Variant report

Variant	nsv515883
Chromosome Location	chr5:42949688-42967215
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:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:42948996..42951624-chr5:43068211..43070769,2	MCF-7	breast:
2	chr5:42962325..42964680-chr5:43067049..43069391,2	K562	blood:
3	chr15:52860677..52861470-chr5:42950399..42950927,2	Hela-S3	cervix:
4	chr5:42950507..42951264-chr5:134475534..134476311,2	Hela-S3	cervix:
5	chr5:42949298..42951347-chr5:43007117..43009700,3	MCF-7	breast:
6	chr15:65587975..65588974-chr5:42950581..42951338,2	Hela-S3	cervix:
7	chr5:42930977..42933954-chr5:42950606..42953206,2	MCF-7	breast:
8	chr17:8023704..8024472-chr5:42950367..42950876,2	Hela-S3	cervix:
9	chr19:49138548..49139536-chr5:42949981..42950933,2	Hela-S3	cervix:
10	chr5:42953773..42956177-chr5:43040486..43043453,2	K562	blood:
11	chr5:42950468..42952623-chr5:43006794..43010300,4	MCF-7	breast:
12	chr5:42958938..42960616-chr5:42961964..42963478,2	MCF-7	breast:
13	chr18:44676633..44677401-chr5:42950458..42951078,2	Hela-S3	cervix:
14	chr1:249167058..249167599-chr5:42950376..42951299,2	Hela-S3	cervix:
15	chr5:42949709..42952302-chr5:42999079..43000906,2	MCF-7	breast:
16	chr5:42958938..42960616-chr5:42961964..42963478,2	MCF-7	breast:
17	chr11:66056545..66057202-chr5:42950293..42951110,2	Hela-S3	cervix:
18	chr5:42961475..42963380-chr5:42978584..42980242,2	K562	blood:
19	chr18:3447374..3450339-chr5:42958722..42960710,2	MCF-7	breast:
20	chr5:42949769..42951285-chr5:42989512..42991530,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF131-4	chr5:42960426-42960649	XLOC_004362
2	lnc-ZNF131-4	chr5:42950963-42959174	XLOC_004362

No data

Variant related genes	Relation type
ENSG00000177738	chromatin interactions
ENSG00000177426	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000177721	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000215068	chromatin interactions
ENSG00000271788	chromatin interactions
ENSG00000128989	chromatin interactions
ENSG00000167220	chromatin interactions

Extended variants
information (count: 778 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:778 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6870664	chr5:42949688-42949689	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185142506	chr5:42949717-42949718	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561620237	chr5:42949756-42949757	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373586531	chr5:42949822-42949823	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2548386	chr5:42949882-42949883	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs570741771	chr5:42949889-42949890	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs190120579	chr5:42949900-42949901	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs549951179	chr5:42949903-42949904	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs568160284	chr5:42949916-42949917	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs192402533	chr5:42949930-42949931	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145398998	chr5:42949931-42949932	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs6890457	chr5:42949962-42949963	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs184849341	chr5:42949974-42949975	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs6890021	chr5:42949983-42949984	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374005698	chr5:42949987-42949988	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs6890469	chr5:42949990-42949991	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs149094817	chr5:42950013-42950014	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs542189959	chr5:42950016-42950017	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs10078792	chr5:42950036-42950037	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs371551899	chr5:42950044-42950045	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370061573	chr5:42950045-42950046	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs35347455	chr5:42950076-42950077	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs541951220	chr5:42950091-42950092	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs539994216	chr5:42950139-42950140	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs565086933	chr5:42950162-42950163	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs148278973	chr5:42950186-42950187	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs116609285	chr5:42950264-42950265	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368255429	chr5:42950372-42950373	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs141310938	chr5:42950399-42950400	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs13187223	chr5:42950413-42950414	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs2548387	chr5:42950416-42950417	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs111359707	chr5:42950434-42950435	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs376784583	chr5:42950449-42950450	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs572965939	chr5:42950472-42950473	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs535667845	chr5:42950480-42950481	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs547579376	chr5:42950536-42950537	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs369092141	chr5:42950542-42950543	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs143830150	chr5:42950589-42950590	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs539491652	chr5:42950687-42950688	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs557830607	chr5:42950703-42950704	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs575935810	chr5:42950704-42950705	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs374131922	chr5:42950730-42950731	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs70991446	chr5:42950744-42950745	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs73754505	chr5:42950775-42950776	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs139757156	chr5:42950785-42950786	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs117563637	chr5:42950786-42950787	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs542036870	chr5:42950834-42950835	ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs189363994	chr5:42950851-42950852	ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs572212076	chr5:42950852-42950853	ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs545889632	chr5:42950862-42950863	ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42944600-42949800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:42944600-42949800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:42945200-42950000	Weak transcription	HSMMtube	muscle
4	chr5:42945200-42951000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:42948600-42952200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:42948800-42950800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
7	chr5:42948800-42950800	Flanking Active TSS	GM12878-XiMat	blood
8	chr5:42948800-42953000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:42949000-42949800	Enhancers	Hela-S3	cervix
10	chr5:42949000-42950000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
11	chr5:42949000-42950400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr5:42949000-42950400	Flanking Active TSS	NHDF-Ad	bronchial
13	chr5:42949000-42950600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:42949000-42950600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:42949000-42950600	Flanking Active TSS	Osteobl	bone
16	chr5:42949000-42950800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
17	chr5:42949000-42950800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:42949000-42950800	Flanking Active TSS	A549	lung
19	chr5:42949000-42950800	Flanking Active TSS	HUVEC	blood vessel
20	chr5:42949000-42950800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr5:42949000-42951000	Flanking Active TSS	Primary B cells from peripheral blood	blood
22	chr5:42949000-42951200	Weak transcription	Spleen	Spleen
23	chr5:42949000-42952200	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr5:42949000-42952400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr5:42949000-42952400	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr5:42949000-42952800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr5:42949000-42953600	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr5:42949200-42949800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
29	chr5:42949200-42949800	Enhancers	HepG2	liver
30	chr5:42949200-42950000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
31	chr5:42949200-42950000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
32	chr5:42949200-42950200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr5:42949200-42950200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
34	chr5:42949200-42950200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr5:42949200-42950200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
36	chr5:42949200-42950200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
37	chr5:42949200-42950400	Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr5:42949200-42950400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:42949200-42950400	Flanking Active TSS	NH-A	brain
40	chr5:42949200-42950600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:42949200-42950600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:42949200-42950600	Bivalent Enhancer	Fetal Intestine Large	intestine
43	chr5:42949200-42950600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
44	chr5:42949200-42950800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr5:42949200-42951000	Active TSS	Colonic Mucosa	Colon
46	chr5:42949200-42951200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr5:42949200-42951800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
48	chr5:42949200-42952000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
49	chr5:42949200-42952400	Active TSS	Aorta	Aorta
50	chr5:42949200-42952800	Bivalent/Poised TSS	Psoas Muscle	Psoas

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