Variant report

Variant	nsv587883
Chromosome Location	chr21:47388151-47398411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47393664-47393787	HepG2	liver:	n/a	n/a
2	ATF3	chr21:47394625-47394810	K562	blood:	n/a	n/a
3	ATF3	chr21:47394657-47394857	K562	blood:	n/a	n/a
4	BACH1	chr21:47393656-47395490	H1-hESC	embryonic stem cell:	n/a	chr21:47394783-47394797
5	BACH1	chr21:47392452-47392645	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr21:47390620-47390835	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr21:47393205-47393220	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr21:47393571-47393856	GM12878	blood:	n/a	chr21:47393827-47393843
9	BHLHE40	chr21:47390644-47390909	K562	blood:	n/a	n/a
10	BHLHE40	chr21:47394614-47394625	K562	blood:	n/a	n/a
11	BHLHE40	chr21:47390596-47390848	HepG2	liver:	n/a	n/a
12	BHLHE40	chr21:47393659-47393859	K562	blood:	n/a	chr21:47393827-47393843
13	CEBPB	chr21:47388211-47388418	A549	lung:	n/a	chr21:47388260-47388271
14	CEBPB	chr21:47388107-47388411	HepG2	liver:	n/a	chr21:47388260-47388271
15	CEBPB	chr21:47388080-47388349	K562	blood:	n/a	chr21:47388260-47388271
16	CEBPB	chr21:47392940-47393214	IMR90	lung:	n/a	n/a
17	CHD1	chr21:47393649-47393845	H1-hESC	embryonic stem cell:	n/a	chr21:47393827-47393837
18	CHD1	chr21:47393752-47393988	GM12878	blood:	n/a	chr21:47393827-47393837
19	CHD1	chr21:47390493-47391023	IMR90	lung:	n/a	n/a
20	CHD1	chr21:47394131-47394225	H1-hESC	embryonic stem cell:	n/a	chr21:47394186-47394196
21	CHD2	chr21:47392485-47392539	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr21:47393619-47393797	GM12878	blood:	n/a	n/a
23	CHD2	chr21:47390574-47390862	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr21:47390631-47390767	K562	blood:	n/a	n/a
25	CHD2	chr21:47393720-47393744	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr21:47397006-47397624	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr21:47392032-47395553	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr21:47393620-47393770	HVMF	connective:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
29	CTCF	chr21:47390582-47390897	H1-hESC	embryonic stem cell:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
30	CTCF	chr21:47390660-47390810	WI-38	lung:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
31	CTCF	chr21:47393579-47393854	GM13977	blood:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
32	CTCF	chr21:47390700-47390850	GM12867	blood:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
33	CTCF	chr21:47390606-47390880	GM12878	blood:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
34	CTCF	chr21:47393619-47393794	SK-N-SH_RA	brain:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
35	CTCF	chr21:47394240-47394390	AG04449	skin:	n/a	n/a
36	CTCF	chr21:47393581-47393855	GM19240	blood:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
37	CTCF	chr21:47393553-47393903	K562	blood:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
38	CTCF	chr21:47393660-47393810	HRE	kidney:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
39	CTCF	chr21:47390420-47390471	GM19239	blood:	n/a	n/a
40	CTCF	chr21:47393660-47393810	WI-38	lung:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
41	CTCF	chr21:47393660-47393810	GM12865	blood:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
42	CTCF	chr21:47393576-47393830	GM10248	blood:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
43	CTCF	chr21:47390660-47390810	HMEC	breast:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
44	CTCF	chr21:47393542-47393904	K562	blood:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
45	CTCF	chr21:47390618-47390879	GM20000	blood:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
46	CTCF	chr21:47393596-47393803	LNCaP	prostate:	n/a	chr21:47393702-47393711 chr21:47393704-47393714
47	CTCF	chr21:47390660-47390810	K562	blood:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
48	CTCF	chr21:47390588-47390888	ProgFib	skin:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
49	CTCF	chr21:47390660-47390810	WERI-Rb-1	eye:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751
50	CTCF	chr21:47390640-47390790	GM12869	blood:	n/a	chr21:47390734-47390750 chr21:47390736-47390749 chr21:47390733-47390751

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47396773-47396823	NHBE	bronchial:	n/a
