Variant report

Variant	nsv1059591
Chromosome Location	chr21:15835325-15969195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1851)
CpG islands
(count:61)
Chromatin interactive
region (count:152)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1851 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15879542-15879724	K562	blood:	n/a	n/a
2	ARID3A	chr21:15900823-15901417	K562	blood:	n/a	n/a
3	ARID3A	chr21:15954023-15954811	K562	blood:	n/a	n/a
4	ARID3A	chr21:15952116-15952196	K562	blood:	n/a	n/a
5	ARID3A	chr21:15920229-15920429	K562	blood:	n/a	n/a
6	ARID3A	chr21:15860343-15860727	K562	blood:	n/a	n/a
7	ARID3A	chr21:15918034-15918949	K562	blood:	n/a	n/a
8	ARID3A	chr21:15867403-15867905	K562	blood:	n/a	n/a
9	ARID3A	chr21:15945870-15945930	K562	blood:	n/a	n/a
10	ARID3A	chr21:15941879-15942072	K562	blood:	n/a	n/a
11	ARID3A	chr21:15962428-15962496	K562	blood:	n/a	n/a
12	ARID3A	chr21:15964200-15964470	K562	blood:	n/a	n/a
13	ARID3A	chr21:15955288-15957571	K562	blood:	n/a	n/a
14	ARID3A	chr21:15864283-15864314	K562	blood:	n/a	n/a
15	ARID3A	chr21:15907258-15907450	K562	blood:	n/a	n/a
16	ARID3A	chr21:15922657-15922941	K562	blood:	n/a	n/a
17	ARID3A	chr21:15921104-15921404	K562	blood:	n/a	n/a
18	ARID3A	chr21:15917206-15917215	K562	blood:	n/a	n/a
19	ARID3A	chr21:15913953-15914685	K562	blood:	n/a	n/a
20	ARID3A	chr21:15863823-15864036	K562	blood:	n/a	n/a
21	ARID3A	chr21:15916297-15916537	K562	blood:	n/a	n/a
22	ARID3A	chr21:15898648-15900165	K562	blood:	n/a	n/a
23	ARID3A	chr21:15915542-15916058	K562	blood:	n/a	n/a
24	ARID3A	chr21:15905866-15906701	K562	blood:	n/a	n/a
25	ARID3A	chr21:15948341-15948537	K562	blood:	n/a	n/a
26	ARID3A	chr21:15922300-15922396	K562	blood:	n/a	n/a
27	ATF1	chr21:15918475-15918878	K562	blood:	n/a	n/a
28	ATF1	chr21:15957026-15957461	K562	blood:	n/a	n/a
29	ATF1	chr21:15937557-15937915	K562	blood:	n/a	n/a
30	ATF1	chr21:15906176-15906571	K562	blood:	n/a	n/a
31	ATF2	chr21:15918292-15918991	GM12878	blood:	n/a	n/a
32	ATF2	chr21:15962106-15962556	GM12878	blood:	n/a	n/a
33	ATF2	chr21:15962120-15962574	GM12878	blood:	n/a	n/a
34	ATF2	chr21:15906051-15906824	GM12878	blood:	n/a	n/a
35	ATF2	chr21:15895437-15896021	GM12878	blood:	n/a	n/a
36	ATF2	chr21:15854378-15854908	GM12878	blood:	n/a	n/a
37	ATF2	chr21:15920084-15920815	GM12878	blood:	n/a	n/a
38	ATF2	chr21:15854334-15854968	GM12878	blood:	n/a	n/a
39	ATF2	chr21:15906055-15906924	GM12878	blood:	n/a	n/a
40	ATF2	chr21:15920092-15920756	GM12878	blood:	n/a	n/a
41	ATF2	chr21:15853089-15853541	GM12878	blood:	n/a	n/a
42	ATF3	chr21:15937541-15937885	K562	blood:	n/a	n/a
43	ATF3	chr21:15918358-15918889	K562	blood:	n/a	n/a
44	ATF3	chr21:15899447-15899839	GM12878	blood:	n/a	n/a
45	ATF3	chr21:15906194-15906673	K562	blood:	n/a	n/a
46	BACH1	chr21:15909350-15909434	K562	blood:	n/a	n/a
47	BACH1	chr21:15860270-15860682	K562	blood:	n/a	n/a
48	BACH1	chr21:15921741-15921941	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr21:15921610-15921978	K562	blood:	n/a	n/a
50	BACH1	chr21:15898648-15899278	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15914403-15914453	NT2-D1	testis:	n/a
2	chr21:15914403-15914453	ovcar-3	ovarian:	n/a
3	chr21:15914403-15914453	NHDF-neo	bronchial:	n/a
4	chr21:15914403-15914453	PFSK-1	brain:	n/a
5	chr21:15914403-15914453	ProgFib	skin:	n/a
6	chr21:15914403-15914453	HIPEpiC	eye:	n/a
7	chr21:15914403-15914453	PANC-1	pancreas:	n/a
8	chr21:15914403-15914453	HL-60	blood:	n/a
9	chr21:15914403-15914453	SKMC	muscle:	n/a
10	chr21:15914403-15914453	HNPCEpiC	eye:	n/a
11	chr21:15914403-15914453	ECC-1	luminal epithelium:	n/a
12	chr21:15914403-15914453	HCT-116	colon:	n/a
13	chr21:15914403-15914453	IMR90	lung:	fetal
14	chr21:15914403-15914453	GM12878	blood:	n/a
15	chr21:15914403-15914453	T-47D	breast:	n/a
16	chr21:15914403-15914453	HRE	kidney:	n/a
17	chr21:15914403-15914453	AG10803	skin:	n/a
18	chr21:15914403-15914453	MCF10A-Er-Src	breast:	n/a
19	chr21:15914403-15914453	K562	blood:	n/a
20	chr21:15914403-15914453	GM12891	blood:	n/a
21	chr21:15914403-15914453	GM12892	blood:	n/a
22	chr21:15914403-15914453	AG09309	skin:	n/a
23	chr21:15914403-15914453	Hepatocyte	liver:	n/a
24	chr21:15914403-15914453	CMK	blood:	n/a
25	chr21:15914403-15914453	SAEC	small airway:	n/a
26	chr21:15914403-15914453	A549	lung:	n/a
27	chr21:15914403-15914453	NHBE	bronchial:	n/a
28	chr21:15914403-15914453	BE2_C	brain:	n/a
29	chr21:15914403-15914453	AG04450	lung:	fetal
30	chr21:15914403-15914453	AG09319	gingival:	n/a
31	chr21:15914403-15914453	U87	brain:	n/a
