Variant report

Variant	nsv510779
Chromosome Location	chr20:1509330-1613962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:821)
CpG islands
(count:854)
Chromatin interactive
region (count:5)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:1550229-1550409	K562	blood:	n/a	n/a
2	ATF1	chr20:1509630-1509690	K562	blood:	n/a	n/a
3	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
4	ATF1	chr20:1518447-1518666	K562	blood:	n/a	n/a
5	ATF1	chr20:1597810-1598006	K562	blood:	n/a	n/a
6	ATF2	chr20:1516254-1516949	GM12878	blood:	n/a	n/a
7	ATF2	chr20:1607520-1607935	GM12878	blood:	n/a	n/a
8	ATF2	chr20:1612733-1613271	GM12878	blood:	n/a	n/a
9	ATF2	chr20:1607411-1607905	GM12878	blood:	n/a	n/a
10	ATF2	chr20:1603058-1603543	GM12878	blood:	n/a	n/a
11	ATF2	chr20:1516090-1517022	GM12878	blood:	n/a	n/a
12	ATF2	chr20:1518341-1518724	GM12878	blood:	n/a	n/a
13	ATF2	chr20:1612776-1613188	GM12878	blood:	n/a	n/a
14	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
15	BATF	chr20:1612769-1613106	GM12878	blood:	n/a	chr20:1612969-1612980
16	BATF	chr20:1516380-1516828	GM12878	blood:	n/a	n/a
17	BATF	chr20:1612731-1613238	GM12878	blood:	n/a	chr20:1612969-1612980
18	BATF	chr20:1543275-1543590	GM12878	blood:	n/a	n/a
19	BATF	chr20:1516454-1516834	GM12878	blood:	n/a	n/a
20	BATF	chr20:1603174-1603482	GM12878	blood:	n/a	n/a
21	BCL11A	chr20:1603111-1603444	GM12878	blood:	n/a	n/a
22	BCL11A	chr20:1516454-1516746	GM12878	blood:	n/a	chr20:1516685-1516694 chr20:1516649-1516658
23	BCL11A	chr20:1612833-1613216	GM12878	blood:	n/a	n/a
24	BCL11A	chr20:1603100-1603339	GM12878	blood:	n/a	n/a
25	BCL11A	chr20:1516369-1516891	GM12878	blood:	n/a	chr20:1516685-1516694 chr20:1516649-1516658
26	BCL3	chr20:1516308-1516866	GM12878	blood:	n/a	chr20:1516685-1516694 chr20:1516649-1516658
27	BCL3	chr20:1603087-1603515	GM12878	blood:	n/a	n/a
28	BCL3	chr20:1612800-1613166	GM12878	blood:	n/a	n/a
29	BCLAF1	chr20:1603036-1603400	GM12878	blood:	n/a	n/a
30	BCLAF1	chr20:1516214-1516962	GM12878	blood:	n/a	chr20:1516685-1516694 chr20:1516649-1516658
31	BCLAF1	chr20:1612776-1613271	GM12878	blood:	n/a	n/a
32	BCLAF1	chr20:1516270-1516971	GM12878	blood:	n/a	chr20:1516685-1516694 chr20:1516649-1516658
33	BCLAF1	chr20:1612842-1613225	GM12878	blood:	n/a	n/a
34	BHLHE40	chr20:1549969-1550250	K562	blood:	n/a	n/a
35	BHLHE40	chr20:1515311-1515463	K562	blood:	n/a	n/a
36	BHLHE40	chr20:1516379-1517024	GM12878	blood:	n/a	n/a
37	BHLHE40	chr20:1518323-1518752	GM12878	blood:	n/a	n/a
38	BHLHE40	chr20:1603122-1603445	GM12878	blood:	n/a	n/a
39	BRCA1	chr20:1550123-1550444	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr20:1603218-1603418	GM12878	blood:	n/a	n/a
41	CEBPB	chr20:1517899-1518225	HepG2	liver:	n/a	chr20:1518052-1518065 chr20:1518053-1518064 chr20:1518052-1518063
42	CEBPB	chr20:1550085-1550450	A549	lung:	n/a	n/a
43	CEBPB	chr20:1550060-1550411	MCF-7	breast:	n/a	n/a
44	CEBPB	chr20:1509472-1509824	HepG2	liver:	n/a	chr20:1509642-1509653
45	CEBPB	chr20:1550076-1550409	HepG2	liver:	n/a	n/a
46	CEBPB	chr20:1509472-1509797	K562	blood:	n/a	chr20:1509642-1509653
47	CEBPB	chr20:1550069-1550318	K562	blood:	n/a	n/a
48	CEBPB	chr20:1596225-1596242	HepG2	liver:	n/a	n/a
49	CEBPB	chr20:1509443-1509821	A549	lung:	n/a	chr20:1509642-1509653
50	CEBPB	chr20:1536352-1536602	HepG2	liver:	n/a	chr20:1536448-1536459

