Variant report

Variant	nsv524920
Chromosome Location	chr20:24639916-24683554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr20:24654325-24654708	A549	lung:	n/a	n/a
2	CEBPB	chr20:24654216-24654750	A549	lung:	n/a	chr20:24654273-24654286
3	CEBPB	chr20:24654123-24654740	IMR90	lung:	n/a	chr20:24654273-24654286
4	CEBPB	chr20:24676202-24676506	IMR90	lung:	n/a	chr20:24676333-24676344 chr20:24676332-24676349 chr20:24676334-24676345 chr20:24676333-24676346 chr20:24676335-24676344
5	CEBPB	chr20:24676194-24676523	HepG2	liver:	n/a	chr20:24676333-24676344 chr20:24676332-24676349 chr20:24676334-24676345 chr20:24676333-24676346 chr20:24676335-24676344
6	CEBPB	chr20:24676162-24676507	A549	lung:	n/a	chr20:24676333-24676344 chr20:24676332-24676349 chr20:24676334-24676345 chr20:24676333-24676346 chr20:24676335-24676344
7	CEBPB	chr20:24671540-24671663	HepG2	liver:	n/a	n/a
8	CEBPB	chr20:24675731-24676542	MCF-7	breast:	n/a	chr20:24676333-24676344 chr20:24676332-24676349 chr20:24676334-24676345 chr20:24676333-24676346 chr20:24675893-24675906 chr20:24676335-24676344
9	CTCF	chr20:24658360-24658510	GM12865	blood:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
10	CTCF	chr20:24653860-24654010	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr20:24654420-24654570	HMF	breast:	n/a	n/a
12	CTCF	chr20:24666020-24666170	MCF-7	breast:	n/a	n/a
13	CTCF	chr20:24658416-24658522	GM12892	blood:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
14	CTCF	chr20:24654446-24654601	NHEK	skin:	n/a	n/a
15	CTCF	chr20:24666055-24666057	MCF-7	breast:	n/a	n/a
16	CTCF	chr20:24665885-24666334	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr20:24666040-24666190	HMEC	breast:	n/a	n/a
18	CTCF	chr20:24666000-24666150	HRE	kidney:	n/a	n/a
19	CTCF	chr20:24665960-24666110	HEK293	kidney:	n/a	n/a
20	CTCF	chr20:24658416-24658534	MCF-7	breast:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
21	CTCF	chr20:24653860-24654010	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr20:24665988-24666288	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr20:24658254-24658591	H1-hESC	embryonic stem cell:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
24	CTCF	chr20:24653060-24653210	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr20:24666159-24666243	K562	blood:	n/a	n/a
26	CTCF	chr20:24669273-24669334	Lung_OC	lung:	n/a	n/a
27	CTCF	chr20:24665940-24666090	HepG2	liver:	n/a	n/a
28	CTCF	chr20:24658402-24658555	H1-hESC	embryonic stem cell:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
29	CTCF	chr20:24665980-24666130	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr20:24658420-24658531	MCF-7	breast:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
31	CTCF	chr20:24658440-24658590	GM06990	blood:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
32	CTCF	chr20:24658433-24658502	MCF-7	breast:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
33	CTCF	chr20:24653500-24653650	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr20:24665950-24666365	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr20:24666040-24666190	GM12872	blood:	n/a	n/a
36	CTCF	chr20:24658400-24658550	HPF	lung:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
37	CTCF	chr20:24666100-24666250	BE2_C	brain:	n/a	n/a
38	CTCF	chr20:24658446-24658492	MCF-7	breast:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
39	CTCF	chr20:24665980-24666130	HRE	kidney:	n/a	n/a
40	CTCF	chr20:24653160-24653310	BJ	skin:	n/a	n/a
41	CTCF	chr20:24653800-24653950	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr20:24666060-24666210	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr20:24675987-24676043	MCF-7	breast:	n/a	n/a
44	CTCF	chr20:24658360-24658510	WERI-Rb-1	eye:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
45	CTCF	chr20:24666151-24666175	GM12878	blood:	n/a	n/a
46	CTCF	chr20:24666169-24666257	NHEK	skin:	n/a	n/a
47	CTCF	chr20:24658404-24658515	MCF-7	breast:	n/a	chr20:24658454-24658475 chr20:24658459-24658477
48	E2F4	chr20:24645619-24645804	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr20:24656921-24657149	GM12878	blood:	n/a	chr20:24657005-24657016 chr20:24657007-24657017 chr20:24657007-24657016 chr20:24657005-24657018
50	EP300	chr20:24653452-24653770	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:24646600-24646650	HIPEpiC	eye:	n/a
2	chr20:24646600-24646650	PFSK-1	brain:	n/a
3	chr20:24646600-24646650	GM12891	blood:	n/a
4	chr20:24646600-24646650	K562	blood:	n/a
5	chr20:24646600-24646650	HepG2	liver:	n/a
6	chr20:24646600-24646650	AoSMC	blood vessel:	n/a
7	chr20:24646600-24646650	T-47D	breast:	n/a
8	chr20:24646600-24646650	HRCEpiC	kidney:	n/a
9	chr20:24646600-24646650	AG10803	skin:	n/a
10	chr20:24646600-24646650	NHDF-neo	bronchial:	n/a
11	chr20:24646600-24646650	MCF-7	breast:	n/a
12	chr20:24646600-24646650	HPAEpiC	pulmonary alveolar:	n/a
13	chr20:24646600-24646650	SK-N-MC	brain:	n/a
14	chr20:24646600-24646650	GM06990	blood:	n/a
15	chr20:24646600-24646650	HMEC	breast:	n/a
16	chr20:24646600-24646650	U87	brain:	n/a
17	chr20:24646600-24646650	HAEpiC	amniotic membrane:	n/a
18	chr20:24646600-24646650	A549	lung:	n/a
19	chr20:24646600-24646650	HL-60	blood:	n/a
20	chr20:24646600-24646650	GM19239	blood:	n/a
21	chr20:24646600-24646650	NHBE	bronchial:	n/a
22	chr20:24646600-24646650	Caco-2	colon:	n/a
23	chr20:24646600-24646650	GM12878	blood:	n/a
24	chr20:24646600-24646650	NB4	blood:	n/a
25	chr20:24646600-24646650	HCT-116	colon:	n/a
