Variant report

Variant	nsv879494
Chromosome Location	chr4:76264496-76337998
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	ATF1	chr4:76294711-76294852	K562	blood:	n/a	n/a
2	BACH1	chr4:76282966-76282978	K562	blood:	n/a	n/a
3	CEBPB	chr4:76321079-76321193	A549	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
4	CEBPB	chr4:76319825-76319934	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:76321013-76321304	HepG2	liver:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
6	CEBPB	chr4:76321118-76321291	K562	blood:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
7	CEBPB	chr4:76264522-76264645	HepG2	liver:	n/a	chr4:76264549-76264560
8	CEBPB	chr4:76321097-76321297	IMR90	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
9	CEBPB	chr4:76319796-76319943	K562	blood:	n/a	n/a
10	CTCF	chr4:76272640-76272790	AG09319	gingival:	n/a	n/a
11	CTCF	chr4:76326520-76326550	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr4:76321800-76321950	GM12866	blood:	n/a	n/a
13	CTCF	chr4:76296510-76296576	Lung_OC	lung:	n/a	n/a
14	CTCF	chr4:76300053-76300083	Lung_OC	lung:	n/a	n/a
15	EBF1	chr4:76265966-76266131	GM12878	blood:	n/a	chr4:76266016-76266027
16	EP300	chr4:76318525-76318629	K562	blood:	n/a	chr4:76318611-76318625
17	FOS	chr4:76270135-76270449	MCF10A-Er-Src	breast:	n/a	chr4:76270296-76270308 chr4:76270316-76270323 chr4:76270314-76270323
18	FOS	chr4:76270186-76270508	MCF10A-Er-Src	breast:	n/a	chr4:76270296-76270308 chr4:76270316-76270323 chr4:76270314-76270323
19	FOS	chr4:76270142-76270501	MCF10A-Er-Src	breast:	n/a	chr4:76270296-76270308 chr4:76270316-76270323 chr4:76270314-76270323
20	FOS	chr4:76270046-76270437	MCF10A-Er-Src	breast:	n/a	chr4:76270296-76270308 chr4:76270316-76270323 chr4:76270314-76270323
21	FOSL2	chr4:76270159-76270535	SK-N-SH	brain:	n/a	chr4:76270296-76270308 chr4:76270316-76270323 chr4:76270314-76270323
22	FOXA1	chr4:76303772-76303984	HepG2	liver:	n/a	n/a
23	FOXA1	chr4:76295879-76296077	T-47D	breast:	n/a	chr4:76296008-76296023
24	FOXA2	chr4:76326697-76326999	A549	lung:	n/a	n/a
25	FOXA2	chr4:76326505-76327199	A549	lung:	n/a	n/a
26	FOXA2	chr4:76316724-76316928	HepG2	liver:	n/a	n/a
27	GATA3	chr4:76270117-76270636	SK-N-SH	brain:	n/a	chr4:76270349-76270356 chr4:76270532-76270542 chr4:76270348-76270358 chr4:76270349-76270356 chr4:76270349-76270356 chr4:76270346-76270356
28	GATA3	chr4:76270136-76270606	SK-N-SH	brain:	n/a	chr4:76270349-76270356 chr4:76270532-76270542 chr4:76270348-76270358 chr4:76270349-76270356 chr4:76270349-76270356 chr4:76270346-76270356
29	HEY1	chr4:76326401-76326590	K562	blood:	n/a	n/a
30	JUND	chr4:76270161-76270464	SK-N-SH	brain:	n/a	chr4:76270296-76270308 chr4:76270316-76270323 chr4:76270314-76270323
31	JUND	chr4:76286023-76286192	HepG2	liver:	n/a	chr4:76286129-76286138
32	KAP1	chr4:76268012-76268868	U2OS	brain:	n/a	n/a
33	MAFF	chr4:76288213-76288353	HepG2	liver:	n/a	n/a
34	MAFK	chr4:76281358-76281555	HepG2	liver:	n/a	n/a
35	MAFK	chr4:76285713-76285839	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAFK	chr4:76288256-76288325	IMR90	lung:	n/a	n/a
37	MAFK	chr4:76288131-76288433	HepG2	liver:	n/a	n/a
38	MAFK	chr4:76298451-76298466	HepG2	liver:	n/a	n/a
39	MAFK	chr4:76270222-76270924	IMR90	lung:	n/a	n/a
40	MAFK	chr4:76324076-76324320	HepG2	liver:	n/a	n/a
41	MXI1	chr4:76264816-76264818	GM12878	blood:	n/a	n/a
42	MYC	chr4:76270152-76270352	MCF10A-Er-Src	breast:	n/a	n/a
43	MYC	chr4:76316716-76316882	HepG2	liver:	n/a	n/a
44	MYC	chr4:76326119-76326187	K562	blood:	n/a	n/a
45	MYC	chr4:76270116-76270449	MCF10A-Er-Src	breast:	n/a	n/a
46	MYC	chr4:76316887-76316891	HepG2	liver:	n/a	n/a
47	NFYB	chr4:76268554-76268661	Hela-S3	cervix:	n/a	n/a
48	NRF1	chr4:76284762-76284865	H1-hESC	embryonic stem cell:	n/a	n/a
49	PBX3	chr4:76270203-76270533	SK-N-SH	brain:	n/a	n/a
50	POLR2A	chr4:76325987-76326068	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76317967-76318017	RPTEC	kidney:	n/a
2	chr4:76264560-76264610	HRPEpiC	eye:	n/a
