Variant report

Variant	esv1845782
Chromosome Location	chr4:78237955-78321598
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	chr4:78268651-78268718	HepG2	liver:	n/a	n/a
2	ATF1	chr4:78267547-78267723	K562	blood:	n/a	n/a
3	BACH1	chr4:78301745-78301818	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:78306645-78306845	K562	blood:	n/a	n/a
5	BHLHE40	chr4:78265976-78266449	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:78306677-78307028	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr4:78263352-78263680	HCT-116	colon:	n/a	n/a
8	CBX3	chr4:78263330-78263629	K562	blood:	n/a	n/a
9	CBX3	chr4:78253824-78254202	K562	blood:	n/a	n/a
10	CBX3	chr4:78253883-78254139	K562	blood:	n/a	n/a
11	CBX3	chr4:78263269-78263765	HCT-116	colon:	n/a	n/a
12	CBX3	chr4:78253746-78254319	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:78296891-78297161	A549	lung:	n/a	chr4:78297047-78297058 chr4:78297049-78297058
14	CEBPB	chr4:78268252-78268595	HepG2	liver:	n/a	chr4:78268368-78268377 chr4:78268366-78268379 chr4:78268368-78268379
15	CEBPB	chr4:78296898-78297215	HepG2	liver:	n/a	chr4:78297047-78297058 chr4:78297049-78297058
16	CEBPB	chr4:78301675-78301828	H1-hESC	embryonic stem cell:	n/a	chr4:78301753-78301766
17	CEBPB	chr4:78296971-78297162	IMR90	lung:	n/a	chr4:78297047-78297058 chr4:78297049-78297058
18	CEBPB	chr4:78268366-78268440	K562	blood:	n/a	chr4:78268368-78268377 chr4:78268366-78268379 chr4:78268368-78268379
19	CEBPB	chr4:78268359-78268485	IMR90	lung:	n/a	chr4:78268368-78268377 chr4:78268366-78268379 chr4:78268368-78268379
20	CHD2	chr4:78254095-78254505	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:78306623-78306852	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr4:78298160-78298310	NHEK	skin:	n/a	n/a
23	CTCF	chr4:78279931-78279957	GM19240	blood:	n/a	n/a
24	CTCF	chr4:78306680-78306830	HRE	kidney:	n/a	chr4:78306711-78306729 chr4:78306713-78306734 chr4:78306714-78306727
25	CTCF	chr4:78279600-78279750	HCPEpiC	choroid plexus:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
26	CTCF	chr4:78279600-78279750	GM12866	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
27	CTCF	chr4:78287920-78288070	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr4:78279860-78280010	HVMF	connective:	n/a	n/a
29	CTCF	chr4:78306521-78306844	SK-N-SH_RA	brain:	n/a	chr4:78306711-78306729 chr4:78306713-78306734 chr4:78306714-78306727
30	CTCF	chr4:78320200-78320350	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr4:78306640-78306790	HPF	lung:	n/a	chr4:78306711-78306729 chr4:78306713-78306734 chr4:78306714-78306727
32	CTCF	chr4:78288000-78288527	K562	blood:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
33	CTCF	chr4:78287940-78288090	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr4:78292760-78292910	HEK293	kidney:	n/a	n/a
35	CTCF	chr4:78287700-78287850	AG10803	skin:	n/a	n/a
36	CTCF	chr4:78288058-78288351	Hela-S3	cervix:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
37	CTCF	chr4:78279360-78279866	HCT-116	colon:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
38	CTCF	chr4:78279620-78279770	GM12868	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
39	CTCF	chr4:78287940-78288090	GM12872	blood:	n/a	n/a
40	CTCF	chr4:78306569-78306854	GM13977	blood:	n/a	chr4:78306711-78306729 chr4:78306713-78306734 chr4:78306714-78306727
41	CTCF	chr4:78279432-78279812	A549	lung:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
42	CTCF	chr4:78274860-78275010	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr4:78279620-78279770	AG09309	skin:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
44	CTCF	chr4:78274580-78274730	HCT-116	colon:	n/a	n/a
45	CTCF	chr4:78306680-78306830	GM12869	blood:	n/a	chr4:78306711-78306729 chr4:78306713-78306734 chr4:78306714-78306727
46	CTCF	chr4:78320267-78320280	GM12878	blood:	n/a	n/a
47	CTCF	chr4:78288340-78288490	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:78238320-78238470	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:78298080-78298230	GM12872	blood:	n/a	n/a
50	CTCF	chr4:78298140-78298290	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78298282-78298332	IMR90	lung:	fetal
2	chr4:78298282-78298332	U87	brain:	n/a
3	chr4:78298282-78298332	HIPEpiC	eye:	n/a
4	chr4:78298282-78298332	HCM	heart:	n/a
5	chr4:78298282-78298332	NHDF-neo	bronchial:	n/a
