Variant report

Variant	nsv1033350
Chromosome Location	chr5:75367809-75538460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1616)
CpG islands
(count:2079)
Chromatin interactive
region (count:35)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:75517243-75517452	K562	blood:	n/a	n/a
2	ATF1	chr5:75442283-75442385	K562	blood:	n/a	n/a
3	ATF1	chr5:75471623-75472170	K562	blood:	n/a	n/a
4	ATF1	chr5:75476928-75477230	K562	blood:	n/a	n/a
5	ATF1	chr5:75458345-75458529	K562	blood:	n/a	n/a
6	ATF1	chr5:75515637-75515837	K562	blood:	n/a	n/a
7	ATF2	chr5:75483142-75483633	GM12878	blood:	n/a	n/a
8	ATF2	chr5:75476882-75477667	GM12878	blood:	n/a	n/a
9	ATF2	chr5:75394969-75395455	GM12878	blood:	n/a	n/a
10	ATF2	chr5:75474597-75475178	GM12878	blood:	n/a	n/a
11	ATF2	chr5:75471452-75472442	GM12878	blood:	n/a	n/a
12	ATF2	chr5:75476912-75477609	GM12878	blood:	n/a	n/a
13	ATF2	chr5:75474650-75475133	GM12878	blood:	n/a	n/a
14	ATF2	chr5:75394893-75395805	GM12878	blood:	n/a	n/a
15	ATF2	chr5:75471604-75472348	GM12878	blood:	n/a	n/a
16	ATF3	chr5:75471599-75472016	K562	blood:	n/a	n/a
17	BACH1	chr5:75380053-75380336	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:75378858-75379581	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:75377746-75378139	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:75380639-75380650	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr5:75395097-75395564	GM12878	blood:	n/a	n/a
22	BATF	chr5:75474748-75475148	GM12878	blood:	n/a	n/a
23	BATF	chr5:75471890-75472287	GM12878	blood:	n/a	n/a
24	BATF	chr5:75476907-75477562	GM12878	blood:	n/a	n/a
25	BATF	chr5:75476903-75477253	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:75476940-75477332	GM12878	blood:	n/a	n/a
27	BCL11A	chr5:75474738-75475112	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:75440843-75440979	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL3	chr5:75476943-75477631	GM12878	blood:	n/a	n/a
30	BCL3	chr5:75471555-75472304	GM12878	blood:	n/a	n/a
31	BCL3	chr5:75474685-75475133	GM12878	blood:	n/a	n/a
32	BCL3	chr5:75473860-75474199	GM12878	blood:	n/a	n/a
33	BCLAF1	chr5:75476931-75477519	GM12878	blood:	n/a	n/a
34	BCLAF1	chr5:75471604-75472393	GM12878	blood:	n/a	n/a
35	BCLAF1	chr5:75470838-75471335	GM12878	blood:	n/a	n/a
36	BCLAF1	chr5:75394943-75395528	GM12878	blood:	n/a	n/a
37	BHLHE40	chr5:75515244-75515285	GM12878	blood:	n/a	n/a
38	BHLHE40	chr5:75476870-75477240	K562	blood:	n/a	n/a
39	BHLHE40	chr5:75471965-75472226	GM12878	blood:	n/a	n/a
40	BHLHE40	chr5:75471619-75472026	K562	blood:	n/a	n/a
41	BHLHE40	chr5:75441876-75442076	K562	blood:	n/a	n/a
42	BHLHE40	chr5:75470933-75471235	GM12878	blood:	n/a	n/a
43	CBX3	chr5:75476823-75477541	K562	blood:	n/a	n/a
44	CBX3	chr5:75505170-75505419	K562	blood:	n/a	n/a
45	CBX3	chr5:75471552-75472056	K562	blood:	n/a	n/a
46	CCNT2	chr5:75383757-75383903	K562	blood:	n/a	n/a
47	CCNT2	chr5:75471729-75471951	K562	blood:	n/a	chr5:75471940-75471949
48	CCNT2	chr5:75530726-75530914	K562	blood:	n/a	n/a
49	CCNT2	chr5:75476951-75477181	K562	blood:	n/a	n/a
50	CEBPB	chr5:75500559-75501070	ECC-1	luminal epithelium:	n/a	chr5:75500852-75500863

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75377755-75377805	HEEpiC	esophagus:	n/a
2	chr5:75376460-75376510	NT2-D1	testis:	n/a
3	chr5:75380303-75380353	MCF-7	breast:	n/a
4	chr5:75378176-75378226	HEK293	kidney:	embryo
5	chr5:75538132-75538182	HIPEpiC	eye:	n/a
6	chr5:75377755-75377805	HEEpiC	esophagus:	n/a
7	chr5:75376460-75376510	NT2-D1	testis:	n/a
8	chr5:75380303-75380353	MCF-7	breast:	n/a
9	chr5:75378176-75378226	HEK293	kidney:	embryo
10	chr5:75538132-75538182	HIPEpiC	eye:	n/a
11	chr5:75377968-75378018	PrEC	prostate:	n/a
12	chr5:75380842-75380892	Jurkat	blood:	n/a
13	chr5:75538132-75538182	T-47D	breast:	n/a
14	chr5:75471166-75471216	NH-A	brain:	n/a
15	chr5:75471166-75471216	MCF10A-Er-Src	breast:	n/a
16	chr5:75381070-75381120	IMR90	lung:	fetal
17	chr5:75469826-75469876	HRCEpiC	kidney:	n/a
18	chr5:75471166-75471216	HCT-116	colon:	n/a
19	chr5:75379748-75379798	NHDF-neo	bronchial:	n/a
20	chr5:75381070-75381120	Hepatocyte	liver:	n/a
21	chr5:75379800-75379850	PFSK-1	brain:	n/a
22	chr5:75380782-75380832	HNPCEpiC	eye:	n/a
23	chr5:75381042-75381092	HAEpiC	amniotic membrane:	n/a
