Variant report

Variant	nsv519814
Chromosome Location	chr8:103778809-103806914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:104)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:103731630..103733859-chr8:103803496..103805362,2	MCF-7	breast:
2	chr6:33377872..33378441-chr8:103802745..103803501,2	Hela-S3	cervix:
3	chr8:103785972..103788764-chr8:103800319..103802177,2	MCF-7	breast:
4	chr8:103751112..103752616-chr8:103777186..103780062,2	MCF-7	breast:
5	chr8:103786553..103789448-chr8:103790120..103793289,3	K562	blood:
6	chr8:103659960..103661632-chr8:103784492..103786905,2	MCF-7	breast:
7	chr8:103801182..103801858-chr8:103818432..103819122,2	MCF-7	breast:
8	chr8:103610542..103615201-chr8:103799392..103803025,12	MCF-7	breast:
9	chr8:103250581..103253575-chr8:103781555..103783212,2	K562	blood:
10	chr8:103798127..103800585-chr8:103873832..103876657,2	MCF-7	breast:
11	chr8:103797903..103806624-chr8:103818327..103823736,14	K562	blood:
12	chr8:103778765..103784253-chr8:103785133..103788553,5	MCF-7	breast:
13	chr8:103768194..103770313-chr8:103790495..103792249,2	K562	blood:
14	chr8:103663783..103664326-chr8:103784923..103785885,2	MCF-7	breast:
15	chr22:26726747..26727625-chr8:103798801..103799435,2	MCF-7	breast:
16	chr8:103672477..103675226-chr8:103793415..103795051,2	MCF-7	breast:
17	chr8:103640822..103642604-chr8:103804689..103806588,2	MCF-7	breast:
18	chr8:103249417..103252086-chr8:103785588..103787097,2	MCF-7	breast:
19	chr8:103779903..103782646-chr8:103802643..103805318,2	MCF-7	breast:
20	chr8:103786553..103789448-chr8:103790011..103792533,3	K562	blood:
21	chr8:103775938..103779802-chr8:103800388..103802850,3	MCF-7	breast:
22	chr8:103668372..103669150-chr8:103798115..103798979,2	MCF-7	breast:
23	chr12:50559613..50562540-chr8:103799738..103802183,2	MCF-7	breast:
24	chr8:103768552..103771616-chr8:103798960..103803059,6	MCF-7	breast:
25	chr8:103761444..103763819-chr8:103803611..103805535,2	MCF-7	breast:
26	chr8:103627127..103628766-chr8:103799309..103800855,2	MCF-7	breast:
27	chr8:103749881..103751632-chr8:103799897..103801405,2	MCF-7	breast:
28	chr8:103801177..103801753-chr8:103822678..103823503,2	MCF-7	breast:
29	chr8:103780128..103782222-chr8:103783334..103787112,5	MCF-7	breast:
30	chr8:103760932..103779637-chr8:103816413..103823932,43	MCF-7	breast:
31	chr8:103749609..103751555-chr8:103780958..103783384,2	MCF-7	breast:
32	chr16:7601160..7603904-chr8:103805589..103808353,2	MCF-7	breast:
33	chr8:103793090..103794674-chr8:103795645..103798018,2	MCF-7	breast:
34	chr8:103778765..103784253-chr8:103785133..103788553,5	MCF-7	breast:
35	chr8:103788996..103790949-chr8:103819445..103820984,2	MCF-7	breast:
36	chr8:103775938..103779802-chr8:103800388..103802850,3	MCF-7	breast:
37	chr8:103612111..103614488-chr8:103776554..103778954,2	MCF-7	breast:
38	chr8:103613738..103615729-chr8:103803530..103805618,2	MCF-7	breast:
39	chr8:103779903..103782646-chr8:103802643..103805318,2	MCF-7	breast:
40	chr8:103801276..103802081-chr8:103821575..103822409,2	MCF-7	breast:
41	chr8:103768858..103770441-chr8:103782319..103784370,2	MCF-7	breast:
42	chr8:103801046..103802242-chr8:103819152..103820867,8	MCF-7	breast:
43	chr8:103612971..103613985-chr8:103800780..103801660,3	MCF-7	breast:
44	chr8:103793293..103798105-chr8:103798745..103802952,14	MCF-7	breast:
45	chr8:103638875..103641204-chr8:103798891..103801842,3	MCF-7	breast:
46	chr8:103664425..103672321-chr8:103786823..103809844,55	MCF-7	breast:
47	chr8:103676147..103677915-chr8:103792093..103794754,2	K562	blood:
48	chr8:103801172..103803123-chr8:103875000..103876524,2	MCF-7	breast:
49	chr8:103793090..103794674-chr8:103795645..103798018,2	MCF-7	breast:
50	chr4:106305169..106307885-chr8:103798334..103800789,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000155096	chromatin interactions
ENSG00000253669	chromatin interactions
ENSG00000048392	chromatin interactions
ENSG00000121897	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000112511	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000139624	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000253320	chromatin interactions

