Variant report

Variant	nsv1062532
Chromosome Location	chr21:15616629-15654501
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	chr21:15643398-15643769	K562	blood:	n/a	n/a
2	ARID3A	chr21:15632038-15632466	K562	blood:	n/a	n/a
3	ARID3A	chr21:15636185-15636385	K562	blood:	n/a	n/a
4	ARID3A	chr21:15632046-15632350	HepG2	liver:	n/a	n/a
5	ATF1	chr21:15636259-15636544	K562	blood:	n/a	n/a
6	ATF1	chr21:15643368-15643726	K562	blood:	n/a	n/a
7	ATF3	chr21:15636281-15636574	K562	blood:	n/a	n/a
8	BACH1	chr21:15632039-15632366	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr21:15646763-15647064	K562	blood:	n/a	chr21:15646984-15646993 chr21:15646984-15646993 chr21:15646983-15646992
10	BHLHE40	chr21:15643413-15643717	K562	blood:	n/a	n/a
11	BHLHE40	chr21:15626679-15626685	GM12878	blood:	n/a	n/a
12	BHLHE40	chr21:15646919-15647015	HepG2	liver:	n/a	chr21:15646984-15646993 chr21:15646984-15646993 chr21:15646983-15646992
13	BHLHE40	chr21:15646075-15646422	K562	blood:	n/a	n/a
14	BRCA1	chr21:15633651-15633671	GM12878	blood:	n/a	n/a
15	CBX3	chr21:15646066-15646407	K562	blood:	n/a	n/a
16	CCNT2	chr21:15646221-15646874	K562	blood:	n/a	n/a
17	CCNT2	chr21:15643026-15643838	K562	blood:	n/a	chr21:15643572-15643592
18	CEBPB	chr21:15647225-15647548	K562	blood:	n/a	chr21:15647385-15647398
19	CEBPB	chr21:15647260-15647457	H1-hESC	embryonic stem cell:	n/a	chr21:15647385-15647398
20	CEBPB	chr21:15643370-15643730	K562	blood:	n/a	chr21:15643550-15643567
21	CEBPB	chr21:15643304-15643758	K562	blood:	n/a	chr21:15643550-15643567
22	CEBPB	chr21:15636263-15636492	K562	blood:	n/a	n/a
23	CEBPB	chr21:15644175-15644343	K562	blood:	n/a	chr21:15644246-15644259
24	CEBPD	chr21:15643312-15643807	K562	blood:	n/a	n/a
25	CEBPD	chr21:15643245-15643803	K562	blood:	n/a	n/a
26	CREB1	chr21:15643320-15643834	K562	blood:	n/a	n/a
27	CREB1	chr21:15643385-15643755	K562	blood:	n/a	n/a
28	CTCF	chr21:15632100-15632250	SAEC	small airway:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
29	CTCF	chr21:15632066-15632340	Gliobla	brain:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
30	CTCF	chr21:15626040-15626190	NHEK	skin:	n/a	n/a
31	CTCF	chr21:15625971-15626225	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr21:15632093-15632306	LNCaP	prostate:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
33	CTCF	chr21:15626080-15626230	HRE	kidney:	n/a	n/a
34	CTCF	chr21:15626060-15626210	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr21:15631660-15631810	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr21:15626070-15626355	Gliobla	brain:	n/a	n/a
37	CTCF	chr21:15624980-15625130	AG09319	gingival:	n/a	n/a
38	CTCF	chr21:15626040-15626190	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr21:15626080-15626230	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr21:15632041-15632332	K562	blood:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
41	CTCF	chr21:15625990-15626191	Lung_OC	lung:	n/a	n/a
42	CTCF	chr21:15632140-15632290	HFF-Myc	foreskin:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
43	CTCF	chr21:15632120-15632270	BE2_C	brain:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
44	CTCF	chr21:15626220-15626370	GM12866	blood:	n/a	n/a
45	CTCF	chr21:15632120-15632270	AG09319	gingival:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
46	CTCF	chr21:15632140-15632290	SAEC	small airway:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
47	CTCF	chr21:15626100-15626250	HCT-116	colon:	n/a	n/a
48	CTCF	chr21:15632038-15632369	T-47D	breast:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
49	CTCF	chr21:15632120-15632270	AG09309	skin:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
50	CTCF	chr21:15625980-15626130	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15646635-15646685	HL-60	blood:	n/a
2	chr21:15645787-15645837	IMR90	lung:	fetal
3	chr21:15646635-15646685	HL-60	blood:	n/a
4	chr21:15645787-15645837	IMR90	lung:	fetal
5	chr21:15646312-15646362	K562	blood:	n/a
6	chr21:15645988-15646038	GM06990	blood:	n/a
7	chr21:15645787-15645837	HPAEpiC	pulmonary alveolar:	n/a
8	chr21:15646635-15646685	PANC-1	pancreas:	n/a
9	chr21:15645810-15645860	HIPEpiC	eye:	n/a
10	chr21:15646187-15646237	Caco-2	colon:	n/a
11	chr21:15645810-15645860	HAEpiC	amniotic membrane:	n/a
12	chr21:15647368-15647418	BE2_C	brain:	n/a
13	chr21:15646187-15646237	K562	blood:	n/a
14	chr21:15645988-15646038	Hela-S3	cervix:	n/a
15	chr21:15645787-15645837	GM12892	blood:	n/a
16	chr21:15645787-15645837	HUVEC	blood vessel:	n/a
17	chr21:15645810-15645860	NT2-D1	testis:	n/a
18	chr21:15647368-15647418	T-47D	breast:	n/a
19	chr21:15645988-15646038	ProgFib	skin:	n/a
20	chr21:15646187-15646237	H1-hESC	embryonic stem cell:	embryo
21	chr21:15646187-15646237	HUVEC	blood vessel:	n/a
22	chr21:15646187-15646237	PFSK-1	brain:	n/a
23	chr21:15646312-15646362	Jurkat	blood:	n/a
24	chr21:15646635-15646685	HEEpiC	esophagus:	n/a
25	chr21:15645988-15646038	HCPEpiC	choroid plexus:	n/a
26	chr21:15645810-15645860	Caco-2	colon:	n/a
27	chr21:15646635-15646685	PrEC	prostate:	n/a
28	chr21:15645649-15645699	HRE	kidney:	n/a
29	chr21:15645649-15645699	ProgFib	skin:	n/a
30	chr21:15645649-15645699	AG09309	skin:	n/a
31	chr21:15645810-15645860	ovcar-3	ovarian:	n/a
32	chr21:15645649-15645699	HUVEC	blood vessel:	n/a
33	chr21:15646187-15646237	HRE	kidney:	n/a
34	chr21:15645649-15645699	PrEC	prostate:	n/a
35	chr21:15646312-15646362	HUVEC	blood vessel:	n/a
36	chr21:15645649-15645699	Hepatocyte	liver:	n/a
37	chr21:15646312-15646362	T-47D	breast:	n/a
38	chr21:15645649-15645699	HepG2	liver:	n/a