24	chr5:75374482-75374532	HRCEpiC	kidney:	n/a
25	chr5:75379273-75379323	HRE	kidney:	n/a
26	chr5:75378102-75378152	PrEC	prostate:	n/a
27	chr5:75379336-75379386	PANC-1	pancreas:	n/a
28	chr5:75379515-75379565	HMEC	breast:	n/a
29	chr5:75379515-75379565	HCPEpiC	choroid plexus:	n/a
30	chr5:75377968-75378018	AG09319	gingival:	n/a
31	chr5:75377755-75377805	AG10803	skin:	n/a
32	chr5:75524056-75524106	RPTEC	kidney:	n/a
33	chr5:75374482-75374532	SK-N-SH	brain:	n/a
34	chr5:75379800-75379850	HRPEpiC	eye:	n/a
35	chr5:75410147-75410197	NB4	blood:	n/a
36	chr5:75378176-75378226	U87	brain:	n/a
37	chr5:75380782-75380832	SKMC	muscle:	n/a
38	chr5:75381070-75381120	NB4	blood:	n/a
39	chr5:75381070-75381120	NHDF-neo	bronchial:	n/a
40	chr5:75465603-75465653	PFSK-1	brain:	n/a
41	chr5:75471166-75471216	GM12878	blood:	n/a
42	chr5:75378176-75378226	ECC-1	luminal epithelium:	n/a
43	chr5:75378102-75378152	GM06990	blood:	n/a
44	chr5:75410147-75410197	Hela-S3	cervix:	n/a
45	chr5:75377922-75377972	NT2-D1	testis:	n/a
46	chr5:75377755-75377805	HL-60	blood:	n/a
47	chr5:75379270-75379320	HEK293	kidney:	embryo
48	chr5:75379273-75379323	ovcar-3	ovarian:	n/a
49	chr5:75524056-75524106	Hela-S3	cervix:	n/a
50	chr5:75538132-75538182	ECC-1	luminal epithelium:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
2	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
3	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
4	chr5:75370241..75371009-chr5:75551554..75552357,4	K562	blood:
5	chr5:75441859..75445534-chr5:75469171..75472141,3	K562	blood:
6	chr5:75470625..75471456-chr5:75551799..75552684,5	MCF-7	breast:
7	chr2:121070497..121071131-chr5:75375493..75376013,2	MCF-7	breast:
8	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
9	chr5:75370056..75370744-chr5:75551849..75552754,4	MCF-7	breast:
10	chr5:75182130..75182669-chr5:75470688..75471450,3	MCF-7	breast:
11	chr5:75031130..75031721-chr5:75470748..75471418,2	MCF-7	breast:
12	chr2:77243462..77244011-chr5:75510913..75511675,2	MCF-7	breast:
13	chr5:75378752..75382586-chr5:75384314..75388337,4	K562	blood:
14	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
15	chr5:75378752..75382586-chr5:75384314..75388337,4	K562	blood:
16	chr5:75011937..75013471-chr5:75474552..75477211,2	MCF-7	breast:
17	chr5:75369710..75371593-chr5:75472300..75473889,2	K562	blood:
18	chr5:75380964..75382586-chr5:75384314..75386293,2	K562	blood:
19	chr5:75534573..75536259-chr5:75552032..75554842,2	K562	blood:
20	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
21	chr5:75370258..75370917-chr5:75470691..75471438,2	MCF-7	breast:
22	chr2:175960283..175962736-chr5:75428852..75431360,2	MCF-7	breast:
23	chr5:75370002..75370997-chr5:75470399..75471572,8	MCF-7	breast:
24	chr5:75520569..75523367-chr5:75540398..75542001,2	K562	blood:
25	chr5:75380964..75382586-chr5:75384314..75386293,2	K562	blood:
26	chr4:144295435..144296093-chr5:75459165..75460000,2	MCF-7	breast:
27	chr5:75370258..75370917-chr5:75470691..75471438,2	MCF-7	breast:
28	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
29	chr5:75370002..75370997-chr5:75470399..75471572,8	MCF-7	breast:
30	chr5:75469938..75472744-chr5:75476639..75478302,2	K562	blood:
31	chr5:75030911..75031730-chr5:75470555..75471416,3	MCF-7	breast:
32	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
33	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
34	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
35	chr5:75370186..75371274-chr5:75551816..75552790,4	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POC5-2	chr5:75379772-75380011	ENSG00000248127
2	lnc-POC5-2	chr5:75377771-75378221	ENSG00000248127
3	lnc-SV2C-1	chr5:75371356-75371745	NONHSAT102226

No data

Variant related genes	Relation type
ENSG00000249777	TF binding region
ENSG00000248127	TF binding region
ENSG00000251668	TF binding region
ENSG00000251342	TF binding region
SV2C	TF binding region
ENSG00000254893	TF binding region
RNA5SP186	TF binding region
HMGN2P4	TF binding region
ENSG00000249777	CpG island
ENSG00000248127	CpG island
ENSG00000251668	CpG island
ENSG00000251342	CpG island
SV2C	CpG island
ENSG00000254893	CpG island
RNA5SP186	CpG island
HMGN2P4	CpG island
