Variant report

Variant	nsv524981
Chromosome Location	chr20:23011468-23021597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:976)
Chromatin interactive
region (count:5)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CREB1	chr20:23020607-23021028	A549	lung:	n/a	n/a
2	CREB1	chr20:23020585-23020934	A549	lung:	n/a	n/a
3	CREB1	chr20:23020327-23020602	A549	lung:	n/a	n/a
4	CTCF	chr20:23021484-23021583	MCF-7	breast:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
5	CTCF	chr20:23021509-23021610	MCF-7	breast:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
6	CTCF	chr20:23021529-23021664	K562	blood:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
7	CTCF	chr20:23021519-23021597	K562	blood:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
8	CTCF	chr20:23021503-23021587	MCF-7	breast:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
9	CTCF	chr20:23021523-23021570	NHEK	skin:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
10	CTCF	chr20:23021519-23021594	GM12892	blood:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
11	CTCF	chr20:23021517-23021604	MCF-7	breast:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
12	CTCF	chr20:23021496-23021589	MCF-7	breast:	n/a	chr20:23021534-23021542 chr20:23021535-23021543
13	FOS	chr20:23020547-23020871	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr20:23020455-23020882	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr20:23020584-23020823	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr20:23020518-23020908	MCF10A-Er-Src	breast:	n/a	n/a
17	FOXA1	chr20:23020279-23020953	A549	lung:	n/a	n/a
18	FOXA1	chr20:23020250-23020912	A549	lung:	n/a	n/a
19	GABPA	chr20:23015856-23016314	H1-hESC	embryonic stem cell:	n/a	n/a
20	GABPA	chr20:23016022-23016424	H1-hESC	embryonic stem cell:	n/a	n/a
21	JUN	chr20:23019290-23019352	H1-hESC	embryonic stem cell:	n/a	n/a
22	KAP1	chr20:23017670-23018142	HEK293	kidney:	n/a	n/a
23	KAP1	chr20:23017703-23018158	U2OS	brain:	n/a	n/a
24	MAX	chr20:23016075-23016689	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAX	chr20:23014024-23014035	NB4	blood:	n/a	n/a
26	MXI1	chr20:23012102-23012170	K562	blood:	n/a	n/a
27	MYC	chr20:23020547-23020875	MCF10A-Er-Src	breast:	n/a	n/a
28	NR3C1	chr20:23020480-23021028	A549	lung:	n/a	n/a
29	NR3C1	chr20:23020277-23021023	A549	lung:	n/a	n/a
30	NR3C1	chr20:23020314-23021010	A549	lung:	n/a	n/a
31	NR3C1	chr20:23020185-23021144	A549	lung:	n/a	chr20:23021089-23021106
32	NR3C1	chr20:23020187-23021067	A549	lung:	n/a	n/a
33	NR3C1	chr20:23020347-23021067	A549	lung:	n/a	n/a
34	POLR2A	chr20:23016439-23016497	MCF-7	breast:	n/a	n/a
35	POLR2A	chr20:23020683-23020869	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr20:23020353-23020473	A549	lung:	n/a	n/a
37	POLR2A	chr20:23016559-23016568	MCF-7	breast:	n/a	n/a
38	POLR2A	chr20:23020452-23020475	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr20:23016532-23016546	MCF-7	breast:	n/a	n/a
40	POLR2A	chr20:23016521-23016528	MCF-7	breast:	n/a	n/a
41	RAD21	chr20:23021444-23021593	K562	blood:	n/a	chr20:23021510-23021522
42	RAD21	chr20:23015821-23016230	H1-hESC	embryonic stem cell:	n/a	n/a
43	STAT3	chr20:23020424-23021000	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr20:23020574-23020933	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr20:23020678-23020910	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr20:23020416-23020962	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr20:23020516-23020962	MCF10A-Er-Src	breast:	n/a	n/a
48	TCF7L2	chr20:23017473-23018450	HEK293	kidney:	n/a	chr20:23018031-23018040 chr20:23018032-23018041 chr20:23018032-23018042 chr20:23018028-23018044 chr20:23018028-23018044
49	USF1	chr20:23020236-23021025	A549	lung:	n/a	n/a
50	ZNF263	chr20:23017379-23018138	HEK293-T-REx	kidney:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23016315-23016365	HEEpiC	esophagus:	n/a
2	chr20:23015908-23015958	BJ	skin:	n/a
3	chr20:23019450-23019500	HNPCEpiC	eye:	n/a
4	chr20:23019450-23019500	GM12891	blood:	n/a
5	chr20:23015906-23015956	NB4	blood:	n/a
6	chr20:23019450-23019500	ECC-1	luminal epithelium:	n/a
7	chr20:23015936-23015986	ECC-1	luminal epithelium:	n/a
8	chr20:23016753-23016803	NHBE	bronchial:	n/a
9	chr20:23015908-23015958	GM12892	blood:	n/a
10	chr20:23014087-23014137	Hepatocyte	liver:	n/a
11	chr20:23016753-23016803	HCPEpiC	choroid plexus:	n/a
12	chr20:23018108-23018158	K562	blood:	n/a
13	chr20:23018108-23018158	AG09319	gingival:	n/a
14	chr20:23012241-23012291	ECC-1	luminal epithelium:	n/a
15	chr20:23018108-23018158	HNPCEpiC	eye:	n/a
16	chr20:23016753-23016803	PFSK-1	brain:	n/a
17	chr20:23019450-23019500	RPTEC	kidney:	n/a
18	chr20:23015091-23015141	NB4	blood:	n/a
19	chr20:23016753-23016803	HCF	heart:	n/a
20	chr20:23016315-23016365	HCF	heart:	n/a
21	chr20:23016753-23016803	HIPEpiC	eye:	n/a
22	chr20:23014087-23014137	LNCaP	prostate:	n/a
23	chr20:23019450-23019500	HEEpiC	esophagus:	n/a
24	chr20:23015932-23015982	PANC-1	pancreas:	n/a
25	chr20:23015908-23015958	T-47D	breast:	n/a
26	chr20:23016315-23016365	AG09319	gingival:	n/a
27	chr20:23015932-23015982	HPAEpiC	pulmonary alveolar:	n/a
28	chr20:23015908-23015958	GM19239	blood:	n/a