32	chr21:15914403-15914453	HRPEpiC	eye:	n/a
33	chr21:15914403-15914453	HCF	heart:	n/a
34	chr21:15914403-15914453	HAEpiC	amniotic membrane:	n/a
35	chr21:15914403-15914453	PrEC	prostate:	n/a
36	chr21:15914403-15914453	BJ	skin:	n/a
37	chr21:15914403-15914453	HEEpiC	esophagus:	n/a
38	chr21:15914403-15914453	AG04449	skin:	fetal
39	chr21:15914403-15914453	HPAEpiC	pulmonary alveolar:	n/a
40	chr21:15914403-15914453	H1-hESC	embryonic stem cell:	embryo
41	chr21:15914403-15914453	HCPEpiC	choroid plexus:	n/a
42	chr21:15914403-15914453	NB4	blood:	n/a
43	chr21:15914403-15914453	SK-N-SH	brain:	n/a
44	chr21:15914403-15914453	HEK293	kidney:	embryo
45	chr21:15914403-15914453	LNCaP	prostate:	n/a
46	chr21:15914403-15914453	Caco-2	colon:	n/a
47	chr21:15914403-15914453	NH-A	brain:	n/a
48	chr21:15914403-15914453	HepG2	liver:	n/a
49	chr21:15914403-15914453	AoSMC	blood vessel:	n/a
50	chr21:15914403-15914453	Jurkat	blood:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr21:15863459..15867536-chr21:15871353..15874494,5	K562	blood:
2	chr20:57606873..57607444-chr21:15903062..15903984,2	MCF-7	breast:
3	chr21:15916866..15918516-chr21:16085549..16087908,2	K562	blood:
4	chr21:15904847..15906603-chr21:16029430..16031380,2	K562	blood:
5	chr21:15893314..15896057-chr21:15897268..15899492,2	K562	blood:
6	chr21:15900972..15903079-chr21:15904912..15907876,2	K562	blood:
7	chr21:15942194..15946580-chr21:15946989..15950349,5	K562	blood:
8	chr21:15878918..15881751-chr21:15882365..15886915,4	K562	blood:
9	chr21:15833864..15836238-chr21:15845488..15848019,2	K562	blood:
10	chr21:15905941..15908063-chr21:15951429..15954293,3	K562	blood:
11	chr21:15876554..15878638-chr21:15883430..15885143,2	K562	blood:
12	chr21:15912730..15916019-chr21:15916425..15919963,12	K562	blood:
13	chr21:15919365..15921468-chr21:16048127..16050377,2	K562	blood:
14	chr21:15870384..15874520-chr21:15900850..15905377,4	K562	blood:
15	chr21:15961455..15963973-chr21:15965969..15968617,3	K562	blood:
16	chr21:15953103..15955709-chr21:15961850..15965268,4	K562	blood:
17	chr21:15834401..15837014-chr21:15837761..15840673,3	K562	blood:
18	chr21:15842218..15844807-chr21:15848260..15850081,2	K562	blood:
19	chr21:15949855..15953983-chr21:15956777..15961120,5	K562	blood:
20	chr21:15962990..15965815-chr21:15973045..15978585,5	K562	blood:
21	chr21:15858969..15860796-chr21:15865823..15868637,2	MCF-7	breast:
22	chr21:15878918..15881751-chr21:15882365..15886915,4	K562	blood:
23	chr21:15888072..15891465-chr21:15894886..15898226,3	K562	blood:
24	chr21:15919672..15922192-chr21:15926866..15928968,2	K562	blood:
25	chr21:15862079..15863579-chr6:26301955..26303620,2	K562	blood:
26	chr21:15867966..15869641-chr21:15871722..15874223,2	K562	blood:
27	chr21:15882752..15884455-chr21:15884908..15886969,2	K562	blood:
28	chr21:15904288..15906853-chr21:15912996..15915455,2	K562	blood:
29	chr21:15863117..15865240-chr21:15875551..15877419,2	K562	blood:
30	chr21:15844220..15846274-chr21:15867274..15869149,2	K562	blood:
31	chr21:15944720..15947651-chr21:15950659..15952358,2	K562	blood:
32	chr21:15886516..15889058-chr21:15891380..15893121,2	K562	blood:
33	chr21:15882543..15884938-chr21:15891850..15893710,2	K562	blood:
34	chr21:15852372..15854683-chr21:15916871..15919423,2	K562	blood:
35	chr21:15882752..15884455-chr21:15884908..15886969,2	K562	blood:
36	chr21:15915978..15918625-chr21:15919465..15922478,3	K562	blood:
37	chr21:15860428..15863237-chr21:15863342..15865579,2	K562	blood:
38	chr21:15940693..15943113-chr21:15945415..15947276,2	K562	blood:
39	chr21:15833864..15836238-chr21:15845488..15848019,2	K562	blood:
40	chr21:15915915..15920125-chr21:15922754..15925442,5	K562	blood:
41	chr21:15919781..15923280-chr21:15954504..15956620,3	K562	blood:
42	chr21:15920671..15923360-chr21:15929340..15932218,2	K562	blood:
43	chr21:15834306..15836856-chr21:16111395..16113784,2	K562	blood:
44	chr21:15852608..15854130-chr21:15861560..15864028,2	K562	blood:
45	chr21:15839769..15841961-chr21:15842594..15844538,2	K562	blood:
46	chr21:15915303..15917955-chr21:15967480..15970218,2	K562	blood:
47	chr21:15870901..15873770-chr21:15873802..15877193,3	K562	blood:
48	chr21:15848828..15851671-chr21:15855558..15857437,2	MCF-7	breast:
49	chr21:15857773..15859999-chr21:15862087..15863944,2	K562	blood:
50	chr21:15857773..15859999-chr21:15862087..15863944,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-3	chr21:15957683-15957859	ENSG00000223662.1
2	lnc-AF165138.7.1-5	chr21:15921236-15921459	l_2170_chr21:15869459-15921459_brain
