Variant report

Variant	esv3353743
Chromosome Location	chr20:52476445-52485443
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:143)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:143 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr20:52482302..52483839-chr20:52727165..52730009,2	MCF-7	breast:
2	chr20:52480563..52482351-chr9:126090029..126091702,2	MCF-7	breast:
3	chr17:57913854..57916854-chr20:52481054..52484411,4	MCF-7	breast:
4	chr20:52481633..52483659-chr3:119812549..119814551,2	MCF-7	breast:
5	chr17:57920817..57923301-chr20:52482910..52485730,2	MCF-7	breast:
6	chr1:26797035..26798935-chr20:52477868..52479858,2	MCF-7	breast:
7	chr20:52403738..52404269-chr20:52481124..52481895,2	MCF-7	breast:
8	chr12:53341666..53344368-chr20:52478824..52481024,2	MCF-7	breast:
9	chr20:52484501..52486317-chr6:34526583..34529198,2	MCF-7	breast:
10	chr20:52480111..52481859-chr6:21593030..21595290,2	MCF-7	breast:
11	chr20:52462487..52463357-chr20:52481724..52482466,3	MCF-7	breast:
12	chr20:52480121..52486257-chr20:55824427..55830996,6	MCF-7	breast:
13	chr20:52480308..52482647-chr3:156271373..156273715,2	MCF-7	breast:
14	chr20:52483064..52485443-chr7:29327053..29329425,2	MCF-7	breast:
15	chr20:49358154..49361002-chr20:52481386..52484444,3	MCF-7	breast:
16	chr20:52471901..52491673-chr20:55835708..55845674,34	MCF-7	breast:
17	chr20:52481918..52484276-chr20:55753867..55756347,2	MCF-7	breast:
18	chr20:52278292..52278903-chr20:52480742..52481616,3	MCF-7	breast:
19	chr20:52484288..52486178-chr4:88957310..88959480,2	MCF-7	breast:
20	chr13:28501323..28502030-chr20:52481842..52482437,2	MCF-7	breast:
21	chr20:52483983..52486847-chr6:26156318..26159151,2	MCF-7	breast:
22	chr19:1214467..1217115-chr20:52481524..52483245,2	MCF-7	breast:
23	chr12:58138537..58140112-chr20:52481997..52483617,2	MCF-7	breast:
24	chr20:52483639..52484202-chr20:52556102..52557084,2	MCF-7	breast:
25	chr17:56707643..56709532-chr20:52480297..52482944,2	MCF-7	breast:
26	chr17:59939092..59941762-chr20:52481316..52482941,2	MCF-7	breast:
27	chr20:45988422..45990533-chr20:52480760..52483220,2	MCF-7	breast:
28	chr20:52482916..52483597-chr20:52531915..52532688,3	MCF-7	breast:
29	chr17:57921050..57924844-chr20:52479420..52483981,7	MCF-7	breast:
30	chr20:52481676..52483648-chr20:52685803..52687304,2	MCF-7	breast:
31	chr20:52481362..52483334-chr4:100456733..100459317,2	MCF-7	breast:
32	chr17:56706335..56710914-chr20:52478718..52484082,7	MCF-7	breast:
33	chr20:52479588..52482520-chr20:52814960..52817385,2	MCF-7	breast:
34	chr20:52210074..52211092-chr20:52482654..52483935,3	MCF-7	breast:
35	chr2:25014323..25015853-chr20:52481121..52482725,2	MCF-7	breast:
36	chr10:104470223..104472461-chr20:52479681..52481593,2	MCF-7	breast:
37	chr16:1020617..1022475-chr20:52480079..52481826,2	MCF-7	breast:
38	chr17:59578043..59580081-chr20:52480934..52483362,2	MCF-7	breast:
39	chr20:52479216..52480867-chr8:63834559..63837540,2	MCF-7	breast:
40	chr17:59652154..59652890-chr20:52480568..52481434,2	MCF-7	breast:
41	chr20:52462474..52463337-chr20:52480867..52481393,2	MCF-7	breast:
42	chr1:113247492..113249614-chr20:52480900..52482881,2	MCF-7	breast:
43	chr20:52195366..52195877-chr20:52484212..52484846,2	MCF-7	breast:
44	chr1:42043636..42046059-chr20:52480512..52482758,2	MCF-7	breast:
45	chr20:52484799..52486540-chr20:52532724..52534997,2	K562	blood:
46	chr20:52390169..52390831-chr20:52481716..52482235,2	MCF-7	breast:
47	chr17:79480745..79482983-chr20:52482594..52484140,2	MCF-7	breast:
48	chr17:43867694..43870674-chr20:52481399..52483362,2	MCF-7	breast:
49	chr20:52195106..52195625-chr20:52482924..52483862,2	MCF-7	breast:
50	chr12:66506885..66508576-chr20:52484476..52487409,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000136492	chromatin interactions
ENSG00000124766	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000103227	chromatin interactions
ENSG00000267100	chromatin interactions
ENSG00000111057	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000267064	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000229848	chromatin interactions
ENSG00000263826	chromatin interactions
ENSG00000155366	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000046647	chromatin interactions
ENSG00000184863	chromatin interactions
ENSG00000129351	chromatin interactions
ENSG00000101115	chromatin interactions
ENSG00000216895	chromatin interactions
ENSG00000135452	chromatin interactions
ENSG00000241721	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000127124	chromatin interactions
ENSG00000235448	chromatin interactions
ENSG00000013288	chromatin interactions
ENSG00000064787	chromatin interactions
ENSG00000260793	chromatin interactions
ENSG00000169564	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000184924	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000170832	chromatin interactions
ENSG00000106069	chromatin interactions
ENSG00000082701	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000184640	chromatin interactions
ENSG00000235527	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000267882	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000179818	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000114850	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000126756	chromatin interactions
ENSG00000150753	chromatin interactions

