Variant report

Variant	nsv1063474
Chromosome Location	chr20:23918394-24048069
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	ARID3A	chr20:23976814-23977193	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:24015537-24015818	HepG2	liver:	n/a	n/a
3	BATF	chr20:23965266-23965679	GM12878	blood:	n/a	n/a
4	BCL11A	chr20:23957003-23957211	GM12878	blood:	n/a	n/a
5	BCL11A	chr20:23959204-23959390	GM12878	blood:	n/a	chr20:23959323-23959332
6	BCL11A	chr20:23965421-23965603	GM12878	blood:	n/a	n/a
7	BCL11A	chr20:23970694-23970943	GM12878	blood:	n/a	n/a
8	BCL11A	chr20:23959584-23959850	GM12878	blood:	n/a	n/a
9	BCL11A	chr20:23965025-23965194	GM12878	blood:	n/a	n/a
10	BCL3	chr20:24015336-24015896	A549	lung:	n/a	n/a
11	BCL3	chr20:23960441-23961293	GM12878	blood:	n/a	chr20:23960654-23960662
12	BCL3	chr20:23983424-23984018	GM12878	blood:	n/a	n/a
13	BCL3	chr20:23960521-23961246	GM12878	blood:	n/a	chr20:23960654-23960662
14	BCL3	chr20:23994598-23994921	GM12878	blood:	n/a	n/a
15	BCL3	chr20:24015286-24015904	A549	lung:	n/a	n/a
16	BCL3	chr20:23983385-23983983	GM12878	blood:	n/a	n/a
17	BCL3	chr20:23980731-23981055	GM12878	blood:	n/a	n/a
18	BCL3	chr20:23994585-23994901	GM12878	blood:	n/a	n/a
19	BHLHE40	chr20:23976881-23977143	GM12878	blood:	n/a	n/a
20	BHLHE40	chr20:24007996-24008127	GM12878	blood:	n/a	n/a
21	CEBPB	chr20:23934284-23934571	A549	lung:	n/a	chr20:23934424-23934435
22	CEBPB	chr20:24039276-24039572	A549	lung:	n/a	chr20:24039429-24039440
23	CEBPB	chr20:24039321-24039570	HepG2	liver:	n/a	chr20:24039429-24039440
24	CEBPB	chr20:23961774-23962025	HepG2	liver:	n/a	n/a
25	CEBPB	chr20:23932569-23932853	A549	lung:	n/a	chr20:23932702-23932715 chr20:23932702-23932715 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932702-23932713 chr20:23932704-23932713 chr20:23932704-23932715
26	CEBPB	chr20:24015397-24015929	MCF-7	breast:	n/a	n/a
27	CEBPB	chr20:23987376-23987576	A549	lung:	n/a	n/a
28	CEBPB	chr20:24015279-24015918	MCF-7	breast:	n/a	n/a
29	CEBPB	chr20:24015525-24015800	HepG2	liver:	n/a	n/a
30	CEBPB	chr20:23997872-23998129	K562	blood:	n/a	chr20:23997983-23997994
31	CEBPB	chr20:24015278-24015926	A549	lung:	n/a	n/a
32	CEBPB	chr20:23997825-23998162	HepG2	liver:	n/a	chr20:23997983-23997994
33	CEBPB	chr20:23961806-23961982	HepG2	liver:	n/a	n/a
34	CEBPB	chr20:23997851-23998167	A549	lung:	n/a	chr20:23997983-23997994
35	CEBPB	chr20:23997821-23998156	IMR90	lung:	n/a	chr20:23997983-23997994
36	CEBPB	chr20:23991495-23991592	HepG2	liver:	n/a	chr20:23991528-23991539
37	CEBPB	chr20:23934298-23934572	HepG2	liver:	n/a	chr20:23934424-23934435
38	CEBPB	chr20:24015398-24015868	HepG2	liver:	n/a	n/a
39	CEBPB	chr20:23932580-23932833	IMR90	lung:	n/a	chr20:23932702-23932715 chr20:23932702-23932715 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932702-23932713 chr20:23932704-23932713 chr20:23932704-23932715
40	CEBPB	chr20:24015433-24015887	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:24015430-24015834	A549	lung:	n/a	n/a
42	CEBPB	chr20:23932543-23932848	HepG2	liver:	n/a	chr20:23932702-23932715 chr20:23932702-23932715 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932702-23932713 chr20:23932704-23932713 chr20:23932704-23932715
43	CHD2	chr20:24032306-24032522	K562	blood:	n/a	n/a
44	CHD2	chr20:24015722-24015770	HepG2	liver:	n/a	n/a
45	CTCF	chr20:23976900-23977050	HCT-116	colon:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
46	CTCF	chr20:23976903-23977079	Fibrobl	skin:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
47	CTCF	chr20:23976920-23977070	GM12872	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
48	CTCF	chr20:23959308-23959504	Gliobla	brain:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959490-23959498 chr20:23959384-23959402 chr20:23959386-23959407
49	CTCF	chr20:23965180-23965330	Hela-S3	cervix:	n/a	chr20:23965234-23965243
50	CTCF	chr20:23965360-23965510	AG10803	skin:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23969432-23969482	T-47D	breast:	n/a
2	chr20:23965841-23965891	HNPCEpiC	eye:	n/a
3	chr20:23965921-23965971	HCM	heart:	n/a
4	chr20:23969397-23969447	SK-N-SH_RA	brain:	n/a
5	chr20:23972451-23972501	HMEC	breast:	n/a
6	chr20:23969432-23969482	HRCEpiC	kidney:	n/a
7	chr20:23969237-23969287	HEEpiC	esophagus:	n/a
8	chr20:23965841-23965891	HepG2	liver:	n/a
9	chr20:23969397-23969447	GM19239	blood:	n/a
10	chr20:23970162-23970212	BE2_C	brain:	n/a
