Variant report

Variant	nsv914097
Chromosome Location	chr21:47445791-47505084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:1161)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47453886-47454184	HepG2	liver:	n/a	n/a
2	ATF1	chr21:47449168-47449491	K562	blood:	n/a	n/a
3	ATF1	chr21:47451381-47451634	K562	blood:	n/a	n/a
4	BACH1	chr21:47469613-47469830	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr21:47480538-47480950	GM12878	blood:	n/a	n/a
6	BCL3	chr21:47489061-47489552	GM12878	blood:	n/a	n/a
7	BCL3	chr21:47489095-47489602	GM12878	blood:	n/a	n/a
8	BCL3	chr21:47499620-47499965	GM12878	blood:	n/a	n/a
9	BCL3	chr21:47499588-47499878	GM12878	blood:	n/a	n/a
10	BHLHE40	chr21:47451370-47451817	K562	blood:	n/a	n/a
11	BHLHE40	chr21:47499569-47499767	K562	blood:	n/a	n/a
12	BHLHE40	chr21:47503034-47503099	HepG2	liver:	n/a	n/a
13	BHLHE40	chr21:47488501-47488504	K562	blood:	n/a	n/a
14	BHLHE40	chr21:47451470-47451654	HepG2	liver:	n/a	n/a
15	BHLHE40	chr21:47502920-47503227	K562	blood:	n/a	n/a
16	CBX3	chr21:47483130-47483459	K562	blood:	n/a	n/a
17	CBX3	chr21:47449419-47449832	K562	blood:	n/a	n/a
18	CBX3	chr21:47449480-47449748	K562	blood:	n/a	n/a
19	CBX3	chr21:47483098-47483540	K562	blood:	n/a	n/a
20	CEBPB	chr21:47469201-47469600	K562	blood:	n/a	n/a
21	CEBPB	chr21:47464653-47464729	K562	blood:	n/a	n/a
22	CEBPB	chr21:47468992-47470110	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr21:47469348-47469712	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr21:47466459-47466659	K562	blood:	n/a	n/a
25	CEBPB	chr21:47473333-47473552	A549	lung:	n/a	n/a
26	CEBPB	chr21:47469242-47469605	HepG2	liver:	n/a	n/a
27	CEBPB	chr21:47492417-47492549	HepG2	liver:	n/a	n/a
28	CEBPB	chr21:47473213-47473667	IMR90	lung:	n/a	n/a
29	CEBPB	chr21:47469269-47469549	A549	lung:	n/a	n/a
30	CEBPB	chr21:47480507-47481116	IMR90	lung:	n/a	n/a
31	CEBPB	chr21:47458811-47459259	IMR90	lung:	n/a	n/a
32	CEBPB	chr21:47468951-47469962	IMR90	lung:	n/a	n/a
33	CEBPB	chr21:47445457-47445829	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr21:47469136-47469927	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr21:47448333-47448708	IMR90	lung:	n/a	n/a
36	CEBPB	chr21:47464685-47464932	IMR90	lung:	n/a	n/a
37	CEBPB	chr21:47464777-47464883	A549	lung:	n/a	n/a
38	CHD1	chr21:47473013-47474761	IMR90	lung:	n/a	n/a
39	CHD1	chr21:47475585-47477580	IMR90	lung:	n/a	chr21:47476798-47476808
40	CHD2	chr21:47460628-47461088	K562	blood:	n/a	n/a
41	CHD2	chr21:47461294-47461390	K562	blood:	n/a	n/a
42	CHD2	chr21:47453830-47453920	HepG2	liver:	n/a	n/a
43	CTCF	chr21:47484934-47485023	H1-hESC	embryonic stem cell:	n/a	chr21:47484980-47484993
44	CTCF	chr21:47503580-47503730	AG10803	skin:	n/a	chr21:47503657-47503670
45	CTCF	chr21:47503380-47503670	AG09319	gingival:	n/a	chr21:47503657-47503670
46	CTCF	chr21:47489293-47489420	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr21:47489301-47489355	MCF-7	breast:	n/a	n/a
48	CTCF	chr21:47476440-47476590	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr21:47489207-47489228	GM12891	blood:	n/a	n/a
50	CTCF	chr21:47485220-47485370	AG10803	skin:	n/a	chr21:47485343-47485356

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47457188-47457238	IMR90	lung:	fetal
2	chr21:47453297-47453347	SAEC	small airway:	n/a
3	chr21:47457188-47457238	IMR90	lung:	fetal
4	chr21:47453297-47453347	SAEC	small airway:	n/a
5	chr21:47455453-47455503	ovcar-3	ovarian:	n/a
6	chr21:47451611-47451661	NH-A	brain:	n/a
7	chr21:47455779-47455829	AG04450	lung:	fetal
8	chr21:47457738-47457788	HIPEpiC	eye:	n/a
9	chr21:47456315-47456365	HepG2	liver:	n/a
10	chr21:47458587-47458637	K562	blood:	n/a
11	chr21:47453656-47453706	MCF10A-Er-Src	breast:	n/a
12	chr21:47457738-47457788	CMK	blood:	n/a
13	chr21:47457738-47457788	BE2_C	brain:	n/a
14	chr21:47453889-47453939	SAEC	small airway:	n/a
15	chr21:47453520-47453570	HMEC	breast:	n/a
16	chr21:47469679-47469729	K562	blood:	n/a
17	chr21:47454892-47454942	HIPEpiC	eye:	n/a
18	chr21:47456404-47456454	CMK	blood:	n/a
19	chr21:47453297-47453347	HMEC	breast:	n/a
20	chr21:47453520-47453570	HCM	heart:	n/a
21	chr21:47456446-47456496	MCF-7	breast:	n/a
22	chr21:47457375-47457425	Hela-S3	cervix:	n/a
23	chr21:47460364-47460414	SKMC	muscle:	n/a