26	chr20:24646600-24646650	NH-A	brain:	n/a
27	chr20:24646600-24646650	HEEpiC	esophagus:	n/a
28	chr20:24646600-24646650	PrEC	prostate:	n/a
29	chr20:24646600-24646650	GM12892	blood:	n/a
30	chr20:24646600-24646650	SAEC	small airway:	n/a
31	chr20:24646600-24646650	LNCaP	prostate:	n/a
32	chr20:24646600-24646650	AG09309	skin:	n/a
33	chr20:24646600-24646650	SKMC	muscle:	n/a
34	chr20:24646600-24646650	PANC-1	pancreas:	n/a
35	chr20:24646600-24646650	MCF10A-Er-Src	breast:	n/a
36	chr20:24646600-24646650	Jurkat	blood:	n/a
37	chr20:24646600-24646650	HCM	heart:	n/a
38	chr20:24646600-24646650	AG09319	gingival:	n/a
39	chr20:24646600-24646650	BJ	skin:	n/a
40	chr20:24646600-24646650	ECC-1	luminal epithelium:	n/a
41	chr20:24646600-24646650	HNPCEpiC	eye:	n/a
42	chr20:24646600-24646650	HCF	heart:	n/a
43	chr20:24646600-24646650	HCPEpiC	choroid plexus:	n/a
44	chr20:24646600-24646650	IMR90	lung:	fetal
45	chr20:24646600-24646650	HEK293	kidney:	embryo
46	chr20:24646600-24646650	Hepatocyte	liver:	n/a
47	chr20:24646600-24646650	ProgFib	skin:	n/a
48	chr20:24646600-24646650	ovcar-3	ovarian:	n/a
49	chr20:24646600-24646650	SK-N-SH_RA	brain:	n/a
50	chr20:24646600-24646650	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:24631399..24634097-chr20:24646074..24647990,2	MCF-7	breast:
2	chr20:24671696..24673797-chr20:24673883..24676356,3	MCF-7	breast:
3	chr20:24671696..24673797-chr20:24673883..24676356,3	MCF-7	breast:
4	chr20:24645518..24647041-chr20:24652515..24654778,2	MCF-7	breast:
5	chr20:24645110..24646856-chr20:24648654..24651485,2	MCF-7	breast:
6	chr20:24645518..24647041-chr20:24652515..24654778,2	MCF-7	breast:
7	chr20:24616131..24617827-chr20:24647064..24649863,2	MCF-7	breast:
8	chr20:24637159..24638708-chr20:24641343..24643289,2	K562	blood:
9	chr20:24651840..24653392-chr20:24727209..24728729,2	MCF-7	breast:
10	chr20:24671407..24673133-chr20:24673157..24675510,2	K562	blood:
11	chr20:24629731..24632578-chr20:24657556..24659618,3	MCF-7	breast:
12	chr20:24654225..24656073-chr20:24661737..24664471,2	MCF-7	breast:
13	chr20:24629448..24631960-chr20:24674530..24677062,2	MCF-7	breast:
14	chr20:24630261..24631279-chr20:24640264..24641332,21	MCF-7	breast:
15	chr20:24654225..24656073-chr20:24661737..24664471,2	MCF-7	breast:
16	chr20:24630253..24631426-chr20:24640312..24641216,7	MCF-7	breast:
17	chr20:24624340..24627189-chr20:24639641..24641542,2	MCF-7	breast:
18	chr20:24671407..24673133-chr20:24673157..24675510,2	K562	blood:
19	chr20:24645110..24646856-chr20:24648654..24651485,2	MCF-7	breast:
20	chr20:24630307..24631279-chr20:24640279..24641332,14	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SYNDIG1-1	chr20:24660183-24660300	XLOC_013498
2	lnc-SYNDIG1-1	chr20:24660941-24661627	XLOC_013498

Variant related genes	Relation type
ENSG00000231015	TF binding region
ENSG00000231015	CpG island

Extended variants
information (count: 2045 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2045 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6076248	chr20:24639916-24639917	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563605766	chr20:24639926-24639927	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs573281750	chr20:24639928-24639929	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs183447813	chr20:24639957-24639958	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs559645427	chr20:24640003-24640004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574987050	chr20:24640006-24640007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188946133	chr20:24640025-24640026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369628066	chr20:24640026-24640027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527642211	chr20:24640054-24640055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34645434	chr20:24640070-24640071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547499199	chr20:24640092-24640093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570580570	chr20:24640173-24640174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112475281	chr20:24640197-24640198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542347673	chr20:24640219-24640220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372334781	chr20:24640227-24640228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539670945	chr20:24640229-24640230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549945872	chr20:24640238-24640239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149646998	chr20:24640242-24640243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535770026	chr20:24640256-24640257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555978714	chr20:24640257-24640258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113199999	chr20:24640269-24640270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534578540	chr20:24640315-24640316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377306373	chr20:24640318-24640319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557910023	chr20:24640330-24640331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577792091	chr20:24640339-24640340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551878537	chr20:24640341-24640342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111775838	chr20:24640345-24640346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112477633	chr20:24640390-24640391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369916436	