Variant report

Variant	nsv1059465
Chromosome Location	chr21:15116712-15347609
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:757)
CpG islands
(count:1464)
Chromatin interactive
region (count:0)
LncRNA
region (count:41)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15346922-15347270	K562	blood:	n/a	n/a
2	ARID3A	chr21:15346022-15346251	K562	blood:	n/a	n/a
3	ARID3A	chr21:15295624-15295648	K562	blood:	n/a	n/a
4	ATF1	chr21:15342677-15342811	K562	blood:	n/a	n/a
5	ATF1	chr21:15249426-15249616	K562	blood:	n/a	n/a
6	BACH1	chr21:15347039-15347218	K562	blood:	n/a	n/a
7	BATF	chr21:15321908-15322326	GM12878	blood:	n/a	chr21:15322062-15322070
8	BATF	chr21:15340450-15340827	GM12878	blood:	n/a	n/a
9	BATF	chr21:15315150-15315618	GM12878	blood:	n/a	n/a
10	BATF	chr21:15341379-15341645	GM12878	blood:	n/a	chr21:15341542-15341553
11	BATF	chr21:15340388-15340909	GM12878	blood:	n/a	n/a
12	BATF	chr21:15295228-15295568	GM12878	blood:	n/a	chr21:15295405-15295416
13	BATF	chr21:15293789-15294118	GM12878	blood:	n/a	chr21:15293876-15293886
14	BATF	chr21:15295169-15295585	GM12878	blood:	n/a	chr21:15295405-15295416
15	BATF	chr21:15293789-15294119	GM12878	blood:	n/a	chr21:15293876-15293886
16	BATF	chr21:15134301-15134500	GM12878	blood:	n/a	n/a
17	BATF	chr21:15321950-15322323	GM12878	blood:	n/a	chr21:15322062-15322070
18	BATF	chr21:15319344-15319735	GM12878	blood:	n/a	n/a
19	BATF	chr21:15302414-15302611	GM12878	blood:	n/a	chr21:15302548-15302559
20	BATF	chr21:15315223-15315545	GM12878	blood:	n/a	n/a
21	BATF	chr21:15315664-15315881	GM12878	blood:	n/a	n/a
22	BATF	chr21:15319369-15319639	GM12878	blood:	n/a	n/a
23	BCL11A	chr21:15340450-15340836	GM12878	blood:	n/a	chr21:15340521-15340530 chr21:15340574-15340583
24	BCL11A	chr21:15315283-15315608	GM12878	blood:	n/a	n/a
25	BCL11A	chr21:15315306-15315658	GM12878	blood:	n/a	chr21:15315610-15315619
26	BCL11A	chr21:15293842-15294225	GM12878	blood:	n/a	n/a
27	BCL11A	chr21:15223481-15223715	GM12878	blood:	n/a	n/a
28	BCL11A	chr21:15340406-15340552	GM12878	blood:	n/a	chr21:15340521-15340530
29	BCL11A	chr21:15322021-15322201	GM12878	blood:	n/a	n/a
30	BCL11A	chr21:15319397-15319586	GM12878	blood:	n/a	n/a
31	BCL11A	chr21:15328745-15328928	GM12878	blood:	n/a	n/a
32	BCL11A	chr21:15319352-15319733	GM12878	blood:	n/a	n/a
33	BCL11A	chr21:15321900-15322332	GM12878	blood:	n/a	n/a
34	BHLHE40	chr21:15295613-15295821	K562	blood:	n/a	n/a
35	BHLHE40	chr21:15145416-15145487	K562	blood:	n/a	chr21:15145432-15145441
36	BHLHE40	chr21:15347507-15347656	K562	blood:	n/a	n/a
37	CCNT2	chr21:15295624-15295806	K562	blood:	n/a	n/a
38	CEBPB	chr21:15277523-15277853	IMR90	lung:	n/a	chr21:15277673-15277684
39	CEBPB	chr21:15277580-15277731	HepG2	liver:	n/a	chr21:15277673-15277684
40	CEBPB	chr21:15277523-15277688	K562	blood:	n/a	chr21:15277673-15277684
41	CEBPB	chr21:15347031-15347099	K562	blood:	n/a	n/a
42	CEBPB	chr21:15130594-15130794	HepG2	liver:	n/a	chr21:15130731-15130742
43	CEBPB	chr21:15168793-15168892	A549	lung:	n/a	n/a
44	CEBPB	chr21:15158571-15158864	IMR90	lung:	n/a	n/a
45	CEBPB	chr21:15346232-15346412	K562	blood:	n/a	n/a
46	CEBPB	chr21:15186322-15186471	HepG2	liver:	n/a	chr21:15186346-15186357
47	CEBPB	chr21:15294348-15294556	IMR90	lung:	n/a	n/a
48	CEBPB	chr21:15186319-15186519	IMR90	lung:	n/a	chr21:15186346-15186357
49	CEBPD	chr21:15295340-15295897	K562	blood:	n/a	n/a
50	CEBPD	chr21:15346361-15346742	K562	blood:	n/a	n/a

