Variant report

Variant	esv3518425
Chromosome Location	chr20:25911125-26051144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:692)
CpG islands
(count:427)
Chromatin interactive
region (count:0)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:692 , 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	ARID3A	chr20:25989422-25989527	HepG2	liver:	n/a	n/a
2	ATF2	chr20:25990276-25990617	GM12878	blood:	n/a	n/a
3	BATF	chr20:25991390-25991666	GM12878	blood:	n/a	n/a
4	BATF	chr20:25914607-25914931	GM12878	blood:	n/a	n/a
5	BATF	chr20:25914679-25914959	GM12878	blood:	n/a	n/a
6	BATF	chr20:25975707-25975907	GM12878	blood:	n/a	n/a
7	BCL11A	chr20:26041793-26041988	GM12878	blood:	n/a	n/a
8	BCL11A	chr20:25990610-25990918	GM12878	blood:	n/a	n/a
9	BCL11A	chr20:26010805-26011025	GM12878	blood:	n/a	n/a
10	BCL3	chr20:25945773-25946163	GM12878	blood:	n/a	n/a
11	BHLHE40	chr20:25975821-25976057	GM12878	blood:	n/a	n/a
12	BHLHE40	chr20:25975281-25975466	GM12878	blood:	n/a	n/a
13	BHLHE40	chr20:25968676-25968796	K562	blood:	n/a	chr20:25968678-25968699 chr20:25968682-25968695
14	BRCA1	chr20:25990208-25990605	Hela-S3	cervix:	n/a	chr20:25990394-25990403
15	BRCA1	chr20:25990237-25990584	HepG2	liver:	n/a	chr20:25990394-25990403
16	BRCA1	chr20:25990247-25990579	GM12878	blood:	n/a	chr20:25990394-25990403
17	CEBPB	chr20:25989351-25989594	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
18	CEBPB	chr20:25989347-25989484	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
19	CEBPB	chr20:25988753-25989639	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
20	CEBPB	chr20:25988884-25989639	Hela-S3	cervix:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
21	CEBPB	chr20:25942378-25942614	HepG2	liver:	n/a	chr20:25942454-25942467 chr20:25942454-25942465
22	CEBPB	chr20:26041786-26041946	K562	blood:	n/a	n/a
23	CEBPB	chr20:25989272-25989628	IMR90	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
24	CEBPB	chr20:25990281-25990629	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr20:25942443-25942488	A549	lung:	n/a	chr20:25942454-25942467 chr20:25942454-25942465
26	CEBPB	chr20:25989230-25989660	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
27	CEBPB	chr20:25989323-25989598	H1-hESC	embryonic stem cell:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
28	CEBPB	chr20:25988927-25989639	A549	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
29	CEBPB	chr20:25989264-25989635	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
30	CEBPB	chr20:25989327-25989510	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
31	CEBPB	chr20:25976255-25976322	HepG2	liver:	n/a	chr20:25976304-25976315
32	CEBPB	chr20:25933076-25933229	HepG2	liver:	n/a	chr20:25933144-25933155
33	CEBPD	chr20:25990293-25990725	HepG2	liver:	n/a	n/a
34	CHD1	chr20:25990580-25990581	GM12878	blood:	n/a	n/a
35	CHD2	chr20:25990208-25990784	GM12878	blood:	n/a	chr20:25990394-25990403
36	CHD2	chr20:25967886-25967927	GM12878	blood:	n/a	n/a
37	CHD2	chr20:25990200-25990660	HepG2	liver:	n/a	chr20:25990394-25990403
38	CHD2	chr20:25990204-25990773	Hela-S3	cervix:	n/a	chr20:25990394-25990403
39	CHD2	chr20:25990214-25990586	K562	blood:	n/a	chr20:25990394-25990403
40	CTCF	chr20:26022800-26022867	Fibrobl	skin:	n/a	n/a
41	CTCF	chr20:25956562-25956683	HepG2	liver:	n/a	n/a
42	CTCF	chr20:25956611-25956681	GM12878	blood:	n/a	n/a
43	CTCF	chr20:25968099-25968222	K562	blood:	n/a	n/a
44	CTCF	chr20:25958301-25958370	GM10266	blood:	n/a	n/a
45	CTCF	chr20:26022765-26022887	HepG2	liver:	n/a	n/a
46	CTCF	chr20:25917798-25917843	Lung_OC	lung:	n/a	n/a
47	CTCF	chr20:25968360-25968510	GM12864	blood:	n/a	n/a
48	CTCF	chr20:25968065-25968138	Lung_OC	lung:	n/a	n/a
49	CTCF	chr20:26022795-26022916	LNCaP	prostate:	n/a	n/a
50	CTCF	chr20:25956616-25956645	NHEK	skin:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25991114-25991164	ovcar-3	ovarian:	n/a
2	chr20:25988266-25988316	GM12878	blood:	n/a
3	chr20:25988266-25988316	HepG2	liver:	n/a
4	chr20:25989674-25989724	T-47D	breast:	n/a
5	chr20:25989775-25989825	SKMC	muscle:	n/a
6	chr20:25988587-25988637	HL-60	blood:	n/a
7	chr20:25989775-25989825	CMK	blood:	n/a
