Variant report

Variant	esv3441285
Chromosome Location	chr20:29579691-29639889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3611)
CpG islands
(count:855)
Chromatin interactive
region (count:39)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3611 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:29583349-29583872	K562	blood:	n/a	n/a
2	ARID3A	chr20:29633241-29633535	K562	blood:	n/a	n/a
3	ARID3A	chr20:29611370-29612771	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:29610993-29612184	K562	blood:	n/a	n/a
5	ARID3A	chr20:29593307-29593371	K562	blood:	n/a	n/a
6	ARID3A	chr20:29604416-29604457	K562	blood:	n/a	n/a
7	ARID3A	chr20:29584419-29584422	K562	blood:	n/a	n/a
8	ARID3A	chr20:29630626-29630814	K562	blood:	n/a	n/a
9	ARID3A	chr20:29633844-29634865	K562	blood:	n/a	n/a
10	ARID3A	chr20:29622471-29622991	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:29629422-29629654	K562	blood:	n/a	n/a
12	ARID3A	chr20:29606728-29606742	K562	blood:	n/a	n/a
13	ARID3A	chr20:29632785-29632962	K562	blood:	n/a	n/a
14	ARID3A	chr20:29591484-29591955	K562	blood:	n/a	n/a
15	ARID3A	chr20:29597481-29597512	K562	blood:	n/a	n/a
16	ARID3A	chr20:29637221-29638826	K562	blood:	n/a	chr20:29637380-29637396
17	ARID3A	chr20:29631123-29631286	K562	blood:	n/a	n/a
18	ARID3A	chr20:29628524-29629135	K562	blood:	n/a	chr20:29628683-29628699
19	ARID3A	chr20:29584438-29584638	HepG2	liver:	n/a	n/a
20	ARID3A	chr20:29613365-29613570	K562	blood:	n/a	n/a
21	ARID3A	chr20:29627540-29627876	K562	blood:	n/a	n/a
22	ARID3A	chr20:29620583-29620956	K562	blood:	n/a	chr20:29620815-29620831
23	ATF1	chr20:29591587-29591950	K562	blood:	n/a	n/a
24	ATF1	chr20:29581710-29581786	K562	blood:	n/a	n/a
25	ATF1	chr20:29582426-29582626	K562	blood:	n/a	n/a
26	ATF1	chr20:29625665-29625843	K562	blood:	n/a	n/a
27	ATF1	chr20:29587204-29587381	K562	blood:	n/a	n/a
28	ATF1	chr20:29630171-29630348	K562	blood:	n/a	n/a
29	ATF1	chr20:29634000-29635084	K562	blood:	n/a	n/a
30	ATF1	chr20:29613285-29613479	K562	blood:	n/a	n/a
31	ATF1	chr20:29597041-29597229	K562	blood:	n/a	n/a
32	ATF1	chr20:29586601-29586746	K562	blood:	n/a	n/a
33	ATF1	chr20:29633094-29633439	K562	blood:	n/a	n/a
34	ATF1	chr20:29626100-29626288	K562	blood:	n/a	n/a
35	ATF1	chr20:29599619-29599729	K562	blood:	n/a	n/a
36	ATF1	chr20:29601011-29601080	K562	blood:	n/a	n/a
37	ATF1	chr20:29631255-29631264	K562	blood:	n/a	n/a
38	ATF1	chr20:29583054-29583253	K562	blood:	n/a	n/a
39	ATF1	chr20:29616245-29616416	K562	blood:	n/a	n/a
40	ATF1	chr20:29635802-29636715	K562	blood:	n/a	n/a
41	ATF1	chr20:29607716-29607882	K562	blood:	n/a	n/a
42	ATF1	chr20:29610930-29612133	K562	blood:	n/a	n/a
43	ATF1	chr20:29593010-29593256	K562	blood:	n/a	n/a
44	ATF1	chr20:29620111-29620173	K562	blood:	n/a	n/a
45	ATF1	chr20:29584425-29584627	K562	blood:	n/a	n/a
46	ATF1	chr20:29606718-29606904	K562	blood:	n/a	n/a
47	ATF1	chr20:29629679-29629821	K562	blood:	n/a	n/a
48	ATF1	chr20:29628542-29628871	K562	blood:	n/a	n/a
49	ATF1	chr20:29627360-29627533	K562	blood:	n/a	n/a
50	ATF1	chr20:29622631-29622824	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:29611785-29611835	H1-hESC	embryonic stem cell:	embryo
2	chr20:29611785-29611835	H1-hESC	embryonic stem cell:	embryo
3	chr20:29610620-29610670	NT2-D1	testis:	n/a
4	chr20:29611810-29611860	U87	brain:	n/a
5	chr20:29610620-29610670	GM12892	blood:	n/a
6	chr20:29611924-29611974	NH-A	brain:	n/a
7	chr20:29611676-29611726	NH-A	brain:	n/a
8	chr20:29608500-29608550	SK-N-SH_RA	brain:	n/a
9	chr20:29610620-29610670	HCPEpiC	choroid plexus:	n/a
10	chr20:29611810-29611860	Jurkat	blood:	n/a
11	chr20:29611810-29611860	NT2-D1	testis:	n/a
12	chr20:29611903-29611953	PFSK-1	brain:	n/a
13	chr20:29611652-29611702	Caco-2	colon:	n/a
14	chr20:29615890-29615940	HCPEpiC	choroid plexus:	n/a
15	chr20:29611676-29611726	HMEC	breast:	n/a
16	chr20:29608500-29608550	H1-hESC	embryonic stem cell:	embryo
17	chr20:29611924-29611974	GM12891	blood:	n/a
18	chr20:29611676-29611726	MCF-7	breast:	n/a
19	chr20:29611909-29611959	Caco-2	colon:	n/a
20	chr20:29610620-29610670	PFSK-1	brain:	n/a
21	chr20:29615890-29615940	PrEC	prostate:	n/a
22	chr20:29611785-29611835	HCPEpiC	choroid plexus:	n/a
23	chr20:29611652-29611702	HCM	heart:	n/a
24	chr20:29610620-29610670	CMK	blood:	n/a
