Variant report

Variant	nsv1035197
Chromosome Location	chr10:52446582-52622349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1259)
CpG islands
(count:1159)
Chromatin interactive
region (count:34)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1259 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52591874-52592317	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:52568206-52568638	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:52592773-52592774	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:52609900-52610100	K562	blood:	n/a	n/a
5	ATF1	chr10:52499751-52500379	K562	blood:	n/a	n/a
6	ATF2	chr10:52499576-52499831	GM12878	blood:	n/a	n/a
7	ATF2	chr10:52499272-52499770	GM12878	blood:	n/a	n/a
8	ATF3	chr10:52499803-52500110	K562	blood:	n/a	n/a
9	BACH1	chr10:52499491-52499981	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:52568322-52568541	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr10:52483591-52483970	GM12878	blood:	n/a	n/a
12	BATF	chr10:52464232-52464555	GM12878	blood:	n/a	n/a
13	BATF	chr10:52500151-52500419	GM12878	blood:	n/a	chr10:52500262-52500272
14	BATF	chr10:52528646-52528833	GM12878	blood:	n/a	chr10:52528772-52528783
15	BATF	chr10:52464214-52464440	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:52483588-52483995	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:52483579-52483874	GM12878	blood:	n/a	n/a
18	BCLAF1	chr10:52499532-52500122	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:52499519-52500222	K562	blood:	n/a	n/a
20	BHLHE40	chr10:52568224-52568499	HepG2	liver:	n/a	n/a
21	BRCA1	chr10:52593658-52593791	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr10:52457565-52457966	K562	blood:	n/a	n/a
23	CBX3	chr10:52610297-52610637	HCT-116	colon:	n/a	n/a
24	CBX3	chr10:52499171-52500475	K562	blood:	n/a	chr10:52499590-52499601
25	CBX3	chr10:52606499-52606981	HCT-116	colon:	n/a	n/a
26	CBX3	chr10:52499234-52500020	K562	blood:	n/a	chr10:52499590-52499601
27	CBX3	chr10:52461543-52462022	K562	blood:	n/a	n/a
28	CBX3	chr10:52609447-52610233	HCT-116	colon:	n/a	n/a
29	CCNT2	chr10:52499496-52499855	K562	blood:	n/a	n/a
30	CEBPB	chr10:52537035-52537243	A549	lung:	n/a	chr10:52537079-52537088 chr10:52537077-52537088 chr10:52537079-52537088 chr10:52537077-52537090 chr10:52537079-52537088 chr10:52537079-52537088
31	CEBPB	chr10:52537035-52537246	K562	blood:	n/a	chr10:52537079-52537088 chr10:52537077-52537088 chr10:52537079-52537088 chr10:52537077-52537090 chr10:52537079-52537088 chr10:52537079-52537088
32	CEBPB	chr10:52615287-52615479	HepG2	liver:	n/a	chr10:52615379-52615390 chr10:52615352-52615365
33	CEBPB	chr10:52475848-52476130	HepG2	liver:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
34	CEBPB	chr10:52475866-52476066	K562	blood:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
35	CEBPB	chr10:52537037-52537245	IMR90	lung:	n/a	chr10:52537079-52537088 chr10:52537077-52537088 chr10:52537079-52537088 chr10:52537077-52537090 chr10:52537079-52537088 chr10:52537079-52537088
36	CEBPB	chr10:52583036-52583253	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:52609472-52609711	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr10:52475847-52476153	A549	lung:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
39	CEBPB	chr10:52539924-52540176	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:52559196-52559199	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr10:52493265-52493366	Hela-S3	cervix:	n/a	chr10:52493296-52493307 chr10:52493273-52493284
42	CEBPB	chr10:52609212-52610317	HCT-116	colon:	n/a	chr10:52610186-52610197
43	CEBPB	chr10:52615359-52615463	A549	lung:	n/a	chr10:52615379-52615390
44	CEBPB	chr10:52475853-52476055	IMR90	lung:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
45	CEBPB	chr10:52589976-52590143	HepG2	liver:	n/a	chr10:52590025-52590036
46	CEBPB	chr10:52568157-52568539	HepG2	liver:	n/a	n/a
47	CEBPB	chr10:52609465-52609700	A549	lung:	n/a	n/a
48	CEBPB	chr10:52585695-52585982	HepG2	liver:	n/a	chr10:52585876-52585887
49	CEBPB	chr10:52609399-52609737	A549	lung:	n/a	n/a
50	CEBPB	chr10:52568153-52568547	HepG2	liver:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52499888-52499938	GM12891	blood:	n/a
2	chr10:52600370-52600420	PrEC	prostate:	n/a
3	chr10:52499562-52499612	HIPEpiC	eye:	n/a
4	chr10:52487619-52487669	BJ	skin:	n/a
5	chr10:52500089-52500139	AG04450	lung:	fetal
6	chr10:52500089-52500139	HCF	heart:	n/a
7	chr10:52500020-52500070	SAEC	small airway:	n/a
8	chr10:52498929-52498979	ProgFib	skin:	n/a
