Variant report

Variant	nsv530822
Chromosome Location	chr5:127777365-127900742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:915)
CpG islands
(count:1464)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:127806610-127806682	K562	blood:	n/a	n/a
2	ATF2	chr5:127882320-127882828	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:127873655-127874250	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr5:127882397-127882834	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr5:127872994-127873173	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr5:127872970-127873223	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr5:127782946-127783265	K562	blood:	n/a	n/a
8	CBX3	chr5:127782979-127783264	K562	blood:	n/a	n/a
9	CEBPB	chr5:127873326-127873777	A549	lung:	n/a	n/a
10	CEBPB	chr5:127806331-127806871	A549	lung:	n/a	chr5:127806590-127806601 chr5:127806840-127806853
11	CEBPB	chr5:127873371-127873769	IMR90	lung:	n/a	n/a
12	CEBPB	chr5:127806344-127806789	ECC-1	luminal epithelium:	n/a	chr5:127806590-127806601
13	CEBPB	chr5:127811720-127811815	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:127793790-127794026	A549	lung:	n/a	n/a
15	CEBPB	chr5:127873328-127874021	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr5:127811646-127811838	A549	lung:	n/a	n/a
17	CEBPB	chr5:127793833-127793982	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:127862880-127863144	A549	lung:	n/a	chr5:127863029-127863040
19	CEBPB	chr5:127806441-127806687	HepG2	liver:	n/a	chr5:127806590-127806601
20	CEBPB	chr5:127873364-127873821	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:127873460-127873807	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr5:127806411-127806785	Hela-S3	cervix:	n/a	chr5:127806590-127806601
23	CEBPB	chr5:127790534-127790630	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:127793786-127794085	IMR90	lung:	n/a	n/a
25	CEBPB	chr5:127807794-127807895	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:127874329-127874580	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr5:127873423-127873762	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:127806376-127806899	IMR90	lung:	n/a	chr5:127806590-127806601 chr5:127806840-127806853
29	CEBPB	chr5:127822981-127823246	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:127827064-127827348	IMR90	lung:	n/a	n/a
31	CEBPB	chr5:127862887-127863170	HepG2	liver:	n/a	chr5:127863029-127863040
32	CEBPB	chr5:127807752-127808076	IMR90	lung:	n/a	n/a
33	CEBPB	chr5:127806417-127806735	ECC-1	luminal epithelium:	n/a	chr5:127806590-127806601
34	CEBPB	chr5:127806448-127806753	A549	lung:	n/a	chr5:127806590-127806601
35	CEBPB	chr5:127873396-127873776	A549	lung:	n/a	n/a
36	CHD1	chr5:127873098-127873907	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr5:127872100-127872579	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr5:127874959-127875045	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr5:127872915-127873565	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr5:127872653-127873279	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr5:127874975-127875004	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr5:127873631-127873796	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr5:127874053-127874474	Hela-S3	cervix:	n/a	chr5:127874378-127874388
44	CHD2	chr5:127874123-127874655	H1-hESC	embryonic stem cell:	n/a	chr5:127874378-127874388
45	CHD2	chr5:127882382-127882841	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr5:127872352-127872825	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr5:127873712-127874982	A549	lung:	n/a	n/a
48	CTBP2	chr5:127871959-127875032	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr5:127834680-127834830	Caco-2	colon:	n/a	chr5:127834742-127834760
50	CTCF	chr5:127872820-127872970	HBMEC	blood vessel:	n/a	n/a

