Variant report

Variant	nsv4412
Chromosome Location	chr4:88237813-88283368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:88253897-88253929	K562	blood:	n/a	n/a
2	ARID3A	chr4:88238747-88239287	HepG2	liver:	n/a	n/a
3	BCLAF1	chr4:88274531-88275047	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:88238776-88238949	HepG2	liver:	n/a	n/a
5	BHLHE40	chr4:88280589-88280606	K562	blood:	n/a	n/a
6	BRCA1	chr4:88274711-88274757	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:88263580-88263749	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr4:88274849-88275046	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr4:88254173-88254833	K562	blood:	n/a	n/a
10	CBX3	chr4:88254322-88254718	K562	blood:	n/a	n/a
11	CEBPB	chr4:88257579-88258049	IMR90	lung:	n/a	chr4:88257687-88257696 chr4:88257685-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257685-88257698
12	CEBPB	chr4:88238743-88239106	MCF-7	breast:	n/a	n/a
13	CEBPB	chr4:88257600-88257870	K562	blood:	n/a	chr4:88257687-88257696 chr4:88257685-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257685-88257698
14	CEBPB	chr4:88246787-88246815	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:88257547-88258074	HepG2	liver:	n/a	chr4:88257687-88257696 chr4:88257685-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257685-88257698
16	CEBPB	chr4:88238169-88239081	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:88238687-88239062	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:88238650-88239170	A549	lung:	n/a	n/a
19	CEBPB	chr4:88280503-88280750	IMR90	lung:	n/a	chr4:88280568-88280579
20	CEBPB	chr4:88274649-88274999	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:88280504-88280678	A549	lung:	n/a	chr4:88280568-88280579
22	CEBPB	chr4:88238773-88238946	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:88262596-88262828	HepG2	liver:	n/a	chr4:88262658-88262669
24	CEBPB	chr4:88238721-88239017	A549	lung:	n/a	n/a
25	CEBPB	chr4:88238754-88238999	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:88263335-88263764	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr4:88274671-88274892	K562	blood:	n/a	n/a
28	CEBPB	chr4:88274621-88275554	IMR90	lung:	n/a	chr4:88275098-88275111
29	CEBPB	chr4:88246514-88246851	MCF-7	breast:	n/a	n/a
30	CEBPB	chr4:88257669-88257948	A549	lung:	n/a	chr4:88257687-88257696 chr4:88257685-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257687-88257696 chr4:88257685-88257698 chr4:88257687-88257698 chr4:88257685-88257698
31	CEBPB	chr4:88274583-88274924	MCF-7	breast:	n/a	n/a
32	CEBPB	chr4:88274643-88274980	A549	lung:	n/a	n/a
33	CEBPB	chr4:88238667-88239136	MCF-7	breast:	n/a	n/a
34	CEBPB	chr4:88274648-88274960	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:88241858-88242058	K562	blood:	n/a	chr4:88241967-88241980 chr4:88241967-88241978
36	CEBPB	chr4:88238748-88239007	A549	lung:	n/a	n/a
37	CEBPB	chr4:88260233-88260502	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:88280405-88280740	HepG2	liver:	n/a	chr4:88280568-88280579
39	CEBPB	chr4:88249280-88249561	HepG2	liver:	n/a	chr4:88249401-88249412
40	CEBPB	chr4:88250534-88250698	A549	lung:	n/a	n/a
41	CEBPB	chr4:88253976-88254261	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:88262614-88262799	IMR90	lung:	n/a	chr4:88262658-88262669
43	CEBPB	chr4:88280524-88280680	H1-hESC	embryonic stem cell:	n/a	chr4:88280568-88280579
44	CEBPB	chr4:88241820-88242139	HepG2	liver:	n/a	chr4:88241967-88241980 chr4:88241967-88241978
45	CEBPB	chr4:88253983-88254237	A549	lung:	n/a	n/a
46	CEBPB	chr4:88274654-88274987	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr4:88280484-88280727	K562	blood:	n/a	chr4:88280568-88280579
48	CEBPB	chr4:88280537-88280635	Hela-S3	cervix:	n/a	chr4:88280568-88280579
49	CEBPD	chr4:88238790-88238923	HepG2	liver:	n/a	n/a
50	CHD2	chr4:88263445-88263748	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88245032-88245082	A549	lung:	n/a