ENSG00000249777	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000254893	chromatin interactions
ENSG00000252833	chromatin interactions
ENSG00000248127	chromatin interactions
ENSG00000122012	chromatin interactions

Extended variants
information (count: 4008 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4008 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561951371	chr5:75369414-75369415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs185691102	chr5:75369481-75369482	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs551182460	chr5:75370043-75370044	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs559767756	chr5:75370051-75370052	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs186049194	chr5:75370063-75370064	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs537561079	chr5:75370093-75370094	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs151028590	chr5:75370110-75370111	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs56342638	chr5:75370111-75370112	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533106074	chr5:75370148-75370149	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs549894310	chr5:75370170-75370171	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs115009898	chr5:75370171-75370172	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs528864024	chr5:75370211-75370212	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs201237128	chr5:75370213-75370214	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs533819763	chr5:75370223-75370224	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs565802112	chr5:75370224-75370225	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs369455979	chr5:75370229-75370230	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs116671820	chr5:75370242-75370243	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs115258727	chr5:75370265-75370266	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs141104918	chr5:75370270-75370271	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs28529745	chr5:75370294-75370295	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs117663256	chr5:75370296-75370297	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs557013248	chr5:75370297-75370298	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs30191	chr5:75370308-75370309	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs150266327	chr5:75370333-75370334	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs553635367	chr5:75370364-75370365	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs573408480	chr5:75370378-75370379	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs117273282	chr5:75370397-75370398	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs74992399	chr5:75370419-75370420	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs71628999	chr5:75370484-75370485	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs191717804	chr5:75370541-75370542	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs30192	chr5:75370597-75370598	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs539268382	chr5:75370659-75370660	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs12513447	chr5:75370737-75370738	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs147937445	chr5:75370787-75370788	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs548662077	chr5:75370791-75370792	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs529309712	chr5:75370820-75370821	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs559603007	chr5:75370837-75370838	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs528418230	chr5:75370879-75370880	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs141747732	chr5:75371025-75371026	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs146967652	chr5:75371043-75371044	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs138023340	chr5:75371095-75371096	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs544784884	chr5:75371368-75371369	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs368170659	chr5:75371373-75371374	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs143039273	chr5:75371389-75371390	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs542705687	chr5:75371397-75371398	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs375181286	chr5:75371412-75371413	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs541977329	chr5:75371444-75371445	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs77889694	chr5:75371446-75371447	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs544922531	chr5:75371487-75371488	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs564800663	chr5:75371501-75371502	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75376000-75376400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