25	chr20:29611903-29611953	HEEpiC	esophagus:	n/a
26	chr20:29612151-29612201	SK-N-SH	brain:	n/a
27	chr20:29611652-29611702	SK-N-SH	brain:	n/a
28	chr20:29613021-29613071	BJ	skin:	n/a
29	chr20:29610042-29610092	T-47D	breast:	n/a
30	chr20:29610042-29610092	SAEC	small airway:	n/a
31	chr20:29610042-29610092	AG10803	skin:	n/a
32	chr20:29611652-29611702	HIPEpiC	eye:	n/a
33	chr20:29608500-29608550	HepG2	liver:	n/a
34	chr20:29611676-29611726	U87	brain:	n/a
35	chr20:29611652-29611702	ovcar-3	ovarian:	n/a
36	chr20:29611652-29611702	LNCaP	prostate:	n/a
37	chr20:29613021-29613071	Hepatocyte	liver:	n/a
38	chr20:29610620-29610670	AoSMC	blood vessel:	n/a
39	chr20:29611924-29611974	AG09319	gingival:	n/a
40	chr20:29611676-29611726	HRPEpiC	eye:	n/a
41	chr20:29610042-29610092	HUVEC	blood vessel:	n/a
42	chr20:29613021-29613071	IMR90	lung:	fetal
43	chr20:29608500-29608550	HCM	heart:	n/a
44	chr20:29611676-29611726	HPAEpiC	pulmonary alveolar:	n/a
45	chr20:29611810-29611860	HepG2	liver:	n/a
46	chr20:29615890-29615940	Hepatocyte	liver:	n/a
47	chr20:29611652-29611702	IMR90	lung:	fetal
48	chr20:29612151-29612201	PrEC	prostate:	n/a
49	chr20:29608500-29608550	Hepatocyte	liver:	n/a
50	chr20:29608500-29608550	GM12891	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:29634644..29639248-chr4:190892116..190896171,7	MCF-7	breast:
2	chr20:29611329..29612191-chr9:68455368..68456077,2	MCF-7	breast:
3	chr20:29636048..29637003-chr4:190893089..190893743,2	MCF-7	breast:
4	chr20:29625984..29631616-chr9:68431406..68435615,4	MCF-7	breast:
5	chr20:29611333..29614057-chr4:190860675..190863034,4	MCF-7	breast:
6	chr20:29637616..29639102-chr4:190894557..190895938,8	MCF-7	breast:
7	chr20:29637498..29638875-chr4:190894757..190896186,13	MCF-7	breast:
8	chr20:29582669..29584786-chr4:190825212..190827819,2	MCF-7	breast:
9	chr20:29611632..29612497-chr4:190861809..190862721,3	MCF-7	breast:
10	chr20:29611128..29612321-chr4:190861463..190862739,6	MCF-7	breast:
11	chr20:29611467..29612118-chr9:68454964..68455886,2	MCF-7	breast:
12	chr20:29636068..29638048-chr4:190894138..190896351,4	K562	blood:
13	chr20:29611384..29612018-chr9:68455093..68455961,3	MCF-7	breast:
14	chr20:29635971..29637948-chr4:190894580..190896098,2	K562	blood:
15	chr20:29583664..29584204-chr20:29847922..29848698,2	MCF-7	breast:
16	chr20:29634371..29640092-chr4:190891314..190895900,7	MCF-7	breast:
17	chr20:29582937..29584194-chr4:190825284..190826211,7	MCF-7	breast:
18	chr20:29633490..29636802-chr9:68424473..68428627,9	MCF-7	breast:
19	chr20:29611070..29612139-chr9:68455176..68456091,3	K562	blood:
20	chr20:29634674..29636233-chr4:190890902..190893775,2	K562	blood:
21	chr20:29609593..29613129-chr4:190859723..190863221,5	K562	blood:
22	chr20:29583336..29584321-chr4:190825209..190826241,11	MCF-7	breast:
23	chr20:29520570..29521135-chr20:29591146..29591730,2	K562	blood:
24	chr20:29610649..29612158-chr9:68453830..68455817,2	K562	blood:
25	chr20:29611427..29612170-chr9:68454810..68455955,3	MCF-7	breast:
26	chr20:29583096..29583858-chr20:29848251..29848776,2	K562	blood:
27	chr20:29582149..29584387-chr4:190823886..190825724,2	MCF-7	breast:
28	chr20:29635538..29636169-chr9:68425739..68426630,2	MCF-7	breast:
29	chr20:29610673..29612888-chr4:190860203..190862511,3	MCF-7	breast:
30	chr20:29611333..29612723-chr4:190861521..190862825,5	HCT-116	colon:
31	chr20:29626530..29628486-chr9:68434110..68435636,2	MCF-7	breast:
32	chr20:29634837..29636605-chr9:68424534..68426260,2	K562	blood:
33	chr20:29609687..29611312-chr4:190860742..190862429,2	MCF-7	breast:
34	chr20:29635757..29636455-chr9:68425529..68426032,2	MCF-7	breast:
35	chr2:133109798..133110355-chr20:29611407..29612129,2	MCF-7	breast:
36	chr20:29637783..29638776-chr4:190894346..190895390,3	MCF-7	breast:
37	chr20:29583334..29584203-chr4:190824893..190826446,5	K562	blood:
38	chr20:29591220..29591720-chr4:190825717..190826283,2	MCF-7	breast:
39	chr20:29610847..29613187-chr4:190860454..190862227,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB116-1	chr20:29591786-29591863	ENSG00000231934.1
2	lnc-DEFB116-1	chr20:29596333-29596406	ENSG00000231934.1
3	lnc-DEFB116-1	chr20:29585008-29585143	ENSG00000231934.1
4	lnc-DEFB116-7	chr20:29637584-29638138	NONHSAT079280
5	lnc-DEFB116-7	chr20:29637799-29638060	NONHSAT147162