24	chr21:47458587-47458637	ovcar-3	ovarian:	n/a
25	chr21:47469104-47469154	NH-A	brain:	n/a
26	chr21:47456404-47456454	A549	lung:	n/a
27	chr21:47458587-47458637	H1-hESC	embryonic stem cell:	embryo
28	chr21:47453889-47453939	HCPEpiC	choroid plexus:	n/a
29	chr21:47454892-47454942	AG09309	skin:	n/a
30	chr21:47451611-47451661	AG04449	skin:	fetal
31	chr21:47469679-47469729	NT2-D1	testis:	n/a
32	chr21:47453297-47453347	IMR90	lung:	fetal
33	chr21:47454892-47454942	SK-N-MC	brain:	n/a
34	chr21:47455779-47455829	HNPCEpiC	eye:	n/a
35	chr21:47455779-47455829	HRE	kidney:	n/a
36	chr21:47460364-47460414	NHDF-neo	bronchial:	n/a
37	chr21:47453656-47453706	NHDF-neo	bronchial:	n/a
38	chr21:47449364-47449414	HL-60	blood:	n/a
39	chr21:47469679-47469729	ProgFib	skin:	n/a
40	chr21:47457375-47457425	NT2-D1	testis:	n/a
41	chr21:47453889-47453939	ovcar-3	ovarian:	n/a
42	chr21:47453520-47453570	HEK293	kidney:	embryo
43	chr21:47453297-47453347	HCF	heart:	n/a
44	chr21:47458587-47458637	ProgFib	skin:	n/a
45	chr21:47457375-47457425	A549	lung:	n/a
46	chr21:47453520-47453570	NB4	blood:	n/a
47	chr21:47453520-47453570	HepG2	liver:	n/a
48	chr21:47469104-47469154	HCT-116	colon:	n/a
49	chr21:47455779-47455829	HCT-116	colon:	n/a
50	chr21:47456446-47456496	ECC-1	luminal epithelium:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47389198..47390888-chr21:47465741..47468426,2	K562	blood:
2	chr21:47464638..47467897-chr21:47467945..47470124,3	K562	blood:
3	chr21:47448813..47450619-chr21:47451876..47453813,2	K562	blood:
4	chr21:47452473..47454142-chr21:47459376..47461918,2	K562	blood:
5	chr21:47467167..47469249-chr21:47470137..47471990,2	K562	blood:
6	chr21:47468918..47472938-chr21:47474374..47476128,3	K562	blood:
7	chr21:47477438..47479279-chr21:47515180..47518074,2	K562	blood:
8	chr21:47486054..47488058-chr21:47490628..47493448,2	MCF-7	breast:
9	chr21:47401486..47403121-chr21:47460352..47462597,2	K562	blood:
10	chr21:47452931..47454985-chr21:47457105..47459208,2	K562	blood:
11	chr21:47476412..47478192-chr21:47563693..47565789,2	K562	blood:
12	chr21:47459712..47462417-chr21:47469068..47471117,2	K562	blood:
13	chr21:47464638..47467897-chr21:47467945..47470124,3	K562	blood:
14	chr21:47448813..47450619-chr21:47451876..47453813,2	K562	blood:
15	chr21:47459145..47461835-chr21:47471631..47473216,2	K562	blood:
16	chr21:47491970..47494495-chr21:47501163..47503528,2	K562	blood:
17	chr21:47447601..47449403-chr21:47486419..47488081,2	K562	blood:
18	chr21:47444128..47447153-chr21:47459721..47462680,3	K562	blood:
19	chr21:47452473..47454142-chr21:47459376..47461918,2	K562	blood:
20	chr21:47444128..47447153-chr21:47459721..47462680,3	K562	blood:
21	chr21:47470351..47471891-chr21:47543505..47546157,2	K562	blood:
22	chr21:47459712..47462417-chr21:47469068..47471117,2	K562	blood:
23	chr21:47498636..47500154-chr21:47500293..47503205,2	MCF-7	breast:
24	chr2:131851141..131852056-chr21:47448788..47449619,2	Hela-S3	cervix:
25	chr21:47456464..47458445-chr21:47465961..47468863,2	MCF-7	breast:
26	chr21:47498636..47500154-chr21:47500293..47503205,2	MCF-7	breast:
27	chr21:47483689..47485600-chr21:47485621..47488078,2	K562	blood:
28	chr21:47464638..47466951-chr21:47467945..47470531,2	K562	blood:
29	chr21:47493601..47495532-chr21:47497650..47499455,2	K562	blood:
30	chr21:47480527..47483405-chr21:47514946..47517801,2	MCF-7	breast:
31	chr21:47447601..47449403-chr21:47486419..47488081,2	K562	blood:
32	chr21:47460724..47462986-chr21:47480949..47482640,2	K562	blood:
33	chr21:47493601..47495532-chr21:47497650..47499455,2	K562	blood:
34	chr21:47439436..47442196-chr21:47457727..47460452,2	MCF-7	breast:
35	chr21:47464638..47466951-chr21:47467945..47470531,2	K562	blood:
36	chr21:47452931..47454985-chr21:47457105..47459208,2	K562	blood:
37	chr21:47467167..47469249-chr21:47470137..47471990,2	K562	blood:
38	chr21:47421697..47423323-chr21:47458853..47461069,2	MCF-7	breast:
39	chr21:47460724..47462986-chr21:47480949..47482640,2	K562	blood:
40	chr21:47483689..47485600-chr21:47485621..47488078,2	K562	blood:
41	chr21:47485799..47487872-chr21:47511862..47514238,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000226115	TF binding region
PSMA6P3	TF binding region
ENSG00000224413	TF binding region
