Variant report

Variant	nsv1065105
Chromosome Location	chr20:1560775-1598990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
2	CEBPB	chr20:1596225-1596242	HepG2	liver:	n/a	n/a
3	CTCF	chr20:1569820-1569970	GM12878	blood:	n/a	n/a
4	CTCF	chr20:1569820-1569970	HEEpiC	esophagus:	n/a	n/a
5	CTCF	chr20:1569820-1569970	HCT-116	colon:	n/a	n/a
6	CTCF	chr20:1569890-1569986	ProgFib	skin:	n/a	n/a
7	CTCF	chr20:1583950-1584135	GM12878	blood:	n/a	chr20:1583996-1584006
8	CTCF	chr20:1569812-1570027	Gliobla	brain:	n/a	n/a
9	CTCF	chr20:1569800-1569950	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr20:1562336-1562338	Gliobla	brain:	n/a	n/a
11	CTCF	chr20:1569800-1569950	GM12864	blood:	n/a	n/a
12	CTCF	chr20:1569840-1569990	HAc	cerebellar:	n/a	n/a
13	CTCF	chr20:1569860-1570007	GM12878	blood:	n/a	n/a
14	CTCF	chr20:1562180-1562330	GM12875	blood:	n/a	n/a
15	CTCF	chr20:1569820-1569970	AG10803	skin:	n/a	n/a
16	CTCF	chr20:1569780-1569930	SAEC	small airway:	n/a	n/a
17	CTCF	chr20:1562235-1562365	GM13977	blood:	n/a	n/a
18	CTCF	chr20:1569900-1570050	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr20:1569840-1569990	HRE	kidney:	n/a	n/a
20	CTCF	chr20:1583918-1584066	GM12878	blood:	n/a	chr20:1583996-1584006
21	CTCF	chr20:1583954-1584054	GM19239	blood:	n/a	chr20:1583996-1584006
22	CTCF	chr20:1585205-1585266	GM10248	blood:	n/a	n/a
23	CTCF	chr20:1562140-1562290	GM12864	blood:	n/a	n/a
24	CTCF	chr20:1594081-1594153	LNCaP	prostate:	n/a	n/a
25	CTCF	chr20:1569840-1569990	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr20:1595313-1595408	GM12878	blood:	n/a	n/a
27	CTCF	chr20:1583974-1584038	GM10266	blood:	n/a	chr20:1583996-1584006
28	CTCF	chr20:1589816-1589866	NHEK	skin:	n/a	n/a
29	CTCF	chr20:1562218-1562407	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr20:1595316-1595438	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr20:1569840-1569990	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr20:1583938-1584013	HUVEC	blood vessel:	n/a	chr20:1583996-1584006
33	CTCF	chr20:1569768-1570055	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr20:1569809-1569981	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr20:1562180-1562330	GM12878	blood:	n/a	n/a
36	CTCF	chr20:1593027-1593071	K562	blood:	n/a	n/a
37	CTCF	chr20:1569844-1569973	GM12878	blood:	n/a	n/a
38	CTCF	chr20:1583993-1584014	H1-hESC	embryonic stem cell:	n/a	chr20:1583996-1584006
39	CTCF	chr20:1583923-1584071	GM12891	blood:	n/a	chr20:1583996-1584006
40	CTCF	chr20:1569860-1570010	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr20:1569880-1570030	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr20:1562235-1562401	GM12878	blood:	n/a	n/a
43	CTCF	chr20:1569840-1569990	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr20:1562236-1562335	Gliobla	brain:	n/a	n/a
45	CTCF	chr20:1569782-1570019	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr20:1569820-1569970	HRE	kidney:	n/a	n/a
47	E2F4	chr20:1596569-1596779	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr20:1575968-1576160	GM12878	blood:	n/a	n/a
49	EBF1	chr20:1576059-1576210	GM12878	blood:	n/a	n/a
50	ELF1	chr20:1575954-1576254	GM12878	blood:	n/a	chr20:1576167-1576178