6	lnc-FRG1B-1	chr20:29638246-29638813	ENSG00000223346

No data

Variant related genes	Relation type
ENSG00000221319	TF binding region
MLLT10P1	TF binding region
ENSG00000231934	TF binding region
FRG1B	TF binding region
ENSG00000221319	CpG island
MLLT10P1	CpG island
ENSG00000231934	CpG island
FRG1B	CpG island
ENSG00000230992	chromatin interactions
ENSG00000249462	chromatin interactions
ENSG00000245685	chromatin interactions
ENSG00000215548	chromatin interactions
ENSG00000109536	chromatin interactions

Extended variants
information (count: 7742 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:7742 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182611016	chr20:29580610-29580611	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73620593	chr20:29580625-29580626	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73620594	chr20:29580635-29580636	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569822737	chr20:29580652-29580653	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535324119	chr20:29580689-29580690	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555417946	chr20:29580690-29580691	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73620595	chr20:29580714-29580715	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565407740	chr20:29580732-29580733	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs68030071	chr20:29580736-29580737	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs67216419	chr20:29580759-29580760	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2116508	chr20:29580764-29580765	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73620596	chr20:29580771-29580772	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111721690	chr20:29580773-29580774	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564456358	chr20:29580775-29580776	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144562895	chr20:29580776-29580777	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534428688	chr20:29580778-29580779	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10451731	chr20:29580789-29580790	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200735345	chr20:29580796-29580797	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73620597	chr20:29580817-29580818	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73620598	chr20:29580822-29580823	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557291567	chr20:29580824-29580825	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62197578	chr20:29580850-29580851	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147442218	chr20:29580865-29580866	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577221614	chr20:29580872-29580873	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76840147	chr20:29580883-29580884	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73620600	chr20:29580886-29580887	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540124151	chr20:29580891-29580892	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73620601	chr20:29580898-29580899	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556626857	chr20:29580912-29580913	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs367770324	chr20:29580915-29580916	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2424866	chr20:29580916-29580917	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs4588262	chr20:29580917-29580918	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138483831	chr20:29580921-29580922	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4315604	chr20:29580922-29580923	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542087708	chr20:29580928-29580929	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73622303	chr20:29580933-29580934	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201138920	chr20:29580946-29580947	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75210704	chr20:29580954-29580955	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73622304	chr20:29580957-29580958	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562292072	chr20:29580958-29580959	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76784683	chr20:29580977-29580978	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10451732	