Variant report

Variant	esv1802303
Chromosome Location	chr21:46580319-46606676
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:197)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:197 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:46587720-46587908	K562	blood:	n/a	n/a
2	BACH1	chr21:46587650-46587885	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr21:46587628-46588015	K562	blood:	n/a	n/a
4	BATF	chr21:46596546-46596739	GM12878	blood:	n/a	n/a
5	BHLHE40	chr21:46589085-46589336	K562	blood:	n/a	n/a
6	BHLHE40	chr21:46587900-46588066	K562	blood:	n/a	n/a
7	CBX3	chr21:46606582-46607003	HCT-116	colon:	n/a	n/a
8	CBX3	chr21:46606603-46606963	K562	blood:	n/a	n/a
9	CEBPB	chr21:46596648-46596939	K562	blood:	n/a	n/a
10	CEBPB	chr21:46596637-46596961	HepG2	liver:	n/a	n/a
11	CEBPB	chr21:46596662-46596973	IMR90	lung:	n/a	n/a
12	CEBPB	chr21:46596670-46596935	A549	lung:	n/a	n/a
13	CTCF	chr21:46599658-46599675	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr21:46587640-46587790	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr21:46587820-46587970	AG09309	skin:	n/a	n/a
16	CTCF	chr21:46587780-46587930	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr21:46587760-46587910	AG10803	skin:	n/a	n/a
18	CTCF	chr21:46587800-46587950	AG04449	skin:	n/a	n/a
19	CTCF	chr21:46587800-46587950	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr21:46587900-46588050	AG04450	lung:	n/a	n/a
21	CTCF	chr21:46587780-46587930	AG10803	skin:	n/a	n/a
22	CTCF	chr21:46587780-46587930	HPF	lung:	n/a	n/a
23	CTCF	chr21:46587780-46587930	AG09309	skin:	n/a	n/a
24	CTCF	chr21:46599160-46599310	HPF	lung:	n/a	n/a
25	CTCF	chr21:46593020-46593170	HVMF	connective:	n/a	n/a
26	CTCF	chr21:46587800-46587950	AG04450	lung:	n/a	n/a
27	CTCF	chr21:46591060-46591210	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr21:46599655-46599683	K562	blood:	n/a	n/a
29	CTCF	chr21:46587780-46587930	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr21:46587840-46587990	BJ	skin:	n/a	n/a
31	CTCF	chr21:46587815-46587926	IMR90	lung:	n/a	n/a
32	CTCF	chr21:46587800-46587950	BJ	skin:	n/a	n/a
33	CTCF	chr21:46587860-46588010	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr21:46587640-46587790	AG04450	lung:	n/a	n/a
35	CTCF	chr21:46587800-46587950	AG09319	gingival:	n/a	n/a
36	CTCF	chr21:46587760-46587910	HPF	lung:	n/a	n/a
37	CTCF	chr21:46596620-46596770	HEK293	kidney:	n/a	chr21:46596695-46596704
38	CTCF	chr21:46587780-46587930	AG09319	gingival:	n/a	n/a
39	CTCF	chr21:46596620-46596770	HepG2	liver:	n/a	chr21:46596695-46596704
40	CTCF	chr21:46599626-46599632	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr21:46587820-46587970	AG04449	skin:	n/a	n/a
42	CTCF	chr21:46587740-46587890	HCFaa	heart:	n/a	n/a
43	CTCF	chr21:46587800-46587950	HMF	breast:	n/a	n/a
44	CUX1	chr21:46592358-46592558	K562	blood:	n/a	n/a
45	EGR1	chr21:46582070-46582601	ECC-1	luminal epithelium:	n/a	n/a
46	EGR1	chr21:46584126-46584334	K562	blood:	n/a	chr21:46584269-46584284 chr21:46584307-46584317 chr21:46584270-46584283 chr21:46584266-46584288 chr21:46584270-46584283 chr21:46584271-46584285 chr21:46584273-46584282
47	EGR1	chr21:46599754-46600018	K562	blood:	n/a	chr21:46599849-46599862 chr21:46599873-46599887 chr21:46599874-46599885 chr21:46599875-46599885 chr21:46599874-46599885 chr21:46599873-46599886
48	EGR1	chr21:46584186-46584315	GM12878	blood:	n/a	chr21:46584269-46584284 chr21:46584270-46584283 chr21:46584266-46584288 chr21:46584270-46584283 chr21:46584271-46584285 chr21:46584273-46584282
49	EGR1	chr21:46582020-46582514	ECC-1	luminal epithelium:	n/a	n/a
50	EGR1	chr21:46584152-46584378	K562	blood:	n/a	chr21:46584269-46584284 chr21:46584307-46584317 chr21:46584270-46584283 chr21:46584266-46584288 chr21:46584270-46584283 chr21:46584271-46584285 chr21:46584273-46584282

