Variant report

Variant	esv3380725
Chromosome Location	chr5:95041824-95049026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:305)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:95046051-95046377	K562	blood:	n/a	n/a
2	ARID3A	chr5:95042591-95042912	K562	blood:	n/a	n/a
3	ARID3A	chr5:95046602-95046683	K562	blood:	n/a	n/a
4	ARID3A	chr5:95047937-95048734	K562	blood:	n/a	n/a
5	ATF1	chr5:95048032-95048542	K562	blood:	n/a	n/a
6	ATF1	chr5:95047327-95047534	K562	blood:	n/a	n/a
7	ATF1	chr5:95046053-95047077	K562	blood:	n/a	n/a
8	ATF2	chr5:95047297-95047567	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr5:95046616-95046896	K562	blood:	n/a	n/a
10	ATF3	chr5:95047944-95048607	K562	blood:	n/a	n/a
11	ATF3	chr5:95047898-95048587	HCT-116	colon:	n/a	n/a
12	ATF3	chr5:95048198-95048492	K562	blood:	n/a	n/a
13	ATF3	chr5:95046588-95047096	K562	blood:	n/a	n/a
14	BACH1	chr5:95046104-95046389	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:95046863-95046974	K562	blood:	n/a	n/a
16	BCL3	chr5:95047977-95048621	K562	blood:	n/a	n/a
17	BCLAF1	chr5:95047853-95048602	K562	blood:	n/a	n/a
18	BCLAF1	chr5:95047922-95048655	K562	blood:	n/a	n/a
19	BCLAF1	chr5:95045878-95046471	K562	blood:	n/a	n/a
20	BHLHE40	chr5:95047985-95048676	K562	blood:	n/a	n/a
21	BHLHE40	chr5:95047340-95047576	K562	blood:	n/a	n/a
22	BHLHE40	chr5:95046699-95046968	K562	blood:	n/a	n/a
23	BHLHE40	chr5:95046041-95046399	K562	blood:	n/a	n/a
24	BRCA1	chr5:95046823-95047023	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:95047993-95048575	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:95046184-95046310	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:95047868-95048604	K562	blood:	n/a	n/a
28	CBX3	chr5:95046026-95046435	K562	blood:	n/a	n/a
29	CBX3	chr5:95045771-95046436	K562	blood:	n/a	n/a
30	CBX3	chr5:95048853-95049357	K562	blood:	n/a	n/a
31	CBX3	chr5:95047853-95048715	HCT-116	colon:	n/a	n/a
32	CBX3	chr5:95041566-95042270	K562	blood:	n/a	n/a
33	CBX3	chr5:95048034-95048558	K562	blood:	n/a	n/a
34	CCNT2	chr5:95048010-95048581	K562	blood:	n/a	n/a
35	CEBPB	chr5:95048047-95048333	K562	blood:	n/a	chr5:95048133-95048144
36	CEBPB	chr5:95046802-95047143	K562	blood:	n/a	n/a
37	CEBPB	chr5:95047963-95048410	IMR90	lung:	n/a	chr5:95048133-95048144
38	CEBPB	chr5:95044353-95044698	MCF-7	breast:	n/a	n/a
39	CEBPB	chr5:95047890-95048441	A549	lung:	n/a	chr5:95048133-95048144
40	CEBPB	chr5:95046678-95047065	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:95046172-95046400	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:95047957-95048331	A549	lung:	n/a	chr5:95048133-95048144
43	CEBPB	chr5:95047915-95048578	Hela-S3	cervix:	n/a	chr5:95048133-95048144
44	CEBPB	chr5:95047815-95048742	HCT-116	colon:	n/a	chr5:95048133-95048144
45	CEBPB	chr5:95047931-95048388	A549	lung:	n/a	chr5:95048133-95048144
46	CEBPB	chr5:95044482-95044647	K562	blood:	n/a	n/a
47	CEBPB	chr5:95047504-95048583	K562	blood:	n/a	chr5:95048133-95048144
48	CEBPB	chr5:95048093-95048272	HepG2	liver:	n/a	chr5:95048133-95048144
49	CEBPB	chr5:95044834-95045239	MCF-7	breast:	n/a	n/a
50	CEBPB	chr5:95047854-95048575	MCF-7	breast:	n/a	chr5:95048133-95048144

