Variant report

Variant	nsv520538
Chromosome Location	chr21:15615220-15660539
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:599)
CpG islands
(count:488)
Chromatin interactive
region (count:30)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15632038-15632466	K562	blood:	n/a	n/a
2	ARID3A	chr21:15656994-15657207	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	ARID3A	chr21:15643398-15643769	K562	blood:	n/a	n/a
6	ATF1	chr21:15643368-15643726	K562	blood:	n/a	n/a
7	ATF1	chr21:15636259-15636544	K562	blood:	n/a	n/a
8	ATF3	chr21:15636281-15636574	K562	blood:	n/a	n/a
9	BACH1	chr21:15632039-15632366	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr21:15626679-15626685	GM12878	blood:	n/a	n/a
11	BHLHE40	chr21:15646763-15647064	K562	blood:	n/a	chr21:15646984-15646993 chr21:15646984-15646993 chr21:15646983-15646992
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	BHLHE40	chr21:15643413-15643717	K562	blood:	n/a	n/a
15	BRCA1	chr21:15660289-15660306	GM12878	blood:	n/a	n/a
16	BRCA1	chr21:15633651-15633671	GM12878	blood:	n/a	n/a
17	CBX3	chr21:15646066-15646407	K562	blood:	n/a	n/a
18	CCNT2	chr21:15646221-15646874	K562	blood:	n/a	n/a
19	CCNT2	chr21:15643026-15643838	K562	blood:	n/a	chr21:15643572-15643592
20	CEBPB	chr21:15643304-15643758	K562	blood:	n/a	chr21:15643550-15643567
21	CEBPB	chr21:15616286-15616521	K562	blood:	n/a	chr21:15616395-15616406
22	CEBPB	chr21:15616281-15616480	H1-hESC	embryonic stem cell:	n/a	chr21:15616395-15616406
23	CEBPB	chr21:15656971-15657124	K562	blood:	n/a	n/a
24	CEBPB	chr21:15643370-15643730	K562	blood:	n/a	chr21:15643550-15643567
25	CEBPB	chr21:15647260-15647457	H1-hESC	embryonic stem cell:	n/a	chr21:15647385-15647398
26	CEBPB	chr21:15644175-15644343	K562	blood:	n/a	chr21:15644246-15644259
27	CEBPB	chr21:15616200-15616596	MCF-7	breast:	n/a	chr21:15616395-15616406
28	CEBPB	chr21:15647225-15647548	K562	blood:	n/a	chr21:15647385-15647398
29	CEBPB	chr21:15616272-15616511	K562	blood:	n/a	chr21:15616395-15616406
30	CEBPB	chr21:15616219-15616581	Hela-S3	cervix:	n/a	chr21:15616395-15616406
31	CEBPB	chr21:15616227-15616543	HepG2	liver:	n/a	chr21:15616395-15616406
32	CEBPB	chr21:15636263-15636492	K562	blood:	n/a	n/a
33	CEBPD	chr21:15643245-15643803	K562	blood:	n/a	n/a
34	CEBPD	chr21:15643312-15643807	K562	blood:	n/a	n/a
35	CREB1	chr21:15643320-15643834	K562	blood:	n/a	n/a
36	CREB1	chr21:15643385-15643755	K562	blood:	n/a	n/a
37	CTCF	chr21:15625360-15625510	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr21:15626060-15626210	HEK293	kidney:	n/a	n/a
39	CTCF	chr21:15632140-15632290	NHDF-neo	bronchial:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
40	CTCF	chr21:15626070-15626355	Gliobla	brain:	n/a	n/a
41	CTCF	chr21:15631019-15631110	Fibrobl	skin:	n/a	n/a
42	CTCF	chr21:15626060-15626210	HMF	breast:	n/a	n/a
43	CTCF	chr21:15626347-15626436	GM12892	blood:	n/a	n/a
44	CTCF	chr21:15632063-15632322	LNCaP	prostate:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
45	CTCF	chr21:15624980-15625130	AG09319	gingival:	n/a	n/a
46	CTCF	chr21:15632120-15632270	HepG2	liver:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
47	CTCF	chr21:15632038-15632369	T-47D	breast:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
48	CTCF	chr21:15626040-15626190	GM12878	blood:	n/a	n/a
49	CTCF	chr21:15626020-15626170	HPF	lung:	n/a	n/a
50	CTCF	chr21:15632160-15632310	GM12869	blood:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15646312-15646362	BJ	skin:	n/a
2	chr21:15646312-15646362	GM12891	blood:	n/a
3	chr21:15647368-15647418	HCM	heart:	n/a
4	chr21:15645787-15645837	HIPEpiC	eye:	n/a
5	chr21:15645810-15645860	PFSK-1	brain:	n/a
6	chr21:15647368-15647418	Caco-2	colon:	n/a
7	chr21:15645787-15645837	AG09319	gingival:	n/a
8	chr21:15647368-15647418	AoSMC	blood vessel:	n/a
9	chr21:15645810-15645860	SKMC	muscle:	n/a
10	chr21:15645787-15645837	HEEpiC	esophagus:	n/a
11	chr21:15647368-15647418	Hepatocyte	liver:	n/a
12	chr21:15645810-15645860	ECC-1	luminal epithelium:	n/a
13	chr21:15645649-15645699	NT2-D1	testis:	n/a
14	chr21:15646187-15646237	K562	blood:	n/a
15	chr21:15645787-15645837	NB4	blood:	n/a
16	chr21:15645787-15645837	IMR90	lung:	fetal
17	chr21:15646312-15646362	ECC-1	luminal epithelium:	n/a
18	chr21:15645810-15645860	NT2-D1	testis:	n/a
19	chr21:15645649-15645699	HCF	heart:	n/a
20	chr21:15646635-15646685	A549	lung:	n/a
21	chr21:15645649-15645699	AG10803	skin:	n/a
22	chr21:15647368-15647418	Hela-S3	cervix:	n/a
23	chr21:15645810-15645860	CMK	blood:	n/a
24	chr21:15646635-15646685	ProgFib	skin:	n/a
25	chr21:15646187-15646237	PrEC	prostate:	n/a
26	chr21:15645787-15645837	BE2_C	brain:	n/a
27	chr21:15647368-15647418	SKMC	muscle:	n/a
28	chr21:15645988-15646038	HAEpiC	amniotic membrane:	n/a
29	chr21:15647368-15647418	PrEC	prostate:	n/a
30	chr21:15645988-15646038	Hepatocyte	liver:	n/a
31	chr21:15646187-15646237	ECC-1	luminal epithelium:	n/a
32	chr21:15645810-15645860	Jurkat	blood:	n/a
33	chr21:15645988-15646038	GM12891	blood:	n/a
34	chr21:15645988-15646038	HEK293	kidney:	embryo
35	chr21:15645810-15645860	SK-N-SH	brain:	n/a
36	chr21:15646635-15646685	GM12892	blood:	n/a
37	chr21:15647368-15647418	HUVEC	blood vessel:	n/a
38	chr21:15645787-15645837	SK-N-SH	brain:	n/a
39	chr21:15645988-15646038	PFSK-1	brain:	n/a
40	chr21:15645787-15645837	AG04450	lung:	fetal
41	chr21:15645810-15645860	Hela-S3	cervix:	n/a
42	chr21:15645988-15646038	RPTEC	kidney:	n/a
43	chr21:15646635-15646685	HRE	kidney:	n/a
44	chr21:15646187-15646237	LNCaP	prostate:	n/a
45	chr21:15645988-15646038	SK-N-SH_RA	brain:	n/a