39	chr21:15645787-15645837	AG04450	lung:	fetal
40	chr21:15647368-15647418	GM06990	blood:	n/a
41	chr21:15646312-15646362	PFSK-1	brain:	n/a
42	chr21:15646312-15646362	BE2_C	brain:	n/a
43	chr21:15645810-15645860	MCF10A-Er-Src	breast:	n/a
44	chr21:15645810-15645860	RPTEC	kidney:	n/a
45	chr21:15645810-15645860	GM19239	blood:	n/a
46	chr21:15645810-15645860	HCPEpiC	choroid plexus:	n/a
47	chr21:15645787-15645837	HL-60	blood:	n/a
48	chr21:15646635-15646685	GM12878	blood:	n/a
49	chr21:15646187-15646237	ovcar-3	ovarian:	n/a
50	chr21:15647368-15647418	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:15647599..15649902-chr21:15656709..15659445,2	K562	blood:
2	chr21:15618985..15621962-chr21:15624169..15625950,3	K562	blood:
3	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:
4	chr21:15642588..15643376-chr21:15678270..15679084,2	MCF-7	breast:
5	chr21:15637737..15639634-chr21:15641854..15644729,2	K562	blood:
6	chr21:15616597..15618358-chr21:15624634..15626645,2	K562	blood:
7	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:
8	chr21:15646421..15649560-chr21:15654356..15655933,3	K562	blood:
9	chr21:15652023..15652746-chr7:152811109..152812098,2	MCF-7	breast:
10	chr21:15645251..15647400-chr21:15754351..15756122,2	K562	blood:
11	chr21:15652280..15654566-chr21:15773386..15776181,2	MCF-7	breast:
12	chr21:15637737..15639634-chr21:15641854..15644729,2	K562	blood:
13	chr21:15637216..15639622-chr21:15681292..15683772,2	MCF-7	breast:
14	chr21:15638970..15641725-chr21:15734559..15736787,2	K562	blood:
15	chr21:15611898..15613509-chr21:15614140..15616953,2	K562	blood:
16	chr21:15637824..15639860-chr21:15661262..15662859,2	MCF-7	breast:
17	chr21:15616597..15618358-chr21:15624634..15626645,2	K562	blood:
18	chr21:15612009..15614501-chr21:15615453..15618275,2	K562	blood:
19	chr21:15646421..15649560-chr21:15654356..15655933,3	K562	blood:
20	chr21:15650981..15652853-chr21:15655632..15658875,3	K562	blood:
21	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:
22	chr21:15646214..15647824-chr21:15649237..15651559,2	MCF-7	breast:
23	chr21:15642588..15643574-chr21:15678270..15679033,2	MCF-7	breast:
24	chr21:15618985..15621962-chr21:15624169..15625950,3	K562	blood:
25	chr21:15644504..15646965-chr21:15652945..15655779,2	K562	blood:
26	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081156
2	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081154
3	lnc-RBM11-5	chr21:15640724-15640913	NONHSAT081153
4	lnc-RBM11-5	chr21:15641808-15641980	NONHSAT081153
5	lnc-RBM11-5	chr21:15642846-15642930	NONHSAT081153
6	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081153
7	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081156
8	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081154

Variant related genes	Relation type
ABCC13	TF binding region
ABCC13	CpG island
ENSG00000155304	chromatin interactions
ENSG00000243064	chromatin interactions

Extended variants
information (count: 1519 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1519 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2822503	chr21:15616629-15616630	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191550264	chr21:15616636-15616637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184648563	chr21:15616660-15616661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73890758	chr21:15616680-15616681	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557649871	chr21:15616711-15616712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9647114	chr21:15616729-15616730	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs9647115	chr21:15616750-15616751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs143856200	chr21:15616766-15616767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2822504	chr21:15616772-15616773	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs542932028	chr21:15616793-15616794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577674455	chr21:15616803-15616804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533615338	chr21:15616870-15616871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553574890	chr21:15616873-15616874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140697422	chr21:15616875-15616876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149862495	chr21:15616893-15616894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527833456	chr21:15616988-15616989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75066708	chr21:15617027-15617028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567665361	chr21:15617058-15617059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12482302	chr21:15617116-15617117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76529132	chr21:15617136-15617137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550177178	chr21:15617142-15617143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569206942	chr21:15617170-15617171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs71330049	chr21:15617177-15617178	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs9979484	chr21:15617178-15617179	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs571305999	chr21:15617191-15617192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533898963	chr21:15617210-15617211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2822505	chr21:15617217-15617218	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs437162	chr21:15617242-15617243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs190041430	