Variant report

Variant	nsv1019518
Chromosome Location	chr8:106923469-106959075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:106945692-106945856	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:106945373-106945613	GM12878	blood:	n/a	n/a
3	CBX3	chr8:106929016-106929303	K562	blood:	n/a	n/a
4	CBX3	chr8:106930473-106930765	K562	blood:	n/a	n/a
5	CEBPB	chr8:106945296-106945660	IMR90	lung:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
6	CEBPB	chr8:106945332-106945750	MCF-7	breast:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
7	CEBPB	chr8:106945296-106945671	MCF-7	breast:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
8	CEBPB	chr8:106952099-106952272	A549	lung:	n/a	n/a
9	CEBPB	chr8:106930368-106930574	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:106941559-106941870	HepG2	liver:	n/a	chr8:106941701-106941712
11	CEBPB	chr8:106945295-106945667	K562	blood:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
12	CEBPB	chr8:106952279-106952485	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:106957833-106958113	A549	lung:	n/a	chr8:106957974-106957985 chr8:106957889-106957902 chr8:106957889-106957902
14	CEBPB	chr8:106952240-106952596	MCF-7	breast:	n/a	n/a
15	CEBPB	chr8:106957798-106958125	IMR90	lung:	n/a	chr8:106957974-106957985 chr8:106957889-106957902 chr8:106957889-106957902
16	CEBPB	chr8:106930362-106930587	A549	lung:	n/a	n/a
17	CEBPB	chr8:106941553-106941884	IMR90	lung:	n/a	chr8:106941701-106941712
18	CEBPB	chr8:106957816-106958144	Hela-S3	cervix:	n/a	chr8:106957974-106957985 chr8:106957889-106957902 chr8:106957889-106957902
19	CEBPB	chr8:106941583-106941835	H1-hESC	embryonic stem cell:	n/a	chr8:106941701-106941712
20	CEBPB	chr8:106941546-106941859	K562	blood:	n/a	chr8:106941701-106941712
21	CEBPB	chr8:106945290-106945700	Hela-S3	cervix:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
22	CEBPB	chr8:106945289-106945669	HepG2	liver:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
23	CEBPB	chr8:106957827-106958110	HepG2	liver:	n/a	chr8:106957974-106957985 chr8:106957889-106957902 chr8:106957889-106957902
24	CEBPB	chr8:106941584-106941859	A549	lung:	n/a	chr8:106941701-106941712
25	CEBPB	chr8:106957831-106958046	K562	blood:	n/a	chr8:106957974-106957985 chr8:106957889-106957902 chr8:106957889-106957902
26	CEBPB	chr8:106945305-106945651	A549	lung:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
27	CEBPB	chr8:106945319-106945647	H1-hESC	embryonic stem cell:	n/a	chr8:106945470-106945483 chr8:106945470-106945481
28	CTCF	chr8:106945283-106945587	K562	blood:	n/a	chr8:106945454-106945472 chr8:106945456-106945477
29	CTCF	chr8:106945400-106945550	HVMF	connective:	n/a	chr8:106945454-106945472 chr8:106945456-106945477
30	CTCF	chr8:106939572-106939591	GM20000	blood:	n/a	n/a
31	CTCF	chr8:106952305-106952465	MCF-7	breast:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
32	CTCF	chr8:106936621-106936742	GM20000	blood:	n/a	n/a
33	CTCF	chr8:106952340-106952490	HAc	cerebellar:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
34	CTCF	chr8:106945520-106945670	NHLF	lung:	n/a	n/a
35	CTCF	chr8:106945380-106945530	HCT-116	colon:	n/a	chr8:106945454-106945472 chr8:106945456-106945477
36	CTCF	chr8:106952320-106952470	HPAF	blood vessel:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
37	CTCF	chr8:106945320-106945470	HVMF	connective:	n/a	n/a
38	CTCF	chr8:106945400-106945550	Hela-S3	cervix:	n/a	chr8:106945454-106945472 chr8:106945456-106945477
39	CTCF	chr8:106952209-106952561	GM12878	blood:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
40	CTCF	chr8:106952440-106952590	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr8:106952280-106952430	NHEK	skin:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
42	CTCF	chr8:106951888-106953231	A549	lung:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
43	CTCF	chr8:106945400-106945550	SAEC	small airway:	n/a	chr8:106945454-106945472 chr8:106945456-106945477
44	CTCF	chr8:106952300-106952450	HRE	kidney:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
45	CTCF	chr8:106945380-106945530	AoAF	blood vessel:	n/a	chr8:106945454-106945472 chr8:106945456-106945477
46	CTCF	chr8:106945280-106945645	K562	blood:	n/a	chr8:106945454-106945472 chr8:106945456-106945477
47	CTCF	chr8:106952251-106952469	K562	blood:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
48	CTCF	chr8:106954020-106954170	AG04450	lung:	n/a	chr8:106954111-106954124
49	CTCF	chr8:106952260-106952410	AoAF	blood vessel:	n/a	chr8:106952378-106952396 chr8:106952380-106952401
50	CTCF	chr8:106945360-106945510	GM12871	blood:	n/a	chr8:106945454-106945472 chr8:106945456-106945477

