Variant report

Variant	nsv1066579
Chromosome Location	chr20:1560240-1597934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:114)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:114 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
2	CEBPB	chr20:1596225-1596242	HepG2	liver:	n/a	n/a
3	CTCF	chr20:1562236-1562335	Gliobla	brain:	n/a	n/a
4	CTCF	chr20:1562235-1562401	GM12878	blood:	n/a	n/a
5	CTCF	chr20:1583950-1584135	GM12878	blood:	n/a	chr20:1583996-1584006
6	CTCF	chr20:1589816-1589866	NHEK	skin:	n/a	n/a
7	CTCF	chr20:1562140-1562290	GM12864	blood:	n/a	n/a
8	CTCF	chr20:1569800-1569950	GM12864	blood:	n/a	n/a
9	CTCF	chr20:1562180-1562330	GM12878	blood:	n/a	n/a
10	CTCF	chr20:1595313-1595408	GM12878	blood:	n/a	n/a
11	CTCF	chr20:1595316-1595438	HUVEC	blood vessel:	n/a	n/a
12	CTCF	chr20:1569840-1569990	HRPEpiC	eye:	n/a	n/a
13	CTCF	chr20:1569840-1569990	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr20:1562180-1562330	GM12875	blood:	n/a	n/a
15	CTCF	chr20:1583974-1584038	GM10266	blood:	n/a	chr20:1583996-1584006
16	CTCF	chr20:1569840-1569990	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr20:1569782-1570019	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr20:1594081-1594153	LNCaP	prostate:	n/a	n/a
19	CTCF	chr20:1583918-1584066	GM12878	blood:	n/a	chr20:1583996-1584006
20	CTCF	chr20:1569900-1570050	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr20:1569880-1570030	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr20:1562218-1562407	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr20:1593027-1593071	K562	blood:	n/a	n/a
24	CTCF	chr20:1569820-1569970	HRE	kidney:	n/a	n/a
25	CTCF	chr20:1562235-1562365	GM13977	blood:	n/a	n/a
26	CTCF	chr20:1569820-1569970	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr20:1569840-1569990	HRE	kidney:	n/a	n/a
28	CTCF	chr20:1569820-1569970	GM12878	blood:	n/a	n/a
29	CTCF	chr20:1583938-1584013	HUVEC	blood vessel:	n/a	chr20:1583996-1584006
30	CTCF	chr20:1569860-1570010	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr20:1569840-1569990	HAc	cerebellar:	n/a	n/a
32	CTCF	chr20:1585205-1585266	GM10248	blood:	n/a	n/a
33	CTCF	chr20:1562336-1562338	Gliobla	brain:	n/a	n/a
34	CTCF	chr20:1569860-1570007	GM12878	blood:	n/a	n/a
35	CTCF	chr20:1569800-1569950	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr20:1569820-1569970	AG10803	skin:	n/a	n/a
37	CTCF	chr20:1569820-1569970	HCT-116	colon:	n/a	n/a
38	CTCF	chr20:1569768-1570055	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr20:1569780-1569930	SAEC	small airway:	n/a	n/a
40	CTCF	chr20:1569812-1570027	Gliobla	brain:	n/a	n/a
41	CTCF	chr20:1569844-1569973	GM12878	blood:	n/a	n/a
42	CTCF	chr20:1569809-1569981	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr20:1583923-1584071	GM12891	blood:	n/a	chr20:1583996-1584006
44	CTCF	chr20:1569890-1569986	ProgFib	skin:	n/a	n/a
45	CTCF	chr20:1583954-1584054	GM19239	blood:	n/a	chr20:1583996-1584006
46	CTCF	chr20:1583993-1584014	H1-hESC	embryonic stem cell:	n/a	chr20:1583996-1584006
47	E2F4	chr20:1596569-1596779	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr20:1576059-1576210	GM12878	blood:	n/a	n/a
49	EBF1	chr20:1575968-1576160	GM12878	blood:	n/a	n/a
50	ELF1	chr20:1575954-1576254	GM12878	blood:	n/a	chr20:1576167-1576178

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1578550-1578600	HRE	kidney:	n/a
2	chr20:1578550-1578600	ECC-1	luminal epithelium:	n/a
3	chr20:1578550-1578600	AG10803	skin:	n/a
4	chr20:1578550-1578600	ovcar-3	ovarian:	n/a
5	chr20:1578550-1578600	HRPEpiC	eye:	n/a
6	chr20:1578550-1578600	HCT-116	colon:	n/a
7	chr20:1578550-1578600	HCPEpiC	choroid plexus:	n/a
8	chr20:1578550-1578600	HRCEpiC	kidney:	n/a
9	chr20:1578550-1578600	K562	blood:	n/a
10	chr20:1578550-1578600	HCM	heart:	n/a
11	chr20:1578550-1578600	Jurkat	blood:	n/a
12	chr20:1578550-1578600	MCF10A-Er-Src	breast:	n/a
13	chr20:1578550-1578600	HPAEpiC	pulmonary alveolar:	n/a
14	chr20:1578550-1578600	HNPCEpiC	eye:	n/a
15	chr20:1578550-1578600	MCF-7	breast:	n/a
16	chr20:1578550-1578600	GM12878	blood:	n/a
17	chr20:1578550-1578600	AG04450	lung:	fetal
18	chr20:1578550-1578600	GM12891	blood:	n/a
19	chr20:1578550-1578600	NB4	blood:	n/a
20	chr20:1578550-1578600	AG04449	skin:	fetal
21	chr20:1578550-1578600	Caco-2	colon:	n/a
22	chr20:1578550-1578600	LNCaP	prostate:	n/a
23	chr20:1578550-1578600	HL-60	blood:	n/a
24	chr20:1578550-1578600	Hela-S3	cervix:	n/a
25	chr20:1578550-1578600	GM19239	blood:	n/a
26	chr20:1578550-1578600	AG09319	gingival:	n/a
27	chr20:1578550-1578600	Hepatocyte	liver:	n/a
28	chr20:1578550-1578600	HEEpiC	esophagus:	n/a
