Variant report

Variant	nsv544206
Chromosome Location	chr20:14964258-15547739
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2856)
CpG islands
(count:244)
Chromatin interactive
region (count:35)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2856 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

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	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:15139111-15139485	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:15144336-15144711	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
8	ATF2	chr20:15180601-15181187	GM12878	blood:	n/a	n/a
9	ATF2	chr20:15142556-15143423	GM12878	blood:	n/a	n/a
10	ATF2	chr20:15299899-15300572	GM12878	blood:	n/a	n/a
11	ATF2	chr20:15313045-15313880	GM12878	blood:	n/a	chr20:15313332-15313343
12	ATF2	chr20:15180324-15181228	GM12878	blood:	n/a	n/a
13	ATF2	chr20:15142645-15143351	GM12878	blood:	n/a	n/a
14	ATF2	chr20:15299283-15299738	GM12878	blood:	n/a	n/a
15	ATF2	chr20:15298201-15298708	GM12878	blood:	n/a	n/a
16	ATF2	chr20:15299152-15299756	GM12878	blood:	n/a	n/a
17	ATF2	chr20:15297929-15299020	GM12878	blood:	n/a	n/a
18	ATF2	chr20:15542293-15542732	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
20	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
21	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
22	BACH1	chr20:15144468-15144534	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr20:15180351-15181277	GM12878	blood:	n/a	chr20:15180905-15180913
24	BATF	chr20:15180677-15181088	GM12878	blood:	n/a	chr20:15180905-15180913
25	BATF	chr20:15217496-15217756	GM12878	blood:	n/a	n/a
26	BATF	chr20:15142669-15143382	GM12878	blood:	n/a	n/a
27	BATF	chr20:15298206-15298537	GM12878	blood:	n/a	n/a
28	BATF	chr20:15142631-15143004	GM12878	blood:	n/a	n/a
29	BATF	chr20:15298174-15298614	GM12878	blood:	n/a	n/a
30	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
31	BATF	chr20:15299346-15299710	GM12878	blood:	n/a	n/a
32	BATF	chr20:15376139-15376425	GM12878	blood:	n/a	n/a
33	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
34	BATF	chr20:15298652-15298919	GM12878	blood:	n/a	n/a
35	BATF	chr20:15313268-15313752	GM12878	blood:	n/a	n/a
36	BATF	chr20:15229264-15229547	GM12878	blood:	n/a	n/a
37	BATF	chr20:15299357-15299730	GM12878	blood:	n/a	n/a
38	BATF	chr20:15143005-15143338	GM12878	blood:	n/a	n/a
39	BCL11A	chr20:15180758-15180983	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:15180658-15181150	GM12878	blood:	n/a	n/a
41	BCL3	chr20:14966411-14967352	A549	lung:	n/a	n/a
42	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
43	BCL3	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
