Variant report

Variant	nsv437397
Chromosome Location	chr4:75077057-75095061
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	ATF2	chr4:75094472-75094740	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:75083263-75083307	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr4:75094377-75094758	GM12878	blood:	n/a	n/a
4	CBX3	chr4:75094278-75094965	HCT-116	colon:	n/a	n/a
5	CCNT2	chr4:75083118-75083643	K562	blood:	n/a	n/a
6	CEBPB	chr4:75089524-75089806	K562	blood:	n/a	n/a
7	CEBPB	chr4:75089525-75089863	A549	lung:	n/a	n/a
8	CEBPB	chr4:75089498-75089864	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:75089499-75089797	K562	blood:	n/a	n/a
10	CEBPB	chr4:75089484-75089870	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:75089465-75089968	HCT-116	colon:	n/a	n/a
12	CEBPB	chr4:75089375-75090037	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:75089403-75089940	A549	lung:	n/a	n/a
14	CEBPB	chr4:75089516-75089856	A549	lung:	n/a	n/a
15	CTCF	chr4:75094449-75094791	SK-N-SH_RA	brain:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
16	CTCF	chr4:75094540-75094690	GM12866	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
17	CTCF	chr4:75094600-75094750	HAc	cerebellar:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
18	CTCF	chr4:75094540-75094690	AoAF	blood vessel:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
19	CTCF	chr4:75094500-75094650	HL-60	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
20	CTCF	chr4:75094500-75094650	GM12865	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
21	CTCF	chr4:75094560-75094710	BJ	skin:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
22	CTCF	chr4:75094220-75094370	GM12870	blood:	n/a	n/a
23	CTCF	chr4:75094520-75094670	AG09319	gingival:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
24	CTCF	chr4:75094476-75094731	Fibrobl	skin:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
25	CTCF	chr4:75094540-75094690	NB4	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
26	CTCF	chr4:75094482-75094744	A549	lung:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
27	CTCF	chr4:75081198-75081281	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:75094540-75094690	HRPEpiC	eye:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
29	CTCF	chr4:75094304-75094885	HCT-116	colon:	n/a	chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094601-75094619 chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094604-75094613 chr4:75094604-75094617
30	CTCF	chr4:75094540-75094690	NHDF-neo	bronchial:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
31	CTCF	chr4:75094500-75094650	SK-N-SH_RA	brain:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
32	CTCF	chr4:75094313-75094898	MCF-7	breast:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
33	CTCF	chr4:75094474-75094737	MCF-7	breast:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
34	CTCF	chr4:75094491-75094725	GM10266	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
35	CTCF	chr4:75094468-75094746	K562	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
36	CTCF	chr4:75094580-75094730	GM12869	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
37	CTCF	chr4:75094238-75094360	K562	blood:	n/a	n/a
38	CTCF	chr4:75094520-75094670	GM12875	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
39	CTCF	chr4:75094488-75094740	LNCaP	prostate:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
40	CTCF	chr4:75094244-75095014	HCT-116	colon:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
41	CTCF	chr4:75094427-75094741	A549	lung:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
42	CTCF	chr4:75094540-75094690	GM12865	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
43	CTCF	chr4:75094520-75094670	HFF	foreskin:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
44	CTCF	chr4:75094479-75094709	H1-hESC	embryonic stem cell:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
45	CTCF	chr4:75094242-75094966	A549	lung:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
46	CTCF	chr4:75094500-75094650	HepG2	liver:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
47	CTCF	chr4:75094580-75094730	GM12872	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
48	CTCF	chr4:75094500-75094650	HCT-116	colon:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
49	CTCF	chr4:75094500-75094650	GM12874	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617
50	CTCF	chr4:75094520-75094670	GM12871	blood:	n/a	chr4:75094602-75094618 chr4:75094606-75094616 chr4:75094601-75094619 chr4:75094604-75094617 chr4:75094603-75094624 chr4:75094604-75094613 chr4:75094604-75094617

No.	Distal block	Cell Line	Cell type
1	chr4:75071138..75073600-chr4:75079457..75081137,2	MCF-7	breast:
2	chr4:75085650..75087545-chr4:75089867..75092462,3	K562	blood:
3	chr4:75093661..75096004-chr4:75147885..75149545,2	K562	blood:
4	chr4:75090793..75093494-chr4:75193558..75196089,2	K562	blood:
5	chr4:75093762..75095528-chr4:75175394..75177161,2	MCF-7	breast:
6	chr4:75055396..75057559-chr4:75092904..75094536,2	K562	blood:
7	chr4:75094222..75095380-chr4:75595823..75596616,3	K562	blood:
8	chr4:75089767..75091947-chr4:75172992..75174863,2	K562	blood:
9	chr4:75054721..75055635-chr4:75094051..75095124,3	K562	blood:
10	chr4:75091219..75093823-chr4:75093870..75096715,2	MCF-7	breast:
11	chr4:75094355..75095090-chr4:75547966..75548494,2	K562	blood:
12	chr4:75091219..75093823-chr4:75093870..75096715,2	MCF-7	breast:
13	chr4:75072066..75073934-chr4:75080235..75082986,2	K562	blood:
14	chr4:75093827..75095059-chr4:75177130..75178054,11	MCF-7	breast:
15	chr4:75081253..75083346-chr4:75120623..75122127,2	K562	blood:
16	chr4:75085650..75087545-chr4:75089867..75092462,3	K562	blood:
17	chr4:75023760..75025591-chr4:75092315..75094784,2	K562	blood:
18	chr4:75092889..75094695-chr4:75179646..75182331,2	K562	blood:
19	chr4:75094225..75095673-chr4:75176947..75177967,4	MCF-7	breast:
20	chr4:75030710..75033406-chr4:75092166..75094201,2	K562	blood:
21	chr4:75088731..75091267-chr4:75171967..75174863,2	K562	blood:

Variant related genes	Relation type
MTHFD2L	TF binding region
ENSG00000163738	chromatin interactions
ENSG00000269559	chromatin interactions
ENSG00000182585	chromatin interactions

Extended variants
information (count: 588 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543582	chr4:75077057-75077058	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs476556	chr4:75077066-75077067	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549797394	chr4:75077105-75077106	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs370536123	chr4:75077112-75077113	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs186844768	chr4:75077141-75077142	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs535396977	chr4:75077142-75077143	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs148908270	chr4:75077148-75077149	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs192419293	chr4:75077157-75077158	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs371123814	chr4:75077160-75077161	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs539574553	chr4:75077200-75077201	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs144245994	chr4:75077216-75077217	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs576765848	chr4:75077255-75077256	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs577313456	chr4:75077285-75077286	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs537930441	chr4:75077428-75077429	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs189925512	chr4:75077448-75077449	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs574850873	chr4:75077452-75077453	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs182142597	chr4:75077473-75077474	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs374315315	chr4:75077488-75077489	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs560717383	chr4:75077542-75077543	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs184752071	chr4:75077655-75077656	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs386676066	chr4:75077658-75077659	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs181316395	chr4:75077659-75077660	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs143584279	chr4:75077677-75077678	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs531465696	chr4:75077759-75077760	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs549598207	chr4:75077795-75077796	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs561363446	chr4:75077819-75077820	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs184948498	chr4:75077823-75077824	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs201879436	chr4:75077841-75077842	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs138116663	chr4:75077851-75077852	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs565598859	chr4:75077892-75077893	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs189808838	chr4:75077898-75077899	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs551580300	chr4:75077934-75077935	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs569735747	chr4:75077938-75077939	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs144603959	chr4:75078011-75078012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367822799	chr4:75078023-75078024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574885863	chr4:75078076-75078077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138622671	chr4:75078119-75078120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6811214	chr4:75078160-75078161	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs181819886	chr4:75078161-75078162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76435517	chr4:75078168-75078169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76919596	chr4:75078194-75078195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79448586	chr4:75078208-75078209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541572994	chr4:75078238-75078239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10034906	chr4:75078263-75078264	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs78688192	chr4:75078293-75078294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186416128	chr4:75078318-75078319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576529528	chr4:75078369-75078370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543526692	chr4:75078413-75078414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561400750	chr4:75078428-75078429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6858809	chr4:75078429-75078430	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

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
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	20952505	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75024800-75080600	Weak transcription	Left Ventricle	heart
2	chr4:75056800-75096600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:75059200-75081000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr4:75060000-75080200	Weak transcription	Dnd41	blood
5	chr4:75064200-75096400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:75065000-75086200	Weak transcription	Psoas Muscle	Psoas
7	chr4:75067800-75097000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr4:75068400-75082400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr4:75068400-75093000	Weak transcription	Thymus	Thymus
10	chr4:75068400-75096600	Weak transcription	Adipose Nuclei	Adipose
11	chr4:75069600-75091000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:75071800-75096400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr4:75072200-75080200	Weak transcription	Fetal Intestine Small	intestine
14	chr4:75072200-75099200	Weak transcription	Ovary	ovary
15	chr4:75072800-75080200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:75072800-75080400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:75073000-75092400	Weak transcription	Primary B cells from cord blood	blood
18	chr4:75073800-75080400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:75073800-75089400	Weak transcription	A549	lung
20	chr4:75073800-75089600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr4:75073800-75094400	Weak transcription	Brain Angular Gyrus	brain
22	chr4:75074000-75082800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr4:75074200-75079800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr4:75074200-75080400	Weak transcription	Fetal Thymus	thymus
25	chr4:75074200-75082800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr4:75074200-75084000	Weak transcription	HMEC	breast
27	chr4:75074400-75083200	Weak transcription	HSMMtube	muscle
28	chr4:75074600-75077400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:75074600-75080200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:75074600-75091200	Weak transcription	Liver	Liver
31	chr4:75075000-75080400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:75075000-75080400	Weak transcription	K562	blood
33	chr4:75075000-75095800	Weak transcription	Primary T cells from cord blood	blood
34	chr4:75075200-75083400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:75076800-75078000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
36	chr4:75076800-75080200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr4:75078000-75084800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr4:75078400-75083600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:75079000-75080400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:75079800-75080800	Enhancers	Placenta Amnion	Placenta Amnion
41	chr4:75080000-75080600	Enhancers	Fetal Intestine Large	intestine
42	chr4:75080000-75081000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:75080000-75081200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:75080000-75081200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:75080000-75081400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:75080200-75080400	Weak transcription	Primary hematopoietic stem cells	blood
47	chr4:75080200-75080600	Genic enhancers	Fetal Intestine Small	intestine
48	chr4:75080200-75080600	Enhancers	Lung	lung
49	chr4:75080200-75080800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr4:75080200-75080800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links