Variant report

Variant	nsv913414
Chromosome Location	chr21:17383785-17459507
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	chr21:17454775-17455077	HepG2	liver:	n/a	chr21:17454915-17454931
2	ARID3A	chr21:17452104-17452625	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:17454805-17455058	K562	blood:	n/a	chr21:17454915-17454931
4	BCL3	chr21:17457869-17458022	GM12878	blood:	n/a	n/a
5	BRCA1	chr21:17452021-17452405	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr21:17441548-17441765	IMR90	lung:	n/a	chr21:17441653-17441664 chr21:17441652-17441663
7	CEBPB	chr21:17405558-17405813	HepG2	liver:	n/a	chr21:17405673-17405684
8	CEBPB	chr21:17452043-17452550	Hela-S3	cervix:	n/a	chr21:17452229-17452240
9	CEBPB	chr21:17444904-17445415	IMR90	lung:	n/a	n/a
10	CEBPB	chr21:17441592-17441700	HepG2	liver:	n/a	chr21:17441653-17441664 chr21:17441652-17441663
11	CEBPB	chr21:17452112-17452490	MCF-7	breast:	n/a	chr21:17452229-17452240
12	CEBPB	chr21:17425250-17425311	HepG2	liver:	n/a	chr21:17425285-17425296
13	CEBPB	chr21:17452092-17452529	A549	lung:	n/a	chr21:17452229-17452240
14	CEBPB	chr21:17452140-17452410	A549	lung:	n/a	chr21:17452229-17452240
15	CEBPB	chr21:17412830-17413513	HepG2	liver:	n/a	chr21:17412969-17412980 chr21:17412968-17412979 chr21:17412970-17412979
16	CEBPB	chr21:17412820-17413512	IMR90	lung:	n/a	chr21:17412969-17412980 chr21:17412968-17412979 chr21:17412970-17412979
17	CEBPB	chr21:17452064-17452599	HepG2	liver:	n/a	chr21:17452229-17452240
18	CEBPB	chr21:17451984-17452511	A549	lung:	n/a	chr21:17452229-17452240
19	CEBPB	chr21:17405654-17405729	Hela-S3	cervix:	n/a	chr21:17405673-17405684
20	CEBPB	chr21:17405647-17405807	A549	lung:	n/a	chr21:17405673-17405684
21	CEBPB	chr21:17452028-17452533	IMR90	lung:	n/a	chr21:17452229-17452240
22	CEBPB	chr21:17419141-17419620	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr21:17412864-17413469	Hela-S3	cervix:	n/a	chr21:17412969-17412980 chr21:17412968-17412979 chr21:17412970-17412979
24	CEBPB	chr21:17405567-17405758	H1-hESC	embryonic stem cell:	n/a	chr21:17405673-17405684
25	CEBPB	chr21:17442502-17442706	MCF-7	breast:	n/a	n/a
26	CTCF	chr21:17442520-17442670	AG04449	skin:	n/a	n/a
27	CTCF	chr21:17454859-17455025	A549	lung:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
28	CTCF	chr21:17454840-17454990	GM12875	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
29	CTCF	chr21:17454808-17455018	Medullo	brain:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
30	CTCF	chr21:17454740-17454890	HVMF	connective:	n/a	n/a
31	CTCF	chr21:17454820-17454970	GM12873	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
32	CTCF	chr21:17442500-17442650	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr21:17454880-17455030	GM06990	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
34	CTCF	chr21:17442540-17442690	HAc	cerebellar:	n/a	n/a
35	CTCF	chr21:17455260-17455410	GM12873	blood:	n/a	n/a
36	CTCF	chr21:17442516-17442667	Medullo	brain:	n/a	n/a
37	CTCF	chr21:17454660-17454810	AG04449	skin:	n/a	n/a
38	CTCF	chr21:17454835-17455060	Spleen_OC	spleen:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
39	CTCF	chr21:17454880-17455030	GM12865	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
40	CTCF	chr21:17446223-17446333	Medullo	brain:	n/a	n/a
41	CTCF	chr21:17442520-17442670	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr21:17454883-17455012	GM10266	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
43	CTCF	chr21:17457372-17457485	LNCaP	prostate:	n/a	n/a
44	CTCF	chr21:17442560-17442710	HAc	cerebellar:	n/a	n/a
45	CTCF	chr21:17457407-17457410	ProgFib	skin:	n/a	n/a
46	CTCF	chr21:17454742-17454784	Gliobla	brain:	n/a	n/a
47	CTCF	chr21:17442500-17442650	AG09319	gingival:	n/a	n/a