46	chr21:15645649-15645699	SK-N-SH	brain:	n/a
47	chr21:15647368-15647418	Jurkat	blood:	n/a
48	chr21:15646312-15646362	HNPCEpiC	eye:	n/a
49	chr21:15645988-15646038	ECC-1	luminal epithelium:	n/a
50	chr21:15646635-15646685	AG10803	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15656047..15658961-chr21:16165584..16168436,2	K562	blood:
2	chr21:15637737..15639634-chr21:15641854..15644729,2	K562	blood:
3	chr21:15616597..15618358-chr21:15624634..15626645,2	K562	blood:
4	chr21:15650981..15652853-chr21:15655632..15658875,3	K562	blood:
5	chr21:15646421..15649560-chr21:15654356..15655933,3	K562	blood:
6	chr21:15616597..15618358-chr21:15624634..15626645,2	K562	blood:
7	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:
8	chr21:15652023..15652746-chr7:152811109..152812098,2	MCF-7	breast:
9	chr21:15647599..15649902-chr21:15656709..15659445,2	K562	blood:
10	chr21:15638970..15641725-chr21:15734559..15736787,2	K562	blood:
11	chr21:15652280..15654566-chr21:15773386..15776181,2	MCF-7	breast:
12	chr21:15642588..15643376-chr21:15678270..15679084,2	MCF-7	breast:
13	chr21:15611898..15613509-chr21:15614140..15616953,2	K562	blood:
14	chr21:15644504..15646965-chr21:15652945..15655779,2	K562	blood:
15	chr21:15637737..15639634-chr21:15641854..15644729,2	K562	blood:
16	chr21:15637824..15639860-chr21:15661262..15662859,2	MCF-7	breast:
17	chr21:15650981..15652853-chr21:15655632..15658875,3	K562	blood:
18	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:
19	chr21:15618985..15621962-chr21:15624169..15625950,3	K562	blood:
20	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:
21	chr21:15637216..15639622-chr21:15681292..15683772,2	MCF-7	breast:
22	chr21:15647599..15649902-chr21:15656709..15659445,2	K562	blood:
23	chr21:15645251..15647400-chr21:15754351..15756122,2	K562	blood:
24	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:
25	chr21:15646421..15649560-chr21:15654356..15655933,3	K562	blood:
26	chr21:15612009..15614501-chr21:15615453..15618275,2	K562	blood:
27	chr21:15642588..15643574-chr21:15678270..15679033,2	MCF-7	breast:
28	chr21:15658088..15660152-chr21:15664037..15665784,2	MCF-7	breast:
29	chr21:15646214..15647824-chr21:15649237..15651559,2	MCF-7	breast:
30	chr21:15618985..15621962-chr21:15624169..15625950,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081156
2	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081154
3	lnc-RBM11-5	chr21:15659871-15660018	NONHSAT081154
4	lnc-RBM11-5	chr21:15641808-15641980	NONHSAT081153
5	lnc-RBM11-5	chr21:15659871-15660018	NONHSAT081156
6	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081154
7	lnc-RBM11-5	chr21:15640724-15640913	NONHSAT081153
8	lnc-RBM11-5	chr21:15642846-15642930	NONHSAT081153
9	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081153
10	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081156

No data

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

Extended variants
information (count: 1842 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs434396	chr21:15615220-15615221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142699673	chr21:15615223-15615224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569041357	chr21:15615283-15615284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537936509	chr21:15615317-15615318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs434081	chr21:15615360-15615361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs35425382	chr21:15615375-15615376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs438336	chr21:15615376-15615377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs143181479	chr21:15615388-15615389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537576970	chr21:15615464-15615465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7275979	chr21:15615500-15615501	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs148259173	chr21:15615527-15615528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568459652	chr21:15615545-15615546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10650898	chr21:15615546-15615547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1739490	chr21:15615548-15615549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71786695	chr21:15615583-15615584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188408217	chr21:15615598-15615599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73160424	chr21:15615615-15615616	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs544278090	chr21:15615616-15615617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568004017	chr21:15615630-15615631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564080515	chr21:15615656-15615657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117226147	chr21:15615661-15615662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546998576	chr21:15615697-15615698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375237023	chr21:15615736-15615737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529544022	chr21:15615747-15615748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549203703	chr21:15615781-15615782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569103995	chr21:15615797-15615798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368132390	chr21:15615803-15615804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553622551	chr21:15615842-15615843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs439146	chr21:15615855-15615856	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545092490	