Variant report

Variant	nsv879532
Chromosome Location	chr4:89811195-89917135
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	chr4:89833021-89833268	GM12878	blood:	n/a	n/a
5	BATF	chr4:89885594-89885893	GM12878	blood:	n/a	chr4:89885728-89885739 chr4:89885705-89885716 chr4:89885750-89885761
6	BCL11A	chr4:89885573-89885913	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:89885729-89885765	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:89859235-89859579	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr4:89870777-89870963	K562	blood:	n/a	n/a
10	CEBPB	chr4:89897274-89897580	HepG2	liver:	n/a	chr4:89897421-89897432
11	CEBPB	chr4:89824859-89824882	A549	lung:	n/a	n/a
12	CEBPB	chr4:89832417-89832779	MCF-7	breast:	n/a	n/a
13	CEBPB	chr4:89874716-89874832	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:89874722-89874868	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:89832423-89832761	A549	lung:	n/a	n/a
16	CEBPB	chr4:89906528-89906906	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:89885069-89885448	IMR90	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
18	CEBPB	chr4:89885137-89885375	H1-hESC	embryonic stem cell:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
19	CEBPB	chr4:89874604-89874958	K562	blood:	n/a	n/a
20	CEBPB	chr4:89832455-89832716	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:89876910-89877110	HepG2	liver:	n/a	chr4:89877032-89877043
22	CEBPB	chr4:89881959-89882394	Hela-S3	cervix:	n/a	chr4:89881983-89881994 chr4:89881983-89881994
23	CEBPB	chr4:89885095-89885403	K562	blood:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
24	CEBPB	chr4:89863394-89863528	H1-hESC	embryonic stem cell:	n/a	chr4:89863416-89863429
25	CEBPB	chr4:89885060-89885416	Hela-S3	cervix:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
26	CEBPB	chr4:89832427-89832767	K562	blood:	n/a	n/a
27	CEBPB	chr4:89870364-89870564	H1-hESC	embryonic stem cell:	n/a	chr4:89870413-89870424
28	CEBPB	chr4:89861072-89861198	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:89885035-89885463	MCF-7	breast:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
30	CEBPB	chr4:89885074-89885441	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
31	CEBPB	chr4:89912413-89912613	IMR90	lung:	n/a	chr4:89912539-89912550
32	CEBPB	chr4:89885166-89885321	HepG2	liver:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
33	CEBPB	chr4:89906601-89906833	A549	lung:	n/a	n/a
34	CEBPB	chr4:89884978-89885499	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
35	CEBPB	chr4:89874632-89874836	K562	blood:	n/a	n/a
36	CEBPB	chr4:89832405-89832770	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:89889271-89889545	MCF-7	breast:	n/a	n/a
38	CEBPB	chr4:89912425-89912616	H1-hESC	embryonic stem cell:	n/a	chr4:89912539-89912550
39	CEBPB	chr4:89832391-89832757	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:89870249-89870592	K562	blood:	n/a	chr4:89870413-89870424
41	CEBPB	chr4:89881808-89882115	H1-hESC	embryonic stem cell:	n/a	chr4:89881983-89881994 chr4:89881983-89881994
42	CEBPB	chr4:89832475-89832676	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:89897320-89897571	A549	lung:	n/a	chr4:89897421-89897432
44	CEBPB	chr4:89859282-89859714	IMR90	lung:	n/a	chr4:89859523-89859535 chr4:89859464-89859477
45	CEBPB	chr4:89870275-89870582	A549	lung:	n/a	chr4:89870413-89870424
46	CEBPB	chr4:89873417-89873576	HepG2	liver:	n/a	chr4:89873529-89873540
47	CEBPB	chr4:89859267-89859714	Hela-S3	cervix:	n/a	chr4:89859523-89859535 chr4:89859464-89859477
48	CEBPB	chr4:89858357-89858612	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:89870278-89870601	HepG2	liver:	n/a	chr4:89870413-89870424