ENSG00000228235	TF binding region
ENSG00000226115	CpG island
PSMA6P3	CpG island
ENSG00000224413	CpG island
ENSG00000228235	CpG island
ENSG00000142173	chromatin interactions
ENSG00000233767	chromatin interactions
ENSG00000227438	chromatin interactions
ENSG00000224413	chromatin interactions
ENSG00000228235	chromatin interactions
ENSG00000142156	chromatin interactions
ENSG00000160282	chromatin interactions

Extended variants
information (count: 3371 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:3371 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4293630	chr21:47445791-47445792	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs541021174	chr21:47445928-47445929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200795454	chr21:47446015-47446016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373475306	chr21:47446030-47446031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574414505	chr21:47446050-47446051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76776737	chr21:47446052-47446053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550509943	chr21:47446066-47446067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56344865	chr21:47446092-47446093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs55982203	chr21:47446094-47446095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs55778509	chr21:47446096-47446097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115050216	chr21:47446154-47446155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575008504	chr21:47446242-47446243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181024394	chr21:47446248-47446249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74769677	chr21:47446292-47446293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79306428	chr21:47446394-47446395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79464142	chr21:47446395-47446396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542480298	chr21:47446439-47446440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7277589	chr21:47446486-47446487	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs201760818	chr21:47446557-47446558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185907291	chr21:47446635-47446636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190300039	chr21:47446645-47446646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539315007	chr21:47446662-47446663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557722440	chr21:47446690-47446691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532592266	chr21:47446738-47446739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569589448	chr21:47446742-47446743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536816666	chr21:47446782-47446783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554869898	chr21:47446791-47446792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572855468	chr21:47446839-47446840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552439232	chr21:47446854-47446855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539994215	chr21:47446858-47446859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530967353	chr21:47446950-47446951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558522339	chr21:47446970-47446971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181043308	chr21:47446988-47446989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576459049	chr21:47446994-47446995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543819843	chr21:47447007-47447008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531847424	chr21:47447058-47447059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185914507	chr21:47447150-47447151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190373973	chr21:47447166-47447167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375772792	chr21:47447208-47447209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs202236003	chr21:47447210-47447211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541966277	chr21:47447214-47447215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28824235	chr21:47447216-47447217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183970008	