Variant report

Variant	nsv1001230
Chromosome Location	chr1:95085184-95108531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:305)
Chromatin interactive
region (count:13)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:95100612-95100993	K562	blood:	n/a	n/a
2	ATF1	chr1:95100599-95100815	K562	blood:	n/a	n/a
3	ATF3	chr1:95100495-95100857	K562	blood:	n/a	n/a
4	BCL3	chr1:95100543-95101039	K562	blood:	n/a	chr1:95100617-95100626
5	BHLHE40	chr1:95087002-95087263	K562	blood:	n/a	n/a
6	BRCA1	chr1:95088263-95088574	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr1:95107642-95108055	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr1:95086951-95087354	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr1:95086670-95087531	HCT-116	colon:	n/a	n/a
10	CBX3	chr1:95100509-95100956	K562	blood:	n/a	n/a
11	CBX3	chr1:95105705-95106261	HCT-116	colon:	n/a	n/a
12	CCNT2	chr1:95100532-95100921	K562	blood:	n/a	n/a
13	CEBPB	chr1:95094803-95095271	Hela-S3	cervix:	n/a	chr1:95094987-95094998
14	CEBPB	chr1:95094826-95095239	HepG2	liver:	n/a	chr1:95094987-95094998
15	CEBPB	chr1:95108476-95108887	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:95102154-95102562	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:95107069-95107999	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:95086952-95087726	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:95100623-95100892	K562	blood:	n/a	n/a
20	CEBPB	chr1:95085154-95085370	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:95098642-95099086	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:95102162-95102546	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:95087383-95087720	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:95094879-95095180	K562	blood:	n/a	chr1:95094987-95094998
25	CEBPB	chr1:95101997-95102670	HCT-116	colon:	n/a	n/a
26	CEBPB	chr1:95089260-95089559	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:95089239-95089597	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:95094803-95095306	HCT-116	colon:	n/a	chr1:95094987-95094998
29	CEBPB	chr1:95100556-95100972	K562	blood:	n/a	n/a
30	CEBPB	chr1:95094827-95095172	IMR90	lung:	n/a	chr1:95094987-95094998
31	CEBPB	chr1:95088315-95088655	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:95094872-95095174	HepG2	liver:	n/a	chr1:95094987-95094998
33	CEBPB	chr1:95094837-95095149	H1-hESC	embryonic stem cell:	n/a	chr1:95094987-95094998
34	CEBPB	chr1:95094848-95095141	K562	blood:	n/a	chr1:95094987-95094998
35	CEBPB	chr1:95102192-95102599	HCT-116	colon:	n/a	n/a
36	CEBPD	chr1:95100452-95101068	K562	blood:	n/a	n/a
37	CEBPD	chr1:95100444-95101044	K562	blood:	n/a	n/a
38	CHD2	chr1:95088289-95088738	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:95102154-95102547	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr1:95089090-95089557	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr1:95086907-95087428	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr1:95107107-95108079	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr1:95089476-95089648	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr1:95100354-95101008	K562	blood:	n/a	n/a
45	CTCF	chr1:95100740-95100890	AG04450	lung:	n/a	n/a
46	CTCF	chr1:95086068-95086079	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:95086005-95086168	MCF-7	breast:	n/a	chr1:95086095-95086116 chr1:95086096-95086104 chr1:95086096-95086109
48	CTCF	chr1:95100720-95100870	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr1:95085960-95086110	MCF-7	breast:	n/a	chr1:95086096-95086104 chr1:95086096-95086109
50	CTCF	chr1:95100840-95100990	HPF	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95101297-95101347	CMK	blood:	n/a
2	chr1:95095221-95095271	MCF10A-Er-Src	breast:	n/a
3	chr1:95089526-95089576	H1-hESC	embryonic stem cell:	embryo
