Variant report

Variant	esv3328348
Chromosome Location	chr20:24095746-24285830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1333)
CpG islands
(count:0)
Chromatin interactive
region (count:48)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1333 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:24145085-24145446	HepG2	liver:	n/a	n/a
2	BCL3	chr20:24188431-24189516	GM12878	blood:	n/a	n/a
3	BCL3	chr20:24188372-24189543	GM12878	blood:	n/a	n/a
4	BHLHE40	chr20:24130785-24130985	K562	blood:	n/a	n/a
5	BHLHE40	chr20:24128975-24129495	GM12878	blood:	n/a	n/a
6	BHLHE40	chr20:24129055-24129401	K562	blood:	n/a	n/a
7	BRCA1	chr20:24266308-24266359	GM12878	blood:	n/a	n/a
8	CEBPB	chr20:24220836-24221404	HepG2	liver:	n/a	chr20:24220948-24220961 chr20:24220948-24220959 chr20:24220948-24220959 chr20:24220948-24220961 chr20:24221258-24221269
9	CEBPB	chr20:24174808-24175062	K562	blood:	n/a	chr20:24174915-24174926
10	CEBPB	chr20:24188434-24189349	A549	lung:	n/a	n/a
11	CEBPB	chr20:24174652-24175273	MCF-7	breast:	n/a	chr20:24174915-24174926
12	CEBPB	chr20:24127059-24127398	HepG2	liver:	n/a	chr20:24127230-24127241 chr20:24127228-24127241 chr20:24127228-24127239
13	CEBPB	chr20:24208163-24208431	A549	lung:	n/a	n/a
14	CEBPB	chr20:24117508-24117661	HepG2	liver:	n/a	n/a
15	CEBPB	chr20:24136176-24136576	A549	lung:	n/a	chr20:24136401-24136412 chr20:24136401-24136414 chr20:24136403-24136412 chr20:24136250-24136263
16	CEBPB	chr20:24161090-24161243	HepG2	liver:	n/a	n/a
17	CEBPB	chr20:24174748-24175100	HepG2	liver:	n/a	chr20:24174915-24174926
18	CEBPB	chr20:24174679-24175143	MCF-7	breast:	n/a	chr20:24174915-24174926
19	CEBPB	chr20:24168991-24169147	HepG2	liver:	n/a	chr20:24169115-24169126
20	CEBPB	chr20:24107992-24108130	HepG2	liver:	n/a	n/a
21	CEBPB	chr20:24281781-24282085	A549	lung:	n/a	chr20:24281907-24281918 chr20:24281908-24281919
22	CEBPB	chr20:24174829-24175039	ECC-1	luminal epithelium:	n/a	chr20:24174915-24174926
23	CEBPB	chr20:24174794-24175082	IMR90	lung:	n/a	chr20:24174915-24174926
24	CEBPB	chr20:24212148-24212313	HepG2	liver:	n/a	n/a
25	CEBPB	chr20:24165620-24165941	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr20:24279108-24279332	HepG2	liver:	n/a	chr20:24279251-24279262
27	CEBPB	chr20:24163078-24163402	HepG2	liver:	n/a	n/a
28	CEBPB	chr20:24208268-24208435	HepG2	liver:	n/a	n/a
29	CEBPB	chr20:24142904-24143103	HepG2	liver:	n/a	n/a
30	CEBPB	chr20:24281789-24282084	HepG2	liver:	n/a	chr20:24281907-24281918 chr20:24281908-24281919
31	CEBPB	chr20:24174804-24175090	A549	lung:	n/a	chr20:24174915-24174926
32	CEBPB	chr20:24188454-24189077	HepG2	liver:	n/a	n/a
33	CEBPB	chr20:24136184-24136571	HepG2	liver:	n/a	chr20:24136401-24136412 chr20:24136401-24136414 chr20:24136403-24136412 chr20:24136250-24136263
34	CHD2	chr20:24148972-24148982	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr20:24145144-24145228	Hela-S3	cervix:	n/a	chr20:24145185-24145206 chr20:24145190-24145208 chr20:24145192-24145205
36	CTCF	chr20:24141340-24141490	HA-sp	spinal cord:	n/a	chr20:24141393-24141411
37	CTCF	chr20:24181580-24181730	Caco-2	colon:	n/a	n/a
38	CTCF	chr20:24145020-24145170	GM12870	blood:	n/a	n/a
39	CTCF	chr20:24130720-24130870	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr20:24145054-24145322	A549	lung:	n/a	chr20:24145185-24145206 chr20:24145190-24145208 chr20:24145192-24145205
41	CTCF	chr20:24130720-24130870	HCT-116	colon:	n/a	n/a
42	CTCF	chr20:24141340-24141490	HPF	lung:	n/a	chr20:24141393-24141411
43	CTCF	chr20:24189397-24189570	Gliobla	brain:	n/a	n/a
44	CTCF	chr20:24141250-24141530	Fibrobl	skin:	n/a	chr20:24141393-24141411
45	CTCF	chr20:24189540-24189690	A549	lung:	n/a	n/a
46	CTCF	chr20:24130740-24130890	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr20:24141320-24141470	HCPEpiC	choroid plexus:	n/a	chr20:24141393-24141411
48	CTCF	chr20:24141280-24141430	GM12874	blood:	n/a	chr20:24141393-24141411
49	CTCF	chr20:24145140-24145290	HMEC	breast:	n/a	chr20:24145185-24145206 chr20:24145190-24145208 chr20:24145192-24145205
50	CTCF	chr20:24186000-24186150	SAEC	small airway:	n/a	chr20:24186079-24186097 chr20:24186082-24186095

No data

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:24283757..24284263-chr20:24761732..24762710,2	MCF-7	breast:
