Variant report

Variant	esv1851038
Chromosome Location	chr21:17412144-17488119
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	chr21:17454805-17455058	K562	blood:	n/a	chr21:17454915-17454931
2	ARID3A	chr21:17452104-17452625	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:17454775-17455077	HepG2	liver:	n/a	chr21:17454915-17454931
4	BACH1	chr21:17479135-17479311	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr21:17457869-17458022	GM12878	blood:	n/a	n/a
6	BRCA1	chr21:17452021-17452405	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr21:17487850-17488164	HepG2	liver:	n/a	n/a
8	CEBPB	chr21:17452092-17452529	A549	lung:	n/a	chr21:17452229-17452240
9	CEBPB	chr21:17441592-17441700	HepG2	liver:	n/a	chr21:17441653-17441664 chr21:17441652-17441663
10	CEBPB	chr21:17451984-17452511	A549	lung:	n/a	chr21:17452229-17452240
11	CEBPB	chr21:17441548-17441765	IMR90	lung:	n/a	chr21:17441653-17441664 chr21:17441652-17441663
12	CEBPB	chr21:17452140-17452410	A549	lung:	n/a	chr21:17452229-17452240
13	CEBPB	chr21:17487848-17488168	IMR90	lung:	n/a	n/a
14	CEBPB	chr21:17425250-17425311	HepG2	liver:	n/a	chr21:17425285-17425296
15	CEBPB	chr21:17452112-17452490	MCF-7	breast:	n/a	chr21:17452229-17452240
16	CEBPB	chr21:17479706-17479963	IMR90	lung:	n/a	n/a
17	CEBPB	chr21:17412864-17413469	Hela-S3	cervix:	n/a	chr21:17412969-17412980 chr21:17412968-17412979 chr21:17412970-17412979
18	CEBPB	chr21:17487898-17488132	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr21:17487823-17488137	A549	lung:	n/a	n/a
20	CEBPB	chr21:17452043-17452550	Hela-S3	cervix:	n/a	chr21:17452229-17452240
21	CEBPB	chr21:17487872-17488049	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr21:17412830-17413513	HepG2	liver:	n/a	chr21:17412969-17412980 chr21:17412968-17412979 chr21:17412970-17412979
23	CEBPB	chr21:17459872-17459920	HepG2	liver:	n/a	chr21:17459876-17459887
24	CEBPB	chr21:17487836-17488122	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr21:17452064-17452599	HepG2	liver:	n/a	chr21:17452229-17452240
26	CEBPB	chr21:17452028-17452533	IMR90	lung:	n/a	chr21:17452229-17452240
27	CEBPB	chr21:17419141-17419620	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr21:17442502-17442706	MCF-7	breast:	n/a	n/a
29	CEBPB	chr21:17412820-17413512	IMR90	lung:	n/a	chr21:17412969-17412980 chr21:17412968-17412979 chr21:17412970-17412979
30	CEBPB	chr21:17444904-17445415	IMR90	lung:	n/a	n/a
31	CTCF	chr21:17454700-17454850	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr21:17454840-17454990	HBMEC	blood vessel:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
33	CTCF	chr21:17455540-17455690	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr21:17442500-17442650	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr21:17454600-17454750	BE2_C	brain:	n/a	n/a
36	CTCF	chr21:17454840-17454990	GM12878	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
37	CTCF	chr21:17454900-17455050	K562	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
38	CTCF	chr21:17442560-17442710	HAc	cerebellar:	n/a	n/a
39	CTCF	chr21:17454840-17454990	GM12875	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
40	CTCF	chr21:17445200-17445350	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr21:17442480-17442630	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr21:17454880-17455030	HMEC	breast:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
43	CTCF	chr21:17427565-17427611	Medullo	brain:	n/a	n/a
44	CTCF	chr21:17454877-17455028	GM12878	blood:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
45	CTCF	chr21:17454560-17454710	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr21:17454800-17454950	GM12864	blood:	n/a	n/a
47	CTCF	chr21:17454900-17455050	AG10803	skin:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
48	CTCF	chr21:17454860-17455010	HPF	lung:	n/a	chr21:17454940-17454961 chr21:17454938-17454956 chr21:17454943-17454951 chr21:17454939-17454955
49	CTCF	chr21:17461871-17461899	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr21:17460320-17460470	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:17442803-17442853	HNPCEpiC	eye:	n/a
2	chr21:17442803-17442853	ProgFib	skin:	n/a
3	chr21:17442803-17442853	BE2_C	brain:	n/a
4	chr21:17442467-17442517	NHDF-neo	bronchial:	n/a
5	chr21:17442663-17442713	SAEC	small airway:	n/a
6	chr21:17441953-17442003	Hepatocyte	liver:	n/a
7	chr21:17442467-17442517	GM19239	blood:	n/a
8	chr21:17441953-17442003	Hela-S3	cervix:	n/a
9	chr21:17442467-17442517	A549	lung:	n/a
10	chr21:17442663-17442713	BE2_C	brain:	n/a
11	chr21:17441953-17442003	AG04449	skin:	fetal
12	chr21:17441953-17442003	AG10803	skin:	n/a
13	chr21:17442803-17442853	HEEpiC	esophagus:	n/a
14	chr21:17442803-17442853	RPTEC	kidney:	n/a
15	chr21:17441953-17442003	BE2_C	brain:	n/a
16	chr21:17442803-17442853	IMR90	lung:	fetal
17	chr21:17442663-17442713	LNCaP	prostate:	n/a
18	chr21:17442663-17442713	HRCEpiC	kidney:	n/a
19	chr21:17441953-17442003	GM12878	blood:	n/a
20	chr21:17441953-17442003	NB4	blood:	n/a
21	chr21:17441953-17442003	AG04450	lung:	fetal
22	chr21:17441953-17442003	HCM	heart:	n/a
23	chr21:17442663-17442713	HEEpiC	esophagus:	n/a
24	chr21:17441953-17442003	IMR90	lung:	fetal
25	chr21:17442663-17442713	HCPEpiC	choroid plexus:	n/a
26	chr21:17441953-17442003	PANC-1	pancreas:	n/a
27	chr21:17442663-17442713	AG09319	gingival:	n/a
28	chr21:17441953-17442003	RPTEC	kidney:	n/a
