Variant report

Variant	esv3453902
Chromosome Location	chr20:1559252-1586450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr20:1569890-1569986	ProgFib	skin:	n/a	n/a
2	CTCF	chr20:1569840-1569990	HRPEpiC	eye:	n/a	n/a
3	CTCF	chr20:1569844-1569973	GM12878	blood:	n/a	n/a
4	CTCF	chr20:1583950-1584135	GM12878	blood:	n/a	chr20:1583996-1584006
5	CTCF	chr20:1562235-1562365	GM13977	blood:	n/a	n/a
6	CTCF	chr20:1562235-1562401	GM12878	blood:	n/a	n/a
7	CTCF	chr20:1569860-1570007	GM12878	blood:	n/a	n/a
8	CTCF	chr20:1569812-1570027	Gliobla	brain:	n/a	n/a
9	CTCF	chr20:1569800-1569950	GM12864	blood:	n/a	n/a
10	CTCF	chr20:1583974-1584038	GM10266	blood:	n/a	chr20:1583996-1584006
11	CTCF	chr20:1569820-1569970	HRE	kidney:	n/a	n/a
12	CTCF	chr20:1583923-1584071	GM12891	blood:	n/a	chr20:1583996-1584006
13	CTCF	chr20:1569820-1569970	GM12878	blood:	n/a	n/a
14	CTCF	chr20:1585205-1585266	GM10248	blood:	n/a	n/a
15	CTCF	chr20:1562180-1562330	GM12875	blood:	n/a	n/a
16	CTCF	chr20:1569782-1570019	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr20:1562140-1562290	GM12864	blood:	n/a	n/a
18	CTCF	chr20:1583954-1584054	GM19239	blood:	n/a	chr20:1583996-1584006
19	CTCF	chr20:1569820-1569970	HCT-116	colon:	n/a	n/a
20	CTCF	chr20:1583918-1584066	GM12878	blood:	n/a	chr20:1583996-1584006
21	CTCF	chr20:1569768-1570055	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr20:1569880-1570030	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr20:1569900-1570050	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr20:1562218-1562407	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr20:1569840-1569990	HAc	cerebellar:	n/a	n/a
26	CTCF	chr20:1562236-1562335	Gliobla	brain:	n/a	n/a
27	CTCF	chr20:1569809-1569981	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr20:1569800-1569950	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr20:1562180-1562330	GM12878	blood:	n/a	n/a
30	CTCF	chr20:1569820-1569970	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr20:1562336-1562338	Gliobla	brain:	n/a	n/a
32	CTCF	chr20:1583993-1584014	H1-hESC	embryonic stem cell:	n/a	chr20:1583996-1584006
33	CTCF	chr20:1569840-1569990	HRE	kidney:	n/a	n/a
34	CTCF	chr20:1569860-1570010	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr20:1569820-1569970	AG10803	skin:	n/a	n/a
36	CTCF	chr20:1569780-1569930	SAEC	small airway:	n/a	n/a
37	CTCF	chr20:1569840-1569990	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr20:1569840-1569990	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr20:1583938-1584013	HUVEC	blood vessel:	n/a	chr20:1583996-1584006
40	EBF1	chr20:1575968-1576160	GM12878	blood:	n/a	n/a
41	EBF1	chr20:1576059-1576210	GM12878	blood:	n/a	n/a
42	ELF1	chr20:1575954-1576254	GM12878	blood:	n/a	chr20:1576167-1576178