2	chr20:24180566..24182316-chr20:24260551..24262639,2	K562	blood:
3	chr20:24153821..24155495-chr20:24158056..24159705,2	MCF-7	breast:
4	chr20:24111886..24113648-chr20:24113789..24115599,2	MCF-7	breast:
5	chr20:24092433..24093240-chr20:24141090..24141875,2	MCF-7	breast:
6	chr20:24115388..24117970-chr20:24118371..24122645,4	MCF-7	breast:
7	chr20:24112072..24114906-chr20:24115605..24118020,3	MCF-7	breast:
8	chr20:24092580..24094161-chr20:24096209..24099117,2	MCF-7	breast:
9	chr20:24082693..24083584-chr20:24144765..24145673,2	MCF-7	breast:
10	chr20:24237902..24238701-chr20:24630250..24631153,4	MCF-7	breast:
11	chr20:24237874..24238722-chr20:24630391..24631249,3	MCF-7	breast:
12	chr20:24185914..24186516-chr20:24277045..24277654,2	MCF-7	breast:
13	chr14:21270235..21271079-chr20:24147176..24148134,2	MCF-7	breast:
14	chr20:24111886..24113648-chr20:24113789..24115599,2	MCF-7	breast:
15	chr20:24112072..24114906-chr20:24115605..24118020,3	MCF-7	breast:
16	chr20:24268351..24270345-chr20:24275470..24277004,2	MCF-7	breast:
17	chr20:23917874..23918575-chr20:24189095..24189921,2	MCF-7	breast:
18	chr20:24160483..24163088-chr20:24164952..24167667,2	MCF-7	breast:
19	chr20:24180566..24182316-chr20:24260551..24262639,2	K562	blood:
20	chr20:24139018..24140898-chr20:24143950..24146165,2	MCF-7	breast:
21	chr20:24284170..24284741-chr20:24580499..24581174,2	MCF-7	breast:
22	chr20:24082767..24083750-chr20:24144753..24145406,4	MCF-7	breast:
23	chr20:24256740..24259048-chr20:24262534..24264205,2	MCF-7	breast:
24	chr20:24153695..24155804-chr20:24157326..24159438,2	K562	blood:
25	chr20:24160483..24163088-chr20:24164952..24167667,2	MCF-7	breast:
26	chr20:23918077..23918602-chr20:24144722..24145283,2	MCF-7	breast:
27	chr20:24153821..24155495-chr20:24158056..24159705,2	MCF-7	breast:
28	chr20:24284269..24286790-chr20:24295761..24298544,3	MCF-7	breast:
29	chr20:24140940..24141858-chr20:24761680..24762579,3	MCF-7	breast:
30	chr20:24113587..24115337-chr20:24123688..24125826,2	MCF-7	breast:
31	chr20:24139018..24140898-chr20:24143950..24146165,2	MCF-7	breast:
32	chr20:24256740..24259048-chr20:24262534..24264205,2	MCF-7	breast:
33	chr20:24268351..24270345-chr20:24275470..24277004,2	MCF-7	breast:
34	chr20:24243101..24245973-chr20:24250065..24252649,2	MCF-7	breast:
35	chr20:24115388..24117970-chr20:24118371..24122645,4	MCF-7	breast:
36	chr20:24283824..24284530-chr20:24761681..24762698,3	MCF-7	breast:
37	chr20:24283582..24284398-chr20:24898678..24899422,2	MCF-7	breast:
38	chr20:24153695..24155804-chr20:24157326..24159438,2	K562	blood:
39	chr20:24189062..24189921-chr20:24297244..24297772,2	MCF-7	breast:
40	chr20:24189074..24189575-chr20:24761714..24762521,2	MCF-7	breast:
41	chr20:24185914..24186516-chr20:24277045..24277654,2	MCF-7	breast:
42	chr20:24243101..24245973-chr20:24250065..24252649,2	MCF-7	breast:
43	chr20:24092635..24093275-chr20:24140955..24141475,2	MCF-7	breast:
44	chr20:24185798..24186480-chr20:24761761..24762538,2	MCF-7	breast:
45	chr20:24147267..24149849-chr20:24336608..24338562,2	MCF-7	breast:
46	chr20:24245404..24247078-chr20:24248670..24250484,2	K562	blood:
47	chr20:24188959..24189575-chr20:24297258..24297884,2	MCF-7	breast:
48	chr20:24245404..24247078-chr20:24248670..24250484,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGTLC1-5	chr20:24278908-24279053	ENSG00000232200.2
2	lnc-GGTLC1-8	chr20:24246707-24246722	NONHSAT079106
3	lnc-SYNDIG1-2	chr20:24180403-24180470	XLOC_013497
4	lnc-GGTLC1-8	chr20:24226221-24226402	NONHSAT079106
5	lnc-SYNDIG1-2	chr20:24200259-24200338	XLOC_013497
6	lnc-GGTLC1-4	chr20:24160867-24161018	XLOC_013699
7	lnc-GGTLC1-8	chr20:24245775-24245843	NONHSAT079106
8	lnc-GGTLC1-8	chr20:24226908-24227053	NONHSAT079106
9	lnc-GGTLC1-5	chr20:24278221-24278402	XLOC_013700
10	lnc-GGTLC1-4	chr20:24164310-24164530	XLOC_013699
11	lnc-SYNDIG1-6	chr20:24139985-24141327	NONHSAT079102
12	lnc-SYNDIG1-6	chr20:24128403-24128470	NONHSAT079102
13	lnc-GGTLC1-8	chr20:24243305-24243394	NONHSAT079106
14	lnc-SYNDIG1-2	chr20:24204340-24205224	XLOC_013497
15	lnc-SYNDIG1-6	chr20:24148259-24148338	NONHSAT079102
16	lnc-SYNDIG1-2	chr20:24191985-24193327	XLOC_013497
17	lnc-SYNDIG1-6	chr20:24152340-24153224	NONHSAT079102
