Variant report

Variant	esv3454858
Chromosome Location	chr20:1545691-1674811
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:872)
CpG islands
(count:732)
Chromatin interactive
region (count:3)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	ARID3A	chr20:1617304-1617678	HepG2	liver:	n/a	n/a
3	ATF1	chr20:1614192-1614501	K562	blood:	n/a	n/a
4	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
5	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
6	ATF2	chr20:1607520-1607935	GM12878	blood:	n/a	n/a
7	ATF2	chr20:1640754-1641281	GM12878	blood:	n/a	n/a
8	ATF2	chr20:1645577-1645900	GM12878	blood:	n/a	n/a
9	ATF2	chr20:1603058-1603543	GM12878	blood:	n/a	n/a
10	ATF2	chr20:1612776-1613188	GM12878	blood:	n/a	n/a
11	ATF2	chr20:1645510-1646022	GM12878	blood:	n/a	n/a
12	ATF2	chr20:1607411-1607905	GM12878	blood:	n/a	n/a
13	ATF2	chr20:1640865-1641393	GM12878	blood:	n/a	n/a
14	ATF2	chr20:1612733-1613271	GM12878	blood:	n/a	n/a
15	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
16	BATF	chr20:1621158-1621494	GM12878	blood:	n/a	n/a
17	BATF	chr20:1628753-1629096	GM12878	blood:	n/a	chr20:1628940-1628951
18	BATF	chr20:1638679-1639013	GM12878	blood:	n/a	n/a
19	BATF	chr20:1640943-1641497	GM12878	blood:	n/a	chr20:1641404-1641414
20	BATF	chr20:1638736-1639011	GM12878	blood:	n/a	n/a
21	BATF	chr20:1641005-1641263	GM12878	blood:	n/a	n/a
22	BATF	chr20:1612731-1613238	GM12878	blood:	n/a	chr20:1612969-1612980
23	BATF	chr20:1603174-1603482	GM12878	blood:	n/a	n/a
24	BATF	chr20:1612769-1613106	GM12878	blood:	n/a	chr20:1612969-1612980
25	BATF	chr20:1642642-1642897	GM12878	blood:	n/a	n/a
26	BATF	chr20:1633644-1633992	GM12878	blood:	n/a	n/a
27	BCL11A	chr20:1640981-1641251	GM12878	blood:	n/a	n/a
28	BCL11A	chr20:1645573-1645931	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
29	BCL11A	chr20:1603111-1603444	GM12878	blood:	n/a	n/a
30	BCL11A	chr20:1612833-1613216	GM12878	blood:	n/a	n/a
31	BCL11A	chr20:1603100-1603339	GM12878	blood:	n/a	n/a
32	BCL3	chr20:1645525-1645977	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
33	BCL3	chr20:1628817-1629045	GM12878	blood:	n/a	n/a
34	BCL3	chr20:1612800-1613166	GM12878	blood:	n/a	n/a
35	BCL3	chr20:1603087-1603515	GM12878	blood:	n/a	n/a
36	BCLAF1	chr20:1640863-1641357	GM12878	blood:	n/a	n/a
37	BCLAF1	chr20:1612842-1613225	GM12878	blood:	n/a	n/a
38	BCLAF1	chr20:1603036-1603400	GM12878	blood:	n/a	n/a
39	BCLAF1	chr20:1612776-1613271	GM12878	blood:	n/a	n/a
40	BCLAF1	chr20:1645421-1645899	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
41	BHLHE40	chr20:1603122-1603445	GM12878	blood:	n/a	n/a
42	BHLHE40	chr20:1674091-1674109	GM12878	blood:	n/a	n/a
43	BHLHE40	chr20:1647508-1647681	GM12878	blood:	n/a	n/a
44	BHLHE40	chr20:1549969-1550250	K562	blood:	n/a	n/a
45	BHLHE40	chr20:1640252-1640311	GM12878	blood:	n/a	n/a
46	BRCA1	chr20:1603218-1603418	GM12878	blood:	n/a	n/a
47	BRCA1	chr20:1550123-1550444	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr20:1549828-1550670	HCT-116	colon:	n/a	chr20:1549945-1549956
49	CEBPB	chr20:1612296-1612538	HepG2	liver:	n/a	n/a
50	CEBPB	chr20:1612280-1612459	H1-hESC	embryonic stem cell:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1639250-1639300	HNPCEpiC	eye:	n/a
2	chr20:1639325-1639375	NHBE	bronchial:	n/a
3	chr20:1639816-1639866	HRE	kidney:	n/a
4	chr20:1601704-1601754	AG10803	skin:	n/a
5	chr20:1600641-1600691	HRCEpiC	kidney:	n/a
6	chr20:1616387-1616437	HAEpiC	amniotic membrane:	n/a
7	chr20:1639250-1639300	MCF-7	breast:	n/a
8	chr20:1601704-1601754	HRE	kidney:	n/a
9	chr20:1638393-1638443	AG04450	lung:	fetal
10	chr20:1546019-1546069	NHBE	bronchial:	n/a
11	chr20:1616387-1616437	HL-60	blood:	n/a
12	chr20:1546019-1546069	U87	brain:	n/a
13	chr20:1639250-1639300	HCF	heart:	n/a
14	chr20:1639250-1639300	HPAEpiC	pulmonary alveolar:	n/a
