Variant report

Variant	nsv998919
Chromosome Location	chr4:47207023-47476876
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1490)
CpG islands
(count:1467)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1490 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:47465478-47465975	HepG2	liver:	n/a	n/a
2	ATF2	chr4:47465413-47465867	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:47466935-47467507	GM12878	blood:	n/a	n/a
4	ATF2	chr4:47465150-47466061	GM12878	blood:	n/a	n/a
5	ATF2	chr4:47465468-47465825	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr4:47465456-47465941	HepG2	liver:	n/a	chr4:47465570-47465579
7	ATF3	chr4:47465578-47465836	GM12878	blood:	n/a	n/a
8	ATF3	chr4:47465525-47465870	HepG2	liver:	n/a	chr4:47465570-47465579
9	ATF3	chr4:47465427-47465908	H1-hESC	embryonic stem cell:	n/a	chr4:47465570-47465579
10	ATF3	chr4:47465491-47465867	H1-hESC	embryonic stem cell:	n/a	chr4:47465570-47465579
11	ATF3	chr4:47465562-47465919	K562	blood:	n/a	chr4:47465570-47465579
12	ATF3	chr4:47465535-47465868	K562	blood:	n/a	chr4:47465570-47465579
13	ATF3	chr4:47465515-47465976	A549	lung:	n/a	chr4:47465570-47465579
14	ATF3	chr4:47465468-47466025	GM12878	blood:	n/a	chr4:47465570-47465579
15	BACH1	chr4:47346367-47346374	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr4:47417739-47418078	GM12878	blood:	n/a	chr4:47417937-47417947 chr4:47417954-47417962 chr4:47417936-47417947
17	BATF	chr4:47393375-47393564	GM12878	blood:	n/a	chr4:47393463-47393474
18	BATF	chr4:47317409-47317707	GM12878	blood:	n/a	chr4:47317561-47317572
19	BATF	chr4:47317343-47317703	GM12878	blood:	n/a	chr4:47317561-47317572
20	BATF	chr4:47393344-47393640	GM12878	blood:	n/a	chr4:47393463-47393474
21	BCL11A	chr4:47317305-47317629	GM12878	blood:	n/a	n/a
22	BCL3	chr4:47406365-47406634	GM12878	blood:	n/a	n/a
23	BCL3	chr4:47406335-47406574	GM12878	blood:	n/a	n/a
24	BCLAF1	chr4:47465140-47466001	GM12878	blood:	n/a	chr4:47465167-47465176
25	BHLHE40	chr4:47421414-47421605	HepG2	liver:	n/a	n/a
26	BHLHE40	chr4:47465138-47466081	K562	blood:	n/a	n/a
27	BHLHE40	chr4:47465595-47465873	A549	lung:	n/a	n/a
28	BHLHE40	chr4:47385969-47386140	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:47465199-47466004	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:47465050-47466041	GM12878	blood:	n/a	n/a
31	BRCA1	chr4:47465505-47465966	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr4:47465511-47465851	HepG2	liver:	n/a	n/a
33	BRCA1	chr4:47465421-47465876	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr4:47465355-47465555	GM12878	blood:	n/a	n/a
35	BRCA1	chr4:47385899-47386193	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr4:47465316-47465918	K562	blood:	n/a	n/a
37	CCNT2	chr4:47465176-47465855	K562	blood:	n/a	n/a
38	CCNT2	chr4:47328026-47328226	K562	blood:	n/a	n/a
39	CEBPB	chr4:47211848-47212003	HepG2	liver:	n/a	chr4:47211941-47211952
40	CEBPB	chr4:47376976-47377143	H1-hESC	embryonic stem cell:	n/a	chr4:47377090-47377103 chr4:47377090-47377103 chr4:47377090-47377101 chr4:47377090-47377103 chr4:47377092-47377103
41	CEBPB	chr4:47438599-47438730	HepG2	liver:	n/a	chr4:47438628-47438639 chr4:47438628-47438641
42	CEBPB	chr4:47376472-47377220	Hela-S3	cervix:	n/a	chr4:47377090-47377103 chr4:47377090-47377103 chr4:47377090-47377101 chr4:47377090-47377103 chr4:47377092-47377103
43	CEBPB	chr4:47384521-47384887	IMR90	lung:	n/a	chr4:47384704-47384715 chr4:47384703-47384714 chr4:47384522-47384533
44	CEBPB	chr4:47384539-47384856	Hela-S3	cervix:	n/a	chr4:47384704-47384715 chr4:47384703-47384714
45	CEBPB	chr4:47260706-47260995	K562	blood:	n/a	chr4:47260839-47260850
46	CEBPB	chr4:47215921-47216519	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:47373928-47374034	A549	lung:	n/a	n/a
48	CEBPB	chr4:47260662-47260999	IMR90	lung:	n/a	chr4:47260839-47260850
49	CEBPB	chr4:47428558-47428779	Hela-S3	cervix:	n/a	chr4:47428673-47428684 chr4:47428672-47428683 chr4:47428672-47428685
50	CEBPB	chr4:47376960-47377201	A549	lung:	n/a	chr4:47377090-47377103 chr4:47377090-47377103 chr4:47377090-47377101 chr4:47377090-47377103 chr4:47377092-47377103

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:47465011-47465061	HNPCEpiC	eye:	n/a
2	chr4:47465763-47465813	BJ	skin:	n/a
3	chr4:47465676-47465726	GM12878	blood:	n/a
4	chr4:47465011-47465061	HNPCEpiC	eye:	n/a
5	chr4:47465763-47465813	BJ	skin:	n/a
6	chr4:47465676-47465726	GM12878	blood:	n/a
