Variant report

Variant	esv3349649
Chromosome Location	chr20:23689538-23834871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr20:23781355-23781508	K562	blood:	n/a	n/a
2	BACH1	chr20:23832673-23832794	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
4	CEBPB	chr20:23747026-23747352	A549	lung:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747029-23747041 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
5	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
6	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
7	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
8	CEBPB	chr20:23747142-23747274	K562	blood:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
9	CEBPB	chr20:23747045-23747345	HepG2	liver:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
10	CEBPB	chr20:23828408-23828598	A549	lung:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
11	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
12	CEBPB	chr20:23828412-23828599	HepG2	liver:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
13	CEBPB	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
14	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
15	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
16	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
17	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
18	CTCF	chr20:23779920-23780070	HFF	foreskin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
19	CTCF	chr20:23763060-23763210	GM12865	blood:	n/a	chr20:23763195-23763204 chr20:23763192-23763210
20	CTCF	chr20:23780260-23780410	HEK293	kidney:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
21	CTCF	chr20:23779902-23780221	Kidney_OC	kidney:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
22	CTCF	chr20:23704351-23704881	H1-hESC	embryonic stem cell:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
23	CTCF	chr20:23779880-23780030	NHEK	skin:	n/a	n/a
24	CTCF	chr20:23704380-23704530	GM12871	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
25	CTCF	chr20:23780260-23780410	RPTEC	kidney:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
26	CTCF	chr20:23779960-23780110	AG09319	gingival:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
27	CTCF	chr20:23704131-23704257	GM12891	blood:	n/a	n/a
28	CTCF	chr20:23779960-23780110	HA-sp	spinal cord:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
29	CTCF	chr20:23780280-23780430	HFF	foreskin:	n/a	chr20:23780320-23780329
30	CTCF	chr20:23704920-23705070	HVMF	connective:	n/a	n/a
31	CTCF	chr20:23704363-23704834	GM13977	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
32	CTCF	chr20:23704655-23704875	H1-hESC	embryonic stem cell:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
33	CTCF	chr20:23704340-23704490	GM12872	blood:	n/a	n/a
34	CTCF	chr20:23779880-23780030	HVMF	connective:	n/a	n/a
35	CTCF	chr20:23754840-23754990	HRE	kidney:	n/a	chr20:23754976-23754989
36	CTCF	chr20:23779878-23780378	GM19238	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
37	CTCF	chr20:23704350-23704892	MCF-7	breast:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
38	CTCF	chr20:23779738-23780632	K562	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
39	CTCF	chr20:23704355-23704664	GM19240	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
40	CTCF	chr20:23763120-23763270	GM12873	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
41	CTCF	chr20:23704308-23704679	GM12878	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
42	CTCF	chr20:23805860-23806010	GM12870	blood:	n/a	n/a
43	CTCF	chr20:23729680-23729830	GM12866	blood:	n/a	n/a
44	CTCF	chr20:23779960-23780110	HMEC	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
45	CTCF	chr20:23704313-23704665	K562	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
46	CTCF	chr20:23704340-23704899	Gliobla	brain:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
47	CTCF	chr20:23826257-23826361	K562	blood:	n/a	n/a
48	CTCF	chr20:23762700-23762850	WI-38	lung:	n/a	n/a
49	CTCF	chr20:23704360-23704510	AG04449	skin:	n/a	chr20:23704496-23704505
50	CTCF	chr20:23763140-23763290	HRPEpiC	eye:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23807359-23807409	GM06990	blood:	n/a
2	chr20:23806999-23807049	SK-N-MC	brain:	n/a
3	chr20:23807359-23807409	GM06990	blood:	n/a
4	chr20:23806999-23807049	SK-N-MC	brain:	n/a
5	chr20:23728432-23728482	ovcar-3	ovarian:	n/a
6	chr20:23807736-23807786	NH-A	brain:	n/a
7	chr20:23732595-23732645	NHBE	bronchial:	n/a
8	chr20:23728432-23728482	AoSMC	blood vessel:	n/a
9	chr20:23807778-23807828	GM12892	blood:	n/a
10	chr20:23806999-23807049	HCPEpiC	choroid plexus:	n/a
11	chr20:23732595-23732645	HEK293	kidney:	embryo
12	chr20:23807306-23807356	HEEpiC	esophagus:	n/a
13	chr20:23807736-23807786	HIPEpiC	eye:	n/a
14	chr20:23807778-23807828	AG10803	skin:	n/a
15	chr20:23807736-23807786	GM12892	blood:	n/a
16	chr20:23807359-23807409	Hepatocyte	liver:	n/a
17	chr20:23728432-23728482	AG04449	skin:	fetal
18	chr20:23806999-23807049	SKMC	muscle:	n/a
19	chr20:23728814-23728864	HEK293	kidney:	embryo
20	chr20:23806999-23807049	LNCaP	prostate:	n/a
21	chr20:23806999-23807049	GM19239	blood:	n/a
22	chr20:23732873-23732923	GM19239	blood:	n/a
23	chr20:23807778-23807828	MCF10A-Er-Src	breast:	n/a
24	chr20:23807359-23807409	NB4	blood:	n/a
25	chr20:23732873-23732923	BJ	skin:	n/a
26	chr20:23806999-23807049	GM12892	blood:	n/a
27	chr20:23807778-23807828	NT2-D1	testis:	n/a
28	chr20:23807359-23807409	SKMC	muscle:	n/a
