Variant report

Variant	nsv833945
Chromosome Location	chr20:24163437-24349462
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:0)
Chromatin interactive
region (count:39)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr20:24188431-24189516	GM12878	blood:	n/a	n/a
2	BCL3	chr20:24188372-24189543	GM12878	blood:	n/a	n/a
3	BRCA1	chr20:24266308-24266359	GM12878	blood:	n/a	n/a
4	CEBPB	chr20:24315141-24315395	A549	lung:	n/a	n/a
5	CEBPB	chr20:24174748-24175100	HepG2	liver:	n/a	chr20:24174915-24174926
6	CEBPB	chr20:24168991-24169147	HepG2	liver:	n/a	chr20:24169115-24169126
7	CEBPB	chr20:24174652-24175273	MCF-7	breast:	n/a	chr20:24174915-24174926
8	CEBPB	chr20:24208268-24208435	HepG2	liver:	n/a	n/a
9	CEBPB	chr20:24281789-24282084	HepG2	liver:	n/a	chr20:24281907-24281918 chr20:24281908-24281919
10	CEBPB	chr20:24220836-24221404	HepG2	liver:	n/a	chr20:24220948-24220961 chr20:24220948-24220959 chr20:24220948-24220959 chr20:24220948-24220961 chr20:24221258-24221269
11	CEBPB	chr20:24174679-24175143	MCF-7	breast:	n/a	chr20:24174915-24174926
12	CEBPB	chr20:24297312-24297858	MCF-7	breast:	n/a	n/a
13	CEBPB	chr20:24295996-24296326	HepG2	liver:	n/a	chr20:24296162-24296173
14	CEBPB	chr20:24279108-24279332	HepG2	liver:	n/a	chr20:24279251-24279262
15	CEBPB	chr20:24293825-24293845	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr20:24212148-24212313	HepG2	liver:	n/a	n/a
17	CEBPB	chr20:24334411-24334508	HepG2	liver:	n/a	chr20:24334472-24334483
18	CEBPB	chr20:24296774-24297024	HepG2	liver:	n/a	n/a
19	CEBPB	chr20:24188454-24189077	HepG2	liver:	n/a	n/a
20	CEBPB	chr20:24298571-24298701	HepG2	liver:	n/a	chr20:24298671-24298682
21	CEBPB	chr20:24174829-24175039	ECC-1	luminal epithelium:	n/a	chr20:24174915-24174926
22	CEBPB	chr20:24174794-24175082	IMR90	lung:	n/a	chr20:24174915-24174926
23	CEBPB	chr20:24208163-24208431	A549	lung:	n/a	n/a
24	CEBPB	chr20:24281781-24282085	A549	lung:	n/a	chr20:24281907-24281918 chr20:24281908-24281919
25	CEBPB	chr20:24315110-24315340	HepG2	liver:	n/a	n/a
26	CEBPB	chr20:24174804-24175090	A549	lung:	n/a	chr20:24174915-24174926
27	CEBPB	chr20:24188434-24189349	A549	lung:	n/a	n/a
28	CEBPB	chr20:24331475-24331764	HepG2	liver:	n/a	chr20:24331619-24331630 chr20:24331618-24331629
29	CEBPB	chr20:24298600-24298706	A549	lung:	n/a	chr20:24298671-24298682
30	CEBPB	chr20:24331452-24331786	IMR90	lung:	n/a	chr20:24331619-24331630 chr20:24331618-24331629
31	CEBPB	chr20:24165620-24165941	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr20:24174808-24175062	K562	blood:	n/a	chr20:24174915-24174926
33	CTCF	chr20:24284140-24284290	AG04449	skin:	n/a	n/a
34	CTCF	chr20:24297214-24297398	MCF-7	breast:	n/a	n/a
35	CTCF	chr20:24270872-24271013	MCF-7	breast:	n/a	chr20:24270923-24270941 chr20:24270918-24270939 chr20:24270925-24270938
36	CTCF	chr20:24270860-24271010	Caco-2	colon:	n/a	chr20:24270923-24270941 chr20:24270918-24270939 chr20:24270925-24270938
37	CTCF	chr20:24290900-24291050	HepG2	liver:	n/a	n/a
38	CTCF	chr20:24206057-24206111	LNCaP	prostate:	n/a	n/a
39	CTCF	chr20:24297197-24297418	MCF-7	breast:	n/a	n/a
40	CTCF	chr20:24331980-24332130	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr20:24283940-24284356	MCF-7	breast:	n/a	chr20:24284034-24284042
42	CTCF	chr20:24284045-24284297	MCF-7	breast:	n/a	n/a
43	CTCF	chr20:24189400-24189550	GM12864	blood:	n/a	n/a
44	CTCF	chr20:24189440-24189590	NB4	blood:	n/a	n/a
45	CTCF	chr20:24205900-24206050	A549	lung:	n/a	n/a
46	CTCF	chr20:24189396-24189571	A549	lung:	n/a	n/a
47	CTCF	chr20:24189342-24189607	LNCaP	prostate:	n/a	n/a
48	CTCF	chr20:24189374-24189616	A549	lung:	n/a	n/a
49	CTCF	chr20:24297173-24297408	MCF-7	breast:	n/a	n/a
50	CTCF	chr20:24284145-24284248	GM12892	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr20:24256740..24259048-chr20:24262534..24264205,2	MCF-7	breast:
2	chr20:24189062..24189921-chr20:24297244..24297772,2	MCF-7	breast:
3	chr20:24185914..24186516-chr20:24277045..24277654,2	MCF-7	breast:
4	chr20:24180566..24182316-chr20:24260551..24262639,2	K562	blood:
5	chr20:24344885..24347176-chr20:24347608..24349903,2	MCF-7	breast:
6	chr20:24311140..24313044-chr20:24313684..24316218,2	MCF-7	breast:
7	chr20:24189062..24189921-chr20:24297244..24297772,2	MCF-7	breast:
8	chr20:24284269..24286790-chr20:24295761..24298544,3	MCF-7	breast:
9	chr20:24256740..24259048-chr20:24262534..24264205,2	MCF-7	breast:
10	chr20:24245404..24247078-chr20:24248670..24250484,2	K562	blood:
11	chr20:24180566..24182316-chr20:24260551..24262639,2	K562	blood:
12	chr20:24188959..24189575-chr20:24297258..24297884,2	MCF-7	breast:
13	chr20:24300357..24302551-chr20:24304498..24306050,2	K562	blood:
14	chr20:24245404..24247078-chr20:24248670..24250484,2	K562	blood:
15	chr20:24311140..24313044-chr20:24313684..24316218,2	MCF-7	breast:
16	chr20:24337993..24340100-chr20:24340194..24343622,3	MCF-7	breast:
17	chr20:24243101..24245973-chr20:24250065..24252649,2	MCF-7	breast:
18	chr20:24188959..24189575-chr20:24297258..24297884,2	MCF-7	breast:
19	chr20:24268351..24270345-chr20:24275470..24277004,2	MCF-7	breast:
20	chr20:24189074..24189575-chr20:24761714..24762521,2	MCF-7	breast:
21	chr20:24346392..24348668-chr20:24354485..24357111,2	MCF-7	breast:
22	chr20:24147267..24149849-chr20:24336608..24338562,2	MCF-7	breast:
23	chr20:24344885..24347176-chr20:24347608..24349903,2	MCF-7	breast:
24	chr20:24337993..24340100-chr20:24340194..24343622,3	MCF-7	breast:
25	chr20:24283582..24284398-chr20:24898678..24899422,2	MCF-7	breast:
26	chr20:24160483..24163088-chr20:24164952..24167667,2	MCF-7	breast:
27	chr20:24283824..24284530-chr20:24761681..24762698,3	MCF-7	breast:
28	chr20:24284269..24286790-chr20:24295761..24298544,3	MCF-7	breast:
29	chr20:24268351..24270345-chr20:24275470..24277004,2	MCF-7	breast:
30	chr20:24185914..24186516-chr20:24277045..24277654,2	MCF-7	breast:
31	chr20:24300357..24302551-chr20:24304498..24306050,2	K562	blood:
32	chr20:24347069..24348854-chr20:24350597..24353212,2	K562	blood:
33	chr20:24237874..24238722-chr20:24630391..24631249,3	MCF-7	breast:
34	chr20:24185798..24186480-chr20:24761761..24762538,2	MCF-7	breast:
35	chr20:23917874..23918575-chr20:24189095..24189921,2	MCF-7	breast:
36	chr20:24237902..24238701-chr20:24630250..24631153,4	MCF-7	breast:
37	chr20:24283757..24284263-chr20:24761732..24762710,2	MCF-7	breast:
38	chr20:24284170..24284741-chr20:24580499..24581174,2	MCF-7	breast:
39	chr20:24243101..24245973-chr20:24250065..24252649,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGTLC1-8	chr20:24246707-24246722	NONHSAT079106
2	lnc-GGTLC1-8	chr20:24245775-24245843	NONHSAT079106
3	lnc-GGTLC1-5	chr20:24278221-24278402	XLOC_013700
4	lnc-SYNDIG1-2	chr20:24204340-24205224	XLOC_013497
5	lnc-GGTLC1-8	chr20:24226221-24226402	NONHSAT079106
6	lnc-GGTLC1-5	chr20:24278908-24279053	ENSG00000232200.2
7	lnc-GGTLC1-5	chr20:24295306-24295394	ENSG00000232200.2
8	lnc-GGTLC1-5	chr20:24298607-24298722	ENSG00000232200.2
9	lnc-GGTLC1-5	chr20:24297775-24297843	ENSG00000232200.2
10	lnc-SYNDIG1-2	chr20:24200259-24200338	XLOC_013497
11	lnc-SYNDIG1-2	chr20:24180403-24180470	XLOC_013497
12	lnc-GGTLC1-5	chr20:24278908-24279053	XLOC_013700
13	lnc-GGTLC1-5	chr20:24295305-24295394	XLOC_013700
14	lnc-GGTLC1-4	chr20:24164310-24164530	XLOC_013699
15	lnc-GGTLC1-5	chr20:24297775-24297843	XLOC_013700
16	lnc-GGTLC1-8	chr20:24243305-24243394	NONHSAT079106
17	lnc-SYNDIG1-2	chr20:24191985-24193327	XLOC_013497
18	lnc-GGTLC1-8	chr20:24226908-24227053	NONHSAT079106
19	lnc-GGTLC1-5	chr20:24298707-24298722	XLOC_013700
20	lnc-GGTLC1-5	chr20:24278221-24278402	ENSG00000232200.2

No data

Variant related genes	Relation type
RNU1-23P	TF binding region
ENSG00000230133	TF binding region
ENSG00000232200	TF binding region
TBX22	miRNA target sites
TCF12	miRNA target sites
TCEB3	miRNA target sites

Extended variants
information (count: 5721 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5721 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548767602	chr20:24164310-24164311	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs191597091	chr20:24164311-24164312	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs527352794	chr20:24164338-24164339	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs182816136	chr20:24164343-24164344	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs564231280	chr20:24164359-24164360	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs186806035	chr20:24164360-24164361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs191316910	chr20:24164413-24164414	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs567338455	chr20:24164436-24164437	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs531596168	chr20:24164466-24164467	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs148184600	chr20:24164499-24164500	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs568140398	chr20:24164503-24164504	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs375769157	chr20:24164510-24164511	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs6106799	chr20:24164521-24164522	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs537577894	chr20:24164527-24164528	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs547496960	chr20:24164534-24164535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368072387	chr20:24164535-24164536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570702908	chr20:24164552-24164553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540072394	chr20:24164567-24164568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556563765	chr20:24164573-24164574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140080189	chr20:24164587-24164588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535794159	chr20:24164607-24164608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370112155	chr20:24164624-24164625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371494725	chr20:24164661-24164662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553065379	chr20:24164664-24164665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555353175	chr20:24164676-24164677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6083424	chr20:24164679-24164680	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs150331711	chr20:24164733-24164734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564212678	chr20:24164754-24164755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577742936	chr20:24164759-24164760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570920794	chr20:24164815-24164816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116493259	chr20:24164830-24164831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183450363	