29	chr20:23016315-23016365	HAEpiC	amniotic membrane:	n/a
30	chr20:23015908-23015958	SAEC	small airway:	n/a
31	chr20:23019450-23019500	HRPEpiC	eye:	n/a
32	chr20:23012235-23012285	AG10803	skin:	n/a
33	chr20:23015899-23015949	Jurkat	blood:	n/a
34	chr20:23015932-23015982	GM12878	blood:	n/a
35	chr20:23015624-23015674	MCF10A-Er-Src	breast:	n/a
36	chr20:23015936-23015986	ovcar-3	ovarian:	n/a
37	chr20:23015908-23015958	Jurkat	blood:	n/a
38	chr20:23014087-23014137	PFSK-1	brain:	n/a
39	chr20:23015932-23015982	GM06990	blood:	n/a
40	chr20:23012235-23012285	GM12892	blood:	n/a
41	chr20:23019450-23019500	HRE	kidney:	n/a
42	chr20:23012241-23012291	AG09319	gingival:	n/a
43	chr20:23015906-23015956	SK-N-SH	brain:	n/a
44	chr20:23018108-23018158	SK-N-SH_RA	brain:	n/a
45	chr20:23012235-23012285	HepG2	liver:	n/a
46	chr20:23012235-23012285	Hela-S3	cervix:	n/a
47	chr20:23017312-23017362	BJ	skin:	n/a
48	chr20:23015908-23015958	HIPEpiC	eye:	n/a
49	chr20:23015899-23015949	AG04450	lung:	fetal
50	chr20:23015624-23015674	ProgFib	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:23021523..23024307-chr20:23024511..23026678,2	MCF-7	breast:
2	chr20:23020985..23023221-chr20:23027756..23029605,2	MCF-7	breast:
3	chr20:23015312..23016906-chr20:23019292..23021304,2	MCF-7	breast:
4	chr20:23017212..23020123-chr20:23028174..23031939,4	MCF-7	breast:
5	chr20:23013696..23015304-chr20:23018702..23020463,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SSTR4-1	chr20:23018860-23018942	ENSG00000234646.1
2	lnc-SSTR4-1	chr20:23018380-23018942	NONHSAT079026
3	lnc-SSTR4-1	chr20:23018357-23019074	NONHSAT079025
4	lnc-SSTR4-1	chr20:23019693-23019865	NONHSAT079026
5	lnc-SSTR4-1	chr20:23019186-23019873	NONHSAT079025
6	lnc-SSTR4-1	chr20:23018860-23018942	ENSG00000234646.1
7	lnc-SSTR4-1	chr20:23019693-23019873	ENSG00000234646.1
8	lnc-SSTR4-1	chr20:23019571-23019873	ENSG00000234646.1
9	lnc-SSTR4-1	chr20:23012179-23012325	ENSG00000234646.1

No data

Variant related genes	Relation type
ENSG00000234646	TF binding region
SSTR4	TF binding region
ENSG00000230492	TF binding region
ENSG00000234646	CpG island
SSTR4	CpG island
ENSG00000230492	CpG island
ENSG00000132671	chromatin interactions
ENSG00000178726	chromatin interactions
ENSG00000234646	chromatin interactions

Extended variants
information (count: 507 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11696134	chr20:23011468-23011469	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542917735	chr20:23011488-23011489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561380683	chr20:23011509-23011510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528897362	chr20:23011581-23011582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114208548	chr20:23011595-23011596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575659954	chr20:23011628-23011629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181448512	chr20:23011639-23011640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184570281	chr20:23011662-23011663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529064508	chr20:23011691-23011692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376953330	chr20:23011706-23011707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147136058	chr20:23011715-23011716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs8120756	chr20:23011718-23011719	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs528394699	chr20:23011741-23011742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551132734	chr20:23011761-23011762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs118048929	chr20:23011762-23011763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188646633	chr20:23011790-23011791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551489657	chr20:23011794-23011795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567532782	chr20:23011858-23011859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115815145	chr20:23011870-23011871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140261086	chr20:23011961-23011962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181461247	chr20:23011984-23011985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186006019	chr20:23012002-23012003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539279918	chr20:23012055-23012056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527444407	chr20:23012058-23012059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558684948	chr20:23012068-23012069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575566909	chr20:23012075-23012076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545398629	chr20:23012098-23012099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544395729	chr20:23012115-23012116	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
29	rs149250548	chr20:23012151-23012152	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
30	rs112982366	chr20:23012155-23012156	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
31	rs148431094	chr20:23012158-23012159	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