48	CTCF	chr21:17454848-17455009	Kidney_OC	kidney:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
49	CTCF	chr21:17442340-17442490	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr21:17442160-17442310	HMF	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:17442467-17442517	LNCaP	prostate:	n/a
2	chr21:17442467-17442517	H1-hESC	embryonic stem cell:	embryo
3	chr21:17442803-17442853	GM19239	blood:	n/a
4	chr21:17442803-17442853	ECC-1	luminal epithelium:	n/a
5	chr21:17442803-17442853	K562	blood:	n/a
6	chr21:17442803-17442853	HRCEpiC	kidney:	n/a
7	chr21:17442467-17442517	HAEpiC	amniotic membrane:	n/a
8	chr21:17441953-17442003	HNPCEpiC	eye:	n/a
9	chr21:17442663-17442713	HPAEpiC	pulmonary alveolar:	n/a
10	chr21:17442467-17442517	GM12892	blood:	n/a
11	chr21:17442803-17442853	AG04449	skin:	fetal
12	chr21:17442803-17442853	Hela-S3	cervix:	n/a
13	chr21:17441953-17442003	CMK	blood:	n/a
14	chr21:17442467-17442517	BJ	skin:	n/a
15	chr21:17442803-17442853	MCF-7	breast:	n/a
16	chr21:17442467-17442517	NT2-D1	testis:	n/a
17	chr21:17442663-17442713	GM12878	blood:	n/a
18	chr21:17442467-17442517	Hela-S3	cervix:	n/a
19	chr21:17442467-17442517	CMK	blood:	n/a
20	chr21:17442803-17442853	A549	lung:	n/a
21	chr21:17442467-17442517	HCF	heart:	n/a
22	chr21:17441953-17442003	SK-N-SH_RA	brain:	n/a
23	chr21:17442663-17442713	AG09319	gingival:	n/a
24	chr21:17441953-17442003	AG09309	skin:	n/a
25	chr21:17442663-17442713	SK-N-SH	brain:	n/a
26	chr21:17442803-17442853	HNPCEpiC	eye:	n/a
27	chr21:17442663-17442713	NH-A	brain:	n/a
28	chr21:17442467-17442517	PANC-1	pancreas:	n/a
29	chr21:17441953-17442003	PFSK-1	brain:	n/a
30	chr21:17442803-17442853	PANC-1	pancreas:	n/a
31	chr21:17442803-17442853	SKMC	muscle:	n/a
32	chr21:17441953-17442003	HPAEpiC	pulmonary alveolar:	n/a
33	chr21:17441953-17442003	NHBE	bronchial:	n/a
34	chr21:17442803-17442853	Jurkat	blood:	n/a
35	chr21:17442663-17442713	HUVEC	blood vessel:	n/a
36	chr21:17442663-17442713	HEEpiC	esophagus:	n/a
37	chr21:17442467-17442517	Jurkat	blood:	n/a
38	chr21:17442467-17442517	HCT-116	colon:	n/a
39	chr21:17442467-17442517	T-47D	breast:	n/a
40	chr21:17441953-17442003	IMR90	lung:	fetal
41	chr21:17442467-17442517	RPTEC	kidney:	n/a
42	chr21:17442803-17442853	NH-A	brain:	n/a
43	chr21:17441953-17442003	AG10803	skin:	n/a
44	chr21:17441953-17442003	H1-hESC	embryonic stem cell:	embryo
45	chr21:17442803-17442853	GM12891	blood:	n/a
46	chr21:17442467-17442517	ProgFib	skin:	n/a
47	chr21:17442803-17442853	HPAEpiC	pulmonary alveolar:	n/a
48	chr21:17442467-17442517	SKMC	muscle:	n/a
49	chr21:17442803-17442853	NB4	blood:	n/a
50	chr21:17442663-17442713	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:17431681..17433944-chr21:17437804..17439810,2	MCF-7	breast:
2	chr21:17379808..17382152-chr21:17382746..17385605,3	MCF-7	breast:
3	chr21:17405738..17408862-chr21:17414467..17417425,3	MCF-7	breast:
4	chr21:17431681..17433944-chr21:17437804..17439810,2	MCF-7	breast:
5	chr21:17457077..17457729-chr21:17702169..17702961,2	MCF-7	breast:
6	chr21:17266810..17267465-chr21:17454846..17455467,2	MCF-7	breast:
7	chr21:17454496..17455374-chr21:17702457..17703273,3	MCF-7	breast:
8	chr21:17409413..17411769-chr21:17412159..17413717,2	MCF-7	breast:
9	chr21:17409413..17411769-chr21:17412159..17413717,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386.6
2	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386.6
3	lnc-USP25-2	chr21:17442853-17442887	ENSG00000215386.6
4	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386
5	lnc-USP25-2	chr21:17443553-17443718	ENSG00000215386
6	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386
7	lnc-USP25-2	chr21:17442842-17442868	ENSG00000215386.6
8	lnc-USP25-2	chr21:17442842-17442868	ENSG00000215386