chr21:15617260-15617261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs63640862	chr21:15617263-15617264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555725591	chr21:15617270-15617271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138151538	chr21:15617271-15617272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79247872	chr21:15617272-15617273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs386816415	chr21:15617274-15617275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77723843	chr21:15617276-15617277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77577997	chr21:15617280-15617281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11910399	chr21:15617284-15617285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181703623	chr21:15617287-15617288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs419398	chr21:15617308-15617309	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541535167	chr21:15617312-15617313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186820039	chr21:15617367-15617368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17208013	chr21:15617406-15617407	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530201744	chr21:15617439-15617440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs926880	chr21:15617444-15617445	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558618857	chr21:15617458-15617459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201966953	chr21:15617469-15617470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368431944	chr21:15617470-15617471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs397742980	chr21:15617471-15617472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113076925	chr21:15617512-15617513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570059693	chr21:15617546-15617547	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15615400-15617000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr21:15616000-15617000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr21:15616200-15616800	Enhancers	H9 Cell Line	embryonic stem cell
4	chr21:15616200-15616800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr21:15616200-15619200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr21:15616400-15616800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr21:15616400-15616800	Enhancers	Hela-S3	cervix
8	chr21:15617600-15618400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr21:15617800-15618600	Enhancers	Primary hematopoietic stem cells	blood
10	chr21:15618200-15618600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr21:15623200-15623400	Enhancers	Brain Substantia Nigra	brain
12	chr21:15623400-15626000	Weak transcription	Brain Substantia Nigra	brain
13	chr21:15623600-15624200	Enhancers	Brain Cingulate Gyrus	brain
14	chr21:15624000-15624200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr21:15624000-15625000	Enhancers	Brain Hippocampus Middle	brain
16	chr21:15624200-15624400	Enhancers	Fetal Brain Male	brain
17	chr21:15624200-15625400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr21:15624400-15626000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr21:15625400-15625800	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr21:15625400-15626400	Enhancers	Brain Cingulate Gyrus	brain
21	chr21:15626000-15626200	Active TSS	Primary T helper cells PMA-I stimulated	--
22	chr21:15626000-15626200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr21:15626000-15626200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr21:15626000-15626200	Active TSS	Brain Substantia Nigra	brain
25	chr21:15626000-15626200	Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr21:15626000-15626200	Active TSS	Dnd41	blood
27	chr21:15626000-15626200	Active TSS	Monocytes-CD14+_RO01746	blood
28	chr21:15626000-15626400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr21:15626000-15626400	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr21:15626000-15626400	Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr21:15626000-15626800	Enhancers	Duodenum Mucosa	Duodenum
32	chr21:15626200-15626400	Enhancers	H9 Cell Line	embryonic stem cell
33	chr21:15626200-15626400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr21:15626200-15626400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr21:15626200-15626400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr21:15626200-15626400	Enhancers	Primary T cells from cord blood	blood
37	chr21:15626200-15626400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr21:15626200-15626400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
39	chr21:15626200-15626400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
40	chr21:15626200-15626400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr21:15626200-15626400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr21:15626200-15626400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr21:15626200-15626400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr21:15626200-15626400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr21:15626200-15626400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr21:15626200-15626400	Enhancers	Adipose Nuclei	Adipose
47	chr21:15626200-15626400	Flanking Active TSS	Liver	Liver
48	chr21:15626200-15626400	Enhancers	Brain Anterior Caudate	brain
49	chr21:15626200-15626400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr21:15626200-15626400	Flanking Active TSS	Brain Substantia Nigra	brain

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