Variant report

Variant	esv1803360
Chromosome Location	chr8:58976889-58986166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58980001-58981335	HepG2	liver:	n/a	chr8:58980592-58980608 chr8:58980591-58980607
2	BATF	chr8:58983819-58984034	GM12878	blood:	n/a	chr8:58983935-58983946
3	BHLHE40	chr8:58980138-58980511	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:58980825-58981187	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:58980137-58980533	HepG2	liver:	n/a	n/a
6	CTCF	chr8:58979060-58979210	HBMEC	blood vessel:	n/a	n/a
7	CTCF	chr8:58980000-58980150	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr8:58979440-58979590	GM12864	blood:	n/a	n/a
9	CTCF	chr8:58980180-58980330	HMEC	breast:	n/a	n/a
10	CTCF	chr8:58980320-58980470	HRE	kidney:	n/a	n/a
11	CTCF	chr8:58980160-58980310	HMF	breast:	n/a	n/a
12	CTCF	chr8:58980120-58980270	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr8:58980220-58980370	AG04450	lung:	n/a	n/a
14	CTCF	chr8:58980220-58980370	HMF	breast:	n/a	n/a
15	CUX1	chr8:58985833-58985843	GM12878	blood:	n/a	n/a
16	EBF1	chr8:58983877-58984082	GM12878	blood:	n/a	n/a
17	EP300	chr8:58982474-58982817	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr8:58979716-58979801	HepG2	liver:	n/a	n/a
19	EP300	chr8:58980747-58981207	HepG2	liver:	n/a	chr8:58980760-58980769
20	EP300	chr8:58980068-58980584	HepG2	liver:	n/a	n/a
21	EP300	chr8:58982446-58982885	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr8:58986008-58986500	T-47D	breast:	n/a	chr8:58986259-58986269 chr8:58986278-58986292 chr8:58986282-58986291
23	EP300	chr8:58979986-58980737	HepG2	liver:	n/a	n/a
24	EP300	chr8:58980155-58980682	HepG2	liver:	n/a	n/a
25	FOS	chr8:58980206-58980517	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:58980111-58980662	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr8:58980098-58980529	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr8:58980109-58980850	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr8:58980062-58980698	HepG2	liver:	n/a	n/a
30	FOSL2	chr8:58980075-58980534	HepG2	liver:	n/a	n/a
31	FOSL2	chr8:58980086-58980661	A549	lung:	n/a	n/a
32	FOSL2	chr8:58980072-58980522	MCF-7	breast:	n/a	n/a
33	FOSL2	chr8:58980197-58980511	A549	lung:	n/a	n/a
34	FOXA1	chr8:58979922-58981136	HepG2	liver:	n/a	chr8:58980482-58980494
35	FOXA1	chr8:58986021-58986533	T-47D	breast:	n/a	chr8:58986254-58986269
36	FOXA1	chr8:58980167-58980552	T-47D	breast:	n/a	chr8:58980482-58980494
37	FOXA1	chr8:58980154-58980529	T-47D	breast:	n/a	chr8:58980482-58980494
38	FOXA1	chr8:58980041-58980672	HepG2	liver:	n/a	chr8:58980482-58980494
39	FOXA1	chr8:58980055-58980720	HepG2	liver:	n/a	chr8:58980482-58980494
40	FOXA1	chr8:58980073-58980763	HepG2	liver:	n/a	chr8:58980482-58980494
41	FOXA2	chr8:58979764-58980869	HepG2	liver:	n/a	chr8:58980482-58980494
42	FOXA2	chr8:58980099-58980594	A549	lung:	n/a	chr8:58980482-58980494
43	FOXA2	chr8:58980094-58980716	A549	lung:	n/a	chr8:58980482-58980494
44	FOXA2	chr8:58980833-58981114	HepG2	liver:	n/a	n/a
45	FOXA2	chr8:58979995-58980653	HepG2	liver:	n/a	chr8:58980482-58980494
46	GATA2	chr8:58980608-58981152	SH-SY5Y	brain:	n/a	n/a
47	GATA2	chr8:58982549-58983028	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr8:58980082-58981010	MCF-7	breast:	n/a	chr8:58980510-58980519 chr8:58980512-58980519 chr8:58980512-58980522 chr8:58980512-58980519 chr8:58980512-58980519 chr8:58980505-58980526
49	GATA3	chr8:58980632-58981159	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr8:58980138-58981519	SK-N-SH	brain:	n/a	chr8:58980510-58980519 chr8:58980512-58980519 chr8:58980512-58980522 chr8:58980512-58980519 chr8:58980512-58980519 chr8:58980505-58980526

