Variant report

Variant	nsv965869
Chromosome Location	chr20:29521699-29570138
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	ARID3A	chr20:29525107-29525240	K562	blood:	n/a	n/a
2	BATF	chr20:29557150-29557425	GM12878	blood:	n/a	n/a
3	BCL11A	chr20:29543803-29543974	GM12878	blood:	n/a	n/a
4	BCL11A	chr20:29523723-29524008	GM12878	blood:	n/a	n/a
5	BHLHE40	chr20:29525056-29525392	K562	blood:	n/a	n/a
6	CBX3	chr20:29524962-29525647	K562	blood:	n/a	n/a
7	CCNT2	chr20:29525150-29525425	K562	blood:	n/a	n/a
8	CTCF	chr20:29525102-29525204	GM20000	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
9	CTCF	chr20:29525120-29525270	HCT-116	colon:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
10	CTCF	chr20:29525060-29525210	GM12864	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
11	CTCF	chr20:29525080-29525230	GM12864	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
12	CTCF	chr20:29525119-29525245	MCF-7	breast:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
13	CTCF	chr20:29525040-29525190	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr20:29525140-29525290	BE2_C	brain:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
15	CTCF	chr20:29531202-29531231	GM20000	blood:	n/a	n/a
16	CTCF	chr20:29525120-29525270	WERI-Rb-1	eye:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
17	CTCF	chr20:29525105-29525267	HepG2	liver:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
18	CTCF	chr20:29525100-29525250	HUVEC	blood vessel:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
19	CTCF	chr20:29525100-29525250	HPF	lung:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
20	CTCF	chr20:29535640-29535790	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr20:29525100-29525250	GM12874	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
22	CTCF	chr20:29525093-29525262	GM19240	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
23	CTCF	chr20:29525058-29525277	K562	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
24	CTCF	chr20:29525120-29525270	HCM	heart:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
25	CTCF	chr20:29525354-29525409	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr20:29525120-29525270	Caco-2	colon:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
27	CTCF	chr20:29525080-29525230	AG04449	skin:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
28	CTCF	chr20:29525060-29525210	HCPEpiC	choroid plexus:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
29	CTCF	chr20:29525120-29525270	GM12874	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
30	CTCF	chr20:29525120-29525257	MCF-7	breast:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
31	CTCF	chr20:29525120-29525270	NHLF	lung:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
32	CTCF	chr20:29525100-29525250	GM12872	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
33	CTCF	chr20:29535629-29535737	K562	blood:	n/a	n/a
34	CTCF	chr20:29525060-29525210	K562	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
35	CTCF	chr20:29525140-29525290	RPTEC	kidney:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
36	CTCF	chr20:29525120-29525270	HepG2	liver:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
37	CTCF	chr20:29525100-29525250	GM12870	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
38	CTCF	chr20:29525094-29525262	GM12891	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
39	CTCF	chr20:29525120-29525270	GM12866	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
40	CTCF	chr20:29560485-29560520	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr20:29525120-29525270	K562	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
42	CTCF	chr20:29525133-29525236	GM10266	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
43	CTCF	chr20:29525120-29525270	GM12871	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
44	CTCF	chr20:29525060-29525210	Caco-2	colon:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
45	CTCF	chr20:29535620-29535770	HepG2	liver:	n/a	n/a
46	CTCF	chr20:29525100-29525250	SK-N-SH_RA	brain:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
47	CTCF	chr20:29535660-29535810	RPTEC	kidney:	n/a	n/a
48	CTCF	chr20:29525137-29525255	MCF-7	breast:	n/a	chr20:29525181-29525191 chr20:29525180-29525193
49	CTCF	chr20:29535620-29535770	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr20:29525100-29525250	GM12871	blood:	n/a	chr20:29525181-29525191 chr20:29525180-29525193

