Variant report

Variant	esv2758821
Chromosome Location	chr21:47243032-47319768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:838)
CpG islands
(count:1588)
Chromatin interactive
region (count:81)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:838 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47300411-47300587	HepG2	liver:	n/a	n/a
2	ATF1	chr21:47312104-47312255	K562	blood:	n/a	n/a
3	BACH1	chr21:47300042-47300646	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr21:47311523-47311813	GM12878	blood:	n/a	n/a
5	BHLHE40	chr21:47300397-47300678	K562	blood:	n/a	n/a
6	BHLHE40	chr21:47296636-47296655	K562	blood:	n/a	n/a
7	BHLHE40	chr21:47257127-47257384	HepG2	liver:	n/a	n/a
8	BHLHE40	chr21:47278675-47278994	K562	blood:	n/a	n/a
9	BHLHE40	chr21:47300411-47300694	GM12878	blood:	n/a	n/a
10	BHLHE40	chr21:47257240-47257241	K562	blood:	n/a	n/a
11	BHLHE40	chr21:47295046-47295376	HepG2	liver:	n/a	n/a
12	BHLHE40	chr21:47300363-47300708	HepG2	liver:	n/a	n/a
13	BHLHE40	chr21:47295064-47295332	K562	blood:	n/a	n/a
14	BHLHE40	chr21:47312164-47312380	K562	blood:	n/a	n/a
15	BHLHE40	chr21:47266627-47266969	HepG2	liver:	n/a	n/a
16	CCNT2	chr21:47295011-47295153	K562	blood:	n/a	n/a
17	CEBPB	chr21:47295180-47295381	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr21:47282613-47282885	HepG2	liver:	n/a	n/a
19	CEBPB	chr21:47294912-47295621	IMR90	lung:	n/a	n/a
20	CEBPB	chr21:47272012-47272152	H1-hESC	embryonic stem cell:	n/a	chr21:47272096-47272107
21	CEBPB	chr21:47251984-47252069	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr21:47279143-47279370	IMR90	lung:	n/a	chr21:47279281-47279292
23	CEBPB	chr21:47248885-47249211	HepG2	liver:	n/a	chr21:47249033-47249044 chr21:47249057-47249068
24	CEBPB	chr21:47271941-47272238	HepG2	liver:	n/a	chr21:47272096-47272107
25	CEBPB	chr21:47251915-47252115	IMR90	lung:	n/a	n/a
26	CEBPB	chr21:47279212-47279333	HepG2	liver:	n/a	chr21:47279281-47279292
27	CEBPB	chr21:47304830-47305050	HepG2	liver:	n/a	chr21:47304949-47304960
28	CEBPB	chr21:47271939-47272246	K562	blood:	n/a	chr21:47272096-47272107
29	CEBPB	chr21:47282732-47282796	K562	blood:	n/a	n/a
30	CEBPB	chr21:47279162-47279361	Hela-S3	cervix:	n/a	chr21:47279281-47279292
31	CEBPB	chr21:47279096-47279469	HepG2	liver:	n/a	chr21:47279281-47279292
32	CEBPB	chr21:47271950-47272246	A549	lung:	n/a	chr21:47272096-47272107
33	CEBPB	chr21:47256378-47256542	IMR90	lung:	n/a	n/a
34	CEBPB	chr21:47264132-47264215	HepG2	liver:	n/a	n/a
35	CEBPB	chr21:47279077-47279475	HepG2	liver:	n/a	chr21:47279281-47279292
36	CEBPB	chr21:47304809-47304949	A549	lung:	n/a	n/a
37	CEBPB	chr21:47248979-47249179	Hela-S3	cervix:	n/a	chr21:47249033-47249044 chr21:47249057-47249068
38	CEBPB	chr21:47279112-47279339	K562	blood:	n/a	chr21:47279281-47279292
39	CEBPB	chr21:47271954-47272243	IMR90	lung:	n/a	chr21:47272096-47272107
40	CEBPB	chr21:47279144-47279397	HepG2	liver:	n/a	chr21:47279281-47279292
41	CEBPB	chr21:47285083-47285596	IMR90	lung:	n/a	n/a
42	CEBPB	chr21:47279277-47279362	H1-hESC	embryonic stem cell:	n/a	chr21:47279281-47279292
43	CEBPB	chr21:47295092-47295422	HepG2	liver:	n/a	n/a
44	CHD2	chr21:47278641-47278906	K562	blood:	n/a	n/a
45	CHD2	chr21:47312425-47312441	HepG2	liver:	n/a	n/a
46	CHD2	chr21:47312410-47312571	K562	blood:	n/a	n/a
47	CHD2	chr21:47252730-47253011	K562	blood:	n/a	n/a
48	CTCF	chr21:47300406-47300622	GM10248	blood:	n/a	n/a
49	CTCF	chr21:47300420-47300570	Caco-2	colon:	n/a	n/a
50	CTCF	chr21:47300440-47300590	AG04449	skin:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47288438-47288488	NHDF-neo	bronchial:	n/a
2	chr21:47269822-47269872	NT2-D1	testis:	n/a
3	chr21:47288438-47288488	NHDF-neo	bronchial:	n/a
4	chr21:47269822-47269872	NT2-D1	testis:	n/a
5	chr21:47287206-47287256	AG09309	skin:	n/a
6	chr21:47294981-47295031	HRCEpiC	kidney:	n/a
7	chr21:47319304-47319354	T-47D	breast:	n/a
8	chr21:47317093-47317143	Caco-2	colon:	n/a
9	chr21:47319304-47319354	PrEC	prostate:	n/a
10	chr21:47269843-47269893	K562	blood:	n/a
11	chr21:47319304-47319354	IMR90	lung:	fetal
12	chr21:47287357-47287407	AG09319	gingival:	n/a
13	chr21:47294762-47294812	HIPEpiC	eye:	n/a
14	chr21:47269627-47269677	H1-hESC	embryonic stem cell:	embryo
15	chr21:47295215-47295265	NHBE	bronchial:	n/a
16	chr21:47317093-47317143	HEEpiC	esophagus:	n/a
17	chr21:47287017-47287067	NH-A	brain:	n/a
18	chr21:47290548-47290598	RPTEC	kidney:	n/a
19	chr21:47288619-47288669	HPAEpiC	pulmonary alveolar:	n/a
20	chr21:47295375-47295425	HepG2	liver:	n/a
21	chr21:47319304-47319354	AG09319	gingival:	n/a
22	chr21:47295375-47295425	HRCEpiC	kidney:	n/a
23	chr21:47294981-47295031	NH-A	brain:	n/a
24	chr21:47319304-47319354	HPAEpiC	pulmonary alveolar:	n/a
