Variant report

Variant	nsv517837
Chromosome Location	chr4:106466588-106502513
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:167)
CpG islands
(count:305)
Chromatin interactive
region (count:16)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:167 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:106476382-106476975	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:106476296-106476927	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:106493463-106493783	GM12878	blood:	n/a	n/a
4	BCL11A	chr4:106476464-106476911	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr4:106476446-106477001	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr4:106476237-106477133	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:106471808-106472196	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:106485558-106485827	HepG2	liver:	n/a	chr4:106485716-106485727
9	CEBPB	chr4:106468143-106468612	HepG2	liver:	n/a	chr4:106468164-106468175 chr4:106468166-106468177
10	CEBPB	chr4:106489734-106490038	HepG2	liver:	n/a	n/a
11	CHD2	chr4:106476478-106476985	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr4:106473460-106473610	MCF-7	breast:	n/a	n/a
13	CTCF	chr4:106473360-106473510	RPTEC	kidney:	n/a	n/a
14	CTCF	chr4:106473436-106473477	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:106501496-106501514	GM13976	blood:	n/a	n/a
16	E2F4	chr4:106481823-106482023	MCF10A-Er-Src	breast:	n/a	n/a
17	EBF1	chr4:106469739-106469781	GM12878	blood:	n/a	n/a
18	EP300	chr4:106469609-106470065	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr4:106472872-106473985	T-47D	breast:	n/a	n/a
20	EP300	chr4:106481432-106482062	SK-N-SH_RA	brain:	n/a	chr4:106481714-106481723 chr4:106481470-106481479
21	EP300	chr4:106476402-106477021	H1-hESC	embryonic stem cell:	n/a	n/a
22	EP300	chr4:106489913-106490596	T-47D	breast:	n/a	chr4:106490228-106490238
23	EP300	chr4:106476514-106476887	H1-hESC	embryonic stem cell:	n/a	n/a
24	EP300	chr4:106481529-106481933	SK-N-SH_RA	brain:	n/a	chr4:106481714-106481723
25	EP300	chr4:106468814-106470014	SK-N-SH	brain:	n/a	n/a
26	EP300	chr4:106469606-106470040	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr4:106473058-106473846	T-47D	breast:	n/a	n/a
28	EP300	chr4:106490159-106490486	T-47D	breast:	n/a	chr4:106490228-106490238
29	EP300	chr4:106470043-106470130	GM12878	blood:	n/a	n/a
30	EP300	chr4:106467323-106467844	SK-N-SH_RA	brain:	n/a	chr4:106467590-106467604
31	ESR1	chr4:106476595-106476909	ECC-1	luminal epithelium:	n/a	n/a
32	ESR1	chr4:106490154-106490523	T-47D	breast:	n/a	n/a
33	ESR1	chr4:106476644-106476887	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr4:106473019-106473719	T-47D	breast:	n/a	n/a
35	ESR1	chr4:106473258-106473667	T-47D	breast:	n/a	n/a
36	ESR1	chr4:106473085-106473611	T-47D	breast:	n/a	n/a
37	FOS	chr4:106473202-106473298	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:106473170-106473217	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:106469676-106469933	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:106469662-106469977	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:106481554-106482074	MCF10A-Er-Src	breast:	n/a	chr4:106481716-106481723 chr4:106481714-106481723
42	FOS	chr4:106473080-106473348	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:106481600-106482033	MCF10A-Er-Src	breast:	n/a	chr4:106481716-106481723 chr4:106481714-106481723
44	FOS	chr4:106481587-106482108	MCF10A-Er-Src	breast:	n/a	chr4:106481716-106481723 chr4:106481714-106481723
45	FOS	chr4:106471858-106472099	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr4:106473064-106473339	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr4:106481544-106482077	MCF10A-Er-Src	breast:	n/a	chr4:106481716-106481723 chr4:106481714-106481723
48	FOS	chr4:106471821-106472085	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr4:106469667-106469971	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr4:106469669-106469967	MCF10A-Er-Src	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:106472990-106473040	NT2-D1	testis:	n/a
2	chr4:106473040-106473090	NT2-D1	testis:	n/a
3	chr4:106477599-106477649	LNCaP	prostate:	n/a
4	chr4:106473233-106473283	ovcar-3	ovarian:	n/a
5	chr4:106473040-106473090	PrEC	prostate:	n/a
6	chr4:106473233-106473283	GM12891	blood:	n/a
7	chr4:106477599-106477649	GM12878	blood:	n/a
8	chr4:106473040-106473090	ProgFib	skin:	n/a
9	chr4:106473806-106473856	ovcar-3	ovarian:	n/a
10	chr4:106473040-106473090	IMR90	lung:	fetal
11	chr4:106473233-106473283	HCM	heart:	n/a
12	chr4:106473233-106473283	LNCaP	prostate:	n/a
13	chr4:106473233-106473283	GM12892	blood:	n/a
14	chr4:106473040-106473090	AG09319	gingival:	n/a
15	chr4:106477599-106477649	MCF10A-Er-Src	breast:	n/a
16	chr4:106473040-106473090	HCPEpiC	choroid plexus:	n/a
17	chr4:106473040-106473090	AG10803	skin:	n/a
18	chr4:106473233-106473283	SAEC	small airway:	n/a
19	chr4:106473806-106473856	Hepatocyte	liver:	n/a
20	chr4:106477599-106477649	H1-hESC	embryonic stem cell:	embryo
21	chr4:106473040-106473090	HCM	heart:	n/a
22	chr4:106473806-106473856	HCT-116	colon:	n/a
23	chr4:106473233-106473283	IMR90	lung:	fetal
24	chr4:106473806-106473856	GM19239	blood:	n/a
25	chr4:106477599-106477649	AG10803	skin:	n/a
26	chr4:106473806-106473856	MCF10A-Er-Src	breast:	n/a
27	chr4:106473233-106473283	ProgFib	skin:	n/a
28	chr4:106473040-106473090	NB4	blood:	n/a
29	chr4:106473040-106473090	Hela-S3	cervix:	n/a
30	chr4:106472990-106473040	HRCEpiC	kidney:	n/a
31	chr4:106477599-106477649	AG04450	lung:	fetal
32	chr4:106477599-106477649	AG09309	skin:	n/a
33	chr4:106473040-106473090	HRPEpiC	eye:	n/a
