Variant report

Variant	nsv585215
Chromosome Location	chr20:1549402-1582388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:156)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:156 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:1550229-1550409	K562	blood:	n/a	n/a
2	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
3	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
4	BHLHE40	chr20:1549969-1550250	K562	blood:	n/a	n/a
5	BRCA1	chr20:1550123-1550444	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr20:1549993-1550495	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr20:1557313-1557606	Hela-S3	cervix:	n/a	chr20:1557460-1557471
8	CEBPB	chr20:1550069-1550318	K562	blood:	n/a	n/a
9	CEBPB	chr20:1549828-1550670	HCT-116	colon:	n/a	chr20:1549945-1549956
10	CEBPB	chr20:1550121-1550426	IMR90	lung:	n/a	n/a
11	CEBPB	chr20:1549987-1550512	A549	lung:	n/a	n/a
12	CEBPB	chr20:1550076-1550409	HepG2	liver:	n/a	n/a
13	CEBPB	chr20:1550085-1550450	A549	lung:	n/a	n/a
14	CEBPB	chr20:1550079-1550429	K562	blood:	n/a	n/a
15	CEBPB	chr20:1549872-1550575	HCT-116	colon:	n/a	chr20:1549945-1549956
16	CEBPB	chr20:1557320-1557574	A549	lung:	n/a	chr20:1557460-1557471
17	CEBPB	chr20:1557318-1557553	HepG2	liver:	n/a	chr20:1557460-1557471
18	CEBPB	chr20:1550060-1550411	MCF-7	breast:	n/a	n/a
19	CEBPB	chr20:1550062-1550405	A549	lung:	n/a	n/a
20	CHD2	chr20:1550074-1550408	Hela-S3	cervix:	n/a	n/a
21	CREB1	chr20:1550008-1550399	K562	blood:	n/a	n/a
22	CTCF	chr20:1550471-1550587	K562	blood:	n/a	n/a
23	CTCF	chr20:1569820-1569970	GM12878	blood:	n/a	n/a
24	CTCF	chr20:1569900-1570050	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr20:1569782-1570019	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr20:1562180-1562330	GM12878	blood:	n/a	n/a
27	CTCF	chr20:1562235-1562365	GM13977	blood:	n/a	n/a
28	CTCF	chr20:1569840-1569990	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr20:1569809-1569981	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr20:1569768-1570055	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr20:1569820-1569970	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr20:1562218-1562407	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr20:1569880-1570030	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr20:1569800-1569950	GM12864	blood:	n/a	n/a
35	CTCF	chr20:1569840-1569990	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr20:1569860-1570007	GM12878	blood:	n/a	n/a
37	CTCF	chr20:1569840-1569990	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr20:1562180-1562330	GM12875	blood:	n/a	n/a
39	CTCF	chr20:1569780-1569930	SAEC	small airway:	n/a	n/a
40	CTCF	chr20:1569860-1570010	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr20:1562236-1562335	Gliobla	brain:	n/a	n/a
42	CTCF	chr20:1552670-1552733	GM10266	blood:	n/a	n/a
43	CTCF	chr20:1562336-1562338	Gliobla	brain:	n/a	n/a
44	CTCF	chr20:1569820-1569970	AG10803	skin:	n/a	n/a
45	CTCF	chr20:1562235-1562401	GM12878	blood:	n/a	n/a
46	CTCF	chr20:1562140-1562290	GM12864	blood:	n/a	n/a
47	CTCF	chr20:1569820-1569970	HRE	kidney:	n/a	n/a
48	CTCF	chr20:1569844-1569973	GM12878	blood:	n/a	n/a
49	CTCF	chr20:1569840-1569990	HRE	kidney:	n/a	n/a
50	CTCF	chr20:1550540-1550690	NB4	blood:	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	PrEC	prostate:	n/a
2	chr20:1578550-1578600	GM12878	blood:	n/a
3	chr20:1578550-1578600	ovcar-3	ovarian:	n/a
4	chr20:1578550-1578600	HEEpiC	esophagus:	n/a
5	chr20:1578550-1578600	HUVEC	blood vessel:	n/a
6	chr20:1578550-1578600	HCPEpiC	choroid plexus:	n/a
7	chr20:1578550-1578600	SK-N-MC	brain:	n/a
8	chr20:1578550-1578600	AoSMC	blood vessel:	n/a
9	chr20:1578550-1578600	HCT-116	colon:	n/a
10	chr20:1578550-1578600	HRCEpiC	kidney:	n/a
11	chr20:1578550-1578600	MCF10A-Er-Src	breast:	n/a
12	chr20:1578550-1578600	K562	blood:	n/a
13	chr20:1578550-1578600	PANC-1	pancreas:	n/a
14	chr20:1578550-1578600	NT2-D1	testis:	n/a
15	chr20:1578550-1578600	HRE	kidney:	n/a
16	chr20:1578550-1578600	HRPEpiC	eye:	n/a
17	chr20:1578550-1578600	GM06990	blood:	n/a
18	chr20:1578550-1578600	SK-N-SH_RA	brain:	n/a
19	chr20:1578550-1578600	LNCaP	prostate:	n/a
20	chr20:1578550-1578600	HIPEpiC	eye:	n/a
21	chr20:1578550-1578600	RPTEC	kidney:	n/a
22	chr20:1578550-1578600	BJ	skin:	n/a
23	chr20:1578550-1578600	GM12892	blood:	n/a
24	chr20:1578550-1578600	CMK	blood:	n/a
25	chr20:1578550-1578600	GM19239	blood:	n/a
26	chr20:1578550-1578600	NHDF-neo	bronchial:	n/a
27	chr20:1578550-1578600	A549	lung:	n/a
28	chr20:1578550-1578600	HL-60	blood:	n/a
29	chr20:1578550-1578600	SKMC	muscle:	n/a
