Variant report

Variant	nsv586006
Chromosome Location	chr20:41157707-41290936
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	ATF2	chr20:41159448-41159852	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr20:41262897-41263215	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr20:41216153-41216346	H1-hESC	embryonic stem cell:	n/a	chr20:41216218-41216232
4	BATF	chr20:41182066-41182418	GM12878	blood:	n/a	n/a
5	BATF	chr20:41181966-41182424	GM12878	blood:	n/a	n/a
6	BATF	chr20:41192599-41192856	GM12878	blood:	n/a	chr20:41192720-41192731
7	CEBPB	chr20:41282814-41283026	HepG2	liver:	n/a	chr20:41282919-41282930
8	CEBPB	chr20:41185337-41185525	K562	blood:	n/a	chr20:41185398-41185407 chr20:41185398-41185409 chr20:41185398-41185407 chr20:41185396-41185409 chr20:41185396-41185407 chr20:41185396-41185409 chr20:41185398-41185407 chr20:41185398-41185407
9	CEBPB	chr20:41218872-41219099	H1-hESC	embryonic stem cell:	n/a	chr20:41219078-41219089
10	CEBPB	chr20:41265532-41265732	HepG2	liver:	n/a	chr20:41265590-41265603 chr20:41265591-41265602
11	CEBPB	chr20:41218912-41219204	A549	lung:	n/a	chr20:41219078-41219089
12	CEBPB	chr20:41203262-41203461	HepG2	liver:	n/a	chr20:41203427-41203438
13	CEBPB	chr20:41218900-41219249	HepG2	liver:	n/a	chr20:41219078-41219089
14	CEBPB	chr20:41185258-41185572	A549	lung:	n/a	chr20:41185398-41185407 chr20:41185398-41185409 chr20:41185398-41185407 chr20:41185396-41185409 chr20:41185396-41185407 chr20:41185396-41185409 chr20:41185398-41185407 chr20:41185398-41185407
15	CEBPB	chr20:41234364-41234717	HepG2	liver:	n/a	n/a
16	CEBPB	chr20:41218909-41219150	K562	blood:	n/a	chr20:41219078-41219089
17	CEBPB	chr20:41240638-41240690	HepG2	liver:	n/a	chr20:41240677-41240688
18	CEBPB	chr20:41201099-41202020	MCF-7	breast:	n/a	chr20:41201766-41201777 chr20:41201766-41201779
19	CEBPB	chr20:41279055-41279225	H1-hESC	embryonic stem cell:	n/a	chr20:41279114-41279125
20	CEBPB	chr20:41201173-41201616	MCF-7	breast:	n/a	n/a
21	CEBPB	chr20:41274989-41275199	HepG2	liver:	n/a	n/a
22	CEBPB	chr20:41251310-41251377	HepG2	liver:	n/a	n/a
23	CEBPB	chr20:41234470-41234614	K562	blood:	n/a	n/a
24	CEBPB	chr20:41203381-41203449	K562	blood:	n/a	chr20:41203427-41203438
25	CEBPB	chr20:41218940-41219204	IMR90	lung:	n/a	chr20:41219078-41219089
26	CEBPB	chr20:41185225-41185588	HepG2	liver:	n/a	chr20:41185398-41185407 chr20:41185398-41185409 chr20:41185398-41185407 chr20:41185396-41185409 chr20:41185396-41185407 chr20:41185396-41185409 chr20:41185398-41185407 chr20:41185398-41185407
27	CEBPB	chr20:41269498-41269701	HepG2	liver:	n/a	chr20:41269631-41269642
28	CEBPB	chr20:41218705-41219269	MCF-7	breast:	n/a	chr20:41219078-41219089
29	CHD2	chr20:41182204-41182321	GM12878	blood:	n/a	n/a
30	CTCF	chr20:41178320-41178470	MCF-7	breast:	n/a	n/a
31	CTCF	chr20:41159600-41159750	AoAF	blood vessel:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
32	CTCF	chr20:41159579-41159777	GM19239	blood:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
33	CTCF	chr20:41159580-41159730	GM12875	blood:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
34	CTCF	chr20:41160147-41160205	GM19238	blood:	n/a	n/a
35	CTCF	chr20:41159560-41159710	GM12873	blood:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
36	CTCF	chr20:41203516-41203540	GM20000	blood:	n/a	n/a
37	CTCF	chr20:41159580-41159730	RPTEC	kidney:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
38	CTCF	chr20:41159600-41159750	GM12872	blood:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
39	CTCF	chr20:41159542-41159810	GM12878	blood:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
40	CTCF	chr20:41159620-41159770	HL-60	blood:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
41	CTCF	chr20:41205882-41206179	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr20:41159560-41159710	NHDF-neo	bronchial:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
43	CTCF	chr20:41159591-41159772	HUVEC	blood vessel:	n/a	chr20:41159672-41159688 chr20:41159666-41159687 chr20:41159671-41159689
44	CTCF	chr20:41160100-41160250	GM12864	blood:	n/a	n/a
45	CTCF	chr20:41160580-41160730	GM12878	blood:	n/a	n/a
46	CTCF	chr20:41159700-41159850	A549	lung:	n/a	n/a
47	CTCF	chr20:41218660-41218810	HRE	kidney:	n/a	n/a
48	CTCF	chr20:41238860-41239010	MCF-7	breast:	n/a	n/a
49	CTCF	chr20:41223860-41224010	GM12873	blood:	n/a	n/a
50	CTCF	chr20:41160281-41160368	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:41112093..41113034-chr20:41158800..41160071,4	MCF-7	breast:
2	chr20:41221842..41223467-chr20:41282056..41284683,2	MCF-7	breast:
3	chr20:41156659..41159808-chr20:41161331..41164447,3	MCF-7	breast:
4	chr20:41219224..41221515-chr20:41224161..41226568,2	MCF-7	breast:
5	chr20:41111361..41112918-chr20:41159329..41160293,5	MCF-7	breast:
6	chr20:40656318..40657155-chr20:41159287..41160221,3	MCF-7	breast:
7	chr20:41235856..41237826-chr20:41240786..41243321,2	K562	blood:
8	chr20:41154320..41156959-chr20:41167704..41169513,2	K562	blood:
9	chr20:41161976..41163501-chr20:41178008..41179846,2	MCF-7	breast:
10	chr20:41156659..41159808-chr20:41161331..41164447,3	MCF-7	breast:
11	chr20:41238748..41239268-chr20:41307296..41307807,2	MCF-7	breast:
12	chr1:115322010..115324923-chr20:41157640..41159690,2	MCF-7	breast:
13	chr20:41183922..41185722-chr20:41188691..41191209,2	K562	blood:
14	chr20:41161976..41163501-chr20:41178008..41179846,2	MCF-7	breast:
