Variant report

Variant	esv3493532
Chromosome Location	chr20:25972821-26045537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:501)
CpG islands
(count:427)
Chromatin interactive
region (count:0)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:501 , 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	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	chr20:25975707-25975907	GM12878	blood:	n/a	n/a
5	BCL11A	chr20:26041793-26041988	GM12878	blood:	n/a	n/a
6	BCL11A	chr20:25990610-25990918	GM12878	blood:	n/a	n/a
7	BCL11A	chr20:26010805-26011025	GM12878	blood:	n/a	n/a
8	BHLHE40	chr20:25975281-25975466	GM12878	blood:	n/a	n/a
9	BHLHE40	chr20:25975821-25976057	GM12878	blood:	n/a	n/a
10	BRCA1	chr20:25990208-25990605	Hela-S3	cervix:	n/a	chr20:25990394-25990403
11	BRCA1	chr20:25990237-25990584	HepG2	liver:	n/a	chr20:25990394-25990403
12	BRCA1	chr20:25990247-25990579	GM12878	blood:	n/a	chr20:25990394-25990403
13	CEBPB	chr20:25989230-25989660	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
14	CEBPB	chr20:25988927-25989639	A549	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
15	CEBPB	chr20:25989264-25989635	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
16	CEBPB	chr20:25988753-25989639	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
17	CEBPB	chr20:25989327-25989510	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
18	CEBPB	chr20:25989272-25989628	IMR90	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
19	CEBPB	chr20:25988884-25989639	Hela-S3	cervix:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
20	CEBPB	chr20:25989351-25989594	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
21	CEBPB	chr20:26041786-26041946	K562	blood:	n/a	n/a
22	CEBPB	chr20:25976255-25976322	HepG2	liver:	n/a	chr20:25976304-25976315
23	CEBPB	chr20:25989323-25989598	H1-hESC	embryonic stem cell:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
24	CEBPB	chr20:25989347-25989484	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
25	CEBPB	chr20:25990281-25990629	Hela-S3	cervix:	n/a	n/a
26	CEBPD	chr20:25990293-25990725	HepG2	liver:	n/a	n/a
27	CHD1	chr20:25990580-25990581	GM12878	blood:	n/a	n/a
28	CHD2	chr20:25990214-25990586	K562	blood:	n/a	chr20:25990394-25990403
29	CHD2	chr20:25990204-25990773	Hela-S3	cervix:	n/a	chr20:25990394-25990403
30	CHD2	chr20:25990208-25990784	GM12878	blood:	n/a	chr20:25990394-25990403
31	CHD2	chr20:25990200-25990660	HepG2	liver:	n/a	chr20:25990394-25990403
32	CTCF	chr20:25990000-25990060	LNCaP	prostate:	n/a	n/a
33	CTCF	chr20:25998384-25998452	LNCaP	prostate:	n/a	n/a
34	CTCF	chr20:25990600-25990750	GM12867	blood:	n/a	n/a
35	CTCF	chr20:26022832-26022906	Medullo	brain:	n/a	n/a
36	CTCF	chr20:26022744-26022916	MCF-7	breast:	n/a	n/a
37	CTCF	chr20:26022765-26022887	HepG2	liver:	n/a	n/a
38	CTCF	chr20:25991586-25991706	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr20:26014290-26014299	GM13977	blood:	n/a	n/a
40	CTCF	chr20:26045218-26045235	LNCaP	prostate:	n/a	n/a
41	CTCF	chr20:25993777-25993844	GM13976	blood:	n/a	n/a
42	CTCF	chr20:26022791-26022793	ProgFib	skin:	n/a	n/a
43	CTCF	chr20:26041346-26041380	GM13976	blood:	n/a	n/a
44	CTCF	chr20:26022795-26022875	ProgFib	skin:	n/a	n/a
45	CTCF	chr20:26029022-26029052	LNCaP	prostate:	n/a	n/a
46	CTCF	chr20:26022764-26022924	MCF-7	breast:	n/a	n/a
47	CTCF	chr20:25999107-25999194	GM20000	blood:	n/a	n/a
48	CTCF	chr20:26009738-26009859	GM20000	blood:	n/a	n/a
49	CTCF	chr20:26040159-26040181	K562	blood:	n/a	n/a
50	CTCF	chr20:26006053-26006100	GM10248	blood:	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	chr20:25989032-25989082	Hepatocyte	liver:	n/a
2	chr20:25991114-25991164	GM06990	blood:	n/a
3	chr20:25988266-25988316	IMR90	lung:	fetal
4	chr20:25990680-25990730	AG04449	skin:	fetal
5	chr20:25989674-25989724	ECC-1	luminal epithelium:	n/a
6	chr20:25988266-25988316	ovcar-3	ovarian:	n/a
7	chr20:25991114-25991164	HEEpiC	esophagus:	n/a
8	chr20:25990680-25990730	HEEpiC	esophagus:	n/a
9	chr20:25989032-25989082	NHBE	bronchial:	n/a
10	chr20:25988266-25988316	NT2-D1	testis:	n/a
11	chr20:25989674-25989724	BJ	skin:	n/a
12	chr20:25989032-25989082	K562	blood:	n/a
13	chr20:25991114-25991164	Jurkat	blood:	n/a
14	chr20:25989775-25989825	PANC-1	pancreas:	n/a
15	chr20:25989032-25989082	MCF-7	breast:	n/a
16	chr20:25989032-25989082	PANC-1	pancreas:	n/a
17	chr20:25990680-25990730	SKMC	muscle:	n/a
18	chr20:25988266-25988316	HRPEpiC	eye:	n/a
19	chr20:25988266-25988316	GM06990	blood:	n/a
20	chr20:25988587-25988637	HCF	heart:	n/a
21	chr20:25988266-25988316	AG04449	skin:	fetal
22	chr20:25990680-25990730	IMR90	lung:	fetal
23	chr20:25988266-25988316	MCF10A-Er-Src	breast:	n/a
24	chr20:25989674-25989724	LNCaP	prostate:	n/a
25	chr20:25990680-25990730	ECC-1	luminal epithelium:	n/a
26	chr20:25989032-25989082	HAEpiC	amniotic membrane:	n/a
27	chr20:25988587-25988637	HPAEpiC	pulmonary alveolar:	n/a
28	chr20:25988266-25988316	LNCaP	prostate:	n/a
29	chr20:25988587-25988637	GM12878	blood:	n/a
30	chr20:25989775-25989825	HepG2	liver:	n/a
31	chr20:25988587-25988637	AG04450	lung:	fetal
32	chr20:25988587-25988637	HMEC	breast:	n/a
33	chr20:25988587-25988637	GM19239	blood:	n/a
34	chr20:25990680-25990730	AG04450	lung:	fetal
35	chr20:25989775-25989825	Hepatocyte	liver:	n/a
36	chr20:25989674-25989724	Hela-S3	cervix:	n/a
37	chr20:25988587-25988637	SK-N-MC	brain:	n/a
38	chr20:25990680-25990730	SK-N-SH_RA	brain:	n/a
39	chr20:25989775-25989825	NHBE	bronchial:	n/a
40	chr20:25989674-25989724	SK-N-MC	brain:	n/a
41	chr20:25989674-25989724	AG10803	skin:	n/a
42	chr20:25991114-25991164	HCM	heart:	n/a
43	chr20:25988587-25988637	MCF10A-Er-Src	breast:	n/a
44	chr20:25989032-25989082	BJ	skin:	n/a
45	chr20:25991114-25991164	NT2-D1	testis:	n/a
46	chr20:25988266-25988316	SK-N-SH	brain:	n/a
47	chr20:25991114-25991164	HNPCEpiC	eye:	n/a
48	chr20:25988266-25988316	RPTEC	kidney:	n/a
49	chr20:25989674-25989724	PrEC	prostate:	n/a
50	chr20:25989032-25989082	HIPEpiC	eye:	n/a

