Variant report

Variant	nsv1063015
Chromosome Location	chr20:1531131-1674430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:940)
CpG islands
(count:1099)
Chromatin interactive
region (count:3)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr20:1550073-1550394	K562	blood:	n/a	n/a
4	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
5	ATF1	chr20:1614192-1614501	K562	blood:	n/a	n/a
6	ATF2	chr20:1612776-1613188	GM12878	blood:	n/a	n/a
7	ATF2	chr20:1640865-1641393	GM12878	blood:	n/a	n/a
8	ATF2	chr20:1645510-1646022	GM12878	blood:	n/a	n/a
9	ATF2	chr20:1645577-1645900	GM12878	blood:	n/a	n/a
10	ATF2	chr20:1607411-1607905	GM12878	blood:	n/a	n/a
11	ATF2	chr20:1603058-1603543	GM12878	blood:	n/a	n/a
12	ATF2	chr20:1640754-1641281	GM12878	blood:	n/a	n/a
13	ATF2	chr20:1607520-1607935	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	chr20:1642642-1642897	GM12878	blood:	n/a	n/a
17	BATF	chr20:1638679-1639013	GM12878	blood:	n/a	n/a
18	BATF	chr20:1612731-1613238	GM12878	blood:	n/a	chr20:1612969-1612980
19	BATF	chr20:1543275-1543590	GM12878	blood:	n/a	n/a
20	BATF	chr20:1640943-1641497	GM12878	blood:	n/a	chr20:1641404-1641414
21	BATF	chr20:1633644-1633992	GM12878	blood:	n/a	n/a
22	BATF	chr20:1628753-1629096	GM12878	blood:	n/a	chr20:1628940-1628951
23	BATF	chr20:1603174-1603482	GM12878	blood:	n/a	n/a
24	BATF	chr20:1621158-1621494	GM12878	blood:	n/a	n/a
25	BATF	chr20:1612769-1613106	GM12878	blood:	n/a	chr20:1612969-1612980
26	BATF	chr20:1641005-1641263	GM12878	blood:	n/a	n/a
27	BATF	chr20:1638736-1639011	GM12878	blood:	n/a	n/a
28	BCL11A	chr20:1645573-1645931	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
29	BCL11A	chr20:1640981-1641251	GM12878	blood:	n/a	n/a
30	BCL11A	chr20:1603100-1603339	GM12878	blood:	n/a	n/a
31	BCL11A	chr20:1603111-1603444	GM12878	blood:	n/a	n/a
32	BCL11A	chr20:1612833-1613216	GM12878	blood:	n/a	n/a
33	BCL3	chr20:1645525-1645977	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
34	BCL3	chr20:1603087-1603515	GM12878	blood:	n/a	n/a
35	BCL3	chr20:1612800-1613166	GM12878	blood:	n/a	n/a
36	BCL3	chr20:1628817-1629045	GM12878	blood:	n/a	n/a
37	BCLAF1	chr20:1645421-1645899	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
38	BCLAF1	chr20:1603036-1603400	GM12878	blood:	n/a	n/a
39	BCLAF1	chr20:1640863-1641357	GM12878	blood:	n/a	n/a
40	BCLAF1	chr20:1612776-1613271	GM12878	blood:	n/a	n/a
41	BCLAF1	chr20:1612842-1613225	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	chr20:1603122-1603445	GM12878	blood:	n/a	n/a
45	BHLHE40	chr20:1549969-1550250	K562	blood:	n/a	n/a
46	BHLHE40	chr20:1640252-1640311	GM12878	blood:	n/a	n/a
47	BRCA1	chr20:1550123-1550444	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr20:1603218-1603418	GM12878	blood:	n/a	n/a
49	CEBPB	chr20:1612296-1612538	HepG2	liver:	n/a	n/a
50	CEBPB	chr20:1619339-1619657	HepG2	liver:	n/a	chr20:1619478-1619489