No.	Distal block	Cell Line	Cell type
1	chr8:106952181..106953106-chr8:107603771..107604489,3	MCF-7	breast:
2	chr8:106956643..106958867-chr8:106976410..106978559,2	K562	blood:
3	chr8:106941329..106943808-chr8:106947861..106949687,2	K562	blood:
4	chr8:106939707..106941922-chr8:106944290..106946976,2	K562	blood:
5	chr8:106945168..106945969-chr8:107205051..107205557,2	K562	blood:
6	chr8:106944949..106945870-chr8:107534079..107534638,3	MCF-7	breast:
7	chr8:106952270..106952820-chr8:107091540..107092239,2	MCF-7	breast:
8	chr8:106951745..106953008-chr8:107603708..107604641,6	MCF-7	breast:
9	chr8:106952696..106955159-chr8:106958008..106960876,3	K562	blood:
10	chr8:106954281..106956416-chr8:106963227..106965068,2	K562	blood:
11	chr8:106917865..106918639-chr8:106952052..106952798,2	MCF-7	breast:
12	chr8:106945007..106945989-chr8:107093330..107093872,2	K562	blood:
13	chr8:106944912..106945818-chr8:107773624..107774542,2	MCF-7	breast:
14	chr8:106952696..106955159-chr8:106958008..106960876,3	K562	blood:
15	chr8:106945057..106945974-chr8:107604226..107604770,2	MCF-7	breast:
16	chr8:106938733..106940433-chr8:106941479..106943648,2	K562	blood:
17	chr8:106952193..106952705-chr8:107868814..107869363,2	MCF-7	breast:
18	chr8:106951964..106952911-chr8:107092917..107093874,3	MCF-7	breast:
19	chr8:106953058..106955739-chr8:107063560..107065111,2	K562	blood:
20	chr8:106957229..106960103-chr8:106961384..106963365,2	K562	blood:
21	chr8:106932622..106934542-chr8:106950174..106953659,3	K562	blood:
22	chr8:106932622..106934542-chr8:106950174..106953659,3	K562	blood:
23	chr8:106945333..106945909-chr8:108791751..108792331,2	MCF-7	breast:
24	chr8:106938733..106940433-chr8:106941479..106943648,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-778D12.2.1-4	chr8:106939879-106939945	ENSG00000251003.2
2	lnc-RP11-778D12.2.1-4	chr8:106924033-106924097	ENSG00000251003.2
3	lnc-RP11-778D12.2.1-4	chr8:106939879-106939945	ENSG00000251003.2
4	lnc-RP11-778D12.2.1-4	chr8:106939879-106939945	ENSG00000251003.2
5	lnc-RP11-778D12.2.1-4	chr8:106939879-106939945	ENSG00000251003.2
6	lnc-RP11-778D12.2.1-4	chr8:106939870-106939945	ENSG00000251003.2

