Variant report

Variant	esv3402705
Chromosome Location	chr8:103821801-103824349
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:83)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:103692803..103694427-chr8:103820243..103822323,2	MCF-7	breast:
2	chr16:78495514..78497334-chr8:103819724..103822286,2	MCF-7	breast:
3	chr8:103597261..103598173-chr8:103822316..103823433,4	MCF-7	breast:
4	chr8:103769141..103772135-chr8:103823545..103826009,2	K562	blood:
5	chr8:103816389..103823057-chr8:103875264..103878654,9	K562	blood:
6	chr8:103604696..103605200-chr8:103823598..103824163,2	MCF-7	breast:
7	chr8:103663750..103664726-chr8:103822777..103823778,9	MCF-7	breast:
8	chr8:103596405..103599934-chr8:103821942..103825203,3	MCF-7	breast:
9	chr8:103241583..103244347-chr8:103821474..103823149,2	K562	blood:
10	chr10:107297880..107298668-chr8:103822352..103823075,2	MCF-7	breast:
11	chr8:103823248..103825038-chr8:103870591..103872347,2	K562	blood:
12	chr8:103696488..103698955-chr8:103820136..103822762,2	MCF-7	breast:
13	chr8:103249572..103251193-chr8:103822778..103825686,2	K562	blood:
14	chr8:103644446..103678119-chr8:103815618..103829807,419	MCF-7	breast:
15	chr8:103659827..103671648-chr8:103816894..103829599,93	K562	blood:
16	chr8:103623532..103635312-chr8:103817499..103824242,24	MCF-7	breast:
17	chr8:103758707..103761141-chr8:103820912..103822776,2	MCF-7	breast:
18	chr8:103672172..103673821-chr8:103821018..103822916,2	K562	blood:
19	chr8:103662408..103663028-chr8:103823124..103823655,2	MCF-7	breast:
20	chr8:103420136..103427906-chr8:103815410..103825210,22	MCF-7	breast:
21	chr8:103823562..103825489-chr8:103874490..103876820,2	K562	blood:
22	chr8:103663361..103664632-chr8:103822267..103823755,10	MCF-7	breast:
23	chr8:103817439..103824960-chr8:103872390..103877790,15	MCF-7	breast:
24	chr8:103801276..103802081-chr8:103821575..103822409,2	MCF-7	breast:
25	chr8:103653489..103674518-chr8:103809987..103832119,275	MCF-7	breast:
26	chr8:103740249..103747213-chr8:103818698..103822838,8	MCF-7	breast:
27	chr7:47751987..47752487-chr8:103822998..103823507,2	K562	blood:
28	chr8:103703111..103704923-chr8:103821705..103823868,2	K562	blood:
29	chr8:103665794..103666765-chr8:103822627..103823731,3	MCF-7	breast:
30	chr8:103666345..103667557-chr8:103822272..103823530,3	MCF-7	breast:
31	chr8:103693070..103695216-chr8:103822636..103825245,2	K562	blood:
32	chr8:103638288..103640009-chr8:103821096..103823943,2	MCF-7	breast:
33	chr8:103817889..103824823-chr8:103872385..103879164,18	MCF-7	breast:
34	chr8:103612874..103613451-chr8:103822619..103823333,2	MCF-7	breast:
35	chr8:103597181..103599862-chr8:103823976..103826204,2	K562	blood:
36	chr8:103667025..103668992-chr8:103822765..103823586,9	MCF-7	breast:
37	chr8:103822430..103824657-chr8:104048690..104050803,2	MCF-7	breast:
38	chr8:103740987..103747065-chr8:103820578..103824576,6	K562	blood:
39	chr8:103705965..103707674-chr8:103821217..103823842,2	K562	blood:
40	chr8:103739412..103741779-chr8:103821663..103824081,2	MCF-7	breast:
41	chr8:103660043..103660805-chr8:103823098..103823789,2	MCF-7	breast:
42	chr8:103713778..103716086-chr8:103819862..103822357,3	MCF-7	breast:
43	chr8:103626178..103629397-chr8:103820874..103826100,7	MCF-7	breast:
44	chr8:103643403..103646605-chr8:103821191..103823533,3	MCF-7	breast:
45	chr8:103422161..103424073-chr8:103822681..103825599,2	MCF-7	breast:
46	chr8:102504262..102506500-chr8:103822604..103825982,3	MCF-7	breast:
47	chr8:103674710..103676295-chr8:103820852..103822638,2	MCF-7	breast:
48	chr8:103592013..103594944-chr8:103820236..103822716,2	MCF-7	breast:
49	chr8:103742324..103745222-chr8:103822758..103824576,2	K562	blood:
50	chr8:103823092..103825494-chr8:103875474..103877752,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KB-1507C5.2.1-3	chr8:103821162-103821967	XLOC_006894