15	chr20:1639325-1639375	T-47D	breast:	n/a
16	chr20:1616387-1616437	GM12892	blood:	n/a
17	chr20:1546019-1546069	ProgFib	skin:	n/a
18	chr20:1638393-1638443	SK-N-MC	brain:	n/a
19	chr20:1546019-1546069	HUVEC	blood vessel:	n/a
20	chr20:1600623-1600673	K562	blood:	n/a
21	chr20:1600623-1600673	NB4	blood:	n/a
22	chr20:1616387-1616437	HIPEpiC	eye:	n/a
23	chr20:1639325-1639375	HNPCEpiC	eye:	n/a
24	chr20:1639325-1639375	HCF	heart:	n/a
25	chr20:1601704-1601754	PrEC	prostate:	n/a
26	chr20:1600705-1600755	NHDF-neo	bronchial:	n/a
27	chr20:1578550-1578600	NT2-D1	testis:	n/a
28	chr20:1616387-1616437	AG09319	gingival:	n/a
29	chr20:1610358-1610408	HAEpiC	amniotic membrane:	n/a
30	chr20:1600641-1600691	BJ	skin:	n/a
31	chr20:1610358-1610408	SKMC	muscle:	n/a
32	chr20:1546019-1546069	ECC-1	luminal epithelium:	n/a
33	chr20:1639816-1639866	K562	blood:	n/a
34	chr20:1638393-1638443	Jurkat	blood:	n/a
35	chr20:1601704-1601754	HPAEpiC	pulmonary alveolar:	n/a
36	chr20:1600623-1600673	ovcar-3	ovarian:	n/a
37	chr20:1639816-1639866	IMR90	lung:	fetal
38	chr20:1610358-1610408	PrEC	prostate:	n/a
39	chr20:1600705-1600755	SAEC	small airway:	n/a
40	chr20:1546019-1546069	SAEC	small airway:	n/a
41	chr20:1638393-1638443	Caco-2	colon:	n/a
42	chr20:1639250-1639300	IMR90	lung:	fetal
43	chr20:1601704-1601754	HEEpiC	esophagus:	n/a
44	chr20:1610358-1610408	ovcar-3	ovarian:	n/a
45	chr20:1578550-1578600	AG09319	gingival:	n/a
46	chr20:1616387-1616437	U87	brain:	n/a
47	chr20:1639250-1639300	Caco-2	colon:	n/a
48	chr20:1600705-1600755	SKMC	muscle:	n/a
49	chr20:1600705-1600755	Jurkat	blood:	n/a
50	chr20:1616387-1616437	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr20:1547054..1548894-chr20:1756067..1757690,2	K562	blood:
2	chr20:1484085..1484840-chr20:1617080..1618039,2	MCF-7	breast:
3	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIRPA-3	chr20:1626682-1629119	NR_110090
2	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
3	lnc-SIRPG-2	chr20:1610868-1610952	NONHSAT078122
4	lnc-SIRPA-3	chr20:1619056-1619100	ENSG00000237914
5	lnc-SIRPA-3	chr20:1614272-1614366	ENSG00000237914
6	lnc-SIRPA-3	chr20:1618264-1618388	ENSG00000237914
7	lnc-SIRPA-3	chr20:1614154-1614366	ENSG00000237914
8	lnc-SIRPG-2	chr20:1610868-1610952	NONHSAT078123
9	lnc-SNPH-5	chr20:1562154-1562366	ucscGeneNc_uc002wfp_1
10	lnc-SNPH-5	chr20:1574682-1577118	ucscGeneNc_uc002wfp_1
11	lnc-SIRPA-3	chr20:1617852-1617996	ENSG00000237914
12	lnc-SIRPA-3	chr20:1626682-1629118	ENSG00000237914
13	lnc-SIRPA-3	chr20:1617852-1617996	ENSG00000237914
14	lnc-SIRPA-3	chr20:1617852-1617996	NR_110090
15	lnc-SIRPA-3	chr20:1614154-1614366	NR_110090
16	lnc-SIRPG-2	chr20:1611341-1611482	NONHSAT078122
17	lnc-SIRPG-2	chr20:1609798-1610282	NONHSAT078122
18	lnc-SIRPG-2	chr20:1610173-1610282	NONHSAT078123
19	lnc-SIRPA-5	chr20:1647006-1647284	NONHSAT078126
20	lnc-SIRPG-2	chr20:1611060-1611289	NONHSAT078123
21	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1
22	lnc-SNPH-4	chr20:1572038-1572494	NONHSAT078121

No data

Variant related genes	Relation type
SIRPB1	TF binding region
ENSG00000236550	TF binding region
ENSG00000271523	TF binding region
SIRPG	TF binding region
RN7SL561P	TF binding region
ENSG00000237914	TF binding region
ENSG00000260861	TF binding region
SIRPB1	CpG island
ENSG00000236550	CpG island
ENSG00000271523	CpG island
SIRPG	CpG island
RN7SL561P	CpG island
ENSG00000237914	CpG island
ENSG00000260861	CpG island
SOX4	miRNA target sites
ENPP4	miRNA target sites
ETV6	miRNA target sites
KIAA0831	miRNA target sites
GOLT1B	miRNA target sites
BMPR2	miRNA target sites

Extended variants
