Variant report

Variant	esv2758509
Chromosome Location	chr20:1476781-1679256
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1961)
CpG islands
(count:1162)
Chromatin interactive
region (count:29)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1961 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

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	chr20:1484276-1484712	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:1484323-1484667	K562	blood:	n/a	n/a
4	ARID3A	chr20:1617304-1617678	HepG2	liver:	n/a	n/a
5	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
6	ATF1	chr20:1518447-1518666	K562	blood:	n/a	n/a
7	ATF1	chr20:1484296-1484644	K562	blood:	n/a	n/a
8	ATF1	chr20:1614192-1614501	K562	blood:	n/a	n/a
9	ATF1	chr20:1504762-1505001	K562	blood:	n/a	n/a
10	ATF1	chr20:1509630-1509690	K562	blood:	n/a	n/a
11	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
12	ATF2	chr20:1484211-1484699	GM12878	blood:	n/a	n/a
13	ATF2	chr20:1516254-1516949	GM12878	blood:	n/a	n/a
14	ATF2	chr20:1640865-1641393	GM12878	blood:	n/a	n/a
15	ATF2	chr20:1607520-1607935	GM12878	blood:	n/a	n/a
16	ATF2	chr20:1603058-1603543	GM12878	blood:	n/a	n/a
17	ATF2	chr20:1612776-1613188	GM12878	blood:	n/a	n/a
18	ATF2	chr20:1645510-1646022	GM12878	blood:	n/a	n/a
19	ATF2	chr20:1518341-1518724	GM12878	blood:	n/a	n/a
20	ATF2	chr20:1640754-1641281	GM12878	blood:	n/a	n/a
21	ATF2	chr20:1484195-1484671	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr20:1516090-1517022	GM12878	blood:	n/a	n/a
23	ATF2	chr20:1607411-1607905	GM12878	blood:	n/a	n/a
24	ATF2	chr20:1645577-1645900	GM12878	blood:	n/a	n/a
25	ATF2	chr20:1612733-1613271	GM12878	blood:	n/a	n/a
26	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
27	BATF	chr20:1641005-1641263	GM12878	blood:	n/a	n/a
28	BATF	chr20:1516380-1516828	GM12878	blood:	n/a	n/a
29	BATF	chr20:1633644-1633992	GM12878	blood:	n/a	n/a
30	BATF	chr20:1603174-1603482	GM12878	blood:	n/a	n/a
31	BATF	chr20:1489950-1490126	GM12878	blood:	n/a	n/a
32	BATF	chr20:1638736-1639011	GM12878	blood:	n/a	n/a
33	BATF	chr20:1612769-1613106	GM12878	blood:	n/a	chr20:1612969-1612980
34	BATF	chr20:1642642-1642897	GM12878	blood:	n/a	n/a
35	BATF	chr20:1638679-1639013	GM12878	blood:	n/a	n/a
36	BATF	chr20:1640943-1641497	GM12878	blood:	n/a	chr20:1641404-1641414
37	BATF	chr20:1612731-1613238	GM12878	blood:	n/a	chr20:1612969-1612980
38	BATF	chr20:1543275-1543590	GM12878	blood:	n/a	n/a
39	BATF	chr20:1516454-1516834	GM12878	blood:	n/a	n/a