No data

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

No.	Distal block	Cell Line	Cell type
1	chr21:46592578..46594651-chr21:46685178..46686890,2	MCF-7	breast:
2	chr21:46578518..46581096-chr21:46581512..46584493,2	K562	blood:
3	chr21:46596742..46598458-chr21:46604486..46606241,2	MCF-7	breast:
4	chr21:46592718..46595098-chr21:46595762..46598236,3	K562	blood:
5	chr21:46574123..46577749-chr21:46583837..46588993,5	K562	blood:
6	chr21:46582653..46585265-chr21:46586911..46589357,3	MCF-7	breast:
7	chr21:46596731..46599349-chr21:46833672..46835345,2	K562	blood:
8	chr21:46586995..46592553-chr21:46595453..46599761,7	K562	blood:
9	chr21:46605915..46607896-chr21:46668846..46670608,2	K562	blood:
10	chr21:46592424..46595013-chr21:46596357..46598792,2	MCF-7	breast:
11	chr21:46592424..46595013-chr21:46596357..46598792,2	MCF-7	breast:
12	chr21:46603421..46605562-chr21:46613527..46615818,2	K562	blood:
13	chr21:46571989..46575021-chr21:46580299..46583331,3	MCF-7	breast:
14	chr21:46588242..46590449-chr21:46597999..46599761,2	K562	blood:
15	chr21:46578518..46581096-chr21:46581512..46584493,2	K562	blood:
16	chr21:46492545..46495031-chr21:46584204..46586224,2	K562	blood:
17	chr21:46451994..46454639-chr21:46586058..46587723,2	K562	blood:
18	chr21:46586995..46592553-chr21:46595453..46599761,7	K562	blood:
19	chr21:46582653..46585265-chr21:46586911..46589357,3	MCF-7	breast:
20	chr21:46588242..46590449-chr21:46597999..46599761,2	K562	blood:
21	chr21:46571468..46573324-chr21:46581267..46583442,2	MCF-7	breast:
22	chr21:46587207..46589418-chr21:46711709..46714315,2	K562	blood:
23	chr21:46593698..46595826-chr21:46858761..46860504,2	K562	blood:
24	chr21:46595186..46597635-chr21:46597682..46599692,2	MCF-7	breast:
25	chr21:46568116..46569843-chr21:46581882..46584158,2	K562	blood:
26	chr21:46586605..46588915-chr21:46675140..46677229,2	K562	blood:
27	chr21:46572313..46573898-chr21:46593543..46595938,2	K562	blood:
28	chr21:46570712..46573836-chr21:46580844..46582723,4	K562	blood:
29	chr21:46596742..46598458-chr21:46604486..46606241,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADARB1-4	chr21:46595646-46595691	NONHSAT082919
2	lnc-ADARB1-4	chr21:46591526-46591599	NONHSAT082919

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ADARB1	hsa-miR-130b-3p	chr21:46596497-46596518

Variant related genes	Relation type
ADARB1	TF binding region
ENSG00000186866	chromatin interactions
ENSG00000223768	chromatin interactions
ENSG00000268856	chromatin interactions
ENSG00000197381	chromatin interactions
ENSG00000235374	chromatin interactions

