Variant report

Variant	nsv1066235
Chromosome Location	chr20:14173771-14389050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1613)
CpG islands
(count:550)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14318093-14318568	HepG2	liver:	n/a	n/a
2	ATF2	chr20:14318056-14318625	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr20:14318135-14318567	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14318094-14318593	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:14318117-14318567	GM12878	blood:	n/a	n/a
6	ATF3	chr20:14386986-14387654	A549	lung:	n/a	n/a
7	ATF3	chr20:14317954-14318560	A549	lung:	n/a	chr20:14318315-14318328 chr20:14318314-14318329
8	ATF3	chr20:14386976-14387666	A549	lung:	n/a	n/a
9	BACH1	chr20:14194646-14195061	H1-hESC	embryonic stem cell:	n/a	chr20:14194846-14194860
10	BACH1	chr20:14200766-14201092	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr20:14194690-14195019	K562	blood:	n/a	chr20:14194846-14194860
12	BATF	chr20:14213355-14213690	GM12878	blood:	n/a	n/a
13	BATF	chr20:14213283-14213671	GM12878	blood:	n/a	n/a
14	BATF	chr20:14382155-14382397	GM12878	blood:	n/a	chr20:14382255-14382266
15	BATF	chr20:14324408-14324687	GM12878	blood:	n/a	n/a
16	BCL11A	chr20:14382168-14382440	GM12878	blood:	n/a	n/a
17	BCL11A	chr20:14382174-14382393	GM12878	blood:	n/a	n/a
18	BCL3	chr20:14386841-14387786	A549	lung:	n/a	n/a
19	BCL3	chr20:14317905-14318638	A549	lung:	n/a	n/a
20	BCL3	chr20:14386930-14387690	A549	lung:	n/a	n/a
21	BCL3	chr20:14317682-14318646	A549	lung:	n/a	n/a
22	BHLHE40	chr20:14213326-14213653	GM12878	blood:	n/a	n/a
23	BHLHE40	chr20:14381953-14382520	GM12878	blood:	n/a	n/a
24	BHLHE40	chr20:14314339-14314730	GM12878	blood:	n/a	n/a
25	BHLHE40	chr20:14383566-14383621	GM12878	blood:	n/a	n/a
26	BHLHE40	chr20:14324311-14324686	GM12878	blood:	n/a	chr20:14324498-14324507 chr20:14324498-14324507
27	BRCA1	chr20:14318252-14318396	HepG2	liver:	n/a	n/a
28	BRCA1	chr20:14245586-14245671	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr20:14372151-14372272	HepG2	liver:	n/a	chr20:14372182-14372193
30	CEBPB	chr20:14215229-14215777	A549	lung:	n/a	n/a
31	CEBPB	chr20:14387170-14387554	A549	lung:	n/a	n/a
32	CEBPB	chr20:14318232-14318503	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr20:14318217-14318476	HepG2	liver:	n/a	n/a
34	CEBPB	chr20:14339388-14339598	HepG2	liver:	n/a	n/a
35	CEBPB	chr20:14260937-14261232	A549	lung:	n/a	chr20:14261071-14261082 chr20:14261072-14261081 chr20:14261072-14261081 chr20:14261072-14261081 chr20:14261072-14261081 chr20:14261070-14261081
36	CEBPB	chr20:14215339-14215664	A549	lung:	n/a	n/a
37	CEBPB	chr20:14269685-14269839	A549	lung:	n/a	n/a
38	CEBPB	chr20:14307461-14307689	A549	lung:	n/a	chr20:14307575-14307586
39	CEBPB	chr20:14215334-14215682	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr20:14260913-14261245	IMR90	lung:	n/a	chr20:14261071-14261082 chr20:14261072-14261081 chr20:14261072-14261081 chr20:14261072-14261081 chr20:14261072-14261081 chr20:14261070-14261081
41	CEBPB	chr20:14315804-14316095	A549	lung:	n/a	chr20:14315943-14315954 chr20:14315942-14315953
42	CEBPB	chr20:14342464-14342775	Hela-S3	cervix:	n/a	chr20:14342630-14342641 chr20:14342628-14342641
43	CEBPB	chr20:14318149-14318540	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr20:14308968-14309277	HepG2	liver:	n/a	chr20:14309135-14309148 chr20:14309137-14309146 chr20:14309135-14309146 chr20:14309136-14309147
45	CEBPB	chr20:14226059-14226423	HepG2	liver:	n/a	chr20:14226239-14226252 chr20:14226240-14226251 chr20:14226238-14226255
46	CEBPB	chr20:14215321-14215673	IMR90	lung:	n/a	n/a
47	CEBPB	chr20:14182865-14183115	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr20:14318156-14318511	HepG2	liver:	n/a	n/a
49	CEBPB	chr20:14373683-14373999	HepG2	liver:	n/a	chr20:14373829-14373840
50	CEBPB	chr20:14216006-14216480	IMR90	lung:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14318231-14318281	PFSK-1	brain:	n/a
