Variant report

Variant	nsv834049
Chromosome Location	chr21:16717421-16905300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1595)
CpG islands
(count:0)
Chromatin interactive
region (count:102)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1595 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:16813157-16814175	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:16773271-16773461	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:16828186-16828544	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:16724367-16724605	HepG2	liver:	n/a	n/a
5	ARID3A	chr21:16815869-16817310	HepG2	liver:	n/a	n/a
6	ARID3A	chr21:16855480-16855834	HepG2	liver:	n/a	n/a
7	ARID3A	chr21:16886505-16887296	HepG2	liver:	n/a	n/a
8	ARID3A	chr21:16855594-16855756	K562	blood:	n/a	n/a
9	ATF2	chr21:16780207-16780920	GM12878	blood:	n/a	n/a
10	ATF2	chr21:16817669-16818132	GM12878	blood:	n/a	n/a
11	ATF2	chr21:16886391-16887018	GM12878	blood:	n/a	n/a
12	ATF2	chr21:16780324-16780815	GM12878	blood:	n/a	n/a
13	ATF2	chr21:16817663-16818064	GM12878	blood:	n/a	n/a
14	ATF2	chr21:16810105-16810674	GM12878	blood:	n/a	n/a
15	ATF2	chr21:16810141-16810588	GM12878	blood:	n/a	n/a
16	ATF3	chr21:16816478-16817197	A549	lung:	n/a	n/a
17	ATF3	chr21:16816433-16817397	A549	lung:	n/a	n/a
18	BACH1	chr21:16816422-16817200	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr21:16738347-16738675	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr21:16884177-16884294	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr21:16816503-16816735	K562	blood:	n/a	n/a
22	BATF	chr21:16794351-16794655	GM12878	blood:	n/a	chr21:16794491-16794502
23	BATF	chr21:16810181-16810596	GM12878	blood:	n/a	chr21:16810356-16810367
24	BATF	chr21:16795072-16795322	GM12878	blood:	n/a	chr21:16795178-16795189 chr21:16795179-16795189 chr21:16795175-16795185
25	BATF	chr21:16817720-16817973	GM12878	blood:	n/a	n/a
26	BATF	chr21:16817678-16818010	GM12878	blood:	n/a	n/a
27	BATF	chr21:16810169-16810645	GM12878	blood:	n/a	chr21:16810356-16810367
28	BCL11A	chr21:16810249-16810537	GM12878	blood:	n/a	n/a
29	BCL11A	chr21:16780425-16780834	GM12878	blood:	n/a	n/a
30	BCL11A	chr21:16810144-16810663	GM12878	blood:	n/a	n/a
31	BCL11A	chr21:16817666-16817886	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr21:16858816-16859137	GM12878	blood:	n/a	n/a
33	BCL3	chr21:16816018-16817462	A549	lung:	n/a	n/a
34	BCL3	chr21:16733140-16733559	GM12878	blood:	n/a	n/a
35	BCL3	chr21:16816387-16817436	A549	lung:	n/a	n/a
36	BCLAF1	chr21:16817668-16818018	GM12878	blood:	n/a	n/a
37	BCLAF1	chr21:16780411-16780924	GM12878	blood:	n/a	n/a
38	BCLAF1	chr21:16810153-16810694	GM12878	blood:	n/a	n/a
39	BCLAF1	chr21:16855410-16855897	GM12878	blood:	n/a	n/a
40	BHLHE40	chr21:16816602-16816781	K562	blood:	n/a	n/a
41	BHLHE40	chr21:16886663-16887142	HepG2	liver:	n/a	n/a
42	BHLHE40	chr21:16810090-16810708	GM12878	blood:	n/a	n/a
43	BHLHE40	chr21:16816506-16817378	HepG2	liver:	n/a	n/a
44	BHLHE40	chr21:16872280-16872474	HepG2	liver:	n/a	n/a
45	BHLHE40	chr21:16780520-16780839	GM12878	blood:	n/a	n/a
46	BHLHE40	chr21:16797384-16797542	GM12878	blood:	n/a	n/a
47	BHLHE40	chr21:16813448-16813856	HepG2	liver:	n/a	n/a
48	BHLHE40	chr21:16738447-16738573	K562	blood:	n/a	n/a
49	BHLHE40	chr21:16738395-16738718	HepG2	liver:	n/a	n/a
50	BHLHE40	chr21:16786617-16786625	GM12878	blood:	n/a	n/a

