Variant report

Variant	nsv914094
Chromosome Location	chr21:47416324-47431031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:1038)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr21:47421798-47422063	K562	blood:	n/a	n/a
2	CBX3	chr21:47428177-47428442	K562	blood:	n/a	n/a
3	CHD1	chr21:47419515-47420005	IMR90	lung:	n/a	n/a
4	CTCF	chr21:47424240-47424390	K562	blood:	n/a	n/a
5	E2F6	chr21:47420613-47420852	K562	blood:	n/a	n/a
6	E2F6	chr21:47420358-47420579	K562	blood:	n/a	n/a
7	EGR1	chr21:47421046-47421308	K562	blood:	n/a	n/a
8	EGR1	chr21:47421052-47421283	K562	blood:	n/a	n/a
9	ELF1	chr21:47422688-47423052	K562	blood:	n/a	chr21:47422922-47422931 chr21:47422921-47422932
10	ELK1	chr21:47416359-47416364	Hela-S3	cervix:	n/a	n/a
11	ESR1	chr21:47422124-47422536	ECC-1	luminal epithelium:	n/a	n/a
12	ESR1	chr21:47422117-47422631	ECC-1	luminal epithelium:	n/a	n/a
13	ESR1	chr21:47422142-47422628	ECC-1	luminal epithelium:	n/a	n/a
14	ESR1	chr21:47422099-47422655	ECC-1	luminal epithelium:	n/a	n/a
15	GABPA	chr21:47422748-47423085	K562	blood:	n/a	n/a
16	HEY1	chr21:47430607-47430991	K562	blood:	n/a	n/a
17	HMGN3	chr21:47419064-47419259	K562	blood:	n/a	n/a
18	MAX	chr21:47420457-47421045	ECC-1	luminal epithelium:	n/a	n/a
19	MAX	chr21:47420635-47420873	K562	blood:	n/a	n/a
20	MAX	chr21:47421009-47421272	K562	blood:	n/a	n/a
21	MAX	chr21:47420352-47420533	K562	blood:	n/a	n/a
22	MAX	chr21:47420573-47421022	ECC-1	luminal epithelium:	n/a	n/a
23	MAX	chr21:47420249-47420969	K562	blood:	n/a	n/a
24	MAZ	chr21:47420757-47421660	IMR90	lung:	n/a	n/a
25	MAZ	chr21:47420939-47421271	K562	blood:	n/a	n/a
26	MYC	chr21:47423282-47423367	MCF-7	breast:	n/a	n/a
27	MYC	chr21:47420781-47420848	K562	blood:	n/a	n/a
28	MYC	chr21:47420324-47420920	K562	blood:	n/a	n/a
29	PBX3	chr21:47430449-47431018	GM12878	blood:	n/a	n/a
30	POLR2A	chr21:47421881-47422134	ProgFib	skin:	n/a	n/a
31	POLR2A	chr21:47423570-47423602	ProgFib	skin:	n/a	n/a
32	POLR2A	chr21:47419658-47420506	U87	brain:	n/a	n/a
33	POLR2A	chr21:47423614-47423625	ProgFib	skin:	n/a	n/a
34	POLR2A	chr21:47425105-47425183	Gliobla	brain:	n/a	n/a
35	POLR2A	chr21:47421582-47421851	IMR90	lung:	n/a	n/a
36	POLR2A	chr21:47425340-47425341	ProgFib	skin:	n/a	n/a
37	POLR2A	chr21:47416934-47417319	U87	brain:	n/a	n/a
38	POLR2A	chr21:47416141-47416799	U87	brain:	n/a	n/a
39	POLR2A	chr21:47422825-47423188	U87	brain:	n/a	n/a
40	POLR2A	chr21:47421127-47421474	ProgFib	skin:	n/a	n/a
41	POLR2A	chr21:47425004-47425331	ProgFib	skin:	n/a	n/a
42	POLR2A	chr21:47423221-47423272	ProgFib	skin:	n/a	n/a
43	POLR2A	chr21:47420038-47420319	IMR90	lung:	n/a	n/a
44	POLR2A	chr21:47421129-47421255	IMR90	lung:	n/a	n/a
45	POLR2A	chr21:47425159-47425247	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr21:47424973-47425197	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr21:47421062-47421563	U87	brain:	n/a	n/a
48	POLR2A	chr21:47419548-47420512	U87	brain:	n/a	n/a
49	POLR2A	chr21:47421101-47421118	ProgFib	skin:	n/a	n/a
50	POLR2A	chr21:47424956-47425806	IMR90	lung:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47421319-47421369	HPAEpiC	pulmonary alveolar:	n/a
2	chr21:47421319-47421369	HPAEpiC	pulmonary alveolar:	n/a
