Variant report

Variant	nsv546857
Chromosome Location	chr1:95134182-95153262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 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	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
5	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
6	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
7	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
13	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
15	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
16	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	n/a	chr1:95150025-95150033
17	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
18	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
19	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
21	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
22	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
23	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr1:95149871-95150217	H1-hESC	embryonic stem cell:	n/a	n/a
25	EP300	chr1:95134844-95134975	K562	blood:	n/a	n/a
26	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
27	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	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	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
31	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
32	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
33	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
34	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
35	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
36	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
37	JUND	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
38	MAFF	chr1:95142755-95142907	K562	blood:	n/a	chr1:95142838-95142856
39	MAFF	chr1:95134814-95135118	K562	blood:	n/a	n/a
40	MAFF	chr1:95142674-95143010	HepG2	liver:	n/a	chr1:95142838-95142856
41	MAFF	chr1:95145041-95145241	K562	blood:	n/a	chr1:95145086-95145104
42	MAFF	chr1:95144917-95145234	HepG2	liver:	n/a	chr1:95145086-95145104
43	MAFK	chr1:95134884-95135098	K562	blood:	n/a	n/a
44	MAFK	chr1:95142749-95143012	Hela-S3	cervix:	n/a	chr1:95142839-95142854
45	MAFK	chr1:95142671-95143004	HepG2	liver:	n/a	chr1:95142839-95142854
46	MAFK	chr1:95144909-95145272	Hela-S3	cervix:	n/a	chr1:95145087-95145102
47	MAFK	chr1:95144922-95145260	HepG2	liver:	n/a	chr1:95145087-95145102
48	MAFK	chr1:95134835-95135141	IMR90	lung:	n/a	n/a
49	MAFK	chr1:95142662-95143011	IMR90	lung:	n/a	chr1:95142839-95142854
50	MAFK	chr1:95144908-95145278	IMR90	lung:	n/a	chr1:95145087-95145102

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95141800-95141850	HMEC	breast:	n/a
2	chr1:95141800-95141850	IMR90	lung:	fetal
3	chr1:95149580-95149630	AG04450	lung:	fetal
4	chr1:95141800-95141850	NHBE	bronchial:	n/a
5	chr1:95141800-95141850	MCF10A-Er-Src	breast:	n/a
6	chr1:95141800-95141850	HL-60	blood:	n/a
7	chr1:95149580-95149630	AG10803	skin:	n/a
8	chr1:95141800-95141850	A549	lung:	n/a
9	chr1:95149580-95149630	Jurkat	blood:	n/a
10	chr1:95149580-95149630	HRE	kidney:	n/a
11	chr1:95141800-95141850	HNPCEpiC	eye:	n/a
12	chr1:95141800-95141850	AoSMC	blood vessel:	n/a
13	chr1:95149580-95149630	MCF10A-Er-Src	breast:	n/a
14	chr1:95141800-95141850	HCT-116	colon:	n/a
15	chr1:95141800-95141850	LNCaP	prostate:	n/a
16	chr1:95149580-95149630	HCM	heart:	n/a
17	chr1:95141800-95141850	HIPEpiC	eye:	n/a
18	chr1:95149580-95149630	GM12891	blood:	n/a
19	chr1:95141800-95141850	GM12891	blood:	n/a
20	chr1:95149580-95149630	AG04449	skin:	fetal
21	chr1:95149580-95149630	MCF-7	breast:	n/a
22	chr1:95141800-95141850	AG09319	gingival:	n/a
23	chr1:95149580-95149630	SKMC	muscle:	n/a
24	chr1:95149580-95149630	H1-hESC	embryonic stem cell:	embryo
25	chr1:95149580-95149630	GM19239	blood:	n/a
26	chr1:95149580-95149630	HUVEC	blood vessel:	n/a
27	chr1:95149580-95149630	PANC-1	pancreas:	n/a
28	chr1:95141800-95141850	AG04450	lung:	fetal
29	chr1:95141800-95141850	AG10803	skin:	n/a
30	chr1:95141800-95141850	SK-N-SH_RA	brain:	n/a
31	chr1:95141800-95141850	T-47D	breast:	n/a
32	chr1:95149580-95149630	Hepatocyte	liver:	n/a
33	chr1:95141800-95141850	ovcar-3	ovarian:	n/a
34	chr1:95141800-95141850	BJ	skin:	n/a
35	chr1:95149580-95149630	CMK	blood:	n/a
36	chr1:95141800-95141850	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:95141800-95141850	SKMC	muscle:	n/a
38	chr1:95141800-95141850	AG04449	skin:	fetal
39	chr1:95149580-95149630	HAEpiC	amniotic membrane:	n/a
40	chr1:95149580-95149630	SK-N-SH	brain:	n/a
41	chr1:95149580-95149630	NT2-D1	testis:	n/a
42	chr1:95141800-95141850	NT2-D1	testis:	n/a
43	chr1:95149580-95149630	HL-60	blood:	n/a
44	chr1:95141800-95141850	HAEpiC	amniotic membrane:	n/a
45	chr1:95141800-95141850	HUVEC	blood vessel:	n/a
46	chr1:95149580-95149630	NHBE	bronchial:	n/a
47	chr1:95149580-95149630	AG09309	skin:	n/a
48	chr1:95149580-95149630	SK-N-SH_RA	brain:	n/a
49	chr1:95149580-95149630	HEK293	kidney:	embryo
50	chr1:95141800-95141850	PFSK-1	brain:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 717 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11165201	chr1:95134182-95134183	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139216621	chr1:95134196-95134197	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs540032039	chr1:95134214-95134215	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs841351	chr1:95134224-95134225	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs72731503	chr1:95134246-95134247	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs841352	chr1:95134267-95134268	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11165202	chr1:95134269-95134270	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs574534212	chr1:95134335-95134336	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs12079632	chr1:95134336-95134337	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs572176259	chr1:95134356-95134357	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs563408509	chr1:95134396-95134397	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs190183413	chr1:95134397-95134398	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs182079125	chr1:95134452-95134453	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376084014	chr1:95134460-95134461	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71483841	chr1:95134463-95134464	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11165204	