18	lnc-GGTLC1-5	chr20:24278908-24279053	XLOC_013700
19	lnc-GGTLC1-5	chr20:24278221-24278402	ENSG00000232200.2

No data

Variant related genes	Relation type
RNU1-23P	TF binding region
ENSG00000230133	TF binding region
ENSG00000236151	TF binding region
ENSG00000129538	chromatin interactions
ENSG00000236151	chromatin interactions
TBX22	miRNA target sites
TCF12	miRNA target sites
TCEB3	miRNA target sites

Extended variants
information (count: 5476 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5476 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182603464	chr20:24095886-24095887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149117482	chr20:24095955-24095956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35444999	chr20:24095981-24095982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs397865990	chr20:24095982-24095983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs59248167	chr20:24095985-24095986	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs562611955	chr20:24095986-24095987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142194278	chr20:24096010-24096011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191304014	chr20:24096017-24096018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146789948	chr20:24096018-24096019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527553931	chr20:24096020-24096021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547675737	chr20:24096028-24096029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140555149	chr20:24096040-24096041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183877256	chr20:24096048-24096049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538688734	chr20:24096049-24096050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116217931	chr20:24096082-24096083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6036654	chr20:24096083-24096084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs145637555	chr20:24096091-24096092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138367233	chr20:24096132-24096133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574986646	chr20:24096157-24096158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs193079097	chr20:24096200-24096201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570534866	chr20:24096220-24096221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554495346	chr20:24096230-24096231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185468123	chr20:24096232-24096233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545847983	chr20:24096256-24096257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188848210	chr20:24096260-24096261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140984360	chr20:24096261-24096262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150247034	chr20:24096265-24096266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528836353	chr20:24096277-24096278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561688531	chr20:24096279-24096280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6049411	chr20:24096373-24096374	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs138858301	chr20:24096414-24096415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191820465	chr20:24096436-24096437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532351691	chr20:24096533-24096534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6132700	chr20:24096547-24096548	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs369866123	chr20:24096592-24096593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527853289	chr20:24096611-24096612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548665826	chr20:24096618-24096619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59960570	chr20:24096624-24096625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs6036655	chr20:24096635-24096636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138528540	chr20:24096650-24096651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554487790	chr20:24096671-24096672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571187703	chr20:24096672-24096673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142724214	