2	chr20:14318231-14318281	PFSK-1	brain:	n/a
3	chr20:14318297-14318347	Caco-2	colon:	n/a
4	chr20:14318410-14318460	SK-N-MC	brain:	n/a
5	chr20:14318174-14318224	T-47D	breast:	n/a
6	chr20:14318297-14318347	CMK	blood:	n/a
7	chr20:14319035-14319085	HepG2	liver:	n/a
8	chr20:14318174-14318224	HCM	heart:	n/a
9	chr20:14318410-14318460	AoSMC	blood vessel:	n/a
10	chr20:14318231-14318281	HRE	kidney:	n/a
11	chr20:14318231-14318281	GM19239	blood:	n/a
12	chr20:14318398-14318448	BJ	skin:	n/a
13	chr20:14318410-14318460	GM12891	blood:	n/a
14	chr20:14307665-14307715	MCF10A-Er-Src	breast:	n/a
15	chr20:14319125-14319175	HepG2	liver:	n/a
16	chr20:14318152-14318202	GM12878	blood:	n/a
17	chr20:14318231-14318281	HEK293	kidney:	embryo
18	chr20:14318398-14318448	H1-hESC	embryonic stem cell:	embryo
19	chr20:14318174-14318224	HRCEpiC	kidney:	n/a
20	chr20:14319035-14319085	MCF10A-Er-Src	breast:	n/a
21	chr20:14319035-14319085	HEK293	kidney:	embryo
22	chr20:14318152-14318202	MCF10A-Er-Src	breast:	n/a
23	chr20:14319035-14319085	Jurkat	blood:	n/a
24	chr20:14307665-14307715	ProgFib	skin:	n/a
25	chr20:14307665-14307715	HCPEpiC	choroid plexus:	n/a
26	chr20:14318231-14318281	PrEC	prostate:	n/a
27	chr20:14318410-14318460	HIPEpiC	eye:	n/a
28	chr20:14318410-14318460	HPAEpiC	pulmonary alveolar:	n/a
29	chr20:14318398-14318448	K562	blood:	n/a
30	chr20:14307665-14307715	GM06990	blood:	n/a
31	chr20:14318231-14318281	SKMC	muscle:	n/a
32	chr20:14318410-14318460	NB4	blood:	n/a
33	chr20:14318152-14318202	SAEC	small airway:	n/a
34	chr20:14318174-14318224	AG04449	skin:	fetal
35	chr20:14307665-14307715	AG09319	gingival:	n/a
36	chr20:14318297-14318347	HIPEpiC	eye:	n/a
37	chr20:14318152-14318202	HAEpiC	amniotic membrane:	n/a
38	chr20:14318410-14318460	PrEC	prostate:	n/a
39	chr20:14318398-14318448	HIPEpiC	eye:	n/a
40	chr20:14318297-14318347	HAEpiC	amniotic membrane:	n/a
41	chr20:14318152-14318202	Caco-2	colon:	n/a
42	chr20:14318297-14318347	HCT-116	colon:	n/a
43	chr20:14319125-14319175	AG09309	skin:	n/a
44	chr20:14318410-14318460	HepG2	liver:	n/a
45	chr20:14318231-14318281	AG09319	gingival:	n/a
46	chr20:14319125-14319175	NT2-D1	testis:	n/a
47	chr20:14318174-14318224	Hela-S3	cervix:	n/a
48	chr20:14319035-14319085	GM06990	blood:	n/a
49	chr20:14318174-14318224	AG09309	skin:	n/a
50	chr20:14318398-14318448	AG09309	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14305353..14307056-chr20:14308528..14310326,2	MCF-7	breast:
2	chr20:14173827..14175153-chr20:14245201..14246183,6	MCF-7	breast:
3	chr20:14349761..14351392-chr20:14353398..14355373,2	K562	blood:
4	chr20:14170212..14170967-chr20:14245501..14246136,3	MCF-7	breast:
5	chr17:41399300..41401884-chr20:14313065..14316065,3	K562	blood:
6	chr20:14335576..14337791-chr20:15315333..15317078,2	MCF-7	breast:
7	chr20:14246857..14249567-chr20:14268278..14270770,2	K562	blood:
8	chr20:14175439..14177996-chr3:730394..733241,2	MCF-7	breast:
9	chr20:14174059..14174890-chr20:16741525..16742040,2	MCF-7	breast:
10	chr20:14305353..14307056-chr20:14308528..14310326,2	MCF-7	breast:
11	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
12	chr20:14199868..14203458-chr20:14204053..14207149,3	MCF-7	breast:
13	chr20:14173827..14175153-chr20:14245201..14246183,6	MCF-7	breast:
14	chr20:14314454..14317198-chr20:14325361..14327046,2	K562	blood:
15	chr20:14349761..14351392-chr20:14353398..14355373,2	K562	blood:
16	chr17:41400138..41401846-chr20:14313045..14314565,2	K562	blood:
17	chr20:14314454..14317198-chr20:14325361..14327046,2	K562	blood:
18	chr20:14246857..14249567-chr20:14268278..14270770,2	K562	blood:
19	chr20:14199868..14203458-chr20:14204053..14207149,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L2-3	chr20:14309568-14309973	NONHSAT078712
2	lnc-SEL1L2-3	chr20:14318050-14318260	NONHSAT078712
3	lnc-C20orf7-2	chr20:14203687-14203976	NONHSAT078711