40	BATF	chr20:1621158-1621494	GM12878	blood:	n/a	n/a
41	BATF	chr20:1628753-1629096	GM12878	blood:	n/a	chr20:1628940-1628951
42	BCL11A	chr20:1645573-1645931	GM12878	blood:	n/a	chr20:1645725-1645734 chr20:1645691-1645700
43	BCL11A	chr20:1603111-1603444	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:1504703-1505016	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:1640981-1641251	GM12878	blood:	n/a	n/a
46	BCL11A	chr20:1516369-1516891	GM12878	blood:	n/a	chr20:1516685-1516694 chr20:1516649-1516658
47	BCL11A	chr20:1516454-1516746	GM12878	blood:	n/a	chr20:1516685-1516694 chr20:1516649-1516658
48	BCL11A	chr20:1504680-1505064	GM12878	blood:	n/a	n/a
49	BCL11A	chr20:1603100-1603339	GM12878	blood:	n/a	n/a
50	BCL11A	chr20:1612833-1613216	GM12878	blood:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1532543-1532593	HPAEpiC	pulmonary alveolar:	n/a
2	chr20:1639325-1639375	HCPEpiC	choroid plexus:	n/a
3	chr20:1639250-1639300	HCM	heart:	n/a
4	chr20:1532543-1532593	HPAEpiC	pulmonary alveolar:	n/a
5	chr20:1639325-1639375	HCPEpiC	choroid plexus:	n/a
6	chr20:1639250-1639300	HCM	heart:	n/a
7	chr20:1546019-1546069	GM12892	blood:	n/a
8	chr20:1639325-1639375	NHBE	bronchial:	n/a
9	chr20:1600641-1600691	ovcar-3	ovarian:	n/a
10	chr20:1600623-1600673	BE2_C	brain:	n/a
11	chr20:1546019-1546069	HAEpiC	amniotic membrane:	n/a
12	chr20:1514929-1514979	PFSK-1	brain:	n/a
13	chr20:1514929-1514979	SK-N-MC	brain:	n/a
14	chr20:1600623-1600673	NT2-D1	testis:	n/a
15	chr20:1601704-1601754	NT2-D1	testis:	n/a
16	chr20:1539702-1539752	GM12892	blood:	n/a
17	chr20:1600623-1600673	HCM	heart:	n/a
18	chr20:1639816-1639866	GM12891	blood:	n/a
19	chr20:1600641-1600691	GM12891	blood:	n/a
20	chr20:1639325-1639375	MCF-7	breast:	n/a
21	chr20:1600641-1600691	Jurkat	blood:	n/a
22	chr20:1600623-1600673	A549	lung:	n/a
23	chr20:1539702-1539752	NHBE	bronchial:	n/a
24	chr20:1539702-1539752	Hela-S3	cervix:	n/a
25	chr20:1538353-1538403	HL-60	blood:	n/a
26	chr20:1532543-1532593	SK-N-SH_RA	brain:	n/a
27	chr20:1639816-1639866	AG04450	lung:	fetal
28	chr20:1601704-1601754	HRPEpiC	eye:	n/a
29	chr20:1532543-1532593	Hela-S3	cervix:	n/a
30	chr20:1546019-1546069	IMR90	lung:	fetal
31	chr20:1514929-1514979	SKMC	muscle:	n/a
32	chr20:1639325-1639375	U87	brain:	n/a
33	chr20:1610358-1610408	GM12878	blood:	n/a
34	chr20:1532543-1532593	HNPCEpiC	eye:	n/a
35	chr20:1539641-1539691	HCT-116	colon:	n/a
36	chr20:1539641-1539691	PANC-1	pancreas:	n/a
37	chr20:1538366-1538416	SKMC	muscle:	n/a