2	chr21:47392592-47392642	SKMC	muscle:	n/a
3	chr21:47394431-47394481	Jurkat	blood:	n/a
4	chr21:47394080-47394130	HCM	heart:	n/a
5	chr21:47394533-47394583	RPTEC	kidney:	n/a
6	chr21:47396773-47396823	SKMC	muscle:	n/a
7	chr21:47393688-47393738	BJ	skin:	n/a
8	chr21:47394431-47394481	HRE	kidney:	n/a
9	chr21:47394354-47394404	HUVEC	blood vessel:	n/a
10	chr21:47394080-47394130	NHBE	bronchial:	n/a
11	chr21:47394533-47394583	HRCEpiC	kidney:	n/a
12	chr21:47394354-47394404	HPAEpiC	pulmonary alveolar:	n/a
13	chr21:47394354-47394404	Caco-2	colon:	n/a
14	chr21:47394015-47394065	SK-N-SH_RA	brain:	n/a
15	chr21:47396773-47396823	PANC-1	pancreas:	n/a
16	chr21:47392916-47392966	H1-hESC	embryonic stem cell:	embryo
17	chr21:47394080-47394130	H1-hESC	embryonic stem cell:	embryo
18	chr21:47394015-47394065	MCF-7	breast:	n/a
19	chr21:47392592-47392642	HCM	heart:	n/a
20	chr21:47392592-47392642	NH-A	brain:	n/a
21	chr21:47390774-47390824	T-47D	breast:	n/a
22	chr21:47394659-47394709	HCT-116	colon:	n/a
23	chr21:47396773-47396823	HAEpiC	amniotic membrane:	n/a
24	chr21:47394354-47394404	GM06990	blood:	n/a
25	chr21:47390774-47390824	CMK	blood:	n/a
26	chr21:47392916-47392966	K562	blood:	n/a
27	chr21:47396773-47396823	HRCEpiC	kidney:	n/a
28	chr21:47393688-47393738	HUVEC	blood vessel:	n/a
29	chr21:47394080-47394130	RPTEC	kidney:	n/a
30	chr21:47392592-47392642	GM12878	blood:	n/a
31	chr21:47394354-47394404	ECC-1	luminal epithelium:	n/a
32	chr21:47390774-47390824	Jurkat	blood:	n/a
33	chr21:47394659-47394709	HEK293	kidney:	embryo
34	chr21:47393322-47393372	HCF	heart:	n/a
35	chr21:47393688-47393738	HNPCEpiC	eye:	n/a
36	chr21:47394354-47394404	HRPEpiC	eye:	n/a
37	chr21:47393322-47393372	SK-N-MC	brain:	n/a
38	chr21:47392592-47392642	PANC-1	pancreas:	n/a
39	chr21:47394354-47394404	H1-hESC	embryonic stem cell:	embryo
40	chr21:47394533-47394583	PFSK-1	brain:	n/a
41	chr21:47392592-47392642	LNCaP	prostate:	n/a
42	chr21:47393322-47393372	AG04449	skin:	fetal
43	chr21:47392916-47392966	AG09319	gingival:	n/a
44	chr21:47394080-47394130	GM06990	blood:	n/a
45	chr21:47394431-47394481	HL-60	blood:	n/a
46	chr21:47394431-47394481	NT2-D1	testis:	n/a
47	chr21:47394431-47394481	HAEpiC	amniotic membrane:	n/a
48	chr21:47394015-47394065	NHBE	bronchial:	n/a
49	chr21:47393322-47393372	HEEpiC	esophagus:	n/a
50	chr21:47394080-47394130	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:47393205..47395473-chr21:47397498..47399697,5	K562	blood:
2	chr21:47391035..47393326-chr21:47704879..47707195,2	MCF-7	breast:
3	chr21:47389572..47393249-chr21:47393676..47397258,4	K562	blood:
4	chr21:47393406..47394151-chr21:47517434..47518087,2	MCF-7	breast:
5	chr21:47388213..47390098-chr21:47396842..47399384,2	MCF-7	breast:
6	chr21:47390231..47390753-chr21:47630052..47630891,2	MCF-7	breast:
7	chr21:47369464..47371619-chr21:47394987..47396620,2	MCF-7	breast:
8	chr21:47384997..47386531-chr21:47397126..47399086,2	MCF-7	breast:
9	chr21:47342692..47343850-chr21:47390349..47391235,3	MCF-7	breast:
10	chr21:47393834..47396182-chr21:47704275..47707193,2	MCF-7	breast:
11	chr21:47393227..47394175-chr21:47566798..47568083,5	MCF-7	breast:
12	chr21:47393731..47395290-chr21:47958756..47960479,2	K562	blood:
13	chr21:47387372..47388982-chr21:47392168..47393871,2	MCF-7	breast:
14	chr21:47388213..47390098-chr21:47396842..47399384,2	MCF-7	breast:
15	chr21:47393160..47394496-chr21:47517520..47518577,7	MCF-7	breast:
16	chr21:47387372..47388982-chr21:47392168..47393871,2	MCF-7	breast:
17	chr21:47389198..47390888-chr21:47465741..47468426,2	K562	blood:
18	chr21:47390651..47391646-chr21:47745274..47746230,2	MCF-7	breast:
19	chr21:47389572..47393249-chr21:47393676..47397258,4	K562	blood:
20	chr21:47393205..47395473-chr21:47397498..47399697,5	K562	blood:
21	chr21:47386674..47388281-chr21:47388690..47390672,2	MCF-7	breast:
22	chr21:47393279..47394087-chr21:47517478..47517993,2	K562	blood:
23	chr21:47390319..47391231-chr21:47563516..47564070,2	MCF-7	breast:
24	chr21:47390635..47391181-chr21:47555465..47556047,2	MCF-7	breast:
25	chr21:47390294..47391149-chr21:47517550..47518205,2	MCF-7	breast:
26	chr21:47386674..47388281-chr21:47388690..47390672,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL6A1-1	chr21:47393595-47393660	XLOC_013986
2	lnc-COL6A1-1	chr21:47394008-47394868	XLOC_013986