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:29522467-29522517	GM12878	blood:	n/a
2	chr20:29535007-29535057	K562	blood:	n/a
3	chr20:29522467-29522517	GM12878	blood:	n/a
4	chr20:29535007-29535057	K562	blood:	n/a
5	chr20:29535007-29535057	RPTEC	kidney:	n/a
6	chr20:29547097-29547147	ECC-1	luminal epithelium:	n/a
7	chr20:29537189-29537239	T-47D	breast:	n/a
8	chr20:29547097-29547147	HUVEC	blood vessel:	n/a
9	chr20:29551422-29551472	GM12878	blood:	n/a
10	chr20:29534074-29534124	HepG2	liver:	n/a
11	chr20:29550850-29550900	AG04450	lung:	fetal
12	chr20:29534074-29534124	RPTEC	kidney:	n/a
13	chr20:29549396-29549446	HRPEpiC	eye:	n/a
14	chr20:29537189-29537239	NT2-D1	testis:	n/a
15	chr20:29547097-29547147	ovcar-3	ovarian:	n/a
16	chr20:29554089-29554139	LNCaP	prostate:	n/a
17	chr20:29535007-29535057	HRPEpiC	eye:	n/a
18	chr20:29547097-29547147	NB4	blood:	n/a
19	chr20:29551622-29551672	NHBE	bronchial:	n/a
20	chr20:29535056-29535106	LNCaP	prostate:	n/a
21	chr20:29535056-29535106	HMEC	breast:	n/a
22	chr20:29554089-29554139	HCPEpiC	choroid plexus:	n/a
23	chr20:29535056-29535106	HIPEpiC	eye:	n/a
24	chr20:29535013-29535063	IMR90	lung:	fetal
25	chr20:29534074-29534124	NT2-D1	testis:	n/a
26	chr20:29535150-29535200	MCF10A-Er-Src	breast:	n/a
27	chr20:29549396-29549446	Hela-S3	cervix:	n/a
28	chr20:29535013-29535063	NHBE	bronchial:	n/a
29	chr20:29535150-29535200	ECC-1	luminal epithelium:	n/a
30	chr20:29547097-29547147	AG09319	gingival:	n/a
31	chr20:29547097-29547147	HCT-116	colon:	n/a
32	chr20:29535150-29535200	SK-N-MC	brain:	n/a
33	chr20:29547097-29547147	HCF	heart:	n/a
34	chr20:29550850-29550900	Hela-S3	cervix:	n/a
35	chr20:29537189-29537239	AG09309	skin:	n/a
36	chr20:29550850-29550900	T-47D	breast:	n/a
37	chr20:29534074-29534124	AG04450	lung:	fetal
38	chr20:29550850-29550900	H1-hESC	embryonic stem cell:	embryo
39	chr20:29547097-29547147	MCF-7	breast:	n/a
40	chr20:29551422-29551472	AoSMC	blood vessel:	n/a
41	chr20:29535013-29535063	RPTEC	kidney:	n/a
42	chr20:29535150-29535200	HRE	kidney:	n/a
43	chr20:29551422-29551472	GM12891	blood:	n/a
44	chr20:29551422-29551472	PFSK-1	brain:	n/a
45	chr20:29554089-29554139	HepG2	liver:	n/a
46	chr20:29537189-29537239	Jurkat	blood:	n/a
47	chr20:29551622-29551672	HCT-116	colon:	n/a
48	chr20:29551622-29551672	K562	blood:	n/a
49	chr20:29550850-29550900	LNCaP	prostate:	n/a
50	chr20:29549396-29549446	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:29523038..29524935-chr20:29609973..29612060,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB116-2	chr20:29521637-29522148	ENSG00000225490
2	lnc-DEFB116-2	chr20:29522947-29522987	ENSG00000225490
3	lnc-DEFB116-1	chr20:29565782-29565935	NONHSAT079273
4	lnc-DEFB116-1	chr20:29559203-29559502	ENSG00000231934.1
5	lnc-DEFB116-1	chr20:29558488-29558622	ENSG00000231934.1
6	lnc-DEFB116-1	chr20:29559468-29559502	XLOC_013717
7	lnc-DEFB116-1	chr20:29565784-29565927	ENSG00000231934.1
8	lnc-DEFB116-1	chr20:29565756-29565927	ENSG00000231934.1
9	lnc-DEFB116-1	chr20:29565784-29565969	XLOC_013717

Variant related genes	Relation type
ENSG00000205611	TF binding region
ENSG00000200325	TF binding region
ENSG00000225490	TF binding region
ENSG00000205611	CpG island
ENSG00000200325	CpG island
ENSG00000225490	CpG island
ENSG00000149531	chromatin interactions
RICTOR	miRNA target sites
RIMS3	miRNA target sites

