brain:	n/a
16	chr1:95141800-95141850	PFSK-1	brain:	n/a
17	chr1:95133907-95133957	PANC-1	pancreas:	n/a
18	chr1:95133907-95133957	SAEC	small airway:	n/a
19	chr1:95141800-95141850	AG09319	gingival:	n/a
20	chr1:95133907-95133957	HMEC	breast:	n/a
21	chr1:95149580-95149630	NT2-D1	testis:	n/a
22	chr1:95149580-95149630	HCT-116	colon:	n/a
23	chr1:95141800-95141850	Caco-2	colon:	n/a
24	chr1:95149580-95149630	SK-N-SH_RA	brain:	n/a
25	chr1:95133907-95133957	AG04449	skin:	fetal
26	chr1:95149580-95149630	HMEC	breast:	n/a
27	chr1:95149580-95149630	MCF-7	breast:	n/a
28	chr1:95149580-95149630	Hela-S3	cervix:	n/a
29	chr1:95133907-95133957	BJ	skin:	n/a
30	chr1:95141800-95141850	AG04450	lung:	fetal
31	chr1:95133907-95133957	SK-N-SH	brain:	n/a
32	chr1:95133907-95133957	NHBE	bronchial:	n/a
33	chr1:95149580-95149630	HepG2	liver:	n/a
34	chr1:95141800-95141850	AG10803	skin:	n/a
35	chr1:95133907-95133957	HRE	kidney:	n/a
36	chr1:95149580-95149630	GM06990	blood:	n/a
37	chr1:95133907-95133957	HCF	heart:	n/a
38	chr1:95141800-95141850	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:95133907-95133957	A549	lung:	n/a
40	chr1:95133907-95133957	NH-A	brain:	n/a
41	chr1:95141800-95141850	HEK293	kidney:	embryo
42	chr1:95141800-95141850	HIPEpiC	eye:	n/a
43	chr1:95141800-95141850	HCF	heart:	n/a
44	chr1:95133907-95133957	PrEC	prostate:	n/a
45	chr1:95149580-95149630	H1-hESC	embryonic stem cell:	embryo
46	chr1:95149580-95149630	SKMC	muscle:	n/a
47	chr1:95141800-95141850	HMEC	breast:	n/a
48	chr1:95133907-95133957	HAEpiC	amniotic membrane:	n/a
49	chr1:95133907-95133957	SK-N-MC	brain:	n/a
50	chr1:95133907-95133957	K562	blood:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 979 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11165192	chr1:95127463-95127464	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577819480	chr1:95127509-95127510	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs34038557	chr1:95127535-95127536	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs397864109	chr1:95127544-95127545	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs562182444	chr1:95127545-95127546	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs536936935	chr1:95127559-95127560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs75190550	chr1:95127566-95127567	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs528127352	chr1:95127579-95127580	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs139107844	chr1:95127645-95127646	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183211929	chr1:95127763-95127764	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs530605089	chr1:95127786-95127787	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs78136403	chr1:95127789-95127790	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs149877518	chr1:95127898-95127899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10159432	chr1:95127996-95127997	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs115509336	chr1:95128040-95128041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546640543	chr1:95128084-95128085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76879403	chr1:95128099-95128100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4847208	chr1:95128100-95128101	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs199738334	chr1:95128104-95128105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72729596	chr1:95128112-95128113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541953150	chr1:95128161-95128162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147573304	chr1:95128171-95128172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187772343	chr1:95128184-95128185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191410699	chr1:95128227-95128228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540634093	chr1:95128275-95128276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4847209	chr1:95128283-95128284	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs578152874	chr1:95128323-95128324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1118429	chr1:95128350-95128351	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs4847210	chr1:95128364-95128365	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562378569	chr1:95128373-95128374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372111327	chr1:95128376-95128377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115618618	chr1:95128381-95128382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140569987	chr1:95128407-95128408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541560342	chr1:95128410-95128411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144523067	chr1:95128469-95128470	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs530666758	chr1:95128544-95128545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4847328	chr1:95128546-95128547	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533497393	chr1:95128627-95128628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533046733	chr1:95128636-95128637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546985610	chr1:95128689-95128690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566784489	chr1:95128720-95128721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529274245	chr1:95128780-95128781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183659769	chr1:95128789-95128790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147817313	chr1:95128798-95128799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4847329	chr1:95128806-95128807	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs558343423	chr1:95128848-95128849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4847330	chr1:95128861-95128862	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs377195905	chr1:95128894-95128895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115867836	chr1:95128914-95128915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529495798	chr1:95128926-95128927	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:343 , 50 per page) page: 1 2 3 4 5 6 7

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	chr1:95125400-95128400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:95125600-95128400	Enhancers	Hela-S3	cervix
5	chr1:95125800-95128800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:95125800-95128800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr1:95126000-95127600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr1:95126000-95128400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr1:95126000-95128600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr1:95126000-95128800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:95126000-95128800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:95126200-95127800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr1:95126400-95127600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:95126400-95127600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:95126400-95127600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:95126400-95127600	Enhancers	Fetal Intestine Small	intestine
17	chr1:95126400-95127800	Enhancers	Fetal Intestine Large	intestine
18	chr1:95126400-95128400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr1:95126800-95128000	Weak transcription	Left Ventricle	heart
20	chr1:95126800-95133000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr1:95126800-95137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr1:95126800-95141600	Weak transcription	Pancreas	Pancrea
23	chr1:95126800-95164200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:95127000-95127600	Enhancers	Duodenum Mucosa	Duodenum
25	chr1:95127000-95130000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:95127200-95127600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr1:95127400-95127600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr1:95127400-95127600	Enhancers	Placenta Amnion	Placenta Amnion
29	chr1:95127400-95128800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:95127400-95129400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr1:95127400-95130000	Weak transcription	Fetal Heart	heart
32	chr1:95127400-95130000	Weak transcription	Stomach Mucosa	stomach
33	chr1:95127600-95128200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:95127600-95128600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr1:95127600-95128800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:95127600-95128800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr1:95127600-95133200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr1:95127600-95133400	Weak transcription	Fetal Intestine Small	intestine
39	chr1:95127600-95134600	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr1:95127800-95128200	Weak transcription	Fetal Intestine Large	intestine
41	chr1:95127800-95128800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr1:95128200-95128400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:95128200-95128400	Enhancers	Fetal Intestine Large	intestine
44	chr1:95128200-95128400	Enhancers	Left Ventricle	heart
45	chr1:95128400-95129600	Weak transcription	Hela-S3	cervix
46	chr1:95128400-95131800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:95128400-95134200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:95128400-95134400	Weak transcription	Fetal Intestine Large	intestine
49	chr1:95128400-95154600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:95128800-95129400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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