Variant report

Variant	nsv1064893
Chromosome Location	chr21:14594223-15088037
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:822)
CpG islands
(count:2015)
Chromatin interactive
region (count:1)
LncRNA
region (count:30)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:822 , 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	BATF	chr21:14607219-14607387	GM12878	blood:	n/a	chr21:14607350-14607360
2	BATF	chr21:15063813-15064156	GM12878	blood:	n/a	chr21:15064016-15064027
3	BCL11A	chr21:15063984-15064146	GM12878	blood:	n/a	n/a
4	BCL11A	chr21:15063819-15064217	GM12878	blood:	n/a	n/a
5	BHLHE40	chr21:15069019-15069264	K562	blood:	n/a	n/a
6	CEBPB	chr21:14748547-14748799	IMR90	lung:	n/a	chr21:14748653-14748664
7	CEBPB	chr21:14748544-14748767	A549	lung:	n/a	chr21:14748653-14748664
8	CEBPB	chr21:14927795-14927928	HepG2	liver:	n/a	n/a
9	CEBPB	chr21:15020469-15020779	K562	blood:	n/a	n/a
10	CEBPB	chr21:15020460-15020823	A549	lung:	n/a	n/a
11	CEBPB	chr21:14616993-14617191	HepG2	liver:	n/a	chr21:14617135-14617146
12	CEBPB	chr21:15020588-15020668	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr21:14616982-14617279	IMR90	lung:	n/a	chr21:14617135-14617146
14	CEBPB	chr21:15020516-15020778	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr21:14748543-14748761	HepG2	liver:	n/a	chr21:14748653-14748664
16	CHD2	chr21:15069161-15069237	K562	blood:	n/a	n/a
17	CTCF	chr21:14797723-14797868	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr21:15080708-15080845	LNCaP	prostate:	n/a	n/a
19	CTCF	chr21:15079620-15079770	K562	blood:	n/a	n/a
20	CTCF	chr21:15069620-15069770	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr21:15069720-15069870	MCF-7	breast:	n/a	n/a
22	CTCF	chr21:14722233-14722326	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr21:15050149-15050256	Spleen_OC	spleen:	n/a	chr21:15050174-15050181
24	CTCF	chr21:15069632-15069909	K562	blood:	n/a	n/a
25	CTCF	chr21:15069060-15069210	GM12865	blood:	n/a	chr21:15069137-15069153 chr21:15069136-15069154 chr21:15069140-15069147
26	CTCF	chr21:15079600-15079750	A549	lung:	n/a	n/a
27	CTCF	chr21:15063581-15063632	MCF-7	breast:	n/a	n/a
28	CTCF	chr21:15069042-15069170	HepG2	liver:	n/a	chr21:15069137-15069153 chr21:15069136-15069154 chr21:15069140-15069147
29	CTCF	chr21:15068960-15069110	RPTEC	kidney:	n/a	n/a
30	CTCF	chr21:15063546-15063661	GM12878	blood:	n/a	n/a
31	CTCF	chr21:14713167-14713284	Hela-S3	cervix:	n/a	chr21:14713204-14713220 chr21:14713198-14713219
32	CTCF	chr21:14713028-14713339	A549	lung:	n/a	chr21:14713204-14713220 chr21:14713198-14713219
33	CTCF	chr21:15031187-15031208	GM13976	blood:	n/a	n/a
34	CTCF	chr21:14951942-14952013	Lung_OC	lung:	n/a	n/a
35	CTCF	chr21:15069080-15069230	HRPEpiC	eye:	n/a	chr21:15069137-15069153 chr21:15069136-15069154 chr21:15069140-15069147
36	CTCF	chr21:14961250-14961273	GM19239	blood:	n/a	n/a
37	CTCF	chr21:15063618-15063665	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr21:14896822-14896844	LNCaP	prostate:	n/a	n/a
39	CTCF	chr21:15069043-15069226	GM10248	blood:	n/a	chr21:15069137-15069153 chr21:15069136-15069154 chr21:15069140-15069147
40	CTCF	chr21:15069004-15069394	MCF-7	breast:	n/a	chr21:15069137-15069153 chr21:15069136-15069154 chr21:15069140-15069147
41	CTCF	chr21:14742700-14742850	HEK293	kidney:	n/a	n/a
42	CTCF	chr21:14683610-14683736	MCF-7	breast:	n/a	n/a
43	CTCF	chr21:14984043-14984115	LNCaP	prostate:	n/a	n/a
44	CTCF	chr21:14980834-14980883	Lung_OC	lung:	n/a	n/a
45	CTCF	chr21:15009027-15009101	GM13976	blood:	n/a	n/a
46	CTCF	chr21:14746915-14746931	LNCaP	prostate:	n/a	n/a
47	CTCF	chr21:14859194-14859318	MCF-7	breast:	n/a	n/a
48	CTCF	chr21:15069003-15069280	LNCaP	prostate:	n/a	chr21:15069137-15069153 chr21:15069136-15069154 chr21:15069140-15069147
49	CTCF	chr21:15067766-15067975	MCF-7	breast:	n/a	chr21:15067857-15067875 chr21:15067859-15067872
50	CTCF	chr21:14911682-14911810	LNCaP	prostate:	n/a	n/a