29	chr20:1578550-1578600	HAEpiC	amniotic membrane:	n/a
30	chr20:1578550-1578600	SAEC	small airway:	n/a
31	chr20:1578550-1578600	PANC-1	pancreas:	n/a
32	chr20:1578550-1578600	AG09309	skin:	n/a
33	chr20:1578550-1578600	RPTEC	kidney:	n/a
34	chr20:1578550-1578600	SK-N-SH	brain:	n/a
35	chr20:1578550-1578600	NT2-D1	testis:	n/a
36	chr20:1578550-1578600	CMK	blood:	n/a
37	chr20:1578550-1578600	NHDF-neo	bronchial:	n/a
38	chr20:1578550-1578600	HepG2	liver:	n/a
39	chr20:1578550-1578600	IMR90	lung:	fetal
40	chr20:1578550-1578600	H1-hESC	embryonic stem cell:	embryo
41	chr20:1578550-1578600	GM06990	blood:	n/a
42	chr20:1578550-1578600	HMEC	breast:	n/a
43	chr20:1578550-1578600	HUVEC	blood vessel:	n/a
44	chr20:1578550-1578600	NHBE	bronchial:	n/a
45	chr20:1578550-1578600	BE2_C	brain:	n/a
46	chr20:1578550-1578600	NH-A	brain:	n/a
47	chr20:1578550-1578600	SK-N-SH_RA	brain:	n/a
48	chr20:1578550-1578600	HCF	heart:	n/a
49	chr20:1578550-1578600	T-47D	breast:	n/a
50	chr20:1578550-1578600	U87	brain:	n/a

No data

(count:4 , 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-4	chr20:1572038-1572494	NONHSAT078121
3	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
4	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: 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	rs577426485	chr20:1560271-1560272	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370112582	chr20:1560291-1560292	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541341780	chr20:1560304-1560305	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182218816	chr20:1560308-1560309	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527271020	chr20:1560313-1560314	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542248801	chr20:1560330-1560331	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560640439	chr20:1560364-1560365	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373530057	chr20:1560375-1560376	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531479101	chr20:1560390-1560391	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547460506	chr20:1560444-1560445	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529662991	chr20:1560491-1560492	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566199837	chr20:1560496-1560497	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549659902	chr20:1560499-1560500	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571427304	chr20:1560502-1560503	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570531179	chr20:1560535-1560536	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532271117	chr20:1560566-1560567	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376628299	chr20:1560603-1560604	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547695312	chr20:1560648-1560649	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539411525	chr20:1560653-1560654	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187184961	chr20:1560736-1560737	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536641413	chr20:1560841-1560842	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555050595	chr20:1560854-1560855	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570007072	chr20:1560861-1560862	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537561902	chr20:1560865-1560866	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142258849	chr20:1560882-1560883	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs55650624	chr20:1560892-1560893	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570375321	chr20:1560901-1560902	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577391168	chr20:1560922-1560923	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190616424	chr20:1560959-1560960	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138828516	chr20:1560969-1560970	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535767897	chr20:1560991-1560992	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370795741	chr20:1560992-1560993	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574833675	chr20:1561026-1561027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181712459	chr20:1561073-1561074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185626126	chr20:1561076-1561077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374198835	chr20:1561089-1561090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190143345	chr20:1561186-1561187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564859575	chr20:1561189-1561190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs66737734	