2	chr4:88244909-88244959	NHDF-neo	bronchial:	n/a
3	chr4:88245032-88245082	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:88245032-88245082	HRPEpiC	eye:	n/a
5	chr4:88245032-88245082	AoSMC	blood vessel:	n/a
6	chr4:88245032-88245082	Jurkat	blood:	n/a
7	chr4:88243818-88243868	ovcar-3	ovarian:	n/a
8	chr4:88243818-88243868	HCM	heart:	n/a
9	chr4:88258112-88258162	K562	blood:	n/a
10	chr4:88243818-88243868	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:88258112-88258162	PANC-1	pancreas:	n/a
12	chr4:88243818-88243868	ProgFib	skin:	n/a
13	chr4:88245032-88245082	MCF10A-Er-Src	breast:	n/a
14	chr4:88245032-88245082	SK-N-SH_RA	brain:	n/a
15	chr4:88258112-88258162	GM12878	blood:	n/a
16	chr4:88258112-88258162	RPTEC	kidney:	n/a
17	chr4:88258112-88258162	HCM	heart:	n/a
18	chr4:88244142-88244192	U87	brain:	n/a
19	chr4:88243818-88243868	AoSMC	blood vessel:	n/a
20	chr4:88243818-88243868	BE2_C	brain:	n/a
21	chr4:88245032-88245082	SK-N-SH	brain:	n/a
22	chr4:88243818-88243868	NHBE	bronchial:	n/a
23	chr4:88245032-88245082	NHBE	bronchial:	n/a
24	chr4:88244909-88244959	Jurkat	blood:	n/a
25	chr4:88258112-88258162	GM12891	blood:	n/a
26	chr4:88243818-88243868	GM12878	blood:	n/a
27	chr4:88244909-88244959	HL-60	blood:	n/a
28	chr4:88243818-88243868	CMK	blood:	n/a
29	chr4:88245032-88245082	AG09319	gingival:	n/a
30	chr4:88243818-88243868	SAEC	small airway:	n/a
31	chr4:88244142-88244192	HEEpiC	esophagus:	n/a
32	chr4:88244142-88244192	GM12891	blood:	n/a
33	chr4:88244142-88244192	PFSK-1	brain:	n/a
34	chr4:88258112-88258162	BE2_C	brain:	n/a
35	chr4:88245032-88245082	GM12891	blood:	n/a
36	chr4:88258112-88258162	SK-N-SH_RA	brain:	n/a
37	chr4:88244909-88244959	T-47D	breast:	n/a
38	chr4:88258112-88258162	GM06990	blood:	n/a
39	chr4:88243818-88243868	GM12891	blood:	n/a
40	chr4:88258112-88258162	HEK293	kidney:	embryo
41	chr4:88245032-88245082	SAEC	small airway:	n/a
42	chr4:88244909-88244959	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:88258112-88258162	SKMC	muscle:	n/a
44	chr4:88244909-88244959	HUVEC	blood vessel:	n/a
45	chr4:88244142-88244192	PANC-1	pancreas:	n/a
46	chr4:88244142-88244192	SKMC	muscle:	n/a
47	chr4:88244909-88244959	HIPEpiC	eye:	n/a
48	chr4:88245032-88245082	NHDF-neo	bronchial:	n/a
49	chr4:88244142-88244192	AG04450	lung:	fetal
50	chr4:88244142-88244192	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:88275401..88278298-chr4:88313681..88315567,2	K562	blood:
2	chr4:88225790..88227669-chr4:88236912..88239118,2	MCF-7	breast:
3	chr4:88242496..88244669-chr4:88248333..88250976,2	MCF-7	breast:
4	chr4:88274380..88275024-chr4:88386955..88387766,2	MCF-7	breast:
5	chr4:88274412..88275303-chr4:88464991..88465582,2	MCF-7	breast:
6	chr4:88274390..88275203-chr4:88387077..88388072,3	K562	blood:
7	chr4:88257535..88259344-chr4:88263879..88265710,2	K562	blood:
8	chr4:88256379..88257982-chr4:88259770..88261744,2	K562	blood:
9	chr4:88275546..88276371-chr4:88386699..88387600,2	MCF-7	breast:
10	chr4:88257214..88259344-chr4:88263879..88266042,3	K562	blood:
11	chr4:88257214..88259344-chr4:88263879..88266042,3	K562	blood:
12	chr4:88241962..88245128-chr4:88247108..88249633,3	MCF-7	breast:
13	chr4:88257535..88259344-chr4:88263879..88265710,2	K562	blood:
14	chr4:88237707..88239445-chr4:88243261..88245305,2	MCF-7	breast:
15	chr4:88141156..88144056-chr4:88277951..88279842,2	MCF-7	breast:
16	chr4:88242503..88244047-chr4:88248462..88250419,2	K562	blood:
17	chr4:88280472..88283090-chr4:88343390..88345468,2	MCF-7	breast:
18	chr4:88256379..88257982-chr4:88259770..88261744,2	K562	blood:
19	chr3:195808128..195810426-chr4:88262608..88264108,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT9-1	chr4:88273499-88273744	expReg_chr4_4651_+

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HSD17B11	hsa-miR-1	chr4:88257896-88257914

Variant related genes	Relation type
ENSG00000255723	TF binding region
HSD17B13	TF binding region
ENSG00000255723	CpG island
HSD17B13	CpG island
