Variant report

Variant	esv1806656
Chromosome Location	chr20:1553470-1651867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:673)
Chromatin interactive
region (count:1)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:1617304-1617678	HepG2	liver:	n/a	n/a
2	ATF1	chr20:1614192-1614501	K562	blood:	n/a	n/a
3	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
4	ATF2	chr20:1607411-1607905	GM12878	blood:	n/a	n/a
5	ATF2	chr20:1640754-1641281	GM12878	blood:	n/a	n/a
6	ATF2	chr20:1607520-1607935	GM12878	blood:	n/a	n/a
7	ATF2	chr20:1640865-1641393	GM12878	blood:	n/a	n/a
8	ATF2	chr20:1603058-1603543	GM12878	blood:	n/a	n/a
9	ATF2	chr20:1612776-1613188	GM12878	blood:	n/a	n/a
10	ATF2	chr20:1645577-1645900	GM12878	blood:	n/a	n/a
11	ATF2	chr20:1612733-1613271	GM12878	blood:	n/a	n/a
12	ATF2	chr20:1645510-1646022	GM12878	blood:	n/a	n/a
13	BATF	chr20:1638679-1639013	GM12878	blood:	n/a	n/a
14	BATF	chr20:1638736-1639011	GM12878	blood:	n/a	n/a
15	BATF	chr20:1642642-1642897	GM12878	blood:	n/a	n/a
16	BATF	chr20:1612769-1613106	GM12878	blood:	n/a	chr20:1612969-1612980
17	BATF	chr20:1641005-1641263	GM12878	blood:	n/a	n/a
18	BATF	chr20:1628753-1629096	GM12878	blood:	n/a	chr20:1628940-1628951
19	BATF	chr20:1603174-1603482	GM12878	blood:	n/a	n/a
20	BATF	chr20:1633644-1633992	GM12878	blood:	n/a	n/a
21	BATF	chr20:1640943-1641497	GM12878	blood:	n/a	chr20:1641404-1641414
22	BATF	chr20:1612731-1613238	GM12878	blood:	n/a	chr20:1612969-1612980
23	BATF	chr20:1621158-1621494	GM12878	blood:	n/a	n/a
24	BCL11A	chr20:1603100-1603339	GM12878	blood:	n/a	n/a
25	BCL11A	chr20:1640981-1641251	GM12878	blood:	n/a	n/a
26	BCL11A	chr20:1612833-1613216	GM12878	blood:	n/a	n/a
27	BCL11A	chr20:1645573-1645931	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
28	BCL11A	chr20:1603111-1603444	GM12878	blood:	n/a	n/a
29	BCL3	chr20:1645525-1645977	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
30	BCL3	chr20:1628817-1629045	GM12878	blood:	n/a	n/a
31	BCL3	chr20:1612800-1613166	GM12878	blood:	n/a	n/a
32	BCL3	chr20:1603087-1603515	GM12878	blood:	n/a	n/a
33	BCLAF1	chr20:1612842-1613225	GM12878	blood:	n/a	n/a
34	BCLAF1	chr20:1612776-1613271	GM12878	blood:	n/a	n/a
35	BCLAF1	chr20:1640863-1641357	GM12878	blood:	n/a	n/a
36	BCLAF1	chr20:1603036-1603400	GM12878	blood:	n/a	n/a
37	BCLAF1	chr20:1645421-1645899	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
38	BHLHE40	chr20:1603122-1603445	GM12878	blood:	n/a	n/a
39	BHLHE40	chr20:1647508-1647681	GM12878	blood:	n/a	n/a
40	BHLHE40	chr20:1640252-1640311	GM12878	blood:	n/a	n/a
41	BRCA1	chr20:1603218-1603418	GM12878	blood:	n/a	n/a
42	CEBPB	chr20:1614183-1614694	HCT-116	colon:	n/a	n/a
43	CEBPB	chr20:1557320-1557574	A549	lung:	n/a	chr20:1557460-1557471
44	CEBPB	chr20:1614267-1614583	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr20:1617435-1617633	HepG2	liver:	n/a	n/a
46	CEBPB	chr20:1614260-1614582	K562	blood:	n/a	n/a
47	CEBPB	chr20:1640773-1641427	GM12878	blood:	n/a	n/a
48	CEBPB	chr20:1612338-1612585	A549	lung:	n/a	n/a
49	CEBPB	chr20:1619387-1619571	HepG2	liver:	n/a	chr20:1619478-1619489
50	CEBPB	chr20:1637825-1637838	H1-hESC	embryonic stem cell:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1578550-1578600	HCM	heart:	n/a
2	chr20:1600623-1600673	GM12891	blood:	n/a
3	chr20:1578550-1578600	HCM	heart:	n/a
4	chr20:1600623-1600673	GM12891	blood:	n/a
5	chr20:1639250-1639300	AG04449	skin:	fetal
6	chr20:1639325-1639375	HRCEpiC	kidney:	n/a
7	chr20:1600641-1600691	AG09319	gingival:	n/a
8	chr20:1600641-1600691	BJ	skin:	n/a
9	chr20:1610358-1610408	T-47D	breast:	n/a
10	chr20:1600623-1600673	SKMC	muscle:	n/a
11	chr20:1638393-1638443	HIPEpiC	eye:	n/a
12	chr20:1600623-1600673	PANC-1	pancreas:	n/a
13	chr20:1639325-1639375	GM12891	blood:	n/a
14	chr20:1639325-1639375	ProgFib	skin:	n/a
15	chr20:1600623-1600673	Hepatocyte	liver:	n/a
16	chr20:1638393-1638443	NHDF-neo	bronchial:	n/a
17	chr20:1578550-1578600	BJ	skin:	n/a
18	chr20:1639816-1639866	K562	blood:	n/a
19	chr20:1616387-1616437	ECC-1	luminal epithelium:	n/a
20	chr20:1610358-1610408	AG04450	lung:	fetal
21	chr20:1600705-1600755	MCF10A-Er-Src	breast:	n/a
22	chr20:1578550-1578600	NH-A	brain:	n/a
23	chr20:1610358-1610408	SAEC	small airway:	n/a
24	chr20:1639325-1639375	SAEC	small airway:	n/a
25	chr20:1600641-1600691	HEK293	kidney:	embryo
26	chr20:1639250-1639300	AoSMC	blood vessel:	n/a
27	chr20:1638393-1638443	BJ	skin:	n/a
