Variant report

Variant	nsv524921
Chromosome Location	chr20:24897355-24932028
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	ATF1	chr20:24929614-24929792	K562	blood:	n/a	n/a
2	ATF2	chr20:24898773-24899088	GM12878	blood:	n/a	n/a
3	BACH1	chr20:24911107-24911328	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr20:24910908-24911117	GM12878	blood:	n/a	n/a
5	BATF	chr20:24898693-24899015	GM12878	blood:	n/a	n/a
6	BCLAF1	chr20:24898684-24899060	GM12878	blood:	n/a	chr20:24899038-24899047 chr20:24898987-24899000 chr20:24899033-24899046 chr20:24898870-24898879
7	BHLHE40	chr20:24898924-24899241	K562	blood:	n/a	n/a
8	BHLHE40	chr20:24930500-24930689	K562	blood:	n/a	n/a
9	BRCA1	chr20:24898953-24899302	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr20:24899054-24899254	HepG2	liver:	n/a	n/a
11	CEBPB	chr20:24899513-24899862	HepG2	liver:	n/a	n/a
12	CEBPB	chr20:24899530-24899847	A549	lung:	n/a	n/a
13	CEBPB	chr20:24898819-24899284	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr20:24911081-24911323	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr20:24911058-24911415	MCF-7	breast:	n/a	n/a
16	CEBPB	chr20:24899521-24899836	IMR90	lung:	n/a	n/a
17	CEBPB	chr20:24911036-24911479	MCF-7	breast:	n/a	n/a
18	CHD2	chr20:24899022-24899314	GM12878	blood:	n/a	n/a
19	CHD2	chr20:24899030-24899279	HepG2	liver:	n/a	n/a
20	CHD2	chr20:24898985-24899212	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr20:24910937-24911101	GM12891	blood:	n/a	n/a
22	CTCF	chr20:24899100-24899250	HA-sp	spinal cord:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
23	CTCF	chr20:24911520-24911670	HRE	kidney:	n/a	n/a
24	CTCF	chr20:24911700-24911850	HCM	heart:	n/a	n/a
25	CTCF	chr20:24911820-24911970	NHEK	skin:	n/a	n/a
26	CTCF	chr20:24899100-24899250	HepG2	liver:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
27	CTCF	chr20:24911680-24911830	HL-60	blood:	n/a	n/a
28	CTCF	chr20:24911840-24911990	GM12878	blood:	n/a	n/a
29	CTCF	chr20:24911680-24911830	SAEC	small airway:	n/a	n/a
30	CTCF	chr20:24899100-24899250	HMF	breast:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
31	CTCF	chr20:24912142-24912243	GM19240	blood:	n/a	n/a
32	CTCF	chr20:24911752-24912044	K562	blood:	n/a	n/a
33	CTCF	chr20:24899100-24899250	GM12869	blood:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
34	CTCF	chr20:24911862-24911935	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr20:24899013-24899284	H1-hESC	embryonic stem cell:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
36	CTCF	chr20:24899060-24899210	HMF	breast:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
37	CTCF	chr20:24898995-24899280	ECC-1	luminal epithelium:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
38	CTCF	chr20:24899014-24899293	Fibrobl	skin:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
39	CTCF	chr20:24910900-24911050	MCF-7	breast:	n/a	n/a
40	CTCF	chr20:24911700-24911850	HCFaa	heart:	n/a	n/a
41	CTCF	chr20:24899080-24899230	GM12868	blood:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
42	CTCF	chr20:24899160-24899310	HCM	heart:	n/a	n/a
43	CTCF	chr20:24930340-24930490	GM12874	blood:	n/a	chr20:24930366-24930379
44	CTCF	chr20:24899500-24899650	GM12866	blood:	n/a	chr20:24899596-24899605 chr20:24899596-24899609
45	CTCF	chr20:24911802-24911982	GM10248	blood:	n/a	n/a
46	CTCF	chr20:24899031-24899273	GM10248	blood:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161
47	CTCF	chr20:24911820-24911970	HCT-116	colon:	n/a	n/a
48	CTCF	chr20:24911440-24911590	AG09319	gingival:	n/a	n/a
49	CTCF	chr20:24899160-24899310	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr20:24899100-24899250	GM12874	blood:	n/a	chr20:24899146-24899162 chr20:24899147-24899160 chr20:24899145-24899163 chr20:24899140-24899161

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:24929687-24929737	AG04449	skin:	fetal
2	chr20:24929687-24929737	AG04449	skin:	fetal
3	chr20:24899180-24899230	NHBE	bronchial:	n/a
4	chr20:24929822-24929872	GM06990	blood:	n/a
5	chr20:24929687-24929737	NH-A	brain:	n/a
6	chr20:24929716-24929766	PANC-1	pancreas:	n/a
7	chr20:24929687-24929737	Jurkat	blood:	n/a
8	chr20:24899180-24899230	GM06990	blood:	n/a
9	chr20:24929695-24929745	AoSMC	blood vessel:	n/a
10	chr20:24929716-24929766	HAEpiC	amniotic membrane:	n/a
11	chr20:24898631-24898681	ProgFib	skin:	n/a
12	chr20:24898990-24899040	NHDF-neo	bronchial:	n/a
13	chr20:24929822-24929872	PFSK-1	brain:	n/a
14	chr20:24898990-24899040	BE2_C	brain:	n/a
15	chr20:24929687-24929737	HIPEpiC	eye:	n/a
16	chr20:24898990-24899040	NHBE	bronchial:	n/a
17	chr20:24929822-24929872	HCF	heart:	n/a
18	chr20:24930099-24930149	HCT-116	colon:	n/a
19	chr20:24929607-24929657	NT2-D1	testis:	n/a
20	chr20:24929687-24929737	U87	brain:	n/a
21	chr20:24898990-24899040	AG10803	skin:	n/a
22	chr20:24929695-24929745	T-47D	breast:	n/a
23	chr20:24929607-24929657	T-47D	breast:	n/a
24	chr20:24929822-24929872	PANC-1	pancreas:	n/a
25	chr20:24899180-24899230	RPTEC	kidney:	n/a
26	chr20:24930099-24930149	AG04449	skin:	fetal
27	chr20:24929687-24929737	GM12891	blood:	n/a
28	chr20:24929695-24929745	ECC-1	luminal epithelium:	n/a
29	chr20:24929716-24929766	ovcar-3	ovarian:	n/a
30	chr20:24898631-24898681	U87	brain:	n/a
31	chr20:24929607-24929657	Caco-2	colon:	n/a
