Variant report

Variant	nsv587936
Chromosome Location	chr21:47410931-47417333
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	CTCF	chr21:47413720-47413870	HMF	breast:	n/a	n/a
2	CTCF	chr21:47413820-47413970	AG09309	skin:	n/a	n/a
3	CTCF	chr21:47413780-47413930	AG10803	skin:	n/a	n/a
4	EGR1	chr21:47411166-47411329	K562	blood:	n/a	n/a
5	ELK1	chr21:47416359-47416364	Hela-S3	cervix:	n/a	n/a
6	FOS	chr21:47415635-47415835	MCF10A-Er-Src	breast:	n/a	chr21:47415707-47415714 chr21:47415706-47415717 chr21:47415708-47415719 chr21:47415707-47415716
7	FOS	chr21:47415690-47415791	MCF10A-Er-Src	breast:	n/a	chr21:47415707-47415714 chr21:47415706-47415717 chr21:47415708-47415719 chr21:47415707-47415716
8	FOS	chr21:47415587-47415767	MCF10A-Er-Src	breast:	n/a	chr21:47415707-47415714 chr21:47415706-47415717 chr21:47415708-47415719 chr21:47415707-47415716
9	FOS	chr21:47415684-47415766	MCF10A-Er-Src	breast:	n/a	chr21:47415707-47415714 chr21:47415706-47415717 chr21:47415708-47415719 chr21:47415707-47415716
10	FOSL2	chr21:47415476-47415885	HepG2	liver:	n/a	chr21:47415707-47415714 chr21:47415706-47415717 chr21:47415708-47415719 chr21:47415707-47415716
11	HMGN3	chr21:47414247-47414393	K562	blood:	n/a	n/a
12	MAX	chr21:47413748-47414132	K562	blood:	n/a	chr21:47413911-47413920 chr21:47413909-47413919 chr21:47413909-47413918 chr21:47413772-47413781 chr21:47413910-47413917 chr21:47413905-47413920
13	MAX	chr21:47415218-47415342	HepG2	liver:	n/a	n/a
14	MAX	chr21:47413797-47413962	K562	blood:	n/a	chr21:47413911-47413920 chr21:47413909-47413919 chr21:47413909-47413918 chr21:47413910-47413917 chr21:47413905-47413920
15	MYC	chr21:47414725-47414853	MCF-7	breast:	n/a	n/a
16	POLR2A	chr21:47414088-47414134	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr21:47414651-47415065	U87	brain:	n/a	n/a
18	POLR2A	chr21:47411966-47412871	U87	brain:	n/a	n/a
19	POLR2A	chr21:47412056-47412767	U87	brain:	n/a	n/a
20	POLR2A	chr21:47416141-47416799	U87	brain:	n/a	n/a
21	POLR2A	chr21:47413988-47415114	U87	brain:	n/a	n/a
22	POLR2A	chr21:47415324-47415649	IMR90	lung:	n/a	n/a
23	POLR2A	chr21:47416940-47417296	U87	brain:	n/a	n/a
24	POLR2A	chr21:47415959-47416107	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr21:47416934-47417319	U87	brain:	n/a	n/a
26	POLR2A	chr21:47414331-47414420	ProgFib	skin:	n/a	n/a
27	POLR2A	chr21:47414701-47414866	ProgFib	skin:	n/a	n/a
28	POLR2A	chr21:47413998-47414030	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr21:47411935-47411958	ProgFib	skin:	n/a	n/a
30	POLR2A	chr21:47416112-47416895	U87	brain:	n/a	n/a
31	POLR2A	chr21:47416212-47416351	ProgFib	skin:	n/a	n/a
32	POLR2A	chr21:47411585-47411727	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr21:47413713-47413722	K562	blood:	n/a	n/a
34	RAD21	chr21:47415673-47415705	IMR90	lung:	n/a	n/a
35	RFX5	chr21:47415585-47415741	HepG2	liver:	n/a	n/a
36	SPI1	chr21:47410586-47410991	HL-60	blood:	n/a	chr21:47410671-47410684 chr21:47410673-47410680 chr21:47410749-47410756 chr21:47410746-47410759
37	UBTF	chr21:47413665-47413731	K562	blood:	n/a	n/a
38	UBTF	chr21:47414407-47414507	K562	blood:	n/a	n/a
39	UBTF	chr21:47411908-47411910	K562	blood:	n/a	n/a
40	USF1	chr21:47415465-47415961	ECC-1	luminal epithelium:	n/a	chr21:47415694-47415705
41	USF1	chr21:47415552-47415775	SK-N-SH_RA	brain:	n/a	chr21:47415694-47415705
42	USF1	chr21:47415383-47416006	HCT-116	colon:	n/a	chr21:47415694-47415705
43	USF1	chr21:47415620-47415781	HepG2	liver:	n/a	chr21:47415694-47415705
44	USF1	chr21:47415503-47415953	ECC-1	luminal epithelium:	n/a	chr21:47415694-47415705
45	USF1	chr21:47415234-47415988	HCT-116	colon:	n/a	chr21:47415275-47415291 chr21:47415694-47415705
46	USF1	chr21:47415611-47415841	A549	lung:	n/a	chr21:47415694-47415705
47	USF1	chr21:47415580-47415793	SK-N-SH_RA	brain:	n/a	chr21:47415694-47415705
48	USF1	chr21:47415590-47415752	K562	blood:	n/a	chr21:47415694-47415705
49	USF1	chr21:47415618-47415799	A549	lung:	n/a	chr21:47415694-47415705
50	USF1	chr21:47415570-47415782	A549	lung:	n/a	chr21:47415694-47415705

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47411200-47411250	HepG2	liver:	n/a
2	chr21:47411200-47411250	CMK	blood:	n/a
3	chr21:47411200-47411250	Jurkat	blood:	n/a
4	chr21:47411200-47411250	Hepatocyte	liver:	n/a
5	chr21:47411200-47411250	K562	blood:	n/a
6	chr21:47411200-47411250	ovcar-3	ovarian:	n/a
7	chr21:47411200-47411250	NHDF-neo	bronchial:	n/a
8	chr21:47411200-47411250	HCPEpiC	choroid plexus:	n/a
9	chr21:47411200-47411250	HRE	kidney:	n/a
10	chr21:47411200-47411250	IMR90	lung:	fetal
11	chr21:47411200-47411250	HIPEpiC	eye:	n/a
12	chr21:47411200-47411250	HRPEpiC	eye:	n/a
13	chr21:47411200-47411250	GM12878	blood:	n/a
14	chr21:47411200-47411250	MCF10A-Er-Src	breast:	n/a
15	chr21:47411200-47411250	NHBE	bronchial:	n/a
16	chr21:47411200-47411250	SKMC	muscle:	n/a
17	chr21:47411200-47411250	LNCaP	prostate:	n/a
18	chr21:47411200-47411250	HEK293	kidney:	embryo
19	chr21:47411200-47411250	GM12892	blood:	n/a
20	chr21:47411200-47411250	Caco-2	colon:	n/a
21	chr21:47411200-47411250	AG09319	gingival:	n/a
22	chr21:47411200-47411250	MCF-7	breast:	n/a
23	chr21:47411200-47411250	HL-60	blood:	n/a
24	chr21:47411200-47411250	SAEC	small airway:	n/a
25	chr21:47411200-47411250	SK-N-MC	brain:	n/a