25	chr21:47295375-47295425	Caco-2	colon:	n/a
26	chr21:47283868-47283918	NT2-D1	testis:	n/a
27	chr21:47269843-47269893	NH-A	brain:	n/a
28	chr21:47317093-47317143	Jurkat	blood:	n/a
29	chr21:47294739-47294789	GM06990	blood:	n/a
30	chr21:47288438-47288488	ECC-1	luminal epithelium:	n/a
31	chr21:47269822-47269872	GM12892	blood:	n/a
32	chr21:47269822-47269872	NH-A	brain:	n/a
33	chr21:47283868-47283918	BE2_C	brain:	n/a
34	chr21:47269627-47269677	HMEC	breast:	n/a
35	chr21:47290548-47290598	IMR90	lung:	fetal
36	chr21:47269877-47269927	PFSK-1	brain:	n/a
37	chr21:47287206-47287256	NHBE	bronchial:	n/a
38	chr21:47290548-47290598	HUVEC	blood vessel:	n/a
39	chr21:47295375-47295425	HCF	heart:	n/a
40	chr21:47290548-47290598	SK-N-MC	brain:	n/a
41	chr21:47294739-47294789	SKMC	muscle:	n/a
42	chr21:47269843-47269893	NHDF-neo	bronchial:	n/a
43	chr21:47294739-47294789	SK-N-SH	brain:	n/a
44	chr21:47317093-47317143	NHDF-neo	bronchial:	n/a
45	chr21:47295375-47295425	NHBE	bronchial:	n/a
46	chr21:47294762-47294812	GM12878	blood:	n/a
47	chr21:47290548-47290598	GM12878	blood:	n/a
48	chr21:47269877-47269927	HMEC	breast:	n/a
49	chr21:47314725-47314775	GM19239	blood:	n/a
50	chr21:47295375-47295425	HAEpiC	amniotic membrane:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:47237289..47239387-chr21:47252638..47254672,2	K562	blood:
2	chr21:46933174..46933795-chr21:47287792..47288661,3	MCF-7	breast:
3	chr21:47248821..47250626-chr21:47254393..47257357,2	MCF-7	breast:
4	chr21:47277116..47279764-chr21:47286679..47288942,2	MCF-7	breast:
5	chr21:47290679..47292853-chr21:47334808..47337713,2	MCF-7	breast:
6	chr21:46294382..46294995-chr21:47312113..47312613,2	Hela-S3	cervix:
7	chr21:47311846..47315136-chr21:47319001..47321928,3	K562	blood:
8	chr21:46974485..46975268-chr21:47299866..47300947,3	MCF-7	breast:
9	chr21:47292108..47294051-chr21:47294662..47296338,2	K562	blood:
10	chr21:47246654..47249179-chr21:47249623..47252084,3	MCF-7	breast:
11	chr21:47298754..47301234-chr21:47302328..47305027,3	K562	blood:
12	chr21:47292095..47293643-chr21:47302560..47304735,2	K562	blood:
13	chr21:47267781..47268663-chr21:47299803..47300649,2	MCF-7	breast:
14	chr21:47283223..47285072-chr21:47288442..47290551,2	MCF-7	breast:
15	chr21:47298754..47301234-chr21:47302328..47305027,3	K562	blood:
16	chr21:47287743..47288527-chr21:47334754..47335348,2	MCF-7	breast:
17	chr21:47263542..47265104-chr21:47266033..47268979,2	K562	blood:
18	chr21:46675057..46677884-chr21:47243864..47245535,2	MCF-7	breast:
19	chr21:47292095..47293643-chr21:47302560..47304735,2	K562	blood:
20	chr21:47273743..47277318-chr21:47278622..47280436,3	K562	blood:
21	chr21:47280971..47284906-chr21:47285301..47288996,5	K562	blood:
22	chr21:47304723..47306559-chr21:47309917..47311783,2	MCF-7	breast:
23	chr21:47286434..47288542-chr21:47340592..47343360,3	MCF-7	breast:
24	chr21:47304723..47306559-chr21:47309917..47311783,2	MCF-7	breast:
25	chr21:47311846..47315136-chr21:47319001..47321928,3	K562	blood:
26	chr21:47282962..47285157-chr21:47294870..47296396,2	K562	blood:
27	chr21:47300090..47300627-chr21:47342032..47342538,2	MCF-7	breast:
28	chr21:47285455..47288368-chr21:47291495..47294082,2	MCF-7	breast:
29	chr21:47300028..47300909-chr21:47342650..47343811,5	MCF-7	breast:
30	chr21:47242790..47243479-chr21:47342941..47343666,2	MCF-7	breast:
31	chr21:47300119..47302715-chr21:47341992..47344397,3	MCF-7	breast:
32	chr21:47286050..47288539-chr21:47292437..47294935,2	K562	blood:
33	chr21:47257190..47260005-chr21:47265923..47268414,2	MCF-7	breast:
34	chr21:47268820..47271027-chr21:47286400..47288109,2	MCF-7	breast:
35	chr21:47295466..47298745-chr21:47300328..47303080,5	MCF-7	breast:
36	chr21:47273162..47275580-chr21:47281088..47283612,2	MCF-7	breast:
37	chr21:47280971..47284906-chr21:47285301..47288996,5	K562	blood:
38	chr21:47293178..47296152-chr21:47298575..47300607,2	K562	blood:
39	chr2:191877174..191879263-chr21:47281698..47283913,2	MCF-7	breast:
40	chr21:47280227..47282087-chr21:47299384..47301576,2	MCF-7	breast:
41	chr17:41464679..41467658-chr21:47312370..47313870,3	K562	blood:
42	chr21:47262614..47265251-chr21:47267241..47269590,2	MCF-7	breast:
43	chr21:46932310..46934674-chr21:47242469..47244429,2	MCF-7	breast:
44	chr21:47308842..47311490-chr21:47321844..47323697,2	MCF-7	breast:
45	chr21:47277593..47281195-chr21:47281258..47286265,4	MCF-7	breast:
46	chr21:46294020..46295642-chr21:47310587..47313582,2	K562	blood:
47	chr21:47263865..47267326-chr21:47272648..47275392,3	K562	blood:
48	chr21:47280227..47282087-chr21:47299384..47301576,2	MCF-7	breast:
49	chr21:47240141..47240932-chr21:47300508..47301042,2	MCF-7	breast:
