Variant report

Variant	nsv587703
Chromosome Location	chr21:45157670-45160625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr21:45158438-45158813	K562	blood:	n/a	n/a
2	BACH1	chr21:45160396-45161112	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr21:45160274-45161086	A549	lung:	n/a	chr21:45160409-45160418
4	BCL3	chr21:45159769-45160260	A549	lung:	n/a	chr21:45159789-45159802
5	BHLHE40	chr21:45158061-45158395	HepG2	liver:	n/a	n/a
6	BHLHE40	chr21:45158311-45158664	K562	blood:	n/a	n/a
7	CBX3	chr21:45159315-45159743	K562	blood:	n/a	n/a
8	CBX3	chr21:45158262-45158880	K562	blood:	n/a	n/a
9	CEBPB	chr21:45157993-45158303	HepG2	liver:	n/a	n/a
10	CEBPB	chr21:45158312-45158814	K562	blood:	n/a	n/a
11	CEBPD	chr21:45158300-45158858	K562	blood:	n/a	n/a
12	CTCF	chr21:45158160-45158310	HepG2	liver:	n/a	n/a
13	CTCF	chr21:45158180-45158330	HepG2	liver:	n/a	n/a
14	CTCF	chr21:45158237-45158340	HepG2	liver:	n/a	n/a
15	CTCF	chr21:45158631-45158670	Kidney_OC	kidney:	n/a	n/a
16	CUX1	chr21:45158443-45158689	K562	blood:	n/a	n/a
17	E2F6	chr21:45158385-45158681	K562	blood:	n/a	n/a
18	E2F6	chr21:45158136-45158703	K562	blood:	n/a	n/a
19	E2F6	chr21:45158372-45158564	K562	blood:	n/a	n/a
20	EP300	chr21:45158326-45158704	K562	blood:	n/a	n/a
21	EP300	chr21:45157986-45158400	HepG2	liver:	n/a	n/a
22	FOSL1	chr21:45158328-45158740	K562	blood:	n/a	n/a
23	FOSL2	chr21:45157993-45158554	HepG2	liver:	n/a	n/a
24	FOXA1	chr21:45158178-45158662	HepG2	liver:	n/a	n/a
25	GABPA	chr21:45158302-45158642	K562	blood:	n/a	n/a
26	GABPA	chr21:45160433-45161012	H1-hESC	embryonic stem cell:	n/a	n/a
27	GATA2	chr21:45158292-45158684	K562	blood:	n/a	n/a
28	GATA2	chr21:45158298-45158887	K562	blood:	n/a	n/a
29	GATA2	chr21:45158441-45158808	K562	blood:	n/a	n/a
30	GTF2B	chr21:45158447-45158809	K562	blood:	n/a	n/a
31	HDAC2	chr21:45158371-45158645	K562	blood:	n/a	n/a
32	HDAC2	chr21:45160497-45161092	MCF-7	breast:	n/a	n/a
33	HDAC2	chr21:45158005-45158351	HepG2	liver:	n/a	n/a
34	HDAC2	chr21:45158337-45158702	K562	blood:	n/a	n/a
35	HNF4A	chr21:45158031-45158419	HepG2	liver:	n/a	chr21:45158224-45158239 chr21:45158188-45158203
36	HNF4A	chr21:45158018-45158412	HepG2	liver:	n/a	chr21:45158224-45158239 chr21:45158188-45158203
37	HNF4A	chr21:45158007-45158355	HepG2	liver:	n/a	chr21:45158224-45158239 chr21:45158188-45158203
38	HNF4G	chr21:45158023-45158383	HepG2	liver:	n/a	chr21:45158187-45158202 chr21:45158225-45158240
39	HNF4G	chr21:45158022-45158389	HepG2	liver:	n/a	chr21:45158187-45158202 chr21:45158225-45158240
40	IRF1	chr21:45158325-45158834	K562	blood:	n/a	n/a
41	IRF1	chr21:45158430-45158837	K562	blood:	n/a	n/a
42	JUND	chr21:45159628-45161057	A549	lung:	n/a	chr21:45159685-45159693
43	JUND	chr21:45157734-45158012	A549	lung:	n/a	n/a
44	JUND	chr21:45158426-45158813	K562	blood:	n/a	n/a
45	MAX	chr21:45160547-45161027	A549	lung:	n/a	n/a
46	MAX	chr21:45158236-45158778	K562	blood:	n/a	n/a
47	MAX	chr21:45159534-45159722	A549	lung:	n/a	n/a
48	MAX	chr21:45159587-45161125	A549	lung:	n/a	chr21:45160229-45160238
49	MAX	chr21:45158296-45158664	K562	blood:	n/a	n/a
50	MAX	chr21:45159521-45159842	K562	blood:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45152139..45163298-chr21:45164540..45174522,16	K562	blood:
2	chr21:45156014..45158647-chr21:45159074..45160757,2	K562	blood:
3	chr21:45156014..45158647-chr21:45159074..45160757,2	K562	blood:
4	chr21:45156014..45158637-chr21:45159074..45161792,2	K562	blood:
5	chr21:45159502..45161246-chr21:45194764..45196763,2	MCF-7	breast:
6	chr21:45156965..45158670-chr21:45174699..45176799,2	K562	blood:
7	chr21:45158615..45161441-chr21:45207897..45210708,2	K562	blood:
8	chr21:45156182..45158069-chr21:45230385..45232004,2	K562	blood:
9	chr21:45159250..45162021-chr21:45208113..45211544,3	MCF-7	breast:

