Variant report

Variant	nsv544374
Chromosome Location	chr21:15624517-15656011
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:545)
CpG islands
(count:488)
Chromatin interactive
region (count:23)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15636185-15636385	K562	blood:	n/a	n/a
2	ARID3A	chr21:15643398-15643769	K562	blood:	n/a	n/a
3	ARID3A	chr21:15632038-15632466	K562	blood:	n/a	n/a
4	ARID3A	chr21:15632046-15632350	HepG2	liver:	n/a	n/a
5	ATF1	chr21:15636259-15636544	K562	blood:	n/a	n/a
6	ATF1	chr21:15643368-15643726	K562	blood:	n/a	n/a
7	ATF3	chr21:15636281-15636574	K562	blood:	n/a	n/a
8	BACH1	chr21:15632039-15632366	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr21:15646763-15647064	K562	blood:	n/a	chr21:15646984-15646993 chr21:15646984-15646993 chr21:15646983-15646992
10	BHLHE40	chr21:15646075-15646422	K562	blood:	n/a	n/a
11	BHLHE40	chr21:15646919-15647015	HepG2	liver:	n/a	chr21:15646984-15646993 chr21:15646984-15646993 chr21:15646983-15646992
12	BHLHE40	chr21:15626679-15626685	GM12878	blood:	n/a	n/a
13	BHLHE40	chr21:15643413-15643717	K562	blood:	n/a	n/a
14	BRCA1	chr21:15633651-15633671	GM12878	blood:	n/a	n/a
15	CBX3	chr21:15646066-15646407	K562	blood:	n/a	n/a
16	CCNT2	chr21:15646221-15646874	K562	blood:	n/a	n/a
17	CCNT2	chr21:15643026-15643838	K562	blood:	n/a	chr21:15643572-15643592
18	CEBPB	chr21:15636263-15636492	K562	blood:	n/a	n/a
19	CEBPB	chr21:15647260-15647457	H1-hESC	embryonic stem cell:	n/a	chr21:15647385-15647398
20	CEBPB	chr21:15643370-15643730	K562	blood:	n/a	chr21:15643550-15643567
21	CEBPB	chr21:15644175-15644343	K562	blood:	n/a	chr21:15644246-15644259
22	CEBPB	chr21:15643304-15643758	K562	blood:	n/a	chr21:15643550-15643567
23	CEBPB	chr21:15647225-15647548	K562	blood:	n/a	chr21:15647385-15647398
24	CEBPD	chr21:15643312-15643807	K562	blood:	n/a	n/a
25	CEBPD	chr21:15643245-15643803	K562	blood:	n/a	n/a
26	CREB1	chr21:15643385-15643755	K562	blood:	n/a	n/a
27	CREB1	chr21:15643320-15643834	K562	blood:	n/a	n/a
28	CTCF	chr21:15632140-15632290	HUVEC	blood vessel:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
29	CTCF	chr21:15626220-15626370	GM12875	blood:	n/a	n/a
30	CTCF	chr21:15632100-15632250	SAEC	small airway:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
31	CTCF	chr21:15632120-15632270	GM12867	blood:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
32	CTCF	chr21:15625971-15626272	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr21:15632140-15632290	AG04450	lung:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
34	CTCF	chr21:15626017-15626191	GM13976	blood:	n/a	n/a
35	CTCF	chr21:15625996-15626197	GM10248	blood:	n/a	n/a
36	CTCF	chr21:15632093-15632306	LNCaP	prostate:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
37	CTCF	chr21:15626020-15626170	HMF	breast:	n/a	n/a
38	CTCF	chr21:15632100-15632250	NHLF	lung:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
39	CTCF	chr21:15626020-15626170	AG04449	skin:	n/a	n/a
40	CTCF	chr21:15626020-15626170	HepG2	liver:	n/a	n/a
41	CTCF	chr21:15626060-15626210	HVMF	connective:	n/a	n/a
42	CTCF	chr21:15631960-15632110	GM12870	blood:	n/a	n/a
43	CTCF	chr21:15632120-15632270	HEK293	kidney:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
44	CTCF	chr21:15631860-15632010	SAEC	small airway:	n/a	n/a
45	CTCF	chr21:15625980-15626130	K562	blood:	n/a	n/a
46	CTCF	chr21:15626040-15626190	GM12864	blood:	n/a	n/a
47	CTCF	chr21:15632160-15632310	GM12868	blood:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
48	CTCF	chr21:15632160-15632310	K562	blood:	n/a	chr21:15632190-15632211 chr21:15632188-15632206 chr21:15632191-15632204 chr21:15632189-15632205
49	CTCF	chr21:15631680-15631830	NHLF	lung:	n/a	n/a
50	CTCF	chr21:15626060-15626210	HEK293	kidney:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15645810-15645860	Jurkat	blood:	n/a
2	chr21:15645988-15646038	GM12891	blood:	n/a
3	chr21:15646635-15646685	NH-A	brain:	n/a
4	chr21:15645649-15645699	Jurkat	blood:	n/a
5	chr21:15646312-15646362	SK-N-MC	brain:	n/a
6	chr21:15645988-15646038	AG10803	skin:	n/a
7	chr21:15646187-15646237	AG09309	skin:	n/a