8	chr20:25989775-25989825	HCT-116	colon:	n/a
9	chr20:25990680-25990730	AG04450	lung:	fetal
10	chr20:25989674-25989724	HUVEC	blood vessel:	n/a
11	chr20:25989674-25989724	Hela-S3	cervix:	n/a
12	chr20:25989775-25989825	Jurkat	blood:	n/a
13	chr20:25989674-25989724	CMK	blood:	n/a
14	chr20:25990680-25990730	IMR90	lung:	fetal
15	chr20:25989775-25989825	HMEC	breast:	n/a
16	chr20:25991114-25991164	HCPEpiC	choroid plexus:	n/a
17	chr20:25990680-25990730	Jurkat	blood:	n/a
18	chr20:25989032-25989082	K562	blood:	n/a
19	chr20:25989032-25989082	Caco-2	colon:	n/a
20	chr20:25988587-25988637	HEK293	kidney:	embryo
21	chr20:25989032-25989082	HEEpiC	esophagus:	n/a
22	chr20:25990680-25990730	Hela-S3	cervix:	n/a
23	chr20:25989674-25989724	Jurkat	blood:	n/a
24	chr20:25989674-25989724	Hepatocyte	liver:	n/a
25	chr20:25988587-25988637	AG09309	skin:	n/a
26	chr20:25988266-25988316	PFSK-1	brain:	n/a
27	chr20:25988266-25988316	RPTEC	kidney:	n/a
28	chr20:25989775-25989825	A549	lung:	n/a
29	chr20:25989674-25989724	GM12892	blood:	n/a
30	chr20:25989674-25989724	HMEC	breast:	n/a
31	chr20:25988266-25988316	HL-60	blood:	n/a
32	chr20:25988587-25988637	AoSMC	blood vessel:	n/a
33	chr20:25989032-25989082	AG10803	skin:	n/a
34	chr20:25989674-25989724	HRE	kidney:	n/a
35	chr20:25989775-25989825	NT2-D1	testis:	n/a
36	chr20:25991114-25991164	SK-N-SH	brain:	n/a
37	chr20:25991114-25991164	U87	brain:	n/a
38	chr20:25988266-25988316	Hela-S3	cervix:	n/a
39	chr20:25990680-25990730	U87	brain:	n/a
40	chr20:25989775-25989825	AG09309	skin:	n/a
41	chr20:25988266-25988316	AG09309	skin:	n/a
42	chr20:25989775-25989825	ProgFib	skin:	n/a
43	chr20:25989032-25989082	GM12878	blood:	n/a
44	chr20:25989032-25989082	AG04449	skin:	fetal
45	chr20:25990680-25990730	MCF-7	breast:	n/a
46	chr20:25988266-25988316	HEK293	kidney:	embryo
47	chr20:25988587-25988637	H1-hESC	embryonic stem cell:	embryo
48	chr20:25991114-25991164	SKMC	muscle:	n/a
49	chr20:25989032-25989082	HepG2	liver:	n/a
50	chr20:25991114-25991164	AG09319	gingival:	n/a

No data

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182A-1	chr20:25945639-25949924	ENSG00000226203
2	lnc-FAM182A-6	chr20:26002406-26002505	ucscGeneNc_uc010gdq_1
3	lnc-FAM182A-4	chr20:26049724-26049840	ENSG00000125804.9
4	lnc-FAM182A-6	chr20:26009800-26010026	ucscGeneNc_uc010gdq_1
5	lnc-FAM182B-10	chr20:25930172-25930528	NONHSAT079203
6	lnc-FAM182B-11	chr20:25937427-25937691	NONHSAT079205
7	lnc-FAM182A-6	chr20:25983291-25983721	ucscGeneNc_uc010gdq_1
8	lnc-FAM182A-4	chr20:26049553-26049840	ENSG00000125804.9
9	lnc-FAM182A-6	chr20:25999468-25999548	NONHSAT147161
10	lnc-FAM182A-4	chr20:26038034-26038238	ENSG00000125804.9
11	lnc-FAM182A-6	chr20:25997553-25997840	ucscGeneNc_uc010gdq_1
12	lnc-FAM182A-4	chr20:26046283-26046420	ENSG00000125804.9
13	lnc-FAM182A-6	chr20:26000465-26000560	NONHSAT147161
14	lnc-FAM182A-1	chr20:25943698-25943832	ENSG00000226203
15	lnc-FAM182B-10	chr20:25930850-25930935	NONHSAT079203
16	lnc-FAM182B-3	chr20:25990891-25991167	XLOC_013712
17	lnc-FAM182B-3	chr20:25989427-25989691	XLOC_013712
18	lnc-FAM182B-2	chr20:25982172-25982528	XLOC_013711
19	lnc-FAM182B-11	chr20:25938891-25939167	NONHSAT079205
20	lnc-FAM182A-4	chr20:26049553-26049796	ENSG00000125804.9
21	lnc-FAM182A-1	chr20:25936722-25936846	ENSG00000226203
22	lnc-FAM182A-4	chr20:26047198-26047273	ENSG00000125804.9
23	lnc-FAM182A-1	chr20:25936722-25936846	XLOC_013502
24	lnc-FAM182A-6	chr20:26001272-26001320	NONHSAT147161
25	lnc-FAM182A-1	chr20:25943698-25943832	XLOC_013502
26	lnc-FAM182A-4	chr20:26047620-26047810	ENSG00000125804.9
27	lnc-FAM182A-1	chr20:25936453-25936505	XLOC_013502
28	lnc-FAM182A-1	chr20:25936448-25936505	ENSG00000226203
29	lnc-FAM182A-1	chr20:25945639-25949923	XLOC_013502
30	lnc-FAM182A-4	chr20:26040299-26040496	ENSG00000125804.9
31	lnc-FAM182A-4	chr20:26049573-26049840	ENSG00000125804.9
32	lnc-FAM182A-6	chr20:25990334-25991091	NONHSAT079206
33	lnc-FAM182A-4	chr20:26049675-26049840	ENSG00000125804.9
34	lnc-FAM182A-6	chr20:25968084-25968225	NONHSAT079206
35	lnc-FAM182A-6	chr20:25999712-25999838	NONHSAT147161
36	lnc-FAM182B-2	chr20:25982850-25982935	XLOC_013711