Extended variants
information (count: 1033 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7841186	chr8:103778809-103778810	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567484647	chr8:103778834-103778835	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534838930	chr8:103778837-103778838	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546784758	chr8:103778845-103778846	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7826496	chr8:103778892-103778893	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538889453	chr8:103778929-103778930	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs145412572	chr8:103778930-103778931	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs376268975	chr8:103778970-103778971	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs568751162	chr8:103778997-103778998	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536382193	chr8:103779015-103779016	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs7827032	chr8:103779027-103779028	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572568540	chr8:103779062-103779063	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs147695606	chr8:103779066-103779067	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs116204575	chr8:103779069-103779070	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577162982	chr8:103779107-103779108	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs536618431	chr8:103779163-103779164	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544566059	chr8:103779171-103779172	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192398705	chr8:103779203-103779204	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530019662	chr8:103779217-103779218	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185541784	chr8:103779250-103779251	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs542180765	chr8:103779258-103779259	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs377197064	chr8:103779303-103779304	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs199889084	chr8:103779377-103779378	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34332325	chr8:103779379-103779380	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560586254	chr8:103779415-103779416	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs386728361	chr8:103779426-103779427	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs559523111	chr8:103779433-103779434	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs73701512	chr8:103779458-103779459	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532490679	chr8:103779470-103779471	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs139615871	chr8:103779563-103779564	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs142638243	chr8:103779580-103779581	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs151006283	chr8:103779623-103779624	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs552372051	chr8:103779740-103779741	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190414029	chr8:103779780-103779781	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs28608974	chr8:103779823-103779824	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs140898323	chr8:103779839-103779840	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs191955052	chr8:103779858-103779859	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184521184	chr8:103779868-103779869	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189228358	chr8:103779945-103779946	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544915924	chr8:103779950-103779951	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562030832	chr8:103779955-103779956	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs573276674	chr8:103779963-103779964	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556602709	chr8:103779968-103779969	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368654028	chr8:103780037-103780038	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575043841	chr8:103780056-103780057	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs150172862	chr8:103780057-103780058	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560479445	chr8:103780085-103780086	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs181200588	chr8:103780145-103780146	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs546310985	chr8:103780148-103780149	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565111372	chr8:103780248-103780249	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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

Chromatin state (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103767200-103779000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr8:103772400-103780200	Weak transcription	A549	lung
3	chr8:103774200-103779600	Weak transcription	Psoas Muscle	Psoas
4	chr8:103774400-103779200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:103774600-103779000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr8:103774600-103779200	Weak transcription	Lung	lung
7	chr8:103774600-103779200	Weak transcription	Pancreas	Pancrea
8	chr8:103774600-103779600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:103774800-103780000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:103775000-103779000	Weak transcription	Aorta	Aorta
11	chr8:103775000-103779000	Weak transcription	Right Atrium	heart
12	chr8:103775000-103779600	Weak transcription	Fetal Lung	lung
13	chr8:103775000-103780000	Weak transcription	Brain Anterior Caudate	brain
14	chr8:103776600-103790600	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr8:103776800-103779600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr8:103777000-103779600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:103777000-103780000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr8:103777200-103779200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr8:103777200-103780400	Weak transcription	Osteobl	bone
20	chr8:103777400-103779400	Weak transcription	Primary T cells from cord blood	blood
21	chr8:103777600-103779000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr8:103777600-103779400	Weak transcription	Adipose Nuclei	Adipose
23	chr8:103777600-103779800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:103777600-103779800	Weak transcription	NHEK	skin
25	chr8:103778600-103779800	Enhancers	Colon Smooth Muscle	Colon
26	chr8:103778600-103781600	Enhancers	Fetal Muscle Leg	muscle
27	chr8:103778800-103780000	Bivalent Enhancer	HepG2	liver
28	chr8:103778800-103782600	Enhancers	Fetal Muscle Trunk	muscle
29	chr8:103778800-103783800	Enhancers	Fetal Thymus	thymus
30	chr8:103779000-103779600	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr8:103779000-103779600	Enhancers	Stomach Smooth Muscle	stomach
32	chr8:103779000-103780000	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr8:103779000-103782600	Enhancers	Placenta	Placenta
34	chr8:103779000-103783600	Enhancers	Right Atrium	heart
35	chr8:103779000-103783800	Enhancers	Aorta	Aorta
36	chr8:103779200-103779600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:103779200-103780000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr8:103779200-103780200	Enhancers	Fetal Heart	heart
39	chr8:103779200-103780400	Enhancers	Colonic Mucosa	Colon
40	chr8:103779200-103780600	Enhancers	Rectal Smooth Muscle	rectum
41	chr8:103779200-103781000	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr8:103779200-103781200	Enhancers	Fetal Stomach	stomach
43	chr8:103779200-103782600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:103779200-103783000	Enhancers	Left Ventricle	heart
45	chr8:103779200-103783000	Enhancers	Lung	lung
46	chr8:103779200-103783400	Enhancers	Right Ventricle	heart
47	chr8:103779200-103783600	Enhancers	Pancreas	Pancrea
48	chr8:103779200-103783800	Enhancers	HMEC	breast
49	chr8:103779400-103780000	Enhancers	Primary T cells from cord blood	blood
50	chr8:103779400-103780600	Enhancers	Monocytes-CD14+_RO01746	blood

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