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58982720-58982770	ProgFib	skin:	n/a
2	chr8:58982720-58982770	HCF	heart:	n/a
3	chr8:58979272-58979322	AG10803	skin:	n/a
4	chr8:58979272-58979322	ECC-1	luminal epithelium:	n/a
5	chr8:58982907-58982957	HEEpiC	esophagus:	n/a
6	chr8:58982907-58982957	SK-N-MC	brain:	n/a
7	chr8:58979272-58979322	PrEC	prostate:	n/a
8	chr8:58979272-58979322	Hepatocyte	liver:	n/a
9	chr8:58979272-58979322	NHBE	bronchial:	n/a
10	chr8:58982907-58982957	A549	lung:	n/a
11	chr8:58979272-58979322	SAEC	small airway:	n/a
12	chr8:58982907-58982957	AoSMC	blood vessel:	n/a
13	chr8:58979272-58979322	HAEpiC	amniotic membrane:	n/a
14	chr8:58982907-58982957	SK-N-SH_RA	brain:	n/a
15	chr8:58982907-58982957	GM12891	blood:	n/a
16	chr8:58982907-58982957	HAEpiC	amniotic membrane:	n/a
17	chr8:58982720-58982770	SAEC	small airway:	n/a
18	chr8:58982907-58982957	HepG2	liver:	n/a
19	chr8:58982720-58982770	SK-N-MC	brain:	n/a
20	chr8:58982907-58982957	HUVEC	blood vessel:	n/a
21	chr8:58979272-58979322	HMEC	breast:	n/a
22	chr8:58979272-58979322	HCF	heart:	n/a
23	chr8:58982907-58982957	Hepatocyte	liver:	n/a
24	chr8:58979272-58979322	AG09319	gingival:	n/a
25	chr8:58982907-58982957	GM12878	blood:	n/a
26	chr8:58982907-58982957	PFSK-1	brain:	n/a
27	chr8:58982907-58982957	NH-A	brain:	n/a
28	chr8:58982720-58982770	NB4	blood:	n/a
29	chr8:58982720-58982770	GM12891	blood:	n/a
30	chr8:58982720-58982770	HNPCEpiC	eye:	n/a
31	chr8:58982720-58982770	HIPEpiC	eye:	n/a
32	chr8:58982907-58982957	LNCaP	prostate:	n/a
33	chr8:58982720-58982770	AG10803	skin:	n/a
34	chr8:58979272-58979322	IMR90	lung:	fetal
35	chr8:58982907-58982957	U87	brain:	n/a
36	chr8:58979272-58979322	LNCaP	prostate:	n/a
37	chr8:58979272-58979322	SK-N-SH_RA	brain:	n/a
38	chr8:58982720-58982770	NH-A	brain:	n/a
39	chr8:58982720-58982770	AG04449	skin:	fetal
40	chr8:58982907-58982957	AG09319	gingival:	n/a
41	chr8:58982907-58982957	ovcar-3	ovarian:	n/a
42	chr8:58982907-58982957	NB4	blood:	n/a
43	chr8:58982720-58982770	AoSMC	blood vessel:	n/a
44	chr8:58982720-58982770	HEK293	kidney:	embryo
45	chr8:58982720-58982770	PANC-1	pancreas:	n/a
46	chr8:58982720-58982770	SK-N-SH_RA	brain:	n/a
47	chr8:58979272-58979322	H1-hESC	embryonic stem cell:	embryo
48	chr8:58982907-58982957	Caco-2	colon:	n/a
49	chr8:58979272-58979322	HRPEpiC	eye:	n/a
50	chr8:58982907-58982957	AG10803	skin:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58906976..58908719-chr8:58984081..58986529,3	MCF-7	breast:
2	chr8:58973927..58975481-chr8:58979211..58981021,2	K562	blood:
3	chr8:58972227..58973828-chr8:58977965..58980354,2	MCF-7	breast:
4	chr8:58964702..58966209-chr8:58978856..58981572,2	K562	blood:
5	chr8:58909602..58910570-chr8:58983968..58984807,2	MCF-7	breast:
6	chr8:58948042..58950902-chr8:58979793..58982678,2	MCF-7	breast:
7	chr8:58980424..58983334-chr8:58985225..58988967,3	MCF-7	breast:
8	chr8:58979230..58980915-chr8:59145278..59146797,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-1	chr8:58982786-58982921	NONHSAT126770
2	lnc-FAM110B-1	chr8:58982766-58982946	NONHSAT126769
3	lnc-FAM110B-1	chr8:58982877-58982921	NONHSAT126771

No data

Variant related genes	Relation type
FAM110B	TF binding region
FAM110B	CpG island
ENSG00000169122	chromatin interactions

