Variant report

Variant	esv1814180
Chromosome Location	chr20:1540847-1601747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:350)
CpG islands
(count:367)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:350 , 50 per page) page: 1 2 3 4 5 6 7

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	chr20:1597810-1598006	K562	blood:	n/a	n/a
3	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
4	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
5	BATF	chr20:1543275-1543590	GM12878	blood:	n/a	n/a
6	BHLHE40	chr20:1549969-1550250	K562	blood:	n/a	n/a
7	BRCA1	chr20:1550123-1550444	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr20:1548089-1548620	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr20:1550121-1550426	IMR90	lung:	n/a	n/a
10	CEBPB	chr20:1549828-1550670	HCT-116	colon:	n/a	chr20:1549945-1549956
11	CEBPB	chr20:1549993-1550495	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr20:1550079-1550429	K562	blood:	n/a	n/a
13	CEBPB	chr20:1557313-1557606	Hela-S3	cervix:	n/a	chr20:1557460-1557471
14	CEBPB	chr20:1549987-1550512	A549	lung:	n/a	n/a
15	CEBPB	chr20:1557318-1557553	HepG2	liver:	n/a	chr20:1557460-1557471
16	CEBPB	chr20:1550069-1550318	K562	blood:	n/a	n/a
17	CEBPB	chr20:1541479-1541541	HepG2	liver:	n/a	chr20:1541509-1541518 chr20:1541509-1541520 chr20:1541507-1541520
18	CEBPB	chr20:1549872-1550575	HCT-116	colon:	n/a	chr20:1549945-1549956
19	CEBPB	chr20:1550085-1550450	A549	lung:	n/a	n/a
20	CEBPB	chr20:1596225-1596242	HepG2	liver:	n/a	n/a
21	CEBPB	chr20:1550076-1550409	HepG2	liver:	n/a	n/a
22	CEBPB	chr20:1557320-1557574	A549	lung:	n/a	chr20:1557460-1557471
23	CEBPB	chr20:1600640-1600781	HepG2	liver:	n/a	chr20:1600734-1600745
24	CEBPB	chr20:1550062-1550405	A549	lung:	n/a	n/a
25	CEBPB	chr20:1550060-1550411	MCF-7	breast:	n/a	n/a
26	CHD1	chr20:1601432-1601474	GM12878	blood:	n/a	n/a
27	CHD1	chr20:1600268-1600351	GM12878	blood:	n/a	n/a
28	CHD2	chr20:1548232-1548651	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr20:1600141-1600445	GM12878	blood:	n/a	n/a
30	CHD2	chr20:1550074-1550408	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr20:1550008-1550399	K562	blood:	n/a	n/a
32	CTCF	chr20:1569840-1569990	HAc	cerebellar:	n/a	n/a
33	CTCF	chr20:1599260-1599410	GM12870	blood:	n/a	n/a
34	CTCF	chr20:1569820-1569970	HRE	kidney:	n/a	n/a
35	CTCF	chr20:1562235-1562401	GM12878	blood:	n/a	n/a
36	CTCF	chr20:1569840-1569990	HRE	kidney:	n/a	n/a
37	CTCF	chr20:1569782-1570019	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr20:1569800-1569950	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr20:1583974-1584038	GM10266	blood:	n/a	chr20:1583996-1584006
40	CTCF	chr20:1569900-1570050	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr20:1583950-1584135	GM12878	blood:	n/a	chr20:1583996-1584006
42	CTCF	chr20:1562180-1562330	GM12878	blood:	n/a	n/a
43	CTCF	chr20:1569820-1569970	AG10803	skin:	n/a	n/a