Extended variants
information (count: 668 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:668 , 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	rs73273910	chr20:52476492-52476493	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs568045319	chr20:52476509-52476510	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs386815147	chr20:52476533-52476534	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs112062134	chr20:52476534-52476535	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs73912530	chr20:52476535-52476536	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs372227844	chr20:52476558-52476559	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs386815148	chr20:52476574-52476575	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs73912532	chr20:52476575-52476576	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs73912533	chr20:52476621-52476622	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs146405604	chr20:52476622-52476623	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs73273912	chr20:52476625-52476626	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs139105881	chr20:52476628-52476629	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs556897791	chr20:52476638-52476639	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs375454154	chr20:52476652-52476653	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs576766410	chr20:52476669-52476670	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs386815149	chr20:52476676-52476677	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs79172558	chr20:52476677-52476678	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs368251470	chr20:52476679-52476680	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs77069881	chr20:52476687-52476688	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs538029878	chr20:52476727-52476728	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs73273914	chr20:52476740-52476741	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs73273916	chr20:52476777-52476778	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs80056881	chr20:52476793-52476794	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs542496644	chr20:52476802-52476803	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs73146544	chr20:52476821-52476822	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs74477165	chr20:52476830-52476831	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs113409360	chr20:52476832-52476833	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs74854063	chr20:52476840-52476841	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs561970789	chr20:52476858-52476859	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs73146547	chr20:52476859-52476860	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs73146548	chr20:52476863-52476864	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs34444378	chr20:52476872-52476873	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs67810428	chr20:52476888-52476889	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs527672055	chr20:52476907-52476908	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs80130005	chr20:52476914-52476915	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs113711840	chr20:52476915-52476916	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs541185030	chr20:52476918-52476919	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs79547894	chr20:52476928-52476929	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs78095871	chr20:52476929-52476930	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs572175097	chr20:52476943-52476944	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs74427507	chr20:52476951-52476952	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs114885943	chr20:52476953-52476954	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs78421131	chr20:52476958-52476959	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs11699038	chr20:52476965-52476966	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs76972629	chr20:52476975-52476976	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs531546789	chr20:52476989-52476990	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs534911960	chr20:52476991-52476992	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs73146553	chr20:52476992-52476993	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs11699059	chr20:52477008-52477009	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs35704771	chr20:52477011-52477012	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myelodysplastic syndrome	21251322	CNVD
Ductal carcinoma	22052326	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Colorectal cancer	16774939	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Ovarian cancer	22174824	CNVD
Lung cancer	16740712	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16620391	CNVD
Okamoto syndrome	17623483	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cervical cancer	16585170	CNVD
Ovarian cancer	20844748	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20459607	CNVD
Gastric cancer	18160780	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Medulloblastoma	16783165	CNVD

Chromatin state (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52453600-52480200	Weak transcription	Small Intestine	intestine
2	chr20:52468800-52481400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr20:52472200-52476600	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr20:52472400-52480800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr20:52473200-52480200	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr20:52474000-52476600	Enhancers	Stomach Mucosa	stomach
7	chr20:52474200-52476600	Enhancers	Duodenum Mucosa	Duodenum
8	chr20:52474600-52480200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:52474600-52480200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr20:52474600-52481600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr20:52474800-52479600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr20:52474800-52480000	Weak transcription	Ovary	ovary
13	chr20:52474800-52480000	Weak transcription	A549	lung
14	chr20:52474800-52480200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr20:52474800-52480200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr20:52474800-52480200	Weak transcription	Fetal Thymus	thymus
17	chr20:52474800-52480200	Weak transcription	Pancreas	Pancrea
18	chr20:52474800-52480800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr20:52474800-52480800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr20:52474800-52482000	Weak transcription	Thymus	Thymus
21	chr20:52474800-52482600	Weak transcription	Left Ventricle	heart
22	chr20:52475000-52479600	Weak transcription	Fetal Kidney	kidney
23	chr20:52475000-52480000	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr20:52475000-52480200	Weak transcription	Primary T cells from cord blood	blood
25	chr20:52475000-52480200	Weak transcription	Colonic Mucosa	Colon
26	chr20:52475200-52482600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr20:52475400-52480000	Weak transcription	Fetal Intestine Large	intestine
28	chr20:52475800-52477200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr20:52476200-52476600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr20:52476200-52476600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr20:52476200-52476600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr20:52476200-52476600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr20:52476200-52476600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr20:52476200-52476600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr20:52476200-52476600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr20:52476200-52476600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr20:52476200-52476600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr20:52476200-52476600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr20:52476200-52476600	ZNF genes & repeats	Fetal Brain Male	brain
40	chr20:52476200-52476600	Enhancers	Fetal Intestine Small	intestine
41	chr20:52476200-52476600	Enhancers	Fetal Muscle Trunk	muscle
42	chr20:52476200-52476600	Enhancers	Fetal Muscle Leg	muscle
43	chr20:52476200-52476600	Enhancers	Placenta	Placenta
44	chr20:52476200-52476600	Enhancers	Fetal Stomach	stomach
45	chr20:52476200-52476600	Enhancers	Gastric	stomach
46	chr20:52476200-52476600	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr20:52476200-52476600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
48	chr20:52476200-52476600	Enhancers	Spleen	Spleen
49	chr20:52476200-52476800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr20:52476200-52476800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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