Variant report

Variant	nsv1061686
Chromosome Location	chr21:15724570-15765777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:908)
CpG islands
(count:915)
Chromatin interactive
region (count:45)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15755173-15756571	K562	blood:	n/a	n/a
2	ARID3A	chr21:15758299-15758479	K562	blood:	n/a	n/a
3	ARID3A	chr21:15753998-15754080	K562	blood:	n/a	n/a
4	ARID3A	chr21:15755268-15756109	HepG2	liver:	n/a	n/a
5	ATF1	chr21:15755085-15755946	K562	blood:	n/a	n/a
6	ATF2	chr21:15755202-15755652	GM12878	blood:	n/a	n/a
7	ATF3	chr21:15755249-15755657	K562	blood:	n/a	chr21:15755481-15755495
8	ATF3	chr21:15734278-15734672	K562	blood:	n/a	n/a
9	BACH1	chr21:15742480-15742584	K562	blood:	n/a	n/a
10	BACH1	chr21:15755261-15755431	K562	blood:	n/a	n/a
11	BACH1	chr21:15755021-15755056	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr21:15760631-15760949	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr21:15760675-15760968	K562	blood:	n/a	n/a
14	BACH1	chr21:15755338-15756042	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr21:15755145-15755665	GM12878	blood:	n/a	chr21:15755330-15755340
16	BATF	chr21:15755303-15755640	GM12878	blood:	n/a	chr21:15755330-15755340
17	BCLAF1	chr21:15755292-15756207	GM12878	blood:	n/a	n/a
18	BCLAF1	chr21:15755245-15755807	GM12878	blood:	n/a	n/a
19	BHLHE40	chr21:15755029-15756177	HepG2	liver:	n/a	chr21:15755215-15755231
20	BHLHE40	chr21:15755039-15756420	GM12878	blood:	n/a	chr21:15755215-15755231
21	BHLHE40	chr21:15755011-15756441	K562	blood:	n/a	chr21:15755215-15755231
22	BRCA1	chr21:15730137-15730553	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr21:15755310-15755866	HepG2	liver:	n/a	n/a
24	BRCA1	chr21:15755229-15756067	GM12878	blood:	n/a	n/a
25	BRCA1	chr21:15755164-15756426	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr21:15755348-15756047	H1-hESC	embryonic stem cell:	n/a	n/a
27	CCNT2	chr21:15755282-15756426	K562	blood:	n/a	n/a
28	CCNT2	chr21:15757539-15757977	K562	blood:	n/a	n/a
29	CEBPB	chr21:15736193-15736376	A549	lung:	n/a	chr21:15736320-15736329
30	CEBPB	chr21:15754739-15755070	K562	blood:	n/a	n/a
31	CEBPB	chr21:15734349-15734628	ECC-1	luminal epithelium:	n/a	chr21:15734491-15734502
32	CEBPB	chr21:15734332-15734638	A549	lung:	n/a	chr21:15734491-15734502
33	CEBPB	chr21:15734315-15734686	HepG2	liver:	n/a	chr21:15734491-15734502
34	CEBPB	chr21:15734383-15734520	HepG2	liver:	n/a	chr21:15734491-15734502
35	CEBPB	chr21:15754813-15755089	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr21:15756026-15756585	GM12878	blood:	n/a	n/a
37	CEBPB	chr21:15736179-15736394	K562	blood:	n/a	chr21:15736320-15736329
38	CEBPB	chr21:15734292-15734601	K562	blood:	n/a	chr21:15734491-15734502
39	CEBPB	chr21:15734330-15734652	K562	blood:	n/a	chr21:15734491-15734502
40	CEBPB	chr21:15755409-15755730	A549	lung:	n/a	n/a
41	CEBPB	chr21:15734305-15734689	K562	blood:	n/a	chr21:15734491-15734502
42	CEBPB	chr21:15734307-15734680	IMR90	lung:	n/a	chr21:15734491-15734502
43	CEBPB	chr21:15734346-15734652	H1-hESC	embryonic stem cell:	n/a	chr21:15734491-15734502
44	CEBPB	chr21:15755328-15755807	K562	blood:	n/a	n/a
45	CEBPB	chr21:15734333-15734656	ECC-1	luminal epithelium:	n/a	chr21:15734491-15734502
46	CEBPB	chr21:15754691-15755984	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr21:15755354-15755995	HepG2	liver:	n/a	n/a
48	CEBPB	chr21:15736204-15736486	HepG2	liver:	n/a	chr21:15736320-15736329
49	CEBPB	chr21:15754746-15755936	IMR90	lung:	n/a	n/a
50	CEBPB	chr21:15755355-15755957	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15756085-15756135	BJ	skin:	n/a
2	chr21:15755986-15756036	AG10803	skin:	n/a
3	chr21:15755986-15756036	AG04450	lung:	fetal
4	chr21:15755706-15755756	Jurkat	blood:	n/a
5	chr21:15755452-15755502	HEK293	kidney:	embryo
6	chr21:15755644-15755694	NHBE	bronchial:	n/a
7	chr21:15755449-15755499	Hepatocyte	liver:	n/a
8	chr21:15755380-15755430	HAEpiC	amniotic membrane:	n/a
9	chr21:15755986-15756036	RPTEC	kidney:	n/a
10	chr21:15755931-15755981	SK-N-SH	brain:	n/a
11	chr21:15755606-15755656	ovcar-3	ovarian:	n/a
12	chr21:15755452-15755502	SK-N-MC	brain:	n/a
13	chr21:15755608-15755658	CMK	blood:	n/a
14	chr21:15756062-15756112	H1-hESC	embryonic stem cell:	embryo
15	chr21:15755606-15755656	HEK293	kidney:	embryo
16	chr21:15756122-15756172	IMR90	lung:	fetal
17	chr21:15756062-15756112	GM12878	blood:	n/a
18	chr21:15755449-15755499	NB4	blood:	n/a
19	chr21:15753565-15753615	HNPCEpiC	eye:	n/a