chr20:24096673-24096674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148859570	chr20:24096725-24096726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371808743	chr20:24096730-24096731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201182030	chr20:24096732-24096733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534491473	chr20:24096733-24096734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539958503	chr20:24096734-24096735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6036656	chr20:24096742-24096743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6036657	chr20:24096746-24096747	Weak transcription	n/a	n/a	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
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24083400-24096200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr20:24094400-24098400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:24095000-24098200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr20:24095600-24096000	Enhancers	Fetal Stomach	stomach
5	chr20:24095800-24096000	Enhancers	Fetal Muscle Leg	muscle
6	chr20:24096000-24096400	Enhancers	HUVEC	blood vessel
7	chr20:24096000-24097000	Weak transcription	Fetal Stomach	stomach
8	chr20:24096200-24096400	Enhancers	Placenta Amnion	Placenta Amnion
9	chr20:24096200-24096600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr20:24096400-24098000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr20:24096400-24098200	Weak transcription	HUVEC	blood vessel
12	chr20:24096600-24097800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr20:24097000-24097200	Enhancers	Fetal Stomach	stomach
14	chr20:24097000-24098200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr20:24097000-24100000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr20:24097200-24098000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr20:24097200-24099200	Bivalent Enhancer	Fetal Stomach	stomach
18	chr20:24097200-24100000	Enhancers	Fetal Muscle Leg	muscle
19	chr20:24097400-24097800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr20:24097400-24097800	Enhancers	Brain Germinal Matrix	brain
21	chr20:24097400-24098400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr20:24097400-24099600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr20:24097600-24099000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr20:24097600-24099400	Enhancers	NH-A	brain
25	chr20:24097800-24098000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr20:24097800-24098000	Enhancers	Esophagus	oesophagus
27	chr20:24097800-24098000	Enhancers	NHLF	lung
28	chr20:24097800-24098400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr20:24097800-24098600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr20:24097800-24099800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr20:24097800-24100000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr20:24097800-24100200	Enhancers	Osteobl	bone
33	chr20:24098000-24098200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr20:24098000-24099200	Weak transcription	NHLF	lung
35	chr20:24098000-24099600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr20:24098000-24099600	Enhancers	Placenta Amnion	Placenta Amnion
37	chr20:24098200-24098800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr20:24098200-24099000	Enhancers	Stomach Smooth Muscle	stomach
39	chr20:24098200-24099200	Weak transcription	Esophagus	oesophagus
40	chr20:24098200-24100200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr20:24098200-24100600	Enhancers	Ovary	ovary
42	chr20:24098200-24100800	Enhancers	HUVEC	blood vessel
43	chr20:24098400-24098600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr20:24098400-24099800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr20:24098400-24099800	Bivalent Enhancer	Adipose Nuclei	Adipose
46	chr20:24098400-24099800	Enhancers	Fetal Lung	lung
47	chr20:24098400-24099800	Enhancers	Rectal Smooth Muscle	rectum
48	chr20:24098400-24100000	Enhancers	Lung	lung
49	chr20:24098400-24100800	Enhancers	Fetal Thymus	thymus
50	chr20:24098600-24099000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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