Variant report

Variant	nsv932106
Chromosome Location	chr20:14964459-15203333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1396)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:15144336-15144711	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:15139111-15139485	HepG2	liver:	n/a	n/a
8	ATF2	chr20:15180324-15181228	GM12878	blood:	n/a	n/a
9	ATF2	chr20:15142645-15143351	GM12878	blood:	n/a	n/a
10	ATF2	chr20:15142556-15143423	GM12878	blood:	n/a	n/a
11	ATF2	chr20:15180601-15181187	GM12878	blood:	n/a	n/a
12	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
13	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
14	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
15	BACH1	chr20:15144468-15144534	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr20:15142669-15143382	GM12878	blood:	n/a	n/a
17	BATF	chr20:15142631-15143004	GM12878	blood:	n/a	n/a
18	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
19	BATF	chr20:15180351-15181277	GM12878	blood:	n/a	chr20:15180905-15180913
20	BATF	chr20:15180677-15181088	GM12878	blood:	n/a	chr20:15180905-15180913
21	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
22	BATF	chr20:15143005-15143338	GM12878	blood:	n/a	n/a
23	BCL11A	chr20:15180658-15181150	GM12878	blood:	n/a	n/a
24	BCL11A	chr20:15180758-15180983	GM12878	blood:	n/a	n/a
25	BCL3	chr20:15180753-15181061	GM12878	blood:	n/a	n/a
26	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
27	BCL3	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
28	BCL3	chr20:14966411-14967352	A549	lung:	n/a	n/a
29	BCLAF1	chr20:15142637-15143439	GM12878	blood:	n/a	n/a
30	BHLHE40	chr20:15180594-15181323	GM12878	blood:	n/a	n/a
31	BHLHE40	chr20:15041038-15041678	HepG2	liver:	n/a	n/a
32	BHLHE40	chr20:14977538-14977786	HepG2	liver:	n/a	n/a
33	BHLHE40	chr20:14965455-14966238	HepG2	liver:	n/a	n/a
34	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
35	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
36	BRCA1	chr20:14965501-14966238	HepG2	liver:	n/a	n/a
37	BRCA1	chr20:15054620-15054671	HepG2	liver:	n/a	n/a
38	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
39	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
40	BRCA1	chr20:14966739-14967191	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:14971689-14972097	HepG2	liver:	n/a	chr20:14971798-14971811
42	CEBPB	chr20:14972648-14973239	A549	lung:	n/a	chr20:14972825-14972837
43	CEBPB	chr20:15169094-15169462	HepG2	liver:	n/a	chr20:15169267-15169284
44	CEBPB	chr20:15013078-15013237	H1-hESC	embryonic stem cell:	n/a	chr20:15013102-15013113
45	CEBPB	chr20:15162823-15163175	IMR90	lung:	n/a	chr20:15162991-15163000 chr20:15162991-15163000 chr20:15162989-15163000 chr20:15162991-15163000 chr20:15162991-15163000 chr20:15162990-15163001
46	CEBPB	chr20:14971613-14972080	HepG2	liver:	n/a	chr20:14971798-14971811
47	CEBPB	chr20:14978443-14978984	A549	lung:	n/a	n/a
48	CEBPB	chr20:15162823-15163186	HepG2	liver:	n/a	chr20:15162991-15163000 chr20:15162991-15163000 chr20:15162989-15163000 chr20:15162991-15163000 chr20:15162991-15163000 chr20:15162990-15163001
49	CEBPB	chr20:14965531-14966128	HepG2	liver:	n/a	n/a
50	CEBPB	chr20:15032344-15032575	H1-hESC	embryonic stem cell:	n/a	chr20:15032453-15032464