29	chr20:23806999-23807049	MCF10A-Er-Src	breast:	n/a
30	chr20:23732873-23732923	NT2-D1	testis:	n/a
31	chr20:23807359-23807409	H1-hESC	embryonic stem cell:	embryo
32	chr20:23732873-23732923	NHDF-neo	bronchial:	n/a
33	chr20:23732595-23732645	GM12892	blood:	n/a
34	chr20:23728814-23728864	AG04450	lung:	fetal
35	chr20:23807359-23807409	Caco-2	colon:	n/a
36	chr20:23732595-23732645	ovcar-3	ovarian:	n/a
37	chr20:23728432-23728482	CMK	blood:	n/a
38	chr20:23807359-23807409	HRE	kidney:	n/a
39	chr20:23732873-23732923	BE2_C	brain:	n/a
40	chr20:23807736-23807786	PFSK-1	brain:	n/a
41	chr20:23731367-23731417	LNCaP	prostate:	n/a
42	chr20:23728814-23728864	HAEpiC	amniotic membrane:	n/a
43	chr20:23732873-23732923	HL-60	blood:	n/a
44	chr20:23807359-23807409	SAEC	small airway:	n/a
45	chr20:23731367-23731417	HEEpiC	esophagus:	n/a
46	chr20:23807359-23807409	A549	lung:	n/a
47	chr20:23732873-23732923	HPAEpiC	pulmonary alveolar:	n/a
48	chr20:23728814-23728864	Hela-S3	cervix:	n/a
49	chr20:23731367-23731417	AG04449	skin:	fetal
50	chr20:23807359-23807409	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
2	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
3	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
4	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
5	chr20:23779854..23780390-chr20:23870001..23870554,2	MCF-7	breast:
6	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
7	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
8	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
9	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
10	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
11	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
12	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
13	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
14	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
15	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
16	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
17	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
18	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-3	chr20:23778778-23778924	XLOC_013494
2	lnc-CST8-5	chr20:23733160-23733281	NONHSAT079083
3	lnc-CST8-5	chr20:23733871-23734300	NONHSAT079083
4	lnc-CST8-5	chr20:23732376-23732473	NONHSAT079083
5	lnc-CST8-5	chr20:23726778-23726924	NONHSAT079083
6	lnc-CST8-3	chr20:23784376-23784473	XLOC_013494
7	lnc-CST8-3	chr20:23785160-23785281	XLOC_013494
8	lnc-CST8-3	chr20:23785871-23786300	XLOC_013494

Variant related genes	Relation type
CST2P1	TF binding region
ENSG00000230908	TF binding region
CST1	TF binding region
CST2	TF binding region
CST2P1	CpG island
ENSG00000230908	CpG island
CST1	CpG island
CST2	CpG island
XIAP	miRNA target sites
WWC2	miRNA target sites
WWP2	miRNA target sites

Extended variants
information (count: 4588 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4588 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146717080	chr20:23692053-23692054	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs528106694	chr20:23692054-23692055	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199526974	chr20:23692067-23692068	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549532977	chr20:23692107-23692108	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs569598519	chr20:23692120-23692121	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs13044018	chr20:23692121-23692122	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs556049373	chr20:23692128-23692129	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs76675555	chr20:23692134-23692135	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs397814444	chr20:23692146-23692147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs140355665	chr20:23692151-23692152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs184011892	chr20:23692182-23692183	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs558316956	chr20:23692187-23692188	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs376321992	chr20:23692218-23692219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs150371787	chr20:23692219-23692220	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs373398047	chr20:23692227-23692228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs111569560	chr20:23692253-23692254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563539472	chr20:23692261-23692262	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs373327051	chr20:23692262-23692263	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs542606877	chr20:23692270-23692271	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs73104372	chr20:23692287-23692288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs73104373	chr20:23692289-23692290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs377471664	chr20:23692295-23692296	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs571126462	chr20:23692304-23692305	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs116394265	chr20:23692332-23692333	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564277507	chr20:23692351-23692352	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs145132998	chr20:23692363-23692364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs188512336	chr20:23692374-23692375	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs569672549	chr20:23692375-23692376	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs559528166	chr20:23693495-23693496	