32	chr20:24898631-24898681	PANC-1	pancreas:	n/a
33	chr20:24929607-24929657	SKMC	muscle:	n/a
34	chr20:24929687-24929737	HAEpiC	amniotic membrane:	n/a
35	chr20:24899048-24899098	HPAEpiC	pulmonary alveolar:	n/a
36	chr20:24899048-24899098	PANC-1	pancreas:	n/a
37	chr20:24899048-24899098	HMEC	breast:	n/a
38	chr20:24898631-24898681	HPAEpiC	pulmonary alveolar:	n/a
39	chr20:24929695-24929745	ovcar-3	ovarian:	n/a
40	chr20:24898631-24898681	Caco-2	colon:	n/a
41	chr20:24930099-24930149	HAEpiC	amniotic membrane:	n/a
42	chr20:24898990-24899040	T-47D	breast:	n/a
43	chr20:24898990-24899040	NH-A	brain:	n/a
44	chr20:24898631-24898681	HCT-116	colon:	n/a
45	chr20:24930099-24930149	PrEC	prostate:	n/a
46	chr20:24929822-24929872	HRE	kidney:	n/a
47	chr20:24899180-24899230	HCF	heart:	n/a
48	chr20:24929695-24929745	HRPEpiC	eye:	n/a
49	chr20:24929716-24929766	HIPEpiC	eye:	n/a
50	chr20:24898990-24899040	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:24909343..24912693-chr20:24913170..24916017,4	MCF-7	breast:
2	chr20:24764889..24765421-chr20:24919390..24920112,2	MCF-7	breast:
3	chr20:24912941..24914562-chr20:24924394..24926104,2	MCF-7	breast:
4	chr20:24763298..24765600-chr20:24898179..24900035,23	MCF-7	breast:
5	chr20:24764506..24765162-chr20:24897617..24898498,2	MCF-7	breast:
6	chr20:24814781..24815580-chr20:24898686..24899395,4	MCF-7	breast:
7	chr20:24914670..24916704-chr20:24919775..24921335,2	MCF-7	breast:
8	chr20:24909343..24912693-chr20:24913170..24916017,4	MCF-7	breast:
9	chr20:24914670..24916704-chr20:24919775..24921335,2	MCF-7	breast:
10	chr20:24910467..24912747-chr20:24972358..24974415,2	MCF-7	breast:
11	chr20:24912941..24914562-chr20:24924394..24926104,2	MCF-7	breast:
12	chr20:24892772..24894924-chr20:24896880..24898878,2	MCF-7	breast:
13	chr20:24771465..24772208-chr20:24898686..24899202,2	MCF-7	breast:
14	chr20:24914439..24915971-chr20:24971852..24973942,2	MCF-7	breast:
15	chr20:24887755..24889606-chr20:24897276..24899425,2	K562	blood:
16	chr20:24764501..24765530-chr20:24898693..24899347,4	MCF-7	breast:
17	chr20:24283582..24284398-chr20:24898678..24899422,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf3-1	chr20:24913047-24913619	ENSG00000250527
2	lnc-C20orf3-1	chr20:24911284-24912866	ENSG00000250527

Variant related genes	Relation type
CST7	TF binding region
CST7	CpG island
ENSG00000101474	chromatin interactions
YOD1	miRNA target sites
ZNF148	miRNA target sites

Extended variants
information (count: 1640 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs914314	chr20:24897355-24897356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113702908	chr20:24897367-24897368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6050126	chr20:24897406-24897407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs570848918	chr20:24897447-24897448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374839222	chr20:24897457-24897458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533415837	chr20:24897477-24897478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367844347	chr20:24897523-24897524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550072220	chr20:24897526-24897527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529317750	chr20:24897537-24897538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569908034	chr20:24897568-24897569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368919216	chr20:24897614-24897615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs944503	chr20:24897626-24897627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs568892720	chr20:24897713-24897714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs914315	chr20:24897716-24897717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs191053154	chr20:24897747-24897748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182202259	chr20:24897751-24897752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557421271	chr20:24897757-24897758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73341267	chr20:24897775-24897776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187925310	chr20:24897844-24897845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557338967	chr20:24897880-24897881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573859446	chr20:24897881-24897882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4502500	chr20:24897897-24897898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs56183883	chr20:24897942-24897943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111932920	chr20:24897959-24897960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6050127	chr20:24897960-24897961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs564284176	chr20:24897973-24897974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140862486	chr20:24898005-24898006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555949136	chr20:24898054-24898055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199747553	chr20:24898116-24898117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs885401	chr20:24898130-24898131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144820696	chr20:24898150-24898151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374420124	chr20:24898198-24898199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567881910	