30	chr20:1578550-1578600	HCM	heart:	n/a
31	chr20:1578550-1578600	AG04450	lung:	fetal
32	chr20:1578550-1578600	MCF-7	breast:	n/a
33	chr20:1578550-1578600	AG09319	gingival:	n/a
34	chr20:1578550-1578600	Jurkat	blood:	n/a
35	chr20:1578550-1578600	AG10803	skin:	n/a
36	chr20:1578550-1578600	SAEC	small airway:	n/a
37	chr20:1578550-1578600	HMEC	breast:	n/a
38	chr20:1578550-1578600	T-47D	breast:	n/a
39	chr20:1578550-1578600	ECC-1	luminal epithelium:	n/a
40	chr20:1578550-1578600	HepG2	liver:	n/a
41	chr20:1578550-1578600	HAEpiC	amniotic membrane:	n/a
42	chr20:1578550-1578600	Caco-2	colon:	n/a
43	chr20:1578550-1578600	HEK293	kidney:	embryo
44	chr20:1578550-1578600	PFSK-1	brain:	n/a
45	chr20:1578550-1578600	ProgFib	skin:	n/a
46	chr20:1578550-1578600	SK-N-SH	brain:	n/a
47	chr20:1578550-1578600	HCF	heart:	n/a
48	chr20:1578550-1578600	Hepatocyte	liver:	n/a
49	chr20:1578550-1578600	Hela-S3	cervix:	n/a
50	chr20:1578550-1578600	NB4	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-4	chr20:1572038-1572494	NONHSAT078121
2	lnc-SNPH-5	chr20:1574682-1577118	ucscGeneNc_uc002wfp_1
3	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1
4	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
5	lnc-SNPH-5	chr20:1562154-1562366	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: 626 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2254194	chr20:1549402-1549403	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188421681	chr20:1549426-1549427	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79699278	chr20:1549548-1549549	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374895236	chr20:1549550-1549551	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572512524	chr20:1549640-1549641	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530653326	chr20:1549642-1549643	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs3848789	chr20:1549654-1549655	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556088320	chr20:1549659-1549660	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564348978	chr20:1549701-1549702	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528337937	chr20:1549758-1549759	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546891710	chr20:1549790-1549791	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370190191	chr20:1549807-1549808	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561896751	chr20:1549820-1549821	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529232065	chr20:1549821-1549822	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112885875	chr20:1549836-1549837	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113460623	chr20:1549936-1549937	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192252316	chr20:1550047-1550048	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373053185	chr20:1550119-1550120	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567058012	chr20:1550140-1550141	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147963521	chr20:1550199-1550200	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114332427	chr20:1550216-1550217	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs574287248	chr20:1550240-1550241	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs149001455	chr20:1550241-1550242	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs557044535	chr20:1550268-1550269	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs183892729	chr20:1550298-1550299	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs545925986	chr20:1550319-1550320	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs16995310	chr20:1550334-1550335	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs573007532	chr20:1550350-1550351	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs115257995	chr20:1550359-1550360	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs188359364	chr20:1550396-1550397	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs181810686	chr20:1550406-1550407	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs560379688	chr20:1550422-1550423	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs550550874	chr20:1550458-1550459	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs143783305	chr20:1550482-1550483	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs148137938	chr20:1550483-1550484	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs551873746	chr20:1550510-1550511	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs115996034	chr20:1550541-1550542	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs368037437	