26	chr21:47411200-47411250	NB4	blood:	n/a
27	chr21:47411200-47411250	GM12891	blood:	n/a
28	chr21:47411200-47411250	HAEpiC	amniotic membrane:	n/a
29	chr21:47411200-47411250	PFSK-1	brain:	n/a
30	chr21:47411200-47411250	HMEC	breast:	n/a
31	chr21:47411200-47411250	AoSMC	blood vessel:	n/a
32	chr21:47411200-47411250	HNPCEpiC	eye:	n/a
33	chr21:47411200-47411250	H1-hESC	embryonic stem cell:	embryo
34	chr21:47411200-47411250	RPTEC	kidney:	n/a
35	chr21:47411200-47411250	GM19239	blood:	n/a
36	chr21:47411200-47411250	HRCEpiC	kidney:	n/a
37	chr21:47411200-47411250	PrEC	prostate:	n/a
38	chr21:47411200-47411250	AG09309	skin:	n/a
39	chr21:47411200-47411250	HEEpiC	esophagus:	n/a
40	chr21:47411200-47411250	AG10803	skin:	n/a
41	chr21:47411200-47411250	HCM	heart:	n/a
42	chr21:47411200-47411250	NT2-D1	testis:	n/a
43	chr21:47411200-47411250	HUVEC	blood vessel:	n/a
44	chr21:47411200-47411250	GM06990	blood:	n/a
45	chr21:47411200-47411250	HPAEpiC	pulmonary alveolar:	n/a
46	chr21:47411200-47411250	HCT-116	colon:	n/a
47	chr21:47411200-47411250	ProgFib	skin:	n/a
48	chr21:47411200-47411250	BJ	skin:	n/a
49	chr21:47411200-47411250	ECC-1	luminal epithelium:	n/a
50	chr21:47411200-47411250	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:47410997..47412945-chr21:47415697..47417959,2	MCF-7	breast:
2	chr21:47409850..47411682-chr21:47705051..47707715,2	K562	blood:
3	chr21:47409518..47412170-chr21:47436887..47438560,2	MCF-7	breast:
4	chr21:47416853..47418859-chr21:47421399..47424312,2	K562	blood:
5	chr21:47407254..47409991-chr21:47416573..47418228,3	K562	blood:
6	chr21:47411553..47415297-chr21:47415530..47420389,6	K562	blood:
7	chr21:47410997..47412945-chr21:47415697..47417959,2	MCF-7	breast:
8	chr21:47407254..47409991-chr21:47416573..47418228,2	K562	blood:
9	chr21:47415907..47418450-chr21:47418722..47421230,2	MCF-7	breast:

Variant related genes	Relation type
COL6A1	TF binding region
COL6A1	CpG island
ENSG00000142156	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000160294	chromatin interactions

Extended variants
information (count: 374 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:374 , 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	rs1980982	chr21:47410931-47410932	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs183994910	chr21:47410932-47410933	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs149338158	chr21:47410951-47410952	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144677931	chr21:47410953-47410954	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs199655304	chr21:47410968-47410969	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374805937	chr21:47410969-47410970	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs367637279	chr21:47410979-47410980	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs74982956	chr21:47410994-47410995	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148314075	chr21:47410995-47410996	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs188448869	chr21:47411007-47411008	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs117529466	chr21:47411046-47411047	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530425387	chr21:47411055-47411056	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs548609837	chr21:47411062-47411063	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs567433737	chr21:47411063-47411064	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534947739	chr21:47411067-47411068	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553015440	chr21:47411124-47411125	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs10154031	chr21:47411144-47411145	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376210029	chr21:47411154-47411155	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111557860	chr21:47411164-47411165	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576649819	chr21:47411183-47411184	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs55726338	chr21:47411216-47411217	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs555824140	chr21:47411225-47411226	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573970524	chr21:47411229-47411230	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs541674672	chr21:47411243-47411244	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs559806183	chr21:47411255-47411256	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs533523929	chr21:47411270-47411271	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs545246543	chr21:47411331-47411332	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563037324	chr21:47411339-47411340	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs530553906	chr21:47411378-47411379	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs377019635	chr21:47411389-47411390	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs556943503	chr21:47411390-47411391	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs559937536	chr21:47411409-47411410	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370514983	chr21:47411413-47411414	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs193058297	chr21:47411417-47411418	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs546824369	