43	MAFF	chr20:1560210-1560695	HepG2	liver:	n/a	n/a
44	MAFK	chr20:1560178-1560655	IMR90	lung:	n/a	n/a
45	MAFK	chr20:1560184-1560754	HepG2	liver:	n/a	n/a
46	MAFK	chr20:1560215-1560626	HepG2	liver:	n/a	n/a
47	MYC	chr20:1586165-1586228	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr20:1585280-1585288	A549	lung:	n/a	n/a
49	POLR2A	chr20:1585301-1585492	A549	lung:	n/a	n/a
50	POLR2A	chr20:1571059-1571375	H1-neurons	neurons:	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	SK-N-MC	brain:	n/a
2	chr20:1578550-1578600	HUVEC	blood vessel:	n/a
3	chr20:1578550-1578600	NHBE	bronchial:	n/a
4	chr20:1578550-1578600	NT2-D1	testis:	n/a
5	chr20:1578550-1578600	Caco-2	colon:	n/a
6	chr20:1578550-1578600	U87	brain:	n/a
7	chr20:1578550-1578600	H1-hESC	embryonic stem cell:	embryo
8	chr20:1578550-1578600	ECC-1	luminal epithelium:	n/a
9	chr20:1578550-1578600	AG09309	skin:	n/a
10	chr20:1578550-1578600	GM06990	blood:	n/a
11	chr20:1578550-1578600	NH-A	brain:	n/a
12	chr20:1578550-1578600	AG09319	gingival:	n/a
13	chr20:1578550-1578600	ovcar-3	ovarian:	n/a
14	chr20:1578550-1578600	LNCaP	prostate:	n/a
15	chr20:1578550-1578600	HCM	heart:	n/a
16	chr20:1578550-1578600	GM12891	blood:	n/a
17	chr20:1578550-1578600	HIPEpiC	eye:	n/a
18	chr20:1578550-1578600	NB4	blood:	n/a
19	chr20:1578550-1578600	PANC-1	pancreas:	n/a
20	chr20:1578550-1578600	HRE	kidney:	n/a
21	chr20:1578550-1578600	Jurkat	blood:	n/a
22	chr20:1578550-1578600	BE2_C	brain:	n/a
23	chr20:1578550-1578600	GM12892	blood:	n/a
24	chr20:1578550-1578600	HepG2	liver:	n/a
25	chr20:1578550-1578600	RPTEC	kidney:	n/a
26	chr20:1578550-1578600	HRCEpiC	kidney:	n/a
27	chr20:1578550-1578600	SKMC	muscle:	n/a
28	chr20:1578550-1578600	GM19239	blood:	n/a
29	chr20:1578550-1578600	K562	blood:	n/a
30	chr20:1578550-1578600	AG04449	skin:	fetal
31	chr20:1578550-1578600	HEEpiC	esophagus:	n/a
32	chr20:1578550-1578600	A549	lung:	n/a
33	chr20:1578550-1578600	GM12878	blood:	n/a
34	chr20:1578550-1578600	Hela-S3	cervix:	n/a
35	chr20:1578550-1578600	HAEpiC	amniotic membrane:	n/a
36	chr20:1578550-1578600	HCT-116	colon:	n/a
37	chr20:1578550-1578600	HL-60	blood:	n/a
38	chr20:1578550-1578600	MCF10A-Er-Src	breast:	n/a
39	chr20:1578550-1578600	T-47D	breast:	n/a
40	chr20:1578550-1578600	HPAEpiC	pulmonary alveolar:	n/a
41	chr20:1578550-1578600	AG10803	skin:	n/a
42	chr20:1578550-1578600	PFSK-1	brain:	n/a
43	chr20:1578550-1578600	ProgFib	skin:	n/a
44	chr20:1578550-1578600	MCF-7	breast:	n/a
45	chr20:1578550-1578600	CMK	blood:	n/a
46	chr20:1578550-1578600	SK-N-SH_RA	brain:	n/a
47	chr20:1578550-1578600	IMR90	lung:	fetal
48	chr20:1578550-1578600	BJ	skin:	n/a
49	chr20:1578550-1578600	HNPCEpiC	eye:	n/a
50	chr20:1578550-1578600	AG04450	lung:	fetal

