Variant report

Variant	esv17842
Chromosome Location	chr21:40918970-40965975
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:177)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:177 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr21:40960796-40961090	K562	blood:	n/a	n/a
2	CEBPB	chr21:40921105-40921163	IMR90	lung:	n/a	chr21:40921130-40921141
3	CEBPB	chr21:40920982-40921249	HepG2	liver:	n/a	chr21:40921130-40921141
4	CEBPB	chr21:40951298-40952147	MCF-7	breast:	n/a	n/a
5	CEBPB	chr21:40965231-40965706	MCF-7	breast:	n/a	n/a
6	CEBPB	chr21:40951432-40952178	MCF-7	breast:	n/a	n/a
7	CHD2	chr21:40940516-40940543	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr21:40945241-40945404	K562	blood:	n/a	n/a
9	CTCF	chr21:40953426-40953590	MCF-7	breast:	n/a	n/a
10	CTCF	chr21:40935120-40935270	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr21:40934819-40934984	MCF-7	breast:	n/a	n/a
12	CTCF	chr21:40953480-40953630	MCF-7	breast:	n/a	n/a
13	CTCF	chr21:40953462-40953518	HepG2	liver:	n/a	n/a
14	CTCF	chr21:40953240-40953390	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr21:40953441-40953581	MCF-7	breast:	n/a	n/a
16	CTCF	chr21:40953398-40953632	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr21:40953375-40953648	K562	blood:	n/a	n/a
18	CTCF	chr21:40953460-40953610	A549	lung:	n/a	n/a
19	CTCF	chr21:40953336-40953601	K562	blood:	n/a	n/a
20	CTCF	chr21:40953440-40953590	HEK293	kidney:	n/a	n/a
21	CTCF	chr21:40953360-40953510	HAc	cerebellar:	n/a	n/a
22	CTCF	chr21:40934780-40934930	MCF-7	breast:	n/a	n/a
23	CTCF	chr21:40945280-40945430	MCF-7	breast:	n/a	n/a
24	CTCF	chr21:40953420-40953593	MCF-7	breast:	n/a	n/a
25	CTCF	chr21:40953460-40953610	K562	blood:	n/a	n/a
26	CTCF	chr21:40934800-40934950	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr21:40945220-40945370	K562	blood:	n/a	n/a
28	CTCF	chr21:40953345-40953757	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr21:40953560-40953710	HCT-116	colon:	n/a	n/a
30	CTCF	chr21:40953420-40953570	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr21:40928453-40928569	Fibrobl	skin:	n/a	n/a
32	CTCF	chr21:40953400-40953550	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr21:40953463-40953546	Gliobla	brain:	n/a	n/a
34	CTCF	chr21:40953372-40953740	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr21:40934797-40935000	MCF-7	breast:	n/a	n/a
36	CTCF	chr21:40953480-40953630	HRE	kidney:	n/a	n/a
37	CTCF	chr21:40953380-40953530	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr21:40953440-40953590	GM12873	blood:	n/a	n/a
39	CTCF	chr21:40945196-40945396	K562	blood:	n/a	n/a
40	CTCF	chr21:40953440-40953590	K562	blood:	n/a	n/a
41	CTCF	chr21:40953380-40953530	AG04449	skin:	n/a	n/a
42	CTCF	chr21:40953444-40953577	MCF-7	breast:	n/a	n/a
43	CTCF	chr21:40953335-40953636	K562	blood:	n/a	n/a
44	CTCF	chr21:40935740-40935890	WERI-Rb-1	eye:	n/a	chr21:40935836-40935849
45	CTCF	chr21:40953420-40953570	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr21:40934900-40935050	MCF-7	breast:	n/a	n/a
47	CTCF	chr21:40953420-40953570	MCF-7	breast:	n/a	n/a
48	CTCF	chr21:40963261-40963292	MCF-7	breast:	n/a	n/a
49	CTCF	chr21:40934847-40934980	MCF-7	breast:	n/a	n/a
50	CTCF	chr21:40945220-40945370	WERI-Rb-1	eye:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:40931914-40931964	AG04449	skin:	fetal
2	chr21:40931914-40931964	HRPEpiC	eye:	n/a
3	chr21:40931914-40931964	CMK	blood:	n/a
4	chr21:40931914-40931964	IMR90	lung:	fetal
5	chr21:40931914-40931964	HCT-116	colon:	n/a
6	chr21:40931914-40931964	AoSMC	blood vessel:	n/a
7	chr21:40931914-40931964	SK-N-MC	brain:	n/a
8	chr21:40931914-40931964	Hela-S3	cervix:	n/a
9	chr21:40931914-40931964	HCM	heart:	n/a
10	chr21:40931914-40931964	AG04450	lung:	fetal
11	chr21:40931914-40931964	AG10803	skin:	n/a
12	chr21:40931914-40931964	Caco-2	colon:	n/a
13	chr21:40931914-40931964	NH-A	brain:	n/a
14	chr21:40931914-40931964	HMEC	breast:	n/a
15	chr21:40931914-40931964	HRE	kidney:	n/a
16	chr21:40931914-40931964	K562	blood:	n/a
17	chr21:40931914-40931964	SK-N-SH_RA	brain:	n/a
18	chr21:40931914-40931964	T-47D	breast:	n/a
19	chr21:40931914-40931964	ovcar-3	ovarian:	n/a
20	chr21:40931914-40931964	H1-hESC	embryonic stem cell:	embryo
21	chr21:40931914-40931964	HPAEpiC	pulmonary alveolar:	n/a
22	chr21:40931914-40931964	HL-60	blood:	n/a
23	chr21:40931914-40931964	PANC-1	pancreas:	n/a
24	chr21:40931914-40931964	GM12892	blood:	n/a
