Variant report

Variant	nsv882622
Chromosome Location	chr5:104717739-104841922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:290)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
2	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
3	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
4	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
5	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
6	BACH1	chr5:104779909-104779930	K562	blood:	n/a	n/a
7	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
8	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
9	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
10	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
11	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
12	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
13	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
14	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
15	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
16	CEBPB	chr5:104780741-104780853	K562	blood:	n/a	n/a
17	CEBPB	chr5:104720876-104721252	K562	blood:	n/a	n/a
18	CEBPB	chr5:104788546-104788789	A549	lung:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
19	CEBPB	chr5:104720977-104721172	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr5:104788448-104788780	HepG2	liver:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
21	CEBPB	chr5:104783657-104783915	HepG2	liver:	n/a	chr5:104783784-104783795
22	CHD2	chr5:104728384-104728863	K562	blood:	n/a	n/a
23	CHD2	chr5:104796530-104796598	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr5:104727637-104727834	K562	blood:	n/a	n/a
25	CTCF	chr5:104824198-104824301	ProgFib	skin:	n/a	n/a
26	CTCF	chr5:104803956-104804039	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr5:104824292-104824367	GM20000	blood:	n/a	n/a
28	CTCF	chr5:104797250-104797319	Medullo	brain:	n/a	n/a
29	CTCF	chr5:104787945-104787991	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr5:104727920-104728070	HepG2	liver:	n/a	n/a
31	CTCF	chr5:104727909-104728007	K562	blood:	n/a	n/a
32	CTCF	chr5:104789240-104789390	HPF	lung:	n/a	n/a
33	CUX1	chr5:104726108-104726579	K562	blood:	n/a	n/a
34	CUX1	chr5:104726999-104727199	K562	blood:	n/a	n/a
35	CUX1	chr5:104727561-104727756	K562	blood:	n/a	n/a
36	E2F4	chr5:104752031-104752136	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr5:104828260-104828440	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr5:104767057-104767257	MCF10A-Er-Src	breast:	n/a	n/a
39	ELF1	chr5:104728319-104729210	HCT-116	colon:	n/a	n/a
40	ELF1	chr5:104728044-104728975	K562	blood:	n/a	n/a
41	ELF1	chr5:104728575-104728905	HepG2	liver:	n/a	n/a
42	ELF1	chr5:104728448-104729083	HCT-116	colon:	n/a	n/a
43	ELF1	chr5:104728406-104728965	K562	blood:	n/a	n/a
44	ELF1	chr5:104728572-104728937	HepG2	liver:	n/a	n/a
45	ELK1	chr5:104728596-104728947	K562	blood:	n/a	n/a
46	EP300	chr5:104728503-104728971	K562	blood:	n/a	n/a
47	EP300	chr5:104728530-104728887	GM12878	blood:	n/a	n/a
48	EP300	chr5:104733154-104733713	MCF-7	breast:	n/a	n/a
49	EP300	chr5:104839677-104840024	SK-N-SH_RA	brain:	n/a	chr5:104839838-104839847 chr5:104839839-104839848 chr5:104839677-104839691
50	EP300	chr5:104839514-104840090	SK-N-SH_RA	brain:	n/a	chr5:104839838-104839847 chr5:104839839-104839848 chr5:104839677-104839691 chr5:104840066-104840076