6	chr4:78298282-78298332	GM19239	blood:	n/a
7	chr4:78298282-78298332	AG09319	gingival:	n/a
8	chr4:78298282-78298332	NB4	blood:	n/a
9	chr4:78298282-78298332	AG10803	skin:	n/a
10	chr4:78298282-78298332	H1-hESC	embryonic stem cell:	embryo
11	chr4:78298282-78298332	HRCEpiC	kidney:	n/a
12	chr4:78298282-78298332	SK-N-SH_RA	brain:	n/a
13	chr4:78298282-78298332	HEK293	kidney:	embryo
14	chr4:78298282-78298332	MCF-7	breast:	n/a
15	chr4:78298282-78298332	HUVEC	blood vessel:	n/a
16	chr4:78298282-78298332	GM12892	blood:	n/a
17	chr4:78298282-78298332	AoSMC	blood vessel:	n/a
18	chr4:78298282-78298332	A549	lung:	n/a
19	chr4:78298282-78298332	HMEC	breast:	n/a
20	chr4:78298282-78298332	GM06990	blood:	n/a
21	chr4:78298282-78298332	GM12891	blood:	n/a
22	chr4:78298282-78298332	HRE	kidney:	n/a
23	chr4:78298282-78298332	AG04450	lung:	fetal
24	chr4:78298282-78298332	CMK	blood:	n/a
25	chr4:78298282-78298332	LNCaP	prostate:	n/a
26	chr4:78298282-78298332	HEEpiC	esophagus:	n/a
27	chr4:78298282-78298332	SK-N-SH	brain:	n/a
28	chr4:78298282-78298332	PrEC	prostate:	n/a
29	chr4:78298282-78298332	T-47D	breast:	n/a
30	chr4:78298282-78298332	ECC-1	luminal epithelium:	n/a
31	chr4:78298282-78298332	BE2_C	brain:	n/a
32	chr4:78298282-78298332	NHBE	bronchial:	n/a
33	chr4:78298282-78298332	HL-60	blood:	n/a
34	chr4:78298282-78298332	HCT-116	colon:	n/a
35	chr4:78298282-78298332	HepG2	liver:	n/a
36	chr4:78298282-78298332	SKMC	muscle:	n/a
37	chr4:78298282-78298332	NT2-D1	testis:	n/a
38	chr4:78298282-78298332	PANC-1	pancreas:	n/a
39	chr4:78298282-78298332	SK-N-MC	brain:	n/a
40	chr4:78298282-78298332	HRPEpiC	eye:	n/a
41	chr4:78298282-78298332	Caco-2	colon:	n/a
42	chr4:78298282-78298332	BJ	skin:	n/a
43	chr4:78298282-78298332	HAEpiC	amniotic membrane:	n/a
44	chr4:78298282-78298332	PFSK-1	brain:	n/a
45	chr4:78298282-78298332	ProgFib	skin:	n/a
46	chr4:78298282-78298332	RPTEC	kidney:	n/a
47	chr4:78298282-78298332	HNPCEpiC	eye:	n/a
48	chr4:78298282-78298332	Hela-S3	cervix:	n/a
49	chr4:78298282-78298332	ovcar-3	ovarian:	n/a
50	chr4:78298282-78298332	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:78306279..78307489-chr4:78353325..78355121,9	MCF-7	breast:
2	chr4:78278110..78280443-chr4:78281438..78283101,2	MCF-7	breast:
3	chr4:78287913..78288436-chr4:78619834..78620825,2	MCF-7	breast:
4	chr4:78230184..78230702-chr4:78278364..78278865,2	MCF-7	breast:
5	chr4:78257188..78259774-chr4:78266144..78268332,2	K562	blood:
6	chr4:78306484..78307565-chr4:78351707..78352604,5	MCF-7	breast:
7	chr4:78306262..78307241-chr4:78353866..78354908,3	MCF-7	breast:
8	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:
9	chr4:78306282..78306818-chr4:78539506..78540132,2	MCF-7	breast:
10	chr4:78307688..78309988-chr4:78313564..78315382,2	K562	blood:
11	chr4:78306259..78307081-chr4:78539517..78540020,2	K562	blood:
12	chr4:78289830..78292754-chr4:78299148..78300754,2	K562	blood:
13	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
14	chr4:78307688..78309988-chr4:78313564..78315382,2	K562	blood:
15	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:
16	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
17	chr4:78289830..78292754-chr4:78299148..78300754,2	K562	blood:
18	chr4:78306597..78307214-chr4:78394387..78394937,2	K562	blood:
19	chr4:78306138..78307360-chr4:78339239..78340037,9	MCF-7	breast:
20	chr4:78306302..78306941-chr4:78521930..78522730,3	MCF-7	breast:
21	chr4:78229797..78230625-chr4:78279333..78280102,3	MCF-7	breast:
22	chr1:118958475..118959178-chr4:78279470..78280113,2	MCF-7	breast:
23	chr4:78270382..78272050-chr4:78274178..78276131,2	K562	blood:
24	chr4:78296565..78297450-chr4:78353933..78354751,2	MCF-7	breast:
25	chr4:78270382..78272050-chr4:78274178..78276131,2	K562	blood:
26	chr4:78257188..78259774-chr4:78266144..78268332,2	K562	blood:
27	chr4:78298658..78300930-chr4:78308885..78310955,2	MCF-7	breast:
28	chr4:78306285..78307276-chr4:78351745..78352760,5	MCF-7	breast:
29	chr4:78298658..78300930-chr4:78308885..78310955,2	MCF-7	breast:
30	chr4:78306456..78307324-chr4:78354247..78354761,2	K562	blood:
31	chr4:78278110..78280443-chr4:78281438..78283101,2	MCF-7	breast:
32	chr4:78269918..78271823-chr4:78272380..78274841,2	MCF-7	breast:
33	chr4:78306158..78306757-chr4:78339536..78340194,2	MCF-7	breast:
34	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