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:95047327-95047377	GM12892	blood:	n/a
2	chr5:95047566-95047616	PANC-1	pancreas:	n/a
3	chr5:95047566-95047616	NHDF-neo	bronchial:	n/a
4	chr5:95047004-95047054	Jurkat	blood:	n/a
5	chr5:95047004-95047054	HRPEpiC	eye:	n/a
6	chr5:95046908-95046958	HCPEpiC	choroid plexus:	n/a
7	chr5:95046908-95046958	CMK	blood:	n/a
8	chr5:95047566-95047616	SAEC	small airway:	n/a
9	chr5:95046908-95046958	Hela-S3	cervix:	n/a
10	chr5:95047004-95047054	HNPCEpiC	eye:	n/a
11	chr5:95047566-95047616	AG10803	skin:	n/a
12	chr5:95046908-95046958	GM12878	blood:	n/a
13	chr5:95046754-95046804	A549	lung:	n/a
14	chr5:95047327-95047377	HL-60	blood:	n/a
15	chr5:95046908-95046958	AoSMC	blood vessel:	n/a
16	chr5:95047566-95047616	H1-hESC	embryonic stem cell:	embryo
17	chr5:95046754-95046804	HNPCEpiC	eye:	n/a
18	chr5:95046754-95046804	AG04450	lung:	fetal
19	chr5:95047566-95047616	AG04449	skin:	fetal
20	chr5:95047004-95047054	LNCaP	prostate:	n/a
21	chr5:95047327-95047377	NHBE	bronchial:	n/a
22	chr5:95046908-95046958	HepG2	liver:	n/a
23	chr5:95047004-95047054	SAEC	small airway:	n/a
24	chr5:95046754-95046804	SAEC	small airway:	n/a
25	chr5:95047327-95047377	K562	blood:	n/a
26	chr5:95047566-95047616	PrEC	prostate:	n/a
27	chr5:95047004-95047054	GM19239	blood:	n/a
28	chr5:95046908-95046958	BJ	skin:	n/a
29	chr5:95047327-95047377	ovcar-3	ovarian:	n/a
30	chr5:95046908-95046958	AG09319	gingival:	n/a
31	chr5:95047566-95047616	GM12891	blood:	n/a
32	chr5:95046754-95046804	AoSMC	blood vessel:	n/a
33	chr5:95047327-95047377	HNPCEpiC	eye:	n/a
34	chr5:95047327-95047377	GM06990	blood:	n/a
35	chr5:95046908-95046958	PANC-1	pancreas:	n/a
36	chr5:95046754-95046804	HRPEpiC	eye:	n/a
37	chr5:95047004-95047054	U87	brain:	n/a
38	chr5:95046754-95046804	NH-A	brain:	n/a
39	chr5:95047327-95047377	BJ	skin:	n/a
40	chr5:95046754-95046804	LNCaP	prostate:	n/a
41	chr5:95047327-95047377	HAEpiC	amniotic membrane:	n/a
42	chr5:95047566-95047616	AG09319	gingival:	n/a
43	chr5:95046908-95046958	A549	lung:	n/a
44	chr5:95047004-95047054	BE2_C	brain:	n/a
45	chr5:95046754-95046804	MCF10A-Er-Src	breast:	n/a
46	chr5:95047566-95047616	HAEpiC	amniotic membrane:	n/a
47	chr5:95046908-95046958	T-47D	breast:	n/a
48	chr5:95046754-95046804	HepG2	liver:	n/a