chr20:24640395-24640396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543678605	chr20:24640403-24640404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193060728	chr20:24640456-24640457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146147651	chr20:24640484-24640485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542562933	chr20:24640491-24640492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559562771	chr20:24640506-24640507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527705441	chr20:24640508-24640509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531310622	chr20:24640544-24640545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62215328	chr20:24640581-24640582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183806470	chr20:24640591-24640592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373388245	chr20:24640613-24640614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188360956	chr20:24640614-24640615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533242608	chr20:24640643-24640644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550008605	chr20:24640648-24640649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191690182	chr20:24640683-24640684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536004825	chr20:24640688-24640689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532417866	chr20:24640689-24640690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566334769	chr20:24640695-24640696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534632472	chr20:24640700-24640701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557773373	chr20:24640707-24640708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577855744	chr20:24640766-24640767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537142500	chr20:24640793-24640794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24620000-24641200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:24629200-24642600	Weak transcription	Right Atrium	heart
3	chr20:24629400-24641000	Weak transcription	Right Ventricle	heart
4	chr20:24634600-24648800	Weak transcription	Gastric	stomach
5	chr20:24637200-24641200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr20:24637400-24640200	Enhancers	Fetal Muscle Leg	muscle
7	chr20:24638400-24640000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr20:24638600-24640000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr20:24638600-24640400	Enhancers	Brain Hippocampus Middle	brain
10	chr20:24638600-24641600	Enhancers	Brain Substantia Nigra	brain
11	chr20:24638600-24643400	Weak transcription	Fetal Kidney	kidney
12	chr20:24639000-24650400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr20:24639200-24641400	Enhancers	Brain Anterior Caudate	brain
14	chr20:24639200-24648600	Weak transcription	Spleen	Spleen
15	chr20:24639400-24640600	Weak transcription	NH-A	brain
16	chr20:24639600-24640200	Enhancers	Brain Cingulate Gyrus	brain
17	chr20:24639600-24641600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr20:24639600-24641800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr20:24639800-24640200	Enhancers	Brain Angular Gyrus	brain
20	chr20:24639800-24640200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr20:24639800-24641000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr20:24640000-24640400	Enhancers	Fetal Muscle Trunk	muscle
23	chr20:24640200-24640400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr20:24640200-24643200	Weak transcription	Brain Angular Gyrus	brain
25	chr20:24640200-24643200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr20:24640400-24640800	Weak transcription	Brain Hippocampus Middle	brain
27	chr20:24640400-24641400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr20:24640400-24646000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr20:24640600-24640800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr20:24640600-24641200	Enhancers	NH-A	brain
31	chr20:24640800-24643600	Enhancers	Brain Hippocampus Middle	brain
32	chr20:24641000-24641200	Enhancers	Right Ventricle	heart
33	chr20:24641000-24641400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr20:24641000-24641600	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr20:24641200-24641400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr20:24641200-24641400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr20:24641200-24641600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr20:24641200-24641600	Weak transcription	Right Ventricle	heart
39	chr20:24641200-24654000	Weak transcription	Aorta	Aorta
40	chr20:24641400-24643000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr20:24641400-24645400	Weak transcription	Brain Anterior Caudate	brain
42	chr20:24641400-24649400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr20:24641600-24641800	Enhancers	Right Ventricle	heart
44	chr20:24641600-24643200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr20:24641600-24643200	Weak transcription	Brain Substantia Nigra	brain
46	chr20:24641600-24643400	Enhancers	Fetal Muscle Trunk	muscle
47	chr20:24641600-24646200	Enhancers	Fetal Muscle Leg	muscle
48	chr20:24641800-24649800	Weak transcription	Right Ventricle	heart
49	chr20:24642600-24642800	Bivalent Enhancer	HSMMtube	muscle
50	chr20:24642600-24643400	Enhancers	Right Atrium	heart

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