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15068553-15068603	AG10803	skin:	n/a
2	chr21:15068826-15068876	Caco-2	colon:	n/a
3	chr21:15068553-15068603	AG10803	skin:	n/a
4	chr21:15068826-15068876	Caco-2	colon:	n/a
5	chr21:14982225-14982275	HRCEpiC	kidney:	n/a
6	chr21:14981404-14981454	GM12878	blood:	n/a
7	chr21:15038629-15038679	HPAEpiC	pulmonary alveolar:	n/a
8	chr21:15052411-15052461	IMR90	lung:	fetal
9	chr21:15038453-15038503	T-47D	breast:	n/a
10	chr21:15077774-15077824	BJ	skin:	n/a
11	chr21:14982779-14982829	AG09309	skin:	n/a
12	chr21:15078554-15078604	BJ	skin:	n/a
13	chr21:15035883-15035933	GM19239	blood:	n/a
14	chr21:15068826-15068876	HIPEpiC	eye:	n/a
15	chr21:15033939-15033989	MCF10A-Er-Src	breast:	n/a
16	chr21:14982779-14982829	PrEC	prostate:	n/a
17	chr21:15080112-15080162	ECC-1	luminal epithelium:	n/a
18	chr21:15038314-15038364	AG10803	skin:	n/a
19	chr21:15039424-15039474	Caco-2	colon:	n/a
20	chr21:15069557-15069607	HPAEpiC	pulmonary alveolar:	n/a
21	chr21:15069557-15069607	HRCEpiC	kidney:	n/a
22	chr21:15069557-15069607	U87	brain:	n/a
23	chr21:15071306-15071356	SK-N-MC	brain:	n/a
24	chr21:15066995-15067045	HCM	heart:	n/a
25	chr21:15035883-15035933	HEK293	kidney:	embryo
26	chr21:15066572-15066622	T-47D	breast:	n/a
27	chr21:15033939-15033989	NH-A	brain:	n/a
28	chr21:15080112-15080162	CMK	blood:	n/a
29	chr21:15035883-15035933	SKMC	muscle:	n/a
30	chr21:15066995-15067045	HRPEpiC	eye:	n/a
31	chr21:14982080-14982130	GM12891	blood:	n/a
32	chr21:14982350-14982400	A549	lung:	n/a
33	chr21:15038314-15038364	LNCaP	prostate:	n/a
34	chr21:15080112-15080162	BE2_C	brain:	n/a
35	chr21:15038314-15038364	ovcar-3	ovarian:	n/a
36	chr21:14981404-14981454	HL-60	blood:	n/a
37	chr21:15038314-15038364	GM12892	blood:	n/a
38	chr21:14981404-14981454	T-47D	breast:	n/a
39	chr21:14982225-14982275	HRE	kidney:	n/a
40	chr21:15033939-15033989	AG09319	gingival:	n/a
41	chr21:14982363-14982413	A549	lung:	n/a
42	chr21:15078554-15078604	PFSK-1	brain:	n/a
43	chr21:15069557-15069607	Caco-2	colon:	n/a
44	chr21:15049206-15049256	Caco-2	colon:	n/a
45	chr21:15069557-15069607	HCM	heart:	n/a
46	chr21:15052411-15052461	CMK	blood:	n/a
47	chr21:15051848-15051898	U87	brain:	n/a
48	chr21:15038629-15038679	NT2-D1	testis:	n/a
49	chr21:15069190-15069240	HEEpiC	esophagus:	n/a
50	chr21:14981404-14981454	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:14629664..14632607-chr21:14899242..14900976,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAGE4-12	chr21:15041937-15042566	NONHSAT081116
2	lnc-BAGE4-12	chr21:15047515-15047653	NONHSAT081117
3	lnc-POTED-12	chr21:14687514-14687778	l_2166_chr21:14677648-14687775_brain
4	lnc-BAGE4-7	chr21:14807106-14807331	expReg_chr21_145_-
5	lnc-BAGE4-10	chr21:15024549-15026514	NONHSAT081113
6	lnc-POTED-1	chr21:14919301-14919449	ENSG00000228159
7	lnc-BAGE4-12	chr21:15045054-15045100	NONHSAT081117
8	lnc-POTED-1	chr21:14918354-14918444	NR_110544
9	lnc-POTED-1	chr21:14928714-14928832	ENSG00000228159
10	lnc-POTED-12	chr21:14677649-14677729	l_2166_chr21:14677648-14687775_brain
11	lnc-POTED-1	chr21:14919301-14919449	NR_110544
12	lnc-BAGE4-5	chr21:14789550-14789761	expReg_chr21_132_-
13	lnc-BAGE4-2	chr21:14783236-14783504	expReg_chr21_122_-
14	lnc-BAGE4-3	chr21:14787066-14787369	expReg_chr21_126_-
15	lnc-BAGE4-12	chr21:15041937-15042566	NONHSAT081117
16	lnc-POTED-1	chr21:14930638-14930781	NR_110544
17	lnc-BAGE4-10	chr21:15023866-15023904	NONHSAT081113
18	lnc-BAGE4-4	chr21:14789321-14789544	expReg_chr21_131_-
19	lnc-POTED-5	chr21:15035025-15035149	NONHSAT081114
20	lnc-POTED-7	chr21:14848692-14849584	NONHSAT081105
21	lnc-POTED-5	chr21:15048216-15048672	NONHSAT081114
22	lnc-POTED-1	chr21:14918354-14918444	ENSG00000228159
23	lnc-BAGE4-12	chr21:15047992-15048057	NONHSAT081116
24	lnc-POTED-1	chr21:14930638-14930782	ENSG00000228159
25	lnc-BAGE4-12	chr21:15045054-15045100	NONHSAT081116
26	lnc-POTED-1	chr21:14928714-14928832	NR_110544
27	lnc-BAGE4-6	chr21:14792037-14792496	expReg_chr21_135_-
28	lnc-POTED-6	chr21:15055902-15056343	NONHSAT081118
29	lnc-BAGE4-13	chr21:15056956-15057423	expReg_chr21_194_-
30	lnc-POTED-6	chr21:15057030-15057282	NONHSAT081118