No data

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182B-3	chr20:25989427-25989691	XLOC_013712
2	lnc-FAM182A-6	chr20:25999712-25999838	NONHSAT147161
3	lnc-FAM182A-6	chr20:25999468-25999548	NONHSAT147161
4	lnc-FAM182A-6	chr20:26000465-26000560	NONHSAT147161
5	lnc-FAM182A-4	chr20:26040299-26040496	ENSG00000125804.9
6	lnc-FAM182B-2	chr20:25982172-25982528	XLOC_013711
7	lnc-FAM182B-2	chr20:25982850-25982935	XLOC_013711
8	lnc-FAM182B-3	chr20:25990891-25991167	XLOC_013712
9	lnc-FAM182A-6	chr20:26011530-26013121	ucscGeneNc_uc010gdq_1
10	lnc-FAM182A-6	chr20:25983291-25983721	ucscGeneNc_uc010gdq_1
11	lnc-FAM182A-6	chr20:26001272-26001320	NONHSAT147161
12	lnc-FAM182A-4	chr20:26038034-26038238	ENSG00000125804.9
13	lnc-FAM182A-6	chr20:26009800-26010026	ucscGeneNc_uc010gdq_1
14	lnc-FAM182A-6	chr20:25997553-25997840	ucscGeneNc_uc010gdq_1
15	lnc-FAM182A-6	chr20:26002406-26002505	ucscGeneNc_uc010gdq_1
16	lnc-FAM182A-6	chr20:25990334-25991091	NONHSAT079206