3	lnc-COL6A1-1	chr21:47394008-47394867	NR_109931
4	lnc-COL6A1-1	chr21:47392863-47393090	XLOC_013986
5	lnc-COL6A1-1	chr21:47392884-47393090	NR_109931
6	lnc-FTCD-2	chr21:47395659-47396732	XLOC_014129
7	lnc-FTCD-2	chr21:47397451-47397653	XLOC_014129
8	lnc-COL6A1-4	chr21:47397218-47397295	NONHSAT083005
9	lnc-COL6A1-1	chr21:47392727-47393090	XLOC_013986

Variant related genes	Relation type
COL6A1	TF binding region
COL6A1	CpG island
ENSG00000227438	chromatin interactions
ENSG00000160282	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000142173	chromatin interactions
AFF4	miRNA target sites

Extended variants
information (count: 399 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8129765	chr21:47388151-47388152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187347175	chr21:47388158-47388159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528865854	chr21:47388184-47388185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368351865	chr21:47388185-47388186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs8129879	chr21:47388196-47388197	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs192487733	chr21:47388211-47388212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574202581	chr21:47388230-47388231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539720693	chr21:47388301-47388302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79496831	chr21:47388302-47388303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183642403	chr21:47388333-47388334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115919515	chr21:47388353-47388354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187895796	chr21:47388383-47388384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574611115	chr21:47388426-47388427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535420647	chr21:47388509-47388510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554143493	chr21:47388537-47388538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs909430	chr21:47388612-47388613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546516668	chr21:47388616-47388617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558054708	chr21:47388617-47388618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530591226	chr21:47388721-47388722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73374730	chr21:47388844-47388845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs199967942	chr21:47388855-47388856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544050452	chr21:47388856-47388857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561731418	chr21:47388871-47388872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57548391	chr21:47388880-47388881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58713630	chr21:47388881-47388882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184254084	chr21:47389055-47389056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190877783	chr21:47389057-47389058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559343680	chr21:47389065-47389066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200844256	chr21:47389089-47389090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533064603	chr21:47389127-47389128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563437017	chr21:47389188-47389189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551686272	chr21:47389290-47389291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569490806	chr21:47389295-47389296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2026285	chr21:47389330-47389331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs201289706	chr21:47389406-47389407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548778464	chr21:47389407-47389408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568173007	chr21:47389410-47389411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535992416	chr21:47389489-47389490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573147157	chr21:47389685-47389686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566101085	chr21:47389756-47389757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373862289	chr21:47389757-47389758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187278847	chr21:47389815-47389816	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191724193	