chr20:24164879-24164880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529160465	chr20:24164893-24164894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs137936172	chr20:24164914-24164915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11698401	chr20:24164937-24164938	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs527720437	chr20:24164976-24164977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547482950	chr20:24164986-24164987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570645416	chr20:24164988-24164989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188033925	chr20:24164999-24165000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs151145078	chr20:24165075-24165076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112820715	chr20:24165108-24165109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373620102	chr20:24165117-24165118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570156923	chr20:24165134-24165135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144732724	chr20:24165172-24165173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554498473	chr20:24165174-24165175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556134974	chr20:24165187-24165188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572065245	chr20:24165219-24165220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6083425	chr20:24165234-24165235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6049484	chr20:24165244-24165245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs557873532	chr20:24165275-24165276	Enhancers	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	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24164400-24165800	Enhancers	Fetal Kidney	kidney
2	chr20:24164600-24166600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr20:24165000-24165800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr20:24165200-24166600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr20:24165200-24167400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr20:24165400-24166600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr20:24165400-24166800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr20:24165600-24166200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr20:24165800-24166600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr20:24166000-24168200	Enhancers	Dnd41	blood
11	chr20:24166600-24167000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr20:24167000-24167400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr20:24174800-24175400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr20:24174800-24175400	Enhancers	Fetal Intestine Large	intestine
15	chr20:24179400-24180200	Enhancers	Placenta Amnion	Placenta Amnion
16	chr20:24179400-24180400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr20:24180000-24180800	Enhancers	Fetal Kidney	kidney
18	chr20:24180400-24180600	Enhancers	Fetal Heart	heart
19	chr20:24180400-24182400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr20:24180800-24181600	Weak transcription	Fetal Heart	heart
21	chr20:24181600-24182000	Enhancers	Fetal Heart	heart
22	chr20:24182400-24182600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr20:24183000-24183200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr20:24184000-24185400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr20:24184800-24188600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr20:24185400-24188800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr20:24185600-24186200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr20:24185800-24186000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr20:24186000-24186600	Enhancers	Dnd41	blood
30	chr20:24186200-24188600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr20:24186200-24188600	Enhancers	Fetal Intestine Large	intestine
32	chr20:24187200-24187400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr20:24187400-24188000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr20:24187400-24188400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr20:24187400-24188600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr20:24187400-24188600	Enhancers	Fetal Intestine Small	intestine
37	chr20:24188000-24192200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr20:24188400-24188800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr20:24188400-24188800	Enhancers	Pancreas	Pancrea
40	chr20:24188400-24192200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr20:24188600-24188800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr20:24188600-24189200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
43	chr20:24188600-24189400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr20:24188600-24189600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
45	chr20:24188600-24190400	Weak transcription	Fetal Intestine Large	intestine
46	chr20:24188600-24190800	Weak transcription	Fetal Intestine Small	intestine
47	chr20:24188600-24192200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr20:24188800-24189000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr20:24188800-24192600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr20:24189000-24189200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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