25	chr21:40931914-40931964	HEK293	kidney:	embryo
26	chr21:40931914-40931964	HepG2	liver:	n/a
27	chr21:40931914-40931964	ProgFib	skin:	n/a
28	chr21:40931914-40931964	GM12891	blood:	n/a
29	chr21:40931914-40931964	RPTEC	kidney:	n/a
30	chr21:40931914-40931964	LNCaP	prostate:	n/a
31	chr21:40931914-40931964	HUVEC	blood vessel:	n/a
32	chr21:40931914-40931964	HCPEpiC	choroid plexus:	n/a
33	chr21:40931914-40931964	Jurkat	blood:	n/a
34	chr21:40931914-40931964	HIPEpiC	eye:	n/a
35	chr21:40931914-40931964	PFSK-1	brain:	n/a
36	chr21:40931914-40931964	NB4	blood:	n/a
37	chr21:40931914-40931964	HEEpiC	esophagus:	n/a
38	chr21:40931914-40931964	AG09309	skin:	n/a
39	chr21:40931914-40931964	SKMC	muscle:	n/a
40	chr21:40931914-40931964	SAEC	small airway:	n/a
41	chr21:40931914-40931964	BJ	skin:	n/a
42	chr21:40931914-40931964	SK-N-SH	brain:	n/a
43	chr21:40931914-40931964	NT2-D1	testis:	n/a
44	chr21:40931914-40931964	GM12878	blood:	n/a
45	chr21:40931914-40931964	GM06990	blood:	n/a
46	chr21:40931914-40931964	NHDF-neo	bronchial:	n/a
47	chr21:40931914-40931964	U87	brain:	n/a
48	chr21:40931914-40931964	GM19239	blood:	n/a
49	chr21:40931914-40931964	HCF	heart:	n/a
50	chr21:40931914-40931964	HAEpiC	amniotic membrane:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:40899001..40900930-chr21:40949117..40954040,4	MCF-7	breast:
2	chr21:40938920..40940719-chr21:40942034..40944243,2	MCF-7	breast:
3	chr21:40918819..40921569-chr21:40925046..40926881,2	K562	blood:
4	chr21:40950947..40952814-chr21:40953410..40955309,2	MCF-7	breast:
5	chr21:40959511..40961499-chr21:40966054..40968109,2	MCF-7	breast:
6	chr21:40895888..40897721-chr21:40949552..40952315,2	MCF-7	breast:
7	chr21:40943694..40945815-chr21:40949884..40952156,3	MCF-7	breast:
8	chr21:40956746..40958740-chr21:40961030..40962712,2	MCF-7	breast:
9	chr21:40919721..40922141-chr21:40925056..40927590,2	MCF-7	breast:
10	chr21:40950925..40952824-chr21:40985213..40987161,2	MCF-7	breast:
11	chr21:40917372..40919952-chr21:40934813..40936673,2	MCF-7	breast:
12	chr21:40894704..40896899-chr21:40951352..40952979,2	MCF-7	breast:
13	chr21:40933376..40935680-chr21:40951136..40954071,2	MCF-7	breast:
14	chr21:40951212..40954090-chr21:41083007..41085637,2	MCF-7	breast:
15	chr21:40951078..40953695-chr21:41039084..41042090,4	MCF-7	breast:
16	chr21:40956746..40958740-chr21:40961030..40962712,2	MCF-7	breast:
17	chr21:40931124..40933238-chr21:40974685..40976833,2	MCF-7	breast:
18	chr21:40816623..40819045-chr21:40951462..40953239,2	MCF-7	breast:
19	chr21:40949058..40951815-chr21:40958704..40961249,3	MCF-7	breast:
20	chr21:40919721..40922141-chr21:40925056..40927590,2	MCF-7	breast:
21	chr21:40938920..40940719-chr21:40942034..40944243,2	MCF-7	breast:
22	chr21:40917372..40919952-chr21:40934813..40936673,2	MCF-7	breast:
23	chr21:40951149..40953987-chr21:41066958..41068611,2	MCF-7	breast:
24	chr21:40950425..40953784-chr21:40975609..40978181,3	MCF-7	breast:
25	chr21:40933376..40935680-chr21:40951136..40954071,2	MCF-7	breast:
26	chr21:40938866..40941607-chr21:40942165..40944706,2	K562	blood:
27	chr21:40928238..40929752-chr21:40932007..40934794,2	MCF-7	breast:
28	chr21:40936564..40938095-chr21:40947433..40949927,2	MCF-7	breast:
29	chr21:40963714..40965931-chr21:40968819..40971403,2	K562	blood:
30	chr21:40932657..40935327-chr21:40936709..40939916,3	MCF-7	breast:
31	chr21:40938866..40941607-chr21:40942165..40944706,2	K562	blood:
32	chr21:40902475..40904077-chr21:40952462..40954060,2	MCF-7	breast:
33	chr21:40938677..40940816-chr21:41079572..41081840,2	MCF-7	breast:
34	chr21:40918819..40921569-chr21:40925046..40926881,2	K562	blood:
35	chr21:40956951..40959069-chr21:40965144..40966734,2	K562	blood:
36	chr21:40950947..40952814-chr21:40953410..40955309,2	MCF-7	breast:
37	chr21:40943694..40945815-chr21:40949884..40952156,3	MCF-7	breast:
38	chr21:40932657..40935327-chr21:40936709..40939916,3	MCF-7	breast:
39	chr21:40936564..40938095-chr21:40947433..40949927,2	MCF-7	breast:
40	chr21:40951091..40953456-chr21:41032196..41036006,4	MCF-7	breast:
41	chr21:40949058..40951815-chr21:40958704..40961249,3	MCF-7	breast:
42	chr21:40843042..40844967-chr21:40948609..40950746,2	MCF-7	breast:
43	chr21:40956951..40959069-chr21:40965144..40966734,2	K562	blood:
44	chr21:40951993..40952513-chr8:27471078..27471638,2	MCF-7	breast:
45	chr21:40913607..40915930-chr21:40942342..40944958,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3BGR-3	chr21:40934881-40935511	NONHSAT082199
