Variant report

Variant	nsv587997
Chromosome Location	chr21:47850405-47863025
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:122)
CpG islands
(count:732)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:122 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:47862928-47863303	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr21:47855134-47855161	K562	blood:	n/a	n/a
3	CEBPB	chr21:47859695-47859943	HepG2	liver:	n/a	n/a
4	CHD2	chr21:47854192-47854246	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr21:47852040-47852190	HL-60	blood:	n/a	chr21:47852134-47852147 chr21:47852137-47852150
6	CTCF	chr21:47855984-47856177	H1-hESC	embryonic stem cell:	n/a	chr21:47856071-47856087
7	ELF1	chr21:47858028-47858469	GM12878	blood:	n/a	n/a
8	HMGN3	chr21:47856590-47856745	K562	blood:	n/a	n/a
9	HMGN3	chr21:47850589-47850651	K562	blood:	n/a	n/a
10	HMGN3	chr21:47862865-47863065	K562	blood:	n/a	n/a
11	MAFF	chr21:47855770-47855908	HepG2	liver:	n/a	chr21:47855860-47855878
12	MAFF	chr21:47862921-47863262	K562	blood:	n/a	n/a
13	MAFK	chr21:47855821-47855893	IMR90	lung:	n/a	n/a
14	MAFK	chr21:47855747-47855881	HepG2	liver:	n/a	n/a
15	MAFK	chr21:47860125-47860312	HepG2	liver:	n/a	n/a
16	MAFK	chr21:47862938-47863168	HepG2	liver:	n/a	chr21:47863091-47863100
17	MAFK	chr21:47855748-47855975	HepG2	liver:	n/a	n/a
18	MAFK	chr21:47862892-47863274	H1-hESC	embryonic stem cell:	n/a	chr21:47863091-47863100
19	MAFK	chr21:47862927-47863253	K562	blood:	n/a	chr21:47863091-47863100
20	MXI1	chr21:47856869-47856889	Hela-S3	cervix:	n/a	n/a
21	MYC	chr21:47857215-47857288	GM12878	blood:	n/a	n/a
22	MYC	chr21:47857214-47857372	MCF-7	breast:	n/a	n/a
23	POLR2A	chr21:47858393-47858402	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr21:47856670-47856680	ProgFib	skin:	n/a	n/a
25	POLR2A	chr21:47849992-47851065	K562	blood:	n/a	n/a
26	POLR2A	chr21:47857156-47857385	MCF-7	breast:	n/a	n/a
27	POLR2A	chr21:47856577-47856841	K562	blood:	n/a	n/a
28	POLR2A	chr21:47860995-47861005	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr21:47854741-47854753	MCF-7	breast:	n/a	n/a
30	POLR2A	chr21:47859239-47859655	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr21:47854146-47854993	K562	blood:	n/a	n/a
32	POLR2A	chr21:47859131-47859551	K562	blood:	n/a	n/a
33	POLR2A	chr21:47860361-47860409	K562	blood:	n/a	n/a
34	POLR2A	chr21:47856536-47857487	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr21:47857068-47857121	MCF-7	breast:	n/a	n/a
36	POLR2A	chr21:47862976-47862998	K562	blood:	n/a	n/a
37	POLR2A	chr21:47854724-47854869	K562	blood:	n/a	n/a
38	POLR2A	chr21:47857262-47857327	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr21:47861753-47862103	MCF-7	breast:	n/a	n/a
40	POLR2A	chr21:47861753-47861799	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr21:47859831-47859931	K562	blood:	n/a	n/a
42	POLR2A	chr21:47860436-47860465	K562	blood:	n/a	n/a
43	POLR2A	chr21:47861849-47861850	GM12878	blood:	n/a	n/a
44	POLR2A	chr21:47861663-47862373	K562	blood:	n/a	n/a
45	POLR2A	chr21:47856797-47857954	K562	blood:	n/a	n/a
46	POLR2A	chr21:47856778-47857193	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr21:47862918-47863400	HepG2	liver:	n/a	n/a
48	POLR2A	chr21:47862801-47863358	SK-N-MC	brain:	n/a	n/a
49	POLR2A	chr21:47855798-47856289	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr21:47849714-47850825	Hela-S3	cervix:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47851742-47851792	K562	blood:	n/a
2	chr21:47855916-47855966	RPTEC	kidney:	n/a
3	chr21:47851470-47851520	NHDF-neo	bronchial:	n/a
4	chr21:47855893-47855943	HL-60	blood:	n/a
5	chr21:47851470-47851520	GM06990	blood:	n/a
6	chr21:47856020-47856070	Jurkat	blood:	n/a
7	chr21:47856020-47856070	HRE	kidney:	n/a
8	chr21:47851742-47851792	Hela-S3	cervix:	n/a
9	chr21:47851621-47851671	HCT-116	colon:	n/a
10	chr21:47859926-47859976	NHDF-neo	bronchial:	n/a
11	chr21:47856215-47856265	SAEC	small airway:	n/a
12	chr21:47856215-47856265	HRCEpiC	kidney:	n/a
13	chr21:47851621-47851671	ovcar-3	ovarian:	n/a
14	chr21:47859926-47859976	CMK	blood:	n/a
15	chr21:47851545-47851595	T-47D	breast:	n/a