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104728220-104728270	PANC-1	pancreas:	n/a
2	chr5:104728427-104728477	RPTEC	kidney:	n/a
3	chr5:104728220-104728270	LNCaP	prostate:	n/a
4	chr5:104728427-104728477	HCPEpiC	choroid plexus:	n/a
5	chr5:104728220-104728270	PFSK-1	brain:	n/a
6	chr5:104728427-104728477	AG04450	lung:	fetal
7	chr5:104728220-104728270	ProgFib	skin:	n/a
8	chr5:104728220-104728270	BJ	skin:	n/a
9	chr5:104728427-104728477	GM12892	blood:	n/a
10	chr5:104728427-104728477	AG10803	skin:	n/a
11	chr5:104728220-104728270	AG04449	skin:	fetal
12	chr5:104728427-104728477	AG09319	gingival:	n/a
13	chr5:104728427-104728477	HEK293	kidney:	embryo
14	chr5:104728220-104728270	A549	lung:	n/a
15	chr5:104728220-104728270	T-47D	breast:	n/a
16	chr5:104728220-104728270	SK-N-SH	brain:	n/a
17	chr5:104728427-104728477	AG04449	skin:	fetal
18	chr5:104728220-104728270	K562	blood:	n/a
19	chr5:104728427-104728477	Hela-S3	cervix:	n/a
20	chr5:104728220-104728270	ovcar-3	ovarian:	n/a
21	chr5:104728220-104728270	GM19239	blood:	n/a
22	chr5:104728427-104728477	K562	blood:	n/a
23	chr5:104728427-104728477	HRPEpiC	eye:	n/a
24	chr5:104728427-104728477	HUVEC	blood vessel:	n/a
25	chr5:104728220-104728270	HRE	kidney:	n/a
26	chr5:104728427-104728477	SK-N-SH_RA	brain:	n/a
27	chr5:104728427-104728477	HAEpiC	amniotic membrane:	n/a
28	chr5:104728220-104728270	MCF10A-Er-Src	breast:	n/a
29	chr5:104728220-104728270	U87	brain:	n/a
30	chr5:104728220-104728270	HAEpiC	amniotic membrane:	n/a
31	chr5:104728427-104728477	Jurkat	blood:	n/a
32	chr5:104728220-104728270	CMK	blood:	n/a
33	chr5:104728427-104728477	GM12878	blood:	n/a
34	chr5:104728220-104728270	HUVEC	blood vessel:	n/a
35	chr5:104728220-104728270	HEK293	kidney:	embryo
36	chr5:104728427-104728477	Caco-2	colon:	n/a
37	chr5:104728427-104728477	HL-60	blood:	n/a
38	chr5:104728220-104728270	SK-N-MC	brain:	n/a
39	chr5:104728427-104728477	PrEC	prostate:	n/a
40	chr5:104728220-104728270	NB4	blood:	n/a
41	chr5:104728427-104728477	SK-N-SH	brain:	n/a
42	chr5:104728220-104728270	ECC-1	luminal epithelium:	n/a
43	chr5:104728220-104728270	Hepatocyte	liver:	n/a
44	chr5:104728427-104728477	CMK	blood:	n/a
45	chr5:104728220-104728270	NHBE	bronchial:	n/a
46	chr5:104728220-104728270	HepG2	liver:	n/a
47	chr5:104728220-104728270	AoSMC	blood vessel:	n/a
48	chr5:104728220-104728270	Hela-S3	cervix:	n/a
49	chr5:104728220-104728270	HRCEpiC	kidney:	n/a
50	chr5:104728220-104728270	SAEC	small airway:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
2	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
3	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
4	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
5	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
6	chr5:104727296..104728816-chr5:104790778..104793743,2	K562	blood:
7	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
8	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
9	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
10	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
11	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
12	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
13	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
14	chr5:104726534..104729492-chr5:107716153..107718681,2	K562	blood:
15	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
16	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
17	chr5:104726359..104728666-chr5:105131284..105132821,2	K562	blood:
18	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
19	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
20	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
21	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
22	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
23	chr1:184434764..184435543-chr5:104792004..104792524,3	MCF-7	breast:
24	chr5:104716167..104718489-chr5:104728063..104729895,2	K562	blood:
25	chr5:104727742..104729434-chr5:104763198..104765492,2	K562	blood:
26	chr18:42792470..42793145-chr5:104821622..104822504,2	MCF-7	breast:
27	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097
2	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574

No data

Variant related genes	Relation type
ENSG00000251574	TF binding region
ENSG00000251574	CpG island
ENSG00000145743	chromatin interactions
ENSG00000132874	chromatin interactions
ENSG00000251574	chromatin interactions