50	CEBPB	chr4:89906512-89906919	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:89841012-89841062	AG09319	gingival:	n/a
2	chr4:89884612-89884662	HNPCEpiC	eye:	n/a
3	chr4:89841012-89841062	NHDF-neo	bronchial:	n/a
4	chr4:89881374-89881424	SK-N-SH_RA	brain:	n/a
5	chr4:89884612-89884662	HL-60	blood:	n/a
6	chr4:89829015-89829065	AG09319	gingival:	n/a
7	chr4:89841012-89841062	MCF10A-Er-Src	breast:	n/a
8	chr4:89829015-89829065	Jurkat	blood:	n/a
9	chr4:89884612-89884662	T-47D	breast:	n/a
10	chr4:89841012-89841062	HNPCEpiC	eye:	n/a
11	chr4:89881374-89881424	HepG2	liver:	n/a
12	chr4:89829015-89829065	HRCEpiC	kidney:	n/a
13	chr4:89841012-89841062	PFSK-1	brain:	n/a
14	chr4:89841012-89841062	Jurkat	blood:	n/a
15	chr4:89829015-89829065	SKMC	muscle:	n/a
16	chr4:89884612-89884662	NT2-D1	testis:	n/a
17	chr4:89881374-89881424	NB4	blood:	n/a
18	chr4:89881374-89881424	GM12892	blood:	n/a
19	chr4:89884612-89884662	BE2_C	brain:	n/a
20	chr4:89829015-89829065	ovcar-3	ovarian:	n/a
21	chr4:89884612-89884662	H1-hESC	embryonic stem cell:	embryo
22	chr4:89881374-89881424	HCT-116	colon:	n/a
23	chr4:89841012-89841062	SK-N-SH_RA	brain:	n/a
24	chr4:89884612-89884662	GM12891	blood:	n/a
25	chr4:89881374-89881424	HCF	heart:	n/a
26	chr4:89884612-89884662	K562	blood:	n/a
27	chr4:89841012-89841062	RPTEC	kidney:	n/a
28	chr4:89829015-89829065	PrEC	prostate:	n/a
29	chr4:89829015-89829065	CMK	blood:	n/a
30	chr4:89884612-89884662	GM19239	blood:	n/a
31	chr4:89829015-89829065	MCF10A-Er-Src	breast:	n/a
32	chr4:89884612-89884662	HIPEpiC	eye:	n/a
33	chr4:89884612-89884662	HCF	heart:	n/a
34	chr4:89881374-89881424	HRPEpiC	eye:	n/a
35	chr4:89829015-89829065	AG04450	lung:	fetal
36	chr4:89841012-89841062	NB4	blood:	n/a
37	chr4:89829015-89829065	ProgFib	skin:	n/a
38	chr4:89881374-89881424	IMR90	lung:	fetal
39	chr4:89884612-89884662	AG04450	lung:	fetal
40	chr4:89881374-89881424	HNPCEpiC	eye:	n/a
41	chr4:89881374-89881424	AG09319	gingival:	n/a
42	chr4:89829015-89829065	AG10803	skin:	n/a
43	chr4:89881374-89881424	NH-A	brain:	n/a
44	chr4:89881374-89881424	Hepatocyte	liver:	n/a
45	chr4:89829015-89829065	GM19239	blood:	n/a
46	chr4:89881374-89881424	SKMC	muscle:	n/a
47	chr4:89841012-89841062	HepG2	liver:	n/a
48	chr4:89884612-89884662	ProgFib	skin:	n/a
49	chr4:89881374-89881424	ProgFib	skin:	n/a
50	chr4:89829015-89829065	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:89883284..89885618-chr4:89895803..89899472,3	K562	blood:
2	chr4:89444433..89447084-chr4:89907641..89909631,2	MCF-7	breast:
3	chr4:89883284..89885618-chr4:89895803..89899472,3	K562	blood:
4	chr4:89916625..89919056-chr4:89920360..89922873,2	MCF-7	breast:
5	chr4:89864109..89865635-chr4:89874326..89876576,2	K562	blood:
6	chr4:89879550..89882970-chr4:89885286..89887934,3	K562	blood:
7	chr4:89853119..89856686-chr4:89857478..89862427,5	K562	blood:
8	chr4:89870700..89873807-chr4:89875689..89877845,3	MCF-7	breast:
9	chr4:89864109..89865635-chr4:89874326..89876576,2	K562	blood:
10	chr4:89870700..89873807-chr4:89875689..89877845,3	MCF-7	breast:
11	chr4:89900502..89902834-chr4:89906493..89908325,2	K562	blood:
12	chr4:89879550..89882970-chr4:89885286..89887934,3	K562	blood:
13	chr4:89900502..89902834-chr4:89906493..89908325,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAP1L5-4	chr4:89826837-89826869	NONHSAT097381
2	lnc-TIGD2-6	chr4:89868009-89870277	refGeneNc_1707_NR_002806
3	lnc-TIGD2-6	chr4:89849963-89850439	refGeneNc_1707_NR_002806
4	lnc-TIGD2-6	chr4:89862325-89862518	refGeneNc_1707_NR_002806
5	lnc-NAP1L5-4	chr4:89827530-89827613	NONHSAT097381
6	lnc-TIGD2-6	chr4:89852029-89852191	refGeneNc_1707_NR_002806
7	lnc-NAP1L5-4	chr4:89857465-89857573	NONHSAT097381
8	lnc-TIGD2-6	chr4:89863383-89863489	refGeneNc_1707_NR_002806

