Variant report

Variant	nsv913405
Chromosome Location	chr21:15875108-15899085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:0)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15898648-15900165	K562	blood:	n/a	n/a
2	ARID3A	chr21:15879542-15879724	K562	blood:	n/a	n/a
3	ATF2	chr21:15895437-15896021	GM12878	blood:	n/a	n/a
4	BACH1	chr21:15898648-15899278	K562	blood:	n/a	n/a
5	BATF	chr21:15895588-15895933	GM12878	blood:	n/a	n/a
6	BCLAF1	chr21:15895456-15896037	GM12878	blood:	n/a	chr21:15895567-15895576
7	BCLAF1	chr21:15895520-15896091	GM12878	blood:	n/a	chr21:15895567-15895576
8	BHLHE40	chr21:15886104-15886131	GM12878	blood:	n/a	n/a
9	BHLHE40	chr21:15895526-15896248	GM12878	blood:	n/a	n/a
10	CCNT2	chr21:15882593-15883685	K562	blood:	n/a	n/a
11	CCNT2	chr21:15885204-15886543	K562	blood:	n/a	n/a
12	CEBPB	chr21:15895273-15895397	K562	blood:	n/a	n/a
13	CEBPB	chr21:15892795-15893073	HepG2	liver:	n/a	n/a
14	CEBPB	chr21:15892330-15892432	K562	blood:	n/a	n/a
15	CEBPB	chr21:15892755-15893032	K562	blood:	n/a	n/a
16	CEBPB	chr21:15892923-15893123	A549	lung:	n/a	n/a
17	CEBPB	chr21:15892771-15893102	K562	blood:	n/a	n/a
18	CEBPB	chr21:15884037-15884291	K562	blood:	n/a	n/a
19	CEBPD	chr21:15886091-15886833	K562	blood:	n/a	n/a
20	CHD1	chr21:15895330-15895513	GM12878	blood:	n/a	n/a
21	CHD1	chr21:15899078-15899108	GM12878	blood:	n/a	n/a
22	CHD2	chr21:15882525-15883631	K562	blood:	n/a	n/a
23	CHD2	chr21:15895580-15896162	GM12878	blood:	n/a	n/a
24	CHD2	chr21:15885082-15886463	K562	blood:	n/a	n/a
25	CTCF	chr21:15883426-15883488	ProgFib	skin:	n/a	n/a
26	CTCF	chr21:15898500-15898650	HCPEpiC	choroid plexus:	n/a	n/a
27	CUX1	chr21:15899029-15899409	GM12878	blood:	n/a	n/a
28	CUX1	chr21:15895314-15896208	GM12878	blood:	n/a	n/a
29	EBF1	chr21:15895562-15895982	GM12878	blood:	n/a	n/a
30	EBF1	chr21:15895559-15895840	GM12878	blood:	n/a	n/a
31	ELK1	chr21:15892877-15893024	GM12878	blood:	n/a	n/a
32	EP300	chr21:15895514-15895895	GM12878	blood:	n/a	chr21:15895562-15895576 chr21:15895548-15895562
33	EP300	chr21:15895491-15896195	GM12878	blood:	n/a	chr21:15896181-15896189 chr21:15895562-15895576 chr21:15895548-15895562
34	EP300	chr21:15895601-15895873	GM12878	blood:	n/a	n/a
35	EP300	chr21:15892984-15893223	GM12878	blood:	n/a	n/a
36	EP300	chr21:15879408-15879728	K562	blood:	n/a	n/a
37	FOS	chr21:15895740-15895982	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr21:15895688-15895985	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr21:15898666-15898856	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr21:15895696-15896000	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr21:15888142-15888387	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXM1	chr21:15895503-15896063	GM12878	blood:	n/a	n/a
43	HMGN3	chr21:15882766-15883425	K562	blood:	n/a	n/a
44	HMGN3	chr21:15898213-15898425	K562	blood:	n/a	n/a
45	IKZF1	chr21:15895316-15896161	GM12878	blood:	n/a	n/a
46	IRF1	chr21:15888274-15888283	K562	blood:	n/a	n/a
47	IRF1	chr21:15886373-15886527	K562	blood:	n/a	n/a
48	IRF1	chr21:15893243-15893398	K562	blood:	n/a	n/a
49	IRF1	chr21:15898382-15900002	K562	blood:	n/a	chr21:15899104-15899118 chr21:15899328-15899335 chr21:15898933-15898946
50	IRF1	chr21:15897426-15898012	K562	blood:	n/a	n/a

