Variant report

Variant	nsv1026110
Chromosome Location	chr4:144239825-144292148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1406)
CpG islands
(count:1283)
Chromatin interactive
region (count:65)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:144267015-144267207	K562	blood:	n/a	n/a
2	ARID3A	chr4:144280180-144281040	K562	blood:	n/a	n/a
3	ARID3A	chr4:144258865-144259787	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:144265750-144266332	K562	blood:	n/a	n/a
5	ARID3A	chr4:144269570-144269910	K562	blood:	n/a	n/a
6	ARID3A	chr4:144242445-144242639	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:144258008-144258074	HepG2	liver:	n/a	n/a
8	ATF2	chr4:144280076-144280559	GM12878	blood:	n/a	n/a
9	ATF2	chr4:144280786-144281305	GM12878	blood:	n/a	n/a
10	ATF2	chr4:144257890-144258135	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:144256761-144257436	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:144279916-144280692	GM12878	blood:	n/a	n/a
13	BACH1	chr4:144258028-144258559	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:144273179-144273375	K562	blood:	n/a	n/a
15	BACH1	chr4:144256935-144257447	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr4:144257893-144258269	GM12878	blood:	n/a	n/a
17	BCLAF1	chr4:144258231-144258725	GM12878	blood:	n/a	chr4:144258477-144258490
18	BHLHE40	chr4:144257177-144257721	K562	blood:	n/a	n/a
19	BHLHE40	chr4:144266006-144266379	K562	blood:	n/a	n/a
20	BHLHE40	chr4:144277673-144277982	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:144269642-144269929	K562	blood:	n/a	n/a
22	BHLHE40	chr4:144280066-144280594	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:144280060-144280403	K562	blood:	n/a	n/a
24	BHLHE40	chr4:144257181-144258110	GM12878	blood:	n/a	chr4:144257737-144257753
25	BHLHE40	chr4:144257991-144258345	K562	blood:	n/a	n/a
26	BRCA1	chr4:144256931-144257355	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr4:144258773-144259088	HepG2	liver:	n/a	n/a
28	BRCA1	chr4:144257195-144257200	GM12878	blood:	n/a	n/a
29	CBX3	chr4:144257861-144258188	K562	blood:	n/a	n/a
30	CBX3	chr4:144256897-144257695	K562	blood:	n/a	n/a
31	CBX3	chr4:144269468-144270132	K562	blood:	n/a	n/a
32	CBX3	chr4:144258204-144258568	K562	blood:	n/a	n/a
33	CCNT2	chr4:144266050-144266630	K562	blood:	n/a	n/a
34	CCNT2	chr4:144269643-144269981	K562	blood:	n/a	n/a
35	CCNT2	chr4:144257041-144259053	K562	blood:	n/a	chr4:144258544-144258553
36	CEBPB	chr4:144291988-144292177	K562	blood:	n/a	chr4:144292145-144292156
37	CEBPB	chr4:144269484-144269910	K562	blood:	n/a	n/a
38	CEBPB	chr4:144255661-144256269	HepG2	liver:	n/a	chr4:144255756-144255767
39	CEBPB	chr4:144277850-144277880	K562	blood:	n/a	n/a
40	CEBPB	chr4:144277715-144277978	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:144276670-144277058	MCF-7	breast:	n/a	n/a
42	CEBPB	chr4:144291985-144292186	HepG2	liver:	n/a	chr4:144292145-144292156
43	CEBPB	chr4:144280130-144280475	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:144268746-144269920	K562	blood:	n/a	n/a
45	CEBPB	chr4:144255677-144255907	A549	lung:	n/a	chr4:144255756-144255767
46	CEBPB	chr4:144267253-144267702	MCF-7	breast:	n/a	chr4:144267477-144267490
47	CEBPB	chr4:144267378-144267619	Hela-S3	cervix:	n/a	chr4:144267477-144267490
48	CEBPB	chr4:144279924-144280461	MCF-7	breast:	n/a	n/a
49	CEBPB	chr4:144267271-144267779	MCF-7	breast:	n/a	chr4:144267477-144267490
50	CEBPB	chr4:144280999-144281265	K562	blood:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:144262077-144262127	AG09309	skin:	n/a
2	chr4:144272609-144272659	SKMC	muscle:	n/a
3	chr4:144262077-144262127	AG09309	skin:	n/a
4	chr4:144272609-144272659	SKMC	muscle:	n/a
5	chr4:144259119-144259169	PrEC	prostate:	n/a
6	chr4:144257692-144257742	SK-N-SH	brain:	n/a
7	chr4:144272609-144272659	PrEC	prostate:	n/a
8	chr4:144262077-144262127	PANC-1	pancreas:	n/a
9	chr4:144257692-144257742	Hepatocyte	liver:	n/a
10	chr4:144258448-144258498	HRPEpiC	eye:	n/a
11	chr4:144258809-144258859	U87	brain:	n/a
12	chr4:144257218-144257268	CMK	blood:	n/a
13	chr4:144266241-144266291	K562	blood:	n/a
14	chr4:144272716-144272766	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:144275126-144275176	HRPEpiC	eye:	n/a
16	chr4:144271265-144271315	SK-N-SH	brain:	n/a
17	chr4:144272716-144272766	BE2_C	brain:	n/a
18	chr4:144277796-144277846	ovcar-3	ovarian:	n/a
19	chr4:144258863-144258913	NHDF-neo	bronchial:	n/a
20	chr4:144258863-144258913	IMR90	lung:	fetal
21	chr4:144258863-144258913	AG09319	gingival:	n/a
22	chr4:144270944-144270994	U87	brain:	n/a
23	chr4:144257692-144257742	NH-A	brain:	n/a
24	chr4:144272609-144272659	NT2-D1	testis:	n/a
