Variant report

Variant	esv3429566
Chromosome Location	chr20:25838143-25848095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:434)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr20:25843689-25844092	HepG2	liver:	n/a	n/a
2	BCL11A	chr20:25846694-25846979	GM12878	blood:	n/a	n/a
3	BCL11A	chr20:25846720-25846953	GM12878	blood:	n/a	n/a
4	BCL11A	chr20:25843000-25843149	GM12878	blood:	n/a	n/a
5	BHLHE40	chr20:25838692-25838875	K562	blood:	n/a	n/a
6	BHLHE40	chr20:25840427-25840668	K562	blood:	n/a	n/a
7	BHLHE40	chr20:25844497-25844502	K562	blood:	n/a	n/a
8	BHLHE40	chr20:25843608-25844126	K562	blood:	n/a	n/a
9	CBX3	chr20:25843839-25844188	K562	blood:	n/a	n/a
10	CCNT2	chr20:25843881-25844128	K562	blood:	n/a	n/a
11	CEBPB	chr20:25846248-25846410	HepG2	liver:	n/a	n/a
12	CEBPB	chr20:25838694-25838720	K562	blood:	n/a	n/a
13	CEBPB	chr20:25843000-25843241	K562	blood:	n/a	n/a
14	CEBPB	chr20:25841958-25842158	K562	blood:	n/a	n/a
15	CEBPB	chr20:25844039-25844135	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr20:25844508-25844516	HepG2	liver:	n/a	n/a
17	CEBPB	chr20:25843063-25843150	K562	blood:	n/a	n/a
18	CEBPB	chr20:25843604-25843807	K562	blood:	n/a	n/a
19	CREB1	chr20:25842055-25842489	A549	lung:	n/a	n/a
20	CTBP2	chr20:25840333-25840793	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr20:25843983-25844066	GM10266	blood:	n/a	n/a
22	CTCF	chr20:25843826-25844192	K562	blood:	n/a	n/a
23	CTCF	chr20:25842292-25842452	A549	lung:	n/a	n/a
24	CTCF	chr20:25843935-25844078	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr20:25843940-25844103	GM12892	blood:	n/a	n/a
26	CTCF	chr20:25843900-25844074	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr20:25842303-25842442	GM10248	blood:	n/a	n/a
28	CTCF	chr20:25843965-25844060	HepG2	liver:	n/a	n/a
29	CTCF	chr20:25842297-25842449	MCF-7	breast:	n/a	n/a
30	CTCF	chr20:25842311-25842461	GM13977	blood:	n/a	n/a
31	CTCF	chr20:25843961-25844070	MCF-7	breast:	n/a	n/a
32	CTCF	chr20:25842281-25842478	GM10266	blood:	n/a	n/a
33	CTCF	chr20:25843953-25844079	MCF-7	breast:	n/a	n/a
34	CTCF	chr20:25843862-25844145	K562	blood:	n/a	n/a
35	CTCF	chr20:25843934-25844117	LNCaP	prostate:	n/a	n/a
36	CTCF	chr20:25842300-25842448	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr20:25842280-25842454	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr20:25842207-25842507	K562	blood:	n/a	n/a
39	CTCF	chr20:25842292-25842446	MCF-7	breast:	n/a	n/a
40	CTCF	chr20:25843740-25844273	K562	blood:	n/a	n/a
41	CTCF	chr20:25842278-25842456	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr20:25843963-25844114	GM10248	blood:	n/a	n/a
43	CTCF	chr20:25842177-25842551	K562	blood:	n/a	n/a
44	CTCF	chr20:25842290-25842469	GM19240	blood:	n/a	n/a
45	CTCF	chr20:25842266-25842494	LNCaP	prostate:	n/a	n/a
46	CTCF	chr20:25842176-25842472	K562	blood:	n/a	n/a
47	CTCF	chr20:25842299-25842462	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr20:25843872-25844162	HepG2	liver:	n/a	n/a
49	CTCF	chr20:25844006-25844022	Fibrobl	skin:	n/a	n/a
50	CTCF	chr20:25842287-25842443	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25846519-25846569	PFSK-1	brain:	n/a
2	chr20:25846519-25846569	AG10803	skin:	n/a
3	chr20:25846519-25846569	IMR90	lung:	fetal
4	chr20:25846519-25846569	GM06990	blood:	n/a
5	chr20:25846519-25846569	HRPEpiC	eye:	n/a
6	chr20:25846519-25846569	CMK	blood:	n/a
7	chr20:25846519-25846569	HL-60	blood:	n/a
8	chr20:25846519-25846569	HUVEC	blood vessel:	n/a
9	chr20:25846519-25846569	H1-hESC	embryonic stem cell:	embryo
10	chr20:25846519-25846569	T-47D	breast:	n/a
11	chr20:25846519-25846569	HNPCEpiC	eye:	n/a
12	chr20:25846519-25846569	AG09319	gingival:	n/a
13	chr20:25846519-25846569	NHDF-neo	bronchial:	n/a
14	chr20:25846519-25846569	A549	lung:	n/a
15	chr20:25846519-25846569	NH-A	brain:	n/a
16	chr20:25846519-25846569	HCF	heart:	n/a
17	chr20:25846519-25846569	PANC-1	pancreas:	n/a
18	chr20:25846519-25846569	NB4	blood:	n/a
19	chr20:25846519-25846569	Jurkat	blood:	n/a
20	chr20:25846519-25846569	HIPEpiC	eye:	n/a
21	chr20:25846519-25846569	HMEC	breast:	n/a
22	chr20:25846519-25846569	ProgFib	skin:	n/a
23	chr20:25846519-25846569	RPTEC	kidney:	n/a
24	chr20:25846519-25846569	HRCEpiC	kidney:	n/a
25	chr20:25846519-25846569	SK-N-SH	brain:	n/a
26	chr20:25846519-25846569	NT2-D1	testis:	n/a
27	chr20:25846519-25846569	BE2_C	brain:	n/a
28	chr20:25846519-25846569	GM19239	blood:	n/a
29	chr20:25846519-25846569	U87	brain:	n/a
30	chr20:25846519-25846569	HEK293	kidney:	embryo
31	chr20:25846519-25846569	SK-N-MC	brain:	n/a
32	chr20:25846519-25846569	AG09309	skin:	n/a
33	chr20:25846519-25846569	AG04450	lung:	fetal
