Variant report

Variant	nsv1067242
Chromosome Location	chr20:1567994-1599142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:101)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:101 , 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	chr20:1569860-1570010	HEEpiC	esophagus:	n/a	n/a
4	CTCF	chr20:1594081-1594153	LNCaP	prostate:	n/a	n/a
5	CTCF	chr20:1589816-1589866	NHEK	skin:	n/a	n/a
6	CTCF	chr20:1583923-1584071	GM12891	blood:	n/a	chr20:1583996-1584006
7	CTCF	chr20:1569820-1569970	AG10803	skin:	n/a	n/a
8	CTCF	chr20:1569840-1569990	HRE	kidney:	n/a	n/a
9	CTCF	chr20:1569809-1569981	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr20:1569844-1569973	GM12878	blood:	n/a	n/a
11	CTCF	chr20:1569840-1569990	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr20:1583938-1584013	HUVEC	blood vessel:	n/a	chr20:1583996-1584006
13	CTCF	chr20:1593027-1593071	K562	blood:	n/a	n/a
14	CTCF	chr20:1595313-1595408	GM12878	blood:	n/a	n/a
15	CTCF	chr20:1583950-1584135	GM12878	blood:	n/a	chr20:1583996-1584006
16	CTCF	chr20:1583918-1584066	GM12878	blood:	n/a	chr20:1583996-1584006
17	CTCF	chr20:1569800-1569950	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr20:1569800-1569950	GM12864	blood:	n/a	n/a
19	CTCF	chr20:1569860-1570007	GM12878	blood:	n/a	n/a
20	CTCF	chr20:1583974-1584038	GM10266	blood:	n/a	chr20:1583996-1584006
21	CTCF	chr20:1569782-1570019	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr20:1569820-1569970	HCT-116	colon:	n/a	n/a
23	CTCF	chr20:1569812-1570027	Gliobla	brain:	n/a	n/a
24	CTCF	chr20:1569780-1569930	SAEC	small airway:	n/a	n/a
25	CTCF	chr20:1595316-1595438	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr20:1569890-1569986	ProgFib	skin:	n/a	n/a
27	CTCF	chr20:1569768-1570055	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr20:1585205-1585266	GM10248	blood:	n/a	n/a
29	CTCF	chr20:1583993-1584014	H1-hESC	embryonic stem cell:	n/a	chr20:1583996-1584006
30	CTCF	chr20:1569900-1570050	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr20:1569840-1569990	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr20:1569880-1570030	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr20:1569840-1569990	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr20:1583954-1584054	GM19239	blood:	n/a	chr20:1583996-1584006
35	CTCF	chr20:1569820-1569970	GM12878	blood:	n/a	n/a
36	CTCF	chr20:1569820-1569970	HRE	kidney:	n/a	n/a
37	CTCF	chr20:1569820-1569970	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr20:1569840-1569990	HAc	cerebellar:	n/a	n/a
39	E2F4	chr20:1596569-1596779	MCF10A-Er-Src	breast:	n/a	n/a
40	EBF1	chr20:1576059-1576210	GM12878	blood:	n/a	n/a
41	EBF1	chr20:1575968-1576160	GM12878	blood:	n/a	n/a
42	ELF1	chr20:1575954-1576254	GM12878	blood:	n/a	chr20:1576167-1576178