29	chr21:17442803-17442853	HAEpiC	amniotic membrane:	n/a
30	chr21:17442803-17442853	K562	blood:	n/a
31	chr21:17442663-17442713	Hepatocyte	liver:	n/a
32	chr21:17442467-17442517	NHBE	bronchial:	n/a
33	chr21:17442467-17442517	AG09319	gingival:	n/a
34	chr21:17442663-17442713	NHBE	bronchial:	n/a
35	chr21:17442467-17442517	HNPCEpiC	eye:	n/a
36	chr21:17442467-17442517	GM06990	blood:	n/a
37	chr21:17442663-17442713	AoSMC	blood vessel:	n/a
38	chr21:17442803-17442853	NB4	blood:	n/a
39	chr21:17442803-17442853	HCT-116	colon:	n/a
40	chr21:17442467-17442517	BE2_C	brain:	n/a
41	chr21:17442663-17442713	Caco-2	colon:	n/a
42	chr21:17441953-17442003	U87	brain:	n/a
43	chr21:17442467-17442517	PFSK-1	brain:	n/a
44	chr21:17442803-17442853	NH-A	brain:	n/a
45	chr21:17442467-17442517	HCPEpiC	choroid plexus:	n/a
46	chr21:17441953-17442003	ovcar-3	ovarian:	n/a
47	chr21:17442803-17442853	NT2-D1	testis:	n/a
48	chr21:17442467-17442517	Caco-2	colon:	n/a
49	chr21:17442467-17442517	IMR90	lung:	fetal
50	chr21:17441953-17442003	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:17431681..17433944-chr21:17437804..17439810,2	MCF-7	breast:
2	chr21:17431681..17433944-chr21:17437804..17439810,2	MCF-7	breast:
3	chr21:17473635..17474615-chr8:88176720..88177423,2	MCF-7	breast:
4	chr21:17467874..17469378-chr21:17482535..17484569,2	K562	blood:
5	chr21:17457077..17457729-chr21:17702169..17702961,2	MCF-7	breast:
6	chr21:17405738..17408862-chr21:17414467..17417425,3	MCF-7	breast:
7	chr21:17466615..17468236-chr21:17471288..17473078,2	K562	blood:
8	chr21:17454496..17455374-chr21:17702457..17703273,3	MCF-7	breast:
9	chr21:17266810..17267465-chr21:17454846..17455467,2	MCF-7	breast:
10	chr21:17409413..17411769-chr21:17412159..17413717,2	MCF-7	breast:
11	chr21:17467874..17469378-chr21:17482535..17484569,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRIP1-12	chr21:17466735-17467692	NONHSAT081224
2	lnc-USP25-2	chr21:17442842-17442868	ENSG00000215386.6
3	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386
4	lnc-USP25-2	chr21:17442842-17442868	ENSG00000215386
5	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386.6
6	lnc-USP25-2	chr21:17442853-17442887	ENSG00000215386.6
7	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386.6
8	lnc-USP25-2	chr21:17443553-17443718	ENSG00000215386
9	lnc-USP25-2	chr21:17443434-17443718	ENSG00000215386

Variant related genes	Relation type
RNU6-426P	TF binding region
VDAC2P1	TF binding region
LINC00478	TF binding region
RNU6-426P	CpG island
VDAC2P1	CpG island
LINC00478	CpG island
ENSG00000214976	chromatin interactions
ENSG00000215386	chromatin interactions
ENSG00000252273	chromatin interactions
DCBLD2	miRNA target sites
ATAD2	miRNA target sites
STAT3	miRNA target sites
MEF2C	miRNA target sites

Extended variants
information (count: 2168 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2823580	chr21:17412144-17412145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376014036	chr21:17412198-17412199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554689483	chr21:17412199-17412200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574136397	chr21:17412216-17412217	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs139049136	chr21:17412217-17412218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs536876702	chr21:17412320-17412321	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs556549606	chr21:17412337-17412338	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs533571350	chr21:17412346-17412347	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs140010449	chr21:17412821-17412822	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs530464933	chr21:17414051-17414052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550683131	chr21:17414062-17414063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144742492	chr21:17414078-17414079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564200706	chr21:17414084-17414085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532727000	chr21:17414116-17414117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529168841	chr21:17414165-17414166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552821807	chr21:17414189-17414190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76641446	chr21:17414243-17414244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370448785	chr21:17414262-17414263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535322819	chr21:17414268-17414269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs193120660	chr21:17414292-17414293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148853958	chr21:17414324-17414325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530165808	chr21:17414326-17414327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376912133	chr21:17414327-17414328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200901165	chr21:17414328-17414329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537075222	chr21:17414329-17414330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567104879	chr21:17414330-17414331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555573810	chr21:17414332-17414333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143747360	chr21:17414355-17414356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553523783	chr21:17414392-17414393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573005056	