Variant report

Variant	esv1829430
Chromosome Location	chr4:89853598-89908308
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	chr4:89888308-89888316	K562	blood:	n/a	n/a
2	ARID3A	chr4:89890408-89890619	HepG2	liver:	n/a	n/a
3	BATF	chr4:89885593-89885832	GM12878	blood:	n/a	chr4:89885728-89885739 chr4:89885705-89885716 chr4:89885750-89885761
4	BATF	chr4:89885594-89885893	GM12878	blood:	n/a	chr4:89885728-89885739 chr4:89885705-89885716 chr4:89885750-89885761
5	BCL11A	chr4:89885573-89885913	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:89885729-89885765	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:89859235-89859579	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr4:89870777-89870963	K562	blood:	n/a	n/a
9	CEBPB	chr4:89885043-89885391	MCF-7	breast:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
10	CEBPB	chr4:89876910-89877110	HepG2	liver:	n/a	chr4:89877032-89877043
11	CEBPB	chr4:89885095-89885403	K562	blood:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
12	CEBPB	chr4:89897265-89897581	IMR90	lung:	n/a	chr4:89897421-89897432
13	CEBPB	chr4:89885074-89885441	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
14	CEBPB	chr4:89885035-89885463	MCF-7	breast:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
15	CEBPB	chr4:89906528-89906906	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:89870283-89870589	IMR90	lung:	n/a	chr4:89870413-89870424
17	CEBPB	chr4:89870275-89870582	A549	lung:	n/a	chr4:89870413-89870424
18	CEBPB	chr4:89876916-89877140	IMR90	lung:	n/a	chr4:89877032-89877043
19	CEBPB	chr4:89885069-89885448	IMR90	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
20	CEBPB	chr4:89892842-89892884	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:89874722-89874868	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:89885067-89885456	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
23	CEBPB	chr4:89885137-89885375	H1-hESC	embryonic stem cell:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
24	CEBPB	chr4:89870278-89870601	HepG2	liver:	n/a	chr4:89870413-89870424
25	CEBPB	chr4:89897320-89897571	A549	lung:	n/a	chr4:89897421-89897432
26	CEBPB	chr4:89863394-89863528	H1-hESC	embryonic stem cell:	n/a	chr4:89863416-89863429
27	CEBPB	chr4:89873417-89873576	HepG2	liver:	n/a	chr4:89873529-89873540
28	CEBPB	chr4:89885166-89885321	HepG2	liver:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
29	CEBPB	chr4:89906512-89906919	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:89906601-89906833	A549	lung:	n/a	n/a
31	CEBPB	chr4:89870364-89870564	H1-hESC	embryonic stem cell:	n/a	chr4:89870413-89870424
32	CEBPB	chr4:89870249-89870592	K562	blood:	n/a	chr4:89870413-89870424
33	CEBPB	chr4:89881959-89882394	Hela-S3	cervix:	n/a	chr4:89881983-89881994 chr4:89881983-89881994
34	CEBPB	chr4:89885060-89885416	Hela-S3	cervix:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
35	CEBPB	chr4:89881808-89882115	H1-hESC	embryonic stem cell:	n/a	chr4:89881983-89881994 chr4:89881983-89881994
36	CEBPB	chr4:89861072-89861198	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:89884978-89885499	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
38	CEBPB	chr4:89892848-89892922	K562	blood:	n/a	n/a
39	CEBPB	chr4:89885062-89885419	HepG2	liver:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
40	CEBPB	chr4:89889271-89889545	MCF-7	breast:	n/a	n/a
41	CEBPB	chr4:89874716-89874832	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:89897290-89897569	K562	blood:	n/a	chr4:89897421-89897432
43	CEBPB	chr4:89859267-89859714	Hela-S3	cervix:	n/a	chr4:89859523-89859535 chr4:89859464-89859477
44	CEBPB	chr4:89858357-89858612	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:89874632-89874836	K562	blood:	n/a	n/a
46	CEBPB	chr4:89897274-89897580	HepG2	liver:	n/a	chr4:89897421-89897432
47	CEBPB	chr4:89874604-89874958	K562	blood:	n/a	n/a
48	CEBPB	chr4:89859282-89859714	IMR90	lung:	n/a	chr4:89859523-89859535 chr4:89859464-89859477
49	CTCF	chr4:89859200-89859350	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr4:89879400-89879550	GM12871	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:89884612-89884662	AG09309	skin:	n/a
2	chr4:89884612-89884662	SAEC	small airway:	n/a
3	chr4:89884612-89884662	HIPEpiC	eye:	n/a
4	chr4:89884612-89884662	BJ	skin:	n/a
5	chr4:89881374-89881424	AG09319	gingival:	n/a
6	chr4:89884612-89884662	IMR90	lung:	fetal
7	chr4:89881374-89881424	H1-hESC	embryonic stem cell:	embryo
8	chr4:89881374-89881424	SK-N-SH_RA	brain:	n/a
9	chr4:89881374-89881424	SKMC	muscle:	n/a
10	chr4:89881374-89881424	NHDF-neo	bronchial:	n/a
11	chr4:89884612-89884662	ECC-1	luminal epithelium:	n/a
12	chr4:89884612-89884662	NT2-D1	testis:	n/a
13	chr4:89884612-89884662	U87	brain:	n/a
14	chr4:89884612-89884662	GM19239	blood:	n/a
15	chr4:89884612-89884662	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:89884612-89884662	MCF10A-Er-Src	breast:	n/a
17	chr4:89884612-89884662	GM06990	blood:	n/a
18	chr4:89884612-89884662	PrEC	prostate:	n/a
19	chr4:89884612-89884662	HCPEpiC	choroid plexus:	n/a
20	chr4:89881374-89881424	HRCEpiC	kidney:	n/a
21	chr4:89881374-89881424	SAEC	small airway:	n/a
22	chr4:89884612-89884662	Jurkat	blood:	n/a
23	chr4:89881374-89881424	Hepatocyte	liver:	n/a
24	chr4:89881374-89881424	HepG2	liver:	n/a
25	chr4:89884612-89884662	ProgFib	skin:	n/a