No data

Variant related genes	Relation type
ENSG00000253320	chromatin interactions
ENSG00000119707	chromatin interactions
ENSG00000254024	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000258813	chromatin interactions
ENSG00000253382	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000104517	chromatin interactions
ENSG00000155096	chromatin interactions
ENSG00000048392	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000266799	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140014442	chr8:103821879-103821880	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
2	rs530157259	chr8:103821884-103821885	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
3	rs548541205	chr8:103821902-103821903	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
4	rs542445232	chr8:103821913-103821914	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
5	rs527802560	chr8:103821940-103821941	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
6	rs182415938	chr8:103821943-103821944	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
7	rs571115330	chr8:103821987-103821988	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs538408572	chr8:103822011-103822012	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs117236286	chr8:103822062-103822063	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs557675675	chr8:103822077-103822078	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs568806584	chr8:103822102-103822103	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs373104978	chr8:103822111-103822112	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs575337532	chr8:103822145-103822146	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs535869450	chr8:103822172-103822173	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs577515495	chr8:103822220-103822221	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs202236268	chr8:103822228-103822229	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs200344007	chr8:103822229-103822230	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs201292074	chr8:103822231-103822232	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs373149910	chr8:103822244-103822245	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs187051858	chr8:103822275-103822276	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs572714329	chr8:103822285-103822286	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs79124005	chr8:103822372-103822373	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs558320630	chr8:103822386-103822387	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs560786262	chr8:103822419-103822420	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs577522554	chr8:103822421-103822422	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs544810201	chr8:103822460-103822461	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs190854859	chr8:103822466-103822467	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs575170483	chr8:103822505-103822506	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs542124682	chr8:103822562-103822563	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs373176446	chr8:103822563-103822564	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs182573792	chr8:103822572-103822573	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs112317252	chr8:103822580-103822581	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs112624174	chr8:103822595-103822596	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs527641857	chr8:103822602-103822603	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs546289692	chr8:103822617-103822618	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs111429166	chr8:103822685-103822686	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs564234034	chr8:103822722-103822723	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs144386167	chr8:103822726-103822727	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs6982674	chr8:103822734-103822735	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs35859001	chr8:103822751-103822752	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs188038544	chr8:103822752-103822753	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs550337562	chr8:103822763-103822764	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs568844057	chr8:103822784-103822785	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs530015442	chr8:103822845-103822846	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs548155655	chr8:103822874-103822875	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs566465382	chr8:103822958-103822959	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs554750954	chr8:103822985-103822986	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs533513008	chr8:103822990-103822991	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs572918607	chr8:103822992-103822993	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs71276479	chr8:103823004-103823005	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	12 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:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103816800-103822400	Enhancers	Spleen	Spleen
2	chr8:103817200-103822800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:103818600-103822200	Enhancers	HUVEC	blood vessel
4	chr8:103819200-103822800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr8:103819400-103822600	Flanking Active TSS	A549	lung
6	chr8:103819400-103822600	Flanking Active TSS	Hela-S3	cervix
7	chr8:103819400-103822800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
8	chr8:103819600-103822200	Enhancers	Primary hematopoietic stem cells	blood
9	chr8:103819600-103822400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:103819600-103822400	Enhancers	Left Ventricle	heart
11	chr8:103819600-103822600	Weak transcription	Ovary	ovary
12	chr8:103819800-103822000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr8:103819800-103822200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
14	chr8:103819800-103822200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:103819800-103822200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:103819800-103822200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:103819800-103822400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:103819800-103822400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr8:103819800-103822400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr8:103819800-103822400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr8:103819800-103822400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr8:103819800-103822400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:103819800-103822400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr8:103819800-103822400	Enhancers	Fetal Stomach	stomach
25	chr8:103819800-103822400	Enhancers	Fetal Thymus	thymus
26	chr8:103819800-103822400	Enhancers	Pancreas	Pancrea
27	chr8:103819800-103822400	Enhancers	Right Atrium	heart
28	chr8:103819800-103823000	Enhancers	Fetal Heart	heart
29	chr8:103819800-103823400	Enhancers	Stomach Mucosa	stomach
30	chr8:103819800-103823800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr8:103820000-103822000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:103820000-103822200	Enhancers	Primary B cells from cord blood	blood
33	chr8:103820000-103822200	Enhancers	K562	blood
34	chr8:103820000-103822400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:103820000-103822400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr8:103820000-103822400	Enhancers	Primary B cells from peripheral blood	blood
37	chr8:103820000-103822400	Enhancers	Primary T cells from cord blood	blood
38	chr8:103820000-103822400	Enhancers	Primary T cells fromperipheralblood	blood
39	chr8:103820000-103822400	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr8:103820000-103822400	Enhancers	Liver	Liver
41	chr8:103820000-103822400	Enhancers	Fetal Muscle Trunk	muscle
42	chr8:103820200-103822200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr8:103820200-103822200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:103820200-103822200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr8:103820200-103822200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr8:103820200-103822200	Enhancers	NHDF-Ad	bronchial
47	chr8:103820200-103822400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr8:103820200-103822400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:103820200-103822400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr8:103820200-103822400	Enhancers	Primary T helper cells fromperipheralblood	blood

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