Extended variants
information (count: 1432 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1432 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1423208	chr5:104717739-104717740	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566461538	chr5:104717744-104717745	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576940562	chr5:104717746-104717747	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550164360	chr5:104717750-104717751	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571607225	chr5:104717764-104717765	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538296745	chr5:104717770-104717771	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372055159	chr5:104717778-104717779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558785224	chr5:104717821-104717822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575535931	chr5:104717824-104717825	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538747739	chr5:104717883-104717884	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547531126	chr5:104717907-104717908	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541964979	chr5:104717923-104717924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554758289	chr5:104717968-104717969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs6860623	chr5:104717974-104717975	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540699321	chr5:104718011-104718012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560426030	chr5:104718026-104718027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566319236	chr5:104718039-104718040	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201720300	chr5:104718045-104718046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545884352	chr5:104718049-104718050	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565126826	chr5:104718054-104718055	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530844659	chr5:104718202-104718203	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs550931465	chr5:104718259-104718260	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567448906	chr5:104718341-104718342	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs141164184	chr5:104718371-104718372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369139216	chr5:104718376-104718377	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555353734	chr5:104718379-104718380	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145653068	chr5:104718383-104718384	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538582259	chr5:104718416-104718417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73196665	chr5:104718441-104718442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182718122	chr5:104718471-104718472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11951892	chr5:104718477-104718478	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556087121	chr5:104722002-104722003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs193213303	chr5:104722034-104722035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11955463	chr5:104722062-104722063	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs72786079	chr5:104722072-104722073	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572127539	chr5:104722079-104722080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375413183	chr5:104722110-104722111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541050877	chr5:104722131-104722132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185562880	chr5:104722136-104722137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564056253	chr5:104722161-104722162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75001211	chr5:104722164-104722165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544123140	chr5:104722172-104722173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187751653	chr5:104722239-104722240	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375479981	chr5:104722252-104722253	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72786080	chr5:104722261-104722262	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559558535	chr5:104722275-104722276	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548857574	chr5:104722285-104722286	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562537092	chr5:104722292-104722293	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528599609	chr5:104722372-104722373	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112591478	chr5:104722426-104722427	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Obesity	20622171	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104722000-104722200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr5:104722200-104722600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr5:104722200-104722800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr5:104722200-104723200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:104722400-104723400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:104722400-104723600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:104722600-104723000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:104724800-104725800	Enhancers	K562	blood
9	chr5:104725800-104726400	Weak transcription	K562	blood
10	chr5:104726400-104729200	Active TSS	K562	blood
11	chr5:104727400-104727600	Enhancers	Placenta	Placenta
12	chr5:104727600-104727800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:104727600-104728000	Flanking Active TSS	Placenta	Placenta
14	chr5:104727600-104729000	Active TSS	HepG2	liver
15	chr5:104727800-104728000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:104727800-104728600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:104728000-104728400	Active TSS	Placenta	Placenta
18	chr5:104728400-104728800	ZNF genes & repeats	Placenta	Placenta
19	chr5:104742400-104743400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:104742400-104743600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:104742400-104743600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:104742600-104743400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:104742800-104743200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:104742800-104743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:104748600-104749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:104748800-104749200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:104749200-104749600	Bivalent Enhancer	Placenta	Placenta
28	chr5:104749200-104749800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:104757800-104758600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:104763400-104764400	Enhancers	Fetal Intestine Large	intestine
31	chr5:104766000-104767600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:104767600-104768600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:104768600-104769000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:104768600-104769200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:104796000-104801800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr5:104811600-104811800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:104817600-104817800	Enhancers	Liver	Liver
38	chr5:104817800-104818200	Active TSS	Liver	Liver
39	chr5:104820000-104820600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:104828000-104828600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:104829400-104829600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:104833800-104834200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:104833800-104834400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:104833800-104834400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:104833800-104834400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:104834000-104834400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:104834000-104834400	Active TSS	Spleen	Spleen
48	chr5:104834400-104836200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr5:104836200-104837000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:104836200-104837200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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