Variant report

Variant	nsv913915
Chromosome Location	chr21:45697755-45712588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:1282)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:45705844-45705867	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr21:45702375-45702509	GM12878	blood:	n/a	n/a
3	CCNT2	chr21:45712225-45712243	K562	blood:	n/a	n/a
4	CHD2	chr21:45705555-45705642	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr21:45702416-45702447	GM12878	blood:	n/a	n/a
6	CTCF	chr21:45710860-45711010	GM12873	blood:	n/a	n/a
7	CTCF	chr21:45705562-45705696	Fibrobl	skin:	n/a	chr21:45705574-45705583
8	CTCF	chr21:45705520-45705670	AG04449	skin:	n/a	chr21:45705574-45705583
9	CTCF	chr21:45705578-45705698	ProgFib	skin:	n/a	n/a
10	CTCF	chr21:45705520-45705670	AG09319	gingival:	n/a	chr21:45705574-45705583
11	CTCF	chr21:45705615-45705675	Gliobla	brain:	n/a	n/a
12	CTCF	chr21:45705780-45705930	AG04449	skin:	n/a	n/a
13	CTCF	chr21:45712420-45712570	K562	blood:	n/a	n/a
14	CTCF	chr21:45705240-45705390	HUVEC	blood vessel:	n/a	chr21:45705376-45705389
15	CTCF	chr21:45705550-45705670	IMR90	lung:	n/a	chr21:45705574-45705583
16	CTCF	chr21:45705480-45705630	HBMEC	blood vessel:	n/a	chr21:45705574-45705583
17	CTCF	chr21:45705420-45705570	BJ	skin:	n/a	n/a
18	CUX1	chr21:45711906-45711909	K562	blood:	n/a	n/a
19	EBF1	chr21:45702237-45702619	GM12878	blood:	n/a	chr21:45702390-45702401 chr21:45702371-45702382 chr21:45702392-45702401
20	EBF1	chr21:45711172-45711389	GM12878	blood:	n/a	n/a
21	EBF1	chr21:45702233-45702688	GM12878	blood:	n/a	chr21:45702390-45702401 chr21:45702371-45702382 chr21:45702392-45702401
22	EGR1	chr21:45712191-45712445	K562	blood:	n/a	n/a
23	EGR1	chr21:45712229-45712418	K562	blood:	n/a	n/a
24	EP300	chr21:45702287-45702564	GM12878	blood:	n/a	chr21:45702389-45702405 chr21:45702555-45702562
25	EP300	chr21:45702352-45702653	GM12878	blood:	n/a	chr21:45702389-45702405 chr21:45702555-45702562
26	EP300	chr21:45699573-45700107	ECC-1	luminal epithelium:	n/a	n/a
27	ESR1	chr21:45699650-45700022	ECC-1	luminal epithelium:	n/a	n/a
28	FOXA2	chr21:45703329-45703649	A549	lung:	n/a	n/a
29	GABPA	chr21:45705372-45706077	H1-hESC	embryonic stem cell:	n/a	chr21:45706029-45706038 chr21:45705875-45705884
30	GABPA	chr21:45705521-45705951	H1-hESC	embryonic stem cell:	n/a	chr21:45705875-45705884
31	GATA2	chr21:45703216-45703480	K562	blood:	n/a	n/a
32	HMGN3	chr21:45709520-45709525	K562	blood:	n/a	n/a
33	HMGN3	chr21:45707436-45707469	K562	blood:	n/a	n/a
34	HMGN3	chr21:45712138-45712213	K562	blood:	n/a	n/a
35	IRF1	chr21:45712264-45712337	K562	blood:	n/a	n/a
36	JUND	chr21:45705526-45705621	H1-hESC	embryonic stem cell:	n/a	chr21:45705584-45705592 chr21:45705582-45705593 chr21:45705582-45705594
37	JUND	chr21:45705457-45705507	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAX	chr21:45712189-45712418	K562	blood:	n/a	n/a
39	MAZ	chr21:45702434-45702551	GM12878	blood:	n/a	n/a
40	MAZ	chr21:45705335-45706044	IMR90	lung:	n/a	chr21:45705740-45705749
41	MYC	chr21:45707981-45708083	MCF-7	breast:	n/a	n/a
42	MYC	chr21:45710978-45711019	MCF-7	breast:	n/a	n/a
43	MYC	chr21:45711021-45711034	MCF-7	breast:	n/a	n/a
44	NFIC	chr21:45699712-45700091	ECC-1	luminal epithelium:	n/a	n/a
45	NR2F2	chr21:45703218-45703741	K562	blood:	n/a	n/a
46	NR2F2	chr21:45703310-45703565	K562	blood:	n/a	n/a
47	POLR2A	chr21:45712557-45712642	K562	blood:	n/a	n/a
48	POLR2A	chr21:45708385-45708464	HepG2	liver:	n/a	n/a
49	RAD21	chr21:45705442-45705735	IMR90	lung:	n/a	n/a
50	RELA	chr21:45702249-45702676	GM12878	blood:	n/a	chr21:45702444-45702453 chr21:45702444-45702453

