Variant report

Variant	esv2758530
Chromosome Location	chr21:16912646-17096678
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1400)
CpG islands
(count:0)
Chromatin interactive
region (count:96)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:16964646-16964900	K562	blood:	n/a	n/a
2	ARID3A	chr21:17000298-17000319	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:16964668-16964944	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:16915871-16916071	HepG2	liver:	n/a	n/a
5	ARID3A	chr21:17054516-17054801	HepG2	liver:	n/a	n/a
6	ARID3A	chr21:17032123-17032416	HepG2	liver:	n/a	n/a
7	ATF1	chr21:17079030-17079390	K562	blood:	n/a	n/a
8	ATF1	chr21:17067875-17067961	K562	blood:	n/a	n/a
9	ATF1	chr21:17074263-17074486	K562	blood:	n/a	n/a
10	ATF1	chr21:16930343-16930672	K562	blood:	n/a	n/a
11	BACH1	chr21:17001048-17001064	K562	blood:	n/a	n/a
12	BCL3	chr21:16997709-16998047	GM12878	blood:	n/a	n/a
13	BCL3	chr21:16997709-16997978	GM12878	blood:	n/a	n/a
14	BHLHE40	chr21:16990974-16990988	GM12878	blood:	n/a	n/a
15	BRCA1	chr21:17039390-17039723	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr21:17041624-17041993	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr21:17054673-17054821	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr21:16930253-16930535	K562	blood:	n/a	n/a
19	CBX3	chr21:17078978-17079442	HCT-116	colon:	n/a	n/a
20	CBX3	chr21:17078887-17079488	HCT-116	colon:	n/a	n/a
21	CEBPB	chr21:16976775-16976996	A549	lung:	n/a	n/a
22	CEBPB	chr21:17060964-17061559	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr21:17039179-17039842	A549	lung:	n/a	chr21:17039307-17039320 chr21:17039459-17039470 chr21:17039562-17039573
24	CEBPB	chr21:16915800-16916185	Hela-S3	cervix:	n/a	chr21:16915992-16916003
25	CEBPB	chr21:16976661-16977123	MCF-7	breast:	n/a	n/a
26	CEBPB	chr21:16925441-16925677	A549	lung:	n/a	chr21:16925570-16925581
27	CEBPB	chr21:16989243-16989588	IMR90	lung:	n/a	chr21:16989394-16989405
28	CEBPB	chr21:17041555-17042095	Hela-S3	cervix:	n/a	chr21:17041795-17041808
29	CEBPB	chr21:16993246-16993594	HepG2	liver:	n/a	n/a
30	CEBPB	chr21:16915791-16916174	A549	lung:	n/a	chr21:16915992-16916003
31	CEBPB	chr21:16976466-16977222	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr21:16915804-16916190	HepG2	liver:	n/a	chr21:16915992-16916003
33	CEBPB	chr21:17059446-17059809	IMR90	lung:	n/a	n/a
34	CEBPB	chr21:16998419-16998620	K562	blood:	n/a	chr21:16998421-16998433 chr21:16998598-16998606
35	CEBPB	chr21:16976606-16977176	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr21:17011435-17011787	K562	blood:	n/a	chr21:17011611-17011622 chr21:17011612-17011621 chr21:17011610-17011623
37	CEBPB	chr21:16976708-16977137	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr21:17011400-17011803	ECC-1	luminal epithelium:	n/a	chr21:17011611-17011622 chr21:17011612-17011621 chr21:17011610-17011623
39	CEBPB	chr21:16937760-16937919	A549	lung:	n/a	n/a
40	CEBPB	chr21:16993282-16993570	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr21:17054533-17055014	K562	blood:	n/a	chr21:17054766-17054777
42	CEBPB	chr21:17011467-17011774	A549	lung:	n/a	chr21:17011611-17011622 chr21:17011612-17011621 chr21:17011610-17011623
43	CEBPB	chr21:17039258-17039676	A549	lung:	n/a	chr21:17039307-17039320 chr21:17039459-17039470 chr21:17039562-17039573
44	CEBPB	chr21:16915722-16916215	HepG2	liver:	n/a	chr21:16915992-16916003
45	CEBPB	chr21:16993249-16993601	IMR90	lung:	n/a	n/a
46	CEBPB	chr21:17039251-17039745	IMR90	lung:	n/a	chr21:17039307-17039320 chr21:17039459-17039470 chr21:17039562-17039573
47	CEBPB	chr21:17054565-17054894	H1-hESC	embryonic stem cell:	n/a	chr21:17054766-17054777
48	CEBPB	chr21:17011428-17011806	Hela-S3	cervix:	n/a	chr21:17011611-17011622 chr21:17011612-17011621 chr21:17011610-17011623
49	CEBPB	chr21:16915910-16916196	A549	lung:	n/a	chr21:16915992-16916003
50	CEBPB	chr21:17011316-17011967	MCF-7	breast:	n/a	chr21:17011611-17011622 chr21:17011612-17011621 chr21:17011610-17011623