8	chr21:15645988-15646038	MCF-7	breast:	n/a
9	chr21:15645649-15645699	HPAEpiC	pulmonary alveolar:	n/a
10	chr21:15646635-15646685	H1-hESC	embryonic stem cell:	embryo
11	chr21:15646187-15646237	NHDF-neo	bronchial:	n/a
12	chr21:15646312-15646362	HRPEpiC	eye:	n/a
13	chr21:15647368-15647418	PANC-1	pancreas:	n/a
14	chr21:15646187-15646237	AG04450	lung:	fetal
15	chr21:15645988-15646038	Jurkat	blood:	n/a
16	chr21:15645787-15645837	U87	brain:	n/a
17	chr21:15646312-15646362	PFSK-1	brain:	n/a
18	chr21:15645787-15645837	HPAEpiC	pulmonary alveolar:	n/a
19	chr21:15645988-15646038	Hepatocyte	liver:	n/a
20	chr21:15646187-15646237	Hela-S3	cervix:	n/a
21	chr21:15646312-15646362	AG09309	skin:	n/a
22	chr21:15645787-15645837	NT2-D1	testis:	n/a
23	chr21:15646635-15646685	HCM	heart:	n/a
24	chr21:15645787-15645837	GM12892	blood:	n/a
25	chr21:15645787-15645837	Hepatocyte	liver:	n/a
26	chr21:15645810-15645860	BJ	skin:	n/a
27	chr21:15647368-15647418	MCF10A-Er-Src	breast:	n/a
28	chr21:15647368-15647418	HRCEpiC	kidney:	n/a
29	chr21:15646312-15646362	AG04449	skin:	fetal
30	chr21:15646635-15646685	ECC-1	luminal epithelium:	n/a
31	chr21:15647368-15647418	T-47D	breast:	n/a
32	chr21:15645810-15645860	U87	brain:	n/a
33	chr21:15647368-15647418	GM19239	blood:	n/a
34	chr21:15646312-15646362	HAEpiC	amniotic membrane:	n/a
35	chr21:15647368-15647418	HNPCEpiC	eye:	n/a
36	chr21:15645988-15646038	T-47D	breast:	n/a
37	chr21:15646187-15646237	HMEC	breast:	n/a
38	chr21:15645988-15646038	A549	lung:	n/a
39	chr21:15645988-15646038	HUVEC	blood vessel:	n/a
40	chr21:15645787-15645837	ECC-1	luminal epithelium:	n/a
41	chr21:15645988-15646038	GM12892	blood:	n/a
42	chr21:15646187-15646237	GM19239	blood:	n/a
43	chr21:15645649-15645699	HCF	heart:	n/a
44	chr21:15645988-15646038	HEEpiC	esophagus:	n/a
45	chr21:15645810-15645860	A549	lung:	n/a
46	chr21:15645988-15646038	NHBE	bronchial:	n/a
47	chr21:15645649-15645699	HRCEpiC	kidney:	n/a
48	chr21:15645988-15646038	Hela-S3	cervix:	n/a
49	chr21:15646312-15646362	Caco-2	colon:	n/a
50	chr21:15645988-15646038	AG04450	lung:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15618985..15621962-chr21:15624169..15625950,3	K562	blood:
2	chr21:15652023..15652746-chr7:152811109..152812098,2	MCF-7	breast:
3	chr21:15652280..15654566-chr21:15773386..15776181,2	MCF-7	breast:
4	chr21:15637216..15639622-chr21:15681292..15683772,2	MCF-7	breast:
5	chr21:15646421..15649560-chr21:15654356..15655933,3	K562	blood:
6	chr21:15645251..15647400-chr21:15754351..15756122,2	K562	blood:
7	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:
8	chr21:15616597..15618358-chr21:15624634..15626645,2	K562	blood:
9	chr21:15650981..15652853-chr21:15655632..15658875,3	K562	blood:
10	chr21:15637824..15639860-chr21:15661262..15662859,2	MCF-7	breast:
11	chr21:15642588..15643376-chr21:15678270..15679084,2	MCF-7	breast:
12	chr21:15637737..15639634-chr21:15641854..15644729,2	K562	blood:
13	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:
14	chr21:15646421..15649560-chr21:15654356..15655933,3	K562	blood:
15	chr21:15642588..15643574-chr21:15678270..15679033,2	MCF-7	breast:
16	chr21:15650981..15652853-chr21:15655632..15658875,3	K562	blood:
17	chr21:15637737..15639634-chr21:15641854..15644729,2	K562	blood:
18	chr21:15644504..15646965-chr21:15652945..15655779,2	K562	blood:
19	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:
20	chr21:15646214..15647824-chr21:15649237..15651559,2	MCF-7	breast:
21	chr21:15638970..15641725-chr21:15734559..15736787,2	K562	blood:
22	chr21:15647599..15649902-chr21:15656709..15659445,2	K562	blood:
23	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081156
2	lnc-RBM11-5	chr21:15640724-15640913	NONHSAT081153
3	lnc-RBM11-5	chr21:15641808-15641980	NONHSAT081153
4	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081153
5	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081156
6	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081154
7	lnc-RBM11-5	chr21:15642846-15642930	NONHSAT081153
8	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081154

No data

Variant related genes	Relation type
