Variant report

Variant	nsv965935
Chromosome Location	chr20:23168139-23175404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:23174714-23174842	K562	blood:	n/a	n/a
2	ATF1	chr20:23174598-23174987	K562	blood:	n/a	n/a
3	BACH1	chr20:23174740-23174743	K562	blood:	n/a	n/a
4	BRCA1	chr20:23168432-23168802	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr20:23174571-23175027	K562	blood:	n/a	n/a
6	CEBPB	chr20:23174679-23174962	K562	blood:	n/a	n/a
7	CEBPB	chr20:23174577-23174972	K562	blood:	n/a	n/a
8	CEBPB	chr20:23174611-23174939	K562	blood:	n/a	n/a
9	CEBPB	chr20:23174839-23174892	Hela-S3	cervix:	n/a	n/a
10	CEBPD	chr20:23174523-23175020	K562	blood:	n/a	n/a
11	CHD2	chr20:23168418-23168683	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr20:23174652-23174670	K562	blood:	n/a	n/a
13	CREB1	chr20:23174531-23175047	K562	blood:	n/a	chr20:23174773-23174786
14	CREB1	chr20:23174536-23175003	K562	blood:	n/a	chr20:23174773-23174786
15	CTCF	chr20:23168640-23168790	HMEC	breast:	n/a	chr20:23168746-23168759
16	CTCF	chr20:23168540-23168690	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr20:23168540-23168690	SAEC	small airway:	n/a	n/a
18	CTCF	chr20:23168560-23168710	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr20:23168660-23168810	HEEpiC	esophagus:	n/a	chr20:23168746-23168759
20	CTCF	chr20:23168600-23168750	NHEK	skin:	n/a	n/a
21	CTCF	chr20:23168633-23168638	MCF-7	breast:	n/a	n/a
22	CTCF	chr20:23168380-23168530	HMEC	breast:	n/a	n/a
23	CTCF	chr20:23168500-23168650	RPTEC	kidney:	n/a	n/a
24	CTCF	chr20:23168520-23168670	HRE	kidney:	n/a	n/a
25	CTCF	chr20:23168540-23168690	NHEK	skin:	n/a	n/a
26	CTCF	chr20:23168560-23168710	SAEC	small airway:	n/a	n/a
27	CTCF	chr20:23168540-23168690	MCF-7	breast:	n/a	n/a
28	CTCF	chr20:23168600-23168750	HMEC	breast:	n/a	n/a
29	CTCF	chr20:23168340-23168490	MCF-7	breast:	n/a	n/a
30	E2F6	chr20:23170638-23170758	K562	blood:	n/a	n/a
31	ELF1	chr20:23174595-23174885	K562	blood:	n/a	n/a
32	ELK1	chr20:23169531-23169693	GM12878	blood:	n/a	n/a
33	EP300	chr20:23174556-23174965	K562	blood:	n/a	n/a
34	FOS	chr20:23168507-23168625	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr20:23168454-23168613	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr20:23174651-23174878	MCF10A-Er-Src	breast:	n/a	chr20:23174775-23174784
37	GATA1	chr20:23174126-23175152	PBDE	blood:	n/a	chr20:23174994-23175005 chr20:23175047-23175055 chr20:23174630-23174647 chr20:23174727-23174737
38	GATA3	chr20:23168316-23168731	MCF-7	breast:	n/a	n/a
39	GATA3	chr20:23170669-23170917	T-47D	breast:	n/a	n/a
40	HA-E2F1	chr20:23168262-23169816	MCF-7	breast:	n/a	chr20:23168548-23168557
41	HCFC1	chr20:23174607-23174958	K562	blood:	n/a	n/a
42	HEY1	chr20:23174532-23174861	K562	blood:	n/a	n/a
43	JUN	chr20:23174190-23175244	K562	blood:	n/a	chr20:23174771-23174784 chr20:23174775-23174784
44	JUN	chr20:23174685-23174916	HepG2	liver:	n/a	chr20:23174771-23174784 chr20:23174775-23174784
45	JUND	chr20:23174599-23174957	K562	blood:	n/a	chr20:23174775-23174784
46	JUND	chr20:23174653-23174916	HepG2	liver:	n/a	chr20:23174775-23174784
47	MAFK	chr20:23168657-23168677	HepG2	liver:	n/a	n/a
48	MAFK	chr20:23168427-23168778	Hela-S3	cervix:	n/a	chr20:23168625-23168636 chr20:23168624-23168639
49	MAFK	chr20:23168548-23168673	H1-hESC	embryonic stem cell:	n/a	chr20:23168625-23168636 chr20:23168624-23168639
50	MAX	chr20:23168430-23168770	Hela-S3	cervix:	n/a	chr20:23168753-23168763

