Variant report

Variant	nsv593621
Chromosome Location	chr4:7943106-7969594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:676)
CpG islands
(count:672)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7946339-7946818	HepG2	liver:	n/a	n/a
2	ATF2	chr4:7962571-7962969	GM12878	blood:	n/a	n/a
3	BACH1	chr4:7960955-7960958	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr4:7962575-7962937	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:7962585-7962926	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:7944018-7944172	HepG2	liver:	n/a	n/a
7	BHLHE40	chr4:7962511-7962995	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:7958116-7959089	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr4:7962423-7962872	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:7966951-7967424	K562	blood:	n/a	chr4:7967146-7967157
11	CEBPB	chr4:7966896-7967382	HCT-116	colon:	n/a	chr4:7967146-7967157
12	CEBPB	chr4:7966940-7967288	HepG2	liver:	n/a	chr4:7967146-7967157
13	CEBPB	chr4:7962442-7962876	A549	lung:	n/a	n/a
14	CEBPB	chr4:7957965-7958357	MCF-7	breast:	n/a	chr4:7958039-7958052
15	CEBPB	chr4:7953248-7953429	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:7966670-7967455	ECC-1	luminal epithelium:	n/a	chr4:7967146-7967157
17	CEBPB	chr4:7966922-7967294	K562	blood:	n/a	chr4:7967146-7967157
18	CEBPB	chr4:7943953-7944141	HepG2	liver:	n/a	chr4:7944074-7944085
19	CEBPB	chr4:7962420-7962823	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr4:7962367-7962952	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr4:7957950-7958265	A549	lung:	n/a	chr4:7958039-7958052
22	CEBPB	chr4:7966896-7967332	A549	lung:	n/a	chr4:7967146-7967157
23	CEBPB	chr4:7958961-7959246	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:7966952-7967473	IMR90	lung:	n/a	chr4:7967146-7967157
25	CEBPB	chr4:7966975-7967244	K562	blood:	n/a	chr4:7967146-7967157
26	CEBPB	chr4:7966803-7967401	ECC-1	luminal epithelium:	n/a	chr4:7967146-7967157
27	CEBPB	chr4:7958665-7959332	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:7958975-7959224	A549	lung:	n/a	n/a
29	CEBPB	chr4:7943186-7943397	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:7957926-7958392	IMR90	lung:	n/a	chr4:7958039-7958052
31	CEBPB	chr4:7962421-7962883	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:7966606-7967577	Hela-S3	cervix:	n/a	chr4:7967146-7967157
33	CEBPB	chr4:7958914-7959247	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr4:7958954-7959203	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:7966762-7967537	A549	lung:	n/a	chr4:7967146-7967157
36	CEBPB	chr4:7966992-7967437	MCF-7	breast:	n/a	chr4:7967146-7967157
37	CEBPB	chr4:7958813-7959326	A549	lung:	n/a	n/a
38	CEBPB	chr4:7957863-7958450	Hela-S3	cervix:	n/a	chr4:7958039-7958052
39	CEBPB	chr4:7962418-7962773	A549	lung:	n/a	n/a
40	CEBPB	chr4:7957833-7958435	A549	lung:	n/a	chr4:7958039-7958052
41	CEBPB	chr4:7962347-7962958	A549	lung:	n/a	n/a
42	CEBPB	chr4:7966962-7967345	HepG2	liver:	n/a	chr4:7967146-7967157
43	CEBPB	chr4:7962164-7963067	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:7949761-7949843	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:7943913-7944265	HepG2	liver:	n/a	chr4:7944074-7944085
46	CEBPB	chr4:7958000-7958301	HepG2	liver:	n/a	chr4:7958039-7958052
47	CEBPB	chr4:7943878-7944274	Hela-S3	cervix:	n/a	chr4:7944074-7944085
48	CEBPB	chr4:7967069-7967252	HepG2	liver:	n/a	chr4:7967146-7967157
49	CEBPB	chr4:7966862-7967341	MCF-7	breast:	n/a	chr4:7967146-7967157
50	CEBPB	chr4:7953282-7953494	A549	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7965818-7965868	PANC-1	pancreas:	n/a
2	chr4:7965818-7965868	PANC-1	pancreas:	n/a
3	chr4:7968351-7968401	HRCEpiC	kidney:	n/a
4	chr4:7965818-7965868	AG09309	skin:	n/a
5	chr4:7968678-7968728	RPTEC	kidney:	n/a
6	chr4:7951330-7951380	AG10803	skin:	n/a
7	chr4:7968351-7968401	HRE	kidney:	n/a
8	chr4:7965715-7965765	HCM	heart:	n/a
9	chr4:7951330-7951380	HCT-116	colon:	n/a
10	chr4:7965818-7965868	BE2_C	brain:	n/a
11	chr4:7967393-7967443	H1-hESC	embryonic stem cell:	embryo
12	chr4:7945149-7945199	ECC-1	luminal epithelium:	n/a
13	chr4:7968678-7968728	ECC-1	luminal epithelium:	n/a
14	chr4:7965818-7965868	AG10803	skin:	n/a
15	chr4:7967625-7967675	K562	blood:	n/a
16	chr4:7967625-7967675	Jurkat	blood:	n/a
17	chr4:7967625-7967675	MCF-7	breast:	n/a
18	chr4:7967275-7967325	SK-N-SH_RA	brain:	n/a
19	chr4:7965818-7965868	HRCEpiC	kidney:	n/a
20	chr4:7968120-7968170	U87	brain:	n/a
21	chr4:7965818-7965868	HL-60	blood:	n/a
22	chr4:7967393-7967443	SK-N-SH_RA	brain:	n/a
23	chr4:7961982-7962032	SK-N-SH_RA	brain:	n/a
24	chr4:7965715-7965765	AG09319	gingival:	n/a
25	chr4:7967393-7967443	SK-N-SH	brain:	n/a
26	chr4:7968120-7968170	LNCaP	prostate:	n/a
27	chr4:7965818-7965868	SK-N-SH	brain:	n/a
28	chr4:7968678-7968728	HCPEpiC	choroid plexus:	n/a
29	chr4:7968351-7968401	NHBE	bronchial:	n/a
30	chr4:7965818-7965868	HIPEpiC	eye:	n/a
31	chr4:7967275-7967325	AG09309	skin:	n/a
32	chr4:7965818-7965868	RPTEC	kidney:	n/a
33	chr4:7965715-7965765	MCF-7	breast:	n/a
34	chr4:7967393-7967443	MCF10A-Er-Src	breast:	n/a
35	chr4:7961982-7962032	HAEpiC	amniotic membrane:	n/a