Extended variants
information (count: 2638 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2638 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373546892	chr20:29521718-29521719	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs190986093	chr20:29521721-29521722	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs537131819	chr20:29521738-29521739	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs534688373	chr20:29521771-29521772	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs143324108	chr20:29521772-29521773	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs536266199	chr20:29521869-29521870	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs556063474	chr20:29521889-29521890	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs183258283	chr20:29521896-29521897	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs377582616	chr20:29521917-29521918	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs188122547	chr20:29521918-29521919	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs34619750	chr20:29521919-29521920	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs377692953	chr20:29521923-29521924	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs578140372	chr20:29521961-29521962	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs6118970	chr20:29521964-29521965	Weak transcription Active TSS Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs557038084	chr20:29521968-29521969	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs573657146	chr20:29521999-29522000	Weak transcription Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs6118971	chr20:29522024-29522025	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs1064148	chr20:29522049-29522050	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs148544598	chr20:29522078-29522079	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs528363855	chr20:29522089-29522090	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs190415533	chr20:29522092-29522093	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs142862805	chr20:29522107-29522108	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs565079104	chr20:29522109-29522110	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs530623450	chr20:29522130-29522131	Weak transcription Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs550658577	chr20:29522175-29522176	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567387529	chr20:29522230-29522231	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs182961132	chr20:29522239-29522240	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs375541255	chr20:29522240-29522241	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs187604720	chr20:29522242-29522243	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs566380568	chr20:29522247-29522248	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs535318732	chr20:29522259-29522260	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs563562776	chr20:29522270-29522271	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs571764738	chr20:29522295-29522296	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs192548147	chr20:29522313-29522314	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs183473301	chr20:29522325-29522326	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs573818087	chr20:29522339-29522340	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs151043354	chr20:29522340-29522341	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs368225001	chr20:29522354-29522355	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs573194643	chr20:29522369-29522370	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs117284715	chr20:29522373-29522374	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs200920440	chr20:29522380-29522381	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs575542587	chr20:29522392-29522393	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs545655546	chr20:29522408-29522409	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187863078	chr20:29522435-29522436	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs56034052	chr20:29522449-29522450	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs397741109	chr20:29522452-29522453	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs544442488	chr20:29522468-29522469	Weak transcription Enhancers Active TSS Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs561096791	chr20:29522473-29522474	Weak transcription Enhancers Active TSS Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs529799340	chr20:29522512-29522513	Weak transcription Enhancers Active TSS Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs140919194	chr20:29522514-29522515	Weak transcription Enhancers Active TSS Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	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
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21806811	CNVD
Melanoma	21693616	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20688871	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:29519000-29523800	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr20:29519000-29524200	Weak transcription	Small Intestine	intestine
3	chr20:29519000-29524400	Weak transcription	Primary T cells from cord blood	blood
4	chr20:29519000-29524400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr20:29519000-29524400	Weak transcription	Aorta	Aorta
6	chr20:29519000-29524800	Weak transcription	Primary B cells from cord blood	blood
7	chr20:29519200-29523000	Weak transcription	Right Atrium	heart
8	chr20:29519200-29523600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr20:29519200-29523800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr20:29519200-29523800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr20:29519200-29523800	Weak transcription	Osteobl	bone
12	chr20:29519200-29524200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr20:29519200-29524200	Weak transcription	HSMMtube	muscle
14	chr20:29519400-29523800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr20:29519400-29523800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr20:29519400-29524200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr20:29519400-29525000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr20:29519600-29522200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr20:29519600-29522800	Weak transcription	Primary hematopoietic stem cells	blood
20	chr20:29519600-29523000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr20:29519600-29523200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr20:29519600-29523200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr20:29519600-29523600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr20:29519600-29523600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr20:29519600-29523600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr20:29519600-29523600	Weak transcription	Thymus	Thymus
27	chr20:29519600-29523600	Weak transcription	NH-A	brain
28	chr20:29519600-29523800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr20:29519600-29523800	Weak transcription	Brain Hippocampus Middle	brain
30	chr20:29519600-29523800	Weak transcription	Left Ventricle	heart
31	chr20:29519600-29523800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr20:29519600-29524600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr20:29519800-29523600	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr20:29520000-29523000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr20:29520600-29524200	Weak transcription	Esophagus	oesophagus
36	chr20:29520800-29523800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr20:29520800-29523800	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr20:29521000-29522000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr20:29521000-29523000	Weak transcription	Stomach Mucosa	stomach
40	chr20:29521000-29523200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr20:29521000-29523200	Weak transcription	K562	blood
42	chr20:29521000-29523800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:29521000-29524000	Weak transcription	Spleen	Spleen
44	chr20:29521000-29534000	Weak transcription	Gastric	stomach
45	chr20:29521200-29521800	Weak transcription	Duodenum Mucosa	Duodenum
46	chr20:29521200-29523600	Weak transcription	Brain Anterior Caudate	brain
47	chr20:29521200-29524400	Weak transcription	Pancreas	Pancrea
48	chr20:29521400-29522400	Enhancers	Dnd41	blood
49	chr20:29521800-29525600	Active TSS	Duodenum Mucosa	Duodenum
50	chr20:29522000-29522200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland

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