34	chr4:106473233-106473283	U87	brain:	n/a
35	chr4:106473040-106473090	PFSK-1	brain:	n/a
36	chr4:106477599-106477649	NHDF-neo	bronchial:	n/a
37	chr4:106473233-106473283	Hepatocyte	liver:	n/a
38	chr4:106477599-106477649	AG04449	skin:	fetal
39	chr4:106473806-106473856	GM12891	blood:	n/a
40	chr4:106473806-106473856	ECC-1	luminal epithelium:	n/a
41	chr4:106473233-106473283	HEEpiC	esophagus:	n/a
42	chr4:106473040-106473090	SK-N-SH	brain:	n/a
43	chr4:106473233-106473283	HUVEC	blood vessel:	n/a
44	chr4:106473040-106473090	GM06990	blood:	n/a
45	chr4:106473806-106473856	NHDF-neo	bronchial:	n/a
46	chr4:106473806-106473856	HRCEpiC	kidney:	n/a
47	chr4:106472990-106473040	AoSMC	blood vessel:	n/a
48	chr4:106473806-106473856	HEK293	kidney:	embryo
49	chr4:106477599-106477649	Caco-2	colon:	n/a
50	chr4:106477599-106477649	NT2-D1	testis:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:106467032..106469606-chr4:106472121..106474204,2	MCF-7	breast:
2	chr4:106479363..106481837-chr4:106485512..106487322,2	MCF-7	breast:
3	chr4:106473010..106475476-chr4:106482085..106484725,2	MCF-7	breast:
4	chr4:106452636..106454650-chr4:106472579..106474364,2	MCF-7	breast:
5	chr4:106474325..106476444-chr4:106476458..106478164,2	MCF-7	breast:
6	chr4:106464275..106466669-chr4:106473220..106476149,3	K562	blood:
7	chr4:106470555..106472304-chr4:106504730..106507228,2	MCF-7	breast:
8	chr4:106479363..106481837-chr4:106485512..106487322,2	MCF-7	breast:
9	chr4:106474325..106476444-chr4:106476458..106478164,2	MCF-7	breast:
10	chr4:106479272..106480860-chr4:106482086..106483907,2	MCF-7	breast:
11	chr4:106473806..106476270-chr4:106501097..106503243,2	MCF-7	breast:
12	chr4:106493186..106495301-chr4:106506579..106508240,2	K562	blood:
13	chr4:106492214..106494083-chr4:106533878..106536037,2	MCF-7	breast:
14	chr4:106471957..106473637-chr4:106475938..106478326,2	MCF-7	breast:
15	chr4:106483518..106485552-chr4:106531782..106533703,2	MCF-7	breast:
16	chr4:106473010..106475476-chr4:106482085..106484725,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSTCD-1	chr4:106491061-106491395	ENSG00000249885.1
2	lnc-GSTCD-1	chr4:106491061-106491392	NR_046840
3	lnc-PPA2-2	chr4:106473350-106473512	XLOC_004036
4	lnc-GSTCD-1	chr4:106484459-106484522	ENSG00000249885.1
5	lnc-GSTCD-1	chr4:106482748-106482804	NR_046840
6	lnc-GSTCD-1	chr4:106484459-106484522	NR_046840
7	lnc-GSTCD-1	chr4:106482748-106482804	ENSG00000249885.1

No data

Variant related genes	Relation type
ARHGEF38	TF binding region
ENSG00000250522	TF binding region
ARHGEF38-IT1	TF binding region
ARHGEF38	CpG island
ENSG00000250522	CpG island
ARHGEF38-IT1	CpG island
ENSG00000236699	chromatin interactions
ENSG00000250922	chromatin interactions
ENSG00000250522	chromatin interactions
ENSG00000249885	chromatin interactions
SF3A1	miRNA target sites

Extended variants
information (count: 1422 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1422 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs730850	chr4:106466588-106466589	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569592741	chr4:106466630-106466631	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs76716514	chr4:106466646-106466647	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs62317353	chr4:106466677-106466678	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs201728367	chr4:106466711-106466712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs70938195	chr4:106466712-106466713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143824747	chr4:106466721-106466722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs397829743	chr4:106466724-106466725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552393274	chr4:106466745-106466746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114680606	chr4:106466752-106466753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534873724	chr4:106466767-106466768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189718843	chr4:106466826-106466827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578185175	chr4:106466854-106466855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145946810	chr4:106466855-106466856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182068646	chr4:106466894-106466895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187914011	chr4:106466896-106466897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543068272	chr4:106466948-106466949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369128694	chr4:106466960-106466961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139828730	chr4:106466965-106466966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541221157	chr4:106466974-106466975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200087370	chr4:106466975-106466976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192277733	chr4:106466976-106466977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564015526	chr4:106466983-106466984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183537875	chr4:106466993-106466994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188588686	chr4:106467018-106467019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575641198	chr4:106467054-106467055	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs6858204	chr4:106467126-106467127	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs141622038	chr4:106467143-106467144	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565428243	chr4:106467229-106467230	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs1490596	chr4:106467306-106467307	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs192830383	