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45705721-45705771	IMR90	lung:	fetal
2	chr21:45705721-45705771	IMR90	lung:	fetal
3	chr21:45705721-45705771	RPTEC	kidney:	n/a
4	chr21:45705267-45705317	SK-N-SH_RA	brain:	n/a
5	chr21:45705740-45705790	AG10803	skin:	n/a
6	chr21:45709604-45709654	ovcar-3	ovarian:	n/a
7	chr21:45705721-45705771	NHDF-neo	bronchial:	n/a
8	chr21:45705618-45705668	AoSMC	blood vessel:	n/a
9	chr21:45705429-45705479	NT2-D1	testis:	n/a
10	chr21:45705686-45705736	LNCaP	prostate:	n/a
11	chr21:45707344-45707394	HAEpiC	amniotic membrane:	n/a
12	chr21:45709676-45709726	MCF-7	breast:	n/a
13	chr21:45705994-45706044	PrEC	prostate:	n/a
14	chr21:45705721-45705771	PANC-1	pancreas:	n/a
15	chr21:45705618-45705668	SAEC	small airway:	n/a
16	chr21:45709604-45709654	HIPEpiC	eye:	n/a
17	chr21:45705694-45705744	HPAEpiC	pulmonary alveolar:	n/a
18	chr21:45709676-45709726	NH-A	brain:	n/a
19	chr21:45702039-45702089	GM12878	blood:	n/a
20	chr21:45705686-45705736	BE2_C	brain:	n/a
21	chr21:45705429-45705479	SKMC	muscle:	n/a
22	chr21:45710296-45710346	AG09319	gingival:	n/a
23	chr21:45705742-45705792	H1-hESC	embryonic stem cell:	embryo
24	chr21:45705740-45705790	K562	blood:	n/a
25	chr21:45710296-45710346	NHDF-neo	bronchial:	n/a
26	chr21:45705429-45705479	AG09319	gingival:	n/a
27	chr21:45705267-45705317	BJ	skin:	n/a
28	chr21:45709604-45709654	IMR90	lung:	fetal
29	chr21:45705699-45705749	AG10803	skin:	n/a
30	chr21:45706101-45706151	LNCaP	prostate:	n/a
31	chr21:45702039-45702089	Hepatocyte	liver:	n/a
32	chr21:45706101-45706151	Hela-S3	cervix:	n/a
33	chr21:45705740-45705790	ECC-1	luminal epithelium:	n/a
34	chr21:45705994-45706044	NT2-D1	testis:	n/a
35	chr21:45706101-45706151	NB4	blood:	n/a
36	chr21:45710225-45710275	CMK	blood:	n/a
37	chr21:45702039-45702089	PFSK-1	brain:	n/a
38	chr21:45710225-45710275	LNCaP	prostate:	n/a
39	chr21:45705699-45705749	HRCEpiC	kidney:	n/a
40	chr21:45705618-45705668	HCM	heart:	n/a
41	chr21:45705742-45705792	HRPEpiC	eye:	n/a
42	chr21:45702039-45702089	HRE	kidney:	n/a
43	chr21:45709595-45709645	HEEpiC	esophagus:	n/a
44	chr21:45709595-45709645	SKMC	muscle:	n/a
45	chr21:45710225-45710275	SK-N-SH_RA	brain:	n/a
46	chr21:45702039-45702089	GM12891	blood:	n/a
47	chr21:45705740-45705790	HRE	kidney:	n/a
48	chr21:45710225-45710275	HRCEpiC	kidney:	n/a
49	chr21:45709595-45709645	GM19239	blood:	n/a
50	chr21:45709595-45709645	RPTEC	kidney:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45659201..45661814-chr21:45711763..45713332,2	MCF-7	breast:
2	chr21:45698387..45700699-chr21:45707290..45709157,2	MCF-7	breast:
3	chr21:45621565..45624005-chr21:45712576..45714212,3	MCF-7	breast:
4	chr21:45675362..45678242-chr21:45707030..45708929,2	K562	blood:
5	chr21:45621144..45622830-chr21:45706293..45708596,2	MCF-7	breast:
6	chr21:45661660..45663213-chr21:45700955..45703674,2	K562	blood:
7	chr21:45598378..45600609-chr21:45712200..45713820,2	MCF-7	breast:
8	chr21:45707047..45709447-chr21:45711047..45712909,2	MCF-7	breast:
9	chr21:45675362..45677457-chr21:45707030..45709484,2	K562	blood:
10	chr21:45644343..45646450-chr21:45701805..45703427,2	MCF-7	breast:
11	chr21:45568318..45571293-chr21:45707823..45709583,2	K562	blood:
12	chr21:45699767..45703911-chr21:45704221..45706771,4	MCF-7	breast:
13	chr21:45689868..45692167-chr21:45702477..45704899,2	K562	blood:
14	chr21:45551834..45580791-chr21:45711953..45732193,97	MCF-7	breast:
15	chr21:45703655..45709073-chr21:45718662..45721905,6	MCF-7	breast:
16	chr21:45707337..45709850-chr21:45719040..45720575,2	K562	blood:
17	chr21:45687866..45689846-chr21:45707604..45709225,2	MCF-7	breast:
18	chr21:45705948..45708747-chr21:45714407..45716597,2	MCF-7	breast:
19	chr21:45698387..45700699-chr21:45707290..45709157,2	MCF-7	breast:
20	chr21:45706192..45708380-chr9:137402919..137404419,2	K562	blood:
21	chr21:45664753..45666308-chr21:45706084..45707885,2	MCF-7	breast:
22	chr21:45620857..45623394-chr21:45709649..45711804,3	MCF-7	breast:
23	chr21:45659418..45662938-chr21:45698078..45703771,5	MCF-7	breast:
24	chr21:45707047..45709447-chr21:45711047..45712909,2	MCF-7	breast:
25	chr21:45703415..45705838-chr21:45706496..45708664,2	K562	blood:

No data

Variant related genes	Relation type
AIRE	TF binding region
AIRE	CpG island
ENSG00000141959	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000225331	chromatin interactions
ENSG00000160224	chromatin interactions
ENSG00000232124	chromatin interactions

Extended variants
information (count: 898 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2105662	chr21:45697755-45697756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150175794	chr21:45697766-45697767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182762048	chr21:45697779-45697780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539357573	chr21:45697792-45697793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188235122	chr21:45697794-45697795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575710354	chr21:45697808-45697809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550050536	chr21:45697832-45697833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs8133277	chr21:45697834-45697835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs368173122	chr21:45697884-45697885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114990855	chr21:45697949-45697950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200289663	chr21:45697950-45697951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111837024	chr21:45697954-45697955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60635693	chr21:45697965-45697966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147564052	chr21:45697969-45697970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367823080	chr21:45697970-45697971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56396676	chr21:45697973-45697974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369613264	chr21:45697974-45697975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386819131	chr21:45697981-45697982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56168471	chr21:45697982-45697983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2329745	chr21:45697983-45697984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559548801	chr21:45697995-45697996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532976857	chr21:45698005-45698006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544914482	chr21:45698014-45698015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563196974	chr21:45698016-45698017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569702223	chr21:45698025-45698026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558658264	chr21:45698027-45698028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35406013	chr21:45698052-45698053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2096859	chr21:45698069-45698070	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs57013428	chr21:45698077-45698078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377158118	chr21:45698089-45698090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567136517	chr21:45698118-45698119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528236366	chr21:45698119-45698120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546366964	chr21:45698121-45698122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35417449	chr21:45698125-45698126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369890378	chr21:45698146-45698147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182699305	chr21:45698175-45698176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538809483	chr21:45698181-45698182	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557705971	chr21:45698185-45698186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs187429069	chr21:45698198-45698199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192208700	chr21:45698214-45698215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184839059	chr21:45698227-45698228	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs530726771	chr21:45698249-45698250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540763612	chr21:45698254-45698255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188881578	chr21:45698341-45698342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143661616	chr21:45698380-45698381	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2776373	chr21:45698393-45698394	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs563257346	chr21:45698411-45698412	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs8129046	chr21:45698427-45698428	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs57281000	chr21:45698488-45698489	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs560977929	chr21:45698515-45698516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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 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
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	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 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
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	21364760	CNVD
Down syndrome	21154855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45662800-45705600	Weak transcription	Right Atrium	heart
2	chr21:45684000-45702000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr21:45693000-45701200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr21:45699400-45699600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr21:45699400-45699800	Enhancers	Fetal Stomach	stomach
6	chr21:45699400-45700000	Enhancers	Fetal Muscle Leg	muscle
7	chr21:45699600-45699800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr21:45699600-45699800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
9	chr21:45699800-45700000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr21:45699800-45700000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr21:45701200-45703000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr21:45701400-45702200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr21:45701400-45702200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr21:45701400-45702800	Enhancers	GM12878-XiMat	blood
15	chr21:45701600-45701800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr21:45701800-45702000	Enhancers	Right Ventricle	heart
17	chr21:45701800-45703600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr21:45702000-45702200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
19	chr21:45702000-45705200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr21:45702000-45705200	Weak transcription	Right Ventricle	heart
21	chr21:45702200-45702400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr21:45702200-45702400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr21:45702200-45702400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr21:45702200-45702400	Bivalent Enhancer	HepG2	liver
25	chr21:45702200-45702800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr21:45702200-45703000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr21:45702200-45704400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr21:45702200-45705200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr21:45702400-45702600	Enhancers	Primary hematopoietic stem cells	blood
30	chr21:45702400-45702800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr21:45702400-45703000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr21:45702400-45703000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr21:45702400-45704200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr21:45702400-45705800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr21:45702600-45703600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr21:45702600-45703800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr21:45702600-45703800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr21:45702800-45703600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr21:45702800-45714000	Weak transcription	GM12878-XiMat	blood
40	chr21:45703000-45703400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr21:45703000-45703400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr21:45703000-45703400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr21:45703000-45703800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr21:45703000-45704600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr21:45703000-45705000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr21:45703000-45705600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr21:45703400-45704000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr21:45703400-45704200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr21:45703400-45704200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr21:45703400-45704600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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