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15199826-15199876	HUVEC	blood vessel:	n/a
2	chr21:15199826-15199876	LNCaP	prostate:	n/a
3	chr21:15199826-15199876	HRE	kidney:	n/a
4	chr21:15134738-15134788	Jurkat	blood:	n/a
5	chr21:15135145-15135195	HRCEpiC	kidney:	n/a
6	chr21:15134738-15134788	HRCEpiC	kidney:	n/a
7	chr21:15307662-15307712	NB4	blood:	n/a
8	chr21:15311594-15311644	CMK	blood:	n/a
9	chr21:15221404-15221454	Jurkat	blood:	n/a
10	chr21:15144580-15144630	HL-60	blood:	n/a
11	chr21:15134491-15134541	HCM	heart:	n/a
12	chr21:15307662-15307712	HRE	kidney:	n/a
13	chr21:15215654-15215704	NH-A	brain:	n/a
14	chr21:15307662-15307712	LNCaP	prostate:	n/a
15	chr21:15149415-15149465	AG09319	gingival:	n/a
16	chr21:15215654-15215704	HMEC	breast:	n/a
17	chr21:15135580-15135630	GM06990	blood:	n/a
18	chr21:15199826-15199876	HL-60	blood:	n/a
19	chr21:15199826-15199876	AG09319	gingival:	n/a
20	chr21:15134491-15134541	AG04449	skin:	fetal
21	chr21:15309846-15309896	SK-N-SH_RA	brain:	n/a
22	chr21:15200106-15200156	ovcar-3	ovarian:	n/a
23	chr21:15199826-15199876	K562	blood:	n/a
24	chr21:15221404-15221454	A549	lung:	n/a
25	chr21:15200106-15200156	SK-N-SH	brain:	n/a
26	chr21:15200106-15200156	U87	brain:	n/a
27	chr21:15309724-15309774	HCM	heart:	n/a
28	chr21:15197291-15197341	MCF10A-Er-Src	breast:	n/a
29	chr21:15309724-15309774	HMEC	breast:	n/a
30	chr21:15131938-15131988	HEEpiC	esophagus:	n/a
31	chr21:15309724-15309774	ECC-1	luminal epithelium:	n/a
32	chr21:15134491-15134541	Hela-S3	cervix:	n/a
33	chr21:15135043-15135093	LNCaP	prostate:	n/a
34	chr21:15220709-15220759	HCT-116	colon:	n/a
35	chr21:15309724-15309774	SAEC	small airway:	n/a
36	chr21:15147467-15147517	SKMC	muscle:	n/a
37	chr21:15221404-15221454	Hepatocyte	liver:	n/a
38	chr21:15131938-15131988	SK-N-SH_RA	brain:	n/a
39	chr21:15199826-15199876	GM12878	blood:	n/a
40	chr21:15199826-15199876	Hela-S3	cervix:	n/a
41	chr21:15149415-15149465	ProgFib	skin:	n/a
42	chr21:15135145-15135195	A549	lung:	n/a
43	chr21:15311594-15311644	AG04450	lung:	fetal
44	chr21:15138802-15138852	Caco-2	colon:	n/a
45	chr21:15148636-15148686	PFSK-1	brain:	n/a
46	chr21:15215654-15215704	ovcar-3	ovarian:	n/a
47	chr21:15135336-15135386	HRCEpiC	kidney:	n/a
48	chr21:15221404-15221454	AG09319	gingival:	n/a
49	chr21:15215654-15215704	GM12891	blood:	n/a
50	chr21:15200106-15200156	BE2_C	brain:	n/a