4	chr1:95101861-95101911	SK-N-MC	brain:	n/a
5	chr1:95101297-95101347	Hepatocyte	liver:	n/a
6	chr1:95101861-95101911	AG04450	lung:	fetal
7	chr1:95089526-95089576	Hela-S3	cervix:	n/a
8	chr1:95101861-95101911	MCF10A-Er-Src	breast:	n/a
9	chr1:95095221-95095271	RPTEC	kidney:	n/a
10	chr1:95088560-95088610	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:95101297-95101347	H1-hESC	embryonic stem cell:	embryo
12	chr1:95101861-95101911	LNCaP	prostate:	n/a
13	chr1:95095221-95095271	IMR90	lung:	fetal
14	chr1:95089526-95089576	HUVEC	blood vessel:	n/a
15	chr1:95089526-95089576	NB4	blood:	n/a
16	chr1:95101297-95101347	HIPEpiC	eye:	n/a
17	chr1:95101297-95101347	HEK293	kidney:	embryo
18	chr1:95101861-95101911	A549	lung:	n/a
19	chr1:95089526-95089576	PrEC	prostate:	n/a
20	chr1:95101297-95101347	GM12878	blood:	n/a
21	chr1:95088560-95088610	GM12891	blood:	n/a
22	chr1:95101861-95101911	HAEpiC	amniotic membrane:	n/a
23	chr1:95088560-95088610	HRCEpiC	kidney:	n/a
24	chr1:95101297-95101347	GM06990	blood:	n/a
25	chr1:95088560-95088610	AG09319	gingival:	n/a
26	chr1:95101861-95101911	SKMC	muscle:	n/a
27	chr1:95101297-95101347	U87	brain:	n/a
28	chr1:95101861-95101911	HCM	heart:	n/a
29	chr1:95089526-95089576	GM12878	blood:	n/a
30	chr1:95088560-95088610	HCM	heart:	n/a
31	chr1:95088560-95088610	U87	brain:	n/a
32	chr1:95101861-95101911	BE2_C	brain:	n/a
33	chr1:95101861-95101911	AoSMC	blood vessel:	n/a
34	chr1:95089526-95089576	HL-60	blood:	n/a
35	chr1:95101297-95101347	HL-60	blood:	n/a
36	chr1:95088560-95088610	BE2_C	brain:	n/a
37	chr1:95095221-95095271	SAEC	small airway:	n/a
38	chr1:95088560-95088610	MCF-7	breast:	n/a
39	chr1:95089526-95089576	HIPEpiC	eye:	n/a
40	chr1:95088560-95088610	HEEpiC	esophagus:	n/a
41	chr1:95088560-95088610	NHBE	bronchial:	n/a
42	chr1:95095221-95095271	SK-N-SH_RA	brain:	n/a
43	chr1:95101297-95101347	HCT-116	colon:	n/a
44	chr1:95095221-95095271	PFSK-1	brain:	n/a
45	chr1:95101861-95101911	SK-N-SH_RA	brain:	n/a
46	chr1:95088560-95088610	GM06990	blood:	n/a
47	chr1:95101861-95101911	IMR90	lung:	fetal
48	chr1:95088560-95088610	HEK293	kidney:	embryo
49	chr1:95089526-95089576	NHBE	bronchial:	n/a
50	chr1:95101861-95101911	Caco-2	colon:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:95100479..95101193-chr1:95267507..95268149,2	MCF-7	breast:
2	chr1:95005520..95008552-chr1:95083214..95086682,3	MCF-7	breast:
3	chr1:95015461..95017197-chr1:95086412..95088142,2	K562	blood:
4	chr1:95080479..95082832-chr1:95086788..95088378,2	K562	blood:
5	chr1:95087249..95089894-chr1:95090024..95092198,2	MCF-7	breast:
6	chr1:95098692..95101011-chr1:95110470..95114437,3	K562	blood:
7	chr1:95079718..95082412-chr1:95085713..95087293,2	MCF-7	breast:
8	chr1:95092034..95094712-chr1:95098482..95100203,2	K562	blood:
9	chr1:95083696..95086099-chr1:95111956..95113779,2	MCF-7	breast:
10	chr1:95092034..95094712-chr1:95098482..95100203,2	K562	blood:
11	chr1:95075515..95077960-chr1:95084097..95086216,2	K562	blood:
12	chr1:95104382..95108045-chr1:95108728..95112831,4	K562	blood:
13	chr1:95084398..95087368-chr1:95088701..95090405,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-2	chr1:95086187-95086543	XLOC_000922
2	lnc-F3-2	chr1:95088565-95088595	NONHSAT004597
3	lnc-F3-2	chr1:95088606-95089355	NONHSAT004597
4	lnc-F3-2	chr1:95088275-95088440	XLOC_000922
5	lnc-F3-2	chr1:95103992-95104114	NONHSAT004602
6	lnc-F3-2	chr1:95086707-95087512	XLOC_000922
7	lnc-F3-2	chr1:95091441-95091887	NONHSAT004597
8	lnc-F3-2	chr1:95088275-95089740	XLOC_000922
9	lnc-F3-2	chr1:95099373-95099414	NONHSAT004599
10	lnc-F3-2	chr1:95088275-95088456	NONHSAT004599
11	lnc-CNN3-3	chr1:95104017-95104114	ENSG00000224081.2
12	lnc-F3-2	chr1:95099361-95099428	NONHSAT004602
13	lnc-F3-2	chr1:95103261-95103386	NONHSAT004602
14	lnc-F3-2	chr1:95101565-95101980	NONHSAT004602