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs528156761	chr20:23693512-23693513	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs7269598	chr20:23693575-23693576	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs143246055	chr20:23693585-23693586	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs146705016	chr20:23693611-23693612	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550820703	chr20:23693629-23693630	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs139296053	chr20:23693633-23693634	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs142640991	chr20:23693653-23693654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs182267717	chr20:23693675-23693676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566990590	chr20:23693680-23693681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs538736736	chr20:23693684-23693685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs552563922	chr20:23693686-23693687	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs11698815	chr20:23693689-23693690	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs569694428	chr20:23693705-23693706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs557249067	chr20:23693708-23693709	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs369555421	chr20:23693712-23693713	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs118171357	chr20:23693715-23693716	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs536482539	chr20:23693725-23693726	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs140861762	chr20:23693730-23693731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs149749845	chr20:23693780-23693781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs544742033	chr20:23693781-23693782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs564905327	chr20:23693789-23693790	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23694000-23694400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:23694200-23694600	Enhancers	HMEC	breast
3	chr20:23695000-23695400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr20:23697800-23698600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:23698600-23698800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr20:23698800-23699400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr20:23700200-23701000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr20:23702200-23702400	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr20:23703600-23704000	Enhancers	Left Ventricle	heart
10	chr20:23713600-23714200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr20:23714200-23719000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr20:23715200-23716000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr20:23715400-23716400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr20:23719000-23719400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr20:23724800-23726600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr20:23725200-23726800	Enhancers	HUVEC	blood vessel
17	chr20:23725400-23725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr20:23725400-23725800	Enhancers	Osteobl	bone
19	chr20:23725400-23726000	Enhancers	NHLF	lung
20	chr20:23725400-23726600	Enhancers	NHDF-Ad	bronchial
21	chr20:23725400-23727000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr20:23725600-23725800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr20:23725800-23726200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr20:23725800-23727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr20:23726800-23727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
27	chr20:23727000-23727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr20:23727000-23729600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr20:23727200-23727800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:23727800-23728000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr20:23727800-23728400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr20:23727800-23728600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr20:23727800-23728800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr20:23728000-23728600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr20:23728600-23728800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr20:23728600-23729200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr20:23728800-23731400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr20:23728800-23735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr20:23729200-23730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr20:23729600-23734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr20:23730600-23730800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr20:23730600-23731000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr20:23730800-23731000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr20:23730800-23731600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr20:23731000-23731200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr20:23731000-23732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr20:23731200-23731400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
48	chr20:23731400-23731600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr20:23731600-23733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr20:23731800-23732000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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