28	chr20:1600705-1600755	Jurkat	blood:	n/a
29	chr20:1639816-1639866	Jurkat	blood:	n/a
30	chr20:1600705-1600755	HRE	kidney:	n/a
31	chr20:1600623-1600673	AG04450	lung:	fetal
32	chr20:1600623-1600673	BJ	skin:	n/a
33	chr20:1610358-1610408	AG09319	gingival:	n/a
34	chr20:1639325-1639375	K562	blood:	n/a
35	chr20:1578550-1578600	HCT-116	colon:	n/a
36	chr20:1600705-1600755	SKMC	muscle:	n/a
37	chr20:1639816-1639866	HRPEpiC	eye:	n/a
38	chr20:1600705-1600755	H1-hESC	embryonic stem cell:	embryo
39	chr20:1610358-1610408	NB4	blood:	n/a
40	chr20:1600705-1600755	Caco-2	colon:	n/a
41	chr20:1600623-1600673	HCF	heart:	n/a
42	chr20:1578550-1578600	H1-hESC	embryonic stem cell:	embryo
43	chr20:1600623-1600673	PrEC	prostate:	n/a
44	chr20:1600641-1600691	AoSMC	blood vessel:	n/a
45	chr20:1638393-1638443	AoSMC	blood vessel:	n/a
46	chr20:1600641-1600691	HRPEpiC	eye:	n/a
47	chr20:1600705-1600755	ECC-1	luminal epithelium:	n/a
48	chr20:1600623-1600673	HEEpiC	esophagus:	n/a
49	chr20:1610358-1610408	K562	blood:	n/a
50	chr20:1578550-1578600	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:1484085..1484840-chr20:1617080..1618039,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 3277 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3277 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541137891	chr20:1553506-1553507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559562258	chr20:1553532-1553533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191433751	chr20:1553570-1553571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529894293	chr20:1553573-1553574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548440301	chr20:1553630-1553631	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184886138	chr20:1553645-1553646	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190781930	chr20:1553657-1553658	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192864614	chr20:1553669-1553670	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112179282	chr20:1553841-1553842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530873321	chr20:1554002-1554003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552240688	chr20:1554262-1554263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570834306	chr20:1554282-1554283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185182800	chr20:1554349-1554350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553451981	chr20:1554397-1554398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568686600	chr20:1554425-1554426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568241413	chr20:1554535-1554536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6135328	chr20:1554639-1554640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6079634	chr20:1554762-1554763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6074827	chr20:1554930-1554931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535634484	chr20:1554948-1554949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2422625	chr20:1554956-1554957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557181264	chr20:1554973-1554974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575488702	chr20:1555412-1555413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2422628	chr20:1555755-1555756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540136753	chr20:1556292-1556293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138682357	chr20:1556325-1556326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2422630	chr20:1556347-1556348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558234966	chr20:1556399-1556400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576795370	chr20:1556431-1556432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540699817	chr20:1556507-1556508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559475096	chr20:1556623-1556624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574626139	chr20:1556646-1556647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542042153	chr20:1556733-1556734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2422631	chr20:1556758-1556759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs2422632	chr20:1556812-1556813	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs71230434	chr20:1556849-1556850	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs7265732	chr20:1556857-1556858	