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15882752..15884455-chr21:15884908..15886969,2	K562	blood:
2	chr21:15898174..15900938-chr21:15917034..15919951,2	K562	blood:
3	chr21:15878918..15881751-chr21:15882365..15886915,4	K562	blood:
4	chr21:15886516..15889058-chr21:15891380..15893121,2	K562	blood:
5	chr21:15885068..15887603-chr21:15887779..15891209,3	K562	blood:
6	chr21:15875519..15877306-chr21:15885573..15888247,2	K562	blood:
7	chr21:15863117..15865240-chr21:15875551..15877419,2	K562	blood:
8	chr21:15883124..15887603-chr21:15889415..15891209,4	K562	blood:
9	chr21:15889503..15891554-chr21:15895441..15898226,3	K562	blood:
10	chr21:15888072..15891465-chr21:15894886..15898226,3	K562	blood:
11	chr21:15886516..15889058-chr21:15891380..15893121,2	K562	blood:
12	chr21:15881208..15883540-chr21:15886975..15889188,2	K562	blood:
13	chr21:15882752..15884455-chr21:15884908..15886969,2	K562	blood:
14	chr21:15885414..15887800-chr21:16108116..16110605,2	K562	blood:
15	chr21:15882543..15884938-chr21:15891850..15893710,2	K562	blood:
16	chr21:15882543..15885229-chr21:15891850..15893526,2	K562	blood:
17	chr21:15875519..15877306-chr21:15885573..15888247,2	K562	blood:
18	chr21:15876554..15878638-chr21:15883430..15885143,2	K562	blood:
19	chr21:15876554..15878638-chr21:15883430..15885143,2	K562	blood:
20	chr21:15872479..15875273-chr21:15885613..15887603,2	K562	blood:
21	chr21:15883124..15887603-chr21:15889415..15891209,4	K562	blood:
22	chr21:15889503..15891554-chr21:15895441..15898226,3	K562	blood:
23	chr21:15893314..15896057-chr21:15897268..15899492,2	K562	blood:
24	chr21:15893314..15896057-chr21:15897268..15899492,2	K562	blood:
25	chr21:15881208..15883540-chr21:15886975..15889188,2	K562	blood:
26	chr21:15870901..15873770-chr21:15873802..15877193,3	K562	blood:
27	chr21:15888072..15891465-chr21:15894886..15898226,3	K562	blood:
28	chr21:15878918..15881751-chr21:15882365..15886915,4	K562	blood:
29	chr21:15882543..15885229-chr21:15891850..15893526,2	K562	blood:
30	chr21:15885068..15887603-chr21:15887779..15891209,3	K562	blood:
31	chr21:15865993..15867759-chr21:15875544..15877082,2	K562	blood:
32	chr21:15882543..15884938-chr21:15891850..15893710,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF165138.7.1-4	chr21:15895592-15895715	NONHSAT081164
2	lnc-AF165138.7.1-4	chr21:15893494-15893542	NONHSAT081164

No data

Variant related genes	Relation type
SAMSN1	TF binding region
ENSG00000155307	chromatin interactions