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:127873552-127873602	MCF10A-Er-Src	breast:	n/a
2	chr5:127872958-127873008	HepG2	liver:	n/a
3	chr5:127872037-127872087	RPTEC	kidney:	n/a
4	chr5:127874466-127874516	MCF10A-Er-Src	breast:	n/a
5	chr5:127805611-127805661	NT2-D1	testis:	n/a
6	chr5:127874463-127874513	HEEpiC	esophagus:	n/a
7	chr5:127874587-127874637	AG04449	skin:	fetal
8	chr5:127874587-127874637	PFSK-1	brain:	n/a
9	chr5:127868982-127869032	IMR90	lung:	fetal
10	chr5:127872200-127872250	A549	lung:	n/a
11	chr5:127872037-127872087	HMEC	breast:	n/a
12	chr5:127873980-127874030	GM06990	blood:	n/a
13	chr5:127873552-127873602	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:127872037-127872087	AG04450	lung:	fetal
15	chr5:127872074-127872124	PFSK-1	brain:	n/a
16	chr5:127872200-127872250	AG09309	skin:	n/a
17	chr5:127873283-127873333	AG04450	lung:	fetal
18	chr5:127873106-127873156	NHDF-neo	bronchial:	n/a
19	chr5:127871606-127871656	HCM	heart:	n/a
20	chr5:127875163-127875213	PANC-1	pancreas:	n/a
21	chr5:127835777-127835827	SK-N-MC	brain:	n/a
22	chr5:127872958-127873008	MCF-7	breast:	n/a
23	chr5:127873106-127873156	AG10803	skin:	n/a
24	chr5:127872767-127872817	BJ	skin:	n/a
25	chr5:127873552-127873602	K562	blood:	n/a
26	chr5:127874466-127874516	NB4	blood:	n/a
27	chr5:127874587-127874637	HIPEpiC	eye:	n/a
28	chr5:127873106-127873156	SK-N-MC	brain:	n/a
29	chr5:127873711-127873761	AoSMC	blood vessel:	n/a
30	chr5:127873552-127873602	ovcar-3	ovarian:	n/a
31	chr5:127874587-127874637	GM19239	blood:	n/a
32	chr5:127868982-127869032	SK-N-SH	brain:	n/a
33	chr5:127875163-127875213	HCT-116	colon:	n/a
34	chr5:127874478-127874528	MCF10A-Er-Src	breast:	n/a
35	chr5:127872074-127872124	HRPEpiC	eye:	n/a
36	chr5:127874466-127874516	RPTEC	kidney:	n/a
37	chr5:127873106-127873156	CMK	blood:	n/a
38	chr5:127835777-127835827	NHDF-neo	bronchial:	n/a
39	chr5:127874587-127874637	HCPEpiC	choroid plexus:	n/a
40	chr5:127875163-127875213	NHBE	bronchial:	n/a
41	chr5:127835777-127835827	K562	blood:	n/a
42	chr5:127868982-127869032	HRE	kidney:	n/a
43	chr5:127873980-127874030	CMK	blood:	n/a
44	chr5:127873552-127873602	SAEC	small airway:	n/a
45	chr5:127874587-127874637	HEEpiC	esophagus:	n/a
46	chr5:127874463-127874513	BE2_C	brain:	n/a
47	chr5:127872037-127872087	HAEpiC	amniotic membrane:	n/a
48	chr5:127874466-127874516	HAEpiC	amniotic membrane:	n/a
49	chr5:127873980-127874030	IMR90	lung:	fetal
50	chr5:127873552-127873602	Caco-2	colon:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:127864261..127866407-chr5:127867220..127868792,2	MCF-7	breast:
2	chr3:62270932..62271598-chr5:127779199..127780071,2	MCF-7	breast:
3	chr5:127536790..127537566-chr5:127834284..127834940,2	MCF-7	breast:
4	chr5:127896126..127898974-chr5:127902072..127903856,2	MCF-7	breast:
5	chr5:127818462..127820464-chr5:127829462..127831068,2	K562	blood:
6	chr5:127548634..127549618-chr5:127834133..127835328,8	MCF-7	breast:
7	chr5:127864261..127866407-chr5:127867220..127868792,2	MCF-7	breast:
8	chr5:127871072..127873305-chr5:127875022..127876615,2	K562	blood:
9	chr5:127871072..127873305-chr5:127875022..127876615,2	K562	blood:
10	chr5:127873521..127875105-chr5:127878457..127880160,2	MCF-7	breast:
11	chr5:127833988..127834810-chr5:128179744..128180636,2	MCF-7	breast:
12	chr5:127881388..127883013-chr5:127901894..127903649,2	MCF-7	breast:
13	chr5:127549084..127549689-chr5:127834386..127835205,3	MCF-7	breast:
14	chr5:127836111..127838712-chr5:127840672..127842489,2	K562	blood:
15	chr5:127836111..127838712-chr5:127840672..127842489,2	K562	blood:
16	chr5:127818462..127820464-chr5:127829462..127831068,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FBN2	hsa-miR-92b-3p	chr5:127777876-127777897

Variant related genes	Relation type
SLC27A6	TF binding region
FBN2	TF binding region
SLC27A6	CpG island
FBN2	CpG island
ENSG00000113396	chromatin interactions
ENSG00000138829	chromatin interactions