Extended variants
information (count: 314 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555826343	chr8:58976938-58976939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11318730	chr8:58976954-58976955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7010934	chr8:58977019-58977020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs535159875	chr8:58977028-58977029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146517422	chr8:58977169-58977170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140796268	chr8:58977199-58977200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543259645	chr8:58977232-58977233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190814314	chr8:58977256-58977257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562104132	chr8:58977351-58977352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73682109	chr8:58977386-58977387	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs180772326	chr8:58977420-58977421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs57157697	chr8:58977486-58977487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528166618	chr8:58977495-58977496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551501494	chr8:58977502-58977503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138432485	chr8:58977665-58977666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73236465	chr8:58977669-58977670	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs111681108	chr8:58977719-58977720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550413771	chr8:58977723-58977724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111799297	chr8:58977762-58977763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148843539	chr8:58977770-58977771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7007800	chr8:58977828-58977829	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs549387770	chr8:58977847-58977848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564208737	chr8:58977851-58977852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566124291	chr8:58977909-58977910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534709655	chr8:58977927-58977928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79544225	chr8:58978009-58978010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571662477	chr8:58978016-58978017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537220163	chr8:58978022-58978023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187269126	chr8:58978099-58978100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573585898	chr8:58978118-58978119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376546069	chr8:58978287-58978288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373038929	chr8:58978314-58978315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542555310	chr8:58978320-58978321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs6988260	chr8:58978322-58978323	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs549828872	chr8:58978391-58978392	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572751974	chr8:58978396-58978397	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563316621	chr8:58978437-58978438	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs12114432	chr8:58978570-58978571	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564959174	chr8:58978602-58978603	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190835664	chr8:58978605-58978606	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549268465	chr8:58978612-58978613	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372783805	chr8:58978638-58978639	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544015962	chr8:58978641-58978642	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567426585	chr8:58978666-58978667	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565734524	chr8:58978670-58978671	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs386725875	chr8:58978804-58978805	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10093645	chr8:58978805-58978806	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs566543420	chr8:58978852-58978853	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529608176	chr8:58978877-58978878	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549649826	chr8:58978954-58978955	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58935600-58988800	Weak transcription	Aorta	Aorta
2	chr8:58952200-58986400	Weak transcription	Adipose Nuclei	Adipose
3	chr8:58952800-58979600	Weak transcription	HSMMtube	muscle
4	chr8:58958000-58979000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:58963600-58978400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:58963800-58978800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr8:58966600-58980000	Weak transcription	Ovary	ovary
8	chr8:58968800-58981000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:58969800-58979800	Weak transcription	HSMM	muscle
10	chr8:58970000-58978600	Weak transcription	Lung	lung
11	chr8:58970000-58978600	Weak transcription	Right Atrium	heart
12	chr8:58970000-58979000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr8:58970400-58978800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:58970600-58978600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:58970600-58979000	Weak transcription	NH-A	brain
16	chr8:58971000-58977600	Weak transcription	Fetal Kidney	kidney
17	chr8:58971200-58982800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:58973200-58979800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr8:58973600-58978600	Weak transcription	Psoas Muscle	Psoas
20	chr8:58973600-58982600	Weak transcription	Spleen	Spleen
21	chr8:58974000-58979800	Weak transcription	NHLF	lung
22	chr8:58974200-58978600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr8:58974200-58979000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:58974400-58978200	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr8:58974400-58979200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:58974400-58979200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr8:58974400-58979200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr8:58974400-58979600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:58974400-58979600	Weak transcription	NHDF-Ad	bronchial
30	chr8:58974600-58977400	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr8:58974600-58978600	Weak transcription	Colon Smooth Muscle	Colon
32	chr8:58974600-58979400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr8:58974800-58978400	Weak transcription	Brain Germinal Matrix	brain
34	chr8:58975600-58978800	Weak transcription	Brain Anterior Caudate	brain
35	chr8:58975800-58978400	Weak transcription	Fetal Muscle Leg	muscle
36	chr8:58975800-58978800	Weak transcription	Left Ventricle	heart
37	chr8:58975800-58978800	Weak transcription	Right Ventricle	heart
38	chr8:58975800-58979000	Weak transcription	Fetal Brain Female	brain
39	chr8:58975800-58982600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:58976000-58977200	Weak transcription	Fetal Heart	heart
41	chr8:58976000-58977600	Weak transcription	Fetal Lung	lung
42	chr8:58976000-58978400	Weak transcription	Fetal Stomach	stomach
43	chr8:58976000-58978800	Weak transcription	Fetal Brain Male	brain
44	chr8:58977200-58980400	Enhancers	Fetal Heart	heart
45	chr8:58977400-58981200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:58977600-58980200	Enhancers	Fetal Kidney	kidney
47	chr8:58977600-58981400	Enhancers	Fetal Lung	lung
48	chr8:58978200-58978400	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr8:58978200-58979200	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr8:58978200-58981400	Enhancers	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links