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
LIMCH1	miRNA target sites

Extended variants
information (count: 567 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115358877	chr20:25972826-25972827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371019033	chr20:25972851-25972852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6138772	chr20:25972858-25972859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372633289	chr20:25972885-25972886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12624435	chr20:25972900-25972901	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs192930071	chr20:25972942-25972943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553028754	chr20:25972954-25972955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567989062	chr20:25972972-25972973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368752759	chr20:25973004-25973005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147920513	chr20:25973044-25973045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565131817	chr20:25973085-25973086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544367895	chr20:25973109-25973110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564791618	chr20:25973117-25973118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183548932	chr20:25973146-25973147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140542384	chr20:25973170-25973171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188087843	chr20:25973245-25973246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367584501	chr20:25973296-25973297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191718846	chr20:25973317-25973318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549249212	chr20:25973388-25973389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541521461	chr20:25973390-25973391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535430735	chr20:25978025-25978026	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs182688368	chr20:25978048-25978049	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs6037311	chr20:25978089-25978090	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs540579400	chr20:25978122-25978123	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs80274446	chr20:25978135-25978136	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs386813613	chr20:25978138-25978139	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs6037313	chr20:25978139-25978140	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs187041654	chr20:25978160-25978161	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562966389	chr20:25978182-25978183	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs112241241	chr20:25978184-25978185	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs75938338	chr20:25978214-25978215	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs144617511	chr20:25978284-25978285	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542198339	chr20:25978298-25978299	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs562327298	chr20:25978337-25978338	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs527688737	chr20:25978355-25978356	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs6115469	chr20:25978363-25978364	Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570973410	chr20:25978364-25978365	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs533294371	chr20:25978374-25978375	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs564489894	chr20:25978397-25978398	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs550246302	chr20:25978417-25978418	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528823079	chr20:25978456-25978457	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150067324	chr20:25978486-25978487	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145311575	chr20:25978494-25978495	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562268403	chr20:25978518-25978519	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535856186	chr20:25978528-25978529	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555247465	chr20:25978562-25978563	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6037314	chr20:25978572-25978573	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548318381	chr20:25978764-25978765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566366447	chr20:25978767-25978768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572881368	chr20:25981612-25981613	Enhancers	n/a	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	chr20:25972600-25973000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr20:25972600-25973400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr20:25972800-25973200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr20:25978000-25978200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr20:25978000-25978400	Active TSS	Brain Anterior Caudate	brain
6	chr20:25978200-25978600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
7	chr20:25978400-25978800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr20:25978600-25978800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr20:25981600-25982400	Enhancers	HepG2	liver
10	chr20:25982400-25983800	Weak transcription	HepG2	liver
11	chr20:25983800-25985600	Enhancers	HepG2	liver
12	chr20:25985600-25989600	Weak transcription	HepG2	liver
13	chr20:25988800-25990200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr20:25989200-25990200	Enhancers	Placenta	Placenta
15	chr20:25989600-25990400	Active TSS	HepG2	liver
16	chr20:25989600-25991600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr20:25989800-25990000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr20:25989800-25990000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr20:25989800-25990000	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr20:25989800-25990000	Enhancers	Fetal Brain Female	brain
21	chr20:25989800-25990000	Enhancers	Fetal Lung	lung
22	chr20:25989800-25990000	Enhancers	Hela-S3	cervix
23	chr20:25989800-25990200	Enhancers	NHDF-Ad	bronchial
24	chr20:25989800-25990400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr20:25989800-25990400	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr20:25989800-25990400	Enhancers	Spleen	Spleen
27	chr20:25989800-25990600	Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr20:25989800-25991600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr20:25989800-25991600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:25989800-25991600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr20:25989800-25991600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr20:25989800-25991600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr20:25989800-25991600	Active TSS	Brain Cingulate Gyrus	brain
34	chr20:25989800-25991600	Active TSS	A549	lung
35	chr20:25990000-25990200	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr20:25990000-25990600	Active TSS	Fetal Lung	lung
37	chr20:25990000-25990600	Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr20:25990000-25990800	Active TSS	Adipose Nuclei	Adipose
39	chr20:25990000-25990800	Active TSS	Fetal Thymus	thymus
40	chr20:25990000-25991000	Active TSS	Fetal Muscle Leg	muscle
41	chr20:25990000-25991000	Active TSS	Fetal Stomach	stomach
42	chr20:25990000-25991000	Active TSS	Rectal Smooth Muscle	rectum
43	chr20:25990000-25991400	Active TSS	Primary hematopoietic stem cells short term culture	blood
44	chr20:25990000-25991400	Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr20:25990000-25991400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr20:25990000-25991400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr20:25990000-25991400	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr20:25990000-25991400	Active TSS	Fetal Brain Female	brain
49	chr20:25990000-25991400	Active TSS	Fetal Kidney	kidney
50	chr20:25990000-25991400	Active TSS	Pancreatic Islets	Pancreatic Islet

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