No data

Variant related genes	Relation type
PDXK	TF binding region
ENSG00000160214	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000160209	chromatin interactions

Extended variants
information (count: 173 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:173 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11702042	chr21:45157670-45157671	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs575541460	chr21:45157671-45157672	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186494824	chr21:45157699-45157700	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534817929	chr21:45157746-45157747	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189298020	chr21:45157759-45157760	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528732856	chr21:45157779-45157780	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540844997	chr21:45157832-45157833	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377089613	chr21:45157838-45157839	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140836126	chr21:45157839-45157840	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs533051038	chr21:45157851-45157852	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551151152	chr21:45157885-45157886	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370403637	chr21:45157920-45157921	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs180872475	chr21:45157929-45157930	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs148070117	chr21:45157942-45157943	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs116696452	chr21:45157981-45157982	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567236428	chr21:45158006-45158007	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs149733837	chr21:45158066-45158067	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552750626	chr21:45158154-45158155	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs145650469	chr21:45158241-45158242	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs539165707	chr21:45158256-45158257	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114334873	chr21:45158280-45158281	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs146800990	chr21:45158300-45158301	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575625943	chr21:45158301-45158302	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs548507872	chr21:45158312-45158313	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs541398476	chr21:45158409-45158410	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs115358733	chr21:45158436-45158437	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs386819069	chr21:45158459-45158460	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs386819070	chr21:45158468-45158469	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs374564336	chr21:45158472-45158473	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112089509	chr21:45158489-45158490	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs114190375	chr21:45158490-45158491	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs35600592	chr21:45158501-45158502	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186542304	chr21:45158504-45158505	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573420572	chr21:45158511-45158512	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565489619	chr21:45158515-45158516	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs9981955	chr21:45158544-45158545	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs147032512	chr21:45158568-45158569	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs563221905	chr21:45158580-45158581	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs530594105	chr21:45158583-45158584	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375428050	chr21:45158596-45158597	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs138324230	chr21:45158598-45158599	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528377443	chr21:45158616-45158617	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546478302	chr21:45158630-45158631	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs571468088	chr21:45158648-45158649	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs142428689	chr21:45158652-45158653	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs538435970	chr21:45158656-45158657	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs199718865	chr21:45158657-45158658	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs557466469	chr21:45158680-45158681	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs569271251	chr21:45158683-45158684	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs536716509	chr21:45158684-45158685	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Hodgkin''s lymphoma	18641027	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
Neuroblastoma	20406844	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
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45146000-45163600	Weak transcription	Dnd41	blood
2	chr21:45149000-45194400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr21:45149400-45175400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr21:45149600-45157800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr21:45149600-45159400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr21:45149600-45163600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr21:45149600-45163600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr21:45149600-45163800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr21:45149600-45164200	Weak transcription	Primary B cells from cord blood	blood
10	chr21:45149800-45160200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr21:45149800-45164200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr21:45149800-45164400	Weak transcription	Fetal Kidney	kidney
13	chr21:45149800-45175200	Weak transcription	HUVEC	blood vessel
14	chr21:45149800-45188200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr21:45150000-45158200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr21:45150000-45161600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr21:45150000-45163600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr21:45150000-45173200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr21:45152200-45160600	Genic enhancers	Fetal Intestine Large	intestine
20	chr21:45152200-45160600	Genic enhancers	Fetal Intestine Small	intestine
21	chr21:45152200-45183400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr21:45152400-45157800	Genic enhancers	HepG2	liver
23	chr21:45152400-45163800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr21:45152400-45173200	Weak transcription	Psoas Muscle	Psoas
25	chr21:45153400-45158400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr21:45153600-45159400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr21:45153600-45163800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr21:45154000-45158400	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr21:45154000-45159200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr21:45154000-45167000	Weak transcription	Small Intestine	intestine
31	chr21:45154200-45158200	Strong transcription	Placenta	Placenta
32	chr21:45154200-45163400	Weak transcription	Colon Smooth Muscle	Colon
33	chr21:45154200-45163800	Weak transcription	NHDF-Ad	bronchial
34	chr21:45154400-45158400	Strong transcription	Stomach Smooth Muscle	stomach
35	chr21:45154400-45160400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr21:45154400-45160600	Strong transcription	Fetal Stomach	stomach
37	chr21:45154400-45184200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr21:45154600-45164200	Weak transcription	Brain Substantia Nigra	brain
39	chr21:45154800-45157800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr21:45154800-45158600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr21:45154800-45164200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr21:45154800-45174600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr21:45155000-45157800	Strong transcription	Colonic Mucosa	Colon
44	chr21:45155000-45158200	Genic enhancers	Adipose Nuclei	Adipose
45	chr21:45155000-45158400	Strong transcription	NHLF	lung
46	chr21:45155000-45158600	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr21:45155000-45160600	Strong transcription	NHEK	skin
48	chr21:45155000-45161400	Weak transcription	Primary B cells from peripheral blood	blood
49	chr21:45155000-45161400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr21:45155000-45163800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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