No data

(count:41 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081131
2	lnc-LIPI-4	chr21:15344317-15344450	NONHSAT081133
3	lnc-POTED-8	chr21:15211439-15211730	NONHSAT081121
4	lnc-LIPI-7	chr21:15216343-15216385	NONHSAT147184
5	lnc-LIPI-4	chr21:15311695-15311749	NONHSAT081132
6	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081133
7	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081133
8	lnc-LIPI-9	chr21:15116918-15118607	l_2168_chr21:15116917-15119815_placenta
9	lnc-LIPI-7	chr21:15215454-15215753	NONHSAT081124
10	lnc-LIPI-4	chr21:15311567-15311749	NONHSAT081131
11	lnc-LIPI-4	chr21:15316065-15316183	NONHSAT081133
12	lnc-LIPI-7	chr21:15217426-15217595	NONHSAT081125
13	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081131
14	lnc-LIPI-7	chr21:15218334-15218713	NONHSAT081125
15	lnc-POTED-11	chr21:15268407-15268509	NONHSAT081129
16	lnc-LIPI-7	chr21:15220411-15220685	NONHSAT081124
17	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081132
18	lnc-LIPI-4	chr21:15339702-15339757	NONHSAT081133
19	lnc-LIPI-4	chr21:15317360-15317464	NONHSAT081132
20	lnc-LIPI-4	chr21:15342294-15342431	NONHSAT081133
21	lnc-POTED-2	chr21:15143886-15144061	XLOC_013860
22	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081132
23	lnc-LIPI-7	chr21:15216343-15216456	NONHSAT081124
24	lnc-LIPI-4	chr21:15335061-15335106	NONHSAT081132
25	lnc-LIPI-7	chr21:15217326-15217595	NONHSAT081124
26	lnc-LIPI-4	chr21:15335061-15335192	NONHSAT081133
27	lnc-POTED-11	chr21:15265662-15265761	NONHSAT081129
28	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081133
29	lnc-POTED-11	chr21:15286426-15287046	NONHSAT081129
30	lnc-POTED-9	chr21:15240747-15241288	NONHSAT081122
31	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081132
32	lnc-LIPI-7	chr21:15219080-15219270	NONHSAT081124
33	lnc-POTED-2	chr21:15142253-15142534	XLOC_013860
34	lnc-LIPI-4	chr21:15310267-15310388	NONHSAT081131
35	lnc-LIPI-9	chr21:15119715-15119817	l_2168_chr21:15116917-15119815_placenta
36	lnc-LIPI-7	chr21:15218334-15218462	NONHSAT081124
37	lnc-LIPI-4	chr21:15342294-15342324	NONHSAT081131
38	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081131
39	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081131
40	lnc-POTED-9	chr21:15212726-15212964	NONHSAT081122
41	lnc-LIPI-7	chr21:15215457-15215753	NONHSAT147184

No data

Variant related genes	Relation type
FEM1AP1	TF binding region
TERF1P1	TF binding region
RNU6-954P	TF binding region
ZNF114P1	TF binding region
ENSG00000224922	TF binding region
SNX18P13	TF binding region
FAM207CP	TF binding region
GXYLT1P2	TF binding region
RHOT1P2	TF binding region
CNN2P7	TF binding region
CYP4F29P	TF binding region
ANKRD20A11P	TF binding region
FEM1AP1	CpG island
TERF1P1	CpG island
RNU6-954P	CpG island
ZNF114P1	CpG island
ENSG00000224922	CpG island
SNX18P13	CpG island
FAM207CP	CpG island
GXYLT1P2	CpG island
RHOT1P2	CpG island
CNN2P7	CpG island
CYP4F29P	CpG island
ANKRD20A11P	CpG island