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3118	chr21:15017105-15017127	MIMAT0014980_5
hsa-miR-3156-5p	chr21:14778752-14778773	MIMAT0015030_2

No data

Variant related genes	Relation type
OR4K11P	TF binding region
ENSG00000269011	TF binding region
RNU6-286P	TF binding region
MIR3156-3	TF binding region
MIR3118-5	TF binding region
GTF2IP2	TF binding region
SNX19P1	TF binding region
VN1R8P	TF binding region
ANKRD30BP1	TF binding region
ENSG00000228159	TF binding region
FGF7P2	TF binding region
CXADRP1	TF binding region
GRAMD4P1	TF binding region
ENSG00000256715	TF binding region
POTED	TF binding region
OR4K12P	TF binding region
OR4K11P	CpG island
ENSG00000269011	CpG island
RNU6-286P	CpG island
MIR3156-3	CpG island
MIR3118-5	CpG island
GTF2IP2	CpG island
SNX19P1	CpG island
VN1R8P	CpG island
ANKRD30BP1	CpG island
ENSG00000228159	CpG island
FGF7P2	CpG island
CXADRP1	CpG island
GRAMD4P1	CpG island
ENSG00000256715	CpG island
POTED	CpG island
OR4K12P	CpG island

Extended variants
information (count: 2376 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2376 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142211526	chr21:14619600-14619601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113971599	chr21:14619616-14619617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141460135	chr21:14619650-14619651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184749096	chr21:14619666-14619667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2997012	chr21:14619682-14619683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2997013	chr21:14619696-14619697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543406096	chr21:14619697-14619698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146970651	chr21:14619767-14619768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201232074	chr21:14619783-14619784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs202154830	chr21:14619837-14619838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545571809	chr21:14619871-14619872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2334427	chr21:14619876-14619877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528655743	chr21:14619880-14619881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548508032	chr21:14619883-14619884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374289918	chr21:14619890-14619891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568383164	chr21:14619895-14619896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200381343	chr21:14619920-14619921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530837093	chr21:14619935-14619936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550516159	chr21:14619961-14619962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532816383	chr21:14620000-14620001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2997014	chr21:14620026-14620027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150232205	chr21:14620043-14620044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2259468	chr21:14620054-14620055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565892189	chr21:14620059-14620060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559337326	chr21:14620075-14620076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534795007	chr21:14620104-14620105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528051472	chr21:14620140-14620141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374908395	chr21:14620165-14620166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574755775	chr21:14620201-14620202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552388077	chr21:14620216-14620217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369683207	chr21:14620224-14620225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537045264	chr21:14620240-14620241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373112936	chr21:14620276-14620277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144688074	chr21:14620278-14620279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576761000	chr21:14620279-14620280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545912476	chr21:14620318-14620319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559168018	chr21:14620320-14620321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573119240	chr21:14620348-14620349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2259427	chr21:14620359-14620360	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs112689261	