chr21:17414401-17414402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112221003	chr21:17414413-17414414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576939695	chr21:17414449-17414450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562522391	chr21:17414474-17414475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185549799	chr21:17414475-17414476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552752890	chr21:17414476-17414477	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573002106	chr21:17414486-17414487	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186818044	chr21:17414488-17414489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191229747	chr21:17414503-17414504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4818251	chr21:17414504-17414505	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs139069081	chr21:17414505-17414506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188634198	chr21:17414519-17414520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564137786	chr21:17414557-17414558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533071186	chr21:17414591-17414592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546762280	chr21:17414624-17414625	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372650929	chr21:17414647-17414648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182124894	chr21:17414653-17414654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550628320	chr21:17414680-17414681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528710663	chr21:17414682-17414683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570535063	chr21:17414683-17414684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548840293	chr21:17414782-17414783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	20409316	CNVD
Gastric cancer	18160780	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17411000-17412200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr21:17412200-17412400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
3	chr21:17414000-17416600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr21:17416400-17417000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr21:17418800-17419000	Enhancers	Osteobl	bone
6	chr21:17418800-17419400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr21:17419000-17419400	Flanking Active TSS	Osteobl	bone
8	chr21:17419000-17419800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr21:17419000-17420000	Enhancers	Hela-S3	cervix
10	chr21:17419200-17419600	Enhancers	A549	lung
11	chr21:17419200-17419800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr21:17419400-17419600	Enhancers	Osteobl	bone
13	chr21:17419800-17420400	Enhancers	Fetal Lung	lung
14	chr21:17419800-17420800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr21:17421000-17421200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr21:17421600-17422200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr21:17428400-17428800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr21:17428800-17431000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr21:17429000-17429200	Enhancers	Fetal Brain Female	brain
20	chr21:17429200-17430200	Weak transcription	Fetal Brain Female	brain
21	chr21:17430200-17431600	Enhancers	Fetal Brain Female	brain
22	chr21:17431000-17431600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr21:17433000-17433800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr21:17433800-17435400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr21:17434400-17434800	Active TSS	Osteobl	bone
26	chr21:17441400-17441600	Enhancers	Brain Hippocampus Middle	brain
27	chr21:17441400-17441600	Enhancers	Fetal Brain Male	brain
28	chr21:17441400-17444000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr21:17441600-17441800	Active TSS	Brain Anterior Caudate	brain
30	chr21:17441600-17441800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr21:17441600-17442000	Enhancers	Brain Cingulate Gyrus	brain
32	chr21:17441600-17442000	Flanking Active TSS	Fetal Brain Male	brain
33	chr21:17441600-17442200	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr21:17441600-17442400	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr21:17441600-17445000	Active TSS	Brain Germinal Matrix	brain
36	chr21:17441600-17446800	Active TSS	Fetal Brain Female	brain
37	chr21:17441800-17442000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr21:17441800-17442000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr21:17441800-17442200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr21:17441800-17442400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr21:17441800-17442400	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr21:17441800-17442400	Enhancers	Brain Substantia Nigra	brain
43	chr21:17441800-17442400	Enhancers	Osteobl	bone
44	chr21:17441800-17442600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr21:17441800-17443200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr21:17441800-17445400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr21:17442000-17442800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr21:17442000-17446200	Active TSS	Brain Angular Gyrus	brain
49	chr21:17442000-17446400	Active TSS	Brain Cingulate Gyrus	brain
50	chr21:17442000-17446800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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