15	chr20:41223845..41225575-chr20:41225576..41227086,2	MCF-7	breast:
16	chr20:41158587..41161005-chr20:41184135..41185897,2	MCF-7	breast:
17	chr20:41183351..41185462-chr20:41211169..41213368,2	MCF-7	breast:
18	chr20:41183922..41185722-chr20:41188691..41191209,2	K562	blood:
19	chr20:41153100..41156959-chr20:41167478..41169513,3	K562	blood:
20	chr20:41190947..41193604-chr20:41196031..41197655,2	MCF-7	breast:
21	chr20:41169178..41171278-chr20:41173910..41175582,2	MCF-7	breast:
22	chr20:41232529..41235268-chr20:41239023..41240669,2	MCF-7	breast:
23	chr20:41219224..41221515-chr20:41224161..41226568,2	MCF-7	breast:
24	chr20:41189320..41191294-chr20:41193549..41196029,2	MCF-7	breast:
25	chr20:41158587..41161005-chr20:41184135..41185897,2	MCF-7	breast:
26	chr1:115223230..115223759-chr20:41159215..41160064,2	MCF-7	breast:
27	chr20:41235856..41237826-chr20:41240786..41243321,2	K562	blood:
28	chr20:41189320..41191294-chr20:41193549..41196029,2	MCF-7	breast:
29	chr20:41190947..41193604-chr20:41196031..41197655,2	MCF-7	breast:
30	chr1:115299061..115301144-chr20:41248782..41252439,3	MCF-7	breast:
31	chr20:40367029..40367531-chr20:41159523..41160164,2	MCF-7	breast:
32	chr20:41186370..41189085-chr20:41189896..41191987,2	MCF-7	breast:
33	chr20:41183351..41185462-chr20:41211169..41213368,2	MCF-7	breast:
34	chr20:41232529..41235268-chr20:41239023..41240669,2	MCF-7	breast:
35	chr1:115296501..115298139-chr20:41277950..41280016,2	MCF-7	breast:
36	chr20:41150606..41154856-chr20:41155913..41160974,4	MCF-7	breast:
37	chr20:41223845..41225575-chr20:41225576..41227086,2	MCF-7	breast:
38	chr20:40832621..40833511-chr20:41158812..41160167,5	MCF-7	breast:
39	chr1:115299122..115302084-chr20:41239351..41241193,2	MCF-7	breast:
40	chr20:41210269..41211939-chr20:41214857..41217644,2	MCF-7	breast:
41	chr20:41169178..41171278-chr20:41173910..41175582,2	MCF-7	breast:
42	chr20:41210269..41211939-chr20:41214857..41217644,2	MCF-7	breast:
43	chr20:41221842..41223467-chr20:41282056..41284683,2	MCF-7	breast:
44	chr20:41186370..41189085-chr20:41189896..41191987,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRSF6-11	chr20:41235334-41235515	NONHSAT079803
2	lnc-SRSF6-11	chr20:41236034-41236199	NONHSAT079803

Variant related genes	Relation type
ENSG00000229892	TF binding region
ENSG00000009307	chromatin interactions
ENSG00000052723	chromatin interactions

Extended variants
information (count: 5322 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5322 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6072770	chr20:41157707-41157708	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115043251	chr20:41157750-41157751	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577390356	chr20:41157751-41157752	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77343420	chr20:41157770-41157771	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559655943	chr20:41157777-41157778	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528791256	chr20:41157778-41157779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570782171	chr20:41157796-41157797	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562035108	chr20:41157806-41157807	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530459269	chr20:41157816-41157817	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550139596	chr20:41157817-41157818	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs62205785	chr20:41157855-41157856	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs140695701	chr20:41157892-41157893	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs545105618	chr20:41157893-41157894	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566502806	chr20:41157902-41157903	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs60918621	chr20:41157924-41157925	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546984201	chr20:41157959-41157960	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145797307	chr20:41157960-41157961	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs6030304	chr20:41157965-41157966	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs535648636	chr20:41157966-41157967	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557171049	chr20:41157982-41157983	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs569155798	chr20:41157986-41157987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537468266	chr20:41157988-41157989	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557363486	chr20:41158037-41158038	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs6124469	chr20:41158041-41158042	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577430945	chr20:41158045-41158046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545935680	chr20:41158052-41158053	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181527808	chr20:41158083-41158084	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138391697	chr20:41158108-41158109	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs6072771	chr20:41158109-41158110	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562073750	chr20:41158137-41158138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539185413	chr20:41158150-41158151	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12481148	chr20:41158156-41158157	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs543822131	chr20:41158157-41158158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563701309	