Variant report

Variant	nsv1033039
Chromosome Location	chr5:177873974-177926244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:694)
CpG islands
(count:1466)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177880009-177880448	K562	blood:	n/a	n/a
2	ARID3A	chr5:177875635-177876882	K562	blood:	n/a	n/a
3	ARID3A	chr5:177877562-177878156	K562	blood:	n/a	n/a
4	ARID3A	chr5:177888233-177888383	HepG2	liver:	n/a	n/a
5	ATF1	chr5:177914943-177915183	K562	blood:	n/a	n/a
6	ATF1	chr5:177876057-177876633	K562	blood:	n/a	n/a
7	BACH1	chr5:177888080-177888450	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:177876133-177876859	K562	blood:	n/a	n/a
9	BACH1	chr5:177886021-177886090	K562	blood:	n/a	n/a
10	BACH1	chr5:177920408-177920532	K562	blood:	n/a	n/a
11	BCLAF1	chr5:177876134-177876491	K562	blood:	n/a	n/a
12	BHLHE40	chr5:177876113-177877870	K562	blood:	n/a	n/a
13	BHLHE40	chr5:177918301-177918460	K562	blood:	n/a	chr5:177918370-177918383
14	BHLHE40	chr5:177880099-177880651	K562	blood:	n/a	n/a
15	BHLHE40	chr5:177895932-177896151	K562	blood:	n/a	n/a
16	BHLHE40	chr5:177921213-177921579	K562	blood:	n/a	n/a
17	BHLHE40	chr5:177910649-177910918	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:177888120-177888558	K562	blood:	n/a	n/a
19	BHLHE40	chr5:177910645-177910908	K562	blood:	n/a	n/a
20	BRCA1	chr5:177888202-177888501	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr5:177888215-177888415	HepG2	liver:	n/a	n/a
22	CBX3	chr5:177876014-177876642	K562	blood:	n/a	n/a
23	CBX3	chr5:177876066-177876600	K562	blood:	n/a	n/a
24	CCNT2	chr5:177882316-177882695	K562	blood:	n/a	n/a
25	CCNT2	chr5:177877417-177877873	K562	blood:	n/a	n/a
26	CCNT2	chr5:177876058-177876813	K562	blood:	n/a	chr5:177876543-177876552 chr5:177876671-177876680 chr5:177876666-177876675
27	CEBPB	chr5:177876094-177876517	K562	blood:	n/a	n/a
28	CEBPB	chr5:177920982-177921242	K562	blood:	n/a	chr5:177921139-177921150
29	CEBPB	chr5:177902443-177902711	K562	blood:	n/a	n/a
30	CEBPB	chr5:177877473-177877742	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:177877467-177877729	K562	blood:	n/a	n/a
32	CEBPB	chr5:177877373-177877776	K562	blood:	n/a	n/a
33	CEBPB	chr5:177888143-177888439	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:177914903-177915241	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr5:177914818-177915372	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr5:177902447-177902754	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:177876019-177876757	K562	blood:	n/a	n/a
38	CEBPB	chr5:177904469-177904775	K562	blood:	n/a	n/a
39	CEBPB	chr5:177876177-177876424	K562	blood:	n/a	n/a
40	CEBPB	chr5:177877353-177877734	K562	blood:	n/a	n/a
41	CEBPD	chr5:177875983-177876671	K562	blood:	n/a	n/a
42	CEBPD	chr5:177875989-177876659	K562	blood:	n/a	n/a
43	CHD2	chr5:177876174-177876982	K562	blood:	n/a	n/a
44	CHD2	chr5:177888031-177888478	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr5:177888188-177888499	K562	blood:	n/a	n/a
46	CHD2	chr5:177888200-177888492	GM12878	blood:	n/a	n/a
47	CHD2	chr5:177924336-177924368	HepG2	liver:	n/a	n/a
48	CHD2	chr5:177888162-177888430	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr5:177886076-177886133	K562	blood:	n/a	n/a
50	CHD2	chr5:177877485-177877502	HepG2	liver:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177915909-177915959	ECC-1	luminal epithelium:	n/a
2	chr5:177875440-177875490	SK-N-SH	brain:	n/a
3	chr5:177915909-177915959	ECC-1	luminal epithelium:	n/a
4	chr5:177875440-177875490	SK-N-SH	brain:	n/a
5	chr5:177891127-177891177	MCF-7	breast:	n/a
6	chr5:177875140-177875190	NH-A	brain:	n/a
7	chr5:177875140-177875190	SK-N-MC	brain:	n/a
8	chr5:177890047-177890097	HMEC	breast:	n/a
9	chr5:177890603-177890653	Jurkat	blood:	n/a
10	chr5:177876930-177876980	U87	brain:	n/a
11	chr5:177890863-177890913	HCF	heart:	n/a
12	chr5:177891127-177891177	RPTEC	kidney:	n/a
13	chr5:177892911-177892961	NHBE	bronchial:	n/a
14	chr5:177891127-177891177	MCF10A-Er-Src	breast:	n/a
15	chr5:177892758-177892808	HRE	kidney:	n/a
16	chr5:177916395-177916445	HAEpiC	amniotic membrane:	n/a
17	chr5:177913485-177913535	AG04450	lung:	fetal
18	chr5:177890863-177890913	HCM	heart:	n/a
19	chr5:177915909-177915959	HepG2	liver:	n/a