2	lnc-SH3BGR-3	chr21:40928411-40928437	NONHSAT082199

No data

Variant related genes	Relation type
B3GALT5	TF binding region
B3GALT5	CpG island
ENSG00000235012	chromatin interactions
ENSG00000183778	chromatin interactions
ENSG00000157578	chromatin interactions
ENSG00000185437	chromatin interactions

Extended variants
information (count: 1709 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566766380	chr21:40919099-40919100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142294215	chr21:40919143-40919144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs490214	chr21:40919144-40919145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs191575044	chr21:40919207-40919208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115369872	chr21:40919238-40919239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557855326	chr21:40919244-40919245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571366758	chr21:40919254-40919255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567461883	chr21:40919266-40919267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77321703	chr21:40919275-40919276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377391424	chr21:40919290-40919291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151211150	chr21:40919301-40919302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs626887	chr21:40919352-40919353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564311356	chr21:40919368-40919369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556455860	chr21:40919382-40919383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77429211	chr21:40919399-40919400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116991330	chr21:40919409-40919410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544597357	chr21:40919411-40919412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571328874	chr21:40919443-40919444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548438754	chr21:40919446-40919447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375681864	chr21:40919460-40919461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538619676	chr21:40919486-40919487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73356089	chr21:40919536-40919537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540376348	chr21:40919553-40919554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563449950	chr21:40919568-40919569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139770108	chr21:40919633-40919634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145205949	chr21:40919650-40919651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs494815	chr21:40919664-40919665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182461492	chr21:40919665-40919666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147619277	chr21:40919676-40919677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185172780	chr21:40919701-40919702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201802223	chr21:40919702-40919703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575799982	chr21:40919708-40919709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115365359	chr21:40919750-40919751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142204397	chr21:40919751-40919752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373735598	chr21:40919765-40919766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62222790	chr21:40919782-40919783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62222791	chr21:40919792-40919793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62222792	chr21:40919801-40919802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs62222793	chr21:40919809-40919810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78128117	chr21:40919810-40919811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62222794	chr21:40919811-40919812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556137680	chr21:40919815-40919816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149687268	chr21:40919850-40919851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71316681	chr21:40919874-40919875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189587237	chr21:40919879-40919880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145538274	chr21:40919908-40919909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577645187	chr21:40919910-40919911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540316486	chr21:40919921-40919922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2837074	chr21:40919955-40919956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs574120405	chr21:40919983-40919984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