43	EP300	chr20:1597685-1598216	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr20:1597667-1598072	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr20:1597694-1598043	Hela-S3	cervix:	n/a	n/a
46	FOS	chr20:1597654-1598180	HUVEC	blood vessel:	n/a	n/a
47	GATA2	chr20:1597568-1598284	HUVEC	blood vessel:	n/a	n/a
48	GATA3	chr20:1597872-1598067	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr20:1597682-1598321	SK-N-SH	brain:	n/a	n/a
50	GATA3	chr20:1597619-1598351	SK-N-SH	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1578550-1578600	ovcar-3	ovarian:	n/a
2	chr20:1578550-1578600	SKMC	muscle:	n/a
3	chr20:1578550-1578600	NT2-D1	testis:	n/a
4	chr20:1578550-1578600	HNPCEpiC	eye:	n/a
5	chr20:1578550-1578600	MCF10A-Er-Src	breast:	n/a
6	chr20:1578550-1578600	HL-60	blood:	n/a
7	chr20:1578550-1578600	AoSMC	blood vessel:	n/a
8	chr20:1578550-1578600	BJ	skin:	n/a
9	chr20:1578550-1578600	HIPEpiC	eye:	n/a
10	chr20:1578550-1578600	HRCEpiC	kidney:	n/a
11	chr20:1578550-1578600	IMR90	lung:	fetal
12	chr20:1578550-1578600	NHDF-neo	bronchial:	n/a
13	chr20:1578550-1578600	PrEC	prostate:	n/a
14	chr20:1578550-1578600	A549	lung:	n/a
15	chr20:1578550-1578600	K562	blood:	n/a
16	chr20:1578550-1578600	PFSK-1	brain:	n/a
17	chr20:1578550-1578600	Caco-2	colon:	n/a
18	chr20:1578550-1578600	HMEC	breast:	n/a
19	chr20:1578550-1578600	NH-A	brain:	n/a
20	chr20:1578550-1578600	Hela-S3	cervix:	n/a
21	chr20:1578550-1578600	U87	brain:	n/a
22	chr20:1578550-1578600	LNCaP	prostate:	n/a
23	chr20:1578550-1578600	GM19239	blood:	n/a
24	chr20:1578550-1578600	Jurkat	blood:	n/a
25	chr20:1578550-1578600	BE2_C	brain:	n/a
26	chr20:1578550-1578600	H1-hESC	embryonic stem cell:	embryo
27	chr20:1578550-1578600	SK-N-MC	brain:	n/a
28	chr20:1578550-1578600	SK-N-SH_RA	brain:	n/a
29	chr20:1578550-1578600	HAEpiC	amniotic membrane:	n/a
30	chr20:1578550-1578600	HRE	kidney:	n/a
31	chr20:1578550-1578600	HCPEpiC	choroid plexus:	n/a
32	chr20:1578550-1578600	NHBE	bronchial:	n/a
33	chr20:1578550-1578600	RPTEC	kidney:	n/a
34	chr20:1578550-1578600	GM06990	blood:	n/a
35	chr20:1578550-1578600	PANC-1	pancreas:	n/a
36	chr20:1578550-1578600	HPAEpiC	pulmonary alveolar:	n/a
37	chr20:1578550-1578600	HCM	heart:	n/a
38	chr20:1578550-1578600	ECC-1	luminal epithelium:	n/a
39	chr20:1578550-1578600	HCF	heart:	n/a
40	chr20:1578550-1578600	CMK	blood:	n/a
41	chr20:1578550-1578600	Hepatocyte	liver:	n/a
42	chr20:1578550-1578600	HCT-116	colon:	n/a
43	chr20:1578550-1578600	ProgFib	skin:	n/a
44	chr20:1578550-1578600	HRPEpiC	eye:	n/a
45	chr20:1578550-1578600	GM12878	blood:	n/a
46	chr20:1578550-1578600	AG04449	skin:	fetal
47	chr20:1578550-1578600	HepG2	liver:	n/a
48	chr20:1578550-1578600	AG09319	gingival:	n/a
49	chr20:1578550-1578600	T-47D	breast:	n/a
50	chr20:1578550-1578600	AG04450	lung:	fetal