chr21:15615869-15615870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571569303	chr21:15615884-15615885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534170880	chr21:15615911-15615912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553714378	chr21:15615922-15615923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111604047	chr21:15615930-15615931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573125935	chr21:15615975-15615976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567473516	chr21:15615978-15615979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112606654	chr21:15616002-15616003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555603996	chr21:15616021-15616022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76808036	chr21:15616070-15616071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76967952	chr21:15616071-15616072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs398061598	chr21:15616072-15616073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192353902	chr21:15616082-15616083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544339399	chr21:15616175-15616176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs118087904	chr21:15616218-15616219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577640569	chr21:15616226-15616227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540255974	chr21:15616287-15616288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559880752	chr21:15616297-15616298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs79207260	chr21:15616324-15616325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141254932	chr21:15616362-15616363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184989429	chr21:15616372-15616373	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:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15614000-15616200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr21:15615400-15617000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr21:15615800-15616600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr21:15615800-15616600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr21:15616000-15617000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr21:15616200-15616600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr21:15616200-15616600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr21:15616200-15616600	Enhancers	Fetal Kidney	kidney
9	chr21:15616200-15616800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr21:15616200-15616800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr21:15616200-15619200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr21:15616400-15616600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr21:15616400-15616800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr21:15616400-15616800	Enhancers	Hela-S3	cervix
15	chr21:15617600-15618400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr21:15617800-15618600	Enhancers	Primary hematopoietic stem cells	blood
17	chr21:15618200-15618600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr21:15623200-15623400	Enhancers	Brain Substantia Nigra	brain
19	chr21:15623400-15626000	Weak transcription	Brain Substantia Nigra	brain
20	chr21:15623600-15624200	Enhancers	Brain Cingulate Gyrus	brain
21	chr21:15624000-15624200	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr21:15624000-15625000	Enhancers	Brain Hippocampus Middle	brain
23	chr21:15624200-15624400	Enhancers	Fetal Brain Male	brain
24	chr21:15624200-15625400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr21:15624400-15626000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr21:15625400-15625800	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr21:15625400-15626400	Enhancers	Brain Cingulate Gyrus	brain
28	chr21:15626000-15626200	Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr21:15626000-15626200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr21:15626000-15626200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr21:15626000-15626200	Active TSS	Brain Substantia Nigra	brain
32	chr21:15626000-15626200	Active TSS	Skeletal Muscle Female	skeletal muscle
33	chr21:15626000-15626200	Active TSS	Dnd41	blood
34	chr21:15626000-15626200	Active TSS	Monocytes-CD14+_RO01746	blood
35	chr21:15626000-15626400	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr21:15626000-15626400	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr21:15626000-15626400	Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr21:15626000-15626800	Enhancers	Duodenum Mucosa	Duodenum
39	chr21:15626200-15626400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr21:15626200-15626400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr21:15626200-15626400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr21:15626200-15626400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr21:15626200-15626400	Enhancers	Primary T cells from cord blood	blood
44	chr21:15626200-15626400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr21:15626200-15626400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr21:15626200-15626400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr21:15626200-15626400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr21:15626200-15626400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr21:15626200-15626400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr21:15626200-15626400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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