chr20:1561205-1561206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182742303	chr20:1561212-1561213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs547656371	chr20:1561220-1561221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2746604	chr20:1561224-1561225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs11087121	chr20:1561257-1561258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs12480823	chr20:1561284-1561285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs12480824	chr20:1561286-1561287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs548562487	chr20:1561337-1561338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570049448	chr20:1561338-1561339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12479784	chr20:1561339-1561340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
49	rs12479785	chr20:1561369-1561370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs12479793	chr20:1561418-1561419	Weak transcription Enhancers	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
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:119 , 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	chr20:1552400-1568000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr20:1552600-1569000	Weak transcription	Spleen	Spleen
6	chr20:1559600-1560400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
7	chr20:1559600-1560600	Weak transcription	Primary T cells from cord blood	blood
8	chr20:1560000-1561000	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr20:1560000-1561000	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr20:1560000-1579200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr20:1560400-1561800	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr20:1560600-1561000	Strong transcription	Primary T cells from cord blood	blood
13	chr20:1561000-1562600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr20:1561000-1563600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr20:1561000-1568000	Weak transcription	Primary T cells from cord blood	blood
16	chr20:1561800-1563800	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr20:1563600-1564600	Genic enhancers	Primary monocytes fromperipheralblood	blood
18	chr20:1563800-1565400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr20:1564600-1565400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr20:1565400-1565600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr20:1565400-1566000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr20:1565600-1565800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr20:1565800-1567000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr20:1566000-1566600	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr20:1566600-1568400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr20:1567000-1569400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
27	chr20:1567600-1570000	Active TSS	Primary B cells from cord blood	blood
28	chr20:1567800-1569600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr20:1568000-1569000	Enhancers	Primary T cells from cord blood	blood
30	chr20:1568000-1570200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr20:1568000-1570200	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr20:1568000-1570400	Enhancers	Primary T cells fromperipheralblood	blood
33	chr20:1568200-1568800	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr20:1568200-1569800	Enhancers	Primary B cells from peripheral blood	blood
35	chr20:1568400-1568600	Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr20:1568400-1569400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr20:1568400-1570200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr20:1568400-1570600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr20:1568600-1568800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr20:1568600-1568800	Enhancers	NHDF-Ad	bronchial
41	chr20:1568600-1569000	Enhancers	Dnd41	blood
42	chr20:1568600-1570200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr20:1568600-1570400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr20:1568800-1569000	Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr20:1568800-1570200	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr20:1568800-1570200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr20:1569000-1569200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr20:1569000-1569200	Flanking Active TSS	Dnd41	blood
49	chr20:1569000-1569400	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr20:1569000-1569400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links