44	BCL3	chr20:15180753-15181061	GM12878	blood:	n/a	n/a
45	BCLAF1	chr20:15142637-15143439	GM12878	blood:	n/a	n/a
46	BCLAF1	chr20:15298185-15298626	GM12878	blood:	n/a	n/a
47	BCLAF1	chr20:15298111-15298900	GM12878	blood:	n/a	n/a
48	BCLAF1	chr20:15313142-15313783	GM12878	blood:	n/a	n/a
49	BHLHE40	chr20:15180594-15181323	GM12878	blood:	n/a	n/a
50	BHLHE40	chr20:15456263-15456376	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:15177509-15177559	PFSK-1	brain:	n/a
2	chr20:15176557-15176607	MCF10A-Er-Src	breast:	n/a
3	chr20:15460804-15460854	HAEpiC	amniotic membrane:	n/a
4	chr20:15176557-15176607	HAEpiC	amniotic membrane:	n/a
5	chr20:15176830-15176880	HEK293	kidney:	embryo
6	chr20:15176830-15176880	K562	blood:	n/a
7	chr20:15176830-15176880	NHBE	bronchial:	n/a
8	chr20:15176830-15176880	HL-60	blood:	n/a
9	chr20:15177509-15177559	NH-A	brain:	n/a
10	chr20:15176830-15176880	AG10803	skin:	n/a
11	chr20:15176557-15176607	PrEC	prostate:	n/a
12	chr20:15176557-15176607	HCF	heart:	n/a
13	chr20:15176557-15176607	HRCEpiC	kidney:	n/a
14	chr20:15177509-15177559	Hepatocyte	liver:	n/a
15	chr20:15177509-15177559	Jurkat	blood:	n/a
16	chr20:15176557-15176607	HUVEC	blood vessel:	n/a
17	chr20:15177509-15177559	NHDF-neo	bronchial:	n/a
18	chr20:15460804-15460854	HRE	kidney:	n/a
19	chr20:15460804-15460854	ProgFib	skin:	n/a
20	chr20:15177509-15177559	GM06990	blood:	n/a
21	chr20:15177509-15177559	HCPEpiC	choroid plexus:	n/a
22	chr20:15177509-15177559	SKMC	muscle:	n/a
23	chr20:15177509-15177559	HCM	heart:	n/a
24	chr20:15460804-15460854	T-47D	breast:	n/a
25	chr20:15176557-15176607	HCM	heart:	n/a
26	chr20:15177509-15177559	BE2_C	brain:	n/a
27	chr20:15176830-15176880	GM06990	blood:	n/a
28	chr20:15176830-15176880	PrEC	prostate:	n/a
29	chr20:15460804-15460854	HIPEpiC	eye:	n/a
30	chr20:15177509-15177559	A549	lung:	n/a
31	chr20:15460804-15460854	SK-N-SH_RA	brain:	n/a
32	chr20:15176557-15176607	A549	lung:	n/a
33	chr20:15176830-15176880	PANC-1	pancreas:	n/a
34	chr20:15176830-15176880	H1-hESC	embryonic stem cell:	embryo
35	chr20:15177509-15177559	GM12892	blood:	n/a
36	chr20:15460804-15460854	AG10803	skin:	n/a
37	chr20:15177509-15177559	HIPEpiC	eye:	n/a
38	chr20:15460804-15460854	HMEC	breast:	n/a
39	chr20:15176557-15176607	BJ	skin:	n/a
40	chr20:15176557-15176607	HEEpiC	esophagus:	n/a
41	chr20:15176830-15176880	T-47D	breast:	n/a
42	chr20:15176830-15176880	HAEpiC	amniotic membrane:	n/a
43	chr20:15176557-15176607	Hepatocyte	liver:	n/a
44	chr20:15176557-15176607	GM19239	blood:	n/a
45	chr20:15177509-15177559	BJ	skin:	n/a
46	chr20:15176557-15176607	NHBE	bronchial:	n/a
47	chr20:15177509-15177559	U87	brain:	n/a
48	chr20:15460804-15460854	NHBE	bronchial:	n/a