information (count: 4647 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4647 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571877913	chr20:1545691-1545692	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536410483	chr20:1545718-1545719	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189597232	chr20:1545727-1545728	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531589523	chr20:1545745-1545746	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372470630	chr20:1545794-1545795	ZNF genes & repeats Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs16995228	chr20:1545857-1545858	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs566308622	chr20:1545941-1545942	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533766481	chr20:1545980-1545981	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145520796	chr20:1545981-1545982	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371415442	chr20:1546012-1546013	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs114721859	chr20:1546020-1546021	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs373144814	chr20:1546030-1546031	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs570931302	chr20:1546035-1546036	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs577419882	chr20:1546086-1546087	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs544878020	chr20:1546093-1546094	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs536615314	chr20:1546135-1546136	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs572287257	chr20:1546148-1546149	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs2253814	chr20:1546175-1546176	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs2253815	chr20:1546207-1546208	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs74321032	chr20:1546229-1546230	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs536542704	chr20:1546233-1546234	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs181521523	chr20:1546248-1546249	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs148842400	chr20:1546256-1546257	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs552931485	chr20:1546263-1546264	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs142523875	chr20:1546274-1546275	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs11907473	chr20:1546350-1546351	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs147557710	chr20:1546352-1546353	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs566340787	chr20:1546353-1546354	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs17721235	chr20:1546373-1546374	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs76482364	chr20:1546378-1546379	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs567160625	chr20:1546386-1546387	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs142664030	chr20:1546423-1546424	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs185973955	chr20:1546429-1546430	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs571076363	chr20:1546430-1546431	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs2253821	chr20:1546450-1546451	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs370361511	chr20:1546452-1546453	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs561332901	chr20:1546498-1546499	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs6135315	chr20:1546506-1546507	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs572292047	chr20:1546544-1546545	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs542564812	chr20:1546548-1546549	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs116264607	chr20:1546564-1546565	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs374752158	chr20:1546595-1546596	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs368544292	chr20:1546613-1546614	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs543901118	chr20:1546641-1546642	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs115564175	chr20:1546689-1546690	