Extended variants
information (count: 1032 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192782811	chr21:46580326-46580327	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558756421	chr21:46580366-46580367	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs381466	chr21:46580370-46580371	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs532230982	chr21:46580382-46580383	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149736217	chr21:46580406-46580407	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562106629	chr21:46580416-46580417	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374778	chr21:46580439-46580440	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs541499400	chr21:46580451-46580452	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560175861	chr21:46580509-46580510	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112450188	chr21:46580515-46580516	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145648217	chr21:46580556-46580557	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564288388	chr21:46580574-46580575	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2838794	chr21:46580651-46580652	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183505647	chr21:46580669-46580670	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550101812	chr21:46580670-46580671	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3788169	chr21:46580779-46580780	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530097107	chr21:46580933-46580934	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548328575	chr21:46580992-46580993	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368119412	chr21:46581026-46581027	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534050749	chr21:46581041-46581042	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11088982	chr21:46581046-46581047	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs77766466	chr21:46581075-46581076	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538105475	chr21:46581078-46581079	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148923411	chr21:46581117-46581118	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147045463	chr21:46581137-46581138	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs384876	chr21:46581167-46581168	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs147691354	chr21:46581196-46581197	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs377524	chr21:46581233-46581234	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs188626188	chr21:46581258-46581259	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs142484819	chr21:46581270-46581271	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs434492	chr21:46581295-46581296	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs372760431	chr21:46581328-46581329	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs561588517	chr21:46581342-46581343	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs115282569	chr21:46581419-46581420	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs146561713	chr21:46581420-46581421	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs548536848	chr21:46581424-46581425	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs530524352	chr21:46581466-46581467	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs111776322	chr21:46581488-46581489	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs181034963	chr21:46581503-46581504	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs527741078	chr21:46581510-46581511	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs552259533	chr21:46581524-46581525	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs570649453	chr21:46581577-46581578	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs386762	chr21:46581634-46581635	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs116798496	chr21:46581672-46581673	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148340992	chr21:46581673-46581674	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2104812	chr21:46581710-46581711	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs373273955	chr21:46581728-46581729	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572073514	chr21:46581737-46581738	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs8130097	chr21:46581762-46581763	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs557877575	chr21:46581764-46581765	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	17426248	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46556600-46581000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr21:46557000-46604800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr21:46557200-46591800	Weak transcription	HUVEC	blood vessel
4	chr21:46557600-46582600	Weak transcription	Psoas Muscle	Psoas
5	chr21:46558600-46588800	Weak transcription	Colonic Mucosa	Colon
6	chr21:46560800-46586400	Weak transcription	Liver	Liver
7	chr21:46563000-46595600	Weak transcription	Pancreas	Pancrea
8	chr21:46566000-46583200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr21:46568400-46581400	Weak transcription	Gastric	stomach
10	chr21:46569000-46587000	Weak transcription	NHEK	skin
11	chr21:46570400-46582600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr21:46571800-46580800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr21:46572000-46581000	Weak transcription	Fetal Brain Male	brain
14	chr21:46572000-46581200	Weak transcription	Lung	lung
15	chr21:46572000-46584000	Weak transcription	Ovary	ovary
16	chr21:46572000-46584000	Weak transcription	Stomach Mucosa	stomach
17	chr21:46572200-46595600	Weak transcription	Brain Germinal Matrix	brain
18	chr21:46572400-46581000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr21:46572400-46601000	Weak transcription	Fetal Brain Female	brain
20	chr21:46572800-46604800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr21:46573000-46582800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr21:46573000-46588400	Weak transcription	Thymus	Thymus
23	chr21:46573600-46591800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr21:46573800-46586800	Weak transcription	Adipose Nuclei	Adipose
25	chr21:46574200-46589200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr21:46574800-46580600	Weak transcription	Fetal Heart	heart
27	chr21:46574800-46583600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr21:46575000-46581000	Weak transcription	Esophagus	oesophagus
29	chr21:46575000-46586400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr21:46575000-46587000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr21:46575000-46595600	Weak transcription	Dnd41	blood
32	chr21:46575000-46601000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr21:46575200-46581400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr21:46575200-46583600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr21:46575200-46586600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr21:46575200-46587000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr21:46575400-46580600	Weak transcription	Colon Smooth Muscle	Colon
38	chr21:46575400-46581400	Weak transcription	Fetal Thymus	thymus
39	chr21:46575400-46582000	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr21:46575400-46583200	Weak transcription	Right Atrium	heart
41	chr21:46575400-46583400	Weak transcription	Left Ventricle	heart
42	chr21:46575400-46583400	Weak transcription	Spleen	Spleen
43	chr21:46575400-46587800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr21:46575400-46588800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr21:46575400-46588800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr21:46575400-46589000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr21:46575400-46604800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr21:46575600-46581600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr21:46575600-46581800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr21:46575600-46588800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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