Variant report

Variant	nsv397168
Chromosome Location	chr8:59488993-59497876
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:171)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:171 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:59492340-59492490	WERI-Rb-1	eye:	n/a	n/a
2	CTCF	chr8:59492340-59492490	HAc	cerebellar:	n/a	n/a
3	CTCF	chr8:59492400-59492550	HA-sp	spinal cord:	n/a	n/a
4	CTCF	chr8:59492420-59492570	SK-N-SH_RA	brain:	n/a	n/a
5	CTCF	chr8:59492250-59492595	K562	blood:	n/a	n/a
6	CTCF	chr8:59492301-59492546	Gliobla	brain:	n/a	n/a
7	CTCF	chr8:59492377-59492462	GM12878	blood:	n/a	n/a
8	CTCF	chr8:59492320-59492470	HFF-Myc	foreskin:	n/a	n/a
9	CTCF	chr8:59492280-59492430	MCF-7	breast:	n/a	n/a
10	CTCF	chr8:59492340-59492490	AoAF	blood vessel:	n/a	n/a
11	CTCF	chr8:59492340-59492498	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr8:59492280-59492430	NHLF	lung:	n/a	n/a
13	CTCF	chr8:59492360-59492510	K562	blood:	n/a	n/a
14	CTCF	chr8:59492321-59492501	K562	blood:	n/a	n/a
15	CTCF	chr8:59492380-59492530	GM06990	blood:	n/a	n/a
16	CTCF	chr8:59492321-59492481	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr8:59492421-59492503	GM12891	blood:	n/a	n/a
18	CTCF	chr8:59492300-59492450	HMF	breast:	n/a	n/a
19	CTCF	chr8:59492391-59492474	Fibrobl	skin:	n/a	n/a
20	CTCF	chr8:59492438-59492486	GM19238	blood:	n/a	n/a
21	CTCF	chr8:59492374-59492437	HepG2	liver:	n/a	n/a
22	CTCF	chr8:59492280-59492430	A549	lung:	n/a	n/a
23	CTCF	chr8:59492280-59492430	HCM	heart:	n/a	n/a
24	CTCF	chr8:59492348-59492512	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:59492380-59492530	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr8:59492385-59492512	GM10266	blood:	n/a	n/a
27	CTCF	chr8:59492301-59492515	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:59492344-59492470	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr8:59492340-59492490	HCFaa	heart:	n/a	n/a
30	CTCF	chr8:59492440-59492590	GM12873	blood:	n/a	n/a
31	CTCF	chr8:59492400-59492550	HCT-116	colon:	n/a	n/a
32	CTCF	chr8:59492380-59492530	BE2_C	brain:	n/a	n/a
33	CTCF	chr8:59492340-59492490	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr8:59492360-59492510	GM12871	blood:	n/a	n/a
35	CTCF	chr8:59492320-59492470	AG09319	gingival:	n/a	n/a
36	CTCF	chr8:59492262-59492559	GM12878	blood:	n/a	n/a
37	CTCF	chr8:59492380-59492530	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr8:59492361-59492481	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:59492240-59492390	RPTEC	kidney:	n/a	n/a
40	CTCF	chr8:59492239-59492296	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr8:59492411-59492482	GM12892	blood:	n/a	n/a
42	CTCF	chr8:59492320-59492470	AG09309	skin:	n/a	n/a
43	CTCF	chr8:59492380-59492530	AG04450	lung:	n/a	n/a
44	CTCF	chr8:59492420-59492437	NHEK	skin:	n/a	n/a
45	CTCF	chr8:59492330-59492528	K562	blood:	n/a	n/a
46	CTCF	chr8:59492320-59492470	HFF	foreskin:	n/a	n/a
47	CTCF	chr8:59492300-59492450	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr8:59492340-59492490	SAEC	small airway:	n/a	n/a
49	CTCF	chr8:59492393-59492519	A549	lung:	n/a	n/a
50	CTCF	chr8:59492395-59492450	Pancreas_OC	pancreas:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:59494306-59494356	A549	lung:	n/a
2	chr8:59494306-59494356	AG09319	gingival:	n/a
3	chr8:59494306-59494356	CMK	blood:	n/a
4	chr8:59494306-59494356	HCT-116	colon:	n/a
5	chr8:59494306-59494356	HL-60	blood:	n/a
6	chr8:59494306-59494356	AG09309	skin:	n/a
7	chr8:59494306-59494356	GM06990	blood:	n/a
8	chr8:59494306-59494356	MCF10A-Er-Src	breast:	n/a
9	chr8:59494306-59494356	HRCEpiC	kidney:	n/a
10	chr8:59494306-59494356	PrEC	prostate:	n/a
11	chr8:59494306-59494356	HNPCEpiC	eye:	n/a
12	chr8:59494306-59494356	HEEpiC	esophagus:	n/a
13	chr8:59494306-59494356	AG04449	skin:	fetal
14	chr8:59494306-59494356	RPTEC	kidney:	n/a
15	chr8:59494306-59494356	U87	brain:	n/a
16	chr8:59494306-59494356	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:59494306-59494356	NB4	blood:	n/a
18	chr8:59494306-59494356	SK-N-SH	brain:	n/a
19	chr8:59494306-59494356	NHBE	bronchial:	n/a
20	chr8:59494306-59494356	HCF	heart:	n/a
21	chr8:59494306-59494356	NT2-D1	testis:	n/a
22	chr8:59494306-59494356	GM12878	blood:	n/a
23	chr8:59494306-59494356	HAEpiC	amniotic membrane:	n/a
24	chr8:59494306-59494356	GM12892	blood:	n/a
25	chr8:59494306-59494356	SK-N-SH_RA	brain:	n/a
26	chr8:59494306-59494356	HepG2	liver:	n/a
27	chr8:59494306-59494356	HRPEpiC	eye:	n/a
28	chr8:59494306-59494356	GM12891	blood:	n/a
29	chr8:59494306-59494356	Hela-S3	cervix:	n/a
30	chr8:59494306-59494356	HEK293	kidney:	embryo
31	chr8:59494306-59494356	HCPEpiC	choroid plexus:	n/a
32	chr8:59494306-59494356	Hepatocyte	liver:	n/a
33	chr8:59494306-59494356	HMEC	breast:	n/a
34	chr8:59494306-59494356	PFSK-1	brain:	n/a
35	chr8:59494306-59494356	AG10803	skin:	n/a
36	chr8:59494306-59494356	BE2_C	brain:	n/a
37	chr8:59494306-59494356	ovcar-3	ovarian:	n/a
38	chr8:59494306-59494356	IMR90	lung:	fetal
39	chr8:59494306-59494356	HIPEpiC	eye:	n/a
40	chr8:59494306-59494356	Caco-2	colon:	n/a
41	chr8:59494306-59494356	T-47D	breast:	n/a
42	chr8:59494306-59494356	HUVEC	blood vessel:	n/a
43	chr8:59494306-59494356	AoSMC	blood vessel:	n/a
44	chr8:59494306-59494356	K562	blood:	n/a
45	chr8:59494306-59494356	MCF-7	breast:	n/a
46	chr8:59494306-59494356	SK-N-MC	brain:	n/a
47	chr8:59494306-59494356	NHDF-neo	bronchial:	n/a
48	chr8:59494306-59494356	AG04450	lung:	fetal
49	chr8:59494306-59494356	SKMC	muscle:	n/a
50	chr8:59494306-59494356	H1-hESC	embryonic stem cell:	embryo