11	chr20:23969429-23969479	ovcar-3	ovarian:	n/a
12	chr20:23969237-23969287	HAEpiC	amniotic membrane:	n/a
13	chr20:23969429-23969479	MCF10A-Er-Src	breast:	n/a
14	chr20:23969237-23969287	HCT-116	colon:	n/a
15	chr20:23970065-23970115	HCT-116	colon:	n/a
16	chr20:23968830-23968880	HCM	heart:	n/a
17	chr20:23969397-23969447	HEK293	kidney:	embryo
18	chr20:23965921-23965971	Caco-2	colon:	n/a
19	chr20:23965841-23965891	RPTEC	kidney:	n/a
20	chr20:23968830-23968880	Caco-2	colon:	n/a
21	chr20:23969832-23969882	T-47D	breast:	n/a
22	chr20:23969832-23969882	NHDF-neo	bronchial:	n/a
23	chr20:23969832-23969882	AoSMC	blood vessel:	n/a
24	chr20:23968830-23968880	GM12892	blood:	n/a
25	chr20:23970065-23970115	GM12878	blood:	n/a
26	chr20:23965841-23965891	AoSMC	blood vessel:	n/a
27	chr20:23969429-23969479	AG04449	skin:	fetal
28	chr20:23969432-23969482	AG04450	lung:	fetal
29	chr20:23969432-23969482	GM12891	blood:	n/a
30	chr20:23968830-23968880	AG09309	skin:	n/a
31	chr20:23969432-23969482	CMK	blood:	n/a
32	chr20:23970065-23970115	ovcar-3	ovarian:	n/a
33	chr20:23972451-23972501	HCPEpiC	choroid plexus:	n/a
34	chr20:23969397-23969447	MCF-7	breast:	n/a
35	chr20:23972451-23972501	AG09309	skin:	n/a
36	chr20:23969237-23969287	ECC-1	luminal epithelium:	n/a
37	chr20:23969397-23969447	U87	brain:	n/a
38	chr20:23972451-23972501	CMK	blood:	n/a
39	chr20:23969832-23969882	AG09309	skin:	n/a
40	chr20:23965841-23965891	MCF10A-Er-Src	breast:	n/a
41	chr20:23969429-23969479	Jurkat	blood:	n/a
42	chr20:23969397-23969447	AG09309	skin:	n/a
43	chr20:23970065-23970115	HNPCEpiC	eye:	n/a
44	chr20:23970162-23970212	SK-N-SH_RA	brain:	n/a
45	chr20:23965921-23965971	AG09309	skin:	n/a
46	chr20:23969397-23969447	HCF	heart:	n/a
47	chr20:23969832-23969882	MCF-7	breast:	n/a
48	chr20:23969429-23969479	SK-N-SH_RA	brain:	n/a
49	chr20:23969429-23969479	GM19239	blood:	n/a
50	chr20:23969429-23969479	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:24001543..24003276-chr20:24005050..24007327,2	MCF-7	breast:
2	chr20:23917806..23918382-chr20:23976746..23977457,2	MCF-7	breast:
3	chr20:24009988..24011988-chr20:24013949..24015486,2	MCF-7	breast:
4	chr20:19198505..19201167-chr20:24035131..24037603,2	MCF-7	breast:
5	chr20:23918328..23919972-chr20:23977586..23980315,2	MCF-7	breast:
6	chr20:23996001..23998841-chr20:24002099..24004850,2	MCF-7	breast:
7	chr20:23870254..23870831-chr20:23976722..23977413,2	MCF-7	breast:
8	chr20:23976507..23978682-chr20:23981230..23983499,2	K562	blood:
9	chr20:23917673..23918874-chr20:23976593..23977514,3	K562	blood:
10	chr20:23979873..23982563-chr20:23986456..23988446,2	MCF-7	breast:
11	chr20:23917874..23918575-chr20:24189095..24189921,2	MCF-7	breast:
12	chr20:23917673..23918874-chr20:23976593..23977514,3	K562	blood:
13	chr20:23993668..23995397-chr20:24015280..24016908,2	MCF-7	breast:
14	chr20:23979873..23982563-chr20:23986456..23988446,2	MCF-7	breast:
15	chr20:23945696..23947620-chr20:23948885..23951214,2	MCF-7	breast:
16	chr20:24015674..24019401-chr20:24025175..24027148,3	MCF-7	breast:
17	chr20:24001543..24003276-chr20:24005050..24007327,2	MCF-7	breast:
18	chr20:23945696..23947620-chr20:23948885..23951214,2	MCF-7	breast:
19	chr20:23870329..23871235-chr20:23976503..23977926,6	MCF-7	breast:
20	chr20:23993668..23995397-chr20:24015280..24016908,2	MCF-7	breast:
21	chr20:24021039..24022886-chr20:24031345..24033382,2	MCF-7	breast:
22	chr20:23918328..23919972-chr20:23977586..23980315,2	MCF-7	breast:
23	chr20:23976507..23978682-chr20:23981230..23983499,2	K562	blood:
24	chr20:23996001..23998841-chr20:24002099..24004850,2	MCF-7	breast:
25	chr20:23918077..23918602-chr20:24144722..24145283,2	MCF-7	breast:
26	chr20:24015674..24019401-chr20:24025175..24027148,3	MCF-7	breast:
27	chr20:24021039..24022886-chr20:24031345..24033382,2	MCF-7	breast:
28	chr20:24009988..24011988-chr20:24013949..24015486,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGTLC1-6	chr20:23982712-23982840	NONHSAT079094
2	lnc-SYNDIG1-4	chr20:24006344-24006652	XLOC_013495
3	lnc-SYNDIG1-3	chr20:24045119-24045145	FPKM1_group_18996_transcript_1
4	lnc-GGTLC1-1	chr20:23979070-23979425	XLOC_013696
5	lnc-SYNDIG1-4	chr20:24003973-24004010	XLOC_013495
6	lnc-SYNDIG1-3	chr20:24046360-24047430	XLOC_013496
7	lnc-GGTLC1-6	chr20:23983714-23983891	NONHSAT079094
8	lnc-GGTLC1-1	chr20:23980262-23980270	XLOC_013696
9	lnc-GGTLC1-7	chr20:24040361-24040525	l_2094_chr20:24022958-24040525_kidney