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1610358-1610408	HRE	kidney:	n/a
2	chr20:1600623-1600673	AG04449	skin:	fetal
3	chr20:1546019-1546069	Hepatocyte	liver:	n/a
4	chr20:1610358-1610408	BJ	skin:	n/a
5	chr20:1538353-1538403	AG09319	gingival:	n/a
6	chr20:1514929-1514979	ProgFib	skin:	n/a
7	chr20:1538353-1538403	GM06990	blood:	n/a
8	chr20:1539641-1539691	GM12892	blood:	n/a
9	chr20:1532543-1532593	HCF	heart:	n/a
10	chr20:1532543-1532593	SKMC	muscle:	n/a
11	chr20:1539702-1539752	Hela-S3	cervix:	n/a
12	chr20:1539702-1539752	AG04449	skin:	fetal
13	chr20:1538671-1538721	HCT-116	colon:	n/a
14	chr20:1600705-1600755	NHDF-neo	bronchial:	n/a
15	chr20:1538671-1538721	Caco-2	colon:	n/a
16	chr20:1538671-1538721	HCM	heart:	n/a
17	chr20:1600641-1600691	H1-hESC	embryonic stem cell:	embryo
18	chr20:1538353-1538403	AG09309	skin:	n/a
19	chr20:1601704-1601754	ECC-1	luminal epithelium:	n/a
20	chr20:1546019-1546069	ECC-1	luminal epithelium:	n/a
21	chr20:1546019-1546069	HEEpiC	esophagus:	n/a
22	chr20:1601704-1601754	HL-60	blood:	n/a
23	chr20:1600705-1600755	GM19239	blood:	n/a
24	chr20:1610358-1610408	HPAEpiC	pulmonary alveolar:	n/a
25	chr20:1546019-1546069	HCM	heart:	n/a
26	chr20:1600623-1600673	AG09309	skin:	n/a
27	chr20:1538366-1538416	MCF10A-Er-Src	breast:	n/a
28	chr20:1600623-1600673	AoSMC	blood vessel:	n/a
29	chr20:1538353-1538403	NH-A	brain:	n/a
30	chr20:1532543-1532593	GM12878	blood:	n/a
31	chr20:1539702-1539752	GM12891	blood:	n/a
32	chr20:1601704-1601754	H1-hESC	embryonic stem cell:	embryo
33	chr20:1538366-1538416	GM12878	blood:	n/a
34	chr20:1532543-1532593	SAEC	small airway:	n/a
35	chr20:1538671-1538721	PANC-1	pancreas:	n/a
36	chr20:1600705-1600755	SAEC	small airway:	n/a
37	chr20:1600641-1600691	T-47D	breast:	n/a
38	chr20:1600705-1600755	HUVEC	blood vessel:	n/a
39	chr20:1539702-1539752	HAEpiC	amniotic membrane:	n/a
40	chr20:1539702-1539752	BJ	skin:	n/a
41	chr20:1514929-1514979	HRPEpiC	eye:	n/a
42	chr20:1538671-1538721	AG10803	skin:	n/a
43	chr20:1601704-1601754	SK-N-SH_RA	brain:	n/a
44	chr20:1600641-1600691	NHDF-neo	bronchial:	n/a
45	chr20:1532543-1532593	HAEpiC	amniotic membrane:	n/a
46	chr20:1578550-1578600	AG04449	skin:	fetal
47	chr20:1539641-1539691	HCPEpiC	choroid plexus:	n/a
48	chr20:1600641-1600691	NH-A	brain:	n/a
49	chr20:1601704-1601754	AG04450	lung:	fetal
50	chr20:1514929-1514979	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:1547054..1548894-chr20:1756067..1757690,2	K562	blood:
2	chr20:1518725..1519225-chr5:637487..638115,2	MCF-7	breast:
3	chr20:1513747..1514348-chr20:1714921..1715422,2	MCF-7	breast:
4	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:
5	chr20:1503830..1506372-chr20:1510373..1512056,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIRPG-2	chr20:1609798-1610282	NONHSAT078122
2	lnc-SNPH-5	chr20:1562154-1562366	ucscGeneNc_uc002wfp_1
3	lnc-SNPH-5	chr20:1565852-1565996	ucscGeneNc_uc002wfp_1
4	lnc-SIRPG-2	chr20:1610868-1610952	NONHSAT078123
5	lnc-SNPH-5	chr20:1574682-1577118	ucscGeneNc_uc002wfp_1
6	lnc-SIRPG-2	chr20:1611341-1611482	NONHSAT078122
7	lnc-SNPH-4	chr20:1572038-1572494	NONHSAT078121
8	lnc-SIRPG-2	chr20:1611060-1611289	NONHSAT078123
9	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1
10	lnc-SIRPG-2	chr20:1610868-1610952	NONHSAT078122
11	lnc-SIRPG-2	chr20:1610173-1610282	NONHSAT078123