No data

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr21:16737684..16740114-chr21:16747406..16749944,2	K562	blood:
2	chr21:16794267..16796207-chr21:16798001..16799584,2	K562	blood:
3	chr21:16583537..16586474-chr21:16857105..16859617,2	MCF-7	breast:
4	chr21:16545130..16546031-chr21:16816305..16817187,2	MCF-7	breast:
5	chr21:16779348..16780934-chr21:16794218..16796513,2	MCF-7	breast:
6	chr21:16435342..16439533-chr21:16847415..16856930,13	MCF-7	breast:
7	chr21:16714501..16715255-chr21:16742984..16743509,2	MCF-7	breast:
8	chr21:16899768..16901686-chr21:16905215..16907866,2	K562	blood:
9	chr21:16742966..16743867-chr21:16816332..16816950,2	MCF-7	breast:
10	chr21:16436680..16438294-chr21:16816997..16819777,2	MCF-7	breast:
11	chr21:16827722..16830026-chr21:16832130..16834284,2	K562	blood:
12	chr21:16737684..16740114-chr21:16747406..16749944,2	K562	blood:
13	chr21:16616918..16617579-chr21:16816270..16816842,2	MCF-7	breast:
14	chr21:16435921..16437860-chr21:16878059..16879589,2	MCF-7	breast:
15	chr21:16851669..16854505-chr21:16929396..16930897,2	MCF-7	breast:
16	chr21:16715385..16717006-chr21:16736563..16738066,2	MCF-7	breast:
17	chr21:16794267..16796207-chr21:16798001..16799584,2	K562	blood:
18	chr21:16796146..16798117-chr21:16798542..16800941,2	MCF-7	breast:
19	chr21:16582443..16583127-chr21:16816309..16817103,2	MCF-7	breast:
20	chr21:16816198..16817284-chr21:16958851..16959824,9	MCF-7	breast:
21	chr21:16732191..16734558-chr21:16742882..16744836,2	MCF-7	breast:
22	chr21:15755923..15757812-chr21:16863949..16865497,2	K562	blood:
23	chr21:16795224..16797113-chr21:16843935..16846229,2	MCF-7	breast:
24	chr21:16434137..16441229-chr21:16850537..16857302,14	MCF-7	breast:
25	chr21:16663401..16665237-chr21:16852171..16854477,2	MCF-7	breast:
26	chr21:16899768..16901686-chr21:16905215..16907866,2	K562	blood:
27	chr21:16777188..16781171-chr21:16781848..16783894,3	K562	blood:
28	chr21:16545039..16545630-chr21:16816325..16817187,2	MCF-7	breast:
29	chr21:16742966..16743867-chr21:16816332..16816950,2	MCF-7	breast:
30	chr21:16435231..16438177-chr21:16847132..16848668,2	MCF-7	breast:
31	chr21:16777188..16781171-chr21:16781848..16783894,3	K562	blood:
32	chr21:16773347..16773877-chr21:16816611..16817237,2	MCF-7	breast:
33	chr21:16580777..16584780-chr21:16852967..16856651,5	MCF-7	breast:
34	chr21:16773347..16773877-chr21:16816611..16817237,2	MCF-7	breast:
35	chr21:16804369..16806411-chr21:16810758..16812985,2	MCF-7	breast:
36	chr21:16614264..16614942-chr21:16855573..16856106,2	MCF-7	breast:
37	chr21:16742888..16745845-chr21:16814324..16816904,2	MCF-7	breast:
38	chr21:16582323..16583272-chr21:16816273..16817233,8	MCF-7	breast:
39	chr21:16827722..16830026-chr21:16832130..16834284,2	K562	blood:
40	chr21:16662853..16665318-chr21:16789620..16791689,2	MCF-7	breast:
41	chr21:16773774..16774316-chr21:16854420..16855168,2	MCF-7	breast:
42	chr21:16713454..16716441-chr21:16762500..16764229,2	MCF-7	breast:
43	chr21:16571993..16572516-chr21:16816311..16817165,2	MCF-7	breast:
44	chr21:16772297..16774137-chr21:16777440..16779221,2	K562	blood:
45	chr21:16880501..16882055-chr21:16883399..16885226,2	MCF-7	breast:
46	chr21:16714779..16715688-chr21:16816321..16817212,3	MCF-7	breast:
47	chr21:16614093..16615068-chr21:16855320..16856108,3	MCF-7	breast:
48	chr21:16804369..16806411-chr21:16810758..16812985,2	MCF-7	breast:
49	chr21:16743337..16743867-chr21:16816332..16817195,2	MCF-7	breast:
50	chr21:16576908..16578947-chr21:16816097..16818886,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRIP1-6	chr21:16862849-16863086	NONHSAT081202
2	lnc-USP25-6	chr21:16808362-16809546	NONHSAT081201
3	lnc-NRIP1-3	chr21:16868035-16868443	XLOC_014007
4	lnc-NRIP1-3	chr21:16866251-16867217	XLOC_014007
5	lnc-USP25-5	chr21:16883544-16883870	l_2173_chr21:16882815-16883978_brain
6	lnc-USP25-6	chr21:16807725-16807828	NONHSAT081201
7	lnc-USP25-5	chr21:16882816-16883306	l_2173_chr21:16882815-16883978_brain
8	lnc-USP25-5	chr21:16883875-16883978	l_2173_chr21:16882815-16883978_brain
9	lnc-USP25-6	chr21:16806721-16807118	NONHSAT081201

