Variant report

Variant	nsv981972
Chromosome Location	chr8:103935652-103937242
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	ARID3A	chr8:103936915-103937705	K562	blood:	n/a	n/a
2	ATF2	chr8:103937145-103937485	GM12878	blood:	n/a	n/a
3	ATF2	chr8:103936977-103937537	GM12878	blood:	n/a	n/a
4	BACH1	chr8:103937084-103937325	K562	blood:	n/a	n/a
5	BACH1	chr8:103937109-103937266	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:103937096-103937421	GM12878	blood:	n/a	n/a
7	BCL3	chr8:103936928-103937579	A549	lung:	n/a	n/a
8	BCL3	chr8:103936982-103937538	A549	lung:	n/a	n/a
9	BHLHE40	chr8:103937222-103937416	K562	blood:	n/a	n/a
10	BRCA1	chr8:103937125-103937358	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr8:103936891-103937738	K562	blood:	n/a	chr8:103936916-103936927
12	CHD2	chr8:103937216-103937459	GM12878	blood:	n/a	n/a
13	CUX1	chr8:103937004-103937644	K562	blood:	n/a	n/a
14	CUX1	chr8:103937080-103937246	GM12878	blood:	n/a	n/a
15	E2F4	chr8:103937000-103937398	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr8:103937161-103937497	GM12878	blood:	n/a	n/a
17	EBF1	chr8:103937115-103937611	GM12878	blood:	n/a	n/a
18	ELK1	chr8:103937132-103937406	GM12878	blood:	n/a	n/a
19	EP300	chr8:103937053-103937491	GM12878	blood:	n/a	n/a
20	EP300	chr8:103937076-103937777	Hela-S3	cervix:	n/a	chr8:103937652-103937666
21	EP300	chr8:103936959-103937937	K562	blood:	n/a	chr8:103937652-103937666
22	EP300	chr8:103936978-103937484	GM12878	blood:	n/a	n/a
23	EP300	chr8:103937175-103937566	GM12878	blood:	n/a	n/a
24	FOS	chr8:103937022-103937899	MCF10A-Er-Src	breast:	n/a	chr8:103937227-103937237 chr8:103937227-103937237 chr8:103937226-103937238 chr8:103937228-103937236 chr8:103937227-103937237
25	FOS	chr8:103937015-103937398	MCF10A-Er-Src	breast:	n/a	chr8:103937227-103937237 chr8:103937227-103937237 chr8:103937226-103937238 chr8:103937228-103937236 chr8:103937227-103937237
26	FOS	chr8:103937056-103937427	MCF10A-Er-Src	breast:	n/a	chr8:103937227-103937237 chr8:103937227-103937237 chr8:103937226-103937238 chr8:103937228-103937236 chr8:103937227-103937237
27	FOS	chr8:103937080-103937875	MCF10A-Er-Src	breast:	n/a	chr8:103937227-103937237 chr8:103937227-103937237 chr8:103937226-103937238 chr8:103937228-103937236 chr8:103937227-103937237
28	FOSL2	chr8:103936877-103938006	A549	lung:	n/a	chr8:103937227-103937237 chr8:103937227-103937237 chr8:103937226-103937238 chr8:103937228-103937236 chr8:103937227-103937237
29	FOSL2	chr8:103936961-103937514	MCF-7	breast:	n/a	chr8:103937227-103937237 chr8:103937227-103937237 chr8:103937226-103937238 chr8:103937228-103937236 chr8:103937227-103937237
30	FOXM1	chr8:103936957-103937565	GM12878	blood:	n/a	n/a
31	FOXM1	chr8:103937046-103937591	GM12878	blood:	n/a	n/a
32	GATA1	chr8:103937033-103937819	PBDE	blood:	n/a	n/a
33	GTF2F1	chr8:103936964-103937314	Hela-S3	cervix:	n/a	n/a
34	JUND	chr8:103936995-103937910	K562	blood:	n/a	chr8:103937227-103937237 chr8:103937227-103937237 chr8:103937226-103937238 chr8:103937228-103937236 chr8:103937227-103937237
35	MAFF	chr8:103936979-103937799	K562	blood:	n/a	n/a
36	MAFK	chr8:103936851-103937902	IMR90	lung:	n/a	chr8:103937226-103937235 chr8:103937226-103937236
37	MAFK	chr8:103936998-103937520	K562	blood:	n/a	chr8:103937226-103937235 chr8:103937226-103937236
38	MAFK	chr8:103937060-103937424	Hela-S3	cervix:	n/a	chr8:103937226-103937235 chr8:103937226-103937236
39	MAFK	chr8:103937040-103937296	H1-hESC	embryonic stem cell:	n/a	chr8:103937226-103937235 chr8:103937226-103937236
40	MAX	chr8:103937006-103938344	A549	lung:	n/a	n/a
41	MAX	chr8:103936882-103938358	A549	lung:	n/a	n/a
42	MAZ	chr8:103937230-103937603	GM12878	blood:	n/a	n/a
43	MAZ	chr8:103937020-103937559	K562	blood:	n/a	n/a
44	MXI1	chr8:103937041-103937411	GM12878	blood:	n/a	n/a
45	MYC	chr8:103937131-103937398	MCF10A-Er-Src	breast:	n/a	n/a
46	MYC	chr8:103937113-103937381	MCF10A-Er-Src	breast:	n/a	n/a
47	NFIC	chr8:103936993-103937516	GM12878	blood:	n/a	n/a
48	NFIC	chr8:103936777-103937603	GM12878	blood:	n/a	n/a
49	NR2F2	chr8:103936961-103937980	K562	blood:	n/a	n/a
50	NR3C1	chr8:103937108-103937512	A549	lung:	n/a	chr8:103937227-103937236