chr21:14667211-14667212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192535622	chr21:14667227-14667228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560316770	chr21:14667233-14667234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7275943	chr21:14667238-14667239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142040374	chr21:14667240-14667241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562798966	chr21:14667242-14667243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145899499	chr21:14667254-14667255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551435107	chr21:14667270-14667271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528259434	chr21:14667296-14667297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568604593	chr21:14667367-14667368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184922724	chr21:14667414-14667415	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	18458336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	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
Myelofibrosis	22110671	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	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
Breast cancer	21364760	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	21785460	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:14619600-14620400	Enhancers	Brain Hippocampus Middle	brain
2	chr21:14667200-14668400	Enhancers	Brain Hippocampus Middle	brain
3	chr21:14676000-14676200	Enhancers	Liver	Liver
4	chr21:14676000-14676800	Enhancers	Brain Anterior Caudate	brain
5	chr21:14676200-14676800	Weak transcription	Liver	Liver
6	chr21:14676800-14677600	Enhancers	Liver	Liver
7	chr21:14677600-14682400	Weak transcription	Liver	Liver
8	chr21:14682400-14682800	Enhancers	Liver	Liver
9	chr21:14733400-14733800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr21:14740600-14741200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr21:14742800-14743200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr21:14742800-14743800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr21:14743000-14743800	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr21:14743400-14743800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr21:14751400-14752800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr21:14752200-14752600	Active TSS	Primary T cells from cord blood	blood
17	chr21:14794200-14795400	Enhancers	Dnd41	blood
18	chr21:14866000-14867000	Enhancers	Dnd41	blood
19	chr21:14867000-14869000	Weak transcription	Dnd41	blood
20	chr21:14869000-14872400	Enhancers	Dnd41	blood
21	chr21:14888000-14888200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr21:14900000-14900400	ZNF genes & repeats	Dnd41	blood
23	chr21:14900400-14901400	Weak transcription	Dnd41	blood
24	chr21:14901400-14904800	Enhancers	Dnd41	blood
25	chr21:14916600-14920000	Enhancers	Dnd41	blood
26	chr21:14917000-14917600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr21:14920000-14922800	Weak transcription	Dnd41	blood
28	chr21:14922800-14923600	Enhancers	Dnd41	blood
29	chr21:14924200-14924400	Enhancers	Dnd41	blood
30	chr21:14965200-14966200	Enhancers	Dnd41	blood
31	chr21:14983000-14983200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr21:15035600-15036200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr21:15056200-15058400	Enhancers	Liver	Liver
34	chr21:15058400-15060200	Weak transcription	Liver	Liver
35	chr21:15060200-15062000	Enhancers	Liver	Liver
36	chr21:15066000-15068800	Weak transcription	Right Atrium	heart
37	chr21:15067000-15070200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr21:15067600-15069600	Enhancers	Liver	Liver
39	chr21:15067600-15069600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
40	chr21:15067800-15070200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr21:15068200-15069600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr21:15068200-15069600	ZNF genes & repeats	Spleen	Spleen
43	chr21:15068400-15069400	Active TSS	Pancreas	Pancrea
44	chr21:15068600-15068800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
45	chr21:15068600-15068800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
46	chr21:15068600-15069800	Enhancers	Placenta	Placenta
47	chr21:15068800-15069000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr21:15068800-15069000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr21:15068800-15069400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
50	chr21:15068800-15069400	Active TSS	Brain Anterior Caudate	brain

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