3	chr4:76317967-76318017	HMEC	breast:	n/a
4	chr4:76264560-76264610	HNPCEpiC	eye:	n/a
5	chr4:76264560-76264610	HRCEpiC	kidney:	n/a
6	chr4:76264560-76264610	AG10803	skin:	n/a
7	chr4:76264560-76264610	K562	blood:	n/a
8	chr4:76264560-76264610	Caco-2	colon:	n/a
9	chr4:76317967-76318017	HCM	heart:	n/a
10	chr4:76317967-76318017	HCT-116	colon:	n/a
11	chr4:76317967-76318017	K562	blood:	n/a
12	chr4:76317967-76318017	Caco-2	colon:	n/a
13	chr4:76264560-76264610	SK-N-SH	brain:	n/a
14	chr4:76264560-76264610	HCM	heart:	n/a
15	chr4:76317967-76318017	HEK293	kidney:	embryo
16	chr4:76264560-76264610	MCF10A-Er-Src	breast:	n/a
17	chr4:76264560-76264610	PrEC	prostate:	n/a
18	chr4:76264560-76264610	H1-hESC	embryonic stem cell:	embryo
19	chr4:76317967-76318017	LNCaP	prostate:	n/a
20	chr4:76317967-76318017	SK-N-SH_RA	brain:	n/a
21	chr4:76317967-76318017	HAEpiC	amniotic membrane:	n/a
22	chr4:76264560-76264610	NHDF-neo	bronchial:	n/a
23	chr4:76264560-76264610	AG09319	gingival:	n/a
24	chr4:76264560-76264610	GM12891	blood:	n/a
25	chr4:76317967-76318017	ovcar-3	ovarian:	n/a
26	chr4:76317967-76318017	HRE	kidney:	n/a
27	chr4:76264560-76264610	NH-A	brain:	n/a
28	chr4:76317967-76318017	SKMC	muscle:	n/a
29	chr4:76264560-76264610	RPTEC	kidney:	n/a
30	chr4:76317967-76318017	AG04449	skin:	fetal
31	chr4:76264560-76264610	HEK293	kidney:	embryo
32	chr4:76264560-76264610	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:76317967-76318017	AG09309	skin:	n/a
34	chr4:76317967-76318017	HL-60	blood:	n/a
35	chr4:76317967-76318017	GM12878	blood:	n/a
36	chr4:76264560-76264610	HAEpiC	amniotic membrane:	n/a
37	chr4:76264560-76264610	GM12878	blood:	n/a
38	chr4:76264560-76264610	SKMC	muscle:	n/a
39	chr4:76264560-76264610	HIPEpiC	eye:	n/a
40	chr4:76264560-76264610	HCPEpiC	choroid plexus:	n/a
41	chr4:76317967-76318017	SAEC	small airway:	n/a
42	chr4:76264560-76264610	HCF	heart:	n/a
43	chr4:76317967-76318017	T-47D	breast:	n/a
44	chr4:76317967-76318017	Hela-S3	cervix:	n/a
45	chr4:76317967-76318017	MCF10A-Er-Src	breast:	n/a
46	chr4:76264560-76264610	ProgFib	skin:	n/a
47	chr4:76264560-76264610	AG09309	skin:	n/a
48	chr4:76317967-76318017	HRCEpiC	kidney:	n/a
49	chr4:76264560-76264610	LNCaP	prostate:	n/a
50	chr4:76317967-76318017	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:76278035..76280636-chr4:76286764..76289463,2	K562	blood:
2	chr4:76277770..76280636-chr4:76287963..76290651,3	K562	blood:
3	chr4:75948889..75950476-chr4:76335747..76337951,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THAP6-2	chr4:76280528-76280597	ENSG00000251383
2	lnc-THAP6-2	chr4:76286934-76287776	ENSG00000251383
3	lnc-RCHY1-6	chr4:76322898-76323124	l_2668_chr4:76322897-76324689_adipose
4	lnc-RCHY1-6	chr4:76324645-76324689	l_2668_chr4:76322897-76324689_adipose
5	lnc-THAP6-2	chr4:76279286-76279325	ENSG00000251383
6	lnc-THAP6-2	chr4:76283191-76283380	ENSG00000251383
7	lnc-THAP6-1	chr4:76326405-76326502	XLOC_003577
8	lnc-THAP6-2	chr4:76280528-76280597	XLOC_003576
9	lnc-THAP6-2	chr4:76286934-76287774	XLOC_003576
10	lnc-THAP6-2	chr4:76280531-76280597	XLOC_003576
11	lnc-RCHY1-2	chr4:76272507-76272663	XLOC_003987
12	lnc-RCHY1-3	chr4:76286352-76286392	XLOC_003986
13	lnc-RCHY1-1	chr4:76286417-76286557	XLOC_003988
14	lnc-RCHY1-2	chr4:76284180-76284234	XLOC_003987
15	lnc-THAP6-2	chr4:76283191-76283380	XLOC_003576
16	lnc-THAP6-2	chr4:76283191-76283545	XLOC_003576
17	lnc-THAP6-1	chr4:76333105-76333222	XLOC_003577
18	lnc-THAP6-2	chr4:76279286-76279325	XLOC_003576
19	lnc-THAP6-1	chr4:76326428-76326502	XLOC_003577
20	lnc-RCHY1-2	chr4:76266672-76266847	XLOC_003987
21	lnc-RCHY1-2	chr4:76266489-76266522	XLOC_003987

Variant related genes	Relation type
ENSG00000250735	TF binding region
ENSG00000251454	TF binding region
ENSG00000251383	TF binding region
ENSG00000251185	TF binding region
ENSG00000250735	CpG island
ENSG00000251454	CpG island
ENSG00000251383	CpG island
ENSG00000251185	CpG island
ENSG00000251383	chromatin interactions
