Variant report

Variant	nsv519997
Chromosome Location	chr1:95083836-95113417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:590)
CpG islands
(count:305)
Chromatin interactive
region (count:16)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	BACH1	chr1:95111892-95111966	K562	blood:	n/a	n/a
5	BCL3	chr1:95100543-95101039	K562	blood:	n/a	chr1:95100617-95100626
6	BHLHE40	chr1:95111706-95111898	K562	blood:	n/a	n/a
7	BHLHE40	chr1:95087002-95087263	K562	blood:	n/a	n/a
8	BRCA1	chr1:95086951-95087354	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr1:95088263-95088574	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr1:95107642-95108055	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr1:95111691-95112631	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr1:95111551-95112517	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:95105705-95106261	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:95086670-95087531	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:95100509-95100956	K562	blood:	n/a	n/a
16	CCNT2	chr1:95100532-95100921	K562	blood:	n/a	n/a
17	CEBPB	chr1:95094803-95095271	Hela-S3	cervix:	n/a	chr1:95094987-95094998
18	CEBPB	chr1:95088315-95088655	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:95107069-95107999	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:95112512-95112599	K562	blood:	n/a	chr1:95112569-95112580
21	CEBPB	chr1:95112385-95112763	IMR90	lung:	n/a	chr1:95112569-95112580
22	CEBPB	chr1:95094837-95095149	H1-hESC	embryonic stem cell:	n/a	chr1:95094987-95094998
23	CEBPB	chr1:95094848-95095141	K562	blood:	n/a	chr1:95094987-95094998
24	CEBPB	chr1:95098642-95099086	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:95094879-95095180	K562	blood:	n/a	chr1:95094987-95094998
26	CEBPB	chr1:95086952-95087726	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:95094826-95095239	HepG2	liver:	n/a	chr1:95094987-95094998
28	CEBPB	chr1:95085154-95085370	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:95094872-95095174	HepG2	liver:	n/a	chr1:95094987-95094998
30	CEBPB	chr1:95089239-95089597	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:95094827-95095172	IMR90	lung:	n/a	chr1:95094987-95094998
32	CEBPB	chr1:95102162-95102546	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:95102192-95102599	HCT-116	colon:	n/a	n/a
34	CEBPB	chr1:95101997-95102670	HCT-116	colon:	n/a	n/a
35	CEBPB	chr1:95102154-95102562	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:95094803-95095306	HCT-116	colon:	n/a	chr1:95094987-95094998
37	CEBPB	chr1:95108476-95108887	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:95111366-95112127	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:95111371-95113060	Hela-S3	cervix:	n/a	chr1:95112840-95112848 chr1:95112569-95112580
40	CEBPB	chr1:95100623-95100892	K562	blood:	n/a	n/a
41	CEBPB	chr1:95112417-95112716	HepG2	liver:	n/a	chr1:95112569-95112580
42	CEBPB	chr1:95100556-95100972	K562	blood:	n/a	n/a
43	CEBPB	chr1:95087383-95087720	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:95112519-95112608	H1-hESC	embryonic stem cell:	n/a	chr1:95112569-95112580
45	CEBPB	chr1:95089260-95089559	IMR90	lung:	n/a	n/a
46	CEBPD	chr1:95100452-95101068	K562	blood:	n/a	n/a
47	CEBPD	chr1:95100444-95101044	K562	blood:	n/a	n/a
48	CHD2	chr1:95089090-95089557	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr1:95088289-95088738	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr1:95107107-95108079	Hela-S3	cervix:	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	chr1:95101861-95101911	GM19239	blood:	n/a
2	chr1:95095221-95095271	IMR90	lung:	fetal
3	chr1:95101297-95101347	AG10803	skin:	n/a
4	chr1:95101297-95101347	Caco-2	colon:	n/a
5	chr1:95089526-95089576	HRE	kidney:	n/a
6	chr1:95095221-95095271	HMEC	breast:	n/a
7	chr1:95089526-95089576	AG10803	skin:	n/a
8	chr1:95101861-95101911	AG04450	lung:	fetal
9	chr1:95101861-95101911	SAEC	small airway:	n/a
10	chr1:95101297-95101347	HEEpiC	esophagus:	n/a
11	chr1:95088560-95088610	HepG2	liver:	n/a
12	chr1:95088560-95088610	PANC-1	pancreas:	n/a
13	chr1:95101297-95101347	CMK	blood:	n/a
14	chr1:95095221-95095271	SKMC	muscle:	n/a
15	chr1:95101861-95101911	HRCEpiC	kidney:	n/a
16	chr1:95095221-95095271	AG04449	skin:	fetal
17	chr1:95095221-95095271	RPTEC	kidney:	n/a
18	chr1:95095221-95095271	Hepatocyte	liver:	n/a
19	chr1:95095221-95095271	BE2_C	brain:	n/a
20	chr1:95088560-95088610	ECC-1	luminal epithelium:	n/a
21	chr1:95095221-95095271	GM19239	blood:	n/a
22	chr1:95088560-95088610	MCF10A-Er-Src	breast:	n/a
23	chr1:95101297-95101347	NH-A	brain:	n/a
24	chr1:95101861-95101911	AG09319	gingival:	n/a
25	chr1:95095221-95095271	GM06990	blood:	n/a
26	chr1:95095221-95095271	SK-N-MC	brain:	n/a
27	chr1:95089526-95089576	SK-N-SH_RA	brain:	n/a
28	chr1:95101861-95101911	U87	brain:	n/a
29	chr1:95089526-95089576	GM19239	blood:	n/a
30	chr1:95101861-95101911	Caco-2	colon:	n/a
31	chr1:95101297-95101347	GM12891	blood:	n/a
32	chr1:95101297-95101347	H1-hESC	embryonic stem cell:	embryo
33	chr1:95095221-95095271	A549	lung:	n/a
34	chr1:95089526-95089576	T-47D	breast:	n/a
35	chr1:95095221-95095271	HCF	heart:	n/a
36	chr1:95088560-95088610	U87	brain:	n/a
37	chr1:95095221-95095271	T-47D	breast:	n/a
38	chr1:95088560-95088610	A549	lung:	n/a
39	chr1:95101297-95101347	HMEC	breast:	n/a
40	chr1:95088560-95088610	AG04449	skin:	fetal
41	chr1:95089526-95089576	NHDF-neo	bronchial:	n/a
42	chr1:95095221-95095271	HCT-116	colon:	n/a
43	chr1:95095221-95095271	ProgFib	skin:	n/a
44	chr1:95095221-95095271	AoSMC	blood vessel:	n/a
45	chr1:95089526-95089576	AG09319	gingival:	n/a
46	chr1:95088560-95088610	HRPEpiC	eye:	n/a
47	chr1:95101861-95101911	ovcar-3	ovarian:	n/a
48	chr1:95101861-95101911	HCM	heart:	n/a
49	chr1:95101297-95101347	IMR90	lung:	fetal
50	chr1:95101297-95101347	HUVEC	blood vessel:	n/a