No data

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:17094914..17097120-chr21:17102062..17104681,2	K562	blood:
2	chr21:16851669..16854505-chr21:16929396..16930897,2	MCF-7	breast:
3	chr21:16999755..17002610-chr21:17103802..17105409,2	MCF-7	breast:
4	chr21:17087926..17089918-chr21:17092657..17095382,2	K562	blood:
5	chr21:16614000..16614891-chr21:16959269..16959857,2	MCF-7	breast:
6	chr21:17044032..17047282-chr21:17048018..17052321,5	K562	blood:
7	chr21:16912535..16914166-chr21:16914818..16917552,2	MCF-7	breast:
8	chr21:16940802..16942430-chr21:16945970..16948560,2	MCF-7	breast:
9	chr21:16912535..16914166-chr21:16914818..16917552,2	MCF-7	breast:
10	chr21:16990382..16992239-chr21:17100657..17103328,2	MCF-7	breast:
11	chr21:16959176..16959732-chr21:17011225..17011757,2	MCF-7	breast:
12	chr21:16235383..16236247-chr21:16959008..16959755,5	MCF-7	breast:
13	chr21:17027863..17030532-chr21:17032881..17035751,2	K562	blood:
14	chr21:16931419..16933182-chr21:16935241..16937836,2	MCF-7	breast:
15	chr21:17064915..17067118-chr21:17101217..17104804,3	MCF-7	breast:
16	chr21:16989283..16990838-chr21:17003947..17006454,2	MCF-7	breast:
17	chr21:16936242..16938072-chr21:16938632..16941243,2	MCF-7	breast:
18	chr21:16919633..16920412-chr21:16959232..16959914,4	MCF-7	breast:
19	chr21:16907370..16908917-chr21:16935643..16937758,2	K562	blood:
20	chr21:16504869..16505637-chr21:16958997..16959745,3	MCF-7	breast:
21	chr21:16919633..16920412-chr21:16959232..16959914,4	MCF-7	breast:
22	chr21:16931419..16933182-chr21:16935241..16937836,2	MCF-7	breast:
23	chr21:16964321..16967062-chr21:17101437..17103786,2	MCF-7	breast:
24	chr21:16714657..16715283-chr21:16959040..16959755,2	MCF-7	breast:
25	chr21:17076130..17076863-chr4:168171748..168172510,2	MCF-7	breast:
26	chr21:16909677..16914012-chr21:16918687..16921004,3	MCF-7	breast:
27	chr21:16930194..16932868-chr21:16938815..16941325,2	K562	blood:
28	chr21:16582204..16583291-chr21:16958900..16960163,20	MCF-7	breast:
29	chr21:17087356..17090819-chr21:17092657..17096162,4	K562	blood:
30	chr21:16918481..16920234-chr21:16923318..16925112,2	MCF-7	breast:
31	chr21:16938516..16940926-chr21:16955755..16957266,2	MCF-7	breast:
32	chr21:16932624..16935111-chr21:16937107..16938655,2	K562	blood:
33	chr21:17087356..17090819-chr21:17092657..17096162,4	K562	blood:
34	chr21:16940802..16942430-chr21:16945970..16948560,2	MCF-7	breast:
35	chr21:17027863..17030532-chr21:17032881..17035751,2	K562	blood:
36	chr21:17025826..17028005-chr21:17208818..17210629,2	MCF-7	breast:
37	chr21:16582273..16583330-chr21:16919552..16920500,4	MCF-7	breast:
38	chr21:16580047..16580567-chr21:16959256..16959831,2	MCF-7	breast:
39	chr21:16936242..16938072-chr21:16938632..16941243,2	MCF-7	breast:
40	chr21:16545107..16545924-chr21:16958930..16959783,5	MCF-7	breast:
41	chr21:16919441..16920015-chr21:16959232..16959755,2	MCF-7	breast:
42	chr21:17077309..17079464-chr21:17110319..17112790,2	K562	blood:
43	chr21:17015627..17017680-chr21:17022587..17025053,2	K562	blood:
44	chr21:16582189..16583291-chr21:16958890..16959931,32	MCF-7	breast:
45	chr21:16930194..16932868-chr21:16938815..16941325,2	K562	blood:
46	chr21:16582221..16583302-chr21:16958882..16959791,8	MCF-7	breast:
47	chr21:17052353..17053898-chr21:17054615..17056835,2	K562	blood:
48	chr21:17015627..17017680-chr21:17022587..17025053,2	K562	blood:
49	chr21:16504814..16505341-chr21:16958945..16959492,2	MCF-7	breast:
50	chr21:16580067..16580933-chr21:16958897..16959756,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRIP1-9	chr21:17049870-17049987	NONHSAT081208
2	lnc-USP25-4	chr21:16934420-16934823	NONHSAT081204
3	lnc-NRIP1-7	chr21:16943559-16943675	NONHSAT081206
4	lnc-NRIP1-8	chr21:17066619-17067073	NONHSAT081210
5	lnc-NRIP1-7	chr21:16947589-16947729	NONHSAT081206
6	lnc-USP25-4	chr21:16925017-16925162	NONHSAT081204
7	lnc-NRIP1-9	chr21:17048709-17048960	NONHSAT081208
8	lnc-NRIP1-8	chr21:17068204-17068900	NONHSAT081210
9	lnc-USP25-4	chr21:16925631-16925679	NONHSAT081205
10	lnc-NRIP1-7	chr21:16999365-16999459	NONHSAT081206
11	lnc-USP25-4	chr21:16934420-16934873	NONHSAT081205