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:59488700..59491214-chr8:59491356..59492898,2	K562	blood:
2	chr8:59492385..59492924-chr8:59613980..59614521,2	K562	blood:
3	chr8:59470291..59472157-chr8:59493284..59495142,2	K562	blood:
4	chr8:59464704..59467459-chr8:59489336..59490887,2	MCF-7	breast:
5	chr8:59488834..59491780-chr8:59497292..59499842,2	MCF-7	breast:
6	chr8:59482062..59484180-chr8:59488026..59489607,2	K562	blood:
7	chr8:59488834..59491780-chr8:59497292..59499842,2	MCF-7	breast:
8	chr8:59465818..59467351-chr8:59492193..59494904,2	MCF-7	breast:
9	chr8:59496245..59498176-chr8:59553071..59554648,2	K562	blood:

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SDCBP	hsa-miR-155-5p	chr8:59494793-59494814
2	SDCBP	hsa-miR-155-5p	chr8:59494807-59494814
3	NSMAF	hsa-miR-92a-3p	chr8:59496577-59496598
4	SDCBP	hsa-miR-155-5p	chr8:59494890-59494914
5	NSMAF	hsa-miR-124-3p	chr8:59496657-59496664
6	NSMAF	hsa-miR-25-3p	chr8:59496583-59496577
7	SDCBP	hsa-miR-103a-3p	chr8:59494399-59494406
8	NSMAF	hsa-miR-92a-3p	chr8:59496583-59496577
9	NSMAF	hsa-miR-124-3p	chr8:59496663-59496657
10	SDCBP	hsa-miR-103a-3p	chr8:59494382-59494406
11	NSMAF	hsa-miR-25-3p	chr8:59496577-59496598
12	SDCBP	hsa-miR-103a-3p	chr8:59494922-59494944