25	chr4:144258448-144258498	PFSK-1	brain:	n/a
26	chr4:144258809-144258859	AG04450	lung:	fetal
27	chr4:144271265-144271315	HUVEC	blood vessel:	n/a
28	chr4:144254752-144254802	Jurkat	blood:	n/a
29	chr4:144258809-144258859	HRE	kidney:	n/a
30	chr4:144272716-144272766	HRCEpiC	kidney:	n/a
31	chr4:144262077-144262127	ovcar-3	ovarian:	n/a
32	chr4:144270944-144270994	CMK	blood:	n/a
33	chr4:144258809-144258859	NH-A	brain:	n/a
34	chr4:144257685-144257735	H1-hESC	embryonic stem cell:	embryo
35	chr4:144272609-144272659	HUVEC	blood vessel:	n/a
36	chr4:144258809-144258859	Hepatocyte	liver:	n/a
37	chr4:144258448-144258498	NT2-D1	testis:	n/a
38	chr4:144277796-144277846	PANC-1	pancreas:	n/a
39	chr4:144256835-144256885	ProgFib	skin:	n/a
40	chr4:144257218-144257268	AG09309	skin:	n/a
41	chr4:144277796-144277846	Hepatocyte	liver:	n/a
42	chr4:144266241-144266291	BJ	skin:	n/a
43	chr4:144277796-144277846	SK-N-SH_RA	brain:	n/a
44	chr4:144257685-144257735	HRE	kidney:	n/a
45	chr4:144271265-144271315	AoSMC	blood vessel:	n/a
46	chr4:144257103-144257153	PFSK-1	brain:	n/a
47	chr4:144275126-144275176	Caco-2	colon:	n/a
48	chr4:144270944-144270994	HUVEC	blood vessel:	n/a
49	chr4:144258863-144258913	GM12878	blood:	n/a
50	chr4:144258809-144258859	SAEC	small airway:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:124524644..124527323-chr4:144255705..144257566,2	MCF-7	breast:
2	chr4:144256119..144259388-chr4:144266158..144269819,4	MCF-7	breast:
3	chr4:144274310..144276106-chr4:144283049..144285599,2	MCF-7	breast:
4	chr4:144104958..144107554-chr4:144256815..144258504,3	K562	blood:
5	chr4:144265483..144268245-chr4:144270502..144272328,2	K562	blood:
6	chr4:144279254..144282177-chr4:144295139..144296728,2	MCF-7	breast:
7	chr4:144283863..144286903-chr4:144287176..144291126,4	K562	blood:
8	chr4:144268435..144271097-chr4:144272609..144275318,3	K562	blood:
9	chr4:144262793..144271335-chr4:144272377..144280163,14	K562	blood:
10	chr4:144282645..144284355-chr4:144296664..144298307,2	MCF-7	breast:
11	chr4:144272183..144275049-chr4:144275578..144277182,2	MCF-7	breast:
12	chr4:144264296..144264969-chr6:30028972..30029813,2	Hela-S3	cervix:
13	chr4:144127423..144129387-chr4:144280177..144281782,2	K562	blood:
14	chr4:144104818..144107585-chr4:144256509..144260468,4	MCF-7	breast:
15	chr4:144256496..144258835-chr4:144281268..144283636,2	MCF-7	breast:
16	chr4:144267296..144268822-chr4:144271997..144274488,2	MCF-7	breast:
17	chr4:144290996..144292995-chr4:144295055..144297084,2	MCF-7	breast:
18	chr4:144263524..144266219-chr4:144271347..144273028,2	MCF-7	breast:
19	chr4:144254627..144258395-chr4:144297952..144301828,4	K562	blood:
20	chr4:144275276..144278433-chr4:144281060..144283410,4	MCF-7	breast:
21	chr4:144235945..144238860-chr4:144239571..144241521,2	K562	blood:
22	chr4:144275276..144278433-chr4:144281060..144283410,4	MCF-7	breast:
23	chr4:144252887..144254426-chr4:144256311..144258181,2	K562	blood:
24	chr4:144284857..144287398-chr4:144288484..144291385,2	K562	blood:
25	chr4:144249067..144251120-chr4:144252809..144255702,2	K562	blood:
26	chr4:144262782..144265192-chr4:144266129..144268644,2	MCF-7	breast:
27	chr4:144251943..144253888-chr4:144255920..144257556,2	MCF-7	breast:
28	chr4:144257935..144259880-chr4:144296110..144298167,2	MCF-7	breast:
29	chr4:144228357..144232212-chr4:144238301..144241767,5	K562	blood:
30	chr4:144255843..144260329-chr4:144275960..144279644,5	MCF-7	breast:
31	chr4:144280022..144283375-chr4:144285064..144288406,3	K562	blood:
32	chr4:144238199..144241165-chr4:144253825..144255392,2	K562	blood:
33	chr4:144256474..144260869-chr4:144433151..144436933,4	K562	blood:
34	chr4:144257782..144259357-chr4:144281420..144283250,2	MCF-7	breast:
35	chr4:144272912..144279199-chr4:144279482..144284125,11	K562	blood:
36	chr4:144106120..144108984-chr4:144259325..144260882,2	K562	blood:
37	chr4:144255276..144259485-chr4:144272162..144275884,5	MCF-7	breast:
38	chr4:144254658..144259448-chr4:144261105..144264742,6	MCF-7	breast:
39	chr4:144268435..144271097-chr4:144272609..144275318,3	K562	blood:
40	chr4:144256714..144259978-chr4:144276972..144280167,4	MCF-7	breast:
41	chr4:144104098..144106648-chr4:144265192..144267593,2	K562	blood:
42	chr4:144279896..144282516-chr4:144316177..144318703,2	K562	blood:
43	chr4:144254658..144259448-chr4:144261105..144264742,6	MCF-7	breast:
44	chr4:144249894..144251809-chr4:144255982..144258797,2	K562	blood:
45	chr4:144104098..144105841-chr4:144264877..144267593,2	K562	blood:
46	chr4:144272912..144279199-chr4:144279482..144284125,11	K562	blood:
47	chr4:144251943..144253888-chr4:144255920..144257556,2	MCF-7	breast:
48	chr4:144249067..144251120-chr4:144252809..144255702,2	K562	blood:
49	chr4:144289833..144291469-chr4:144294402..144296058,2	K562	blood:
50	chr4:144257678..144260213-chr4:144284163..144287062,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FREM3-6	chr4:144256418-144258970	NONHSAT098553
2	lnc-GAB1-1	chr4:144250432-144251011	XLOC_003715

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3139	chr4:144264622-144264644	MIMAT0015007

No data

Variant related genes	Relation type
MIR3139	TF binding region
GAB1	TF binding region
ENSG00000228981	TF binding region
ENSG00000178972	TF binding region
MIR3139	CpG island
GAB1	CpG island
ENSG00000228981	CpG island
ENSG00000178972	CpG island
ENSG00000250326	chromatin interactions
ENSG00000228981	chromatin interactions
ENSG00000245112	chromatin interactions
ENSG00000265623	chromatin interactions
ENSG00000170185	chromatin interactions
ENSG00000200049	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000109458	chromatin interactions
ENSG00000153147	chromatin interactions
ENSG00000178972	chromatin interactions
ENSG00000204623	chromatin interactions

Extended variants
information (count: 1768 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1768 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs300904	chr4:144239825-144239826	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149609477	chr4:144239892-144239893	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535281370	chr4:144239893-144239894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181449950	chr4:144239918-144239919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576292246	chr4:144239954-144239955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs35027946	chr4:144239971-144239972	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs66507425	chr4:144240025-144240026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34853779	chr4:144240038-144240039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200328932	chr4:144240039-144240040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185275472	chr4:144240057-144240058	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34364385	chr4:144240104-144240105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs535276230	chr4:144240131-144240132	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550821217	chr4:144240139-144240140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568944046	chr4:144240147-144240148	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565355223	chr4:144240156-144240157	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539553114	chr4:144240180-144240181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114282845	chr4:144240241-144240242	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs13118863	chr4:144240270-144240271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112620700	chr4:144240339-144240340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181239680	chr4:144240399-144240400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555709035	chr4:144240411-144240412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184552606	chr4:144240433-144240434	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78591363	chr4:144240444-144240445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs76756247	chr4:144240448-144240449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs300905	chr4:144240473-144240474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs559744616	chr4:144240498-144240499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563564243	chr4:144240515-144240516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560288375	chr4:144240528-144240529	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575301104	chr4:144240539-144240540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545903636	chr4:144240542-144240543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547528865	chr4:144240559-144240560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186066334	chr4:144240589-144240590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs79099267	chr4:144240590-144240591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561811739	chr4:144240595-144240596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529207846	chr4:144240636-144240637	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377403177	chr4:144240649-144240650	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs300906	chr4:144240657-144240658	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs11941986	chr4:144240672-144240673	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs995836	chr4:144240673-144240674	