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1600623-1600673	HepG2	liver:	n/a
2	chr20:1600623-1600673	HepG2	liver:	n/a
3	chr20:1538353-1538403	SK-N-SH_RA	brain:	n/a
4	chr20:1610358-1610408	CMK	blood:	n/a
5	chr20:1600641-1600691	NT2-D1	testis:	n/a
6	chr20:1532543-1532593	AG10803	skin:	n/a
7	chr20:1601704-1601754	NT2-D1	testis:	n/a
8	chr20:1578550-1578600	HNPCEpiC	eye:	n/a
9	chr20:1639250-1639300	Caco-2	colon:	n/a
10	chr20:1601704-1601754	T-47D	breast:	n/a
11	chr20:1639250-1639300	MCF-7	breast:	n/a
12	chr20:1639250-1639300	U87	brain:	n/a
13	chr20:1600705-1600755	HRE	kidney:	n/a
14	chr20:1610358-1610408	NH-A	brain:	n/a
15	chr20:1546019-1546069	HRCEpiC	kidney:	n/a
16	chr20:1578550-1578600	RPTEC	kidney:	n/a
17	chr20:1538671-1538721	T-47D	breast:	n/a
18	chr20:1610358-1610408	PFSK-1	brain:	n/a
19	chr20:1578550-1578600	HRE	kidney:	n/a
20	chr20:1600641-1600691	PANC-1	pancreas:	n/a
21	chr20:1532543-1532593	HCF	heart:	n/a
22	chr20:1539702-1539752	HCM	heart:	n/a
23	chr20:1600705-1600755	NT2-D1	testis:	n/a
24	chr20:1539641-1539691	HL-60	blood:	n/a
25	chr20:1538671-1538721	SK-N-MC	brain:	n/a
26	chr20:1578550-1578600	MCF-7	breast:	n/a
27	chr20:1539641-1539691	RPTEC	kidney:	n/a
28	chr20:1600641-1600691	PFSK-1	brain:	n/a
29	chr20:1616387-1616437	GM06990	blood:	n/a
30	chr20:1539641-1539691	BE2_C	brain:	n/a
31	chr20:1600705-1600755	PrEC	prostate:	n/a
32	chr20:1639250-1639300	MCF10A-Er-Src	breast:	n/a
33	chr20:1538353-1538403	HUVEC	blood vessel:	n/a
34	chr20:1600705-1600755	HL-60	blood:	n/a
35	chr20:1578550-1578600	HL-60	blood:	n/a
36	chr20:1600641-1600691	HMEC	breast:	n/a
37	chr20:1601704-1601754	AG09309	skin:	n/a
38	chr20:1616387-1616437	Hela-S3	cervix:	n/a
39	chr20:1539641-1539691	HEK293	kidney:	embryo
40	chr20:1601704-1601754	ECC-1	luminal epithelium:	n/a
41	chr20:1639250-1639300	SK-N-SH	brain:	n/a
42	chr20:1639250-1639300	IMR90	lung:	fetal
43	chr20:1601704-1601754	HMEC	breast:	n/a
44	chr20:1578550-1578600	ovcar-3	ovarian:	n/a
45	chr20:1578550-1578600	AG04450	lung:	fetal
46	chr20:1539641-1539691	MCF10A-Er-Src	breast:	n/a
47	chr20:1638393-1638443	HAEpiC	amniotic membrane:	n/a
48	chr20:1546019-1546069	HRPEpiC	eye:	n/a
49	chr20:1546019-1546069	RPTEC	kidney:	n/a
50	chr20:1546019-1546069	BJ	skin:	n/a

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

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

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

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

No data

Variant related genes	Relation type
SIRPB1	TF binding region
SIRPD	TF binding region
ENSG00000236550	TF binding region
ENSG00000260861	TF binding region
ENSG00000242324	TF binding region
ENSG00000271523	TF binding region
SIRPG	TF binding region
RN7SL561P	TF binding region
ENSG00000237914	TF binding region
SIRPB1	CpG island
SIRPD	CpG island
ENSG00000236550	CpG island
ENSG00000260861	CpG island
ENSG00000242324	CpG island
ENSG00000271523	CpG island
SIRPG	CpG island
RN7SL561P	CpG island
ENSG00000237914	CpG island
KIAA0831	miRNA target sites
ENPP4	miRNA target sites
SOX4	miRNA target sites
GOLT1B	miRNA target sites
ETV6	miRNA target sites
BMPR2	miRNA target sites