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:15176830-15176880	SK-N-SH_RA	brain:	n/a
2	chr20:15177509-15177559	ProgFib	skin:	n/a
3	chr20:15177509-15177559	SK-N-SH_RA	brain:	n/a
4	chr20:15177509-15177559	U87	brain:	n/a
5	chr20:15177509-15177559	SK-N-SH	brain:	n/a
6	chr20:15176830-15176880	MCF-7	breast:	n/a
7	chr20:15176557-15176607	PANC-1	pancreas:	n/a
8	chr20:15176830-15176880	HCM	heart:	n/a
9	chr20:15176557-15176607	AG09319	gingival:	n/a
10	chr20:15176557-15176607	Caco-2	colon:	n/a
11	chr20:15176557-15176607	HCM	heart:	n/a
12	chr20:15176557-15176607	A549	lung:	n/a
13	chr20:15177509-15177559	AG04450	lung:	fetal
14	chr20:15176830-15176880	HAEpiC	amniotic membrane:	n/a
15	chr20:15177509-15177559	PFSK-1	brain:	n/a
16	chr20:15176557-15176607	U87	brain:	n/a
17	chr20:15176830-15176880	Jurkat	blood:	n/a
18	chr20:15177509-15177559	RPTEC	kidney:	n/a
19	chr20:15177509-15177559	A549	lung:	n/a
20	chr20:15176557-15176607	SK-N-MC	brain:	n/a
21	chr20:15176830-15176880	HIPEpiC	eye:	n/a
22	chr20:15176557-15176607	HUVEC	blood vessel:	n/a
23	chr20:15176830-15176880	AG09319	gingival:	n/a
24	chr20:15177509-15177559	HRPEpiC	eye:	n/a
25	chr20:15176557-15176607	HepG2	liver:	n/a
26	chr20:15177509-15177559	HPAEpiC	pulmonary alveolar:	n/a
27	chr20:15177509-15177559	HRE	kidney:	n/a
28	chr20:15176830-15176880	GM06990	blood:	n/a
29	chr20:15176830-15176880	GM12891	blood:	n/a
30	chr20:15176830-15176880	GM19239	blood:	n/a
31	chr20:15176830-15176880	Caco-2	colon:	n/a
32	chr20:15177509-15177559	Jurkat	blood:	n/a
33	chr20:15177509-15177559	HCF	heart:	n/a
34	chr20:15176557-15176607	AoSMC	blood vessel:	n/a
35	chr20:15177509-15177559	AoSMC	blood vessel:	n/a
36	chr20:15176557-15176607	Jurkat	blood:	n/a
37	chr20:15176830-15176880	BJ	skin:	n/a
38	chr20:15176557-15176607	AG04450	lung:	fetal
39	chr20:15176557-15176607	H1-hESC	embryonic stem cell:	embryo
40	chr20:15176830-15176880	HRPEpiC	eye:	n/a
41	chr20:15176557-15176607	MCF10A-Er-Src	breast:	n/a
42	chr20:15176830-15176880	HMEC	breast:	n/a
43	chr20:15176830-15176880	PFSK-1	brain:	n/a
44	chr20:15177509-15177559	HL-60	blood:	n/a
45	chr20:15176557-15176607	HEK293	kidney:	embryo
46	chr20:15177509-15177559	PrEC	prostate:	n/a
47	chr20:15177509-15177559	HCM	heart:	n/a
48	chr20:15176557-15176607	PFSK-1	brain:	n/a
49	chr20:15177509-15177559	BE2_C	brain:	n/a
50	chr20:15176830-15176880	HepG2	liver:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
2	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
3	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:

No data

Variant related genes	Relation type
MACROD2	TF binding region
RNU6-1159P	TF binding region
RNU6-115P	TF binding region
MACROD2	CpG island
RNU6-1159P	CpG island
RNU6-115P	CpG island