No data

Variant related genes	Relation type
FLRT3	TF binding region
RN7SL864P	TF binding region
RNU6-228P	TF binding region
FLRT3	CpG island
RN7SL864P	CpG island
RNU6-228P	CpG island

Extended variants
information (count: 6064 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:6064 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553989244	chr20:14173780-14173781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567299166	chr20:14173879-14173880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190273534	chr20:14173993-14173994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117411140	chr20:14174050-14174051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370394092	chr20:14174056-14174057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373769457	chr20:14174065-14174066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568949970	chr20:14174076-14174077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575948553	chr20:14174117-14174118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544516606	chr20:14174126-14174127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558060680	chr20:14174194-14174195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115922158	chr20:14174228-14174229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540470638	chr20:14174259-14174260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560726806	chr20:14174266-14174267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529377408	chr20:14174267-14174268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543061078	chr20:14174278-14174279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181588940	chr20:14174309-14174310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113850551	chr20:14174321-14174322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73259200	chr20:14174339-14174340	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs75648273	chr20:14174340-14174341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537509285	chr20:14174350-14174351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565207889	chr20:14174356-14174357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76401763	chr20:14174374-14174375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537868650	chr20:14174396-14174397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6105222	chr20:14174431-14174432	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs141765024	chr20:14174437-14174438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549811703	chr20:14174625-14174626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576085665	chr20:14174682-14174683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569393108	chr20:14174703-14174704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538273552	chr20:14174787-14174788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539502974	chr20:14174811-14174812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7362987	chr20:14174898-14174899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185997187	chr20:14175036-14175037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567717308	chr20:14175061-14175062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117169208	chr20:14175088-14175089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577957726	chr20:14175097-14175098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6079347	chr20:14175117-14175118	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554075202	chr20:14175136-14175137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574149228	chr20:14175142-14175143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542771271	chr20:14175145-14175146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188848168	chr20:14175179-14175180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576584451	chr20:14175193-14175194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545466395	chr20:14175268-14175269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144858911	chr20:14175275-14175276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565272574	chr20:14175303-14175304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150088317	chr20:14175397-14175398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs80288067	chr20:14175410-14175411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6110190	chr20:14175481-14175482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551325844	chr20:14175500-14175501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6110191	chr20:14175579-14175580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6042579	chr20:14175596-14175597	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

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
Schizophrenia	23813976	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1355 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14169400-14174400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr20:14169600-14175000	Weak transcription	Brain Substantia Nigra	brain
3	chr20:14170000-14174600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr20:14170800-14175000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr20:14172400-14177200	Weak transcription	HMEC	breast
6	chr20:14174000-14174600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr20:14174400-14175000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr20:14174400-14175400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:14174600-14176000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr20:14174800-14175000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr20:14174800-14175000	Enhancers	Fetal Intestine Small	intestine
12	chr20:14174800-14175000	Enhancers	Spleen	Spleen
13	chr20:14174800-14175400	Enhancers	Lung	lung
14	chr20:14175000-14175200	Enhancers	HSMMtube	muscle
15	chr20:14175000-14175400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr20:14175000-14175400	Enhancers	Brain Substantia Nigra	brain
17	chr20:14175000-14175400	Enhancers	Stomach Mucosa	stomach
18	chr20:14175000-14175600	Enhancers	Brain Angular Gyrus	brain
19	chr20:14175000-14175800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr20:14175000-14179600	Weak transcription	Fetal Intestine Small	intestine
21	chr20:14175200-14175400	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr20:14175200-14176000	Weak transcription	Spleen	Spleen
23	chr20:14175200-14176000	Weak transcription	HSMMtube	muscle
24	chr20:14175200-14177000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr20:14175400-14175800	Weak transcription	Lung	lung
26	chr20:14175400-14177200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr20:14175400-14179000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr20:14175800-14176200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr20:14175800-14176200	Enhancers	Lung	lung
30	chr20:14175800-14176400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr20:14176000-14176200	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr20:14176000-14176400	Enhancers	Gastric	stomach
33	chr20:14176000-14176400	Enhancers	Spleen	Spleen
34	chr20:14176000-14177200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr20:14176000-14177800	Enhancers	HSMMtube	muscle
36	chr20:14176200-14177000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr20:14176200-14178800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr20:14176600-14176800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr20:14176600-14178000	Enhancers	Fetal Stomach	stomach
40	chr20:14176600-14178800	Enhancers	NHLF	lung
41	chr20:14176600-14179400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr20:14176800-14177200	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr20:14176800-14177800	Enhancers	Fetal Heart	heart
44	chr20:14176800-14177800	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr20:14176800-14177800	Enhancers	HSMM	muscle
46	chr20:14176800-14178800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr20:14176800-14178800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr20:14176800-14179000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr20:14176800-14184400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr20:14177000-14177400	Enhancers	Adipose Nuclei	Adipose

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