20	chr21:15755449-15755499	SK-N-SH_RA	brain:	n/a
21	chr21:15755538-15755588	AG09319	gingival:	n/a
22	chr21:15756085-15756135	HIPEpiC	eye:	n/a
23	chr21:15755644-15755694	ECC-1	luminal epithelium:	n/a
24	chr21:15756062-15756112	HCF	heart:	n/a
25	chr21:15755449-15755499	U87	brain:	n/a
26	chr21:15755931-15755981	Caco-2	colon:	n/a
27	chr21:15755606-15755656	HEEpiC	esophagus:	n/a
28	chr21:15755538-15755588	NH-A	brain:	n/a
29	chr21:15753565-15753615	NB4	blood:	n/a
30	chr21:15755986-15756036	NB4	blood:	n/a
31	chr21:15755644-15755694	SK-N-SH	brain:	n/a
32	chr21:15756062-15756112	PFSK-1	brain:	n/a
33	chr21:15755986-15756036	SKMC	muscle:	n/a
34	chr21:15755538-15755588	SAEC	small airway:	n/a
35	chr21:15755986-15756036	NHBE	bronchial:	n/a
36	chr21:15755986-15756036	A549	lung:	n/a
37	chr21:15755538-15755588	NHBE	bronchial:	n/a
38	chr21:15756085-15756135	GM12892	blood:	n/a
39	chr21:15755608-15755658	SK-N-SH	brain:	n/a
40	chr21:15755608-15755658	NH-A	brain:	n/a
41	chr21:15755644-15755694	Hela-S3	cervix:	n/a
42	chr21:15755644-15755694	CMK	blood:	n/a
43	chr21:15755538-15755588	MCF-7	breast:	n/a
44	chr21:15756062-15756112	ovcar-3	ovarian:	n/a
45	chr21:15755608-15755658	HAEpiC	amniotic membrane:	n/a
46	chr21:15755606-15755656	GM12878	blood:	n/a
47	chr21:15752932-15752982	HRCEpiC	kidney:	n/a
48	chr21:15755706-15755756	AG10803	skin:	n/a
49	chr21:15755449-15755499	MCF-7	breast:	n/a
50	chr21:15752932-15752982	GM12878	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15725447..15727391-chr21:15735609..15737943,2	K562	blood:
2	chr21:15738236..15741206-chr21:15753262..15755404,2	K562	blood:
3	chr21:15740980..15743787-chr21:15748039..15750871,3	K562	blood:
4	chr21:15725447..15727391-chr21:15735609..15737943,2	K562	blood:
5	chr21:15759229..15762199-chr21:15825176..15826732,2	K562	blood:
6	chr21:15738341..15740358-chr21:15745168..15748188,3	MCF-7	breast:
7	chr21:15738236..15741507-chr21:15753904..15757362,3	K562	blood:
8	chr21:15741032..15742950-chr21:15746679..15748662,2	MCF-7	breast:
9	chr21:15764391..15766947-chr21:15768713..15771374,3	K562	blood:
10	chr21:15750689..15753216-chr21:15754882..15756987,2	MCF-7	breast:
11	chr21:15709976..15712134-chr21:15731857..15734703,2	K562	blood:
12	chr21:15754842..15757143-chr21:15757991..15759672,2	MCF-7	breast:
13	chr21:15751469..15753501-chr21:15755651..15758117,2	K562	blood:
14	chr21:15725007..15727450-chr21:15727478..15730890,3	K562	blood:
15	chr21:15733160..15735734-chr21:15743714..15745323,2	K562	blood:
16	chr21:15732454..15736809-chr21:15737344..15740819,4	K562	blood:
17	chr21:15753622..15756331-chr21:15761576..15764249,2	MCF-7	breast:
18	chr21:15733246..15736908-chr21:15755835..15758351,3	K562	blood:
19	chr21:15721000..15722814-chr21:15730165..15732273,2	K562	blood:
20	chr21:15738341..15740358-chr21:15745168..15748188,3	MCF-7	breast:
21	chr12:56122664..56123207-chr21:15755194..15755994,2	Hela-S3	cervix:
22	chr21:15755923..15757812-chr21:16863949..16865497,2	K562	blood:
23	chr21:15748798..15750660-chr21:15754088..15755961,2	K562	blood:
24	chr21:15733160..15735734-chr21:15743714..15745323,2	K562	blood:
25	chr21:15739043..15741032-chr21:15755736..15757362,2	K562	blood:
26	chr21:15761527..15763962-chr21:15764673..15767332,2	K562	blood:
27	chr21:15732454..15736809-chr21:15737344..15740819,4	K562	blood:
28	chr21:15754870..15757296-chr21:16435942..16438083,2	K562	blood:
29	chr21:15738717..15742131-chr21:15743462..15746963,4	K562	blood:
30	chr21:15733062..15735967-chr21:15740026..15741975,2	MCF-7	breast:
31	chr21:15740980..15743787-chr21:15748039..15750871,3	K562	blood:
32	chr21:15738717..15742131-chr21:15743462..15746963,4	K562	blood:
33	chr21:15755528..15756150-chr5:33440838..33441550,2	Hela-S3	cervix:
34	chr21:15638970..15641725-chr21:15734559..15736787,2	K562	blood:
35	chr21:15645251..15647400-chr21:15754351..15756122,2	K562	blood:
36	chr21:15757559..15759154-chr21:16437032..16438993,2	K562	blood:
37	chr21:15750287..15752845-chr21:15753558..15756230,2	MCF-7	breast:
38	chr21:15761527..15763962-chr21:15764673..15767332,2	K562	blood:
39	chr11:65265638..65266483-chr21:15738427..15738927,2	NB4	blood:
40	chr21:15733062..15735967-chr21:15740026..15741975,2	MCF-7	breast:
41	chr21:15743793..15747020-chr21:15754018..15757060,4	K562	blood:
42	chr21:15725007..15727450-chr21:15727478..15730890,3	K562	blood:
43	chr21:15741032..15742950-chr21:15746679..15748662,2	MCF-7	breast:
44	chr21:15733246..15736908-chr21:15755835..15758351,3	K562	blood:
45	chr21:15738236..15741206-chr21:15753262..15755404,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-1	chr21:15764891-15764967	ENSG00000242342
2	lnc-RBM11-1	chr21:15765643-15765753	ENSG00000242342

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HSPA13	hsa-miR-590-3p	chr21:15745175-15745195
2	HSPA13	hsa-miR-374b-5p	chr21:15745406-15745427
3	HSPA13	hsa-miR-374b-5p	chr21:15743825-15743845
4	HSPA13	hsa-miR-590-3p	chr21:15743537-15743557
5	HSPA13	hsa-miR-181a-5p	chr21:15744415-15744438
6	HSPA13	hsa-miR-374b-5p	chr21:15744626-15744647
7	HSPA13	hsa-miR-590-3p	chr21:15745703-15745724
8	HSPA13	hsa-miR-590-3p	chr21:15743724-15743744

Variant related genes	Relation type
HSPA13	TF binding region
HSPA13	CpG island
ENSG00000113407	chromatin interactions
ENSG00000258056	chromatin interactions
ENSG00000180530	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000243064	chromatin interactions
ENSG00000135404	chromatin interactions
ENSG00000155304	chromatin interactions

Extended variants
information (count: 1387 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187185823	chr21:15725610-15725611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2205254	chr21:15725642-15725643	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544123969	chr21:15725657-15725658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141024831	chr21:15725694-15725695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113998430	chr21:15725702-15725703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540323978	chr21:15725722-15725723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79439970	chr21:15725733-15725734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559784664	chr21:15725734-15725735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs398101490	chr21:15725735-15725736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528894066	chr21:15725739-15725740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536268012	chr21:15725744-15725745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571045596	chr21:15725746-15725747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373563631	chr21:15725805-15725806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532024385	chr21:15725819-15725820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2822618	chr21:15725868-15725869	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs571815528	chr21:15725885-15725886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376667576	chr21:15725933-15725934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527853374	chr21:15725987-15725988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547884642	chr21:15725996-15725997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs13048016	chr21:15726002-15726003	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs536672107	chr21:15726093-15726094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190119533	chr21:15726134-15726135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73157759	chr21:15726155-15726156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2822619	chr21:15726161-15726162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs199684367	chr21:15726173-15726174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113953828	chr21:15726193-15726194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200806659	chr21:15726299-15726300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538150688	chr21:15726404-15726405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557718946	chr21:15726412-15726413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577787519	chr21:15726439-15726440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540041895	chr21:15726443-15726444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs8127673	chr21:15726466-15726467	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs573400627	chr21:15726486-15726487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141833220	chr21:15726506-15726507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199772145	chr21:15726522-15726523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150329079	chr21:15726527-15726528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562154334	chr21:15726539-15726540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182742837	chr21:15726551-15726552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373638725	chr21:15726559-15726560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188719630	