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM13A	hsa-miR-10b-5p	chr4:89911301-89911325

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

Extended variants
information (count: 4013 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4013 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2609255	chr4:89811195-89811196	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs530465812	chr4:89811196-89811197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570638644	chr4:89811200-89811201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534568481	chr4:89811291-89811292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35988187	chr4:89811299-89811300	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs377540597	chr4:89811504-89811505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563702079	chr4:89811518-89811519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530772250	chr4:89811519-89811520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552721422	chr4:89811528-89811529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35794341	chr4:89811563-89811564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145286083	chr4:89811567-89811568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181943266	chr4:89811584-89811585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373995788	chr4:89811622-89811623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185267884	chr4:89811623-89811624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568154524	chr4:89811672-89811673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553255766	chr4:89811732-89811733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147631746	chr4:89811759-89811760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190026523	chr4:89811847-89811848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555879191	chr4:89811864-89811865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142282778	chr4:89811869-89811870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572635117	chr4:89811897-89811898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145908506	chr4:89811929-89811930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542227504	chr4:89811936-89811937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181191368	chr4:89811937-89811938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574443754	chr4:89811953-89811954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542518744	chr4:89811982-89811983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563796339	chr4:89812091-89812092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530952258	chr4:89812092-89812093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552631752	chr4:89812110-89812111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142472113	chr4:89812207-89812208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138872055	chr4:89812219-89812220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528640171	chr4:89812234-89812235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1458551	chr4:89812242-89812243	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs186501068	chr4:89812246-89812247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140984731	chr4:89812284-89812285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2704572	chr4:89812294-89812295	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs528687096	chr4:89812301-89812302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569083284	chr4:89812343-89812344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539329785	chr4:89812349-89812350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574445063	chr4:89812350-89812351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557369194	chr4:89812352-89812353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111633446	chr4:89812417-89812418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2704570	chr4:89812418-89812419	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562391283	chr4:89812442-89812443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376538885	chr4:89812502-89812503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533644436	chr4:89812507-89812508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112873916	chr4:89812515-89812516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369479352	chr4:89812518-89812519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555127541	chr4:89812567-89812568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574993230	chr4:89812584-89812585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Breast cancer	22522925	CNVD
Obesity	20622171	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89802200-89820600	Weak transcription	Aorta	Aorta
2	chr4:89802600-89812800	Weak transcription	K562	blood
3	chr4:89802600-89825600	Weak transcription	Ovary	ovary
4	chr4:89805400-89817600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:89809200-89828800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:89809400-89813400	Enhancers	Fetal Intestine Small	intestine
7	chr4:89810000-89811400	Enhancers	Placenta	Placenta
8	chr4:89810200-89811400	Enhancers	Psoas Muscle	Psoas
9	chr4:89810200-89811400	Enhancers	HepG2	liver
10	chr4:89810400-89811600	Enhancers	Fetal Intestine Large	intestine
11	chr4:89810800-89811400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:89810800-89811600	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr4:89811000-89811400	Enhancers	Gastric	stomach
14	chr4:89811000-89813200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr4:89811400-89814400	Weak transcription	Placenta	Placenta
16	chr4:89811400-89814400	Weak transcription	Psoas Muscle	Psoas
17	chr4:89811600-89813000	Weak transcription	Fetal Intestine Large	intestine
18	chr4:89812400-89812800	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr4:89812400-89813200	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr4:89813000-89813200	Enhancers	Fetal Intestine Large	intestine
21	chr4:89813400-89821400	Weak transcription	Fetal Intestine Small	intestine
22	chr4:89814400-89814600	Enhancers	Psoas Muscle	Psoas
23	chr4:89814400-89815200	Enhancers	Placenta	Placenta
24	chr4:89815000-89815400	Enhancers	NHEK	skin
25	chr4:89815000-89816000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:89815200-89815600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:89815200-89815600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:89815200-89815800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:89815200-89815800	Weak transcription	Placenta	Placenta
30	chr4:89815600-89818200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:89815800-89816000	Enhancers	Placenta	Placenta
32	chr4:89816000-89825600	Weak transcription	Placenta	Placenta
33	chr4:89816000-89829000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:89816600-89827400	Weak transcription	Fetal Kidney	kidney
35	chr4:89816800-89818400	Weak transcription	Fetal Lung	lung
36	chr4:89816800-89827800	Weak transcription	Fetal Brain Male	brain
37	chr4:89817600-89819200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr4:89818000-89829000	Weak transcription	Pancreas	Pancrea
39	chr4:89818200-89818600	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr4:89818200-89818800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:89818200-89818800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr4:89818200-89819000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:89818400-89818800	Strong transcription	Fetal Lung	lung
44	chr4:89818400-89818800	Enhancers	NHDF-Ad	bronchial
45	chr4:89818800-89820800	Weak transcription	Fetal Lung	lung
46	chr4:89818800-89821400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:89818800-89828800	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr4:89819200-89820200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr4:89820000-89825400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr4:89820000-89859200	Weak transcription	Rectal Smooth Muscle	rectum

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