10	lnc-SYNDIG1-3	chr20:24045119-24045145	NONHSAT079097
11	lnc-SYNDIG1-4	chr20:24010292-24011949	XLOC_013495
12	lnc-SYNDIG1-3	chr20:24045243-24046314	FPKM1_group_18996_transcript_1
13	lnc-SYNDIG1-3	chr20:24045120-24045145	XLOC_013496
14	lnc-GGTLC1-7	chr20:24022959-24023650	l_2094_chr20:24022958-24040525_kidney
15	lnc-SYNDIG1-3	chr20:24046359-24047430	NONHSAT079097

Variant related genes	Relation type
ENSG00000236168	TF binding region
GGTLC1	TF binding region
POM121L3P	TF binding region
ENSG00000236168	CpG island
GGTLC1	CpG island
POM121L3P	CpG island
BACH2	miRNA target sites
SNCA	miRNA target sites
BAG2	miRNA target sites

Extended variants
information (count: 4554 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4554 , 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	rs568192255	chr20:23918396-23918397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73322843	chr20:23918429-23918430	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150910144	chr20:23918449-23918450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2258909	chr20:23918454-23918455	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs539412528	chr20:23918465-23918466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556922671	chr20:23918490-23918491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139385468	chr20:23918498-23918499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113793358	chr20:23918574-23918575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144064146	chr20:23919400-23919401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533058655	chr20:23919403-23919404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532714588	chr20:23919413-23919414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73610769	chr20:23919414-23919415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76655726	chr20:23919419-23919420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146443869	chr20:23919420-23919421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141033496	chr20:23919451-23919452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35057606	chr20:23919473-23919474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566342866	chr20:23919491-23919492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111963281	chr20:23919497-23919498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73322847	chr20:23919505-23919506	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs561789429	chr20:23919539-23919540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530837864	chr20:23919545-23919546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574641114	chr20:23919585-23919586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543056060	chr20:23919629-23919630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567118202	chr20:23919662-23919663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573972488	chr20:23919753-23919754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542985577	chr20:23919776-23919777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537859916	chr20:23919799-23919800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555407038	chr20:23919829-23919830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs58688400	chr20:23919848-23919849	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs561222229	chr20:23919851-23919852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564278253	chr20:23919901-23919902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533120504	chr20:23919946-23919947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115982442	chr20:23919993-23919994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181456520	chr20:23934236-23934237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs74399090	chr20:23934239-23934240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547200521	chr20:23934242-23934243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561952657	chr20:23934244-23934245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567026943	chr20:23934276-23934277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115336935	chr20:23934291-23934292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2983542	chr20:23934297-23934298	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs544713907	chr20:23934355-23934356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568872228	