3	chr21:47421319-47421369	SK-N-SH_RA	brain:	n/a
4	chr21:47422158-47422208	Hela-S3	cervix:	n/a
5	chr21:47419697-47419747	K562	blood:	n/a
6	chr21:47423074-47423124	HCF	heart:	n/a
7	chr21:47428846-47428896	GM12878	blood:	n/a
8	chr21:47419697-47419747	HPAEpiC	pulmonary alveolar:	n/a
9	chr21:47422158-47422208	NHBE	bronchial:	n/a
10	chr21:47431010-47431060	GM19239	blood:	n/a
11	chr21:47428846-47428896	HRCEpiC	kidney:	n/a
12	chr21:47421177-47421227	NH-A	brain:	n/a
13	chr21:47423639-47423689	RPTEC	kidney:	n/a
14	chr21:47422158-47422208	GM12891	blood:	n/a
15	chr21:47430821-47430871	SK-N-SH	brain:	n/a
16	chr21:47421270-47421320	AG10803	skin:	n/a
17	chr21:47421947-47421997	MCF-7	breast:	n/a
18	chr21:47423882-47423932	HPAEpiC	pulmonary alveolar:	n/a
19	chr21:47424543-47424593	HCF	heart:	n/a
20	chr21:47423882-47423932	GM12891	blood:	n/a
21	chr21:47422158-47422208	PrEC	prostate:	n/a
22	chr21:47424543-47424593	SK-N-MC	brain:	n/a
23	chr21:47421947-47421997	BE2_C	brain:	n/a
24	chr21:47420301-47420351	SK-N-SH_RA	brain:	n/a
25	chr21:47424543-47424593	AG10803	skin:	n/a
26	chr21:47423074-47423124	T-47D	breast:	n/a
27	chr21:47418282-47418332	HCM	heart:	n/a
28	chr21:47422158-47422208	ovcar-3	ovarian:	n/a
29	chr21:47424543-47424593	HRPEpiC	eye:	n/a
30	chr21:47421270-47421320	AG09309	skin:	n/a
31	chr21:47421177-47421227	NT2-D1	testis:	n/a
32	chr21:47431010-47431060	ovcar-3	ovarian:	n/a
33	chr21:47428846-47428896	HepG2	liver:	n/a
34	chr21:47421177-47421227	AG09319	gingival:	n/a
35	chr21:47422158-47422208	GM19239	blood:	n/a
36	chr21:47418282-47418332	AG10803	skin:	n/a
37	chr21:47422158-47422208	NB4	blood:	n/a
38	chr21:47419697-47419747	Hepatocyte	liver:	n/a
39	chr21:47419697-47419747	GM12878	blood:	n/a
40	chr21:47431010-47431060	NHDF-neo	bronchial:	n/a
41	chr21:47422537-47422587	BE2_C	brain:	n/a
42	chr21:47422537-47422587	HEEpiC	esophagus:	n/a
43	chr21:47421319-47421369	ovcar-3	ovarian:	n/a
44	chr21:47422537-47422587	ovcar-3	ovarian:	n/a
45	chr21:47423074-47423124	K562	blood:	n/a
46	chr21:47421319-47421369	AG09309	skin:	n/a
47	chr21:47420301-47420351	NH-A	brain:	n/a
48	chr21:47424543-47424593	BE2_C	brain:	n/a
49	chr21:47421270-47421320	AG04449	skin:	fetal
50	chr21:47428846-47428896	AG09309	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47415907..47418450-chr21:47418722..47421230,2	MCF-7	breast:
2	chr21:47422093..47424938-chr21:47427545..47430029,2	K562	blood:
3	chr21:47422053..47425475-chr21:47428591..47432005,3	MCF-7	breast:
4	chr21:47416853..47418859-chr21:47421399..47424312,2	K562	blood:
5	chr21:47427092..47429709-chr21:47442410..47444749,2	K562	blood:
6	chr21:47427326..47428898-chr21:47432670..47434533,2	K562	blood:
7	chr21:47410997..47412945-chr21:47415697..47417959,2	MCF-7	breast:
8	chr21:47407254..47409991-chr21:47416573..47418228,2	K562	blood:
9	chr21:46961078..46962785-chr21:47417789..47420284,2	K562	blood:
10	chr21:47407254..47409991-chr21:47416573..47418228,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCBP3-3	chr21:47420245-47420281	NONHSAT083008
2	lnc-PCBP3-3	chr21:47420673-47420842	NONHSAT083008
3	lnc-PCBP3-3	chr21:47419314-47419606	NONHSAT083008