20	chr5:177891127-177891177	LNCaP	prostate:	n/a
21	chr5:177891221-177891271	AG04450	lung:	fetal
22	chr5:177890816-177890866	SAEC	small airway:	n/a
23	chr5:177892911-177892961	GM19239	blood:	n/a
24	chr5:177876830-177876880	RPTEC	kidney:	n/a
25	chr5:177890816-177890866	HCM	heart:	n/a
26	chr5:177889945-177889995	GM06990	blood:	n/a
27	chr5:177889945-177889995	HAEpiC	amniotic membrane:	n/a
28	chr5:177891221-177891271	SAEC	small airway:	n/a
29	chr5:177882221-177882271	HRE	kidney:	n/a
30	chr5:177915909-177915959	Caco-2	colon:	n/a
31	chr5:177915909-177915959	HRE	kidney:	n/a
32	chr5:177876930-177876980	T-47D	breast:	n/a
33	chr5:177890863-177890913	U87	brain:	n/a
34	chr5:177891127-177891177	CMK	blood:	n/a
35	chr5:177890863-177890913	HEK293	kidney:	embryo
36	chr5:177916395-177916445	GM06990	blood:	n/a
37	chr5:177913468-177913518	RPTEC	kidney:	n/a
38	chr5:177890047-177890097	GM12891	blood:	n/a
39	chr5:177876930-177876980	K562	blood:	n/a
40	chr5:177915909-177915959	AG04450	lung:	fetal
41	chr5:177892911-177892961	HepG2	liver:	n/a
42	chr5:177890863-177890913	GM19239	blood:	n/a
43	chr5:177913434-177913484	K562	blood:	n/a
44	chr5:177890047-177890097	HRE	kidney:	n/a
45	chr5:177890047-177890097	H1-hESC	embryonic stem cell:	embryo
46	chr5:177876863-177876913	IMR90	lung:	fetal
47	chr5:177913434-177913484	MCF-7	breast:	n/a
48	chr5:177875140-177875190	HNPCEpiC	eye:	n/a
49	chr5:177890816-177890866	MCF-7	breast:	n/a
50	chr5:177889945-177889995	K562	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:177873433..177876156-chr5:177880110..177882555,2	K562	blood:
2	chr5:177912045..177914389-chr5:177919098..177921696,2	MCF-7	breast:
3	chr5:177865902..177866648-chr5:177887888..177888885,2	K562	blood:
4	chr5:177861655..177863245-chr5:177875652..177877153,2	K562	blood:
5	chr5:177915163..177917911-chr5:177920254..177922621,2	K562	blood:
6	chr5:177879886..177881970-chr5:177890471..177892015,2	K562	blood:
7	chr5:177881991..177885625-chr5:177886030..177888202,3	MCF-7	breast:
8	chr5:177876265..177878231-chr5:177880241..177881910,2	K562	blood:
9	chr5:177780201..177782328-chr5:177897256..177899348,2	MCF-7	breast:
10	chr5:177706996..177707580-chr5:177887844..177888573,2	K562	blood:
11	chr5:177888252..177888759-chr5:177978244..177978784,2	K562	blood:
12	chr5:177879886..177881970-chr5:177890471..177892015,2	K562	blood:
13	chr5:177882178..177883994-chr5:177886180..177888676,2	K562	blood:
14	chr5:177912045..177914389-chr5:177919098..177921696,2	MCF-7	breast:
15	chr5:177885956..177889656-chr5:177894667..177897889,3	MCF-7	breast:
16	chr5:177633748..177635466-chr5:177877015..177878524,2	K562	blood:
17	chr15:91426417..91426918-chr5:177903850..177904350,2	NB4	blood:
18	chr5:177873433..177876156-chr5:177880110..177882555,2	K562	blood:
19	chr5:177885956..177889656-chr5:177894667..177897889,3	MCF-7	breast:
20	chr5:177881991..177885625-chr5:177886030..177888202,3	MCF-7	breast:
21	chr5:177887719..177888721-chr5:177977307..177978270,3	MCF-7	breast:
22	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:
23	chr5:177876265..177878231-chr5:177880241..177881910,2	K562	blood:
24	chr5:177888015..177888839-chr5:177977833..177978735,3	MCF-7	breast:
25	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
26	chr5:177887805..177889193-chr5:178016576..178017370,3	MCF-7	breast:
27	chr5:177894292..177896063-chr5:177897258..177899224,2	K562	blood:
28	chr5:177893036..177895122-chr5:177964444..177967291,2	K562	blood:
29	chr5:177876786..177879529-chr5:177883377..177886367,2	K562	blood:
30	chr5:177882178..177883994-chr5:177886180..177888676,2	K562	blood:
31	chr5:177879706..177881386-chr5:177883345..177884930,2	K562	blood:
32	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
33	chr5:177894292..177896063-chr5:177897258..177899224,2	K562	blood:
34	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:
35	chr5:177887745..177890184-chr5:177903224..177905118,2	K562	blood:
36	chr5:177876786..177879529-chr5:177883377..177886367,2	K562	blood:
37	chr5:177861063..177863215-chr5:177895852..177898464,2	K562	blood:
38	chr5:177871515..177874034-chr5:177875821..177877688,2	MCF-7	breast:
39	chr5:177915163..177917911-chr5:177920254..177922621,2	K562	blood:
40	chr5:177871515..177874034-chr5:177875821..177877688,2	MCF-7	breast:
41	chr5:177887745..177890184-chr5:177903224..177905118,2	K562	blood:
42	chr5:177768665..177770480-chr5:177878843..177880879,2	K562	blood:
43	chr5:177879706..177881386-chr5:177883345..177884930,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000245688	TF binding region
ENSG00000245688	CpG island

Extended variants
information (count: 2168 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6886832	chr5:177874003-177874004	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190507080	chr5:177874030-177874031	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536020627	chr5:177874066-177874067	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs147252409	chr5:177874090-177874091	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572122794	chr5:177874093-177874094	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs545879852	chr5:177874099-177874100	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs530147758	chr5:177874100-177874101	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs6887010	chr5:177874102-177874103	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs398065445	chr5:177874110-177874111	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111438237	chr5:177874131-177874132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550247374	chr5:177874198-177874199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570227983	chr5:177874205-177874206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6874268	chr5:177874219-177874220	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs560189465	chr5:177874222-177874223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561983163	chr5:177874227-177874228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532415253	chr5:177874271-177874272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182267474	chr5:177874286-177874287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540782914	chr5:177874339-177874340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186883703	chr5:177874426-177874427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549480427	chr5:177874432-177874433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527824126	chr5:177874451-177874452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376188668	chr5:177874461-177874462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552628014	chr5:177874468-177874469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570782508	chr5:177874479-177874480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190826949	chr5:177874560-177874561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531699699	chr5:177874593-177874594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367613733	chr5:177874600-177874601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150906644	chr5:177874650-177874651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568728095	chr5:177874664-177874665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536057943	chr5:177874722-177874723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554452688	chr5:177874748-177874749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566266871	chr5:177874768-177874769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539193149	chr5:177874839-177874840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182650309	chr5:177874852-177874853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575964343	chr5:177874895-177874896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552279517	chr5:177874900-177874901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543367469	chr5:177874938-177874939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73336690	chr5:177874984-177874985	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573647168	chr5:177875000-177875001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371881775	chr5:177875032-177875033	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540919908	chr5:177875035-177875036	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559158822	chr5:177875089-177875090	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532937156	chr5:177875094-177875095	