Variant related genes	Relation type
SDCBP	TF binding region
SDCBP	CpG island
ENSG00000137575	chromatin interactions
ENSG00000035681	chromatin interactions

Extended variants
information (count: 346 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:346 , 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	rs79629779	chr8:59488993-59488994	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs565975869	chr8:59488997-59488998	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs528422108	chr8:59489014-59489015	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs189820766	chr8:59489074-59489075	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs372310921	chr8:59489108-59489109	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs181927634	chr8:59489126-59489127	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs186263792	chr8:59489237-59489238	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs556790117	chr8:59489267-59489268	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs567395472	chr8:59489292-59489293	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs535870359	chr8:59489355-59489356	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs552963413	chr8:59489369-59489370	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs572391075	chr8:59489382-59489383	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs541343666	chr8:59489387-59489388	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557900634	chr8:59489400-59489401	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs190987294	chr8:59489464-59489465	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs4574832	chr8:59489465-59489466	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs115969418	chr8:59489476-59489477	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs529434923	chr8:59489478-59489479	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs542634375	chr8:59489499-59489500	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs559817526	chr8:59489521-59489522	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs4282557	chr8:59489542-59489543	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs4400367	chr8:59489549-59489550	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs376630494	chr8:59489592-59489593	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs571428146	chr8:59489613-59489614	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs530609501	chr8:59489620-59489621	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs116004085	chr8:59489621-59489622	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs574746775	chr8:59489632-59489633	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs567230033	chr8:59489721-59489722	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs536384268	chr8:59489775-59489776	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs145070566	chr8:59489836-59489837	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs114073590	chr8:59489841-59489842	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs534937738	chr8:59489882-59489883	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs201437986	chr8:59489896-59489897	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs558037875	chr8:59489899-59489900	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs578224568	chr8:59489902-59489903	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs185213571	chr8:59489914-59489915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs149121280	chr8:59489937-59489938	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs543651282	chr8:59489946-59489947	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs143194444	chr8:59489985-59489986	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs574033405	chr8:59490005-59490006	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs78451107	chr8:59490008-59490009	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs148180928	chr8:59490095-59490096	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs17264556	chr8:59490096-59490097	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546445901	chr8:59490132-59490133	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs371510703	chr8:59490148-59490149	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs368963536	chr8:59490171-59490172	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs545460079	chr8:59490208-59490209	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs565175365	chr8:59490225-59490226	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs17264577	chr8:59490241-59490242	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs550489942	chr8:59490268-59490269	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	22522925	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59467400-59559400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:59471600-59489200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr8:59472800-59515800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:59473000-59489400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr8:59473000-59493200	Weak transcription	Fetal Heart	heart
6	chr8:59473000-59493400	Weak transcription	Esophagus	oesophagus
7	chr8:59473000-59497400	Weak transcription	Stomach Mucosa	stomach
8	chr8:59473000-59506400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr8:59473200-59493400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:59473200-59508600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr8:59473400-59492200	Weak transcription	Aorta	Aorta
12	chr8:59473400-59495400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:59474000-59497000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:59476600-59505600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:59476800-59489400	Weak transcription	Psoas Muscle	Psoas
16	chr8:59476800-59490800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr8:59476800-59495400	Weak transcription	Pancreas	Pancrea
18	chr8:59476800-59500600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:59477000-59508200	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr8:59477200-59489800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:59477200-59490600	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr8:59477200-59490600	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr8:59477200-59503000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr8:59477200-59503400	Strong transcription	NHDF-Ad	bronchial
25	chr8:59477200-59506200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr8:59477600-59493400	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr8:59477600-59496800	Strong transcription	Placenta	Placenta
28	chr8:59477600-59500600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:59477600-59503600	Strong transcription	Osteobl	bone
30	chr8:59477600-59514200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:59477800-59508800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr8:59478000-59497000	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr8:59478000-59500400	Strong transcription	NH-A	brain
34	chr8:59478000-59500800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr8:59478000-59502800	Strong transcription	Fetal Thymus	thymus
36	chr8:59478000-59503000	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr8:59478000-59503200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:59478000-59506400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr8:59478000-59508200	Strong transcription	Primary B cells from peripheral blood	blood
40	chr8:59478000-59508600	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr8:59478000-59508800	Strong transcription	Fetal Intestine Large	intestine
42	chr8:59479000-59503800	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr8:59479200-59499400	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr8:59479200-59505600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:59479600-59500600	Strong transcription	HUVEC	blood vessel
46	chr8:59479600-59508000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr8:59480400-59503000	Strong transcription	Adipose Nuclei	Adipose
48	chr8:59480600-59515800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr8:59481200-59498000	Weak transcription	Brain Substantia Nigra	brain
50	chr8:59481400-59502000	Weak transcription	Fetal Brain Male	brain

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