chr20:23934362-23934363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537888039	chr20:23934379-23934380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568154974	chr20:23934430-23934431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78523930	chr20:23934479-23934480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189422392	chr20:23934483-23934484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142684510	chr20:23934574-23934575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577027683	chr20:23934597-23934598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180982314	chr20:23934651-23934652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62193649	chr20:23934659-23934660	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23917800-23918600	Enhancers	Primary T cells fromperipheralblood	blood
2	chr20:23918200-23918600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr20:23918200-23918600	Enhancers	Dnd41	blood
4	chr20:23919400-23919800	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr20:23919600-23920000	Enhancers	Right Atrium	heart
6	chr20:23919800-23920000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr20:23934200-23934600	Enhancers	Fetal Lung	lung
8	chr20:23934600-23934800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr20:23934600-23935000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr20:23934800-23935600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr20:23935000-23935400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr20:23935400-23935800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr20:23935400-23936600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr20:23935400-23937600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr20:23935600-23935800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr20:23935600-23937600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr20:23935800-23936600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr20:23935800-23936800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr20:23936400-23937400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr20:23936600-23936800	Enhancers	Brain Angular Gyrus	brain
21	chr20:23936600-23937000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr20:23936600-23937000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr20:23936600-23937000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr20:23936600-23937000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr20:23936600-23937000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr20:23936600-23937200	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr20:23936600-23937400	Enhancers	Primary hematopoietic stem cells	blood
28	chr20:23936600-23938000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr20:23936600-23938800	Enhancers	Brain Substantia Nigra	brain
30	chr20:23936600-23939200	Enhancers	Brain Cingulate Gyrus	brain
31	chr20:23936600-23940400	Enhancers	Brain Hippocampus Middle	brain
32	chr20:23936800-23937400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr20:23936800-23937600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr20:23937000-23937600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr20:23937200-23937600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr20:23937600-23939000	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr20:23938000-23938400	Enhancers	Brain Anterior Caudate	brain
38	chr20:23938800-23939800	Weak transcription	Brain Substantia Nigra	brain
39	chr20:23939000-23939600	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr20:23939200-23939600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr20:23939200-23940800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr20:23939600-23939800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr20:23939600-23940400	Enhancers	Brain Cingulate Gyrus	brain
44	chr20:23939800-23940000	Enhancers	Brain Substantia Nigra	brain
45	chr20:23940600-23940800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr20:23946200-23948600	Enhancers	Left Ventricle	heart
47	chr20:23947000-23948200	Enhancers	Placenta	Placenta
48	chr20:23947200-23948600	Enhancers	Right Atrium	heart
49	chr20:23947600-23947800	Enhancers	Spleen	Spleen
50	chr20:23947600-23948000	Enhancers	Right Ventricle	heart

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