16	chr21:47856020-47856070	AG04450	lung:	fetal
17	chr21:47851742-47851792	HCT-116	colon:	n/a
18	chr21:47856140-47856190	AG09309	skin:	n/a
19	chr21:47851941-47851991	NB4	blood:	n/a
20	chr21:47856140-47856190	AG04449	skin:	fetal
21	chr21:47856215-47856265	RPTEC	kidney:	n/a
22	chr21:47856020-47856070	ovcar-3	ovarian:	n/a
23	chr21:47856020-47856070	HCF	heart:	n/a
24	chr21:47855916-47855966	SAEC	small airway:	n/a
25	chr21:47851941-47851991	GM06990	blood:	n/a
26	chr21:47851545-47851595	ovcar-3	ovarian:	n/a
27	chr21:47856215-47856265	HRPEpiC	eye:	n/a
28	chr21:47856020-47856070	GM12892	blood:	n/a
29	chr21:47856140-47856190	ProgFib	skin:	n/a
30	chr21:47856020-47856070	HL-60	blood:	n/a
31	chr21:47859926-47859976	NB4	blood:	n/a
32	chr21:47855916-47855966	HRCEpiC	kidney:	n/a
33	chr21:47859926-47859976	NT2-D1	testis:	n/a
34	chr21:47856020-47856070	H1-hESC	embryonic stem cell:	embryo
35	chr21:47856140-47856190	Hepatocyte	liver:	n/a
36	chr21:47856020-47856070	GM06990	blood:	n/a
37	chr21:47859926-47859976	A549	lung:	n/a
38	chr21:47856215-47856265	PANC-1	pancreas:	n/a
39	chr21:47851742-47851792	U87	brain:	n/a
40	chr21:47851941-47851991	HMEC	breast:	n/a
41	chr21:47851470-47851520	PrEC	prostate:	n/a
42	chr21:47856215-47856265	ovcar-3	ovarian:	n/a
43	chr21:47855893-47855943	AG10803	skin:	n/a
44	chr21:47851941-47851991	PFSK-1	brain:	n/a
45	chr21:47851742-47851792	T-47D	breast:	n/a
46	chr21:47851545-47851595	CMK	blood:	n/a
47	chr21:47855049-47855099	HUVEC	blood vessel:	n/a
48	chr21:47851470-47851520	GM12891	blood:	n/a
49	chr21:47851545-47851595	SK-N-MC	brain:	n/a
50	chr21:47851941-47851991	HRCEpiC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47848467..47851272-chr21:47852866..47855440,2	K562	blood:
2	chr21:47854363..47856833-chr21:47869358..47873122,3	MCF-7	breast:
3	chr21:47858571..47860642-chr21:47862519..47864961,2	MCF-7	breast:
4	chr21:47857857..47859725-chr21:47876652..47878543,2	MCF-7	breast:
5	chr21:47856507..47858157-chr21:47860635..47863396,2	MCF-7	breast:
6	chr21:47856273..47858659-chr21:47860032..47862884,2	K562	blood:
7	chr21:47858462..47860394-chr21:47879147..47880997,2	MCF-7	breast:
8	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
9	chr21:47857792..47859466-chr21:47861182..47863133,2	MCF-7	breast:
10	chr21:47858571..47860642-chr21:47862519..47864961,2	MCF-7	breast:
11	chr21:47861367..47863286-chr21:48054038..48055974,2	K562	blood:
12	chr21:47854459..47856094-chr21:47859695..47861438,2	K562	blood:
13	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
14	chr21:47853352..47856633-chr21:47878140..47880096,4	MCF-7	breast:
15	chr21:47862980..47864520-chr21:47866153..47868184,2	MCF-7	breast:
16	chr21:47860237..47862414-chr21:47862765..47864935,2	K562	blood:
17	chr21:47851003..47853080-chr21:47856086..47858235,2	K562	blood:
18	chr21:47857792..47859466-chr21:47861182..47863133,2	MCF-7	breast:
19	chr21:47847865..47850685-chr21:47852500..47855672,4	K562	blood:
20	chr21:47844449..47847171-chr21:47854131..47855917,2	K562	blood:
21	chr21:47863005..47865990-chr21:47875934..47878581,2	MCF-7	breast:
22	chr21:47862357..47865195-chr21:47870982..47877612,5	K562	blood:
23	chr21:47746558..47749011-chr21:47851647..47853522,2	K562	blood:
24	chr21:47829908..47831983-chr21:47862794..47864924,2	K562	blood:
25	chr21:47856273..47858659-chr21:47860032..47862884,2	K562	blood:
26	chr21:47850253..47852501-chr21:47862918..47865915,2	MCF-7	breast:
27	chr21:47848817..47851368-chr21:47861813..47863381,2	K562	blood:
28	chr21:47857607..47860157-chr21:47877897..47880411,2	MCF-7	breast:
29	chr21:47856507..47858157-chr21:47860635..47863396,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIP2A-1	chr21:47862410-47863085	NONHSAT083069
2	lnc-DIP2A-1	chr21:47860907-47860997	NONHSAT083069

No data

Variant related genes	Relation type
PCNT	TF binding region
PCNT	CpG island
ENSG00000160310	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000160299	chromatin interactions

Extended variants