2	chr5:75376200-75376400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
3	chr5:75376200-75376800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr5:75376600-75377000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
5	chr5:75376800-75377600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:75377400-75377600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
7	chr5:75377400-75377800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
8	chr5:75377400-75381400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
9	chr5:75377600-75377800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
10	chr5:75377600-75377800	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:75377600-75377800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:75377600-75377800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
13	chr5:75377600-75377800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr5:75377600-75377800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:75377600-75377800	Active TSS	Brain Anterior Caudate	brain
16	chr5:75377600-75377800	Bivalent Enhancer	Brain Germinal Matrix	brain
17	chr5:75377600-75377800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
18	chr5:75377600-75377800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
19	chr5:75377600-75378000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr5:75377600-75378000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
21	chr5:75377600-75378000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:75377600-75378000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr5:75377600-75378200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr5:75377600-75378600	Enhancers	Spleen	Spleen
25	chr5:75377600-75380000	Bivalent Enhancer	Fetal Brain Male	brain
26	chr5:75377600-75381000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr5:75377600-75381000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
28	chr5:75377600-75381200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
29	chr5:75377600-75381400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
30	chr5:75377600-75381600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
31	chr5:75377800-75378000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr5:75377800-75378000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:75377800-75378000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
34	chr5:75377800-75378000	Bivalent Enhancer	Primary T cells from cord blood	blood
35	chr5:75377800-75378000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
36	chr5:75377800-75378000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:75377800-75378000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:75377800-75378000	Flanking Active TSS	Brain Angular Gyrus	brain
39	chr5:75377800-75378000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
40	chr5:75377800-75378000	Bivalent Enhancer	Brain Hippocampus Middle	brain
41	chr5:75377800-75378000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
42	chr5:75377800-75378000	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr5:75377800-75378000	Bivalent Enhancer	Fetal Stomach	stomach
44	chr5:75377800-75378000	Enhancers	Right Ventricle	heart
45	chr5:75377800-75378000	Bivalent Enhancer	Thymus	Thymus
46	chr5:75377800-75378200	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:75377800-75378200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:75377800-75378200	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
49	chr5:75377800-75378200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
50	chr5:75377800-75378200	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links