No data

Variant related genes	Relation type
COL6A1	TF binding region
COL6A1	CpG island
ENSG00000173638	chromatin interactions
ENSG00000142156	chromatin interactions

Extended variants
information (count: 1135 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9978314	chr21:47416324-47416325	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114469764	chr21:47416325-47416326	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs532335824	chr21:47416335-47416336	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550827372	chr21:47416344-47416345	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs377395164	chr21:47416364-47416365	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs372589207	chr21:47416372-47416373	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs529551166	chr21:47416439-47416440	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78234426	chr21:47416440-47416441	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs192508740	chr21:47416445-47416446	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs528949061	chr21:47416453-47416454	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs530880485	chr21:47416490-47416491	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11701952	chr21:47416493-47416494	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12482416	chr21:47416496-47416497	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184555467	chr21:47416519-47416520	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs553249834	chr21:47416523-47416524	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs571650894	chr21:47416530-47416531	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375098712	chr21:47416540-47416541	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs555417089	chr21:47416548-47416549	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369883259	chr21:47416563-47416564	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538834030	chr21:47416572-47416573	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557302743	chr21:47416575-47416576	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114135405	chr21:47416582-47416583	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568045533	chr21:47416610-47416611	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs78052477	chr21:47416612-47416613	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs572870978	chr21:47416641-47416642	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs76758905	chr21:47416648-47416649	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368986565	chr21:47416649-47416650	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565161659	chr21:47416666-47416667	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532476042	chr21:47416672-47416673	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs114175056	chr21:47416681-47416682	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs562508831	chr21:47416682-47416683	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529909858	chr21:47416752-47416753	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549161590	chr21:47416777-47416778	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567795671	chr21:47416838-47416839	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528459633	chr21:47416883-47416884	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs75200965	chr21:47416903-47416904	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs571588667	chr21:47416938-47416939	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs538921019	chr21:47416943-47416944	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs533594599	chr21:47416962-47416963	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs188238761	chr21:47416993-47416994	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536894938	chr21:47416995-47416996	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs554357145	chr21:47417000-47417001	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573008650	chr21:47417014-47417015	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs558559633	chr21:47417026-47417027	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576928795	chr21:47417032-47417033	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544138299	chr21:47417037-47417038	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs112124422	chr21:47417051-47417052	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562805451	chr21:47417052-47417053	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs574545284	chr21:47417063-47417064	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542049728	chr21:47417068-47417069	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 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:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47403200-47424600	Weak transcription	Small Intestine	intestine
2	chr21:47403200-47425000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr21:47404000-47424200	Strong transcription	H1 Cell Line	embryonic stem cell
4	chr21:47404000-47424600	Strong transcription	Aorta	Aorta
5	chr21:47404200-47425200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr21:47404200-47425200	Strong transcription	Muscle Satellite Cultured Cells	--
7	chr21:47404400-47419200	Strong transcription	Left Ventricle	heart
8	chr21:47405000-47417400	Weak transcription	Stomach Mucosa	stomach
9	chr21:47405000-47419400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr21:47405000-47423800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr21:47405000-47425400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr21:47405200-47425400	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr21:47405200-47425400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
14	chr21:47405200-47425800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr21:47405400-47423800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr21:47405400-47424800	Strong transcription	Fetal Brain Female	brain
17	chr21:47405400-47425200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr21:47405600-47419800	Strong transcription	Fetal Stomach	stomach
19	chr21:47405600-47423000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr21:47406400-47421400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr21:47406600-47425400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr21:47407600-47416400	Weak transcription	Esophagus	oesophagus
23	chr21:47407600-47425000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr21:47408400-47416400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr21:47408400-47416800	Genic enhancers	Stomach Smooth Muscle	stomach
26	chr21:47408400-47425800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr21:47408600-47419800	Strong transcription	Brain Germinal Matrix	brain
28	chr21:47408800-47417800	Strong transcription	H9 Cell Line	embryonic stem cell
29	chr21:47409000-47425200	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr21:47409200-47425000	Strong transcription	Ovary	ovary
31	chr21:47409400-47416400	Strong transcription	Fetal Lung	lung
32	chr21:47409400-47419400	Strong transcription	Gastric	stomach
33	chr21:47409800-47426600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr21:47410000-47422600	Weak transcription	Liver	Liver
35	chr21:47410200-47416400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr21:47410800-47416600	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr21:47411200-47432800	Weak transcription	Right Atrium	heart
38	chr21:47412400-47423000	Strong transcription	Colonic Mucosa	Colon
39	chr21:47412400-47426400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr21:47412600-47422400	Weak transcription	Brain Hippocampus Middle	brain
41	chr21:47412600-47425800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr21:47413400-47417000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr21:47413600-47420200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr21:47413800-47416600	Strong transcription	Pancreas	Pancrea
45	chr21:47413800-47416800	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr21:47413800-47425200	Strong transcription	NHLF	lung
47	chr21:47414000-47416600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr21:47414000-47421200	Strong transcription	Spleen	Spleen
49	chr21:47414200-47416400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr21:47414200-47424800	Strong transcription	Right Ventricle	heart

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