chr21:15726581-15726582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs118029338	chr21:15729024-15729025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551058448	chr21:15729025-15729026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76266107	chr21:15729042-15729043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534654572	chr21:15729114-15729115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142110937	chr21:15729198-15729199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2223050	chr21:15729200-15729201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs537349626	chr21:15729224-15729225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145824641	chr21:15729284-15729285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376472593	chr21:15729300-15729301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577383405	chr21:15729323-15729324	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Sudden cardiac death	19188705	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
Breast cancer	20409316	CNVD
Autism	18414403	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15725600-15726600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr21:15725800-15726000	Enhancers	Fetal Stomach	stomach
3	chr21:15726000-15726400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
4	chr21:15729000-15729400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr21:15729000-15729600	Enhancers	HMEC	breast
6	chr21:15729000-15729600	Enhancers	NHEK	skin
7	chr21:15729200-15729600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr21:15729200-15729600	Enhancers	Esophagus	oesophagus
9	chr21:15729400-15730000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr21:15729400-15730400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr21:15729600-15731000	Weak transcription	HMEC	breast
12	chr21:15729600-15731000	Weak transcription	NHEK	skin
13	chr21:15729600-15733600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr21:15730400-15731600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr21:15730800-15731600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr21:15730800-15731600	Enhancers	Hela-S3	cervix
17	chr21:15731000-15731400	Enhancers	NHEK	skin
18	chr21:15731000-15731600	Enhancers	HMEC	breast
19	chr21:15731200-15731400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr21:15731200-15731400	Enhancers	HUVEC	blood vessel
21	chr21:15731400-15733600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr21:15731400-15733600	Weak transcription	NHEK	skin
23	chr21:15731600-15733400	Weak transcription	HMEC	breast
24	chr21:15731600-15733600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr21:15731600-15733600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr21:15731600-15734400	Weak transcription	HUVEC	blood vessel
27	chr21:15731600-15744800	Weak transcription	Hela-S3	cervix
28	chr21:15733400-15734600	Enhancers	HMEC	breast
29	chr21:15733600-15734400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr21:15733600-15734400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr21:15733600-15734600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr21:15733600-15734600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr21:15733600-15735200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr21:15733600-15735200	Enhancers	NHEK	skin
35	chr21:15733800-15734600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr21:15733800-15734800	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr21:15734000-15734600	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr21:15734200-15734800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr21:15734400-15734600	Enhancers	HUVEC	blood vessel
40	chr21:15734400-15745600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr21:15734600-15735000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr21:15734600-15735000	Weak transcription	HMEC	breast
43	chr21:15734600-15739200	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr21:15734600-15744800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr21:15734600-15744800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr21:15734600-15745400	Weak transcription	HUVEC	blood vessel
47	chr21:15734800-15739200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr21:15734800-15745400	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr21:15735000-15735200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr21:15735000-15735200	Enhancers	HMEC	breast

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