Variant report

Variant	nsv1057099
Chromosome Location	chr20:1557178-1593837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:89)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:89 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr20:1557313-1557606	Hela-S3	cervix:	n/a	chr20:1557460-1557471
2	CEBPB	chr20:1557318-1557553	HepG2	liver:	n/a	chr20:1557460-1557471
3	CEBPB	chr20:1557320-1557574	A549	lung:	n/a	chr20:1557460-1557471
4	CTCF	chr20:1569782-1570019	HUVEC	blood vessel:	n/a	n/a
5	CTCF	chr20:1569860-1570007	GM12878	blood:	n/a	n/a
6	CTCF	chr20:1569820-1569970	HCT-116	colon:	n/a	n/a
7	CTCF	chr20:1583974-1584038	GM10266	blood:	n/a	chr20:1583996-1584006
8	CTCF	chr20:1585205-1585266	GM10248	blood:	n/a	n/a
9	CTCF	chr20:1569900-1570050	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr20:1589816-1589866	NHEK	skin:	n/a	n/a
11	CTCF	chr20:1562336-1562338	Gliobla	brain:	n/a	n/a
12	CTCF	chr20:1569800-1569950	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr20:1562140-1562290	GM12864	blood:	n/a	n/a
14	CTCF	chr20:1562180-1562330	GM12875	blood:	n/a	n/a
15	CTCF	chr20:1569840-1569990	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr20:1569880-1570030	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr20:1569840-1569990	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr20:1583923-1584071	GM12891	blood:	n/a	chr20:1583996-1584006
19	CTCF	chr20:1569840-1569990	HAc	cerebellar:	n/a	n/a
20	CTCF	chr20:1562235-1562401	GM12878	blood:	n/a	n/a
21	CTCF	chr20:1583950-1584135	GM12878	blood:	n/a	chr20:1583996-1584006
22	CTCF	chr20:1562218-1562407	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr20:1562235-1562365	GM13977	blood:	n/a	n/a
24	CTCF	chr20:1562180-1562330	GM12878	blood:	n/a	n/a
25	CTCF	chr20:1569809-1569981	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr20:1569860-1570010	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr20:1569820-1569970	AG10803	skin:	n/a	n/a
28	CTCF	chr20:1569890-1569986	ProgFib	skin:	n/a	n/a
29	CTCF	chr20:1569840-1569990	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr20:1583954-1584054	GM19239	blood:	n/a	chr20:1583996-1584006
31	CTCF	chr20:1569840-1569990	HRE	kidney:	n/a	n/a
32	CTCF	chr20:1583993-1584014	H1-hESC	embryonic stem cell:	n/a	chr20:1583996-1584006
33	CTCF	chr20:1569812-1570027	Gliobla	brain:	n/a	n/a
34	CTCF	chr20:1569768-1570055	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr20:1583918-1584066	GM12878	blood:	n/a	chr20:1583996-1584006
36	CTCF	chr20:1569800-1569950	GM12864	blood:	n/a	n/a
37	CTCF	chr20:1569820-1569970	HRE	kidney:	n/a	n/a
38	CTCF	chr20:1569844-1569973	GM12878	blood:	n/a	n/a
39	CTCF	chr20:1569820-1569970	GM12878	blood:	n/a	n/a
40	CTCF	chr20:1593027-1593071	K562	blood:	n/a	n/a
41	CTCF	chr20:1562236-1562335	Gliobla	brain:	n/a	n/a
42	CTCF	chr20:1569780-1569930	SAEC	small airway:	n/a	n/a
43	CTCF	chr20:1569820-1569970	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr20:1583938-1584013	HUVEC	blood vessel:	n/a	chr20:1583996-1584006
45	EBF1	chr20:1575968-1576160	GM12878	blood:	n/a	n/a
46	EBF1	chr20:1576059-1576210	GM12878	blood:	n/a	n/a
47	ELF1	chr20:1575954-1576254	GM12878	blood:	n/a	chr20:1576167-1576178
48	FOS	chr20:1557393-1557685	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr20:1557387-1557630	MCF10A-Er-Src	breast:	n/a	n/a
50	MAFF	chr20:1560210-1560695	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1578550-1578600	Caco-2	colon:	n/a
2	chr20:1578550-1578600	T-47D	breast:	n/a
3	chr20:1578550-1578600	SKMC	muscle:	n/a
4	chr20:1578550-1578600	GM12891	blood:	n/a
5	chr20:1578550-1578600	GM19239	blood:	n/a
6	chr20:1578550-1578600	HUVEC	blood vessel:	n/a
7	chr20:1578550-1578600	PANC-1	pancreas:	n/a
8	chr20:1578550-1578600	BE2_C	brain:	n/a
9	chr20:1578550-1578600	ECC-1	luminal epithelium:	n/a
10	chr20:1578550-1578600	BJ	skin:	n/a
11	chr20:1578550-1578600	HMEC	breast:	n/a
12	chr20:1578550-1578600	GM12878	blood:	n/a
13	chr20:1578550-1578600	HRCEpiC	kidney:	n/a
14	chr20:1578550-1578600	HepG2	liver:	n/a
15	chr20:1578550-1578600	GM12892	blood:	n/a
16	chr20:1578550-1578600	MCF10A-Er-Src	breast:	n/a
17	chr20:1578550-1578600	U87	brain:	n/a
18	chr20:1578550-1578600	Hepatocyte	liver:	n/a
19	chr20:1578550-1578600	MCF-7	breast:	n/a
20	chr20:1578550-1578600	ovcar-3	ovarian:	n/a
21	chr20:1578550-1578600	AG10803	skin:	n/a
22	chr20:1578550-1578600	HIPEpiC	eye:	n/a
23	chr20:1578550-1578600	HRE	kidney:	n/a
24	chr20:1578550-1578600	H1-hESC	embryonic stem cell:	embryo
25	chr20:1578550-1578600	K562	blood:	n/a
26	chr20:1578550-1578600	PFSK-1	brain:	n/a
27	chr20:1578550-1578600	HNPCEpiC	eye:	n/a
28	chr20:1578550-1578600	NT2-D1	testis:	n/a
29	chr20:1578550-1578600	HEK293	kidney:	embryo
30	chr20:1578550-1578600	AG09309	skin:	n/a
31	chr20:1578550-1578600	LNCaP	prostate:	n/a