information (count: 692 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839257	chr21:47850405-47850406	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373126441	chr21:47850408-47850409	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs114120845	chr21:47850416-47850417	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs76287849	chr21:47850417-47850418	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs574092034	chr21:47850439-47850440	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs373282346	chr21:47850453-47850454	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs375738301	chr21:47850456-47850457	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2070426	chr21:47850484-47850485	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs553815033	chr21:47850490-47850491	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572073194	chr21:47850492-47850493	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370099497	chr21:47850500-47850501	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs374592885	chr21:47850531-47850532	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs116217795	chr21:47850631-47850632	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs577571392	chr21:47850639-47850640	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs544921248	chr21:47850641-47850642	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs188976954	chr21:47850650-47850651	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs199878784	chr21:47850651-47850652	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs11285369	chr21:47850652-47850653	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs398081653	chr21:47850654-47850655	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs397867780	chr21:47850655-47850656	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs201565149	chr21:47850656-47850657	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs370487305	chr21:47850691-47850692	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs530103719	chr21:47850701-47850702	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs548324454	chr21:47850711-47850712	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs560608392	chr21:47850742-47850743	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs527800236	chr21:47850764-47850765	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs371510445	chr21:47850803-47850804	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs570317776	chr21:47850807-47850808	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531448810	chr21:47850808-47850809	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs549655294	chr21:47850809-47850810	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs568047140	chr21:47850815-47850816	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535407858	chr21:47850817-47850818	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs553508494	chr21:47850856-47850857	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs565733981	chr21:47850857-47850858	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs35185847	chr21:47850858-47850859	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs539167112	chr21:47850876-47850877	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559144862	chr21:47850933-47850934	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs144667745	chr21:47850989-47850990	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs181590086	chr21:47850995-47850996	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs551307141	chr21:47851041-47851042	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs79203677	chr21:47851175-47851176	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