chr1:95134464-95134465	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs568011128	chr1:95134507-95134508	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs841353	chr1:95134516-95134517	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs1602831	chr1:95134522-95134523	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548004660	chr1:95134525-95134526	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568113144	chr1:95134526-95134527	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149927859	chr1:95134562-95134563	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539519261	chr1:95134582-95134583	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1602832	chr1:95134589-95134590	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532093284	chr1:95134603-95134604	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1845241	chr1:95134610-95134611	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370536825	chr1:95134633-95134634	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556102150	chr1:95134698-95134699	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1845242	chr1:95134728-95134729	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543423005	chr1:95134805-95134806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556657102	chr1:95134807-95134808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576752353	chr1:95134808-95134809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145004507	chr1:95134820-95134821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148942326	chr1:95134883-95134884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6668794	chr1:95134903-95134904	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs541578013	chr1:95134907-95134908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144316632	chr1:95134939-95134940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530680857	chr1:95134997-95134998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186804732	chr1:95135007-95135008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543903607	chr1:95135061-95135062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs57146533	chr1:95135091-95135092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34702033	chr1:95135135-95135136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146536390	chr1:95135164-95135165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11165205	chr1:95135185-95135186	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs546816554	chr1:95135186-95135187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566927683	chr1:95135246-95135247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192491952	chr1:95135258-95135259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549566300	chr1:95135346-95135347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11165206	chr1:95135395-95135396	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs570062314	chr1:95135396-95135397	Enhancers Weak 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:227 , 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	chr1:95127600-95134600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr1:95128400-95134200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr1:95128400-95134400	Weak transcription	Fetal Intestine Large	intestine
7	chr1:95128400-95154600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:95128800-95134200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:95131400-95135200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr1:95131400-95135400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:95131800-95135600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr1:95132400-95135000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:95132600-95134400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:95133000-95134600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr1:95133000-95134800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr1:95133200-95134400	Enhancers	Gastric	stomach
17	chr1:95133200-95135000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:95133400-95134400	ZNF genes & repeats	Fetal Intestine Small	intestine
19	chr1:95133400-95134800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr1:95133400-95134800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:95133400-95135400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:95133400-95135600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr1:95133400-95136000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:95133400-95141200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr1:95133600-95134200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr1:95133600-95141600	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:95133800-95134200	Weak transcription	Stomach Mucosa	stomach
28	chr1:95133800-95136200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:95133800-95136200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:95133800-95137400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:95134000-95135200	Enhancers	Hela-S3	cervix
32	chr1:95134000-95142800	Weak transcription	Small Intestine	intestine
33	chr1:95134200-95134800	Enhancers	Primary hematopoietic stem cells	blood
34	chr1:95134200-95135200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr1:95134200-95135200	Enhancers	NH-A	brain
36	chr1:95134200-95135400	Enhancers	Stomach Mucosa	stomach
37	chr1:95134200-95135800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:95134400-95135000	Enhancers	HepG2	liver
39	chr1:95134400-95135200	Enhancers	Fetal Intestine Large	intestine
40	chr1:95134400-95135600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:95134400-95136000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:95134400-95137400	Weak transcription	Fetal Intestine Small	intestine
43	chr1:95134400-95141600	Weak transcription	Gastric	stomach
44	chr1:95134600-95135000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:95134600-95135000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:95134600-95135200	Enhancers	NHEK	skin
47	chr1:95134600-95135600	Enhancers	Placenta Amnion	Placenta Amnion
48	chr1:95134800-95135000	Enhancers	NHLF	lung
49	chr1:95134800-95135200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:95134800-95135400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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