35	chr4:78306562..78308497-chr4:78334856..78338257,3	MCF-7	breast:
36	chr4:78266632..78268344-chr4:78268869..78271315,2	K562	blood:
37	chr4:78266632..78268344-chr4:78268869..78271315,2	K562	blood:
38	chr4:78287667..78288571-chr4:78353781..78354626,3	MCF-7	breast:
39	chr4:78287359..78291622-chr4:78351702..78357008,5	MCF-7	breast:
40	chr4:78292160..78295150-chr4:78297091..78299092,2	MCF-7	breast:
41	chr4:78292160..78295150-chr4:78297091..78299092,2	MCF-7	breast:
42	chr4:78307066..78309627-chr4:78338398..78341247,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6L-1	chr4:78320747-78320948	XLOC_003994
2	lnc-CNOT6L-1	chr4:78315645-78315891	XLOC_003994
3	lnc-CCNG2-1	chr4:78305791-78305921	NONHSAT097050
4	lnc-CCNI-6	chr4:78271523-78272388	NONHSAT097053

Variant related genes	Relation type
ENSG00000248831	TF binding region
ENSG00000250006	TF binding region
ENSG00000248831	CpG island
ENSG00000250006	CpG island
ENSG00000248831	chromatin interactions

Extended variants
information (count: 3667 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3667 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4859487	chr4:78237955-78237956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs4859488	chr4:78237977-78237978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs542995608	chr4:78237979-78237980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78248357	chr4:78238000-78238001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4859489	chr4:78238031-78238032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs563256693	chr4:78238060-78238061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528592095	chr4:78238085-78238086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4859801	chr4:78238100-78238101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs375547451	chr4:78238107-78238108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571977660	chr4:78238124-78238125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111814614	chr4:78238138-78238139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550914311	chr4:78238157-78238158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114402204	chr4:78238285-78238286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12651366	chr4:78238290-78238291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs555320095	chr4:78238402-78238403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10003077	chr4:78238410-78238411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs534327099	chr4:78238425-78238426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9991635	chr4:78238517-78238518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566213364	chr4:78238522-78238523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567152178	chr4:78238588-78238589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10003257	chr4:78238620-78238621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs556912883	chr4:78238621-78238622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574060525	chr4:78238635-78238636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542803984	chr4:78238658-78238659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559686236	chr4:78238663-78238664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117234480	chr4:78238668-78238669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140336674	chr4:78238699-78238700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188056099	chr4:78238704-78238705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113217190	chr4:78238723-78238724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs17401714	chr4:78238724-78238725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191593702	chr4:78238752-78238753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184117545	chr4:78238776-78238777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572633544	chr4:78238778-78238779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143312512	chr4:78238790-78238791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187263126	chr4:78238798-78238799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528973927	chr4:78238805-78238806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9884375	chr4:78238884-78238885	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs565442668	