3	lnc-RBM11-3	chr21:15963643-15963789	ENSG00000223662.1
4	lnc-RBM11-3	chr21:15967015-15967061	ENSG00000223662.1
5	lnc-AF165138.7.1-4	chr21:15893494-15893542	NONHSAT081164
6	lnc-AF165138.7.1-5	chr21:15869460-15869600	l_2170_chr21:15869459-15921459_brain
7	lnc-AF165138.7.1-4	chr21:15895592-15895715	NONHSAT081164
8	lnc-RBM11-3	chr21:15954523-15954612	ENSG00000223662.1
9	lnc-AF165138.7.1-4	chr21:15918526-15918634	NONHSAT081164

No data

Variant related genes	Relation type
SAMSN1-AS1	TF binding region
SAMSN1	TF binding region
SAMSN1-AS1	CpG island
SAMSN1	CpG island
ENSG00000223662	chromatin interactions
ENSG00000228600	chromatin interactions
ENSG00000243440	chromatin interactions
ENSG00000155307	chromatin interactions
ENSG00000124172	chromatin interactions
ENSG00000232884	chromatin interactions

Extended variants
information (count: 5431 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:5431 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371496463	chr21:15836864-15836865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs80139048	chr21:15836867-15836868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536228596	chr21:15836878-15836879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368927908	chr21:15836954-15836955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372640526	chr21:15836957-15836958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546701891	chr21:15836975-15836976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560598334	chr21:15836994-15836995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150051242	chr21:15837214-15837215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551639490	chr21:15837240-15837241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541512610	chr21:15837241-15837242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146377911	chr21:15837259-15837260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370219982	chr21:15837260-15837261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200942318	chr21:15837267-15837268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78437689	chr21:15837333-15837334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571634502	chr21:15837341-15837342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190194667	chr21:15837364-15837365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75083972	chr21:15837402-15837403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573637221	chr21:15837415-15837416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535965673	chr21:15837417-15837418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556265624	chr21:15837420-15837421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576288502	chr21:15837428-15837429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545253127	chr21:15837436-15837437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565150891	chr21:15837471-15837472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145361613	chr21:15837473-15837474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540580046	chr21:15837488-15837489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560288870	chr21:15837538-15837539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62229750	chr21:15837578-15837579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs183437911	chr21:15837596-15837597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs57489910	chr21:15837618-15837619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs188372242	chr21:15837633-15837634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116996724	chr21:15837644-15837645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112881609	chr21:15837709-15837710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114352420	chr21:15837736-15837737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534229723	chr21:15837745-15837746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371002567	chr21:15837777-15837778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548117679	chr21:15837787-15837788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148763207	chr21:15837808-15837809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373495569	chr21:15837812-15837813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs62229751	chr21:15837825-15837826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs535695426	chr21:15837852-15837853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193022313	chr21:15837857-15837858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185200694	