32	chr20:1578550-1578600	HAEpiC	amniotic membrane:	n/a
33	chr20:1578550-1578600	Hela-S3	cervix:	n/a
34	chr20:1578550-1578600	SK-N-SH	brain:	n/a
35	chr20:1578550-1578600	SK-N-SH_RA	brain:	n/a
36	chr20:1578550-1578600	AG09319	gingival:	n/a
37	chr20:1578550-1578600	HEEpiC	esophagus:	n/a
38	chr20:1578550-1578600	NHDF-neo	bronchial:	n/a
39	chr20:1578550-1578600	CMK	blood:	n/a
40	chr20:1578550-1578600	HRPEpiC	eye:	n/a
41	chr20:1578550-1578600	AoSMC	blood vessel:	n/a
42	chr20:1578550-1578600	HCF	heart:	n/a
43	chr20:1578550-1578600	HCPEpiC	choroid plexus:	n/a
44	chr20:1578550-1578600	A549	lung:	n/a
45	chr20:1578550-1578600	NHBE	bronchial:	n/a
46	chr20:1578550-1578600	SK-N-MC	brain:	n/a
47	chr20:1578550-1578600	HCM	heart:	n/a
48	chr20:1578550-1578600	AG04450	lung:	fetal
49	chr20:1578550-1578600	ProgFib	skin:	n/a
50	chr20:1578550-1578600	NH-A	brain:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-5	chr20:1574682-1577118	ucscGeneNc_uc002wfp_1
2	lnc-SNPH-5	chr20:1562154-1562366	ucscGeneNc_uc002wfp_1
3	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
4	lnc-SNPH-4	chr20:1572038-1572494	NONHSAT078121
5	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1

No data

Variant related genes	Relation type
SIRPB1	TF binding region
ENSG00000260861	TF binding region
ENSG00000271523	TF binding region
SIRPB1	CpG island
ENSG00000260861	CpG island
ENSG00000271523	CpG island

Extended variants
information (count: 672 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:672 , 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	rs188147189	chr20:1557290-1557291	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs367952285	chr20:1557324-1557325	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs6131635	chr20:1557335-1557336	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs534601711	chr20:1557365-1557366	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs553050587	chr20:1557420-1557421	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs574538156	chr20:1557448-1557449	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs180995711	chr20:1557497-1557498	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs563438152	chr20:1557520-1557521	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs34700632	chr20:1557537-1557538	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs140437054	chr20:1557552-1557553	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545706407	chr20:1557574-1557575	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115754775	chr20:1557636-1557637	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528412967	chr20:1557647-1557648	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186192588	chr20:1557652-1557653	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538011509	chr20:1557721-1557722	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548402432	chr20:1557722-1557723	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386811629	chr20:1557742-1557743	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2243425	chr20:1557744-1557745	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs550684905	chr20:1557822-1557823	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569281550	chr20:1557823-1557824	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183967949	chr20:1557844-1557845	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368872086	chr20:1557869-1557870	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540009377	chr20:1557885-1557886	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551728219	chr20:1557915-1557916	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567151560	chr20:1557916-1557917	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142747130	chr20:1557927-1557928	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552964617	chr20:1557932-1557933	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568076787	chr20:1557948-1557949	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2244133	chr20:1557954-1557955	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs115127273	chr20:1557970-1557971	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563490494	chr20:1557980-1557981	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6110506	chr20:1558008-1558009	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186828339	chr20:1558020-1558021	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191608203	chr20:1558048-1558049	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573054798	chr20:1558067-1558068	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148404046	chr20:1558247-1558248	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182496710	chr20:1558248-1558249	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6135335	chr20:1558363-1558364	Genic enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs377231037	chr20:1558364-1558365	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544235260	chr20:1558392-1558393	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535837370	chr20:1558417-1558418	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142488238	chr20:1558425-1558426	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74928022	chr20:1558427-1558428	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79772942	chr20:1558428-1558429	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187333750	chr20:1558429-1558430	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551905856	chr20:1558434-1558435	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539769358	chr20:1558459-1558460	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551835712	chr20:1558505-1558506	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6110507	chr20:1558508-1558509	Genic enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs576574599	chr20:1558539-1558540	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
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
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr20:1550000-1568200	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr20:1552400-1558000	Weak transcription	Primary T cells from cord blood	blood
5	chr20:1552400-1568000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr20:1552600-1569000	Weak transcription	Spleen	Spleen
7	chr20:1552800-1558400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr20:1556800-1557200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr20:1556800-1557400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr20:1556800-1557600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr20:1556800-1557600	Enhancers	NHEK	skin
12	chr20:1556800-1558200	Enhancers	Hela-S3	cervix
13	chr20:1556800-1558600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
14	chr20:1556800-1560000	Genic enhancers	Primary monocytes fromperipheralblood	blood
15	chr20:1556800-1560000	Genic enhancers	Monocytes-CD14+_RO01746	blood
16	chr20:1557000-1557400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr20:1558000-1559600	Strong transcription	Primary T cells from cord blood	blood
18	chr20:1558400-1560000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr20:1558600-1559600	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr20:1559600-1560400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
21	chr20:1559600-1560600	Weak transcription	Primary T cells from cord blood	blood
22	chr20:1560000-1561000	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr20:1560000-1561000	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr20:1560000-1579200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr20:1560400-1561800	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr20:1560600-1561000	Strong transcription	Primary T cells from cord blood	blood
27	chr20:1561000-1562600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr20:1561000-1563600	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr20:1561000-1568000	Weak transcription	Primary T cells from cord blood	blood
30	chr20:1561800-1563800	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr20:1563600-1564600	Genic enhancers	Primary monocytes fromperipheralblood	blood
32	chr20:1563800-1565400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr20:1564600-1565400	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr20:1565400-1565600	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr20:1565400-1566000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr20:1565600-1565800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
37	chr20:1565800-1567000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr20:1566000-1566600	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr20:1566600-1568400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr20:1567000-1569400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
41	chr20:1567600-1570000	Active TSS	Primary B cells from cord blood	blood
42	chr20:1567800-1569600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr20:1568000-1569000	Enhancers	Primary T cells from cord blood	blood
44	chr20:1568000-1570200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr20:1568000-1570200	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr20:1568000-1570400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr20:1568200-1568800	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr20:1568200-1569800	Enhancers	Primary B cells from peripheral blood	blood
49	chr20:1568400-1568600	Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr20:1568400-1569400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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