chr20:1550574-1550575	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs577031258	chr20:1550585-1550586	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs549341292	chr20:1550594-1550595	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs567959012	chr20:1550674-1550675	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141015957	chr20:1550690-1550691	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556959123	chr20:1550728-1550729	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145055610	chr20:1550762-1550763	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114460475	chr20:1550802-1550803	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115550343	chr20:1550832-1550833	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545946549	chr20:1550854-1550855	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373738755	chr20:1550881-1550882	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540418132	chr20:1550891-1550892	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561773014	chr20:1550931-1550932	Enhancers 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:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1537000-1551600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr20:1543200-1550400	Weak transcription	Thymus	Thymus
3	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr20:1546600-1551200	Enhancers	Hela-S3	cervix
6	chr20:1546600-1551400	Weak transcription	Spleen	Spleen
7	chr20:1546800-1550800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr20:1546800-1551000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr20:1547000-1550800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr20:1547000-1551000	Enhancers	HMEC	breast
11	chr20:1547200-1551000	Enhancers	HUVEC	blood vessel
12	chr20:1547800-1550200	Enhancers	NHDF-Ad	bronchial
13	chr20:1548200-1551400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr20:1548400-1550200	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr20:1548600-1550600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr20:1548600-1550600	Enhancers	A549	lung
17	chr20:1548800-1551000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr20:1548800-1551000	Enhancers	NHEK	skin
19	chr20:1548800-1552400	Strong transcription	Primary T cells from cord blood	blood
20	chr20:1549000-1550000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr20:1549000-1550000	Weak transcription	Esophagus	oesophagus
22	chr20:1549200-1549600	Enhancers	Primary B cells from cord blood	blood
23	chr20:1549400-1550200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr20:1549400-1550400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr20:1549600-1550800	Weak transcription	Primary B cells from cord blood	blood
26	chr20:1550000-1550200	Enhancers	Esophagus	oesophagus
27	chr20:1550000-1550400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr20:1550000-1550800	Enhancers	K562	blood
29	chr20:1550000-1568200	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr20:1550200-1550400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr20:1550200-1550400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr20:1550200-1550600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr20:1550200-1551400	Weak transcription	Esophagus	oesophagus
34	chr20:1550400-1550600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr20:1550400-1550600	Enhancers	Thymus	Thymus
36	chr20:1550400-1550800	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr20:1550600-1552400	Genic enhancers	Primary monocytes fromperipheralblood	blood
38	chr20:1550600-1552400	Genic enhancers	Monocytes-CD14+_RO01746	blood
39	chr20:1550800-1551200	Enhancers	Primary B cells from cord blood	blood
40	chr20:1550800-1551600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr20:1550800-1552200	Genic enhancers	Primary neutrophils fromperipheralblood	blood
42	chr20:1551200-1552200	Weak transcription	Hela-S3	cervix
43	chr20:1551400-1552600	Strong transcription	Spleen	Spleen
44	chr20:1551400-1552800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr20:1551600-1552400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr20:1551800-1552000	Enhancers	Esophagus	oesophagus
47	chr20:1552200-1553000	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr20:1552400-1553000	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr20:1552400-1553400	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr20:1552400-1558000	Weak transcription	Primary T cells from cord blood	blood

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