Extended variants
information (count: 4748 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:4748 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555167828	chr5:127777370-127777371	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs11741832	chr5:127777397-127777398	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541817876	chr5:127777430-127777431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs331078	chr5:127777463-127777464	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570329613	chr5:127777479-127777480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539321578	chr5:127777493-127777494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541261559	chr5:127777545-127777546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181303208	chr5:127777567-127777568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532123629	chr5:127777582-127777583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10067405	chr5:127777607-127777608	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs376981696	chr5:127777690-127777691	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560220459	chr5:127777716-127777717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577666120	chr5:127777764-127777765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568820595	chr5:127777780-127777781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531343015	chr5:127777782-127777783	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547851271	chr5:127777904-127777905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568377374	chr5:127777916-127777917	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17697995	chr5:127777928-127777929	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs554036197	chr5:127777970-127777971	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17164115	chr5:127777978-127777979	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs539587071	chr5:127777996-127777997	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs13180243	chr5:127777997-127777998	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs576412812	chr5:127778024-127778025	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376678476	chr5:127778078-127778079	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376184592	chr5:127778079-127778080	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542228845	chr5:127778086-127778087	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555461891	chr5:127778112-127778113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539741267	chr5:127778141-127778142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73347134	chr5:127778169-127778170	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541323457	chr5:127778241-127778242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575367455	chr5:127778284-127778285	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544337736	chr5:127778387-127778388	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577827968	chr5:127778405-127778406	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368299918	chr5:127778410-127778411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115972013	chr5:127778428-127778429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531276849	chr5:127778444-127778445	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548200213	chr5:127778451-127778452	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7712466	chr5:127778457-127778458	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs140361317	chr5:127778504-127778505	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149250115	chr5:127778550-127778551	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570716691	chr5:127778573-127778574	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144429959	chr5:127778577-127778578	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549681957	chr5:127778578-127778579	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562371026	chr5:127778669-127778670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372979909	chr5:127778708-127778709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531020565	chr5:127778715-127778716	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570166729	chr5:127778734-127778735	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73347136	chr5:127778751-127778752	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190857085	chr5:127778773-127778774	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7733090	chr5:127778810-127778811	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:77)

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
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1380 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127739200-127789000	Weak transcription	Left Ventricle	heart
2	chr5:127746000-127777600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:127747600-127784400	Weak transcription	Placenta	Placenta
4	chr5:127758400-127781800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr5:127759800-127778800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:127760600-127783200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr5:127760600-127791400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:127772600-127807600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:127772800-127781800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:127772800-127782000	Weak transcription	NHDF-Ad	bronchial
11	chr5:127772800-127787200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:127772800-127799800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:127773000-127783600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:127773000-127783800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:127773000-127785600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:127773000-127788600	Weak transcription	Fetal Heart	heart
17	chr5:127773000-127809400	Weak transcription	HMEC	breast
18	chr5:127773200-127783600	Weak transcription	NH-A	brain
19	chr5:127773200-127785600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr5:127773400-127830000	Weak transcription	NHEK	skin
21	chr5:127776000-127778400	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr5:127776000-127785600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:127776200-127777400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr5:127776200-127783600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr5:127776600-127778800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:127776800-127777400	Enhancers	Fetal Stomach	stomach
27	chr5:127776800-127777800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr5:127777000-127780200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:127777200-127777600	Weak transcription	Fetal Lung	lung
30	chr5:127777200-127778000	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr5:127777200-127782000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:127777200-127793000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr5:127777400-127780200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:127777400-127789000	Weak transcription	Fetal Stomach	stomach
35	chr5:127777600-127778200	Enhancers	Fetal Lung	lung
36	chr5:127777800-127778200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr5:127777800-127778200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:127777800-127778400	Enhancers	Colon Smooth Muscle	Colon
39	chr5:127777800-127779400	Enhancers	Fetal Kidney	kidney
40	chr5:127777800-127780200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr5:127777800-127782000	Weak transcription	Fetal Muscle Leg	muscle
42	chr5:127778000-127778800	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr5:127778200-127780400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:127778200-127783000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr5:127778400-127778600	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr5:127778400-127778800	Weak transcription	Colon Smooth Muscle	Colon
47	chr5:127778600-127780600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr5:127778800-127779200	Enhancers	Colon Smooth Muscle	Colon
49	chr5:127778800-127780200	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr5:127778800-127780400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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