7	chr4:47465011-47465061	HUVEC	blood vessel:	n/a
8	chr4:47465727-47465777	K562	blood:	n/a
9	chr4:47423779-47423829	LNCaP	prostate:	n/a
10	chr4:47465727-47465777	ECC-1	luminal epithelium:	n/a
11	chr4:47427774-47427824	HRE	kidney:	n/a
12	chr4:47428108-47428158	MCF-7	breast:	n/a
13	chr4:47380248-47380298	NB4	blood:	n/a
14	chr4:47423779-47423829	NT2-D1	testis:	n/a
15	chr4:47465676-47465726	HUVEC	blood vessel:	n/a
16	chr4:47427774-47427824	CMK	blood:	n/a
17	chr4:47427752-47427802	HCF	heart:	n/a
18	chr4:47465732-47465782	SKMC	muscle:	n/a
19	chr4:47465732-47465782	GM12891	blood:	n/a
20	chr4:47465763-47465813	NHBE	bronchial:	n/a
21	chr4:47465606-47465656	AG04450	lung:	fetal
22	chr4:47463168-47463218	SK-N-MC	brain:	n/a
23	chr4:47465606-47465656	HIPEpiC	eye:	n/a
24	chr4:47427904-47427954	Hepatocyte	liver:	n/a
25	chr4:47428108-47428158	HUVEC	blood vessel:	n/a
26	chr4:47465011-47465061	HCPEpiC	choroid plexus:	n/a
27	chr4:47380165-47380215	SK-N-SH	brain:	n/a
28	chr4:47428108-47428158	Hepatocyte	liver:	n/a
29	chr4:47427537-47427587	IMR90	lung:	fetal
30	chr4:47380248-47380298	HRCEpiC	kidney:	n/a
31	chr4:47380248-47380298	HCM	heart:	n/a
32	chr4:47465676-47465726	HEK293	kidney:	embryo
33	chr4:47465732-47465782	ECC-1	luminal epithelium:	n/a
34	chr4:47463168-47463218	HEK293	kidney:	embryo
35	chr4:47465455-47465505	LNCaP	prostate:	n/a
36	chr4:47465818-47465868	PrEC	prostate:	n/a
37	chr4:47463168-47463218	HUVEC	blood vessel:	n/a
38	chr4:47463168-47463218	PrEC	prostate:	n/a
39	chr4:47380165-47380215	Hepatocyte	liver:	n/a
40	chr4:47465676-47465726	HMEC	breast:	n/a
41	chr4:47465763-47465813	IMR90	lung:	fetal
42	chr4:47430173-47430223	GM06990	blood:	n/a
43	chr4:47380165-47380215	HRCEpiC	kidney:	n/a
44	chr4:47427774-47427824	SKMC	muscle:	n/a
45	chr4:47465818-47465868	CMK	blood:	n/a
46	chr4:47465732-47465782	HIPEpiC	eye:	n/a
47	chr4:47465727-47465777	HRE	kidney:	n/a
48	chr4:47423779-47423829	HCM	heart:	n/a
49	chr4:47380248-47380298	HCF	heart:	n/a
50	chr4:47465455-47465505	Caco-2	colon:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:47385250..47388057-chr4:47402693..47405064,2	K562	blood:
2	chr4:44762003..44763242-chr4:47385909..47386537,3	K562	blood:
3	chr4:47455346..47457832-chr4:47566680..47568849,2	K562	blood:
4	chr4:47465829..47468286-chr4:47470252..47472768,2	K562	blood:
5	chr4:47425451..47428331-chr4:47428663..47430199,2	MCF-7	breast:
6	chr4:47468877..47471001-chr4:47471871..47473913,2	K562	blood:
7	chr4:47459303..47460947-chr4:47464140..47467077,2	K562	blood:
8	chr4:47460523..47463508-chr4:47463640..47467389,5	MCF-7	breast:
9	chr4:47460857..47463494-chr4:47464329..47466944,2	MCF-7	breast:
10	chr4:46845685..46846601-chr4:47385587..47386221,2	MCF-7	breast:
11	chr4:47397863..47399973-chr4:47459020..47461928,2	K562	blood:
12	chr4:47464157..47465926-chr4:47473253..47475014,2	MCF-7	breast:
13	chr4:47437562..47440498-chr4:47441242..47443779,2	K562	blood:
14	chr4:46939431..46940150-chr4:47385690..47386236,2	MCF-7	breast:
15	chr4:47389212..47391216-chr4:47392667..47395533,2	K562	blood:
16	chr4:47437562..47440498-chr4:47441242..47443779,2	K562	blood:
17	chr4:46846275..46847133-chr4:47386047..47386599,2	K562	blood:
18	chr4:47386562..47388237-chr4:47450427..47451934,2	K562	blood:
19	chr4:47389212..47391216-chr4:47392667..47395533,2	K562	blood:
20	chr4:47468877..47471001-chr4:47471871..47473913,2	K562	blood:
21	chr4:47386562..47388237-chr4:47450427..47451934,2	K562	blood:
22	chr4:47447254..47449925-chr4:47463916..47465485,2	MCF-7	breast:
23	chr4:47467618..47470444-chr4:47476083..47477741,2	MCF-7	breast:
24	chr4:47447254..47449925-chr4:47463916..47465485,2	MCF-7	breast:
25	chr4:47411634..47414417-chr4:47418360..47422576,3	K562	blood:
26	chr4:47425451..47428331-chr4:47428663..47430199,2	MCF-7	breast:
27	chr4:47472104..47474705-chr4:47476405..47478497,2	K562	blood:
28	chr4:47425951..47428140-chr4:47431003..47433353,2	K562	blood:
29	chr4:47447345..47449625-chr4:47449993..47452895,2	K562	blood:
30	chr4:47425951..47428140-chr4:47431003..47433353,2	K562	blood:
31	chr4:47472104..47474705-chr4:47476405..47478497,2	K562	blood:
32	chr4:47447345..47449625-chr4:47449993..47452895,2	K562	blood:
33	chr4:47378164..47380614-chr4:47492887..47494813,2	K562	blood:
34	chr4:47464764..47466968-chr8:67973543..67975836,2	MCF-7	breast:
35	chr4:47427677..47430366-chr4:47433913..47436003,2	K562	blood:
36	chr4:47411634..47414417-chr4:47418360..47422576,3	K562	blood:
37	chr4:47465829..47468286-chr4:47470252..47472768,2	K562	blood:
38	chr4:47467618..47470444-chr4:47476083..47477741,2	MCF-7	breast:
39	chr4:47412888..47414417-chr4:47420196..47422576,2	K562	blood:
40	chr4:47385250..47388057-chr4:47402693..47405064,2	K562	blood:
41	chr4:47397863..47399973-chr4:47459020..47461928,2	K562	blood:
42	chr4:47412888..47414417-chr4:47420196..47422576,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GABRB1-1	chr4:47433977-47440976	ENSG00000260918.1
2	lnc-GABRB1-1	chr4:47438484-47440426	NONHSAT096250

No data

Variant related genes	Relation type
ENSG00000238301	TF binding region
COMMD8	TF binding region
ENSG00000260918	TF binding region
ENSG00000238301	CpG island
COMMD8	CpG island
ENSG00000260918	CpG island
ENSG00000242431	chromatin interactions
ENSG00000169019	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000260918	chromatin interactions
ENSG00000121022	chromatin interactions

Extended variants
information (count: 6723 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:6723 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531607131	chr4:47207036-47207037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7660544	chr4:47207052-47207053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561825209	chr4:47207084-47207085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529142751	chr4:47207096-47207097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548699247	chr4:47207118-47207119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115576337	chr4:47207177-47207178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7660765	chr4:47207185-47207186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527666012	chr4:47207203-47207204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139619209	chr4:47207230-47207231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570760156	chr4:47207255-47207256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7684997	chr4:47207265-47207266	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs556477134	chr4:47207275-47207276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565154024	chr4:47207278-47207279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190681703	chr4:47207297-47207298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535678620	chr4:47207387-47207388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73247668	chr4:47207391-47207392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368505507	chr4:47207418-47207419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572077027	chr4:47207480-47207481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557429176	chr4:47207496-47207497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2351297	chr4:47207541-47207542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557691182	chr4:47207594-47207595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576117684	chr4:47207597-47207598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9762551	chr4:47207616-47207617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs562010793	chr4:47207617-47207618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184118448	chr4:47207622-47207623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541184945	chr4:47207643-47207644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576292029	chr4:47207644-47207645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527737578	chr4:47207669-47207670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78686495	chr4:47207675-47207676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187140978	chr4:47207686-47207687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570106600	chr4:47207732-47207733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531640525	chr4:47207747-47207748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550037110	chr4:47207755-47207756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568446573	chr4:47207756-47207757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1372496	chr4:47207808-47207809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543402746	chr4:47207860-47207861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369677316	chr4:47207896-47207897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1372495	chr4:47207941-47207942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557608948	chr4:47208000-47208001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547856806	