Variant report

Variant	nsv8660
Chromosome Location	chr10:52328259-52346278
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:616)
CpG islands
(count:122)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52331690-52332242	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:52334069-52334485	K562	blood:	n/a	n/a
3	ARID3A	chr10:52336811-52338299	K562	blood:	n/a	n/a
4	ARID3A	chr10:52336324-52336374	K562	blood:	n/a	n/a
5	ARID3A	chr10:52342572-52343135	K562	blood:	n/a	n/a
6	ARID3A	chr10:52339275-52340080	K562	blood:	n/a	n/a
7	ARID3A	chr10:52334786-52335470	K562	blood:	n/a	n/a
8	ARID3A	chr10:52345577-52345762	K562	blood:	n/a	n/a
9	ATF1	chr10:52337408-52337934	K562	blood:	n/a	n/a
10	ATF1	chr10:52335441-52335481	K562	blood:	n/a	n/a
11	ATF1	chr10:52346212-52346616	K562	blood:	n/a	n/a
12	ATF1	chr10:52342536-52343457	K562	blood:	n/a	n/a
13	ATF3	chr10:52337417-52337950	K562	blood:	n/a	n/a
14	ATF3	chr10:52343084-52343380	K562	blood:	n/a	n/a
15	ATF3	chr10:52343104-52343599	K562	blood:	n/a	n/a
16	BACH1	chr10:52337537-52337914	K562	blood:	n/a	n/a
17	BACH1	chr10:52342593-52342712	K562	blood:	n/a	n/a
18	BCLAF1	chr10:52337422-52338026	K562	blood:	n/a	n/a
19	BCLAF1	chr10:52337238-52338019	K562	blood:	n/a	n/a
20	BHLHE40	chr10:52339283-52340032	K562	blood:	n/a	n/a
21	BHLHE40	chr10:52336767-52338178	K562	blood:	n/a	n/a
22	BHLHE40	chr10:52342481-52343477	K562	blood:	n/a	n/a
23	BHLHE40	chr10:52345958-52346690	K562	blood:	n/a	n/a
24	BHLHE40	chr10:52335819-52336534	K562	blood:	n/a	chr10:52336343-52336364 chr10:52336348-52336357
25	BRCA1	chr10:52346019-52346655	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr10:52345962-52346743	HCT-116	colon:	n/a	n/a
27	CBX3	chr10:52337329-52338095	K562	blood:	n/a	n/a
28	CBX3	chr10:52343043-52343595	K562	blood:	n/a	n/a
29	CBX3	chr10:52346002-52346614	K562	blood:	n/a	n/a
30	CBX3	chr10:52337374-52338049	K562	blood:	n/a	n/a
31	CBX3	chr10:52345999-52346700	HCT-116	colon:	n/a	n/a
32	CCNT2	chr10:52337039-52337999	K562	blood:	n/a	n/a
33	CEBPB	chr10:52337434-52337828	K562	blood:	n/a	n/a
34	CEBPB	chr10:52346182-52346672	A549	lung:	n/a	n/a
35	CEBPB	chr10:52340385-52340774	K562	blood:	n/a	chr10:52340597-52340608
36	CEBPB	chr10:52331770-52332150	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr10:52337537-52337836	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:52346248-52346724	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr10:52340512-52340689	K562	blood:	n/a	chr10:52340597-52340608
40	CEBPB	chr10:52346278-52346673	K562	blood:	n/a	n/a
41	CEBPB	chr10:52331633-52332165	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:52337204-52338017	K562	blood:	n/a	n/a
43	CEBPB	chr10:52331716-52332040	K562	blood:	n/a	n/a
44	CEBPB	chr10:52346207-52346689	K562	blood:	n/a	n/a
45	CEBPB	chr10:52331629-52332111	K562	blood:	n/a	n/a
46	CEBPB	chr10:52331643-52332247	HepG2	liver:	n/a	n/a
47	CEBPB	chr10:52331660-52332214	K562	blood:	n/a	n/a
48	CEBPB	chr10:52346020-52346901	HCT-116	colon:	n/a	n/a
49	CEBPB	chr10:52340449-52340693	A549	lung:	n/a	chr10:52340597-52340608
50	CEBPB	chr10:52340449-52340751	HepG2	liver:	n/a	chr10:52340597-52340608