49	chr20:15176830-15176880	HCF	heart:	n/a
50	chr20:15177509-15177559	AG10803	skin:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:79167275..79169229-chr20:15379751..15381953,2	MCF-7	breast:
2	chr20:15354524..15357487-chr20:15359360..15362240,2	MCF-7	breast:
3	chr20:15279663..15281630-chr20:15285386..15287786,2	MCF-7	breast:
4	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
5	chr1:153462091..153462609-chr20:15426696..15427544,2	MCF-7	breast:
6	chr20:15213744..15214594-chr5:107680986..107681674,2	MCF-7	breast:
7	chr20:15400360..15402078-chr20:15403721..15405394,2	K562	blood:
8	chr20:15474862..15477622-chr20:15478016..15479786,2	MCF-7	breast:
9	chr20:15279663..15281630-chr20:15285386..15287786,2	MCF-7	breast:
10	chr20:15400360..15402078-chr20:15403721..15405394,2	K562	blood:
11	chr20:15222565..15225391-chr20:15228675..15231649,2	MCF-7	breast:
12	chr20:15472191..15472832-chr20:15689360..15689915,3	MCF-7	breast:
13	chr20:15471920..15472855-chr20:15634516..15635330,3	MCF-7	breast:
14	chr20:15354524..15357487-chr20:15359360..15362240,2	MCF-7	breast:
15	chr20:15280200..15282422-chr20:15286811..15288380,2	MCF-7	breast:
16	chr20:15293454..15295061-chr20:15304426..15306908,2	MCF-7	breast:
17	chr20:14335576..14337791-chr20:15315333..15317078,2	MCF-7	breast:
18	chr20:15468580..15470107-chr20:15474953..15477651,2	MCF-7	breast:
19	chr20:15430826..15432876-chr20:15434681..15437679,2	MCF-7	breast:
20	chr20:15349649..15350459-chr6:35465170..35465747,2	MCF-7	breast:
21	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
22	chr20:15474862..15477622-chr20:15478016..15479786,2	MCF-7	breast:
23	chr20:15430826..15432876-chr20:15434681..15437679,2	MCF-7	breast:
24	chr20:15421139..15421682-chr20:16522882..16523464,2	MCF-7	breast:
25	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
26	chr20:15420870..15421552-chr20:15477062..15477568,2	MCF-7	breast:
27	chr20:15293454..15295061-chr20:15304426..15306908,2	MCF-7	breast:
28	chr20:15222565..15225391-chr20:15228675..15231649,2	MCF-7	breast:
29	chr20:15467907..15471393-chr20:15474157..15477058,3	MCF-7	breast:
30	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
31	chr20:15420870..15421552-chr20:15477062..15477568,2	MCF-7	breast:
32	chr20:15280200..15282422-chr20:15286811..15288380,2	MCF-7	breast:
33	chr20:15468580..15470107-chr20:15474953..15477651,2	MCF-7	breast:
34	chr20:15467907..15471393-chr20:15474157..15477058,3	MCF-7	breast:
35	chr20:14316387..14318274-chr20:15215878..15217670,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF16B-4	chr20:15532802-15533046	ENSG00000225181.1
2	lnc-KIF16B-4	chr20:15533257-15533530	ENSG00000225181.1