ABCC13	TF binding region
ABCC13	CpG island
ENSG00000155304	chromatin interactions
ENSG00000243064	chromatin interactions

Extended variants
information (count: 1412 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1412 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540881414	chr21:15624578-15624579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560762578	chr21:15624579-15624580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529868907	chr21:15624599-15624600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543227433	chr21:15624601-15624602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563429011	chr21:15624646-15624647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2822511	chr21:15624647-15624648	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs185613316	chr21:15624648-15624649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139501460	chr21:15624685-15624686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75551826	chr21:15624742-15624743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114572122	chr21:15624747-15624748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145478017	chr21:15624748-15624749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189383288	chr21:15624767-15624768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548866665	chr21:15624772-15624773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568583249	chr21:15624774-15624775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537679805	chr21:15624777-15624778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550879516	chr21:15624809-15624810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528288375	chr21:15624815-15624816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570968695	chr21:15624885-15624886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148821292	chr21:15624895-15624896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552953779	chr21:15624911-15624912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572863167	chr21:15624967-15624968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548552654	chr21:15624973-15624974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10222083	chr21:15624975-15624976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145321552	chr21:15624979-15624980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180968058	chr21:15625017-15625018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568369307	chr21:15625026-15625027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574626890	chr21:15625061-15625062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530795636	chr21:15625096-15625097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368309628	chr21:15625117-15625118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543640508	chr21:15625131-15625132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56686645	chr21:15625139-15625140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs576874551	chr21:15625154-15625155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs405396	chr21:15625180-15625181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs58050746	chr21:15625191-15625192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59480822	chr21:15625192-15625193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559407552	chr21:15625228-15625229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs414651	chr21:15625241-15625242	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs548187362	chr21:15625242-15625243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562440258	chr21:15625257-15625258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531104388	chr21:15625337-15625338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551205147	chr21:15625359-15625360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570911320	chr21:15625406-15625407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs454346	chr21:15625422-15625423	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546659857	chr21:15625467-15625468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534892068	chr21:15625515-15625516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554703050	chr21:15625534-15625535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142175984	chr21:15625577-15625578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535488166	chr21:15625596-15625597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555464345	chr21:15625624-15625625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575044930	chr21:15625661-15625662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15623400-15626000	Weak transcription	Brain Substantia Nigra	brain