chr20:29580978-29580979	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78139974	chr20:29580985-29580986	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73622305	chr20:29580986-29580987	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73622306	chr20:29580987-29580988	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs62197579	chr20:29581010-29581011	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142205641	chr20:29581011-29581012	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78121221	chr20:29581019-29581020	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77564733	chr20:29581021-29581022	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34720771	chr20:29581024-29581025	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21806811	CNVD
Melanoma	21693616	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:29580600-29584800	Enhancers	Dnd41	blood
2	chr20:29580600-29602600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr20:29580800-29581000	Enhancers	Adipose Nuclei	Adipose
4	chr20:29580800-29584800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr20:29581000-29582600	Weak transcription	Spleen	Spleen
6	chr20:29581200-29582000	Weak transcription	Adipose Nuclei	Adipose
7	chr20:29581800-29598800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr20:29582000-29583000	ZNF genes & repeats	Fetal Brain Male	brain
9	chr20:29582000-29583200	ZNF genes & repeats	Adipose Nuclei	Adipose
10	chr20:29582200-29582400	Active TSS	Gastric	stomach
11	chr20:29582200-29583000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr20:29582200-29583000	ZNF genes & repeats	Aorta	Aorta
13	chr20:29582200-29585000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr20:29582400-29582600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
15	chr20:29582400-29582800	Bivalent/Poised TSS	Gastric	stomach
16	chr20:29582400-29583000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
17	chr20:29582400-29583000	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
18	chr20:29582600-29583000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr20:29582600-29583000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
20	chr20:29582600-29583000	ZNF genes & repeats	Spleen	Spleen
21	chr20:29582800-29583000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr20:29582800-29583000	Bivalent Enhancer	Brain Angular Gyrus	brain
23	chr20:29582800-29583000	Bivalent Enhancer	Esophagus	oesophagus
24	chr20:29582800-29583000	Flanking Bivalent TSS/Enh	Gastric	stomach
25	chr20:29582800-29583000	Bivalent Enhancer	Left Ventricle	heart
26	chr20:29582800-29583000	ZNF genes & repeats	Pancreas	Pancrea
27	chr20:29582800-29583000	ZNF genes & repeats	Psoas Muscle	Psoas
28	chr20:29583000-29583800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr20:29583000-29584200	Weak transcription	Gastric	stomach
30	chr20:29583000-29584200	Weak transcription	Pancreas	Pancrea
31	chr20:29583800-29585000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr20:29584200-29584400	Bivalent Enhancer	Esophagus	oesophagus
33	chr20:29584200-29584600	ZNF genes & repeats	Gastric	stomach
34	chr20:29584200-29584600	ZNF genes & repeats	Pancreas	Pancrea
35	chr20:29584400-29588200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
36	chr20:29584600-29586200	Weak transcription	Pancreas	Pancrea
37	chr20:29584800-29586000	Weak transcription	Dnd41	blood
38	chr20:29586000-29587400	ZNF genes & repeats	Dnd41	blood
39	chr20:29586200-29586600	ZNF genes & repeats	Pancreas	Pancrea
40	chr20:29586400-29586600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr20:29586400-29587400	ZNF genes & repeats	Fetal Lung	lung
42	chr20:29586600-29591000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:29586600-29591000	Weak transcription	Pancreas	Pancrea
44	chr20:29586800-29587000	Weak transcription	Gastric	stomach
45	chr20:29587200-29587400	Flanking Active TSS	Small Intestine	intestine
46	chr20:29587200-29587800	Enhancers	Aorta	Aorta
47	chr20:29587400-29590600	Enhancers	Dnd41	blood
48	chr20:29587800-29588000	Flanking Active TSS	Aorta	Aorta
49	chr20:29588000-29588200	Weak transcription	Gastric	stomach
50	chr20:29588000-29588800	Active TSS	Aorta	Aorta

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