(count:16 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 1213 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10874867	chr1:95083836-95083837	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534469750	chr1:95083839-95083840	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548522729	chr1:95083887-95083888	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185843215	chr1:95083907-95083908	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs115252683	chr1:95083949-95083950	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557440728	chr1:95083958-95083959	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs79430637	chr1:95083982-95083983	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562791697	chr1:95084038-95084039	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs539933736	chr1:95084064-95084065	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553146241	chr1:95084112-95084113	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531684837	chr1:95084129-95084130	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190648525	chr1:95084133-95084134	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561930028	chr1:95084161-95084162	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113972137	chr1:95084232-95084233	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs575560202	chr1:95084235-95084236	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs368755417	chr1:95084248-95084249	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567052817	chr1:95084261-95084262	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs531969841	chr1:95084265-95084266	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7526391	chr1:95084281-95084282	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559153458	chr1:95084333-95084334	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs528302362	chr1:95084473-95084474	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs548436154	chr1:95084492-95084493	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568261661	chr1:95084493-95084494	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537385543	chr1:95084531-95084532	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs374780133	chr1:95084537-95084538	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs527455824	chr1:95084539-95084540	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181212447	chr1:95084552-95084553	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547290542	chr1:95084566-95084567	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs112646001	chr1:95084568-95084569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs186665094	chr1:95084572-95084573	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs539423537	chr1:95084575-95084576	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150063736	chr1:95084586-95084587	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs191266400	chr1:95084629-95084630	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs182667201	chr1:95084631-95084632	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536159311	chr1:95084634-95084635	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540771530	chr1:95084635-95084636	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs186823521	chr1:95084636-95084637	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs575422677	chr1:95084689-95084690	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190847235	chr1:95084768-95084769	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs55887124	chr1:95084769-95084770	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs4847206	chr1:95084776-95084777	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545445256	chr1:95084777-95084778	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs183557228	chr1:95084804-95084805	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs34196999	chr1:95084813-95084814	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs376309920	chr1:95084818-95084819	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs369584940	chr1:95084862-95084863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs11165184	chr1:95084940-95084941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs111455441	chr1:95084955-95084956	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573273678	chr1:95084962-95084963	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192299046	chr1:95084977-95084978	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr1:95082000-95084000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr1:95082000-95084000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:95082000-95084200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:95082000-95084200	Enhancers	Placenta Amnion	Placenta Amnion
14	chr1:95082200-95084200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:95082400-95084000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:95082400-95084400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:95082400-95086200	Weak transcription	Fetal Heart	heart
18	chr1:95082600-95088200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:95082800-95088200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:95083000-95084000	Enhancers	Colonic Mucosa	Colon
21	chr1:95083000-95084000	Enhancers	HepG2	liver
22	chr1:95083000-95087600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:95083000-95087800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:95083200-95086400	Weak transcription	A549	lung
25	chr1:95083400-95085200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:95083400-95085800	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:95083400-95086200	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr1:95083400-95086200	Weak transcription	Small Intestine	intestine
29	chr1:95083400-95087000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:95083400-95088600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:95083600-95084400	ZNF genes & repeats	HMEC	breast
32	chr1:95083600-95084800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:95083600-95085400	Weak transcription	HSMM	muscle
34	chr1:95083800-95084000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:95083800-95084000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr1:95083800-95084000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:95083800-95084200	ZNF genes & repeats	NHEK	skin
38	chr1:95083800-95085200	Weak transcription	Hela-S3	cervix
39	chr1:95083800-95085200	Weak transcription	NH-A	brain
40	chr1:95083800-95086400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:95083800-95086800	Weak transcription	NHLF	lung
42	chr1:95083800-95087200	Weak transcription	Osteobl	bone
43	chr1:95083800-95088600	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr1:95084000-95084200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:95084000-95085200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr1:95084000-95085200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr1:95084000-95086400	Weak transcription	Colonic Mucosa	Colon
48	chr1:95084000-95086600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr1:95084000-95086800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:95084000-95086800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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