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
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	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
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Down syndrome	20877625	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21147910	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40914600-40923600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr21:40918600-40920200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr21:40920200-40920400	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr21:40920200-40921000	Enhancers	Fetal Heart	heart
5	chr21:40921000-40925000	Weak transcription	Fetal Heart	heart
6	chr21:40922800-40926200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr21:40923400-40924400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr21:40923600-40924400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr21:40923800-40924800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
10	chr21:40924000-40924400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr21:40924400-40925600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr21:40924800-40925400	Enhancers	Adipose Nuclei	Adipose
13	chr21:40924800-40926200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr21:40924800-40926400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr21:40925000-40925600	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr21:40925000-40926200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr21:40925000-40926600	Enhancers	Fetal Heart	heart
18	chr21:40925200-40925400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr21:40925200-40925400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr21:40925200-40925600	Enhancers	Brain Anterior Caudate	brain
21	chr21:40925200-40927000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr21:40925400-40925600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr21:40925400-40926600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr21:40925400-40926600	Enhancers	Fetal Muscle Leg	muscle
25	chr21:40925600-40926200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr21:40925600-40927800	Weak transcription	Brain Anterior Caudate	brain
27	chr21:40926000-40926800	Enhancers	Right Ventricle	heart
28	chr21:40926200-40926600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr21:40926200-40926600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr21:40926200-40926800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr21:40926200-40926800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr21:40926400-40926600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr21:40926400-40927000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr21:40926600-40926800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr21:40926600-40926800	Enhancers	Fetal Muscle Trunk	muscle
36	chr21:40926600-40927800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr21:40926600-40927800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr21:40926600-40928000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr21:40926600-40928200	Weak transcription	Fetal Muscle Leg	muscle
40	chr21:40926800-40927800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr21:40926800-40928000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr21:40926800-40928000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr21:40926800-40932600	Weak transcription	Right Ventricle	heart
44	chr21:40927000-40927400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr21:40927000-40927400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr21:40927400-40928000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr21:40927400-40928800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr21:40927400-40928800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr21:40927800-40928200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr21:40927800-40928200	Enhancers	Brain Anterior Caudate	brain

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