Variant report

Variant	esv1831533
Chromosome Location	chr21:15442382-15477876
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:1038)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr21:15458789-15459416	GM12878	blood:	n/a	n/a
2	ATF2	chr21:15458823-15459284	GM12878	blood:	n/a	n/a
3	ATF2	chr21:15468353-15468867	GM12878	blood:	n/a	n/a
4	ATF2	chr21:15448799-15449234	GM12878	blood:	n/a	n/a
5	ATF2	chr21:15468299-15468933	GM12878	blood:	n/a	n/a
6	BACH1	chr21:15451014-15451054	K562	blood:	n/a	n/a
7	BATF	chr21:15465685-15465956	GM12878	blood:	n/a	n/a
8	BATF	chr21:15468478-15468902	GM12878	blood:	n/a	n/a
9	BATF	chr21:15448785-15449256	GM12878	blood:	n/a	n/a
10	BATF	chr21:15468538-15468846	GM12878	blood:	n/a	n/a
11	BATF	chr21:15457224-15457512	GM12878	blood:	n/a	chr21:15457321-15457332
12	BATF	chr21:15457207-15457515	GM12878	blood:	n/a	chr21:15457321-15457332
13	BATF	chr21:15458863-15459259	GM12878	blood:	n/a	n/a
14	BATF	chr21:15458844-15459210	GM12878	blood:	n/a	n/a
15	BCL11A	chr21:15458877-15459240	GM12878	blood:	n/a	chr21:15459096-15459105
16	BCL11A	chr21:15457191-15457441	GM12878	blood:	n/a	n/a
17	BCL11A	chr21:15457216-15457530	GM12878	blood:	n/a	n/a
18	BCL11A	chr21:15468433-15468873	GM12878	blood:	n/a	n/a
19	BCL11A	chr21:15468452-15468916	GM12878	blood:	n/a	n/a
20	BCL3	chr21:15468347-15468850	GM12878	blood:	n/a	n/a
21	BCLAF1	chr21:15448869-15449191	GM12878	blood:	n/a	n/a
22	BHLHE40	chr21:15455959-15456330	K562	blood:	n/a	n/a
23	BHLHE40	chr21:15457367-15457395	GM12878	blood:	n/a	n/a
24	BHLHE40	chr21:15450842-15451042	K562	blood:	n/a	n/a
25	BHLHE40	chr21:15468350-15468916	GM12878	blood:	n/a	n/a
26	BHLHE40	chr21:15458854-15459269	GM12878	blood:	n/a	n/a
27	BRCA1	chr21:15450841-15451212	GM12878	blood:	n/a	n/a
28	BRCA1	chr21:15455960-15456265	GM12878	blood:	n/a	n/a
29	CEBPB	chr21:15476909-15477047	K562	blood:	n/a	n/a
30	CEBPB	chr21:15476926-15477037	K562	blood:	n/a	n/a
31	CEBPB	chr21:15456133-15456159	K562	blood:	n/a	n/a
32	CEBPB	chr21:15456731-15456885	HepG2	liver:	n/a	chr21:15456796-15456813
33	CEBPB	chr21:15455654-15455686	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPD	chr21:15476918-15477232	K562	blood:	n/a	n/a
35	CHD1	chr21:15455655-15455686	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr21:15454516-15454533	GM12878	blood:	n/a	n/a
37	CHD2	chr21:15468548-15468815	GM12878	blood:	n/a	n/a
38	CHD2	chr21:15450923-15451042	K562	blood:	n/a	n/a
39	CHD2	chr21:15454515-15454717	K562	blood:	n/a	n/a
40	CHD2	chr21:15450844-15451073	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr21:15458946-15459275	GM12878	blood:	n/a	n/a
42	CHD2	chr21:15456125-15456330	K562	blood:	n/a	n/a
43	CREB1	chr21:15448667-15449270	GM12878	blood:	n/a	n/a
44	CTCF	chr21:15456083-15456304	IMR90	lung:	n/a	n/a
45	CTCF	chr21:15470521-15470670	GM19239	blood:	n/a	n/a