36	chr4:7968120-7968170	HRPEpiC	eye:	n/a
37	chr4:7968120-7968170	GM12892	blood:	n/a
38	chr4:7951330-7951380	HRPEpiC	eye:	n/a
39	chr4:7965715-7965765	NT2-D1	testis:	n/a
40	chr4:7965818-7965868	A549	lung:	n/a
41	chr4:7967625-7967675	NHDF-neo	bronchial:	n/a
42	chr4:7968678-7968728	HepG2	liver:	n/a
43	chr4:7945149-7945199	HIPEpiC	eye:	n/a
44	chr4:7968678-7968728	HUVEC	blood vessel:	n/a
45	chr4:7967625-7967675	PrEC	prostate:	n/a
46	chr4:7968120-7968170	HAEpiC	amniotic membrane:	n/a
47	chr4:7968351-7968401	SK-N-SH_RA	brain:	n/a
48	chr4:7968351-7968401	HUVEC	blood vessel:	n/a
49	chr4:7968678-7968728	SKMC	muscle:	n/a
50	chr4:7945149-7945199	HMEC	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7948820..7951616-chr4:7956556..7958489,2	MCF-7	breast:
2	chr4:7965044..7967214-chr4:7970387..7972613,2	MCF-7	breast:
3	chr4:7946085..7948166-chr4:7952831..7955364,2	MCF-7	breast:
4	chr4:7939921..7943801-chr4:7946020..7949690,5	MCF-7	breast:
5	chr4:7940858..7944255-chr4:7948731..7952415,4	MCF-7	breast:
6	chr4:7939933..7942553-chr4:7951940..7953774,2	MCF-7	breast:
7	chr4:7943913..7945893-chr4:7981237..7983380,2	MCF-7	breast:
8	chr4:7940292..7942827-chr4:7945120..7947736,2	MCF-7	breast:
9	chr4:7953204..7956072-chr4:7960320..7962500,2	MCF-7	breast:
10	chr4:7958027..7960096-chr4:7963574..7966311,3	MCF-7	breast:
11	chr4:7961563..7964655-chr4:7964819..7967108,3	K562	blood:
12	chr4:7961563..7964655-chr4:7964819..7967108,3	K562	blood:
13	chr4:7939022..7943379-chr4:7955959..7960860,7	MCF-7	breast:
14	chr4:7948820..7951616-chr4:7956556..7958489,2	MCF-7	breast:
15	chr4:7958027..7960096-chr4:7963574..7966311,3	MCF-7	breast:
16	chr4:7943385..7945490-chr4:7973996..7976275,2	MCF-7	breast:
17	chr4:7938506..7945813-chr4:7968503..7977501,21	MCF-7	breast:
18	chr4:7946085..7948166-chr4:7952831..7955364,2	MCF-7	breast:
19	chr4:7959441..7961778-chr4:7964289..7966996,2	K562	blood:
20	chr4:7900242..7903106-chr4:7943268..7945113,2	MCF-7	breast:
21	chr20:52208463..52210138-chr4:7967818..7969882,2	MCF-7	breast:
22	chr4:7959441..7961778-chr4:7964289..7966996,2	K562	blood:
23	chr4:7968293..7969808-chr4:7972289..7974865,2	MCF-7	breast:
24	chr4:7724746..7727084-chr4:7966375..7967893,2	K562	blood:
25	chr4:7966853..7969531-chr4:7971692..7973616,2	MCF-7	breast:
26	chr4:7953204..7956072-chr4:7960320..7962500,2	MCF-7	breast:

No data

Variant related genes	Relation type
AFAP1	TF binding region
AFAP1	CpG island
ENSG00000196526	chromatin interactions
ENSG00000228919	chromatin interactions

Extended variants
information (count: 1240 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6447872	chr4:7943106-7943107	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs71601896	chr4:7943171-7943172	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs113164280	chr4:7943178-7943179	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs576300199	chr4:7943200-7943201	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs143723779	chr4:7943202-7943203	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs564739138	chr4:7943205-7943206	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs532170713	chr4:7943227-7943228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147231373	chr4:7943238-7943239	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs140483380	chr4:7943268-7943269	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs142829121	chr4:7943278-7943279	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs12696835	chr4:7943284-7943285	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs569918625	chr4:7943303-7943304	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs537760171	chr4:7943328-7943329	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537549010	chr4:7943331-7943332	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs552549657	chr4:7943349-7943350	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs4696825	chr4:7943397-7943398	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs368463142	chr4:7943398-7943399	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139749515	chr4:7943399-7943400	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs553936324	chr4:7943455-7943456	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs572192387	chr4:7943527-7943528	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs544743896	chr4:7943532-7943533	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs201613070	chr4:7943533-7943534	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs535931994	chr4:7943556-7943557	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs115688901	chr4:7943599-7943600	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149799793	chr4:7943617-7943618	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs543745643	chr4:7943628-7943629	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs28711584	chr4:7943639-7943640	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576658874	chr4:7943659-7943660	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs540807807	chr4:7943706-7943707	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544853630	