37	lnc-FAM182A-6	chr20:26011530-26013121	ucscGeneNc_uc010gdq_1

No data

Variant related genes	Relation type
FAM182A	TF binding region
ENSG00000231081	TF binding region
ENSG00000204556	TF binding region
ENSG00000226203	TF binding region
FAM182A	CpG island
ENSG00000231081	CpG island
ENSG00000204556	CpG island
ENSG00000226203	CpG island
MUC17	miRNA target sites
LIMCH1	miRNA target sites

Extended variants
information (count: 1766 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:1766 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76689718	chr20:25912635-25912636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77840049	chr20:25912640-25912641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6138736	chr20:25912643-25912644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572540800	chr20:25912670-25912671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73350133	chr20:25912744-25912745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541160939	chr20:25912750-25912751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557968868	chr20:25912752-25912753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148765602	chr20:25912775-25912776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs57047656	chr20:25912776-25912777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375167648	chr20:25912779-25912780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577731179	chr20:25912806-25912807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6138737	chr20:25912820-25912821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6138738	chr20:25912825-25912826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6138739	chr20:25912849-25912850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs62212328	chr20:25912867-25912868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534546334	chr20:25912892-25912893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74896916	chr20:25912903-25912904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76053327	chr20:25912913-25912914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542685968	chr20:25912928-25912929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76622651	chr20:25912936-25912937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559388958	chr20:25912953-25912954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4091153	chr20:25912962-25912963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144099661	chr20:25912970-25912971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76561039	chr20:25912981-25912982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4003064	chr20:25912997-25912998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs8184613	chr20:25913015-25913016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1821148	chr20:25913027-25913028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4003066	chr20:25913028-25913029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551173055	chr20:25913065-25913066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4003067	chr20:25913084-25913085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112746238	chr20:25913095-25913096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4003068	chr20:25913142-25913143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76715694	chr20:25913186-25913187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149775130	chr20:25913190-25913191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76629916	chr20:25913195-25913196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs3956078	chr20:25913240-25913241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79748965	chr20:25913274-25913275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79949712	chr20:25913287-25913288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149000685	chr20:25913321-25913322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201752087	chr20:25913339-25913340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs3956079	chr20:25913340-25913341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs3956080	chr20:25913389-25913390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs202196246	