Extended variants
information (count: 7934 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:7934 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7283616	chr21:15116946-15116947	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs368076026	chr21:15116953-15116954	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs200592755	chr21:15117026-15117027	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs201340692	chr21:15117032-15117033	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs112705231	chr21:15117123-15117124	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs372268542	chr21:15117187-15117188	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs374112249	chr21:15117190-15117191	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs149602458	chr21:15117233-15117234	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs536341232	chr21:15117285-15117286	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs111945897	chr21:15117486-15117487	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs62215161	chr21:15117601-15117602	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs112562456	chr21:15117944-15117945	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs61599323	chr21:15117946-15117947	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs374909278	chr21:15118216-15118217	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs61670535	chr21:15118264-15118265	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs372637413	chr21:15118390-15118391	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs377262574	chr21:15118428-15118429	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs200389683	chr21:15118431-15118432	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs374469179	chr21:15119739-15119740	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs199680306	chr21:15130108-15130109	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs368983383	chr21:15130756-15130757	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs368881290	chr21:15130779-15130780	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs62215166	chr21:15132793-15132794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs373881568	chr21:15132794-15132795	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs370455268	chr21:15133017-15133018	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs114401614	chr21:15134369-15134370	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs369455872	chr21:15134379-15134380	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs374158911	chr21:15134386-15134387	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs8130717	chr21:15134577-15134578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs370156690	chr21:15134602-15134603	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371785422	chr21:15134614-15134615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs376850196	chr21:15134650-15134651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs146554625	chr21:15137578-15137579	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs532601820	chr21:15138477-15138478	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs145562005	chr21:15138490-15138491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs200709159	chr21:15144585-15144586	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs201713340	chr21:15145427-15145428	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374978950	chr21:15145484-15145485	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs371531204	chr21:15145505-15145506	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs113925516	chr21:15146879-15146880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371959170	chr21:15146964-15146965	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs3875046	chr21:15147043-15147044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375976857	chr21:15147692-15147693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369875193	chr21:15147720-15147721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112956751	chr21:15147826-15147827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374885872	chr21:15147897-15147898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112319826	chr21:15148024-15148025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117090124	chr21:15148130-15148131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368372247	chr21:15148290-15148291	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs57431843	chr21:15148366-15148367	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Multiple myeloma	17550852	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15147000-15148800	Enhancers	Dnd41	blood
2	chr21:15164800-15165400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr21:15165400-15165800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr21:15165400-15167200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr21:15165600-15167400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr21:15165800-15167400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr21:15166200-15167200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr21:15167400-15169600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr21:15169200-15170800	Enhancers	Dnd41	blood
10	chr21:15169600-15171000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr21:15170000-15170800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr21:15179200-15179600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr21:15182400-15182800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr21:15186800-15187800	Enhancers	Dnd41	blood
15	chr21:15191600-15193200	Enhancers	Placenta	Placenta
16	chr21:15196200-15197400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr21:15197400-15197600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr21:15197600-15198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr21:15198000-15198200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr21:15223800-15224000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
21	chr21:15235200-15235800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr21:15244800-15245200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
23	chr21:15245200-15246200	Weak transcription	Dnd41	blood
24	chr21:15246200-15247600	Enhancers	Dnd41	blood
25	chr21:15247600-15256200	Weak transcription	Dnd41	blood
26	chr21:15249400-15250200	Enhancers	K562	blood
27	chr21:15250200-15250600	Weak transcription	K562	blood
28	chr21:15250600-15250800	Enhancers	K562	blood
29	chr21:15250800-15252400	Weak transcription	K562	blood
30	chr21:15252400-15253000	Enhancers	K562	blood
31	chr21:15254400-15254800	Active TSS	Fetal Heart	heart
32	chr21:15254800-15258800	Weak transcription	Fetal Heart	heart
33	chr21:15256200-15256600	Enhancers	Dnd41	blood
34	chr21:15256600-15265600	Weak transcription	Dnd41	blood
35	chr21:15258800-15259200	ZNF genes & repeats	Fetal Heart	heart
36	chr21:15265600-15267000	Enhancers	Dnd41	blood
37	chr21:15269000-15269400	Enhancers	K562	blood
38	chr21:15269200-15269400	Enhancers	Lung	lung
39	chr21:15269200-15269400	Enhancers	A549	lung
40	chr21:15270000-15270400	Active TSS	Fetal Heart	heart
41	chr21:15275200-15276000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr21:15276000-15278800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr21:15277000-15281400	Weak transcription	Esophagus	oesophagus
44	chr21:15277000-15292200	Weak transcription	Dnd41	blood
45	chr21:15292200-15296200	Enhancers	Dnd41	blood
46	chr21:15292800-15293200	Enhancers	K562	blood
47	chr21:15293200-15293600	Weak transcription	K562	blood
48	chr21:15293600-15296200	Enhancers	K562	blood
49	chr21:15295200-15295800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr21:15295200-15296200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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