chr21:47447226-47447227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138523598	chr21:47447236-47447237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528581190	chr21:47447250-47447251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548880894	chr21:47447270-47447271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62211786	chr21:47447294-47447295	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs532517570	chr21:47447353-47447354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200030994	chr21:47447389-47447390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191917494	chr21:47447415-47447416	Weak transcription Enhancers	n/a	n/a	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:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47439600-47445800	Enhancers	Fetal Stomach	stomach
2	chr21:47441600-47449200	Enhancers	Fetal Intestine Large	intestine
3	chr21:47442600-47446000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr21:47442800-47447800	Weak transcription	Adipose Nuclei	Adipose
5	chr21:47442800-47449600	Enhancers	Rectal Smooth Muscle	rectum
6	chr21:47443200-47446200	Enhancers	Colon Smooth Muscle	Colon
7	chr21:47443400-47446200	Enhancers	NHLF	lung
8	chr21:47443600-47445800	Enhancers	Fetal Intestine Small	intestine
9	chr21:47443600-47448000	Weak transcription	Fetal Muscle Leg	muscle
10	chr21:47443800-47446800	Enhancers	NHDF-Ad	bronchial
11	chr21:47444000-47447800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr21:47444200-47448200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr21:47444400-47449400	Enhancers	Fetal Lung	lung
14	chr21:47444600-47447600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr21:47444800-47446000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr21:47445000-47446000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr21:47445000-47446200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr21:47445200-47445800	Enhancers	NH-A	brain
19	chr21:47445200-47446000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr21:47445200-47446000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr21:47445400-47445800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr21:47445400-47449200	Weak transcription	Left Ventricle	heart
23	chr21:47445600-47446000	Enhancers	Osteobl	bone
24	chr21:47445600-47446400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr21:47445600-47447200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr21:47445600-47447600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr21:47445600-47447800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr21:47445600-47448000	Weak transcription	Ovary	ovary
29	chr21:47445600-47448000	Weak transcription	HSMM	muscle
30	chr21:47445600-47448000	Weak transcription	HSMMtube	muscle
31	chr21:47445600-47448200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr21:47445600-47448200	Weak transcription	Aorta	Aorta
33	chr21:47445600-47448200	Weak transcription	Fetal Kidney	kidney
34	chr21:47445600-47448400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr21:47445600-47458600	Weak transcription	Stomach Mucosa	stomach
36	chr21:47445800-47447600	Weak transcription	Fetal Intestine Small	intestine
37	chr21:47445800-47447800	Weak transcription	Fetal Stomach	stomach
38	chr21:47445800-47448000	Weak transcription	NH-A	brain
39	chr21:47446000-47446400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr21:47446000-47447800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr21:47446000-47447800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr21:47446000-47447800	Weak transcription	Osteobl	bone
43	chr21:47446200-47447400	Weak transcription	Colon Smooth Muscle	Colon
44	chr21:47446200-47447600	Weak transcription	NHLF	lung
45	chr21:47446400-47446800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr21:47446400-47449400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr21:47446800-47447600	Weak transcription	NHDF-Ad	bronchial
48	chr21:47446800-47449400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr21:47447200-47447400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr21:47447400-47447600	Enhancers	Small Intestine	intestine

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