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1578550-1578600	H1-hESC	embryonic stem cell:	embryo
2	chr20:1578550-1578600	IMR90	lung:	fetal
3	chr20:1578550-1578600	HPAEpiC	pulmonary alveolar:	n/a
4	chr20:1578550-1578600	K562	blood:	n/a
5	chr20:1578550-1578600	SK-N-SH_RA	brain:	n/a
6	chr20:1578550-1578600	HL-60	blood:	n/a
7	chr20:1578550-1578600	MCF-7	breast:	n/a
8	chr20:1578550-1578600	LNCaP	prostate:	n/a
9	chr20:1578550-1578600	HCM	heart:	n/a
10	chr20:1578550-1578600	Caco-2	colon:	n/a
11	chr20:1578550-1578600	MCF10A-Er-Src	breast:	n/a
12	chr20:1578550-1578600	GM12878	blood:	n/a
13	chr20:1578550-1578600	HEEpiC	esophagus:	n/a
14	chr20:1578550-1578600	NH-A	brain:	n/a
15	chr20:1578550-1578600	HCPEpiC	choroid plexus:	n/a
16	chr20:1578550-1578600	PrEC	prostate:	n/a
17	chr20:1578550-1578600	AoSMC	blood vessel:	n/a
18	chr20:1578550-1578600	AG09309	skin:	n/a
19	chr20:1578550-1578600	AG04449	skin:	fetal
20	chr20:1578550-1578600	ECC-1	luminal epithelium:	n/a
21	chr20:1578550-1578600	AG04450	lung:	fetal
22	chr20:1578550-1578600	NHBE	bronchial:	n/a
23	chr20:1578550-1578600	HUVEC	blood vessel:	n/a
24	chr20:1578550-1578600	HRCEpiC	kidney:	n/a
25	chr20:1578550-1578600	HRE	kidney:	n/a
26	chr20:1578550-1578600	HCF	heart:	n/a
27	chr20:1578550-1578600	GM19239	blood:	n/a
28	chr20:1578550-1578600	HCT-116	colon:	n/a
29	chr20:1578550-1578600	HEK293	kidney:	embryo
30	chr20:1578550-1578600	CMK	blood:	n/a
31	chr20:1578550-1578600	U87	brain:	n/a
32	chr20:1578550-1578600	NHDF-neo	bronchial:	n/a
33	chr20:1578550-1578600	T-47D	breast:	n/a
34	chr20:1578550-1578600	Jurkat	blood:	n/a
35	chr20:1578550-1578600	SK-N-MC	brain:	n/a
36	chr20:1578550-1578600	HRPEpiC	eye:	n/a
37	chr20:1578550-1578600	Hepatocyte	liver:	n/a
38	chr20:1578550-1578600	SKMC	muscle:	n/a
39	chr20:1578550-1578600	RPTEC	kidney:	n/a
40	chr20:1578550-1578600	BJ	skin:	n/a
41	chr20:1578550-1578600	HIPEpiC	eye:	n/a
42	chr20:1578550-1578600	A549	lung:	n/a
43	chr20:1578550-1578600	GM12892	blood:	n/a
44	chr20:1578550-1578600	ovcar-3	ovarian:	n/a
45	chr20:1578550-1578600	HepG2	liver:	n/a
46	chr20:1578550-1578600	NT2-D1	testis:	n/a
47	chr20:1578550-1578600	NB4	blood:	n/a
48	chr20:1578550-1578600	PFSK-1	brain:	n/a
49	chr20:1578550-1578600	Hela-S3	cervix:	n/a
50	chr20:1578550-1578600	ProgFib	skin:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-5	chr20:1574682-1577118	ucscGeneNc_uc002wfp_1
2	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
3	lnc-SNPH-5	chr20:1562154-1562366	ucscGeneNc_uc002wfp_1
4	lnc-SNPH-4	chr20:1572038-1572494	NONHSAT078121

No data

Variant related genes	Relation type
SIRPB1	TF binding region
ENSG00000260861	TF binding region
ENSG00000271523	TF binding region
SIRPB1	CpG island
ENSG00000260861	CpG island
ENSG00000271523	CpG island