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52340628-52340678	BE2_C	brain:	n/a
2	chr10:52336353-52336403	Hepatocyte	liver:	n/a
3	chr10:52336353-52336403	AG04449	skin:	fetal
4	chr10:52340628-52340678	HCT-116	colon:	n/a
5	chr10:52336353-52336403	PFSK-1	brain:	n/a
6	chr10:52336353-52336403	BE2_C	brain:	n/a
7	chr10:52336353-52336403	HUVEC	blood vessel:	n/a
8	chr10:52336353-52336403	NB4	blood:	n/a
9	chr10:52340628-52340678	GM12892	blood:	n/a
10	chr10:52336353-52336403	SK-N-SH	brain:	n/a
11	chr10:52340628-52340678	Caco-2	colon:	n/a
12	chr10:52336353-52336403	NH-A	brain:	n/a
13	chr10:52340628-52340678	IMR90	lung:	fetal
14	chr10:52340628-52340678	NHBE	bronchial:	n/a
15	chr10:52340628-52340678	Hepatocyte	liver:	n/a
16	chr10:52340628-52340678	HIPEpiC	eye:	n/a
17	chr10:52340628-52340678	NHDF-neo	bronchial:	n/a
18	chr10:52336353-52336403	IMR90	lung:	fetal
19	chr10:52336353-52336403	HCPEpiC	choroid plexus:	n/a
20	chr10:52340628-52340678	SK-N-MC	brain:	n/a
21	chr10:52336353-52336403	GM12878	blood:	n/a
22	chr10:52340628-52340678	AoSMC	blood vessel:	n/a
23	chr10:52340628-52340678	A549	lung:	n/a
24	chr10:52336353-52336403	NHBE	bronchial:	n/a
25	chr10:52340628-52340678	HRE	kidney:	n/a
26	chr10:52336353-52336403	A549	lung:	n/a
27	chr10:52336353-52336403	HEK293	kidney:	embryo
28	chr10:52336353-52336403	HepG2	liver:	n/a
29	chr10:52336353-52336403	HL-60	blood:	n/a
30	chr10:52340628-52340678	HCPEpiC	choroid plexus:	n/a
31	chr10:52336353-52336403	HNPCEpiC	eye:	n/a
32	chr10:52340628-52340678	T-47D	breast:	n/a
33	chr10:52340628-52340678	H1-hESC	embryonic stem cell:	embryo
34	chr10:52340628-52340678	HRPEpiC	eye:	n/a
35	chr10:52336353-52336403	H1-hESC	embryonic stem cell:	embryo
36	chr10:52336353-52336403	HCT-116	colon:	n/a
37	chr10:52340628-52340678	U87	brain:	n/a
38	chr10:52340628-52340678	GM19239	blood:	n/a
39	chr10:52336353-52336403	BJ	skin:	n/a
40	chr10:52340628-52340678	ProgFib	skin:	n/a
41	chr10:52340628-52340678	SK-N-SH	brain:	n/a
42	chr10:52336353-52336403	HEEpiC	esophagus:	n/a
43	chr10:52336353-52336403	AG09319	gingival:	n/a
44	chr10:52336353-52336403	NHDF-neo	bronchial:	n/a
45	chr10:52340628-52340678	HRCEpiC	kidney:	n/a
46	chr10:52340628-52340678	ECC-1	luminal epithelium:	n/a
47	chr10:52340628-52340678	HEK293	kidney:	embryo
48	chr10:52340628-52340678	HL-60	blood:	n/a
49	chr10:52336353-52336403	HCF	heart:	n/a
50	chr10:52340628-52340678	Hela-S3	cervix:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:52322894..52324648-chr10:52337430..52339164,2	K562	blood:
2	chr10:52342133..52345402-chr10:52352257..52355042,3	MCF-7	breast:
3	chr10:52324915..52329170-chr10:52337236..52340296,3	K562	blood:
4	chr10:52305032..52307353-chr10:52341275..52344217,2	K562	blood:
5	chr10:52337504..52339571-chr10:52355930..52358209,2	K562	blood:
6	chr10:52337504..52344093-chr10:52356709..52361052,9	K562	blood:
7	chr10:52319893..52329540-chr10:52377624..52388129,20	MCF-7	breast:
8	chr10:52331050..52332991-chr10:52337513..52339073,2	K562	blood:
9	chr10:52328331..52329887-chr10:52343313..52346143,2	K562	blood:
10	chr10:52339840..52341425-chr10:52350029..52352294,2	K562	blood:
11	chr10:52337416..52340160-chr10:52383643..52385478,2	MCF-7	breast:
12	chr10:52346124..52348507-chr10:52350618..52352666,3	K562	blood:
13	chr10:52331050..52332991-chr10:52337513..52339073,2	K562	blood:
14	chr10:52340909..52343314-chr10:52378678..52381107,3	K562	blood:
15	chr10:52317228..52319701-chr10:52328035..52331029,3	K562	blood:
16	chr10:52333380..52335821-chr10:52336012..52337715,2	K562	blood:
17	chr10:52337499..52341708-chr10:52345297..52349387,5	K562	blood:
18	chr10:52323633..52328946-chr10:52382781..52388541,7	K562	blood:
19	chr10:52330729..52340229-chr10:52381715..52386294,12	K562	blood:
20	chr10:52331558..52333625-chr10:52337015..52339577,2	MCF-7	breast:
21	chr10:52335825..52337405-chr10:52342195..52344591,2	K562	blood:
22	chr10:52342227..52348125-chr10:52381237..52386507,8	K562	blood:
23	chr10:52335825..52337405-chr10:52342195..52344591,2	K562	blood:
24	chr10:52331777..52334924-chr10:52380252..52384970,6	MCF-7	breast:
25	chr10:52340514..52343109-chr10:52378678..52380936,3	K562	blood:
26	chr10:52331103..52333638-chr10:52341359..52343782,2	K562	blood:
27	chr10:52333380..52335821-chr10:52336012..52337715,2	K562	blood:
28	chr10:52334364..52340801-chr10:52380166..52385556,10	K562	blood:
29	chr10:52331103..52333638-chr10:52341359..52343782,2	K562	blood:
30	chr10:52342059..52344112-chr10:52362150..52364434,3	K562	blood:
31	chr10:52345136..52347979-chr10:52349121..52350897,2	MCF-7	breast:
32	chr10:52324915..52329170-chr10:52335171..52340296,4	K562	blood:
33	chr10:52336198..52337725-chr10:52386422..52388764,2	K562	blood:
34	chr10:52331558..52333625-chr10:52337015..52339577,2	MCF-7	breast:
35	chr10:52342671..52345197-chr10:52362617..52364673,2	MCF-7	breast:
36	chr10:52324915..52329170-chr10:52337236..52340296,3	K562	blood:
37	chr10:52335773..52337467-chr10:52361237..52363170,2	K562	blood:
38	chr10:52343264..52344901-chr10:52348884..52350629,3	K562	blood:
39	chr10:52336186..52338969-chr10:52390237..52392466,2	K562	blood:
40	chr10:52310656..52316983-chr10:52334408..52339466,9	K562	blood:
41	chr10:52331790..52334326-chr10:52382272..52386294,4	K562	blood:
42	chr10:52343887..52348125-chr10:52383719..52386062,5	K562	blood:
43	chr10:52313555..52316104-chr10:52337795..52339466,2	K562	blood:
44	chr10:52311229..52315083-chr10:52335257..52337670,4	K562	blood:
45	chr10:52318973..52324648-chr10:52334040..52339164,5	K562	blood:
46	chr10:52335913..52338170-chr10:52340995..52342949,2	MCF-7	breast:
47	chr10:52340715..52342372-chr10:52372792..52375032,2	MCF-7	breast:
48	chr10:52338053..52345279-chr10:52380666..52386211,11	MCF-7	breast:
49	chr10:52335913..52338170-chr10:52340995..52342949,2	MCF-7	breast:
50	chr10:52324915..52329170-chr10:52335171..52340296,4	K562	blood:

No data

Variant related genes	Relation type
RMRPP4	TF binding region
RMRPP4	CpG island
ENSG00000198964	chromatin interactions
ENSG00000251950	chromatin interactions
ENSG00000238523	chromatin interactions
ENSG00000231588	chromatin interactions
ENSG00000226200	chromatin interactions

Extended variants
information (count: 604 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572013998	chr10:52328263-52328264	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs11006160	chr10:52328430-52328431	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs564188660	chr10:52328439-52328440	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535640816	chr10:52328447-52328448	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs373950118	chr10:52328455-52328456	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs371470575	chr10:52328466-52328467	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs548167279	chr10:52328473-52328474	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs549885868	chr10:52328491-52328492	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs563500807	chr10:52328526-52328527	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs529073754	chr10:52328589-52328590	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs549299045	chr10:52328595-52328596	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs572479284	chr10:52328614-52328615	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs565795938	chr10:52328615-52328616	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs535020715	chr10:52328638-52328639	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs533657593	chr10:52328641-52328642	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs551334391	chr10:52328711-52328712	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs148367810	chr10:52328760-52328761	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs568163581	chr10:52328761-52328762	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs112480663	chr10:52328766-52328767	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs557015514	chr10:52328794-52328795	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs141587173	chr10:52328824-52328825	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs150811855	chr10:52328854-52328855	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs553629241	chr10:52328873-52328874	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs573427005	chr10:52328910-52328911	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs536719354	chr10:52328911-52328912	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs11006161	chr10:52328934-52328935	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556744285	chr10:52328956-52328957	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs145394173	chr10:52328959-52328960	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs543588851	chr10:52328962-52328963	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs543742596	chr10:52329026-52329027	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs561791431	chr10:52329033-52329034	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs373748949	chr10:52329059-52329060	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs72066798	chr10:52329060-52329061	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs61433452	chr10:52329077-52329078	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs183812265	chr10:52329092-52329093	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs576543324	chr10:52329147-52329148	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs12262564	chr10:52329187-52329188	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs147266905	chr10:52329203-52329204	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs547244263	chr10:52329204-52329205	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs559622551	chr10:52329214-52329215	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs140853090	chr10:52329281-52329282	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs188733853	chr10:52329335-52329336	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551248320	chr10:52329336-52329337	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs571337400	chr10:52329359-52329360	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs538986920	chr10:52329371-52329372	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539134403	chr10:52329456-52329457	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs550706014	chr10:52329457-52329458	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs567602631	chr10:52329461-52329462	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs190534852	chr10:52329510-52329511	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs558818869	chr10:52329607-52329608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD

Chromatin state (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52305400-52329600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr10:52306000-52331800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr10:52308000-52337200	Weak transcription	Primary T cells from cord blood	blood
4	chr10:52311000-52335800	Weak transcription	Esophagus	oesophagus
5	chr10:52312800-52335800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:52312800-52335800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr10:52313200-52333200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr10:52313600-52337400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr10:52315000-52329600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr10:52315200-52337400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr10:52315600-52336000	Weak transcription	GM12878-XiMat	blood
12	chr10:52316400-52331800	Weak transcription	Lung	lung
13	chr10:52316800-52332000	Weak transcription	Aorta	Aorta
14	chr10:52316800-52332600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr10:52318200-52331800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr10:52318400-52329600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr10:52319200-52335800	Weak transcription	Spleen	Spleen
18	chr10:52319600-52335600	Weak transcription	NHEK	skin
19	chr10:52321600-52335600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr10:52321800-52331600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:52321800-52331600	Weak transcription	Psoas Muscle	Psoas
22	chr10:52321800-52335600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr10:52321800-52335600	Weak transcription	Adipose Nuclei	Adipose
24	chr10:52322000-52330200	Weak transcription	Hela-S3	cervix
25	chr10:52322000-52331000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:52322000-52335800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr10:52322000-52337200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:52322000-52348600	Weak transcription	Fetal Stomach	stomach
29	chr10:52322200-52335600	Weak transcription	NHLF	lung
30	chr10:52322800-52333800	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr10:52322800-52335600	Weak transcription	Fetal Lung	lung
32	chr10:52322800-52336000	Weak transcription	Placenta	Placenta
33	chr10:52324000-52329200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr10:52324000-52331800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:52324000-52336600	Weak transcription	Thymus	Thymus
36	chr10:52324000-52337400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr10:52324200-52329600	Weak transcription	Fetal Intestine Large	intestine
38	chr10:52324400-52330400	Weak transcription	Fetal Intestine Small	intestine
39	chr10:52324400-52331800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr10:52324400-52336800	Weak transcription	Primary B cells from cord blood	blood
41	chr10:52324400-52336800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr10:52325400-52336000	Weak transcription	Stomach Mucosa	stomach
43	chr10:52325600-52328400	Enhancers	Brain Anterior Caudate	brain
44	chr10:52325600-52331800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr10:52325800-52331000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr10:52325800-52331800	Weak transcription	Gastric	stomach
47	chr10:52325800-52331800	Weak transcription	Left Ventricle	heart
48	chr10:52325800-52331800	Weak transcription	Ovary	ovary
49	chr10:52325800-52331800	Weak transcription	Right Atrium	heart
50	chr10:52325800-52335200	Weak transcription	Right Ventricle	heart

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