Variant report

Variant	nsv1018174
Chromosome Location	chr8:58404809-58548970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1105)
CpG islands
(count:0)
Chromatin interactive
region (count:25)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58462919-58463233	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58499788-58500142	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:58492647-58493411	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:58500894-58501389	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:58476520-58477283	HepG2	liver:	n/a	n/a
6	ATF2	chr8:58492953-58493463	GM12878	blood:	n/a	n/a
7	BACH1	chr8:58428447-58428496	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr8:58493059-58493347	GM12878	blood:	n/a	chr8:58493204-58493215
9	BATF	chr8:58431541-58431841	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:58510285-58510560	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr8:58431714-58432065	GM12878	blood:	n/a	chr8:58431723-58431732
12	BCL3	chr8:58476576-58477390	A549	lung:	n/a	n/a
13	BHLHE40	chr8:58431585-58431909	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:58500849-58501230	HepG2	liver:	n/a	n/a
15	CBX3	chr8:58510249-58510452	K562	blood:	n/a	n/a
16	CBX3	chr8:58510232-58510480	HCT-116	colon:	n/a	n/a
17	CEBPB	chr8:58499731-58500732	MCF-7	breast:	n/a	chr8:58500451-58500464
18	CEBPB	chr8:58514301-58514448	A549	lung:	n/a	n/a
19	CEBPB	chr8:58500276-58500614	HepG2	liver:	n/a	chr8:58500451-58500464
20	CEBPB	chr8:58472080-58472400	A549	lung:	n/a	n/a
21	CEBPB	chr8:58500963-58501204	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:58476753-58477143	HCT-116	colon:	n/a	n/a
23	CEBPB	chr8:58476786-58477197	A549	lung:	n/a	n/a
24	CEBPB	chr8:58449571-58449863	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:58449165-58449365	A549	lung:	n/a	n/a
26	CEBPB	chr8:58476611-58477352	A549	lung:	n/a	n/a
27	CEBPB	chr8:58463015-58463318	MCF-7	breast:	n/a	n/a
28	CEBPB	chr8:58471381-58471619	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:58494550-58494740	HepG2	liver:	n/a	chr8:58494697-58494708
30	CEBPB	chr8:58540717-58540946	A549	lung:	n/a	chr8:58540781-58540792
31	CEBPB	chr8:58499687-58500231	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:58500565-58500597	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr8:58476582-58477291	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:58495747-58495758	K562	blood:	n/a	n/a
35	CEBPB	chr8:58506299-58506568	HepG2	liver:	n/a	chr8:58506491-58506504 chr8:58506397-58506408
36	CEBPB	chr8:58500915-58501211	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:58471379-58471748	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:58442628-58442636	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:58463050-58463218	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:58500390-58500522	A549	lung:	n/a	chr8:58500451-58500464
41	CEBPB	chr8:58510239-58510577	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:58471399-58471681	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:58518966-58519006	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:58463011-58463359	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:58492944-58493340	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:58528378-58528615	A549	lung:	n/a	chr8:58528492-58528503
47	CEBPB	chr8:58528410-58528618	HepG2	liver:	n/a	chr8:58528492-58528503
48	CEBPB	chr8:58510291-58510461	MCF-7	breast:	n/a	n/a
49	CEBPB	chr8:58506312-58506591	A549	lung:	n/a	chr8:58506491-58506504 chr8:58506397-58506408
50	CEBPB	chr8:58540627-58540916	HepG2	liver:	n/a	chr8:58540781-58540792

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
2	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
3	chr8:58487549..58488499-chr8:59307870..59308447,3	MCF-7	breast:
4	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
5	chr8:58489820..58490346-chr8:59307522..59308461,2	MCF-7	breast:
6	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
7	chr8:58489931..58492018-chr8:58907170..58909246,2	MCF-7	breast:
8	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
9	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
10	chr8:58487590..58488096-chr8:59301318..59302266,2	MCF-7	breast:
11	chr8:58489495..58490193-chr8:58651461..58652081,3	MCF-7	breast:
12	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
13	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
14	chr8:58487534..58488381-chr8:59156649..59157508,2	MCF-7	breast:
15	chr3:27395027..27395631-chr8:58500130..58500818,2	MCF-7	breast:
16	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
17	chr8:58489621..58490358-chr8:58651676..58652569,4	MCF-7	breast:
18	chr4:139291348..139291947-chr8:58507526..58508108,2	MCF-7	breast:
19	chr8:58499798..58502598-chr8:59323213..59325065,2	MCF-7	breast:
20	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
21	chr8:58404877..58405459-chr8:58487377..58488213,3	MCF-7	breast:
22	chr8:58332657..58333329-chr8:58487609..58488171,2	MCF-7	breast:
23	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
24	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
25	chr8:58487606..58488471-chr8:58651601..58652426,3	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-4	chr8:58405402-58405534	NONHSAT126757
2	lnc-FAM110B-10	chr8:58432559-58432637	ucscGeneNc_uc003xth_2
3	lnc-FAM110B-4	chr8:58405427-58405506	XLOC_006808
4	lnc-FAM110B-4	chr8:58405443-58405534	ENSG00000253821
5	lnc-FAM110B-4	chr8:58405458-58405534	ENSG00000253821
6	lnc-FAM110B-10	chr8:58427573-58427690	ucscGeneNc_uc003xth_2
7	lnc-FAM110B-10	chr8:58422335-58422521	ucscGeneNc_uc003xth_2
8	lnc-IMPAD1-2	chr8:58506725-58507021	ENSG00000253322
9	lnc-FAM110B-4	chr8:58458029-58463564	NONHSAT126757
10	lnc-FAM110B-10	chr8:58423482-58423699	ucscGeneNc_uc003xth_2
11	lnc-FAM110B-4	chr8:58504039-58504118	ENSG00000253821
12	lnc-FAM110B-10	chr8:58439655-58439967	ucscGeneNc_uc003xth_2
13	lnc-FAM110B-10	chr8:58418900-58419128	ucscGeneNc_uc003xth_2
14	lnc-FAM110B-10	chr8:58421807-58422176	ucscGeneNc_uc003xth_2
15	lnc-FAM110B-4	chr8:58458028-58458502	ENSG00000253821
16	lnc-FAM110B-10	chr8:58428384-58428521	ucscGeneNc_uc003xth_2
17	lnc-FAM110B-4	chr8:58405426-58405506	NONHSAT126755
18	lnc-FAM110B-10	chr8:58420077-58420253	ucscGeneNc_uc003xth_2