38	chr20:1600623-1600673	HUVEC	blood vessel:	n/a
39	chr20:1616387-1616437	MCF10A-Er-Src	breast:	n/a
40	chr20:1610358-1610408	HIPEpiC	eye:	n/a
41	chr20:1514929-1514979	K562	blood:	n/a
42	chr20:1538366-1538416	HepG2	liver:	n/a
43	chr20:1610358-1610408	HCF	heart:	n/a
44	chr20:1539641-1539691	AG10803	skin:	n/a
45	chr20:1539641-1539691	AG04449	skin:	fetal
46	chr20:1539702-1539752	SK-N-MC	brain:	n/a
47	chr20:1514929-1514979	SK-N-SH_RA	brain:	n/a
48	chr20:1601704-1601754	HCF	heart:	n/a
49	chr20:1600641-1600691	GM12892	blood:	n/a
50	chr20:1514929-1514979	NB4	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:1484052..1484617-chr20:1714858..1715446,2	MCF-7	breast:
2	chr20:1446728..1449286-chr20:1481542..1483927,2	K562	blood:
3	chr20:1294272..1294825-chr20:1484072..1484878,2	MCF-7	breast:
4	chr20:1190167..1190684-chr20:1484004..1484618,2	MCF-7	breast:
5	chr20:1484085..1484840-chr20:1617080..1618039,2	MCF-7	breast:
6	chr20:1455226..1456302-chr20:1484020..1485065,7	MCF-7	breast:
7	chr20:1503830..1506372-chr20:1510373..1512056,2	K562	blood:
8	chr20:1404065..1404923-chr20:1483919..1484896,2	K562	blood:
9	chr20:1445622..1448578-chr20:1487118..1490074,2	MCF-7	breast:
10	chr20:1293822..1294756-chr20:1484015..1484976,4	K562	blood:
11	chr20:1469550..1472466-chr20:1483678..1485476,2	K562	blood:
12	chr20:1418412..1420201-chr20:1482742..1485316,2	K562	blood:
13	chr20:1459193..1460384-chr20:1484138..1484789,4	MCF-7	breast:
14	chr20:1420415..1421693-chr20:1484065..1484901,6	MCF-7	breast:
15	chr20:1503830..1506372-chr20:1510373..1512056,2	K562	blood:
16	chr20:1489470..1490474-chr20:1714544..1715733,6	MCF-7	breast:
17	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:
18	chr20:1547054..1548894-chr20:1756067..1757690,2	K562	blood:
19	chr20:1455104..1456167-chr20:1483834..1485085,9	MCF-7	breast:
20	chr20:1453675..1455747-chr20:1479938..1482254,2	MCF-7	breast:
21	chr20:1407808..1408337-chr20:1484352..1484862,2	MCF-7	breast:
22	chr20:1518725..1519225-chr5:637487..638115,2	MCF-7	breast:
23	chr20:1513747..1514348-chr20:1714921..1715422,2	MCF-7	breast:
24	chr20:1293995..1294735-chr20:1483999..1484561,2	MCF-7	breast:
25	chr20:1450508..1451201-chr20:1483798..1484780,3	MCF-7	breast:
26	chr20:1484085..1484840-chr20:1617080..1618039,2	MCF-7	breast:
27	chr20:1495247..1497047-chr20:1498389..1500531,2	MCF-7	breast:
28	chr20:1495247..1497047-chr20:1498389..1500531,2	MCF-7	breast:
29	chr20:1447786..1449793-chr20:1482427..1484376,2	K562	blood:

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

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

No data

Variant related genes	Relation type
SIRPB1	TF binding region
SIRPD	TF binding region
ENSG00000236550	TF binding region
SIRPB2	TF binding region
ENSG00000271523	TF binding region
SIRPG	TF binding region
RN7SL561P	TF binding region
ENSG00000237914	TF binding region
RNU6-917P	TF binding region
ENSG00000260861	TF binding region
ENSG00000242324	TF binding region
SIRPB1	CpG island
SIRPD	CpG island
ENSG00000236550	CpG island
SIRPB2	CpG island
ENSG00000271523	CpG island
SIRPG	CpG island
RN7SL561P	CpG island
ENSG00000237914	CpG island
RNU6-917P	CpG island
ENSG00000260861	CpG island
ENSG00000242324	CpG island
ENSG00000196209	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000088833	chromatin interactions
ENPP4	miRNA target sites
BMPR2	miRNA target sites
KIAA0831	miRNA target sites
SOX4	miRNA target sites
GOLT1B	miRNA target sites
ETV6	miRNA target sites

Extended variants
information (count: 7697 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7697 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541921267	chr20:1476820-1476821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556849223	chr20:1476906-1476907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569356417	chr20:1476910-1476911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148009125	chr20:1476930-1476931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370925090	chr20:1476940-1476941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187946545	chr20:1476957-1476958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2422575	chr20:1476976-1476977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs150096199	chr20:1476977-1476978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191899641	chr20:1476994-1476995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528416222	chr20:1477032-1477033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6110215	chr20:1477051-1477052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs562129509	chr20:1477058-1477059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs8115674	chr20:1477155-1477156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs147533520	chr20:1477183-1477184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569435441	chr20:1477199-1477200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374103267	chr20:1477230-1477231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533558723	chr20:1477288-1477289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567248079	chr20:1477319-1477320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552053953	chr20:1477322-1477323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6033923	chr20:1477412-1477413	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs6105233	chr20:1477434-1477435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs113444151	chr20:1477444-1477445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs67784641	chr20:1477457-1477458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568511189	chr20:1477499-1477500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73567340	chr20:1477503-1477504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs6105234	chr20:1477661-1477662	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs185214904	chr20:1477662-1477663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545590369	chr20:1477679-1477680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189719013	chr20:1477696-1477697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572767120	chr20:1477700-1477701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6135103	chr20:1477709-1477710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539721310	chr20:1477734-1477735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79157246	chr20:1477735-1477736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6110218	chr20:1477743-1477744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs562969621	chr20:1477779-1477780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147291527	chr20:1477789-1477790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192754462	chr20:1477797-1477798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544073357	chr20:1477823-1477824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527947878	chr20:1477875-1477876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549652494	chr20:1477882-1477883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567921407	chr20:1477910-1477911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535421017	chr20:1477922-1477923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550351120	chr20:1477933-1477934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144231596	chr20:1477953-1477954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs57556915	chr20:1477957-1477958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538287124	chr20:1478039-1478040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6105235	chr20:1478043-1478044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148747965	chr20:1478075-1478076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568589723	chr20:1478106-1478107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539162686	chr20:1478109-1478110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Ovarian clear cell carcinoma	21343371	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
Lung cancer	18438408	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	21551127	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Medulloblastoma	21163964	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:1694 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1471600-1478400	Weak transcription	NHEK	skin
2	chr20:1471600-1478800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr20:1473000-1479000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr20:1474000-1479800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr20:1475400-1480800	Weak transcription	Fetal Thymus	thymus
6	chr20:1475600-1480800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr20:1476000-1480800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr20:1476000-1480800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr20:1476200-1481000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr20:1476200-1481400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr20:1476600-1484000	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr20:1478400-1480000	Enhancers	NHEK	skin
13	chr20:1478800-1480200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr20:1478800-1480800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr20:1479000-1482200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr20:1479600-1482200	Enhancers	HMEC	breast
17	chr20:1479800-1482200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr20:1480000-1480200	Enhancers	Esophagus	oesophagus
19	chr20:1480000-1481200	Flanking Active TSS	NHEK	skin
20	chr20:1480000-1481800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr20:1480000-1482000	Enhancers	Placenta	Placenta
22	chr20:1480200-1481000	Enhancers	Hela-S3	cervix
23	chr20:1480200-1481200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr20:1480200-1481600	Weak transcription	Esophagus	oesophagus
25	chr20:1480200-1481800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr20:1480600-1481800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr20:1480600-1482000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr20:1480800-1481000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr20:1480800-1481000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr20:1480800-1481000	Bivalent Enhancer	Primary B cells from cord blood	blood
31	chr20:1480800-1481000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr20:1480800-1481000	Bivalent Enhancer	Fetal Intestine Large	intestine
33	chr20:1480800-1481200	Enhancers	Fetal Thymus	thymus
34	chr20:1480800-1481400	Bivalent Enhancer	HepG2	liver
35	chr20:1480800-1481600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr20:1480800-1481800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr20:1480800-1481800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr20:1480800-1482000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
39	chr20:1480800-1482000	Enhancers	H9 Cell Line	embryonic stem cell
40	chr20:1480800-1482000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr20:1480800-1482000	Enhancers	Fetal Intestine Small	intestine
42	chr20:1481000-1481400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr20:1481000-1481600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr20:1481000-1481800	Enhancers	Fetal Intestine Large	intestine
45	chr20:1481000-1482000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr20:1481000-1482200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr20:1481000-1482200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr20:1481000-1482200	Enhancers	Dnd41	blood
49	chr20:1481000-1486000	Weak transcription	Hela-S3	cervix
50	chr20:1481200-1481600	Enhancers	Thymus	Thymus

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