No data

Variant related genes	Relation type
CYCSP42	TF binding region
ENSG00000224247	TF binding region
ENSG00000229425	TF binding region
ENSG00000236471	chromatin interactions
ENSG00000180530	chromatin interactions

Extended variants
information (count: 7518 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:7518 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576080182	chr21:16717431-16717432	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559630405	chr21:16717447-16717448	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537284548	chr21:16717468-16717469	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188206312	chr21:16717484-16717485	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567493494	chr21:16717493-16717494	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2823237	chr21:16717526-16717527	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs556373904	chr21:16717532-16717533	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs200686971	chr21:16717533-16717534	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs193253581	chr21:16717538-16717539	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201748263	chr21:16717539-16717540	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs139584806	chr21:16717540-16717541	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs16982064	chr21:16717570-16717571	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs372685700	chr21:16717640-16717641	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs367916681	chr21:16717642-16717643	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147113645	chr21:16717656-16717657	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375787698	chr21:16717661-16717662	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs117342659	chr21:16717776-16717777	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs369957594	chr21:16717790-16717791	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77258638	chr21:16717806-16717807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543617301	chr21:16717816-16717817	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544812220	chr21:16717825-16717826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs531702249	chr21:16717834-16717835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185433873	chr21:16717840-16717841	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545491555	chr21:16717860-16717861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564682261	chr21:16717901-16717902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78801189	chr21:16717927-16717928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1735232	chr21:16717942-16717943	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs80049886	chr21:16717949-16717950	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115787944	chr21:16717960-16717961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149193762	chr21:16717985-16717986	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143323564	chr21:16717987-16717988	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs189515740	chr21:16718023-16718024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148013308	chr21:16718026-16718027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs557575624	chr21:16718039-16718040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141669456	chr21:16718055-16718056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534594641	chr21:16718060-16718061	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554630549	chr21:16718061-16718062	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34900978	chr21:16718065-16718066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs397772709	chr21:16718078-16718079	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs180967685	chr21:16718135-16718136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537383473	chr21:16718136-16718137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183547523	chr21:16718150-16718151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs535616233	chr21:16718157-16718158	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs545145265	chr21:16718213-16718214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs145949198	chr21:16718216-16718217	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188726608	chr21:16718219-16718220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138522930	chr21:16718283-16718284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560997133	chr21:16718315-16718316	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs62220318	chr21:16718322-16718323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530322069	chr21:16718343-16718344	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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	22522925	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Acute myeloid leukemia	20962326	CNVD

Chromatin state (count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16717400-16717800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr21:16717800-16720000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr21:16718400-16720000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr21:16720000-16721200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr21:16721200-16723400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr21:16723400-16725800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr21:16723800-16724000	Enhancers	HepG2	liver
8	chr21:16724000-16725000	Flanking Active TSS	HepG2	liver
9	chr21:16724000-16726600	Enhancers	Primary hematopoietic stem cells	blood
10	chr21:16724200-16724600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr21:16724200-16726800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr21:16725000-16725200	Enhancers	HepG2	liver
13	chr21:16725200-16738200	Weak transcription	HepG2	liver
14	chr21:16725600-16726200	Enhancers	NHEK	skin
15	chr21:16725600-16728600	Enhancers	HUVEC	blood vessel
16	chr21:16725800-16726200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr21:16725800-16726800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr21:16725800-16728000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr21:16726400-16727000	Enhancers	Spleen	Spleen
20	chr21:16726600-16727600	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr21:16726800-16727600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
22	chr21:16726800-16727600	Enhancers	Fetal Stomach	stomach
23	chr21:16726800-16727800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr21:16727000-16727800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr21:16727200-16727600	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr21:16727200-16727600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr21:16727200-16727800	Enhancers	Fetal Kidney	kidney
28	chr21:16727600-16727800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr21:16727600-16727800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr21:16727600-16727800	Enhancers	Rectal Smooth Muscle	rectum
31	chr21:16727600-16729200	Enhancers	Primary hematopoietic stem cells	blood
32	chr21:16727800-16729200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr21:16728000-16731400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr21:16728600-16732000	Weak transcription	HUVEC	blood vessel
35	chr21:16729200-16730200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr21:16729200-16730400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr21:16730200-16731200	Enhancers	Primary hematopoietic stem cells	blood
38	chr21:16730400-16731200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr21:16730600-16732600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr21:16731200-16735400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr21:16731600-16732000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr21:16731600-16732400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr21:16732000-16732600	Enhancers	Fetal Brain Male	brain
44	chr21:16732000-16734000	Enhancers	HUVEC	blood vessel
45	chr21:16732600-16733600	Weak transcription	Fetal Brain Male	brain
46	chr21:16733800-16734000	Enhancers	Fetal Brain Male	brain
47	chr21:16734000-16736200	Weak transcription	HUVEC	blood vessel
48	chr21:16736200-16736600	Enhancers	HUVEC	blood vessel
49	chr21:16737200-16738000	Weak transcription	Psoas Muscle	Psoas
50	chr21:16737400-16739000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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