Variant report

Variant	esv14698
Chromosome Location	chr20:25989773-26056362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:504)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr20:25990276-25990617	GM12878	blood:	n/a	n/a
2	BATF	chr20:25991390-25991666	GM12878	blood:	n/a	n/a
3	BCL11A	chr20:26041793-26041988	GM12878	blood:	n/a	n/a
4	BCL11A	chr20:25990610-25990918	GM12878	blood:	n/a	n/a
5	BCL11A	chr20:26010805-26011025	GM12878	blood:	n/a	n/a
6	BRCA1	chr20:25990208-25990605	Hela-S3	cervix:	n/a	chr20:25990394-25990403
7	BRCA1	chr20:25990237-25990584	HepG2	liver:	n/a	chr20:25990394-25990403
8	BRCA1	chr20:25990247-25990579	GM12878	blood:	n/a	chr20:25990394-25990403
9	CEBPB	chr20:25990281-25990629	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr20:26041786-26041946	K562	blood:	n/a	n/a
11	CEBPD	chr20:25990293-25990725	HepG2	liver:	n/a	n/a
12	CHD1	chr20:25990580-25990581	GM12878	blood:	n/a	n/a
13	CHD2	chr20:25990204-25990773	Hela-S3	cervix:	n/a	chr20:25990394-25990403
14	CHD2	chr20:25990200-25990660	HepG2	liver:	n/a	chr20:25990394-25990403
15	CHD2	chr20:25990214-25990586	K562	blood:	n/a	chr20:25990394-25990403
16	CHD2	chr20:25990208-25990784	GM12878	blood:	n/a	chr20:25990394-25990403
17	CTCF	chr20:26022832-26022906	Medullo	brain:	n/a	n/a
18	CTCF	chr20:26014290-26014299	GM13977	blood:	n/a	n/a
19	CTCF	chr20:26022760-26022911	K562	blood:	n/a	n/a
20	CTCF	chr20:26022744-26022916	MCF-7	breast:	n/a	n/a
21	CTCF	chr20:26014302-26014317	GM13977	blood:	n/a	n/a
22	CTCF	chr20:26054740-26054890	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr20:25990600-25990750	GM12867	blood:	n/a	n/a
24	CTCF	chr20:26040159-26040181	K562	blood:	n/a	n/a
25	CTCF	chr20:26022795-26022875	ProgFib	skin:	n/a	n/a
26	CTCF	chr20:26022800-26022867	Fibrobl	skin:	n/a	n/a
27	CTCF	chr20:26022742-26022934	MCF-7	breast:	n/a	n/a
28	CTCF	chr20:26022795-26022916	LNCaP	prostate:	n/a	n/a
29	CTCF	chr20:26022775-26022911	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr20:26022765-26022887	HepG2	liver:	n/a	n/a
31	CTCF	chr20:26022756-26022904	MCF-7	breast:	n/a	n/a
32	CTCF	chr20:26045593-26045679	LNCaP	prostate:	n/a	chr20:26045642-26045650
33	CTCF	chr20:26022771-26022938	LNCaP	prostate:	n/a	n/a
34	CTCF	chr20:26022754-26022923	MCF-7	breast:	n/a	n/a
35	CTCF	chr20:25991586-25991706	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr20:26045218-26045235	LNCaP	prostate:	n/a	n/a
37	CTCF	chr20:26042994-26043053	GM10248	blood:	n/a	chr20:26043006-26043019
38	CTCF	chr20:26006053-26006100	GM10248	blood:	n/a	n/a
39	CTCF	chr20:26022781-26022894	A549	lung:	n/a	n/a
40	CTCF	chr20:25993777-25993844	GM13976	blood:	n/a	n/a
41	CTCF	chr20:26045269-26045273	LNCaP	prostate:	n/a	n/a
42	CTCF	chr20:26022764-26022924	MCF-7	breast:	n/a	n/a