chr4:7943749-7943750	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs184590197	chr4:7943773-7943774	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs188251783	chr4:7943804-7943805	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs541920140	chr4:7943813-7943814	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs180783076	chr4:7943824-7943825	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs368800595	chr4:7943853-7943854	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs4696827	chr4:7943885-7943886	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552873570	chr4:7943891-7943892	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs12642714	chr4:7943944-7943945	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs145703522	chr4:7943950-7943951	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs568627914	chr4:7943989-7943990	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536347848	chr4:7943997-7943998	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs139562527	chr4:7944070-7944071	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs184130012	chr4:7944099-7944100	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs536624462	chr4:7944106-7944107	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558450539	chr4:7944164-7944165	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576751478	chr4:7944169-7944170	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs540895584	chr4:7944175-7944176	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs34904252	chr4:7944216-7944217	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs552760814	chr4:7944266-7944267	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs144480706	chr4:7944288-7944289	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	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
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7941600-7943200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:7941600-7944000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:7941600-7944400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:7941600-7951200	Weak transcription	Small Intestine	intestine
5	chr4:7941800-7943600	Enhancers	Fetal Heart	heart
6	chr4:7942000-7943200	Enhancers	Esophagus	oesophagus
7	chr4:7942000-7943200	Enhancers	Fetal Muscle Trunk	muscle
8	chr4:7942000-7943200	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr4:7942000-7943200	Enhancers	HSMMtube	muscle
10	chr4:7942000-7943400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:7942000-7943400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:7942000-7943400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:7942000-7943400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:7942000-7943400	Enhancers	HMEC	breast
15	chr4:7942000-7943600	Enhancers	Osteobl	bone
16	chr4:7942000-7943800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr4:7942000-7943800	Enhancers	Adipose Nuclei	Adipose
18	chr4:7942000-7943800	Enhancers	Pancreas	Pancrea
19	chr4:7942000-7943800	Enhancers	Stomach Mucosa	stomach
20	chr4:7942000-7943800	Enhancers	HepG2	liver
21	chr4:7942000-7943800	Enhancers	HSMM	muscle
22	chr4:7942000-7944000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:7942000-7944000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr4:7942000-7944200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:7942000-7944200	Enhancers	Fetal Intestine Large	intestine
26	chr4:7942000-7944200	Enhancers	NHDF-Ad	bronchial
27	chr4:7942000-7944400	Enhancers	Fetal Intestine Small	intestine
28	chr4:7942000-7944600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:7942000-7945200	Enhancers	A549	lung
30	chr4:7942000-7945400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:7942000-7945400	Enhancers	Placenta	Placenta
32	chr4:7942000-7945400	Enhancers	Placenta Amnion	Placenta Amnion
33	chr4:7942000-7946200	Weak transcription	Liver	Liver
34	chr4:7942000-7946400	Weak transcription	Colon Smooth Muscle	Colon
35	chr4:7942000-7946400	Weak transcription	Fetal Stomach	stomach
36	chr4:7942000-7950400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr4:7942000-7951000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr4:7942000-7951400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:7942200-7943200	Enhancers	HUVEC	blood vessel
40	chr4:7942200-7943400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:7942200-7943400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:7942200-7943600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:7942200-7943800	Enhancers	H9 Cell Line	embryonic stem cell
44	chr4:7942200-7944000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr4:7942200-7944000	Enhancers	NHEK	skin
46	chr4:7942200-7944800	Weak transcription	Fetal Muscle Leg	muscle
47	chr4:7942200-7947400	Weak transcription	Fetal Brain Male	brain
48	chr4:7942200-7950600	Weak transcription	Stomach Smooth Muscle	stomach
49	chr4:7942600-7943400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:7942600-7943400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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