chr20:41158159-41158160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533052973	chr20:41158170-41158171	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546422000	chr20:41158171-41158172	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6130157	chr20:41158173-41158174	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79759472	chr20:41158178-41158179	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529108883	chr20:41158203-41158204	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs6124470	chr20:41158229-41158230	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141306702	chr20:41158236-41158237	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187013916	chr20:41158254-41158255	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190676396	chr20:41158262-41158263	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183195148	chr20:41158288-41158289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs367648924	chr20:41158375-41158376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551003301	chr20:41158413-41158414	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570812487	chr20:41158434-41158435	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs140817588	chr20:41158488-41158489	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs539811372	chr20:41158498-41158499	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540475434	chr20:41158501-41158502	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	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
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ovarian cancer	19193619	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelodysplastic syndrome	17634407	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ductal carcinoma	22052326	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Cervical cancer	21062161	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
early-passage human iPS cells	21368824	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41158800-41161000	Enhancers	Fetal Brain Male	brain
2	chr20:41158800-41161200	Enhancers	Fetal Brain Female	brain
3	chr20:41159000-41161000	Enhancers	Pancreas	Pancrea
4	chr20:41159000-41161200	Enhancers	Brain Germinal Matrix	brain
5	chr20:41159200-41160000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr20:41159200-41160800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr20:41159200-41161000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr20:41159200-41161000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr20:41159200-41161200	Enhancers	Adipose Nuclei	Adipose
10	chr20:41159400-41160400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr20:41159400-41160800	Enhancers	Brain Hippocampus Middle	brain
12	chr20:41159400-41161000	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr20:41159400-41161000	Enhancers	Fetal Muscle Leg	muscle
14	chr20:41159400-41161000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr20:41159800-41160800	Enhancers	Colon Smooth Muscle	Colon
16	chr20:41159800-41161000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr20:41160000-41160200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr20:41160000-41160800	Enhancers	Brain Cingulate Gyrus	brain
19	chr20:41160000-41160800	Enhancers	Fetal Muscle Trunk	muscle
20	chr20:41160000-41160800	Enhancers	Placenta	Placenta
21	chr20:41160000-41161000	Enhancers	GM12878-XiMat	blood
22	chr20:41160200-41160400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr20:41160200-41161000	Enhancers	Brain Anterior Caudate	brain
24	chr20:41160200-41161000	Enhancers	Fetal Thymus	thymus
25	chr20:41160400-41160600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr20:41160400-41160800	Enhancers	Brain Substantia Nigra	brain
27	chr20:41160600-41161200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr20:41160800-41173000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr20:41161000-41163000	Weak transcription	Pancreas	Pancrea
30	chr20:41163600-41164000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr20:41173000-41174200	Enhancers	Pancreas	Pancrea
32	chr20:41173000-41174400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr20:41173600-41174200	Enhancers	Gastric	stomach
34	chr20:41174200-41178000	Weak transcription	Pancreas	Pancrea
35	chr20:41178200-41178400	Enhancers	Brain Germinal Matrix	brain
36	chr20:41178200-41179000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr20:41178400-41179200	Weak transcription	Brain Germinal Matrix	brain
38	chr20:41179200-41181000	Enhancers	Brain Germinal Matrix	brain
39	chr20:41181600-41182000	Enhancers	Duodenum Mucosa	Duodenum
40	chr20:41181800-41182200	Active TSS	GM12878-XiMat	blood
41	chr20:41182000-41182400	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr20:41182000-41182600	Active TSS	Duodenum Mucosa	Duodenum
43	chr20:41182200-41182600	Flanking Active TSS	GM12878-XiMat	blood
44	chr20:41182200-41182800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr20:41182400-41182600	Enhancers	Right Atrium	heart
46	chr20:41182600-41187400	Weak transcription	Right Atrium	heart
47	chr20:41182800-41184000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr20:41184000-41185800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr20:41185800-41197800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr20:41187400-41187600	ZNF genes & repeats	Right Atrium	heart

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