Extended variants
information (count: 5296 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5296 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532926118	chr20:1531157-1531158	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140132400	chr20:1531195-1531196	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6110434	chr20:1531196-1531197	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375424293	chr20:1531232-1531233	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546947487	chr20:1531242-1531243	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568748817	chr20:1531259-1531260	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538041250	chr20:1531278-1531279	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535777010	chr20:1531293-1531294	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547758813	chr20:1531306-1531307	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569361748	chr20:1531318-1531319	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185986445	chr20:1531354-1531355	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6110435	chr20:1531356-1531357	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558631094	chr20:1531360-1531361	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4522683	chr20:1531365-1531366	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73569175	chr20:1531413-1531414	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs142382304	chr20:1531421-1531422	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76373388	chr20:1531432-1531433	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574768367	chr20:1531485-1531486	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542191471	chr20:1531495-1531496	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563663995	chr20:1531514-1531515	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367915706	chr20:1531518-1531519	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376090732	chr20:1531563-1531564	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554514584	chr20:1531573-1531574	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575718365	chr20:1531576-1531577	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76487631	chr20:1531614-1531615	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191642279	chr20:1531627-1531628	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528641368	chr20:1531650-1531651	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181116857	chr20:1531669-1531670	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561969886	chr20:1531687-1531688	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529543095	chr20:1531695-1531696	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550906345	chr20:1531709-1531710	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6135262	chr20:1531744-1531745	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568236034	chr20:1531748-1531749	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151278466	chr20:1531764-1531765	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186358914	chr20:1531774-1531775	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560063962	chr20:1531775-1531776	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551958750	chr20:1531780-1531781	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370410291	chr20:1531834-1531835	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140484588	chr20:1531872-1531873	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534454757	chr20:1531925-1531926	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553112240	chr20:1531948-1531949	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149991008	chr20:1531962-1531963	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191014367	chr20:1531985-1531986	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557294173	chr20:1532072-1532073	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73569178	chr20:1532150-1532151	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577188243	chr20:1532241-1532242	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539411426	chr20:1532252-1532253	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370029585	chr20:1532309-1532310	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377202945	chr20:1532310-1532311	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528800367	chr20:1532314-1532315	Strong transcription	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	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1529600-1533800	Strong transcription	Primary monocytes fromperipheralblood	blood
2	chr20:1529800-1533800	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr20:1529800-1536400	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr20:1532600-1532800	Enhancers	Spleen	Spleen
5	chr20:1532800-1545400	Weak transcription	Spleen	Spleen
6	chr20:1533800-1535800	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr20:1533800-1536400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr20:1535800-1539200	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr20:1536400-1537400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
10	chr20:1536400-1538400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
11	chr20:1536800-1537000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr20:1537000-1541200	Weak transcription	Primary T cells from cord blood	blood
13	chr20:1537000-1551600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr20:1537400-1542800	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr20:1538400-1539600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr20:1538600-1538800	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr20:1539200-1541200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr20:1539600-1542600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr20:1540000-1544800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr20:1540200-1543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr20:1541200-1541800	Strong transcription	Primary T cells from cord blood	blood
22	chr20:1541200-1543000	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr20:1541600-1542200	Enhancers	HUVEC	blood vessel
24	chr20:1541800-1545200	Weak transcription	Primary T cells from cord blood	blood
25	chr20:1542400-1543800	Enhancers	Dnd41	blood
26	chr20:1542600-1543200	Genic enhancers	Primary monocytes fromperipheralblood	blood
27	chr20:1542800-1543000	Genic enhancers	Monocytes-CD14+_RO01746	blood
28	chr20:1543000-1543200	Enhancers	Thymus	Thymus
29	chr20:1543000-1543800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr20:1543000-1545000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
31	chr20:1543200-1543600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr20:1543200-1550400	Weak transcription	Thymus	Thymus
33	chr20:1543400-1544000	Enhancers	Primary B cells from cord blood	blood
34	chr20:1543600-1544000	Enhancers	GM12878-XiMat	blood
35	chr20:1543600-1548600	Genic enhancers	Primary monocytes fromperipheralblood	blood
36	chr20:1543800-1544000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr20:1544000-1545000	Genic enhancers	Monocytes-CD14+_RO01746	blood
39	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr20:1544800-1548200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr20:1545000-1545400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
42	chr20:1545000-1548000	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr20:1545200-1547400	Strong transcription	Primary T cells from cord blood	blood
44	chr20:1545400-1546200	Genic enhancers	Monocytes-CD14+_RO01746	blood
45	chr20:1545400-1546600	Strong transcription	Spleen	Spleen
46	chr20:1545600-1545800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr20:1545800-1546800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr20:1545800-1549400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr20:1546000-1547000	ZNF genes & repeats	Lung	lung
50	chr20:1546200-1547800	Strong transcription	Monocytes-CD14+_RO01746	blood

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