chr4:78238897-78238898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558348610	chr4:78238916-78238917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147536866	chr4:78238934-78238935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140040913	chr4:78238954-78238955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150039859	chr4:78238997-78238998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145232613	chr4:78239032-78239033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557119197	chr4:78239076-78239077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148738164	chr4:78239092-78239093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114021940	chr4:78239108-78239109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9884379	chr4:78239114-78239115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs75427370	chr4:78239138-78239139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545386450	chr4:78239148-78239149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565312234	chr4:78239159-78239160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78233200-78240600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:78240600-78241200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:78241200-78251400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:78252800-78254000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:78253400-78254800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
6	chr4:78255400-78256400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:78256400-78259000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:78256800-78257000	ZNF genes & repeats	HMEC	breast
9	chr4:78256800-78259200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:78257000-78257400	Weak transcription	HMEC	breast
11	chr4:78257200-78258000	Enhancers	NHEK	skin
12	chr4:78257400-78259200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:78257400-78259200	Enhancers	HMEC	breast
14	chr4:78258000-78258400	Flanking Active TSS	NHEK	skin
15	chr4:78258400-78259200	Enhancers	NHEK	skin
16	chr4:78259000-78263000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:78259200-78263000	Weak transcription	NHEK	skin
18	chr4:78263000-78264400	ZNF genes & repeats	NHEK	skin
19	chr4:78263000-78265000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:78263400-78263800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:78263400-78264000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
22	chr4:78264200-78265200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:78264400-78264600	Weak transcription	NHEK	skin
24	chr4:78264600-78264800	Enhancers	NHEK	skin
25	chr4:78264600-78266600	Enhancers	HMEC	breast
26	chr4:78264800-78265000	Flanking Active TSS	NHEK	skin
27	chr4:78264800-78265600	ZNF genes & repeats	GM12878-XiMat	blood
28	chr4:78264800-78266400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr4:78264800-78266400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:78265000-78265400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:78265000-78266600	Enhancers	NHEK	skin
32	chr4:78265200-78266200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:78265400-78270200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:78265600-78266000	Weak transcription	GM12878-XiMat	blood
35	chr4:78266000-78266400	Enhancers	GM12878-XiMat	blood
36	chr4:78266200-78270000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:78266400-78269400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:78266600-78269800	Weak transcription	HMEC	breast
39	chr4:78267400-78269800	Enhancers	Fetal Intestine Small	intestine
40	chr4:78267400-78270000	Enhancers	Stomach Mucosa	stomach
41	chr4:78267400-78270200	Enhancers	Fetal Intestine Large	intestine
42	chr4:78267600-78268800	Enhancers	Pancreas	Pancrea
43	chr4:78268000-78268400	Enhancers	HepG2	liver
44	chr4:78268200-78269200	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr4:78268400-78268600	Enhancers	Colonic Mucosa	Colon
46	chr4:78268400-78268800	Enhancers	A549	lung
47	chr4:78268400-78268800	Flanking Active TSS	HepG2	liver
48	chr4:78268400-78269000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:78268400-78269000	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr4:78268400-78269400	Enhancers	Duodenum Mucosa	Duodenum

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