2	chr21:15624000-15625000	Enhancers	Brain Hippocampus Middle	brain
3	chr21:15624200-15625400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr21:15624400-15626000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr21:15625400-15625800	Enhancers	Duodenum Smooth Muscle	Duodenum
6	chr21:15625400-15626400	Enhancers	Brain Cingulate Gyrus	brain
7	chr21:15626000-15626200	Active TSS	Primary T helper cells PMA-I stimulated	--
8	chr21:15626000-15626200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr21:15626000-15626200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr21:15626000-15626200	Active TSS	Brain Substantia Nigra	brain
11	chr21:15626000-15626200	Active TSS	Skeletal Muscle Female	skeletal muscle
12	chr21:15626000-15626200	Active TSS	Dnd41	blood
13	chr21:15626000-15626200	Active TSS	Monocytes-CD14+_RO01746	blood
14	chr21:15626000-15626400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr21:15626000-15626400	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr21:15626000-15626400	Active TSS	Skeletal Muscle Male	skeletal muscle
17	chr21:15626000-15626800	Enhancers	Duodenum Mucosa	Duodenum
18	chr21:15626200-15626400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr21:15626200-15626400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr21:15626200-15626400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr21:15626200-15626400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr21:15626200-15626400	Enhancers	Primary T cells from cord blood	blood
23	chr21:15626200-15626400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
24	chr21:15626200-15626400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr21:15626200-15626400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
26	chr21:15626200-15626400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
27	chr21:15626200-15626400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
28	chr21:15626200-15626400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
29	chr21:15626200-15626400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr21:15626200-15626400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr21:15626200-15626400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr21:15626200-15626400	Enhancers	Adipose Nuclei	Adipose
33	chr21:15626200-15626400	Flanking Active TSS	Liver	Liver
34	chr21:15626200-15626400	Enhancers	Brain Anterior Caudate	brain
35	chr21:15626200-15626400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr21:15626200-15626400	Flanking Active TSS	Brain Substantia Nigra	brain
37	chr21:15626200-15626400	Enhancers	Fetal Muscle Leg	muscle
38	chr21:15626200-15626400	Flanking Active TSS	Ovary	ovary
39	chr21:15626200-15626400	Enhancers	Pancreas	Pancrea
40	chr21:15626200-15626400	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr21:15626200-15626400	Enhancers	Right Atrium	heart
42	chr21:15626200-15626400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr21:15626200-15626400	Flanking Active TSS	Dnd41	blood
44	chr21:15626200-15626400	Enhancers	Hela-S3	cervix
45	chr21:15626200-15626400	Enhancers	HUVEC	blood vessel
46	chr21:15626200-15626400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr21:15626200-15626600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr21:15626200-15626600	Enhancers	Colon Smooth Muscle	Colon
49	chr21:15626200-15626600	Enhancers	Fetal Brain Male	brain
50	chr21:15626200-15626600	Enhancers	Fetal Lung	lung

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