43	CTCF	chr20:25990360-25990510	HepG2	liver:	n/a	n/a
44	CTCF	chr20:26005438-26005533	GM10248	blood:	n/a	n/a
45	CTCF	chr20:26054800-26054950	Caco-2	colon:	n/a	n/a
46	CTCF	chr20:26036162-26036246	LNCaP	prostate:	n/a	n/a
47	CTCF	chr20:26022791-26022793	ProgFib	skin:	n/a	n/a
48	CTCF	chr20:26048294-26048345	GM13976	blood:	n/a	n/a
49	CTCF	chr20:26039870-26040409	K562	blood:	n/a	n/a
50	CTCF	chr20:25999107-25999194	GM20000	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25989775-25989825	AoSMC	blood vessel:	n/a
2	chr20:25991114-25991164	SK-N-MC	brain:	n/a
3	chr20:25990680-25990730	NHDF-neo	bronchial:	n/a
4	chr20:25989775-25989825	NH-A	brain:	n/a
5	chr20:25990680-25990730	Jurkat	blood:	n/a
6	chr20:25991114-25991164	PrEC	prostate:	n/a
7	chr20:25991114-25991164	HIPEpiC	eye:	n/a
8	chr20:25990680-25990730	AG04450	lung:	fetal
9	chr20:25989775-25989825	GM12891	blood:	n/a
10	chr20:25991114-25991164	HCM	heart:	n/a
11	chr20:25989775-25989825	U87	brain:	n/a
12	chr20:25990680-25990730	U87	brain:	n/a
13	chr20:25990680-25990730	LNCaP	prostate:	n/a
14	chr20:25989775-25989825	HRCEpiC	kidney:	n/a
15	chr20:25989775-25989825	GM19239	blood:	n/a
16	chr20:25991114-25991164	HRCEpiC	kidney:	n/a
17	chr20:25990680-25990730	PrEC	prostate:	n/a
18	chr20:25989775-25989825	AG04450	lung:	fetal
19	chr20:25990680-25990730	ovcar-3	ovarian:	n/a
20	chr20:25989775-25989825	NT2-D1	testis:	n/a
21	chr20:25989775-25989825	HMEC	breast:	n/a
22	chr20:25989775-25989825	HepG2	liver:	n/a
23	chr20:25990680-25990730	HepG2	liver:	n/a
24	chr20:25991114-25991164	AG09319	gingival:	n/a
25	chr20:25991114-25991164	K562	blood:	n/a
26	chr20:25990680-25990730	HRCEpiC	kidney:	n/a
27	chr20:25990680-25990730	AG09319	gingival:	n/a
28	chr20:25991114-25991164	SAEC	small airway:	n/a
29	chr20:25990680-25990730	HUVEC	blood vessel:	n/a
30	chr20:25989775-25989825	SK-N-SH_RA	brain:	n/a
31	chr20:25989775-25989825	HRE	kidney:	n/a
32	chr20:25989775-25989825	ovcar-3	ovarian:	n/a
33	chr20:25989775-25989825	AG09309	skin:	n/a
34	chr20:25989775-25989825	HCM	heart:	n/a
35	chr20:25990680-25990730	SK-N-SH	brain:	n/a
36	chr20:25991114-25991164	SKMC	muscle:	n/a
37	chr20:25989775-25989825	BJ	skin:	n/a
38	chr20:25991114-25991164	GM06990	blood:	n/a
39	chr20:25989775-25989825	IMR90	lung:	fetal
40	chr20:25990680-25990730	Caco-2	colon:	n/a
41	chr20:25991114-25991164	Hela-S3	cervix:	n/a
42	chr20:25990680-25990730	HL-60	blood:	n/a
43	chr20:25989775-25989825	Hepatocyte	liver:	n/a
44	chr20:25989775-25989825	GM06990	blood:	n/a
45	chr20:25991114-25991164	NHBE	bronchial:	n/a
46	chr20:25990680-25990730	Hela-S3	cervix:	n/a
47	chr20:25990680-25990730	BJ	skin:	n/a
48	chr20:25989775-25989825	HRPEpiC	eye:	n/a
49	chr20:25990680-25990730	HEK293	kidney:	embryo
50	chr20:25991114-25991164	U87	brain:	n/a