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs190691374	chr20:1546705-1546706	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs527585630	chr20:1546723-1546724	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs2243602	chr20:1546742-1546743	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs78745462	chr20:1546769-1546770	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs146905696	chr20:1546780-1546781	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	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:1364 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

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	chr20:1543600-1548600	Genic enhancers	Primary monocytes fromperipheralblood	blood
4	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr20:1544800-1548200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr20:1545000-1548000	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr20:1545200-1547400	Strong transcription	Primary T cells from cord blood	blood
9	chr20:1545400-1546200	Genic enhancers	Monocytes-CD14+_RO01746	blood
10	chr20:1545400-1546600	Strong transcription	Spleen	Spleen
11	chr20:1545600-1545800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr20:1545800-1546800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr20:1545800-1549400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr20:1546000-1547000	ZNF genes & repeats	Lung	lung
15	chr20:1546200-1547800	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr20:1546600-1551200	Enhancers	Hela-S3	cervix
17	chr20:1546600-1551400	Weak transcription	Spleen	Spleen
18	chr20:1546800-1550800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr20:1546800-1551000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr20:1547000-1547800	Enhancers	NHEK	skin
21	chr20:1547000-1550800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr20:1547000-1551000	Enhancers	HMEC	breast
23	chr20:1547200-1549000	Enhancers	NH-A	brain
24	chr20:1547200-1549400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr20:1547200-1551000	Enhancers	HUVEC	blood vessel
26	chr20:1547400-1548000	Enhancers	A549	lung
27	chr20:1547400-1548800	Weak transcription	Primary T cells from cord blood	blood
28	chr20:1547400-1549000	Enhancers	Osteobl	bone
29	chr20:1547800-1548000	Genic enhancers	Monocytes-CD14+_RO01746	blood
30	chr20:1547800-1548200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr20:1547800-1548600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr20:1547800-1548800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr20:1547800-1548800	Flanking Active TSS	NHEK	skin
34	chr20:1547800-1550200	Enhancers	NHDF-Ad	bronchial
35	chr20:1548000-1548200	Active TSS	A549	lung
36	chr20:1548000-1548400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr20:1548000-1548400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
38	chr20:1548000-1548400	Enhancers	Esophagus	oesophagus
39	chr20:1548000-1548400	Enhancers	NHLF	lung
40	chr20:1548000-1548800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr20:1548000-1549000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr20:1548000-1549000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr20:1548000-1549000	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
44	chr20:1548200-1548600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr20:1548200-1548600	Flanking Active TSS	A549	lung
46	chr20:1548200-1551400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr20:1548400-1548600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr20:1548400-1548800	Weak transcription	Esophagus	oesophagus
49	chr20:1548400-1550200	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr20:1548600-1549000	Enhancers	Primary hematopoietic stem cells	blood

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