46	CTCF	chr21:15457220-15457495	T-47D	breast:	n/a	n/a
47	CTCF	chr21:15456154-15456303	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr21:15445687-15445818	MCF-7	breast:	n/a	n/a
49	CTCF	chr21:15456139-15456303	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr21:15455430-15455478	Spleen_OC	spleen:	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	chr21:15456343-15456393	HAEpiC	amniotic membrane:	n/a
2	chr21:15456343-15456393	HAEpiC	amniotic membrane:	n/a
3	chr21:15457266-15457316	PFSK-1	brain:	n/a
4	chr21:15448544-15448594	GM12891	blood:	n/a
5	chr21:15448544-15448594	AG04450	lung:	fetal
6	chr21:15451401-15451451	ECC-1	luminal epithelium:	n/a
7	chr21:15444237-15444287	AG10803	skin:	n/a
8	chr21:15442816-15442866	HPAEpiC	pulmonary alveolar:	n/a
9	chr21:15442816-15442866	HMEC	breast:	n/a
10	chr21:15456343-15456393	CMK	blood:	n/a
11	chr21:15442957-15443007	GM12892	blood:	n/a
12	chr21:15443107-15443157	U87	brain:	n/a
13	chr21:15456789-15456839	HPAEpiC	pulmonary alveolar:	n/a
14	chr21:15445421-15445471	LNCaP	prostate:	n/a
15	chr21:15451292-15451342	SAEC	small airway:	n/a
16	chr21:15450528-15450578	MCF-7	breast:	n/a
17	chr21:15445421-15445471	HCPEpiC	choroid plexus:	n/a
18	chr21:15455710-15455760	HEEpiC	esophagus:	n/a
19	chr21:15452938-15452988	GM12878	blood:	n/a
20	chr21:15451242-15451292	K562	blood:	n/a
21	chr21:15457266-15457316	BJ	skin:	n/a
22	chr21:15456343-15456393	HRCEpiC	kidney:	n/a
23	chr21:15442816-15442866	MCF-7	breast:	n/a
24	chr21:15442957-15443007	PANC-1	pancreas:	n/a
25	chr21:15445421-15445471	Jurkat	blood:	n/a
26	chr21:15450528-15450578	GM19239	blood:	n/a
27	chr21:15456789-15456839	PFSK-1	brain:	n/a
28	chr21:15444237-15444287	HPAEpiC	pulmonary alveolar:	n/a
29	chr21:15451242-15451292	IMR90	lung:	fetal
30	chr21:15443107-15443157	NHDF-neo	bronchial:	n/a
31	chr21:15456343-15456393	BE2_C	brain:	n/a
32	chr21:15451401-15451451	Caco-2	colon:	n/a
33	chr21:15455198-15455248	HEK293	kidney:	embryo
34	chr21:15455710-15455760	ECC-1	luminal epithelium:	n/a
35	chr21:15448544-15448594	NT2-D1	testis:	n/a
36	chr21:15451401-15451451	HPAEpiC	pulmonary alveolar:	n/a
37	chr21:15442957-15443007	HEEpiC	esophagus:	n/a
38	chr21:15456343-15456393	Caco-2	colon:	n/a
39	chr21:15445421-15445471	NHDF-neo	bronchial:	n/a
40	chr21:15456605-15456655	H1-hESC	embryonic stem cell:	embryo
41	chr21:15452938-15452988	HepG2	liver:	n/a
42	chr21:15456605-15456655	GM12892	blood:	n/a
43	chr21:15443107-15443157	HCM	heart:	n/a
44	chr21:15451292-15451342	HPAEpiC	pulmonary alveolar:	n/a
45	chr21:15451242-15451292	SKMC	muscle:	n/a
46	chr21:15450528-15450578	T-47D	breast:	n/a
47	chr21:15457266-15457316	MCF-7	breast:	n/a
48	chr21:15456789-15456839	HEEpiC	esophagus:	n/a
49	chr21:15457266-15457316	SAEC	small airway:	n/a
50	chr21:15456789-15456839	HIPEpiC	eye:	n/a