34	chr20:25846519-25846569	BJ	skin:	n/a
35	chr20:25846519-25846569	AoSMC	blood vessel:	n/a
36	chr20:25846519-25846569	ECC-1	luminal epithelium:	n/a
37	chr20:25846519-25846569	MCF10A-Er-Src	breast:	n/a
38	chr20:25846519-25846569	ovcar-3	ovarian:	n/a
39	chr20:25846519-25846569	HCPEpiC	choroid plexus:	n/a
40	chr20:25846519-25846569	SK-N-SH_RA	brain:	n/a
41	chr20:25846519-25846569	Caco-2	colon:	n/a
42	chr20:25846519-25846569	GM12878	blood:	n/a
43	chr20:25846519-25846569	Hela-S3	cervix:	n/a
44	chr20:25846519-25846569	K562	blood:	n/a
45	chr20:25846519-25846569	Hepatocyte	liver:	n/a
46	chr20:25846519-25846569	HPAEpiC	pulmonary alveolar:	n/a
47	chr20:25846519-25846569	NHBE	bronchial:	n/a
48	chr20:25846519-25846569	GM12892	blood:	n/a
49	chr20:25846519-25846569	MCF-7	breast:	n/a
50	chr20:25846519-25846569	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:25604447..25606097-chr20:25837225..25840203,2	MCF-7	breast:

No data

Variant related genes	Relation type
FAM182B	TF binding region
FAM182B	CpG island
ENSG00000170191	chromatin interactions
ENSG00000213742	chromatin interactions

Extended variants
information (count: 941 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111506236	chr20:25838160-25838161	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs529874995	chr20:25838178-25838179	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146354360	chr20:25838192-25838193	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141352774	chr20:25838194-25838195	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200607591	chr20:25838201-25838202	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs546480334	chr20:25838202-25838203	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs566476331	chr20:25838215-25838216	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs201052485	chr20:25838216-25838217	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs147518763	chr20:25838226-25838227	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs139884742	chr20:25838250-25838251	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs375306983	chr20:25838255-25838256	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368198443	chr20:25838257-25838258	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200935328	chr20:25838263-25838264	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs551848749	chr20:25838283-25838284	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs80260539	chr20:25838287-25838288	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs75112672	chr20:25838289-25838290	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs371998599	chr20:25838290-25838291	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201510474	chr20:25838293-25838294	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568855025	chr20:25838295-25838296	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs112947918	chr20:25838302-25838303	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376472358	chr20:25838374-25838375	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs199761443	chr20:25838378-25838379	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537520588	chr20:25838380-25838381	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375359265	chr20:25838382-25838383	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560669159	chr20:25838390-25838391	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368610437	chr20:25838405-25838406	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs372321254	chr20:25838412-25838413	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs533967689	chr20:25838413-25838414	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs374690402	chr20:25838415-25838416	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs192416277	chr20:25838425-25838426	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs368990684	chr20:25838428-25838429	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs533080342	chr20:25838429-25838430	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371502247	chr20:25838436-25838437	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs79382155	chr20:25838447-25838448	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs375278361	chr20:25838448-25838449	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs184367236	chr20:25838454-25838455	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139866061	chr20:25838470-25838471	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs188850760	chr20:25838475-25838476	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs535037983	