chr21:47411422-47411423	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571497184	chr21:47411459-47411460	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538827293	chr21:47411473-47411474	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs557226767	chr21:47411521-47411522	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs150463888	chr21:47411553-47411554	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs549445013	chr21:47411587-47411588	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs532239390	chr21:47411595-47411596	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs185093319	chr21:47411600-47411601	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs555593045	chr21:47411654-47411655	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs541840522	chr21:47411668-47411669	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs138263497	chr21:47411679-47411680	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs534713793	chr21:47411682-47411683	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs73159606	chr21:47411695-47411696	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577961749	chr21:47411755-47411756	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545181287	chr21:47411757-47411758	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190779876	chr21:47411767-47411768	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	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:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47403200-47414600	Weak transcription	Brain Substantia Nigra	brain
2	chr21:47403200-47415200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr21:47403200-47424600	Weak transcription	Small Intestine	intestine
4	chr21:47403200-47425000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr21:47403600-47414800	Strong transcription	Fetal Intestine Small	intestine
6	chr21:47404000-47424200	Strong transcription	H1 Cell Line	embryonic stem cell
7	chr21:47404000-47424600	Strong transcription	Aorta	Aorta
8	chr21:47404200-47414400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr21:47404200-47425200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr21:47404200-47425200	Strong transcription	Muscle Satellite Cultured Cells	--
11	chr21:47404400-47414600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr21:47404400-47419200	Strong transcription	Left Ventricle	heart
13	chr21:47405000-47414600	Weak transcription	Fetal Kidney	kidney
14	chr21:47405000-47417400	Weak transcription	Stomach Mucosa	stomach
15	chr21:47405000-47419400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr21:47405000-47423800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr21:47405000-47425400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr21:47405200-47425400	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr21:47405200-47425400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
20	chr21:47405200-47425800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr21:47405400-47423800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr21:47405400-47424800	Strong transcription	Fetal Brain Female	brain
23	chr21:47405400-47425200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr21:47405600-47413200	Strong transcription	Osteobl	bone
25	chr21:47405600-47419800	Strong transcription	Fetal Stomach	stomach
26	chr21:47405600-47423000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr21:47405800-47414400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr21:47406200-47412400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr21:47406400-47411600	Strong transcription	Adipose Nuclei	Adipose
30	chr21:47406400-47421400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr21:47406600-47425400	Weak transcription	Brain Cingulate Gyrus	brain
32	chr21:47407000-47411600	Weak transcription	Brain Hippocampus Middle	brain
33	chr21:47407000-47414400	Strong transcription	Fetal Intestine Large	intestine
34	chr21:47407400-47411800	Weak transcription	Pancreas	Pancrea
35	chr21:47407400-47413800	Weak transcription	HSMM	muscle
36	chr21:47407600-47414000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr21:47407600-47416400	Weak transcription	Esophagus	oesophagus
38	chr21:47407600-47425000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr21:47407800-47412000	Strong transcription	NHLF	lung
40	chr21:47408200-47412800	Strong transcription	Right Ventricle	heart
41	chr21:47408400-47411000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr21:47408400-47411200	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr21:47408400-47412000	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr21:47408400-47416400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr21:47408400-47416800	Genic enhancers	Stomach Smooth Muscle	stomach
46	chr21:47408400-47425800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr21:47408600-47415400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
48	chr21:47408600-47419800	Strong transcription	Brain Germinal Matrix	brain
49	chr21:47408800-47411200	Strong transcription	Colonic Mucosa	Colon
50	chr21:47408800-47414400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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