No data

Variant related genes	Relation type
RNA5SP488	TF binding region
RNA5SP488	CpG island

Extended variants
information (count: 1990 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1990 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372796970	chr21:15442383-15442384	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs149519673	chr21:15442388-15442389	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs376053546	chr21:15442408-15442409	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs371830003	chr21:15442409-15442410	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs540492421	chr21:15442410-15442411	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs560612601	chr21:15442447-15442448	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529405951	chr21:15442451-15442452	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs398036070	chr21:15442460-15442461	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200021355	chr21:15442461-15442462	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs370143809	chr21:15442491-15442492	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs543001649	chr21:15442529-15442530	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs142872619	chr21:15442548-15442549	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs531745887	chr21:15442550-15442551	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs576763553	chr21:15442562-15442563	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs115292755	chr21:15442578-15442579	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564392609	chr21:15442594-15442595	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs71315760	chr21:15442625-15442626	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs533126026	chr21:15442633-15442634	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs546511898	chr21:15442634-15442635	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs566551912	chr21:15442662-15442663	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs142673015	chr21:15442682-15442683	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs34574140	chr21:15442684-15442685	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs34306203	chr21:15442788-15442789	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180870135	chr21:15442819-15442820	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs373854661	chr21:15442832-15442833	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs368546396	chr21:15442859-15442860	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs568475216	chr21:15442868-15442869	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs537464672	chr21:15442900-15442901	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558001448	chr21:15442914-15442915	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113482289	chr21:15442952-15442953	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7280081	chr21:15442955-15442956	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534391942	chr21:15442960-15442961	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs563192456	chr21:15442969-15442970	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs186398824	chr21:15442978-15442979	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs12483418	chr21:15442979-15442980	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	mRNA abundance
36	rs12483548	chr21:15442980-15442981	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs34079862	chr21:15442981-15442982	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs562984076	chr21:15443008-15443009	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs182829739	chr21:15443026-15443027	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs545443984	chr21:15443046-15443047	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs564354089	chr21:15443052-15443053	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs187471180	chr21:15443053-15443054	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs75701724	chr21:15443087-15443088	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs374173405	chr21:15443127-15443128	Weak transcription Strong transcription ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs548710412	chr21:15443160-15443161	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs138855932	chr21:15443189-15443190	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs548634761	chr21:15443227-15443228	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs557632721	chr21:15443252-15443253	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs34412176	chr21:15443264-15443265	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs368360413	chr21:15443285-15443286	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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	20435627	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
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
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
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD

Chromatin state (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15401800-15452000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr21:15402600-15442400	Weak transcription	Dnd41	blood
3	chr21:15423400-15455600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr21:15423600-15443000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr21:15425800-15443400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr21:15428800-15449000	Weak transcription	Fetal Lung	lung
7	chr21:15430400-15442400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr21:15433000-15442400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr21:15436400-15442400	Weak transcription	Thymus	Thymus
10	chr21:15437000-15442400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr21:15437000-15442600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr21:15437000-15443200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr21:15437000-15448800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr21:15438400-15442400	Weak transcription	Esophagus	oesophagus
15	chr21:15439800-15442400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr21:15441000-15470200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr21:15442000-15442600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr21:15442000-15442600	Enhancers	Gastric	stomach
19	chr21:15442000-15444200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr21:15442000-15448000	ZNF genes & repeats	Fetal Brain Female	brain
21	chr21:15442000-15448200	ZNF genes & repeats	Brain Germinal Matrix	brain
22	chr21:15442200-15442600	Enhancers	Fetal Heart	heart
23	chr21:15442200-15442600	Enhancers	Pancreas	Pancrea
24	chr21:15442200-15442800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr21:15442200-15444000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr21:15442200-15445200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr21:15442400-15442600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr21:15442400-15442800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr21:15442400-15443000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr21:15442400-15443800	ZNF genes & repeats	Thymus	Thymus
31	chr21:15442400-15444600	ZNF genes & repeats	Esophagus	oesophagus
32	chr21:15442400-15445800	Strong transcription	Dnd41	blood
33	chr21:15442400-15446200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr21:15442400-15447800	ZNF genes & repeats	Fetal Stomach	stomach
35	chr21:15442400-15448000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr21:15442600-15445000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr21:15442600-15445600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr21:15442600-15446800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr21:15442600-15447600	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr21:15442800-15443600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr21:15442800-15445600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr21:15443000-15443400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr21:15443000-15447400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr21:15443200-15443600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
45	chr21:15443200-15445000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr21:15443400-15443600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr21:15443400-15444400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr21:15443400-15445600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
49	chr21:15443600-15444000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr21:15443600-15444400	Strong transcription	Cortex derived primary cultured neurospheres	brain

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