No.	Distal block	Cell Line	Cell type
1	chr8:103875112..103878223-chr8:103936319..103939684,4	K562	blood:
2	chr8:103876310..103878750-chr8:103935739..103937868,3	MCF-7	breast:
3	chr8:103937164..103938846-chr8:103972423..103974367,2	MCF-7	breast:
4	chr8:103874816..103877664-chr8:103936329..103938732,4	MCF-7	breast:
5	chr8:103936608..103938218-chr8:104032062..104033919,2	MCF-7	breast:
6	chr8:103936331..103939322-chr8:103948640..103950158,2	K562	blood:

Variant related genes	Relation type
ENSG00000253320	TF binding region
RPL5P24	TF binding region
ENSG00000155096	chromatin interactions
ENSG00000155097	chromatin interactions
ENSG00000265898	chromatin interactions
ENSG00000254236	chromatin interactions
ENSG00000253320	chromatin interactions

Extended variants
information (count: 58 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:58 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532059975	chr8:103935686-103935687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185449244	chr8:103935687-103935688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190258232	chr8:103935735-103935736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78697150	chr8:103935737-103935738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553706248	chr8:103935747-103935748	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs565849170	chr8:103935787-103935788	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs539509823	chr8:103935798-103935799	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558348928	chr8:103935799-103935800	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs576938325	chr8:103935817-103935818	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs544527594	chr8:103935838-103935839	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs556174271	chr8:103935843-103935844	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs548859001	chr8:103935866-103935867	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373549584	chr8:103935897-103935898	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541462852	chr8:103935911-103935912	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs62526535	chr8:103935912-103935913	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs527404995	chr8:103935924-103935925	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs545893237	chr8:103935935-103935936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs564705446	chr8:103935961-103935962	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370320905	chr8:103935974-103935975	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs182153943	chr8:103936048-103936049	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550499173	chr8:103936056-103936057	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs530938000	chr8:103936167-103936168	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs529553362	chr8:103936193-103936194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs547405724	chr8:103936229-103936230	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186760439	chr8:103936255-103936256	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs539571390	chr8:103936304-103936305	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs550959949	chr8:103936308-103936309	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530261430	chr8:103936321-103936322	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs570665200	chr8:103936331-103936332	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs193051250	chr8:103936340-103936341	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs556276179	chr8:103936350-103936351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2668877	chr8:103936429-103936430	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs558503889	chr8:103936487-103936488	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535714337	chr8:103936499-103936500	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs6988956	chr8:103936501-103936502	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564024106	chr8:103936540-103936541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs184120003	chr8:103936588-103936589	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543665869	chr8:103936627-103936628	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs531065675	chr8:103936686-103936687	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs188214465	chr8:103936689-103936690	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs193158187	chr8:103936691-103936692	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs534659647	chr8:103936711-103936712	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs547660912	chr8:103936788-103936789	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs559354245	chr8:103936809-103936810	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs71930792	chr8:103936851-103936852	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs200094734	chr8:103936855-103936856	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs2513878	chr8:103936856-103936857	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs574352405	chr8:103936912-103936913	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs61244485	chr8:103936924-103936925	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs397977108	chr8:103936931-103936932	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103923200-103935800	Weak transcription	Fetal Lung	lung
2	chr8:103926400-103937400	Weak transcription	Lung	lung
3	chr8:103926600-103936600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr8:103927800-103939800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:103927800-103941600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:103930000-103938000	Weak transcription	Gastric	stomach
7	chr8:103931200-103936800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:103931400-103936800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:103931800-103937000	Weak transcription	Colon Smooth Muscle	Colon
10	chr8:103931800-103941600	Weak transcription	Fetal Kidney	kidney
11	chr8:103932000-103936800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr8:103932000-103937200	Weak transcription	Brain Hippocampus Middle	brain
13	chr8:103932000-103939400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr8:103932200-103936000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr8:103932200-103959400	Weak transcription	Fetal Brain Female	brain
16	chr8:103932400-103937000	Weak transcription	Aorta	Aorta
17	chr8:103932400-103937200	Weak transcription	Placenta	Placenta
18	chr8:103932400-103939800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr8:103932600-103937200	Weak transcription	Small Intestine	intestine
20	chr8:103932800-103937200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr8:103932800-103937400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr8:103932800-103938800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:103932800-103939400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr8:103932800-103939600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr8:103933000-103936200	Weak transcription	Fetal Stomach	stomach
26	chr8:103933000-103936600	Weak transcription	GM12878-XiMat	blood
27	chr8:103933000-103937200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr8:103933000-103937200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:103933000-103937200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:103933000-103937200	Weak transcription	Right Atrium	heart
31	chr8:103933000-103937400	Weak transcription	Pancreas	Pancrea
32	chr8:103933000-103939800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr8:103933200-103937000	Weak transcription	Fetal Intestine Large	intestine
34	chr8:103933200-103937000	Weak transcription	Ovary	ovary
35	chr8:103933200-103937200	Weak transcription	Right Ventricle	heart
36	chr8:103933400-103935800	Weak transcription	A549	lung
37	chr8:103933400-103935800	Weak transcription	NHLF	lung
38	chr8:103933400-103936600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr8:103933400-103937000	Weak transcription	Fetal Intestine Small	intestine
40	chr8:103933400-103937000	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr8:103933400-103937200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr8:103933400-103937200	Weak transcription	Stomach Mucosa	stomach
43	chr8:103933400-103940000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:103933600-103936000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr8:103933600-103936200	Weak transcription	Fetal Heart	heart
46	chr8:103933600-103936400	Weak transcription	NHDF-Ad	bronchial
47	chr8:103933600-103936600	Weak transcription	Osteobl	bone
48	chr8:103933600-103937200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr8:103934000-103935800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr8:103934200-103937000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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