No data

Variant related genes	Relation type
MACROD2	TF binding region
ENSG00000225181	TF binding region
RNU6-1159P	TF binding region
RNU6-115P	TF binding region
ENSG00000212111	TF binding region
RNA5SP475	TF binding region
MACROD2	CpG island
ENSG00000225181	CpG island
RNU6-1159P	CpG island
RNU6-115P	CpG island
ENSG00000212111	CpG island
RNA5SP475	CpG island
ENSG00000185787	chromatin interactions
ENSG00000125848	chromatin interactions

Extended variants
information (count: 16956 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:16956 , 50 per page) page: 1 2 3 4 5 6 7 ... 340

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569412552	chr20:14964261-14964262	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536583253	chr20:14964262-14964263	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554807359	chr20:14964269-14964270	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6110479	chr20:14964300-14964301	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182139478	chr20:14964332-14964333	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534274316	chr20:14964355-14964356	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552985494	chr20:14964475-14964476	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs36050787	chr20:14964489-14964490	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs552659273	chr20:14964497-14964498	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs76486858	chr20:14964537-14964538	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs77901532	chr20:14964538-14964539	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs189132018	chr20:14964546-14964547	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs7508885	chr20:14964562-14964563	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs374298660	chr20:14964571-14964572	Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs13043061	chr20:14964602-14964603	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs436699	chr20:14964657-14964658	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs143119278	chr20:14964702-14964703	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs375057948	chr20:14964739-14964740	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs528508152	chr20:14964754-14964755	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs547059348	chr20:14964821-14964822	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs191788415	chr20:14964839-14964840	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs147471072	chr20:14964871-14964872	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs557175174	chr20:14964914-14964915	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs551040175	chr20:14964934-14964935	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs2423900	chr20:14964945-14964946	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs367804635	chr20:14964946-14964947	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs536419531	chr20:14964949-14964950	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs183831230	chr20:14965000-14965001	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs138133643	chr20:14965053-14965054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188376460	chr20:14965067-14965068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542942235	chr20:14965076-14965077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111993813	chr20:14965145-14965146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577543184	chr20:14965152-14965153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191807999	chr20:14965158-14965159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538386686	chr20:14965172-14965173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556992104	chr20:14965220-14965221	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575514369	chr20:14965227-14965228	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559671622	chr20:14965295-14965296	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs542806517	chr20:14965300-14965301	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs557310558	chr20:14965350-14965351	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs536351215	chr20:14965352-14965353	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs117869237	chr20:14965392-14965393	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs573222310	chr20:14965414-14965415	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs173295	chr20:14965447-14965448	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565170996	chr20:14965474-14965475	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs143590156	chr20:14965499-14965500	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs544400022	chr20:14965532-14965533	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs562952749	chr20:14965583-14965584	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs113885813	chr20:14965587-14965588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs183923464	chr20:14965636-14965637	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:1412 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

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	chr20:14964000-14964400	Enhancers	HepG2	liver
7	chr20:14964200-14964600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr20:14964400-14964600	ZNF genes & repeats	A549	lung
9	chr20:14964400-14964600	Flanking Active TSS	HepG2	liver
10	chr20:14964600-14965200	Weak transcription	A549	lung
11	chr20:14964600-14965200	Enhancers	HepG2	liver
12	chr20:14964600-14966800	Enhancers	Fetal Intestine Large	intestine
13	chr20:14964600-14971600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr20:14964800-14967800	Enhancers	HUVEC	blood vessel
15	chr20:14965000-14965200	Weak transcription	Fetal Intestine Small	intestine
16	chr20:14965000-14965600	Enhancers	Stomach Mucosa	stomach
17	chr20:14965000-14968000	Enhancers	Liver	Liver
18	chr20:14965200-14965600	Enhancers	A549	lung
19	chr20:14965200-14965800	Flanking Active TSS	HepG2	liver
20	chr20:14965200-14966000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr20:14965200-14967200	Enhancers	Fetal Intestine Small	intestine
22	chr20:14965400-14966000	Enhancers	Duodenum Mucosa	Duodenum
23	chr20:14965400-14966800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr20:14965400-14967400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr20:14965400-14967600	Enhancers	Pancreas	Pancrea
26	chr20:14965400-14968000	Enhancers	Fetal Kidney	kidney
27	chr20:14965400-14968000	Enhancers	Hela-S3	cervix
28	chr20:14965600-14966000	Flanking Active TSS	Stomach Mucosa	stomach
29	chr20:14965600-14966200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr20:14965600-14966200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr20:14965600-14966200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr20:14965600-14966200	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr20:14965600-14966200	Flanking Active TSS	A549	lung
34	chr20:14965600-14966400	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr20:14965800-14966200	Enhancers	HepG2	liver
36	chr20:14965800-14966600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr20:14965800-14967200	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr20:14966000-14966200	Enhancers	Stomach Mucosa	stomach
39	chr20:14966000-14966400	Enhancers	Aorta	Aorta
40	chr20:14966000-14967200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr20:14966000-14967400	Enhancers	HMEC	breast
42	chr20:14966200-14966600	Enhancers	A549	lung
43	chr20:14966200-14966800	Flanking Active TSS	HepG2	liver
44	chr20:14966200-14967400	Weak transcription	Stomach Mucosa	stomach
45	chr20:14966400-14967000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr20:14966600-14966800	Flanking Active TSS	A549	lung
47	chr20:14966600-14967000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr20:14966600-14967000	Enhancers	Aorta	Aorta
49	chr20:14966600-14967400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr20:14966800-14967200	Active TSS	A549	lung

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