No data

Variant related genes	Relation type
ENSG00000238591	TF binding region
ENSG00000221497	TF binding region
RNU6-1326P	TF binding region
RAD23BLP	TF binding region
ENSG00000155313	chromatin interactions
ENSG00000212564	chromatin interactions
ENSG00000085733	chromatin interactions
ENSG00000180530	chromatin interactions

Extended variants
information (count: 6610 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6610 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573300697	chr21:16912649-16912650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs117625578	chr21:16912703-16912704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs62217440	chr21:16912724-16912725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528201155	chr21:16912763-16912764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555435362	chr21:16912817-16912818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575597315	chr21:16912878-16912879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547768777	chr21:16912886-16912887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140477010	chr21:16912934-16912935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144531035	chr21:16912947-16912948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144313217	chr21:16912970-16912971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs202183628	chr21:16912978-16912979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562429144	chr21:16912979-16912980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199968767	chr21:16912981-16912982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28368766	chr21:16912982-16912983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79832235	chr21:16912983-16912984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200390010	chr21:16912984-16912985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200187992	chr21:16912986-16912987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74822686	chr21:16912987-16912988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13047618	chr21:16912988-16912989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs60164076	chr21:16912990-16912991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78450827	chr21:16912991-16912992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs55722423	chr21:16912996-16912997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373221921	chr21:16912997-16912998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57202572	chr21:16913000-16913001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201376308	chr21:16913001-16913002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549074211	chr21:16913002-16913003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs79093399	chr21:16913004-16913005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562300929	chr21:16913005-16913006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs58583903	chr21:16913009-16913010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531219815	chr21:16913035-16913036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192062303	chr21:16913079-16913080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571234520	chr21:16913092-16913093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182896229	chr21:16913147-16913148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77437564	chr21:16913167-16913168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567462278	chr21:16913177-16913178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535532919	chr21:16913200-16913201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533283483	chr21:16915232-16915233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181966322	chr21:16915244-16915245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186188877	chr21:16915257-16915258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540662740	chr21:16915263-16915264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377603959	chr21:16915269-16915270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554509726	chr21:16915310-16915311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9981901	chr21:16915341-16915342	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs375067737	chr21:16915347-16915348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543714260	chr21:16915358-16915359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73892650	chr21:16915365-16915366	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs61412083	chr21:16915366-16915367	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs73348660	chr21:16915388-16915389	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs61193814	chr21:16915409-16915410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs527742102	chr21:16915424-16915425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Autism	20841430	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:625 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16911400-16913000	Enhancers	Dnd41	blood
2	chr21:16911800-16912800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr21:16911800-16913000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr21:16912600-16913200	Enhancers	Primary hematopoietic stem cells	blood
5	chr21:16915200-16915400	Enhancers	Colon Smooth Muscle	Colon
6	chr21:16915400-16922200	Weak transcription	Colon Smooth Muscle	Colon
7	chr21:16915600-16916000	Active TSS	Hela-S3	cervix
8	chr21:16915600-16916000	Enhancers	HepG2	liver
9	chr21:16915800-16916000	Enhancers	Esophagus	oesophagus
10	chr21:16921600-16922200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr21:16921600-16922400	Enhancers	HSMMtube	muscle
12	chr21:16921800-16922400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr21:16921800-16922400	Enhancers	Adipose Nuclei	Adipose
14	chr21:16921800-16922600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr21:16922000-16922400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr21:16922200-16922400	Enhancers	Colon Smooth Muscle	Colon
17	chr21:16922200-16922600	Enhancers	HSMM	muscle
18	chr21:16923400-16926000	Enhancers	Dnd41	blood
19	chr21:16924200-16925000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr21:16924400-16925600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr21:16924400-16925600	Enhancers	Fetal Thymus	thymus
22	chr21:16924400-16926200	Enhancers	Primary hematopoietic stem cells	blood
23	chr21:16924400-16926200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr21:16924600-16925600	Enhancers	Primary T cells from cord blood	blood
25	chr21:16924600-16925600	Enhancers	Primary T cells fromperipheralblood	blood
26	chr21:16924600-16925600	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr21:16924600-16925600	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr21:16924600-16925600	Enhancers	Thymus	Thymus
29	chr21:16924600-16925800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr21:16924800-16925600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr21:16924800-16925600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr21:16924800-16925600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr21:16924800-16925600	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr21:16924800-16925800	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr21:16924800-16925800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr21:16925000-16925200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr21:16925200-16925400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr21:16925200-16925600	Enhancers	Liver	Liver
39	chr21:16925400-16925600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr21:16925600-16926000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr21:16925600-16930200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr21:16930000-16930800	Enhancers	K562	blood
43	chr21:16931200-16932000	Enhancers	Fetal Intestine Large	intestine
44	chr21:16931200-16932600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr21:16931200-16932800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr21:16931400-16932600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr21:16932000-16932400	Weak transcription	Fetal Intestine Large	intestine
48	chr21:16932000-16932800	Enhancers	H1 Cell Line	embryonic stem cell
49	chr21:16932000-16932800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr21:16932000-16933000	Enhancers	HUES64 Cell Line	embryonic stem cell

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