ENSG00000170502	chromatin interactions
ENSG00000170509	chromatin interactions
ENSG00000072274	chromatin interactions
ENSG00000145332	chromatin interactions

Extended variants
information (count: 1736 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1736 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542271790	chr4:88237883-88237884	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs547196902	chr4:88237891-88237892	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568528411	chr4:88237896-88237897	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549360028	chr4:88237898-88237899	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536183147	chr4:88237905-88237906	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550843245	chr4:88237954-88237955	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs115151963	chr4:88237969-88237970	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7662471	chr4:88238013-88238014	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541432605	chr4:88238045-88238046	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs557291565	chr4:88238055-88238056	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148231707	chr4:88238061-88238062	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533617174	chr4:88238117-88238118	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555569080	chr4:88238179-88238180	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112952768	chr4:88238181-88238182	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373050717	chr4:88238193-88238194	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200335722	chr4:88238196-88238197	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370325280	chr4:88238199-88238200	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544563177	chr4:88238200-88238201	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374101728	chr4:88238220-88238221	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370289965	chr4:88238237-88238238	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs61748262	chr4:88238244-88238245	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142525792	chr4:88238256-88238257	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201763274	chr4:88238293-88238294	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372936841	chr4:88238313-88238314	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190310719	chr4:88238346-88238347	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372816850	chr4:88238363-88238364	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564292392	chr4:88238385-88238386	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371923490	chr4:88238391-88238392	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376964857	chr4:88238406-88238407	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547893464	chr4:88238408-88238409	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528603881	chr4:88238416-88238417	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34419567	chr4:88238430-88238431	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs6531975	chr4:88238448-88238449	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs193051604	chr4:88238482-88238483	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562338105	chr4:88238508-88238509	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185706108	chr4:88238532-88238533	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550904243	chr4:88238550-88238551	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs115628949	chr4:88238556-88238557	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539697967	chr4:88238560-88238561	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550976236	chr4:88238639-88238640	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566327090	chr4:88238682-88238683	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs73839189	chr4:88238693-88238694	