Extended variants
information (count: 694 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536641413	chr20:1560841-1560842	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555050595	chr20:1560854-1560855	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570007072	chr20:1560861-1560862	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537561902	chr20:1560865-1560866	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142258849	chr20:1560882-1560883	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs55650624	chr20:1560892-1560893	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570375321	chr20:1560901-1560902	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577391168	chr20:1560922-1560923	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190616424	chr20:1560959-1560960	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138828516	chr20:1560969-1560970	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535767897	chr20:1560991-1560992	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370795741	chr20:1560992-1560993	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574833675	chr20:1561026-1561027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181712459	chr20:1561073-1561074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185626126	chr20:1561076-1561077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374198835	chr20:1561089-1561090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190143345	chr20:1561186-1561187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564859575	chr20:1561189-1561190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs66737734	chr20:1561205-1561206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182742303	chr20:1561212-1561213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
21	rs547656371	chr20:1561220-1561221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2746604	chr20:1561224-1561225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
23	rs11087121	chr20:1561257-1561258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
24	rs12480823	chr20:1561284-1561285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs12480824	chr20:1561286-1561287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
26	rs548562487	chr20:1561337-1561338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570049448	chr20:1561338-1561339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12479784	chr20:1561339-1561340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs12479785	chr20:1561369-1561370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs12479793	chr20:1561418-1561419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75732437	chr20:1561427-1561428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77190014	chr20:1561440-1561441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184041442	chr20:1561559-1561560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570890440	chr20:1561649-1561650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112994906	chr20:1561655-1561656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112397436	chr20:1561681-1561682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs112944697	chr20:1561717-1561718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
38	rs2746605	chr20:1561776-1561777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
39	rs2746606	chr20:1561879-1561880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2746607	chr20:1561932-1561933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs2746608	chr20:1562043-1562044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs2746609	chr20:1562047-1562048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs187449616	chr20:1562067-1562068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191540587	chr20:1562197-1562198	Weak transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
45	rs184795249	chr20:1562353-1562354	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs535752372	chr20:1562435-1562436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113355567	chr20:1562456-1562457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149462786	chr20:1562749-1562750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34992319	chr20:1562775-1562776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576008711	chr20:1562809-1562810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
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
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr20:1550000-1568200	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr20:1552400-1568000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr20:1552600-1569000	Weak transcription	Spleen	Spleen
6	chr20:1560000-1561000	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr20:1560000-1561000	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr20:1560000-1579200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr20:1560400-1561800	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr20:1560600-1561000	Strong transcription	Primary T cells from cord blood	blood
11	chr20:1561000-1562600	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr20:1561000-1563600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr20:1561000-1568000	Weak transcription	Primary T cells from cord blood	blood
14	chr20:1561800-1563800	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr20:1563600-1564600	Genic enhancers	Primary monocytes fromperipheralblood	blood
16	chr20:1563800-1565400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr20:1564600-1565400	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr20:1565400-1565600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr20:1565400-1566000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr20:1565600-1565800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
21	chr20:1565800-1567000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr20:1566000-1566600	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr20:1566600-1568400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr20:1567000-1569400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
25	chr20:1567600-1570000	Active TSS	Primary B cells from cord blood	blood
26	chr20:1567800-1569600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr20:1568000-1569000	Enhancers	Primary T cells from cord blood	blood
28	chr20:1568000-1570200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr20:1568000-1570200	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr20:1568000-1570400	Enhancers	Primary T cells fromperipheralblood	blood
31	chr20:1568200-1568800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr20:1568200-1569800	Enhancers	Primary B cells from peripheral blood	blood
33	chr20:1568400-1568600	Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr20:1568400-1569400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr20:1568400-1570200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr20:1568400-1570600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr20:1568600-1568800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr20:1568600-1568800	Enhancers	NHDF-Ad	bronchial
39	chr20:1568600-1569000	Enhancers	Dnd41	blood
40	chr20:1568600-1570200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr20:1568600-1570400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr20:1568800-1569000	Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr20:1568800-1570200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr20:1568800-1570200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr20:1569000-1569200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr20:1569000-1569200	Flanking Active TSS	Dnd41	blood
47	chr20:1569000-1569400	Flanking Active TSS	Primary T cells from cord blood	blood
48	chr20:1569000-1569400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr20:1569000-1569800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr20:1569000-1569800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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