chr21:47389836-47389837	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145223446	chr21:47389837-47389838	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542257200	chr21:47389863-47389864	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs367639507	chr21:47389914-47389915	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148773502	chr21:47389951-47389952	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2065336	chr21:47389993-47389994	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs2026286	chr21:47390001-47390002	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs546867006	chr21:47390004-47390005	Enhancers Weak transcription Bivalent Enhancer Active TSS	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:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47379800-47392000	Weak transcription	Right Atrium	heart
2	chr21:47383600-47390400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr21:47385000-47390000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr21:47385400-47389800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr21:47385800-47390400	Weak transcription	Liver	Liver
6	chr21:47386000-47390000	Weak transcription	Fetal Muscle Leg	muscle
7	chr21:47386000-47390400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr21:47387200-47390200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr21:47389800-47390200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr21:47389800-47390800	Enhancers	Fetal Stomach	stomach
11	chr21:47390000-47390200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr21:47390000-47390200	Enhancers	Fetal Muscle Trunk	muscle
13	chr21:47390000-47390400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr21:47390000-47390600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr21:47390000-47391200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr21:47390000-47392000	Enhancers	Placenta	Placenta
17	chr21:47390000-47392400	Enhancers	Fetal Muscle Leg	muscle
18	chr21:47390200-47390400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr21:47390200-47390400	Enhancers	Stomach Smooth Muscle	stomach
20	chr21:47390200-47390400	Bivalent Enhancer	HepG2	liver
21	chr21:47390200-47390600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr21:47390200-47391000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr21:47390200-47391400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr21:47390200-47391400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr21:47390200-47391400	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr21:47390200-47391600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr21:47390200-47392000	Enhancers	Colon Smooth Muscle	Colon
28	chr21:47390200-47392000	Enhancers	Rectal Smooth Muscle	rectum
29	chr21:47390200-47392200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr21:47390200-47393400	Enhancers	Fetal Lung	lung
31	chr21:47390200-47393800	Enhancers	Fetal Heart	heart
32	chr21:47390400-47390600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr21:47390400-47390600	Bivalent Enhancer	Colonic Mucosa	Colon
34	chr21:47390400-47390600	Enhancers	Esophagus	oesophagus
35	chr21:47390400-47390800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr21:47390400-47390800	Enhancers	Pancreas	Pancrea
37	chr21:47390400-47390800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
38	chr21:47390400-47390800	Flanking Bivalent TSS/Enh	HepG2	liver
39	chr21:47390400-47391000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
40	chr21:47390400-47391000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr21:47390400-47391000	Enhancers	Liver	Liver
42	chr21:47390400-47391000	Enhancers	Right Ventricle	heart
43	chr21:47390400-47391200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr21:47390400-47391200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
45	chr21:47390400-47391400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr21:47390400-47391400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr21:47390400-47391400	Enhancers	Fetal Brain Male	brain
48	chr21:47390400-47391600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr21:47390400-47392000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr21:47390400-47392000	Enhancers	Adipose Nuclei	Adipose

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