No data

(count:2 , 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-4	chr20:1572038-1572494	NONHSAT078121

No data

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

Extended variants
information (count: 594 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547499250	chr20:1568383-1568384	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs55894619	chr20:1568541-1568542	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183284759	chr20:1569481-1569482	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs6079692	chr20:1569540-1569541	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs6079693	chr20:1569563-1569564	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
6	rs529481512	chr20:1569605-1569606	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6074853	chr20:1569643-1569644	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6079694	chr20:1569704-1569705	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
9	rs550942617	chr20:1569708-1569709	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
10	rs151069299	chr20:1569809-1569810	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
11	rs187233061	chr20:1569893-1569894	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
12	rs558493048	chr20:1569938-1569939	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
13	rs570485292	chr20:1570398-1570399	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534632590	chr20:1570548-1570549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553089601	chr20:1571442-1571443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574624116	chr20:1571446-1571447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542003075	chr20:1571450-1571451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556880105	chr20:1571467-1571468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111962716	chr20:1571490-1571491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201390207	chr20:1571545-1571546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113296065	chr20:1571547-1571548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140979173	chr20:1571863-1571864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3859626	chr20:1571874-1571875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192105963	chr20:1571885-1571886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528444095	chr20:1571899-1571900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540272302	chr20:1571920-1571921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561845873	chr20:1572018-1572019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529373689	chr20:1572188-1572189	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs145705854	chr20:1572256-1572257	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs1883935	chr20:1572374-1572375	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs6074855	chr20:1572408-1572409	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs372514247	chr20:1572585-1572586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111622289	chr20:1572957-1572958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184869554	chr20:1573092-1573093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188136308	chr20:1573164-1573165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112066061	chr20:1573174-1573175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146169245	chr20:1573253-1573254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552082660	chr20:1573347-1573348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192650290	chr20:1573761-1573762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534589304	chr20:1573960-1573961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184204353	chr20:1574057-1574058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553050433	chr20:1574212-1574213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568115302	chr20:1574304-1574305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188349613	chr20:1574368-1574369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192384927	chr20:1574521-1574522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184937736	chr20:1574591-1574592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575368533	chr20:1574651-1574652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189069759	chr20:1574745-1574746	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs569937413	chr20:1574837-1574838	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs111574569	chr20:1574845-1574846	Weak transcription	lncRNA	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:116 , 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	chr20:1560000-1579200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr20:1561000-1568000	Weak transcription	Primary T cells from cord blood	blood
8	chr20:1566600-1568400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr20:1567000-1569400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
10	chr20:1567600-1570000	Active TSS	Primary B cells from cord blood	blood
11	chr20:1567800-1569600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr20:1568000-1569000	Enhancers	Primary T cells from cord blood	blood
13	chr20:1568000-1570200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr20:1568000-1570200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr20:1568000-1570400	Enhancers	Primary T cells fromperipheralblood	blood
16	chr20:1568200-1568800	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr20:1568200-1569800	Enhancers	Primary B cells from peripheral blood	blood
18	chr20:1568400-1568600	Active TSS	Primary neutrophils fromperipheralblood	blood
19	chr20:1568400-1569400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr20:1568400-1570200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr20:1568400-1570600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr20:1568600-1568800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr20:1568600-1568800	Enhancers	NHDF-Ad	bronchial
24	chr20:1568600-1569000	Enhancers	Dnd41	blood
25	chr20:1568600-1570200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr20:1568600-1570400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr20:1568800-1569000	Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr20:1568800-1570200	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr20:1568800-1570200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr20:1569000-1569200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr20:1569000-1569200	Flanking Active TSS	Dnd41	blood
32	chr20:1569000-1569400	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr20:1569000-1569400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr20:1569000-1569800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr20:1569000-1569800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr20:1569000-1569800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr20:1569000-1569800	Enhancers	Spleen	Spleen
38	chr20:1569200-1569400	Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr20:1569200-1569600	Enhancers	Dnd41	blood
40	chr20:1569400-1569600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr20:1569400-1570400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr20:1569400-1571000	Enhancers	Primary T cells from cord blood	blood
43	chr20:1569400-1572600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr20:1569600-1569800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr20:1569600-1569800	Enhancers	NHDF-Ad	bronchial
46	chr20:1569600-1570000	Flanking Active TSS	Dnd41	blood
47	chr20:1569600-1570400	Enhancers	Liver	Liver
48	chr20:1569800-1570000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr20:1569800-1570200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr20:1569800-1587000	Weak transcription	Spleen	Spleen

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