Variant related genes	Relation type
ENSG00000251003	TF binding region
ENSG00000201627	TF binding region
ENSG00000201627	chromatin interactions

Extended variants
information (count: 696 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16873937	chr8:106923469-106923470	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183598448	chr8:106923516-106923517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189370059	chr8:106923546-106923547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541353255	chr8:106923574-106923575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181724588	chr8:106923579-106923580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185250310	chr8:106923584-106923585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545093442	chr8:106923638-106923639	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs140593478	chr8:106923666-106923667	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs530916601	chr8:106923682-106923683	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs549135248	chr8:106923736-106923737	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs567378790	chr8:106923753-106923754	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs150412168	chr8:106923756-106923757	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs190093335	chr8:106923825-106923826	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs374482761	chr8:106923864-106923865	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs571260135	chr8:106923900-106923901	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs538829177	chr8:106923905-106923906	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs181667816	chr8:106923926-106923927	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs556692234	chr8:106923981-106923982	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs138311199	chr8:106923996-106923997	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs535984463	chr8:106924007-106924008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555905324	chr8:106924013-106924014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552556890	chr8:106924035-106924036	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs9297373	chr8:106924117-106924118	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs541316914	chr8:106924140-106924141	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs553296779	chr8:106924160-106924161	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs9297374	chr8:106924171-106924172	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs74394489	chr8:106924196-106924197	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs186675373	chr8:106924253-106924254	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531015104	chr8:106924287-106924288	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542791595	chr8:106924295-106924296	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs190231667	chr8:106924303-106924304	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs528344036	chr8:106924356-106924357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546819758	chr8:106924360-106924361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374262861	chr8:106924371-106924372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181014828	chr8:106924483-106924484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149522453	chr8:106924543-106924544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185146383	chr8:106924562-106924563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144015558	chr8:106924607-106924608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534399407	chr8:106924610-106924611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540658446	chr8:106924616-106924617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200808960	chr8:106924617-106924618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565127301	chr8:106924725-106924726	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs368798758	chr8:106924727-106924728	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs554408272	chr8:106924745-106924746	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs567514390	chr8:106924760-106924761	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs73698373	chr8:106924764-106924765	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191122036	chr8:106924777-106924778	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs577880925	chr8:106924881-106924882	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs183924620	chr8:106924904-106924905	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs557310718	chr8:106924922-106924923	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
Gastric cancer	17908304	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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106915200-106930200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:106921000-106929800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:106921200-106923600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:106921600-106925200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:106922600-106925000	Weak transcription	Fetal Kidney	kidney
6	chr8:106922800-106923800	Enhancers	NHDF-Ad	bronchial
7	chr8:106923200-106924800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:106923600-106924000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:106924000-106925800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:106924800-106925000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:106924800-106925200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:106925000-106925600	Enhancers	Fetal Kidney	kidney
13	chr8:106929800-106931200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:106945600-106946000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:106947200-106947600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:106951800-106952000	Enhancers	Osteobl	bone
17	chr8:106952000-106952200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr8:106952000-106952400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:106952000-106952400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:106952000-106952400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr8:106952000-106952400	Flanking Active TSS	Osteobl	bone
22	chr8:106952200-106952400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:106952200-106952400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr8:106952200-106952600	Enhancers	Brain Angular Gyrus	brain
25	chr8:106952400-106952800	Enhancers	Osteobl	bone
26	chr8:106952400-106954000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:106952400-106957200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr8:106952800-106957400	Weak transcription	Osteobl	bone
29	chr8:106954000-106954400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:106954400-106957200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:106955200-106955400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr8:106955400-106967200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:106957200-106957600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:106957200-106957600	Enhancers	NH-A	brain
35	chr8:106957200-106958000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr8:106957200-106958000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr8:106957200-106958000	Enhancers	Aorta	Aorta
38	chr8:106957200-106958400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr8:106957400-106958400	Enhancers	Osteobl	bone

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