chr20:25838484-25838485	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200070371	chr20:25838508-25838509	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs74592468	chr20:25838510-25838511	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs6132877	chr20:25838518-25838519	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201666031	chr20:25838527-25838528	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs71185314	chr20:25838563-25838564	Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs536890530	chr20:25838614-25838615	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531269761	chr20:25838619-25838620	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs72490885	chr20:25838623-25838624	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549448540	chr20:25838635-25838636	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs74222706	chr20:25838650-25838651	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs545532284	chr20:25838668-25838669	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25835000-25838600	Weak transcription	Gastric	stomach
2	chr20:25835000-25840200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr20:25835200-25838400	Weak transcription	K562	blood
4	chr20:25835200-25838600	Weak transcription	Liver	Liver
5	chr20:25835200-25838600	Weak transcription	Fetal Heart	heart
6	chr20:25835200-25838600	Weak transcription	Psoas Muscle	Psoas
7	chr20:25835400-25838600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr20:25835400-25838600	Weak transcription	Right Atrium	heart
9	chr20:25835400-25838600	Weak transcription	Right Ventricle	heart
10	chr20:25835600-25838400	Weak transcription	Fetal Brain Male	brain
11	chr20:25835600-25838600	Weak transcription	Left Ventricle	heart
12	chr20:25836600-25838600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr20:25836800-25838600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr20:25837000-25838200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr20:25837200-25838600	Weak transcription	Spleen	Spleen
16	chr20:25837600-25839600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr20:25837800-25838200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr20:25837800-25838400	Enhancers	Brain Anterior Caudate	brain
19	chr20:25837800-25840200	Active TSS	Brain Germinal Matrix	brain
20	chr20:25837800-25840200	Active TSS	Fetal Brain Female	brain
21	chr20:25838000-25838200	Enhancers	Brain Angular Gyrus	brain
22	chr20:25838000-25838600	Weak transcription	Brain Hippocampus Middle	brain
23	chr20:25838200-25838400	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr20:25838200-25838600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr20:25838200-25838600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
26	chr20:25838200-25839200	Active TSS	Brain Cingulate Gyrus	brain
27	chr20:25838200-25839200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr20:25838200-25839800	Active TSS	Brain Angular Gyrus	brain
29	chr20:25838400-25838600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr20:25838400-25838600	Active TSS	Brain Anterior Caudate	brain
31	chr20:25838400-25838600	Enhancers	Esophagus	oesophagus
32	chr20:25838400-25838600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
33	chr20:25838400-25838600	Enhancers	K562	blood
34	chr20:25838400-25839000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
35	chr20:25838400-25839000	Enhancers	Fetal Brain Male	brain
36	chr20:25838400-25839000	Bivalent Enhancer	Placenta	Placenta
37	chr20:25838400-25839000	Bivalent/Poised TSS	NHEK	skin
38	chr20:25838400-25839200	Active TSS	Brain Substantia Nigra	brain
39	chr20:25838400-25839600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
40	chr20:25838400-25840400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
41	chr20:25838400-25842000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
42	chr20:25838400-25842200	ZNF genes & repeats	Dnd41	blood
43	chr20:25838600-25838800	Flanking Bivalent TSS/Enh	ES-WA7 Cell Line	embryonic stem cell
44	chr20:25838600-25838800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr20:25838600-25838800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr20:25838600-25838800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr20:25838600-25838800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr20:25838600-25838800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr20:25838600-25838800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr20:25838600-25838800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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