32	rs6515299	chr20:23012177-23012178	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs530993294	chr20:23012195-23012196	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs142610514	chr20:23012213-23012214	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs146499427	chr20:23012242-23012243	Weak transcription Enhancers	CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs377425608	chr20:23012255-23012256	Weak transcription Enhancers	CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs564747837	chr20:23012304-23012305	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs7262749	chr20:23012305-23012306	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs139961615	chr20:23012328-23012329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115455040	chr20:23012378-23012379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190923821	chr20:23012401-23012402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546829294	chr20:23012445-23012446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556317549	chr20:23012512-23012513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180979431	chr20:23012552-23012553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571298596	chr20:23012562-23012563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143520811	chr20:23012563-23012564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187088897	chr20:23012592-23012593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561511662	chr20:23012595-23012596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146761451	chr20:23012597-23012598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs220979	chr20:23012609-23012610	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23001000-23015800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr20:23008600-23011800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr20:23009000-23011600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr20:23010200-23011600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr20:23010200-23012600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr20:23010200-23012800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr20:23010600-23011800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr20:23010600-23012800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr20:23011000-23011800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr20:23011200-23011600	Enhancers	H9 Cell Line	embryonic stem cell
11	chr20:23011200-23012600	Enhancers	Fetal Heart	heart
12	chr20:23011200-23013800	Enhancers	Left Ventricle	heart
13	chr20:23011400-23011800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr20:23011400-23014600	Enhancers	Dnd41	blood
15	chr20:23011600-23012800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr20:23011600-23013000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr20:23011800-23012200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr20:23011800-23012200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr20:23011800-23013400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr20:23012000-23014800	Enhancers	Right Ventricle	heart
21	chr20:23012200-23014000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr20:23012600-23012800	Flanking Active TSS	Fetal Heart	heart
23	chr20:23012600-23014600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr20:23012800-23013000	Enhancers	Fetal Heart	heart
25	chr20:23012800-23013200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr20:23012800-23013200	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr20:23012800-23013400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr20:23012800-23014000	Enhancers	Primary hematopoietic stem cells	blood
29	chr20:23012800-23014400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr20:23013000-23013200	Flanking Active TSS	Fetal Heart	heart
31	chr20:23013000-23013200	Enhancers	Lung	lung
32	chr20:23013000-23013800	Enhancers	Fetal Muscle Trunk	muscle
33	chr20:23013000-23013800	Enhancers	Fetal Thymus	thymus
34	chr20:23013000-23014200	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr20:23013000-23014200	Enhancers	Fetal Stomach	stomach
36	chr20:23013200-23014000	Enhancers	Fetal Muscle Leg	muscle
37	chr20:23013200-23014000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
38	chr20:23013200-23016200	Weak transcription	Lung	lung
39	chr20:23013200-23017400	Enhancers	Fetal Heart	heart
40	chr20:23013400-23013800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr20:23013400-23014000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr20:23014000-23014200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr20:23014000-23015600	Weak transcription	Primary hematopoietic stem cells	blood
44	chr20:23014000-23015800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr20:23014200-23014400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr20:23014200-23014400	Bivalent Enhancer	Fetal Stomach	stomach
47	chr20:23014600-23016200	Weak transcription	Dnd41	blood
48	chr20:23015200-23015800	Weak transcription	Spleen	Spleen
49	chr20:23015400-23015800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr20:23015400-23016000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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