SMAP2	miRNA target sites
ESRRA	miRNA target sites
ESYT1	miRNA target sites
IL6R	miRNA target sites
ANXA5	miRNA target sites
SIX4	miRNA target sites

Extended variants
information (count: 1664 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1664 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1493716	chr4:76264496-76264497	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552390846	chr4:76264509-76264510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570692554	chr4:76264516-76264517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544726107	chr4:76264524-76264525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537918752	chr4:76264534-76264535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373258435	chr4:76264552-76264553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570799354	chr4:76264561-76264562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139115075	chr4:76264562-76264563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199514806	chr4:76264633-76264634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561203998	chr4:76264667-76264668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149906599	chr4:76264695-76264696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535438594	chr4:76264717-76264718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554916612	chr4:76264736-76264737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573200264	chr4:76264747-76264748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143911311	chr4:76264772-76264773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140941269	chr4:76264831-76264832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs118110364	chr4:76264834-76264835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144786846	chr4:76264896-76264897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186587656	chr4:76264912-76264913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530003598	chr4:76264938-76264939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs36026923	chr4:76264948-76264949	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1873969	chr4:76264984-76264985	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs553851704	chr4:76265010-76265011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189284820	chr4:76265041-76265042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552527010	chr4:76265050-76265051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114840745	chr4:76265058-76265059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181628185	chr4:76265106-76265107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549567730	chr4:76265107-76265108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568149134	chr4:76265122-76265123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs879054	chr4:76265123-76265124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553345785	chr4:76265158-76265159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571745346	chr4:76265182-76265183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528399084	chr4:76265185-76265186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534202484	chr4:76265222-76265223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558847740	chr4:76265225-76265226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs57994898	chr4:76265234-76265235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544800862	chr4:76265279-76265280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185965716	chr4:76265296-76265297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9992408	chr4:76265330-76265331	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541991657	chr4:76265347-76265348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56195780	chr4:76265351-76265352	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs191514616	chr4:76265392-76265393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552465596	