No data

Variant related genes	Relation type
ENSG00000235565	TF binding region
ENSG00000235565	CpG island
ENSG00000117525	chromatin interactions
ENSG00000235565	chromatin interactions

Extended variants
information (count: 960 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:960 , 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	rs370005997	chr1:95085219-95085220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs569110153	chr1:95085230-95085231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs10782983	chr1:95085258-95085259	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs143232133	chr1:95085259-95085260	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531148346	chr1:95085278-95085279	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs578210848	chr1:95085306-95085307	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540921011	chr1:95085325-95085326	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552737289	chr1:95085409-95085410	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572838038	chr1:95085438-95085439	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs376210787	chr1:95085456-95085457	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs554079085	chr1:95085529-95085530	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs114714202	chr1:95085533-95085534	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs11165185	chr1:95085592-95085593	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs112228932	chr1:95085626-95085627	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs146690588	chr1:95085627-95085628	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184291204	chr1:95085648-95085649	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs188180897	chr1:95085702-95085703	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs148857413	chr1:95085717-95085718	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142508457	chr1:95085720-95085721	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181836870	chr1:95085721-95085722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs115509466	chr1:95085724-95085725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12064943	chr1:95085728-95085729	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs111844810	chr1:95085740-95085741	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537930233	chr1:95085762-95085763	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs76686959	chr1:95085777-95085778	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs571805371	chr1:95085830-95085831	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs184813071	chr1:95085831-95085832	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs554401041	chr1:95085926-95085927	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs1539622	chr1:95085927-95085928	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs12065028	chr1:95085936-95085937	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs555387966	chr1:95085955-95085956	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs72541887	chr1:95085958-95085959	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs1539623	chr1:95085959-95085960	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs544292323	chr1:95086000-95086001	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140862053	chr1:95086007-95086008	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs146164053	chr1:95086073-95086074	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540157789	chr1:95086077-95086078	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs560970847	chr1:95086089-95086090	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574111397	chr1:95086095-95086096	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs559984132	chr1:95086097-95086098	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543015293	chr1:95086100-95086101	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529990833	chr1:95086139-95086140	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548997343	chr1:95086152-95086153	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs370693434	chr1:95086164-95086165	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs1245483	chr1:95086175-95086176	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78929856	chr1:95086178-95086179	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs181675528	chr1:95086186-95086187	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs186810395	chr1:95086187-95086188	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs189685583	chr1:95086217-95086218	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs7532777	chr1:95086225-95086226	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95065600-95087200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:95075200-95088400	Weak transcription	Fetal Lung	lung
3	chr1:95075600-95086000	Weak transcription	Fetal Stomach	stomach
4	chr1:95078600-95085200	Weak transcription	Pancreas	Pancrea
5	chr1:95078600-95086000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:95080800-95085200	Weak transcription	Gastric	stomach
7	chr1:95080800-95085200	Weak transcription	Lung	lung
8	chr1:95080800-95086800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr1:95081000-95085400	Weak transcription	Stomach Mucosa	stomach
10	chr1:95082400-95086200	Weak transcription	Fetal Heart	heart
11	chr1:95082600-95088200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:95082800-95088200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:95083000-95087600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:95083000-95087800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:95083200-95086400	Weak transcription	A549	lung
16	chr1:95083400-95085200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:95083400-95085800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr1:95083400-95086200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr1:95083400-95086200	Weak transcription	Small Intestine	intestine
20	chr1:95083400-95087000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:95083400-95088600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:95083600-95085400	Weak transcription	HSMM	muscle
23	chr1:95083800-95085200	Weak transcription	Hela-S3	cervix
24	chr1:95083800-95085200	Weak transcription	NH-A	brain
25	chr1:95083800-95086400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:95083800-95086800	Weak transcription	NHLF	lung
27	chr1:95083800-95087200	Weak transcription	Osteobl	bone
28	chr1:95083800-95088600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr1:95084000-95085200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:95084000-95085200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr1:95084000-95086400	Weak transcription	Colonic Mucosa	Colon
32	chr1:95084000-95086600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr1:95084000-95086800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:95084000-95086800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr1:95084000-95087000	Weak transcription	HepG2	liver
36	chr1:95084000-95087600	Weak transcription	NHDF-Ad	bronchial
37	chr1:95084000-95088200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr1:95084200-95085200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr1:95084200-95085200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:95084200-95085200	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr1:95084400-95085200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr1:95084800-95090200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:95085000-95086200	Enhancers	NHEK	skin
44	chr1:95085000-95090200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:95085000-95090600	Enhancers	HMEC	breast
46	chr1:95085200-95085400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:95085200-95085600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr1:95085200-95085800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:95085200-95086800	Enhancers	Hela-S3	cervix
50	chr1:95085200-95087200	Enhancers	Gastric	stomach

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