Extended variants
information (count: 6891 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6891 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552985494	chr20:14964475-14964476	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs36050787	chr20:14964489-14964490	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs552659273	chr20:14964497-14964498	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs76486858	chr20:14964537-14964538	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs77901532	chr20:14964538-14964539	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs189132018	chr20:14964546-14964547	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7508885	chr20:14964562-14964563	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs374298660	chr20:14964571-14964572	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs13043061	chr20:14964602-14964603	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs436699	chr20:14964657-14964658	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs143119278	chr20:14964702-14964703	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs375057948	chr20:14964739-14964740	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs528508152	chr20:14964754-14964755	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs547059348	chr20:14964821-14964822	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs191788415	chr20:14964839-14964840	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs147471072	chr20:14964871-14964872	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs557175174	chr20:14964914-14964915	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs551040175	chr20:14964934-14964935	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs2423900	chr20:14964945-14964946	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs367804635	chr20:14964946-14964947	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs536419531	chr20:14964949-14964950	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs183831230	chr20:14965000-14965001	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs138133643	chr20:14965053-14965054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188376460	chr20:14965067-14965068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542942235	chr20:14965076-14965077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111993813	chr20:14965145-14965146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577543184	chr20:14965152-14965153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191807999	chr20:14965158-14965159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538386686	chr20:14965172-14965173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556992104	chr20:14965220-14965221	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs575514369	chr20:14965227-14965228	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559671622	chr20:14965295-14965296	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542806517	chr20:14965300-14965301	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs557310558	chr20:14965350-14965351	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs536351215	chr20:14965352-14965353	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs117869237	chr20:14965392-14965393	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs573222310	chr20:14965414-14965415	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs173295	chr20:14965447-14965448	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs565170996	chr20:14965474-14965475	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs143590156	chr20:14965499-14965500	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544400022	chr20:14965532-14965533	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs562952749	chr20:14965583-14965584	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs113885813	chr20:14965587-14965588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs183923464	chr20:14965636-14965637	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs144019731	chr20:14965660-14965661	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs148697635	chr20:14965665-14965666	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528003877	chr20:14965672-14965673	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs552818557	chr20:14965675-14965676	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs571168710	chr20:14965686-14965687	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs139549162	chr20:14965807-14965808	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
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
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	17363583	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21272361	CNVD
Schizophrenia	19805367	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14960600-14965400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr20:14960800-14965400	Weak transcription	Hela-S3	cervix
3	chr20:14961000-14964800	Weak transcription	HUVEC	blood vessel
4	chr20:14962000-14965000	ZNF genes & repeats	Fetal Intestine Small	intestine
5	chr20:14963600-14965800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr20:14964200-14964600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:14964400-14964600	ZNF genes & repeats	A549	lung
8	chr20:14964400-14964600	Flanking Active TSS	HepG2	liver
9	chr20:14964600-14965200	Weak transcription	A549	lung
10	chr20:14964600-14965200	Enhancers	HepG2	liver
11	chr20:14964600-14966800	Enhancers	Fetal Intestine Large	intestine
12	chr20:14964600-14971600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr20:14964800-14967800	Enhancers	HUVEC	blood vessel
14	chr20:14965000-14965200	Weak transcription	Fetal Intestine Small	intestine
15	chr20:14965000-14965600	Enhancers	Stomach Mucosa	stomach
16	chr20:14965000-14968000	Enhancers	Liver	Liver
17	chr20:14965200-14965600	Enhancers	A549	lung
18	chr20:14965200-14965800	Flanking Active TSS	HepG2	liver
19	chr20:14965200-14966000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr20:14965200-14967200	Enhancers	Fetal Intestine Small	intestine
21	chr20:14965400-14966000	Enhancers	Duodenum Mucosa	Duodenum
22	chr20:14965400-14966800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr20:14965400-14967400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr20:14965400-14967600	Enhancers	Pancreas	Pancrea
25	chr20:14965400-14968000	Enhancers	Fetal Kidney	kidney
26	chr20:14965400-14968000	Enhancers	Hela-S3	cervix
27	chr20:14965600-14966000	Flanking Active TSS	Stomach Mucosa	stomach
28	chr20:14965600-14966200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr20:14965600-14966200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:14965600-14966200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr20:14965600-14966200	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr20:14965600-14966200	Flanking Active TSS	A549	lung
33	chr20:14965600-14966400	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr20:14965800-14966200	Enhancers	HepG2	liver
35	chr20:14965800-14966600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr20:14965800-14967200	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr20:14966000-14966200	Enhancers	Stomach Mucosa	stomach
38	chr20:14966000-14966400	Enhancers	Aorta	Aorta
39	chr20:14966000-14967200	Weak transcription	Duodenum Mucosa	Duodenum
40	chr20:14966000-14967400	Enhancers	HMEC	breast
41	chr20:14966200-14966600	Enhancers	A549	lung
42	chr20:14966200-14966800	Flanking Active TSS	HepG2	liver
43	chr20:14966200-14967400	Weak transcription	Stomach Mucosa	stomach
44	chr20:14966400-14967000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr20:14966600-14966800	Flanking Active TSS	A549	lung
46	chr20:14966600-14967000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr20:14966600-14967000	Enhancers	Aorta	Aorta
48	chr20:14966600-14967400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr20:14966800-14967200	Active TSS	A549	lung
50	chr20:14966800-14967200	Enhancers	HepG2	liver

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