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:23128680..23132693-chr20:23173285..23175662,3	K562	blood:
2	chr20:23173550..23175379-chr20:23179178..23180724,2	K562	blood:
3	chr20:23029649..23032465-chr20:23170734..23172386,2	MCF-7	breast:
4	chr20:23127669..23129280-chr20:23170551..23172653,2	K562	blood:
5	chr20:23135912..23138297-chr20:23172308..23174497,2	K562	blood:
6	chr20:23169059..23171573-chr20:23172797..23175263,2	K562	blood:
7	chr20:23169059..23171573-chr20:23172797..23175263,2	K562	blood:
8	chr20:23139207..23141620-chr20:23172771..23174787,2	K562	blood:
9	chr20:23029838..23032400-chr20:23167323..23168960,2	MCF-7	breast:
10	chr20:23167380..23172469-chr20:23172590..23175556,6	K562	blood:
11	chr20:23173550..23175441-chr20:23179224..23181550,2	K562	blood:
12	chr20:23159913..23161586-chr20:23172008..23174904,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SSTR4-2	chr20:23168765-23168795	XLOC_013489
2	lnc-CD93-3	chr20:23168344-23169272	XLOC_013690
3	lnc-SSTR4-2	chr20:23168598-23170942	NONHSAT079044
4	lnc-SSTR4-2	chr20:23167850-23168277	XLOC_013489
5	lnc-SSTR4-2	chr20:23168699-23168795	NONHSAT079045
6	lnc-SSTR4-2	chr20:23170420-23170907	XLOC_013489
7	lnc-SSTR4-2	chr20:23167850-23168277	XLOC_013489
8	lnc-SSTR4-2	chr20:23170420-23170904	NONHSAT079045
9	lnc-SSTR4-2	chr20:23170420-23170935	XLOC_013489
10	lnc-SSTR4-2	chr20:23167850-23168277	XLOC_013489
11	lnc-SSTR4-2	chr20:23170420-23170944	XLOC_013489
12	lnc-CD93-3	chr20:23169415-23169661	XLOC_013690
13	lnc-SSTR4-2	chr20:23170420-23170935	XLOC_013489

No data

Variant related genes	Relation type
ENSG00000230387	TF binding region
ENSG00000201527	chromatin interactions
ENSG00000178726	chromatin interactions
ENSG00000230387	chromatin interactions
FOXF2	miRNA target sites
ZNF609	miRNA target sites
FILIP1L	miRNA target sites
FOXJ3	miRNA target sites
VDAC1	miRNA target sites