26	chr4:89881374-89881424	HUVEC	blood vessel:	n/a
27	chr4:89881374-89881424	NB4	blood:	n/a
28	chr4:89884612-89884662	Hepatocyte	liver:	n/a
29	chr4:89881374-89881424	AG10803	skin:	n/a
30	chr4:89884612-89884662	HEEpiC	esophagus:	n/a
31	chr4:89881374-89881424	SK-N-SH	brain:	n/a
32	chr4:89884612-89884662	NB4	blood:	n/a
33	chr4:89881374-89881424	NT2-D1	testis:	n/a
34	chr4:89881374-89881424	HL-60	blood:	n/a
35	chr4:89884612-89884662	HMEC	breast:	n/a
36	chr4:89884612-89884662	PANC-1	pancreas:	n/a
37	chr4:89881374-89881424	HMEC	breast:	n/a
38	chr4:89881374-89881424	Jurkat	blood:	n/a
39	chr4:89881374-89881424	MCF-7	breast:	n/a
40	chr4:89881374-89881424	HRPEpiC	eye:	n/a
41	chr4:89884612-89884662	NHBE	bronchial:	n/a
42	chr4:89884612-89884662	NH-A	brain:	n/a
43	chr4:89881374-89881424	HCPEpiC	choroid plexus:	n/a
44	chr4:89881374-89881424	MCF10A-Er-Src	breast:	n/a
45	chr4:89884612-89884662	HCF	heart:	n/a
46	chr4:89881374-89881424	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:89881374-89881424	HEK293	kidney:	embryo
48	chr4:89884612-89884662	PFSK-1	brain:	n/a
49	chr4:89881374-89881424	RPTEC	kidney:	n/a
50	chr4:89881374-89881424	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:89900502..89902834-chr4:89906493..89908325,2	K562	blood:
2	chr4:89883284..89885618-chr4:89895803..89899472,3	K562	blood:
3	chr4:89870700..89873807-chr4:89875689..89877845,3	MCF-7	breast:
4	chr4:89879550..89882970-chr4:89885286..89887934,3	K562	blood:
5	chr4:89864109..89865635-chr4:89874326..89876576,2	K562	blood:
6	chr4:89900502..89902834-chr4:89906493..89908325,2	K562	blood:
7	chr4:89879550..89882970-chr4:89885286..89887934,3	K562	blood:
8	chr4:89853119..89856686-chr4:89857478..89862427,5	K562	blood:
9	chr4:89444433..89447084-chr4:89907641..89909631,2	MCF-7	breast:
10	chr4:89870700..89873807-chr4:89875689..89877845,3	MCF-7	breast:
11	chr4:89864109..89865635-chr4:89874326..89876576,2	K562	blood:
12	chr4:89883284..89885618-chr4:89895803..89899472,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIGD2-6	chr4:89862325-89862518	refGeneNc_1707_NR_002806
2	lnc-TIGD2-6	chr4:89863383-89863489	refGeneNc_1707_NR_002806
3	lnc-NAP1L5-4	chr4:89857465-89857573	NONHSAT097381
4	lnc-TIGD2-6	chr4:89868009-89870277	refGeneNc_1707_NR_002806

Variant related genes	Relation type
FAM13A	TF binding region
FAM13A	CpG island
ENSG00000138641	chromatin interactions
ENSG00000138640	chromatin interactions
ENSG00000145337	chromatin interactions

Extended variants
information (count: 2027 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2027 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1458562	chr4:89853598-89853599	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538918265	chr4:89853689-89853690	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575515761	chr4:89853752-89853753	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565396892	chr4:89853787-89853788	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534128896	chr4:89853796-89853797	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549163216	chr4:89853797-89853798	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs567991133	chr4:89853812-89853813	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537775712	chr4:89853834-89853835	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538133629	chr4:89853846-89853847	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556787003	chr4:89853860-89853861	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs72665832	chr4:89853877-89853878	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs538992736	chr4:89853889-89853890	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554307885	chr4:89853924-89853925	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572565831	chr4:89854017-89854018	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs4693977	chr4:89854079-89854080	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs533746731	chr4:89854090-89854091	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs190744967	chr4:89854104-89854105	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs13118412	chr4:89854133-89854134	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs543376245	chr4:89854147-89854148	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs374231397	chr4:89854162-89854163	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532023814	chr4:89854165-89854166	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368159169	chr4:89854166-89854167	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4693978	chr4:89854167-89854168	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs529732223	chr4:89854185-89854186	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10008568	chr4:89854192-89854193	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs138577218	chr4:89854234-89854235	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538400709	chr4:89854235-89854236	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577324982	chr4:89854281-89854282	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141305964	chr4:89854323-89854324	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571860240	chr4:89854328-89854329	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539079058	chr4:89854486-89854487	