50	chr21:46973481..46977035-chr21:47238682..47244036,11	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTCD-6	chr21:47318759-47318789	NONHSAT082999
2	lnc-FTCD-6	chr21:47318001-47318626	NONHSAT082999
3	lnc-SLC19A1-3	chr21:47247755-47251155	NONHSAT082996
4	lnc-SLC19A1-3	chr21:47256200-47256333	ENSG00000205424.1
5	lnc-SLC19A1-3	chr21:47252522-47252572	ENSG00000205424.1
6	lnc-COL6A1-8	chr21:47278595-47278724	NONHSAT082997
7	lnc-COL6A1-8	chr21:47279616-47279691	NONHSAT082997
8	lnc-COL6A1-8	chr21:47278809-47278917	NONHSAT082997
9	lnc-COL6A1-8	chr21:47273885-47273922	NONHSAT082997
10	lnc-SLC19A1-3	chr21:47256200-47256333	NONHSAT082996
11	lnc-SLC19A1-3	chr21:47252522-47252572	NONHSAT082996
12	lnc-SLC19A1-3	chr21:47247875-47251155	ENSG00000205424.1
13	lnc-COL6A1-8	chr21:47278250-47278372	NONHSAT082997

No data

Variant related genes	Relation type
ENSG00000205424	TF binding region
PCBP3	TF binding region
ENSG00000205424	CpG island
PCBP3	CpG island
ENSG00000115415	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000183570	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000205424	chromatin interactions

Extended variants
information (count: 3588 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:3588 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839010	chr21:47243032-47243033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs542390678	chr21:47243043-47243044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145982548	chr21:47243044-47243045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572899623	chr21:47243049-47243050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2839011	chr21:47243074-47243075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78673368	chr21:47243086-47243087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139859542	chr21:47243089-47243090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550749472	chr21:47243094-47243095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371627014	chr21:47243179-47243180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562582030	chr21:47243202-47243203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200883175	chr21:47243204-47243205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181814309	chr21:47243330-47243331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7279479	chr21:47243348-47243349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185403750	chr21:47243378-47243379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534707038	chr21:47243389-47243390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113686599	chr21:47243391-47243392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577577185	chr21:47243395-47243396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556149483	chr21:47243415-47243416	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs117201199	chr21:47243424-47243425	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs149720906	chr21:47243425-47243426	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs557513662	chr21:47243427-47243428	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs145539304	chr21:47243432-47243433	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs148909401	chr21:47243433-47243434	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs554385646	chr21:47243509-47243510	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs73380609	chr21:47243520-47243521	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188883316	chr21:47243535-47243536	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs540238074	chr21:47243538-47243539	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs147637703	chr21:47243569-47243570	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs577201298	chr21:47243626-47243627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544215562	chr21:47243634-47243635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200546984	chr21:47243636-47243637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75118413	chr21:47243646-47243647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386365934	chr21:47243647-47243648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7283756	chr21:47243648-47243649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529862186	chr21:47243660-47243661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543065386	chr21:47243685-47243686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560409762	chr21:47243706-47243707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561050280	chr21:47243712-47243713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528608739	