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551495573	chr4:144240691-144240692	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566605479	chr4:144240723-144240724	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376596122	chr4:144240727-144240728	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189343373	chr4:144240803-144240804	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552384319	chr4:144240851-144240852	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181915383	chr4:144240918-144240919	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535762558	chr4:144240925-144240926	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs148381418	chr4:144240986-144240987	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs557093162	chr4:144241103-144241104	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111743153	chr4:144241146-144241147	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs370665045	chr4:144241152-144241153	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2094 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:144235000-144247000	Weak transcription	Right Atrium	heart
2	chr4:144235600-144241000	Weak transcription	Left Ventricle	heart
3	chr4:144238800-144240400	Weak transcription	Fetal Heart	heart
4	chr4:144239000-144240200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:144239000-144240200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:144239000-144240400	Weak transcription	Colon Smooth Muscle	Colon
7	chr4:144239000-144241000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr4:144239000-144241200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr4:144240200-144240400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:144240200-144240400	Enhancers	Rectal Smooth Muscle	rectum
11	chr4:144240200-144242800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr4:144240400-144240600	Enhancers	Brain Substantia Nigra	brain
13	chr4:144240400-144241200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:144240400-144241200	Enhancers	Colon Smooth Muscle	Colon
15	chr4:144240400-144242200	Enhancers	Fetal Heart	heart
16	chr4:144240600-144241000	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr4:144240600-144241200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:144240600-144241400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:144240600-144241600	Enhancers	Brain Cingulate Gyrus	brain
20	chr4:144240800-144241600	Enhancers	Stomach Mucosa	stomach
21	chr4:144240800-144241800	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr4:144241000-144241400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:144241000-144241600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:144241000-144241600	Enhancers	Left Ventricle	heart
25	chr4:144241000-144242400	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr4:144241200-144241600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr4:144241200-144241800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:144241400-144241600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:144241400-144241600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:144241400-144241600	Enhancers	Brain Substantia Nigra	brain
31	chr4:144241400-144242000	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr4:144241600-144242600	Weak transcription	Stomach Mucosa	stomach
33	chr4:144242200-144242600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:144242200-144242600	Flanking Active TSS	Fetal Heart	heart
35	chr4:144242600-144242800	Enhancers	Fetal Heart	heart
36	chr4:144242600-144243000	Enhancers	Stomach Mucosa	stomach
37	chr4:144247600-144250200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:144249000-144249200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:144249400-144250800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr4:144250800-144251400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:144255400-144255800	Enhancers	Fetal Muscle Trunk	muscle
42	chr4:144255600-144256600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:144255800-144256000	Enhancers	Fetal Kidney	kidney
44	chr4:144255800-144256000	Enhancers	Ovary	ovary
45	chr4:144255800-144256600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:144255800-144256600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr4:144255800-144256600	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr4:144255800-144256600	Weak transcription	Fetal Muscle Trunk	muscle
49	chr4:144256000-144256200	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr4:144256000-144256600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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