chr4:47208007-47208008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74894218	chr4:47208033-47208034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537071813	chr4:47208043-47208044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192000582	chr4:47208048-47208049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573954681	chr4:47208062-47208063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548727702	chr4:47208073-47208074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142712255	chr4:47208074-47208075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144249589	chr4:47208083-47208084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559457097	chr4:47208139-47208140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566261990	chr4:47208191-47208192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577800820	chr4:47208200-47208201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:1348 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47205200-47211600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:47208000-47208200	Enhancers	Fetal Heart	heart
3	chr4:47208200-47209000	Weak transcription	Fetal Heart	heart
4	chr4:47208200-47209200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr4:47209000-47209200	Enhancers	Fetal Heart	heart
6	chr4:47209200-47209400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:47209200-47209600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:47209200-47209600	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr4:47209200-47210000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:47209200-47210200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:47209200-47210200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:47209200-47210200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:47209200-47210200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:47209200-47210400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:47209200-47215600	Weak transcription	Fetal Heart	heart
16	chr4:47209400-47210200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr4:47209600-47210000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr4:47210800-47211000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr4:47211000-47211600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:47211200-47211600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:47211200-47213200	Enhancers	NH-A	brain
22	chr4:47211400-47213400	Enhancers	Osteobl	bone
23	chr4:47211400-47213800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr4:47211600-47211800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:47211600-47211800	Enhancers	NHLF	lung
26	chr4:47211600-47212000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr4:47211600-47212000	Enhancers	HSMMtube	muscle
28	chr4:47211600-47212600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:47211600-47212600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:47211600-47213200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:47211600-47213200	Enhancers	HMEC	breast
32	chr4:47211600-47213200	Enhancers	HSMM	muscle
33	chr4:47211600-47217400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:47211800-47212000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:47211800-47212800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:47211800-47213200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:47211800-47216200	Weak transcription	NHLF	lung
38	chr4:47212000-47213000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:47212000-47213400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr4:47212000-47216200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr4:47212000-47216200	Weak transcription	HSMMtube	muscle
42	chr4:47212600-47215400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr4:47212600-47215800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr4:47212800-47213200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:47212800-47213600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:47213000-47214800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:47213200-47214200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr4:47213200-47214200	Weak transcription	NH-A	brain
49	chr4:47213200-47215200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:47213200-47216200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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