Extended variants
information (count: 1102 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17240640	chr21:15875108-15875109	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115765421	chr21:15875157-15875158	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs192467763	chr21:15875168-15875169	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs113972103	chr21:15875280-15875281	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576380363	chr21:15875336-15875337	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs8129951	chr21:15875342-15875343	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183435594	chr21:15875343-15875344	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs373177190	chr21:15875344-15875345	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548005890	chr21:15875349-15875350	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs561491946	chr21:15875406-15875407	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs187759770	chr21:15875452-15875453	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs550232795	chr21:15875461-15875462	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs191116988	chr21:15875481-15875482	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs144793096	chr21:15875494-15875495	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs79977972	chr21:15875510-15875511	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376231834	chr21:15875522-15875523	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs558950927	chr21:15875551-15875552	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534440883	chr21:15875552-15875553	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs201907902	chr21:15875556-15875557	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147170159	chr21:15875558-15875559	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140355116	chr21:15875576-15875577	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572719206	chr21:15875578-15875579	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs115179588	chr21:15875579-15875580	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs149666814	chr21:15875580-15875581	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145457372	chr21:15875608-15875609	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545408822	chr21:15875618-15875619	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs559038302	chr21:15875664-15875665	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs73344137	chr21:15875701-15875702	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs541569534	chr21:15875743-15875744	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs561507279	chr21:15875744-15875745	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs541226251	chr21:15875766-15875767	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561525409	chr21:15875806-15875807	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs148912725	chr21:15875844-15875845	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs544055930	chr21:15875880-15875881	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376131229	chr21:15875913-15875914	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs73344139	chr21:15875928-15875929	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532888602	chr21:15875961-15875962	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs73171390	chr21:15875980-15875981	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35958469	chr21:15875996-15875997	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs116501166	chr21:15876010-15876011	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs528141033	chr21:15876026-15876027	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547220657	chr21:15876027-15876028	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs76400844	chr21:15876057-15876058	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373978067	chr21:15876058-15876059	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs536862953	chr21:15876127-15876128	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs557159953	chr21:15876147-15876148	Strong transcription ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs112741771	chr21:15876201-15876202	Strong transcription Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184402281	chr21:15876206-15876207	Strong transcription Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539770287	chr21:15876209-15876210	Strong transcription Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs28585611	chr21:15876216-15876217	Strong transcription Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15853200-15885800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr21:15853400-15905400	Weak transcription	HUVEC	blood vessel
3	chr21:15854800-15875600	Weak transcription	Thymus	Thymus
4	chr21:15856200-15875400	Weak transcription	Spleen	Spleen
5	chr21:15857200-15882600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr21:15861600-15881000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr21:15862600-15889400	Strong transcription	Dnd41	blood
8	chr21:15864800-15878400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr21:15864800-15881600	Strong transcription	Primary B cells from peripheral blood	blood
10	chr21:15865000-15878600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr21:15866200-15876800	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr21:15866800-15877800	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr21:15867000-15877400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr21:15867000-15890600	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr21:15867200-15876800	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr21:15867600-15875600	Strong transcription	GM12878-XiMat	blood
17	chr21:15869200-15876800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr21:15869400-15878400	Strong transcription	K562	blood
19	chr21:15870600-15875200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr21:15871000-15876800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
21	chr21:15871200-15875400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr21:15872000-15877000	Strong transcription	Primary T cells from cord blood	blood
23	chr21:15872200-15875800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr21:15872200-15876000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr21:15872800-15875800	Strong transcription	Primary hematopoietic stem cells	blood
26	chr21:15872800-15876400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr21:15872800-15876400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr21:15873200-15875600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr21:15873400-15881200	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr21:15873400-15891000	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr21:15873600-15875600	Weak transcription	Primary B cells from cord blood	blood
32	chr21:15874000-15875400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr21:15874200-15876800	Strong transcription	Fetal Thymus	thymus
34	chr21:15874800-15877800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr21:15875200-15875800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
36	chr21:15875400-15876400	Strong transcription	Spleen	Spleen
37	chr21:15875400-15876600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr21:15875400-15876600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr21:15875600-15876200	ZNF genes & repeats	Primary B cells from cord blood	blood
40	chr21:15875600-15876200	ZNF genes & repeats	GM12878-XiMat	blood
41	chr21:15875600-15876400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
42	chr21:15875600-15876400	Strong transcription	Thymus	Thymus
43	chr21:15875800-15878200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
44	chr21:15875800-15882000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:15875800-15894000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr21:15876000-15878800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr21:15876200-15878400	Strong transcription	GM12878-XiMat	blood
48	chr21:15876200-15879600	Weak transcription	Primary B cells from cord blood	blood
49	chr21:15876400-15879400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr21:15876400-15881000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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