49	chr5:95047004-95047054	HRE	kidney:	n/a
50	chr5:95047004-95047054	ProgFib	skin:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:95047903..95048629-chr5:95063452..95064037,2	MCF-7	breast:
2	chr5:95040226..95041921-chr5:95045124..95047420,2	MCF-7	breast:
3	chr5:94981368..94988467-chr5:95046173..95051252,17	K562	blood:
4	chr5:95007975..95008581-chr5:95047856..95048470,2	MCF-7	breast:
5	chr5:95040226..95041921-chr5:95045124..95047420,2	MCF-7	breast:
6	chr5:95048213..95048773-chr5:95063343..95064037,2	MCF-7	breast:
7	chr20:58386688..58388847-chr5:95046568..95048310,2	MCF-7	breast:
8	chr5:95033605..95034598-chr5:95048081..95048733,4	MCF-7	breast:
9	chr5:94983092..94984851-chr5:95042672..95044978,2	K562	blood:
10	chr5:95046797..95048565-chr5:95053368..95055074,3	MCF-7	breast:
11	chr5:95033758..95034493-chr5:95047911..95048509,2	MCF-7	breast:
12	chr5:95042298..95044229-chr5:95053844..95055562,2	MCF-7	breast:
13	chr5:95033709..95034228-chr5:95048220..95048728,2	MCF-7	breast:
14	chr5:95007953..95008475-chr5:95047970..95048751,2	MCF-7	breast:
15	chr5:95047472..95051247-chr5:95051726..95054261,3	MCF-7	breast:
16	chr5:94982459..94985191-chr5:95042644..95044600,2	MCF-7	breast:
17	chr5:95031841..95037563-chr5:95043452..95050597,14	MCF-7	breast:
18	chr5:95043022..95045914-chr5:95047072..95049996,3	MCF-7	breast:
19	chr5:94997256..95000202-chr5:95046139..95048093,2	MCF-7	breast:
20	chr5:94982238..94984113-chr5:95046187..95048295,2	MCF-7	breast:
21	chr5:95040975..95044012-chr5:95044306..95047616,3	MCF-7	breast:
22	chr5:95044657..95047785-chr5:95094774..95097386,3	MCF-7	breast:
23	chr5:95034519..95036217-chr5:95040591..95042975,2	MCF-7	breast:
24	chr5:94982722..94985316-chr5:95040916..95043420,2	K562	blood:
25	chr5:94982379..94987076-chr5:95045372..95049493,6	K562	blood:
26	chr5:95002978..95007140-chr5:95040184..95043277,3	MCF-7	breast:
27	chr5:94982383..94984588-chr5:95046353..95049787,5	MCF-7	breast:
28	chr5:95047866..95048729-chr5:95064074..95064653,3	MCF-7	breast:
29	chr5:95032657..95035811-chr5:95043701..95049648,10	MCF-7	breast:
30	chr5:95045599..95047743-chr5:95114139..95116293,2	MCF-7	breast:
31	chr5:95040975..95044012-chr5:95044306..95047616,3	MCF-7	breast:
32	chr5:95047860..95048671-chr5:95063373..95064152,4	MCF-7	breast:

No data

Variant related genes	Relation type
RHOBTB3	TF binding region
RHOBTB3	CpG island
ENSG00000175449	chromatin interactions
ENSG00000145757	chromatin interactions
ENSG00000164292	chromatin interactions

Extended variants
information (count: 267 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2348610	chr5:95041838-95041839	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375285458	chr5:95041849-95041850	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550932840	chr5:95041851-95041852	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs139626575	chr5:95041856-95041857	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs28582459	chr5:95041913-95041914	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547787607	chr5:95041953-95041954	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs386690186	chr5:95042010-95042011	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs11747231	chr5:95042012-95042013	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs184069560	chr5:95042021-95042022	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147233082	chr5:95042039-95042040	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565719917	chr5:95042040-95042041	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370616733	chr5:95042047-95042048	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538828954	chr5:95042062-95042063	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558340851	chr5:95042094-95042095	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565782349	chr5:95042123-95042124	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570227931	chr5:95042125-95042126	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2545637	chr5:95042134-95042135	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574384404	chr5:95042136-95042137	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556033795	chr5:95042142-95042143	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2548129	chr5:95042169-95042170	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185069763	chr5:95042225-95042226	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs61060540	chr5:95042230-95042231	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545607917	chr5:95042348-95042349	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565202833	chr5:95042405-95042406	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572528260	chr5:95042406-95042407	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558150006	chr5:95042408-95042409	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs33981605	chr5:95042409-95042410	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs4869247	chr5:95042438-95042439	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs2909877	chr5:95042456-95042457	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2910655	chr5:95042490-95042491	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560985076	chr5:95042532-95042533	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530044213	chr5:95042535-95042536	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201781595	chr5:95042540-95042541	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs33959300	chr5:95042542-95042543	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571626321	chr5:95042553-95042554	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549616314	chr5:95042583-95042584	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563263206	chr5:95042689-95042690	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs62366975	chr5:95042739-95042740	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs568517088	chr5:95042764-95042765	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552383161	chr5:95042822-95042823	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565617621	chr5:95042854-95042855	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543811407	chr5:95042888-95042889	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs56822333	chr5:95042915-95042916	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548199351	chr5:95042937-95042938	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568020408	chr5:95042952-95042953	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs4130725	chr5:95043008-95043009	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs534167254	chr5:95043049-95043050	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs576692880	chr5:95043050-95043051	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538844908	chr5:95043055-95043056	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs60566082	chr5:95043069-95043070	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

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
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95031400-95046000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr5:95033200-95047000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:95033400-95044400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:95034000-95045800	Weak transcription	Ovary	ovary
5	chr5:95034200-95045800	Weak transcription	Fetal Kidney	kidney
6	chr5:95034400-95043000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr5:95037800-95045800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr5:95039800-95048000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr5:95040200-95046000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:95040600-95046000	Weak transcription	HSMMtube	muscle
11	chr5:95040600-95053400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:95041200-95045800	Weak transcription	Fetal Stomach	stomach
13	chr5:95041600-95043800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:95041800-95042000	Enhancers	K562	blood
15	chr5:95042000-95042200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr5:95042000-95042800	Weak transcription	K562	blood
17	chr5:95042200-95051800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr5:95042800-95043000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr5:95042800-95043200	Flanking Active TSS	K562	blood
20	chr5:95043000-95043600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr5:95043200-95043400	Enhancers	Fetal Heart	heart
22	chr5:95043200-95045200	Enhancers	K562	blood
23	chr5:95043600-95045800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr5:95043800-95045600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:95044000-95044400	Active TSS	Placenta	Placenta
26	chr5:95044400-95044800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:95044400-95045800	Enhancers	Hela-S3	cervix
28	chr5:95044400-95046000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:95044400-95048400	Enhancers	Placenta	Placenta
30	chr5:95044800-95045600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr5:95045200-95046200	Flanking Active TSS	K562	blood
32	chr5:95045400-95045600	Enhancers	Brain Substantia Nigra	brain
33	chr5:95045400-95046800	Enhancers	Fetal Heart	heart
34	chr5:95045600-95045800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:95045600-95045800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr5:95045600-95045800	Enhancers	Brain Cingulate Gyrus	brain
37	chr5:95045600-95045800	Active TSS	Brain Hippocampus Middle	brain
38	chr5:95045600-95046000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
39	chr5:95045600-95046000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
40	chr5:95045600-95046000	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr5:95045600-95046200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:95045600-95046200	Enhancers	Right Ventricle	heart
43	chr5:95045600-95046400	Flanking Active TSS	Brain Substantia Nigra	brain
44	chr5:95045600-95046400	Enhancers	HepG2	liver
45	chr5:95045600-95048200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:95045600-95048600	Enhancers	Fetal Intestine Small	intestine
47	chr5:95045800-95046000	Enhancers	H9 Cell Line	embryonic stem cell
48	chr5:95045800-95046000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:95045800-95046000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr5:95045800-95046000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell

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