No data

Variant related genes	Relation type
SIRPB1	TF binding region
SIRPD	TF binding region
RNU6-917P	TF binding region
ENSG00000260861	TF binding region
ENSG00000242324	TF binding region
ENSG00000271523	TF binding region
SIRPG	TF binding region
ENSG00000237914	TF binding region
SIRPB1	CpG island
SIRPD	CpG island
RNU6-917P	CpG island
ENSG00000260861	CpG island
ENSG00000242324	CpG island
ENSG00000271523	CpG island
SIRPG	CpG island
ENSG00000237914	CpG island

Extended variants
information (count: 3450 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3450 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370912549	chr20:1509377-1509378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73569112	chr20:1509389-1509390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs375059240	chr20:1509475-1509476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567586490	chr20:1509504-1509505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113658378	chr20:1509533-1509534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538134267	chr20:1509566-1509567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150675437	chr20:1509580-1509581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368132693	chr20:1509586-1509587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140909466	chr20:1509618-1509619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568399210	chr20:1509650-1509651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574890892	chr20:1509661-1509662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79946443	chr20:1509740-1509741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557792875	chr20:1509843-1509844	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs180828658	chr20:1509942-1509943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533983295	chr20:1509949-1509950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs55899201	chr20:1509953-1509954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117391956	chr20:1509964-1509965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186062530	chr20:1509974-1509975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561877830	chr20:1509984-1509985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6135187	chr20:1509997-1509998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573913502	chr20:1510010-1510011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544493528	chr20:1510022-1510023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2252400	chr20:1510048-1510049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs533321347	chr20:1510052-1510053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545079123	chr20:1510063-1510064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144491487	chr20:1510069-1510070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560608409	chr20:1510116-1510117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2252401	chr20:1510138-1510139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs139943667	chr20:1510178-1510179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567500184	chr20:1510192-1510193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6074760	chr20:1510194-1510195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149989553	chr20:1510201-1510202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373163436	chr20:1510205-1510206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56286817	chr20:1510247-1510248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116214604	chr20:1510288-1510289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145175932	chr20:1510324-1510325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557488848	chr20:1510360-1510361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566524749	chr20:1510361-1510362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148912160	chr20:1510363-1510364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13045197	chr20:1510411-1510412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6042800	chr20:1510432-1510433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs527725102	chr20:1510458-1510459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13041062	chr20:1510484-1510485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13045225	chr20:1510486-1510487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142683145	chr20:1510487-1510488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13045368	chr20:1510501-1510502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs13040607	chr20:1510503-1510504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13039436	chr20:1510520-1510521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146500249	chr20:1510522-1510523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13039437	chr20:1510523-1510524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Prostate cancer	21551127	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Medulloblastoma	21163964	CNVD
Glioma	20126413	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1508000-1513800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr20:1508000-1515200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr20:1508200-1513800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr20:1509600-1510000	Enhancers	NHEK	skin
5	chr20:1510000-1513600	Weak transcription	NHEK	skin
6	chr20:1513600-1514000	Enhancers	NHEK	skin
7	chr20:1513800-1514800	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr20:1513800-1516400	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr20:1513800-1517200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr20:1514000-1514600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
11	chr20:1514000-1519000	Weak transcription	NHEK	skin
12	chr20:1514600-1517800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr20:1514800-1515800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr20:1514800-1519400	Enhancers	Primary hematopoietic stem cells	blood
15	chr20:1514800-1519400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr20:1515000-1517800	Enhancers	Primary B cells from cord blood	blood
17	chr20:1515200-1515400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr20:1515200-1518200	Enhancers	GM12878-XiMat	blood
19	chr20:1515400-1515800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr20:1515800-1518200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr20:1516000-1516200	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr20:1516000-1519600	Enhancers	Primary B cells from peripheral blood	blood
23	chr20:1516400-1516800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr20:1516600-1516800	Enhancers	Placenta	Placenta
25	chr20:1516600-1518200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr20:1516800-1517400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr20:1516800-1518000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr20:1517000-1517400	Enhancers	Fetal Thymus	thymus
29	chr20:1517200-1518400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
30	chr20:1517200-1518400	Enhancers	Liver	Liver
31	chr20:1517200-1519200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr20:1517400-1517800	Weak transcription	Fetal Thymus	thymus
33	chr20:1517400-1518200	Enhancers	Spleen	Spleen
34	chr20:1517400-1519400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr20:1517400-1519400	Enhancers	Placenta	Placenta
36	chr20:1517800-1518800	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr20:1517800-1518800	Enhancers	Fetal Thymus	thymus
38	chr20:1517800-1519000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr20:1518000-1518600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr20:1518200-1518400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr20:1518200-1518800	Weak transcription	Spleen	Spleen
42	chr20:1518200-1519000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr20:1518200-1519000	Flanking Active TSS	GM12878-XiMat	blood
44	chr20:1518400-1518600	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr20:1518400-1519000	Active TSS	Hela-S3	cervix
46	chr20:1518400-1520400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr20:1518600-1518800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr20:1518600-1519800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr20:1518600-1519800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr20:1518600-1519800	Enhancers	HMEC	breast

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