chr20:24898210-24898211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368257512	chr20:24898229-24898230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6050128	chr20:24898235-24898236	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529555034	chr20:24898257-24898258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549280224	chr20:24898298-24898299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138586006	chr20:24898331-24898332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75353095	chr20:24898378-24898379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557128289	chr20:24898385-24898386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575156801	chr20:24898418-24898419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557874244	chr20:24898471-24898472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6050129	chr20:24898485-24898486	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs149331125	chr20:24898493-24898494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557277760	chr20:24898539-24898540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573947206	chr20:24898556-24898557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536573828	chr20:24898579-24898580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79713279	chr20:24898654-24898655	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs6083679	chr20:24898657-24898658	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs556288960	chr20:24898681-24898682	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Oral cancer	21386901	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24892600-24898600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr20:24894000-24898400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:24895800-24898400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr20:24898000-24899600	Enhancers	Brain Hippocampus Middle	brain
5	chr20:24898400-24899800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr20:24898400-24900600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr20:24898600-24898800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr20:24898600-24898800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr20:24898600-24898800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr20:24898600-24898800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr20:24898600-24899000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr20:24898600-24899000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
13	chr20:24898600-24899200	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr20:24898600-24899600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr20:24898600-24899600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr20:24898600-24899800	Enhancers	Fetal Lung	lung
17	chr20:24898600-24899800	Bivalent Enhancer	Fetal Stomach	stomach
18	chr20:24898600-24899800	Enhancers	GM12878-XiMat	blood
19	chr20:24898600-24900000	Enhancers	Adipose Nuclei	Adipose
20	chr20:24898600-24901400	Enhancers	Placenta	Placenta
21	chr20:24898800-24899000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr20:24898800-24899000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr20:24898800-24899000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr20:24898800-24899000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr20:24898800-24899000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
26	chr20:24898800-24899200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr20:24898800-24899200	Enhancers	Primary B cells from peripheral blood	blood
28	chr20:24898800-24899200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr20:24898800-24899200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr20:24898800-24899200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr20:24898800-24899200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr20:24898800-24899200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr20:24898800-24899200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
34	chr20:24898800-24899200	Active TSS	Rectal Mucosa Donor 31	rectum
35	chr20:24898800-24899200	Bivalent/Poised TSS	HepG2	liver
36	chr20:24898800-24899400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr20:24898800-24899400	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr20:24898800-24899400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr20:24898800-24899400	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr20:24898800-24899400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
41	chr20:24898800-24899400	Enhancers	Fetal Brain Female	brain
42	chr20:24898800-24899600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr20:24898800-24899600	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr20:24898800-24899600	Enhancers	Brain Angular Gyrus	brain
45	chr20:24898800-24899600	Enhancers	Fetal Brain Male	brain
46	chr20:24898800-24899600	Flanking Active TSS	Stomach Smooth Muscle	stomach
47	chr20:24898800-24899600	Enhancers	Thymus	Thymus
48	chr20:24898800-24899600	Enhancers	HSMM	muscle
49	chr20:24898800-24899600	Bivalent Enhancer	Osteobl	bone
50	chr20:24898800-24899800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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