chr4:106467343-106467344	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs531467504	chr4:106467489-106467490	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs537266157	chr4:106467543-106467544	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs376042282	chr4:106467544-106467545	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541183438	chr4:106467559-106467560	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs184251953	chr4:106467599-106467600	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559771407	chr4:106467618-106467619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574283140	chr4:106467638-106467639	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs73837976	chr4:106467645-106467646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553448593	chr4:106467648-106467649	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146225297	chr4:106467656-106467657	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187023304	chr4:106467682-106467683	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs191592558	chr4:106467700-106467701	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577738088	chr4:106467703-106467704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs549634958	chr4:106467709-106467710	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs548598838	chr4:106467730-106467731	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543280232	chr4:106467739-106467740	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563583747	chr4:106467753-106467754	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs17617811	chr4:106467767-106467768	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs139299218	chr4:106467831-106467832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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
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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	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
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106464600-106466600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:106464600-106471200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:106465600-106466600	Enhancers	Fetal Intestine Large	intestine
4	chr4:106465600-106466600	Enhancers	Fetal Kidney	kidney
5	chr4:106465600-106467400	Enhancers	Brain Hippocampus Middle	brain
6	chr4:106465800-106466600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:106465800-106466600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr4:106466000-106467000	Weak transcription	Brain Substantia Nigra	brain
9	chr4:106466000-106469000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:106466000-106471400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr4:106466200-106466600	Enhancers	Duodenum Mucosa	Duodenum
12	chr4:106466200-106467000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:106466400-106467000	Weak transcription	Brain Anterior Caudate	brain
14	chr4:106466400-106470600	Weak transcription	Fetal Intestine Small	intestine
15	chr4:106466600-106467000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr4:106466600-106469600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:106466600-106471400	Weak transcription	Fetal Intestine Large	intestine
18	chr4:106466600-106471600	Weak transcription	Duodenum Mucosa	Duodenum
19	chr4:106466600-106472600	Weak transcription	Fetal Kidney	kidney
20	chr4:106467000-106467400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr4:106467000-106467600	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr4:106467000-106467600	Enhancers	Brain Substantia Nigra	brain
23	chr4:106467000-106468000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:106467000-106468000	Enhancers	Brain Anterior Caudate	brain
25	chr4:106467400-106467600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr4:106467400-106467600	Enhancers	HMEC	breast
27	chr4:106467600-106469200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr4:106467600-106471600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:106467800-106469000	Weak transcription	HMEC	breast
30	chr4:106468000-106472600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr4:106468800-106470000	Enhancers	NHEK	skin
32	chr4:106469000-106470200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:106469000-106470200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:106469000-106470200	Enhancers	HMEC	breast
35	chr4:106469200-106470200	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr4:106469400-106469600	Enhancers	NHDF-Ad	bronchial
37	chr4:106469400-106470000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:106469400-106470000	Enhancers	HSMM	muscle
39	chr4:106469400-106470200	Enhancers	A549	lung
40	chr4:106469600-106469800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:106469600-106470000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:106469600-106470000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:106469800-106470200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:106470000-106471800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:106470000-106471800	Weak transcription	Gastric	stomach
46	chr4:106470000-106471800	Weak transcription	NHEK	skin
47	chr4:106470000-106472600	Weak transcription	HSMM	muscle
48	chr4:106470000-106472800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:106470000-106473000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr4:106470000-106476600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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