chr21:47243725-47243726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546578187	chr21:47243732-47243733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142360970	chr21:47243749-47243750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532816823	chr21:47243807-47243808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551010395	chr21:47243812-47243813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569401931	chr21:47243813-47243814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536456669	chr21:47243830-47243831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146356342	chr21:47243835-47243836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575081570	chr21:47243844-47243845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566572503	chr21:47243846-47243847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139185642	chr21:47243853-47243854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182013190	chr21:47243903-47243904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1427 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47217800-47260400	Weak transcription	Right Atrium	heart
2	chr21:47236400-47243800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr21:47239400-47247200	Weak transcription	Primary T cells from cord blood	blood
4	chr21:47240200-47243600	Enhancers	Liver	Liver
5	chr21:47240600-47256600	Weak transcription	Dnd41	blood
6	chr21:47240800-47244800	Weak transcription	Thymus	Thymus
7	chr21:47241000-47243200	Weak transcription	HSMM	muscle
8	chr21:47241000-47251800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr21:47241000-47255400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr21:47241200-47250200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr21:47241400-47249600	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr21:47241600-47257400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr21:47241800-47246200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr21:47241800-47246400	Weak transcription	Fetal Thymus	thymus
15	chr21:47241800-47257600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr21:47242600-47244000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr21:47242600-47246800	Weak transcription	Spleen	Spleen
18	chr21:47242800-47243200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr21:47243200-47243600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr21:47243200-47243600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr21:47243200-47243600	Enhancers	HSMM	muscle
22	chr21:47243400-47243600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr21:47243400-47243600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr21:47243800-47244200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr21:47244000-47245400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr21:47244200-47244600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr21:47244600-47244800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr21:47244600-47245200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr21:47244800-47245000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr21:47244800-47249200	Strong transcription	Thymus	Thymus
31	chr21:47245200-47245400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr21:47245200-47245400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr21:47245400-47245800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr21:47245400-47247000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr21:47245800-47247000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr21:47246200-47247000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr21:47246400-47248200	Enhancers	Fetal Thymus	thymus
38	chr21:47246600-47247400	Enhancers	Primary T cells fromperipheralblood	blood
39	chr21:47246800-47247200	Enhancers	Spleen	Spleen
40	chr21:47246800-47248200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr21:47246800-47248400	Enhancers	Primary B cells from peripheral blood	blood
42	chr21:47247000-47247200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr21:47247000-47247600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr21:47247000-47248000	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr21:47247000-47248000	Enhancers	GM12878-XiMat	blood
46	chr21:47247000-47248400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr21:47247000-47248400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr21:47247000-47257600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr21:47247200-47247600	Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr21:47247200-47248000	Enhancers	Primary T cells from cord blood	blood

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