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182022551	chr4:89854488-89854489	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572604986	chr4:89854530-89854531	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112393419	chr4:89854577-89854578	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139101923	chr4:89854598-89854599	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576175596	chr4:89854651-89854652	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs61415747	chr4:89854700-89854701	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553809017	chr4:89854749-89854750	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs75544096	chr4:89854757-89854758	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs185856056	chr4:89854775-89854776	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs35620540	chr4:89854788-89854789	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577065394	chr4:89854892-89854893	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540667979	chr4:89854933-89854934	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558909594	chr4:89854940-89854941	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143115604	chr4:89854948-89854949	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2609280	chr4:89854961-89854962	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs13149750	chr4:89854994-89854995	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs144678861	chr4:89855023-89855024	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2704602	chr4:89855031-89855032	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148095270	chr4:89855079-89855080	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89820000-89859200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr4:89825600-89878400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:89840800-89862800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:89845400-89859600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr4:89845400-89866400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr4:89845600-89857600	Weak transcription	Gastric	stomach
7	chr4:89847000-89853600	Weak transcription	Right Ventricle	heart
8	chr4:89847200-89854400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr4:89847200-89858800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:89847400-89858200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:89847800-89855400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr4:89848400-89861000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:89850200-89878800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr4:89850400-89861200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr4:89850600-89853800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr4:89851400-89859200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr4:89851400-89883600	Weak transcription	Fetal Intestine Large	intestine
18	chr4:89852000-89855200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr4:89852400-89856000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:89852400-89856000	Weak transcription	Aorta	Aorta
21	chr4:89852400-89856000	Weak transcription	Ovary	ovary
22	chr4:89852400-89857400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:89852400-89857600	Weak transcription	Pancreas	Pancrea
24	chr4:89852400-89885000	Weak transcription	Fetal Lung	lung
25	chr4:89852600-89854400	Weak transcription	Fetal Intestine Small	intestine
26	chr4:89852600-89865400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:89852600-89877800	Weak transcription	Fetal Muscle Leg	muscle
28	chr4:89852600-89879200	Weak transcription	Fetal Stomach	stomach
29	chr4:89852600-89879400	Weak transcription	Fetal Muscle Trunk	muscle
30	chr4:89852800-89856200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr4:89853000-89853600	Enhancers	Primary T cells from cord blood	blood
32	chr4:89853000-89853800	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr4:89853200-89853600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:89853200-89853800	Weak transcription	Stomach Mucosa	stomach
35	chr4:89853200-89854600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr4:89853200-89857600	Active TSS	Placenta	Placenta
37	chr4:89853400-89854400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr4:89853600-89854000	Weak transcription	Primary T cells from cord blood	blood
39	chr4:89853600-89859000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:89853800-89855000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr4:89853800-89855200	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr4:89854000-89855000	Enhancers	Primary T cells from cord blood	blood
43	chr4:89854400-89854800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr4:89854400-89855000	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr4:89854400-89855000	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr4:89854400-89855600	Enhancers	Fetal Intestine Small	intestine
47	chr4:89854400-89860200	Weak transcription	Fetal Heart	heart
48	chr4:89854600-89855000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr4:89854800-89855600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr4:89854800-89865200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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