44	CTCF	chr20:1569840-1569990	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr20:1569860-1570010	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr20:1583954-1584054	GM19239	blood:	n/a	chr20:1583996-1584006
47	CTCF	chr20:1562140-1562290	GM12864	blood:	n/a	n/a
48	CTCF	chr20:1569880-1570030	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr20:1569780-1569930	SAEC	small airway:	n/a	n/a
50	CTCF	chr20:1595313-1595408	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1600705-1600755	AG09309	skin:	n/a
2	chr20:1600705-1600755	AG09309	skin:	n/a
3	chr20:1546019-1546069	AG09319	gingival:	n/a
4	chr20:1600705-1600755	AG09319	gingival:	n/a
5	chr20:1600641-1600691	K562	blood:	n/a
6	chr20:1600641-1600691	U87	brain:	n/a
7	chr20:1600623-1600673	T-47D	breast:	n/a
8	chr20:1600623-1600673	Jurkat	blood:	n/a
9	chr20:1546019-1546069	GM19239	blood:	n/a
10	chr20:1600623-1600673	GM12891	blood:	n/a
11	chr20:1578550-1578600	SK-N-SH_RA	brain:	n/a
12	chr20:1600641-1600691	AoSMC	blood vessel:	n/a
13	chr20:1546019-1546069	GM12892	blood:	n/a
14	chr20:1600705-1600755	HPAEpiC	pulmonary alveolar:	n/a
15	chr20:1600623-1600673	HPAEpiC	pulmonary alveolar:	n/a
16	chr20:1546019-1546069	MCF10A-Er-Src	breast:	n/a
17	chr20:1601704-1601754	NB4	blood:	n/a
18	chr20:1578550-1578600	AG04450	lung:	fetal
19	chr20:1578550-1578600	HRCEpiC	kidney:	n/a
20	chr20:1578550-1578600	SK-N-SH	brain:	n/a
21	chr20:1578550-1578600	U87	brain:	n/a
22	chr20:1601704-1601754	PANC-1	pancreas:	n/a
23	chr20:1600705-1600755	T-47D	breast:	n/a
24	chr20:1600641-1600691	Jurkat	blood:	n/a
25	chr20:1578550-1578600	ECC-1	luminal epithelium:	n/a
26	chr20:1600705-1600755	SK-N-SH	brain:	n/a
27	chr20:1600641-1600691	LNCaP	prostate:	n/a
28	chr20:1600705-1600755	BE2_C	brain:	n/a
29	chr20:1600705-1600755	HCPEpiC	choroid plexus:	n/a
30	chr20:1600623-1600673	SK-N-SH_RA	brain:	n/a
31	chr20:1600705-1600755	SK-N-MC	brain:	n/a
32	chr20:1600705-1600755	SK-N-SH_RA	brain:	n/a
33	chr20:1546019-1546069	BJ	skin:	n/a
34	chr20:1600623-1600673	HUVEC	blood vessel:	n/a
35	chr20:1601704-1601754	AoSMC	blood vessel:	n/a
36	chr20:1578550-1578600	HNPCEpiC	eye:	n/a
37	chr20:1600623-1600673	HEK293	kidney:	embryo
38	chr20:1601704-1601754	LNCaP	prostate:	n/a
39	chr20:1546019-1546069	HCPEpiC	choroid plexus:	n/a
40	chr20:1600705-1600755	HUVEC	blood vessel:	n/a
41	chr20:1600705-1600755	AG10803	skin:	n/a
42	chr20:1601704-1601754	Hepatocyte	liver:	n/a
43	chr20:1600623-1600673	MCF-7	breast:	n/a
44	chr20:1600705-1600755	MCF-7	breast:	n/a
45	chr20:1600705-1600755	Hela-S3	cervix:	n/a
46	chr20:1601704-1601754	HMEC	breast:	n/a
47	chr20:1601704-1601754	HRE	kidney:	n/a
48	chr20:1546019-1546069	PrEC	prostate:	n/a
49	chr20:1546019-1546069	HMEC	breast:	n/a
50	chr20:1546019-1546069	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:
2	chr20:1547054..1548894-chr20:1756067..1757690,2	K562	blood:

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

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

No data

Variant related genes	Relation type
SIRPB1	TF binding region
SIRPD	TF binding region
ENSG00000271523	TF binding region
ENSG00000260861	TF binding region
ENSG00000242324	TF binding region
SIRPB1	CpG island
SIRPD	CpG island
ENSG00000271523	CpG island
ENSG00000260861	CpG island
ENSG00000242324	CpG island

Extended variants
information (count: 1558 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1558 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536214966	chr20:1540855-1540856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555143886	chr20:1540879-1540880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35922329	chr20:1540914-1540915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375310983	chr20:1540941-1540942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34340716	chr20:1540964-1540965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112881786	chr20:1540965-1540966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369372449	chr20:1540995-1540996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148155892	chr20:1540999-1541000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565501942	chr20:1541004-1541005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536427552	chr20:1541105-1541106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144006525	chr20:1541108-1541109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544568165	chr20:1541112-1541113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114430738	chr20:1541184-1541185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543392532	chr20:1541209-1541210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558950139	chr20:1541220-1541221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577314523	chr20:1541269-1541270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375193767	chr20:1541272-1541273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11698344	chr20:1541295-1541296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2263663	chr20:1541301-1541302	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs559901880	chr20:1541317-1541318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557634741	chr20:1541318-1541319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542390269	chr20:1541319-1541320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563778309	chr20:1541329-1541330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531229724	chr20:1541350-1541351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552606976	chr20:1541371-1541372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140843193	chr20:1541373-1541374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6042972	chr20:1541391-1541392	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs118109524	chr20:1541402-1541403	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs73604176	chr20:1541433-1541434	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs188691987	chr20:1541434-1541435	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs150837564	chr20:1541488-1541489	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs79612744	chr20:1541546-1541547	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs537303668	chr20:1541604-1541605	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs180765366	chr20:1541613-1541614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185843593	chr20:1541657-1541658	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73570817	chr20:1541705-1541706	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs386811624	chr20:1541750-1541751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112068647	chr20:1541751-1541752	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199732367	chr20:1541752-1541753	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139256466	chr20:1541762-1541763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542000008	chr20:1541767-1541768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189523983	chr20:1541835-1541836	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181949968	chr20:1541931-1541932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149973544	chr20:1541937-1541938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531513854	chr20:1541952-1541953	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372577556	chr20:1541957-1541958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2422614	chr20:1541969-1541970	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs73570821	chr20:1541982-1541983	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187404654	chr20:1541986-1541987	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558964755	chr20:1541991-1541992	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Prostate cancer	21551127	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1532800-1545400	Weak transcription	Spleen	Spleen
2	chr20:1537000-1541200	Weak transcription	Primary T cells from cord blood	blood
3	chr20:1537000-1551600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr20:1537400-1542800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr20:1539200-1541200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr20:1539600-1542600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr20:1540000-1544800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr20:1540200-1543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr20:1541200-1541800	Strong transcription	Primary T cells from cord blood	blood
10	chr20:1541200-1543000	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr20:1541600-1542200	Enhancers	HUVEC	blood vessel
12	chr20:1541800-1545200	Weak transcription	Primary T cells from cord blood	blood
13	chr20:1542400-1543800	Enhancers	Dnd41	blood
14	chr20:1542600-1543200	Genic enhancers	Primary monocytes fromperipheralblood	blood
15	chr20:1542800-1543000	Genic enhancers	Monocytes-CD14+_RO01746	blood
16	chr20:1543000-1543200	Enhancers	Thymus	Thymus
17	chr20:1543000-1543800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr20:1543000-1545000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
19	chr20:1543200-1543600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr20:1543200-1550400	Weak transcription	Thymus	Thymus
21	chr20:1543400-1544000	Enhancers	Primary B cells from cord blood	blood
22	chr20:1543600-1544000	Enhancers	GM12878-XiMat	blood
23	chr20:1543600-1548600	Genic enhancers	Primary monocytes fromperipheralblood	blood
24	chr20:1543800-1544000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr20:1544000-1545000	Genic enhancers	Monocytes-CD14+_RO01746	blood
27	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr20:1544800-1548200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr20:1545000-1545400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
30	chr20:1545000-1548000	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr20:1545200-1547400	Strong transcription	Primary T cells from cord blood	blood
32	chr20:1545400-1546200	Genic enhancers	Monocytes-CD14+_RO01746	blood
33	chr20:1545400-1546600	Strong transcription	Spleen	Spleen
34	chr20:1545600-1545800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr20:1545800-1546800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr20:1545800-1549400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr20:1546000-1547000	ZNF genes & repeats	Lung	lung
38	chr20:1546200-1547800	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr20:1546600-1551200	Enhancers	Hela-S3	cervix
40	chr20:1546600-1551400	Weak transcription	Spleen	Spleen
41	chr20:1546800-1550800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr20:1546800-1551000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr20:1547000-1547800	Enhancers	NHEK	skin
44	chr20:1547000-1550800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr20:1547000-1551000	Enhancers	HMEC	breast
46	chr20:1547200-1549000	Enhancers	NH-A	brain
47	chr20:1547200-1549400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr20:1547200-1551000	Enhancers	HUVEC	blood vessel
49	chr20:1547400-1548000	Enhancers	A549	lung
50	chr20:1547400-1548800	Weak transcription	Primary T cells from cord blood	blood

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