chr20:25913393-25913394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200963707	chr20:25913437-25913438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201800177	chr20:25913439-25913440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199980380	chr20:25913440-25913441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201085988	chr20:25913443-25913444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs3956081	chr20:25913448-25913449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550064011	chr20:25913456-25913457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs3956082	chr20:25913464-25913465	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25912600-25913200	Enhancers	Osteobl	bone
2	chr20:25912600-25913800	Enhancers	NHEK	skin
3	chr20:25912800-25913400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr20:25913000-25913800	Enhancers	HMEC	breast
5	chr20:25913600-25914000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr20:25913600-25914000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr20:25934800-25935200	Enhancers	Fetal Intestine Large	intestine
8	chr20:25934800-25935200	Enhancers	Fetal Intestine Small	intestine
9	chr20:25945800-25946200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr20:25946000-25946400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr20:25956000-25956400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr20:25957200-25957600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr20:25957600-25964200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr20:25961000-25961400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr20:25964200-25964400	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr20:25964200-25965400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr20:25964400-25965400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr20:25965000-25965600	Enhancers	Fetal Stomach	stomach
19	chr20:25965000-25968600	Active TSS	Brain Germinal Matrix	brain
20	chr20:25965200-25965800	Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr20:25965200-25966600	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr20:25965200-25966600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr20:25965200-25966800	Active TSS	Fetal Brain Female	brain
24	chr20:25965400-25965600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr20:25965400-25965600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
26	chr20:25965400-25965600	Active TSS	Fetal Muscle Trunk	muscle
27	chr20:25965400-25965600	Bivalent Enhancer	Placenta	Placenta
28	chr20:25965400-25965800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr20:25965400-25965800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr20:25965400-25965800	Active TSS	Muscle Satellite Cultured Cells	--
31	chr20:25965400-25966000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr20:25965400-25966000	Active TSS	Left Ventricle	heart
33	chr20:25965400-25966000	Active TSS	Ovary	ovary
34	chr20:25965400-25966000	Active TSS	Psoas Muscle	Psoas
35	chr20:25965400-25966000	Active TSS	HSMM	muscle
36	chr20:25965400-25966000	Active TSS	NH-A	brain
37	chr20:25965400-25966000	Active TSS	Osteobl	bone
38	chr20:25965400-25966200	Active TSS	Primary T cells fromperipheralblood	blood
39	chr20:25965400-25966200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr20:25965400-25966200	Active TSS	Colon Smooth Muscle	Colon
41	chr20:25965400-25966200	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr20:25965400-25966200	Active TSS	Right Ventricle	heart
43	chr20:25965400-25966200	Active TSS	Stomach Smooth Muscle	stomach
44	chr20:25965400-25966200	Active TSS	Thymus	Thymus
45	chr20:25965400-25966400	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr20:25965400-25966400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr20:25965400-25966400	Active TSS	Brain Anterior Caudate	brain
48	chr20:25965400-25966400	Active TSS	Brain Hippocampus Middle	brain
49	chr20:25965400-25966400	Active TSS	Brain Substantia Nigra	brain
50	chr20:25965400-25966600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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