chr4:76265431-76265432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530605633	chr4:76265439-76265440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113444173	chr4:76265440-76265441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564379855	chr4:76265464-76265465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368235872	chr4:76265477-76265478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183125618	chr4:76265480-76265481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531356919	chr4:76265497-76265498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147965008	chr4:76265604-76265605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
Autism	18414403	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76263200-76265000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr4:76263200-76266600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:76263600-76264600	Enhancers	HSMM	muscle
4	chr4:76263600-76264800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:76264200-76264600	Enhancers	NHLF	lung
6	chr4:76264400-76265200	Enhancers	Aorta	Aorta
7	chr4:76264600-76264800	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr4:76264600-76265600	Weak transcription	HSMM	muscle
9	chr4:76264600-76270600	Weak transcription	NHLF	lung
10	chr4:76264800-76265600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:76265000-76265400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr4:76265400-76266200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr4:76265600-76265800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:76265600-76266200	Enhancers	HSMM	muscle
15	chr4:76265800-76266200	Enhancers	NHDF-Ad	bronchial
16	chr4:76265800-76267600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr4:76266200-76267800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr4:76266200-76269200	Weak transcription	NHDF-Ad	bronchial
19	chr4:76266200-76270200	Weak transcription	HSMM	muscle
20	chr4:76266600-76269800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:76267600-76269400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:76267800-76270400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr4:76268000-76269400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr4:76269200-76269400	Enhancers	NHDF-Ad	bronchial
25	chr4:76269200-76271800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr4:76269400-76270000	Weak transcription	NHDF-Ad	bronchial
27	chr4:76269400-76270400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr4:76269400-76270600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:76269800-76271200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:76269800-76271800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:76270000-76271000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr4:76270000-76272000	Enhancers	NHDF-Ad	bronchial
33	chr4:76270200-76271400	Enhancers	HSMM	muscle
34	chr4:76270400-76270800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr4:76270400-76270800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr4:76270600-76271000	Enhancers	Osteobl	bone
37	chr4:76270600-76271200	Enhancers	NH-A	brain
38	chr4:76270600-76271400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:76270600-76272400	Enhancers	NHLF	lung
40	chr4:76270800-76273200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr4:76271400-76272400	Weak transcription	HSMM	muscle
42	chr4:76272000-76272600	Weak transcription	NHDF-Ad	bronchial
43	chr4:76272600-76272800	Enhancers	HSMM	muscle
44	chr4:76272600-76272800	Enhancers	NHDF-Ad	bronchial
45	chr4:76284000-76285000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:76284200-76285000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:76284400-76285000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:76290000-76290400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:76296400-76296600	Enhancers	Gastric	stomach
50	chr4:76296400-76296800	Enhancers	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links