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs552459128	chr20:1556858-1556859	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs564292365	chr20:1556871-1556872	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs528462591	chr20:1556880-1556881	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs2422633	chr20:1556882-1556883	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs568203463	chr20:1556938-1556939	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190051092	chr20:1556942-1556943	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557173941	chr20:1556946-1556947	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374916726	chr20:1557006-1557007	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs137979932	chr20:1557010-1557011	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181057070	chr20:1557016-1557017	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185485696	chr20:1557036-1557037	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74709685	chr20:1557168-1557169	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188147189	chr20:1557290-1557291	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr20:1553000-1556800	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr20:1553000-1556800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr20:1553400-1553600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr20:1553600-1553800	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr20:1553800-1556800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr20:1555600-1556800	Weak transcription	Hela-S3	cervix
14	chr20:1556800-1557200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr20:1556800-1557400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr20:1556800-1557600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr20:1556800-1557600	Enhancers	NHEK	skin
18	chr20:1556800-1558200	Enhancers	Hela-S3	cervix
19	chr20:1556800-1558600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
20	chr20:1556800-1560000	Genic enhancers	Primary monocytes fromperipheralblood	blood
21	chr20:1556800-1560000	Genic enhancers	Monocytes-CD14+_RO01746	blood
22	chr20:1557000-1557400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr20:1558000-1559600	Strong transcription	Primary T cells from cord blood	blood
24	chr20:1558400-1560000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr20:1558600-1559600	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr20:1559600-1560400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
27	chr20:1559600-1560600	Weak transcription	Primary T cells from cord blood	blood
28	chr20:1560000-1561000	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr20:1560000-1561000	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr20:1560000-1579200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr20:1560400-1561800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr20:1560600-1561000	Strong transcription	Primary T cells from cord blood	blood
33	chr20:1561000-1562600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr20:1561000-1563600	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr20:1561000-1568000	Weak transcription	Primary T cells from cord blood	blood
36	chr20:1561800-1563800	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr20:1563600-1564600	Genic enhancers	Primary monocytes fromperipheralblood	blood
38	chr20:1563800-1565400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr20:1564600-1565400	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr20:1565400-1565600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr20:1565400-1566000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr20:1565600-1565800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
43	chr20:1565800-1567000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr20:1566000-1566600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr20:1566600-1568400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr20:1567000-1569400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
47	chr20:1567600-1570000	Active TSS	Primary B cells from cord blood	blood
48	chr20:1567800-1569600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr20:1568000-1569000	Enhancers	Primary T cells from cord blood	blood
50	chr20:1568000-1570200	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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