42	rs575055405	chr21:47851183-47851184	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530487433	chr21:47851191-47851192	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138721694	chr21:47851236-47851237	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs201171629	chr21:47851237-47851238	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527739788	chr21:47851251-47851252	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550282599	chr21:47851257-47851258	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs545978474	chr21:47851259-47851260	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564282706	chr21:47851264-47851265	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2073375	chr21:47851369-47851370	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	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:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47775600-47857600	Weak transcription	Stomach Mucosa	stomach
2	chr21:47803200-47872400	Weak transcription	Fetal Kidney	kidney
3	chr21:47814400-47861000	Weak transcription	Fetal Brain Male	brain
4	chr21:47820400-47851200	Weak transcription	NH-A	brain
5	chr21:47827400-47866600	Strong transcription	Fetal Stomach	stomach
6	chr21:47828000-47863200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr21:47828600-47872400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr21:47829400-47862600	Strong transcription	Skeletal Muscle Female	skeletal muscle
9	chr21:47829400-47867800	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr21:47829600-47862800	Strong transcription	Skeletal Muscle Male	skeletal muscle
11	chr21:47829600-47864000	Strong transcription	Fetal Intestine Small	intestine
12	chr21:47830200-47862800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr21:47830400-47862800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr21:47831000-47857600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr21:47833400-47863400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr21:47834000-47868200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr21:47834200-47868200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr21:47836800-47872400	Weak transcription	Right Atrium	heart
19	chr21:47837800-47854800	Weak transcription	K562	blood
20	chr21:47838000-47853600	Strong transcription	Lung	lung
21	chr21:47838400-47852200	Strong transcription	NHLF	lung
22	chr21:47838800-47862800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr21:47841200-47852400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr21:47842800-47855800	Weak transcription	A549	lung
25	chr21:47843400-47867400	Strong transcription	Dnd41	blood
26	chr21:47843600-47856800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr21:47843600-47857000	Weak transcription	Primary B cells from cord blood	blood
28	chr21:47843800-47857600	Weak transcription	HSMM	muscle
29	chr21:47843800-47862400	Strong transcription	Brain Hippocampus Middle	brain
30	chr21:47843800-47867600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr21:47843800-47868400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr21:47844000-47864400	Strong transcription	Gastric	stomach
33	chr21:47844200-47852800	Strong transcription	H9 Cell Line	embryonic stem cell
34	chr21:47844200-47853200	Strong transcription	Adipose Nuclei	Adipose
35	chr21:47844200-47854400	Strong transcription	Esophagus	oesophagus
36	chr21:47844200-47862200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr21:47844200-47866800	Strong transcription	Brain Germinal Matrix	brain
38	chr21:47844200-47867400	Strong transcription	Fetal Brain Female	brain
39	chr21:47844800-47851400	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr21:47844800-47856800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr21:47844800-47862400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr21:47844800-47865800	Strong transcription	Duodenum Mucosa	Duodenum
43	chr21:47844800-47867400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr21:47845000-47852600	Strong transcription	Brain Cingulate Gyrus	brain
45	chr21:47845000-47852800	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr21:47845000-47853200	Strong transcription	Placenta Amnion	Placenta Amnion
47	chr21:47845000-47854000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr21:47845000-47856800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr21:47845000-47857000	Strong transcription	Spleen	Spleen
50	chr21:47845000-47857200	Strong transcription	Placenta	Placenta

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