No data

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-4	chr20:1572038-1572494	NONHSAT078121
2	lnc-SNPH-5	chr20:1562154-1562366	ucscGeneNc_uc002wfp_1
3	lnc-SNPH-5	chr20:1574682-1577118	ucscGeneNc_uc002wfp_1
4	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
5	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1

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: 334 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2746603	chr20:1559259-1559260	Genic enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143134459	chr20:1559260-1559261	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532011284	chr20:1559263-1559264	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200282498	chr20:1559270-1559271	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200657161	chr20:1559271-1559272	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202017659	chr20:1559300-1559301	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148239911	chr20:1559305-1559306	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199531018	chr20:1559318-1559319	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141367120	chr20:1559320-1559321	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369732461	chr20:1559323-1559324	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73893765	chr20:1559324-1559325	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199835818	chr20:1559330-1559331	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567138961	chr20:1559333-1559334	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538114205	chr20:1559380-1559381	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373987403	chr20:1559383-1559384	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556162165	chr20:1559385-1559386	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577901799	chr20:1559398-1559399	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538644535	chr20:1559413-1559414	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111975078	chr20:1559506-1559507	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180762110	chr20:1559572-1559573	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562761101	chr20:1559616-1559617	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543151409	chr20:1559617-1559618	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561441268	chr20:1559622-1559623	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2243529	chr20:1559696-1559697	Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs184337933	chr20:1559699-1559700	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149142921	chr20:1559725-1559726	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532888398	chr20:1559765-1559766	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544631561	chr20:1559846-1559847	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559727915	chr20:1559852-1559853	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143223440	chr20:1559888-1559889	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548689769	chr20:1559918-1559919	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2243423	chr20:1559989-1559990	Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs531389347	chr20:1559994-1559995	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549986341	chr20:1560047-1560048	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571444349	chr20:1560065-1560066	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538926002	chr20:1560080-1560081	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371524487	chr20:1560151-1560152	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566103574	chr20:1560152-1560153	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536674296	chr20:1560184-1560185	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555087634	chr20:1560197-1560198	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576523865	chr20:1560205-1560206	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543651537	chr20:1560207-1560208	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62186924	chr20:1560222-1560223	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577426485	chr20:1560271-1560272	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370112582	chr20:1560291-1560292	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541341780	chr20:1560304-1560305	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182218816	chr20:1560308-1560309	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527271020	chr20:1560313-1560314	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542248801	chr20:1560330-1560331	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560640439	chr20:1560364-1560365	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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

Chromatin state (count:98 , 50 per page) page: 1 2

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	chr20:1556800-1560000	Genic enhancers	Primary monocytes fromperipheralblood	blood
7	chr20:1556800-1560000	Genic enhancers	Monocytes-CD14+_RO01746	blood
8	chr20:1558000-1559600	Strong transcription	Primary T cells from cord blood	blood
9	chr20:1558400-1560000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr20:1558600-1559600	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr20:1559600-1560400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
12	chr20:1559600-1560600	Weak transcription	Primary T cells from cord blood	blood
13	chr20:1560000-1561000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr20:1560000-1561000	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr20:1560000-1579200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr20:1560400-1561800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr20:1560600-1561000	Strong transcription	Primary T cells from cord blood	blood
18	chr20:1561000-1562600	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr20:1561000-1563600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr20:1561000-1568000	Weak transcription	Primary T cells from cord blood	blood
21	chr20:1561800-1563800	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr20:1563600-1564600	Genic enhancers	Primary monocytes fromperipheralblood	blood
23	chr20:1563800-1565400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr20:1564600-1565400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr20:1565400-1565600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr20:1565400-1566000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr20:1565600-1565800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
28	chr20:1565800-1567000	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr20:1566000-1566600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr20:1566600-1568400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr20:1567000-1569400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr20:1567600-1570000	Active TSS	Primary B cells from cord blood	blood
33	chr20:1567800-1569600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr20:1568000-1569000	Enhancers	Primary T cells from cord blood	blood
35	chr20:1568000-1570200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr20:1568000-1570200	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr20:1568000-1570400	Enhancers	Primary T cells fromperipheralblood	blood
38	chr20:1568200-1568800	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr20:1568200-1569800	Enhancers	Primary B cells from peripheral blood	blood
40	chr20:1568400-1568600	Active TSS	Primary neutrophils fromperipheralblood	blood
41	chr20:1568400-1569400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr20:1568400-1570200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr20:1568400-1570600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr20:1568600-1568800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr20:1568600-1568800	Enhancers	NHDF-Ad	bronchial
46	chr20:1568600-1569000	Enhancers	Dnd41	blood
47	chr20:1568600-1570200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr20:1568600-1570400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr20:1568800-1569000	Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr20:1568800-1570200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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