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs374148861	chr4:88238708-88238709	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs13139110	chr4:88238716-88238717	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7668535	chr4:88238729-88238730	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs150725645	chr4:88238761-88238762	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573817340	chr4:88238800-88238801	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs115143274	chr4:88238806-88238807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556345226	chr4:88238827-88238828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs56293231	chr4:88238850-88238851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88228000-88239600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:88229000-88245000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:88230000-88240000	Weak transcription	Brain Angular Gyrus	brain
4	chr4:88230600-88239600	Weak transcription	Primary T cells from cord blood	blood
5	chr4:88235200-88243800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:88235600-88241400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:88235800-88238400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:88235800-88242600	Weak transcription	Adipose Nuclei	Adipose
9	chr4:88236800-88239000	Weak transcription	Pancreas	Pancrea
10	chr4:88236800-88243200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:88237400-88238400	Strong transcription	Left Ventricle	heart
12	chr4:88237800-88238800	Genic enhancers	Liver	Liver
13	chr4:88237800-88239800	Enhancers	Hela-S3	cervix
14	chr4:88238200-88238600	Enhancers	HepG2	liver
15	chr4:88238400-88238600	Enhancers	Fetal Intestine Small	intestine
16	chr4:88238400-88239200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:88238400-88239600	Weak transcription	Left Ventricle	heart
18	chr4:88238600-88239200	Weak transcription	Fetal Intestine Small	intestine
19	chr4:88238600-88253400	Weak transcription	HepG2	liver
20	chr4:88238800-88239000	Weak transcription	Liver	Liver
21	chr4:88239000-88239600	Genic enhancers	Liver	Liver
22	chr4:88239200-88239400	Enhancers	Fetal Intestine Small	intestine
23	chr4:88239200-88239400	Enhancers	A549	lung
24	chr4:88239400-88239600	Enhancers	Pancreas	Pancrea
25	chr4:88239400-88239800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:88239400-88239800	Enhancers	Placenta	Placenta
27	chr4:88239400-88248000	Weak transcription	Fetal Intestine Small	intestine
28	chr4:88239400-88255400	Weak transcription	A549	lung
29	chr4:88239600-88239800	Active TSS	Left Ventricle	heart
30	chr4:88239600-88240400	Weak transcription	Liver	Liver
31	chr4:88239800-88240200	Weak transcription	Hela-S3	cervix
32	chr4:88240200-88241000	Enhancers	Hela-S3	cervix
33	chr4:88240400-88240600	Enhancers	Liver	Liver
34	chr4:88240600-88241000	Flanking Active TSS	Liver	Liver
35	chr4:88241000-88244200	Active TSS	Liver	Liver
36	chr4:88242600-88244200	Active TSS	Adipose Nuclei	Adipose
37	chr4:88243200-88243600	Active TSS	Ovary	ovary
38	chr4:88243200-88243600	Enhancers	NHLF	lung
39	chr4:88243200-88244000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:88243200-88244200	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr4:88243400-88244200	Enhancers	Colon Smooth Muscle	Colon
42	chr4:88243600-88244200	Enhancers	Ovary	ovary
43	chr4:88243800-88244200	Enhancers	Rectal Smooth Muscle	rectum
44	chr4:88244200-88244600	Enhancers	Liver	Liver
45	chr4:88245000-88245200	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr4:88247800-88249200	Enhancers	Fetal Intestine Large	intestine
47	chr4:88248000-88248600	Enhancers	Fetal Intestine Small	intestine
48	chr4:88248600-88249800	Weak transcription	Fetal Intestine Small	intestine
49	chr4:88250600-88259400	Weak transcription	Fetal Heart	heart
50	chr4:88252200-88254200	Weak transcription	Stomach Smooth Muscle	stomach

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