No data

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182A-4	chr20:26049553-26049840	ENSG00000125804.9
2	lnc-FAM182A-4	chr20:26049573-26049840	ENSG00000125804.9
3	lnc-FAM182A-6	chr20:26011530-26013121	ucscGeneNc_uc010gdq_1
4	lnc-FAM182A-4	chr20:26054406-26054448	ENSG00000125804.9
5	lnc-FAM182A-6	chr20:26002406-26002505	ucscGeneNc_uc010gdq_1
6	lnc-FAM182A-4	chr20:26049553-26049796	ENSG00000125804.9
7	lnc-FAM182A-4	chr20:26040299-26040496	ENSG00000125804.9
8	lnc-FAM182A-4	chr20:26049724-26049840	ENSG00000125804.9
9	lnc-FAM182A-6	chr20:26009800-26010026	ucscGeneNc_uc010gdq_1
10	lnc-FAM182A-4	chr20:26054406-26054495	ENSG00000125804.9
11	lnc-FAM182A-4	chr20:26047198-26047273	ENSG00000125804.9
12	lnc-FAM182B-3	chr20:25990891-25991167	XLOC_013712
13	lnc-FAM182A-4	chr20:26046283-26046420	ENSG00000125804.9
14	lnc-FAM182A-6	chr20:26000465-26000560	NONHSAT147161
15	lnc-FAM182A-4	chr20:26047620-26047810	ENSG00000125804.9
16	lnc-FAM182A-6	chr20:25999468-25999548	NONHSAT147161
17	lnc-FAM182A-6	chr20:25990334-25991091	NONHSAT079206
18	lnc-FAM182A-4	chr20:26049675-26049840	ENSG00000125804.9
19	lnc-FAM182A-6	chr20:26001272-26001320	NONHSAT147161
20	lnc-FAM182A-4	chr20:26038034-26038238	ENSG00000125804.9
21	lnc-FAM182A-6	chr20:25999712-25999838	NONHSAT147161
22	lnc-FAM182A-6	chr20:25997553-25997840	ucscGeneNc_uc010gdq_1
23	lnc-FAM182A-4	chr20:26054406-26054505	ENSG00000125804.9

No data

Variant related genes	Relation type
ENSG00000231081	TF binding region
ENSG00000204556	TF binding region
FAM182A	TF binding region
ENSG00000231081	CpG island
ENSG00000204556	CpG island
FAM182A	CpG island
MUC17	miRNA target sites

Extended variants
information (count: 158 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:158 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139726857	chr20:25989789-25989790	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527444506	chr20:25989875-25989876	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530356445	chr20:25989876-25989877	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6084041	chr20:25989898-25989899	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78217349	chr20:25989942-25989943	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547262097	chr20:25989975-25989976	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112172757	chr20:25989994-25989995	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6051087	chr20:25990002-25990003	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs552725751	chr20:25990009-25990010	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569335923	chr20:25990027-25990028	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184920846	chr20:25990063-25990064	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201206145	chr20:25990088-25990089	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114795197	chr20:25990123-25990124	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554829549	chr20:25990228-25990229	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112887778	chr20:25990230-25990231	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533884986	chr20:25990241-25990242	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553996296	chr20:25990259-25990260	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576769064	chr20:25990269-25990270	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189459021	chr20:25990307-25990308	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192772436	chr20:25990346-25990347	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs575767480	chr20:25990356-25990357	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs8182807	chr20:25990385-25990386	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs541502794	chr20:25990386-25990387	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs369709644	chr20:25990397-25990398	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs561194462	chr20:25990463-25990464	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
26	rs372649755	chr20:25990474-25990475	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
27	rs74175409	chr20:25990501-25990502	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
28	rs540571699	chr20:25990506-25990507	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
29	rs560810151	chr20:25990523-25990524	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
30	rs535339722	chr20:25990546-25990547	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
31	rs531818622	chr20:25990581-25990582	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
32	rs532414868	chr20:25990634-25990635	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
33	rs200218002	chr20:25990717-25990718	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
34	rs552635737	chr20:25990752-25990753	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
35	rs550183177	chr20:25990759-25990760	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
36	rs562845744	chr20:25990813-25990814	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
37	rs571548124	chr20:25990817-25990818	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
38	rs6138778	chr20:25990819-25990820	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs568172915	chr20:25990826-25990827	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
40	rs533944330	chr20:25990841-25990842	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
41	rs547400834	chr20:25990843-25990844	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
42	rs570691890	chr20:25990908-25990909	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
43	rs117378874	chr20:25990927-25990928	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
44	rs370583219	chr20:25990936-25990937	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
45	rs6115479	chr20:25990957-25990958	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
46	rs115354885	chr20:25990971-25990972	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
47	rs535184143	chr20:25990978-25990979	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
48	rs6115480	chr20:25990995-25990996	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
49	rs6115481	chr20:25991008-25991009	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
50	rs6115482	chr20:25991080-25991081	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:47)