No data

Variant related genes	Relation type
RNU7-174P	TF binding region
ENSG00000253821	TF binding region
ENSG00000215114	chromatin interactions
ENSG00000253821	chromatin interactions

Extended variants
information (count: 4018 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4018 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553540046	chr8:58404840-58404841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573304842	chr8:58404844-58404845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545438980	chr8:58404848-58404849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149679499	chr8:58404899-58404900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549291848	chr8:58404928-58404929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145507543	chr8:58404929-58404930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188007674	chr8:58404937-58404938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10106519	chr8:58404965-58404966	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192239471	chr8:58404972-58404973	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs140294534	chr8:58404982-58404983	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs374116106	chr8:58404998-58404999	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs10106533	chr8:58405008-58405009	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551161469	chr8:58405067-58405068	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs4737459	chr8:58405076-58405077	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs552215177	chr8:58405077-58405078	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs145748146	chr8:58405082-58405083	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs531361890	chr8:58405165-58405166	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs146613741	chr8:58405177-58405178	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs527353715	chr8:58405213-58405214	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs184344073	chr8:58405226-58405227	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs188840169	chr8:58405341-58405342	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs550592655	chr8:58405344-58405345	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs192344354	chr8:58405351-58405352	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs570587684	chr8:58405380-58405381	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs112904655	chr8:58405382-58405383	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558982607	chr8:58405421-58405422	Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs575628968	chr8:58405437-58405438	Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs376928089	chr8:58405477-58405478	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs7843806	chr8:58405517-58405518	Weak transcription Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs143385339	chr8:58405530-58405531	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs575213036	chr8:58405551-58405552	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs148383803	chr8:58405564-58405565	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs560535749	chr8:58405570-58405571	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs141413108	chr8:58405592-58405593	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs55799021	chr8:58405593-58405594	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs562634950	chr8:58405617-58405618	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs150412677	chr8:58405633-58405634	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs547826798	chr8:58405644-58405645	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs143914251	chr8:58405722-58405723	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs572925982	chr8:58405764-58405765	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs548592239	chr8:58405795-58405796	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs7843986	chr8:58405819-58405820	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs184357060	chr8:58405827-58405828	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs188931510	chr8:58405927-58405928	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs7844016	chr8:58405928-58405929	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549696576	chr8:58405938-58405939	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs117608089	chr8:58405945-58405946	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs139649509	chr8:58405956-58405957	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs59177812	chr8:58405964-58405965	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs369336587	chr8:58405965-58405966	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58404000-58408000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr8:58404200-58405200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr8:58405200-58405600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr8:58405600-58406800	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr8:58406800-58407000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr8:58406800-58407000	Enhancers	HSMM	muscle
7	chr8:58407000-58408000	Weak transcription	HSMM	muscle
8	chr8:58407000-58418000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr8:58407600-58409400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:58407800-58408600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr8:58407800-58409000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:58408000-58408600	Enhancers	Osteobl	bone
13	chr8:58408000-58408800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr8:58408000-58409200	Enhancers	HSMM	muscle
15	chr8:58409400-58414800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr8:58411400-58411800	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:58411400-58412400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:58413600-58423200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr8:58413800-58415200	Enhancers	HSMMtube	muscle
20	chr8:58414000-58416800	Enhancers	HSMM	muscle
21	chr8:58414600-58414800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:58414600-58416400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr8:58414600-58416400	Enhancers	NHDF-Ad	bronchial
24	chr8:58414800-58415400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:58414800-58416000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr8:58415000-58416000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:58415200-58415600	Flanking Active TSS	HSMMtube	muscle
28	chr8:58415200-58416000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:58415400-58415800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:58415600-58416600	Enhancers	HSMMtube	muscle
31	chr8:58415800-58416000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:58416000-58418800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:58416400-58416800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr8:58416400-58418600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr8:58416600-58418400	Weak transcription	HSMMtube	muscle
36	chr8:58418000-58418400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
37	chr8:58418400-58419000	Enhancers	HSMMtube	muscle
38	chr8:58418400-58419400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:58418600-58418800	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr8:58418600-58419400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr8:58419000-58424000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:58419000-58424400	Weak transcription	HSMMtube	muscle
43	chr8:58419400-58423200	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr8:58423200-58423400	Enhancers	Rectal Smooth Muscle	rectum
45	chr8:58423200-58424000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr8:58423400-58423600	Enhancers	Ovary	ovary
47	chr8:58423400-58423800	Enhancers	Fetal Stomach	stomach
48	chr8:58423400-58424000	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr8:58423400-58424400	Enhancers	HSMM	muscle
50	chr8:58423400-58424400	Enhancers	NHDF-Ad	bronchial

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