chr21:15837911-15837912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538803717	chr21:15837946-15837947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558794170	chr21:15837962-15837963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572257077	chr21:15837969-15837970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555079547	chr21:15837989-15837990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374107214	chr21:15838013-15838014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142393235	chr21:15838073-15838074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79492079	chr21:15838074-15838075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76649410	chr21:15838078-15838079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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	17122850	CNVD
XY gonadal dysgenesis	20685758	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1518 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15836800-15837000	Enhancers	K562	blood
2	chr21:15837200-15838600	Weak transcription	K562	blood
3	chr21:15838600-15839400	Enhancers	K562	blood
4	chr21:15838800-15839400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr21:15847800-15874800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr21:15849200-15849600	Enhancers	K562	blood
7	chr21:15849200-15854600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr21:15849600-15851800	Weak transcription	K562	blood
9	chr21:15849600-15854200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr21:15850200-15850400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr21:15850200-15850400	Enhancers	Brain Substantia Nigra	brain
12	chr21:15850200-15850400	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr21:15850200-15850800	Enhancers	Colon Smooth Muscle	Colon
14	chr21:15850400-15851800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr21:15850600-15851600	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr21:15850600-15853000	Weak transcription	Brain Substantia Nigra	brain
17	chr21:15850800-15851000	Enhancers	Brain Germinal Matrix	brain
18	chr21:15851000-15852000	Weak transcription	Brain Germinal Matrix	brain
19	chr21:15851000-15854800	Enhancers	Fetal Brain Male	brain
20	chr21:15851600-15853200	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr21:15851600-15856400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr21:15851800-15852000	Enhancers	Fetal Brain Female	brain
23	chr21:15851800-15852000	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr21:15851800-15855800	Enhancers	K562	blood
25	chr21:15852000-15852600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr21:15852000-15853000	Weak transcription	Fetal Brain Female	brain
27	chr21:15852000-15853400	Enhancers	Brain Germinal Matrix	brain
28	chr21:15852400-15860400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr21:15852600-15852800	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr21:15852600-15853000	Enhancers	Primary B cells from cord blood	blood
31	chr21:15852600-15853000	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr21:15852600-15855600	Enhancers	Primary hematopoietic stem cells	blood
33	chr21:15852800-15853000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr21:15852800-15853000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
35	chr21:15852800-15853200	Enhancers	Adipose Nuclei	Adipose
36	chr21:15852800-15853400	Enhancers	Stomach Smooth Muscle	stomach
37	chr21:15852800-15853400	Enhancers	HUVEC	blood vessel
38	chr21:15852800-15853800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr21:15852800-15854000	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr21:15852800-15854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr21:15852800-15854200	Enhancers	Fetal Stomach	stomach
42	chr21:15852800-15854400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr21:15853000-15853200	Enhancers	Brain Substantia Nigra	brain
44	chr21:15853000-15853200	Enhancers	GM12878-XiMat	blood
45	chr21:15853000-15853200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr21:15853000-15853400	Enhancers	Fetal Brain Female	brain
47	chr21:15853000-15853600	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr21:15853000-15853800	Enhancers	Brain Hippocampus Middle	brain
49	chr21:15853000-15853800	Enhancers	Fetal Muscle Leg	muscle
50	chr21:15853000-15854000	Weak transcription	Primary B cells from cord blood	blood

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