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs185545176	chr5:177875111-177875112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564568473	chr5:177875117-177875118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112235660	chr5:177875121-177875122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375218079	chr5:177875147-177875148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113268776	chr5:177875151-177875152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs56410177	chr5:177875179-177875180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113538687	chr5:177875181-177875182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177856800-177887200	Weak transcription	Right Atrium	heart
2	chr5:177866600-177876200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr5:177869400-177876200	Weak transcription	Brain Angular Gyrus	brain
4	chr5:177870200-177874600	Weak transcription	K562	blood
5	chr5:177871200-177875600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr5:177871800-177880600	Weak transcription	Fetal Thymus	thymus
7	chr5:177874400-177874600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:177874600-177875400	Enhancers	K562	blood
9	chr5:177874600-177888200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:177874800-177876200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:177875400-177875800	Flanking Active TSS	K562	blood
12	chr5:177875600-177876400	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr5:177875600-177876400	Enhancers	Right Ventricle	heart
14	chr5:177875800-177876000	Active TSS	K562	blood
15	chr5:177876000-177876200	Flanking Active TSS	K562	blood
16	chr5:177876200-177876400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr5:177876200-177876400	Active TSS	Brain Cingulate Gyrus	brain
18	chr5:177876200-177876400	Enhancers	Brain Hippocampus Middle	brain
19	chr5:177876200-177876400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr5:177876200-177876400	Bivalent Enhancer	Placenta	Placenta
21	chr5:177876200-177876400	Active TSS	K562	blood
22	chr5:177876200-177876400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
23	chr5:177876200-177876600	Enhancers	Brain Angular Gyrus	brain
24	chr5:177876200-177876800	Bivalent Enhancer	Primary B cells from cord blood	blood
25	chr5:177876200-177877000	Enhancers	Left Ventricle	heart
26	chr5:177876200-177877400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr5:177876200-177877600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr5:177876200-177877600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:177876200-177877600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:177876200-177877600	Enhancers	Gastric	stomach
31	chr5:177876200-177877600	Enhancers	Spleen	Spleen
32	chr5:177876200-177877800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr5:177876200-177877800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr5:177876200-177878000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr5:177876400-177876600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:177876400-177876600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:177876400-177876600	Flanking Active TSS	Brain Cingulate Gyrus	brain
38	chr5:177876400-177876600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
39	chr5:177876400-177876800	Active TSS	Brain Hippocampus Middle	brain
40	chr5:177876400-177877000	Bivalent Enhancer	Stomach Mucosa	stomach
41	chr5:177876400-177877200	Enhancers	Fetal Heart	heart
42	chr5:177876400-177877400	Weak transcription	Right Ventricle	heart
43	chr5:177876400-177877800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
44	chr5:177876400-177877800	Flanking Active TSS	K562	blood
45	chr5:177876600-177876800	Active TSS	Brain Cingulate Gyrus	brain
46	chr5:177876600-177877000	Flanking Active TSS	Brain Angular Gyrus	brain
47	chr5:177876600-177877200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
48	chr5:177876800-177877000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:177876800-177877000	Flanking Active TSS	Brain Cingulate Gyrus	brain
50	chr5:177876800-177877000	Flanking Active TSS	Brain Hippocampus Middle	brain

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