Variant related genes	Relation type
RNU6-426P	TF binding region
LINC00478	TF binding region
RNU6-426P	CpG island
LINC00478	CpG island
ENSG00000252273	chromatin interactions
ENSG00000215386	chromatin interactions
STAT3	miRNA target sites
DCBLD2	miRNA target sites
ATAD2	miRNA target sites
MEF2C	miRNA target sites

Extended variants
information (count: 1657 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1657 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2823547	chr21:17383785-17383786	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571276396	chr21:17383798-17383799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533829309	chr21:17383906-17383907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs66837398	chr21:17383941-17383942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs374959875	chr21:17383952-17383953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552254220	chr21:17383971-17383972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367561775	chr21:17383991-17383992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372369497	chr21:17384002-17384003	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs10482877	chr21:17384024-17384025	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555713137	chr21:17384032-17384033	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs140762153	chr21:17384066-17384067	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs141266481	chr21:17384107-17384108	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs146608592	chr21:17384108-17384109	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs71185524	chr21:17384128-17384129	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs534405377	chr21:17384176-17384177	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs16992557	chr21:17384227-17384228	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73894709	chr21:17384277-17384278	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs532250353	chr21:17384305-17384306	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs200908389	chr21:17384355-17384356	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs72547890	chr21:17384357-17384358	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs34986570	chr21:17384358-17384359	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs200350799	chr21:17384359-17384360	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs199502332	chr21:17384361-17384362	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs540278226	chr21:17384377-17384378	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs376645884	chr21:17384449-17384450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78853264	chr21:17384453-17384454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573828651	chr21:17384468-17384469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542785008	chr21:17384480-17384481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201214291	chr21:17384489-17384490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12483594	chr21:17384520-17384521	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs56141957	chr21:17384534-17384535	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551392658	chr21:17384571-17384572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12483611	chr21:17384580-17384581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12483563	chr21:17384638-17384639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs149693424	chr21:17384647-17384648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138131072	chr21:17384695-17384696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397971644	chr21:17384702-17384703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187707442	chr21:17384709-17384710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535987895	chr21:17384717-17384718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541514315	chr21:17384718-17384719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369416875	chr21:17384734-17384735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74975712	chr21:17384750-17384751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372706669	chr21:17384819-17384820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569364218	chr21:17384828-17384829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191612008	chr21:17384848-17384849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558027677	chr21:17384917-17384918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58297914	chr21:17384921-17384922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574848856	chr21:17384939-17384940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76869320	chr21:17384950-17384951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202133766	chr21:17384952-17384953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	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
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
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
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	20409316	CNVD
Gastric cancer	18160780	CNVD

Chromatin state (count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17380800-17384000	Weak transcription	Osteobl	bone
2	chr21:17384000-17384400	Active TSS	Osteobl	bone
3	chr21:17384200-17384400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr21:17384400-17386000	Weak transcription	Osteobl	bone
5	chr21:17384400-17386200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr21:17386000-17386400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr21:17386000-17387000	Active TSS	Osteobl	bone
8	chr21:17386200-17386400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr21:17386200-17386600	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr21:17386200-17386800	Active TSS	Ovary	ovary
11	chr21:17386200-17387000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr21:17386200-17387000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr21:17386400-17386800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr21:17386400-17387000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr21:17386600-17387000	Active TSS	Adipose Nuclei	Adipose
16	chr21:17386600-17387000	Active TSS	Colon Smooth Muscle	Colon
17	chr21:17386600-17387000	Active TSS	Stomach Smooth Muscle	stomach
18	chr21:17386800-17387000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr21:17387000-17389200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr21:17389000-17390000	Active TSS	NHDF-Ad	bronchial
21	chr21:17389200-17390000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr21:17394600-17394800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr21:17406400-17407600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr21:17406400-17407800	Enhancers	Fetal Brain Female	brain
25	chr21:17407600-17407800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr21:17407600-17409400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr21:17408000-17409200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr21:17408600-17409600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr21:17408600-17409800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr21:17409200-17409600	Enhancers	Primary hematopoietic stem cells	blood
31	chr21:17409200-17410000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr21:17409400-17410400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr21:17409600-17410000	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr21:17409600-17410400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr21:17409800-17410200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr21:17409800-17410400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
37	chr21:17410000-17410200	Enhancers	Primary hematopoietic stem cells	blood
38	chr21:17410000-17410400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr21:17410000-17410800	Enhancers	HMEC	breast
40	chr21:17410200-17410400	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr21:17410400-17410800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr21:17410400-17411000	Enhancers	Primary hematopoietic stem cells	blood
43	chr21:17410400-17411000	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr21:17410400-17411200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr21:17410400-17411200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr21:17411000-17412200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr21:17412200-17412400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
48	chr21:17414000-17416600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr21:17416400-17417000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr21:17418800-17419000	Enhancers	Osteobl	bone

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