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
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25988800-25990200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr20:25989200-25990200	Enhancers	Placenta	Placenta
3	chr20:25989600-25990400	Active TSS	HepG2	liver
4	chr20:25989600-25991600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr20:25989800-25990000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr20:25989800-25990000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr20:25989800-25990000	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr20:25989800-25990000	Enhancers	Fetal Brain Female	brain
9	chr20:25989800-25990000	Enhancers	Fetal Lung	lung
10	chr20:25989800-25990000	Enhancers	Hela-S3	cervix
11	chr20:25989800-25990200	Enhancers	NHDF-Ad	bronchial
12	chr20:25989800-25990400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr20:25989800-25990400	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr20:25989800-25990400	Enhancers	Spleen	Spleen
15	chr20:25989800-25990600	Active TSS	Skeletal Muscle Female	skeletal muscle
16	chr20:25989800-25991600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr20:25989800-25991600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr20:25989800-25991600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr20:25989800-25991600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr20:25989800-25991600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr20:25989800-25991600	Active TSS	Brain Cingulate Gyrus	brain
22	chr20:25989800-25991600	Active TSS	A549	lung
23	chr20:25990000-25990200	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr20:25990000-25990600	Active TSS	Fetal Lung	lung
25	chr20:25990000-25990600	Active TSS	Skeletal Muscle Male	skeletal muscle
26	chr20:25990000-25990800	Active TSS	Adipose Nuclei	Adipose
27	chr20:25990000-25990800	Active TSS	Fetal Thymus	thymus
28	chr20:25990000-25991000	Active TSS	Fetal Muscle Leg	muscle
29	chr20:25990000-25991000	Active TSS	Fetal Stomach	stomach
30	chr20:25990000-25991000	Active TSS	Rectal Smooth Muscle	rectum
31	chr20:25990000-25991400	Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr20:25990000-25991400	Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr20:25990000-25991400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr20:25990000-25991400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr20:25990000-25991400	Active TSS	Duodenum Smooth Muscle	Duodenum
36	chr20:25990000-25991400	Active TSS	Fetal Brain Female	brain
37	chr20:25990000-25991400	Active TSS	Fetal Kidney	kidney
38	chr20:25990000-25991400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr20:25990000-25991400	Active TSS	Psoas Muscle	Psoas
40	chr20:25990000-25991400	Active TSS	Right Atrium	heart
41	chr20:25990000-25991600	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr20:25990000-25991600	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr20:25990000-25991600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr20:25990000-25991600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr20:25990000-25991600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr20:25990000-25991600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr20:25990000-25991600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr20:25990000-25991600	Active TSS	Muscle Satellite Cultured Cells	--
49	chr20:25990000-25991600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr20:25990000-25991600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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