Extended variants
information (count: 292 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62206881	chr20:23168140-23168141	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368338191	chr20:23168143-23168144	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs533093457	chr20:23168171-23168172	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs543332100	chr20:23168214-23168215	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs844940	chr20:23168232-23168233	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs142220207	chr20:23168237-23168238	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs188412803	chr20:23168248-23168249	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs565684116	chr20:23168251-23168252	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs528167217	chr20:23168259-23168260	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs552036049	chr20:23168330-23168331	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs139575356	chr20:23168334-23168335	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373922973	chr20:23168336-23168337	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376160532	chr20:23168343-23168344	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs146398639	chr20:23168380-23168381	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs557691672	chr20:23168418-23168419	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs139805991	chr20:23168430-23168431	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs114515555	chr20:23168444-23168445	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs553331326	chr20:23168461-23168462	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs62206882	chr20:23168486-23168487	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs545084788	chr20:23168487-23168488	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs548791704	chr20:23168494-23168495	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs79388863	chr20:23168500-23168501	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	mRNA abundance
23	rs62206883	chr20:23168504-23168505	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543171056	chr20:23168508-23168509	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs117390891	chr20:23168526-23168527	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	mRNA abundance
26	rs143197178	chr20:23168540-23168541	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs563852671	chr20:23168551-23168552	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs529181961	chr20:23168552-23168553	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs372175192	chr20:23168569-23168570	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs542286221	chr20:23168600-23168601	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs559284949	chr20:23168637-23168638	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs528055307	chr20:23168646-23168647	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs551522174	chr20:23168665-23168666	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs571317826	chr20:23168681-23168682	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs569493159	chr20:23168714-23168715	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs531138615	chr20:23168720-23168721	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs145511588	chr20:23168749-23168750	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs567911643	chr20:23168779-23168780	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs536931843	chr20:23168798-23168799	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs553129832	chr20:23168800-23168801	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs201450394	chr20:23168858-23168859	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs192223539	chr20:23168860-23168861	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs113397640	chr20:23168864-23168865	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs373283122	chr20:23168865-23168866	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs74400915	chr20:23168868-23168869	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs575322139	chr20:23168880-23168881	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs536889459	chr20:23168904-23168905	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs557096668	chr20:23168912-23168913	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs538293929	chr20:23168919-23168920	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs573886163	chr20:23168924-23168925	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Cancer	20164919	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23162000-23174200	Weak transcription	Left Ventricle	heart
2	chr20:23166200-23168600	Enhancers	Placenta	Placenta
3	chr20:23167200-23168600	Enhancers	Esophagus	oesophagus
4	chr20:23167200-23168600	Enhancers	Fetal Muscle Trunk	muscle
5	chr20:23167200-23170000	Weak transcription	Gastric	stomach
6	chr20:23167400-23168200	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr20:23167400-23168400	Enhancers	Hela-S3	cervix
8	chr20:23167400-23169000	Enhancers	Stomach Mucosa	stomach
9	chr20:23167600-23169400	Enhancers	Fetal Muscle Leg	muscle
10	chr20:23167800-23168600	Weak transcription	Lung	lung
11	chr20:23167800-23168600	Weak transcription	HSMM	muscle
12	chr20:23167800-23168600	Enhancers	HSMMtube	muscle
13	chr20:23167800-23169600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
14	chr20:23168000-23168200	Weak transcription	Spleen	Spleen
15	chr20:23168000-23168800	Enhancers	Right Ventricle	heart
16	chr20:23168000-23169000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr20:23168200-23168800	Enhancers	Psoas Muscle	Psoas
18	chr20:23168200-23169200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr20:23168400-23168600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr20:23168400-23168800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr20:23168400-23168800	Enhancers	Placenta Amnion	Placenta Amnion
22	chr20:23168400-23169200	Enhancers	Duodenum Mucosa	Duodenum
23	chr20:23168400-23169400	Flanking Active TSS	Hela-S3	cervix
24	chr20:23168400-23169800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
25	chr20:23168600-23168800	Flanking Active TSS	Placenta	Placenta
26	chr20:23168600-23168800	Flanking Active TSS	HSMMtube	muscle
27	chr20:23168600-23169000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr20:23168600-23169000	Flanking Active TSS	Fetal Muscle Trunk	muscle
29	chr20:23168600-23169200	Flanking Active TSS	Esophagus	oesophagus
30	chr20:23168600-23169400	Enhancers	HSMM	muscle
31	chr20:23168600-23169800	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr20:23168600-23170000	Enhancers	Pancreas	Pancrea
33	chr20:23168600-23170800	Enhancers	Lung	lung
34	chr20:23168800-23169000	Active TSS	Fetal Kidney	kidney
35	chr20:23168800-23169000	Enhancers	Placenta	Placenta
36	chr20:23168800-23169000	Weak transcription	Spleen	Spleen
37	chr20:23168800-23169000	Enhancers	HSMMtube	muscle
38	chr20:23168800-23170200	Weak transcription	Right Ventricle	heart
39	chr20:23169000-23169200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr20:23169000-23169200	Flanking Active TSS	Fetal Kidney	kidney
41	chr20:23169000-23169200	Active TSS	Fetal Muscle Trunk	muscle
42	chr20:23169000-23169200	Flanking Active TSS	Placenta	Placenta
43	chr20:23169000-23169200	Flanking Active TSS	HSMMtube	muscle
44	chr20:23169000-23169600	Enhancers	Spleen	Spleen
45	chr20:23169000-23170400	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr20:23169200-23169400	Enhancers	Placenta	Placenta
47	chr20:23169200-23169400	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr20:23169200-23169600	ZNF genes & repeats	Fetal Kidney	kidney
49	chr20:23169200-23169600	Enhancers	HSMMtube	muscle
50	chr20:23169200-23171000	Enhancers	Esophagus	oesophagus

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