9	chr10:52566320-52566370	HCPEpiC	choroid plexus:	n/a
10	chr10:52498929-52498979	AG04450	lung:	fetal
11	chr10:52500187-52500237	NHBE	bronchial:	n/a
12	chr10:52500187-52500237	T-47D	breast:	n/a
13	chr10:52508516-52508566	ProgFib	skin:	n/a
14	chr10:52487619-52487669	T-47D	breast:	n/a
15	chr10:52499562-52499612	T-47D	breast:	n/a
16	chr10:52487693-52487743	NB4	blood:	n/a
17	chr10:52612019-52612069	NH-A	brain:	n/a
18	chr10:52500020-52500070	HRE	kidney:	n/a
19	chr10:52499888-52499938	Jurkat	blood:	n/a
20	chr10:52499562-52499612	SKMC	muscle:	n/a
21	chr10:52487693-52487743	GM06990	blood:	n/a
22	chr10:52499568-52499618	NHBE	bronchial:	n/a
23	chr10:52487693-52487743	AG09309	skin:	n/a
24	chr10:52600370-52600420	CMK	blood:	n/a
25	chr10:52499571-52499621	T-47D	breast:	n/a
26	chr10:52500020-52500070	SK-N-MC	brain:	n/a
27	chr10:52500187-52500237	AG09309	skin:	n/a
28	chr10:52487619-52487669	RPTEC	kidney:	n/a
29	chr10:52499562-52499612	HCM	heart:	n/a
30	chr10:52496341-52496391	HCM	heart:	n/a
31	chr10:52498929-52498979	NT2-D1	testis:	n/a
32	chr10:52487693-52487743	RPTEC	kidney:	n/a
33	chr10:52487619-52487669	HRCEpiC	kidney:	n/a
34	chr10:52487619-52487669	HAEpiC	amniotic membrane:	n/a
35	chr10:52499393-52499443	HRE	kidney:	n/a
36	chr10:52499888-52499938	HL-60	blood:	n/a
37	chr10:52612019-52612069	HIPEpiC	eye:	n/a
38	chr10:52499562-52499612	HCPEpiC	choroid plexus:	n/a
39	chr10:52500020-52500070	T-47D	breast:	n/a
40	chr10:52500425-52500475	NHDF-neo	bronchial:	n/a
41	chr10:52500425-52500475	NH-A	brain:	n/a
42	chr10:52500020-52500070	HCPEpiC	choroid plexus:	n/a
43	chr10:52566320-52566370	AoSMC	blood vessel:	n/a
44	chr10:52612019-52612069	AG09319	gingival:	n/a
45	chr10:52566320-52566370	HCT-116	colon:	n/a
46	chr10:52499571-52499621	SK-N-SH_RA	brain:	n/a
47	chr10:52499888-52499938	PrEC	prostate:	n/a
48	chr10:52498929-52498979	HEEpiC	esophagus:	n/a
49	chr10:52499571-52499621	ovcar-3	ovarian:	n/a
50	chr10:52499747-52499797	Hela-S3	cervix:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:52596553..52598355-chr10:52599614..52601320,2	MCF-7	breast:
2	chr10:52613650..52616242-chr10:52616525..52618352,2	K562	blood:
3	chr10:52476123..52479908-chr10:52500945..52503926,3	K562	blood:
4	chr10:52553280..52555784-chr10:52575135..52577429,2	K562	blood:
5	chr10:52473460..52475005-chr10:52487754..52490480,2	K562	blood:
6	chr10:52560442..52563105-chr10:52574617..52576331,2	K562	blood:
7	chr10:52560442..52563105-chr10:52574617..52576331,2	K562	blood:
8	chr10:52568068..52571258-chr10:52571525..52575297,5	K562	blood:
9	chr10:52382538..52386733-chr10:52497918..52501112,4	MCF-7	breast:
10	chr10:52579245..52582235-chr10:52611318..52613230,2	K562	blood:
11	chr10:52568484..52571195-chr10:52609335..52611357,3	K562	blood:
12	chr10:52553366..52555784-chr10:52575135..52576660,2	K562	blood:
13	chr10:52548941..52549489-chr10:52650690..52651378,2	MCF-7	breast:
14	chr10:52579245..52582235-chr10:52611318..52613230,2	K562	blood:
15	chr10:52489655..52491941-chr10:52496784..52498508,2	K562	blood:
16	chr10:52596553..52598355-chr10:52599614..52601320,2	MCF-7	breast:
17	chr10:52553366..52555784-chr10:52575135..52576660,2	K562	blood:
18	chr10:52569217..52570756-chr10:52572677..52575297,2	K562	blood:
19	chr10:52568484..52571195-chr10:52609335..52611357,3	K562	blood:
20	chr10:52383161..52385801-chr10:52551039..52553128,2	K562	blood:
21	chr10:52603109..52605010-chr10:52608525..52610040,2	K562	blood:
22	chr10:52548462..52549320-chr10:52748178..52748838,2	MCF-7	breast:
23	chr10:52573478..52574380-chr9:83098647..83099182,2	MCF-7	breast:
24	chr10:52489655..52491941-chr10:52496784..52498508,2	K562	blood:
25	chr10:52495633..52497465-chr10:52497957..52500428,2	K562	blood:
26	chr10:52569217..52570756-chr10:52572677..52575297,2	K562	blood:
27	chr10:52476123..52479908-chr10:52500945..52503926,3	K562	blood:
28	chr10:52568068..52571258-chr10:52571525..52575297,5	K562	blood:
29	chr10:52553280..52555784-chr10:52575135..52577429,2	K562	blood:
30	chr10:52494752..52497133-chr10:52497800..52500428,2	K562	blood:
31	chr10:52603109..52605010-chr10:52608525..52610040,2	K562	blood:
32	chr10:52473460..52475005-chr10:52487754..52490480,2	K562	blood:
33	chr10:52548632..52549305-chr10:52650692..52651261,3	MCF-7	breast:
34	chr10:52613650..52616242-chr10:52616525..52618352,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SGMS1-1	chr10:52582452-52582744	ENSG00000229711.1
2	lnc-SGMS1-1	chr10:52583253-52583355	ENSG00000229711.1
3	lnc-A1CF-4	chr10:52559793-52562438	NONHSAT013400
4	lnc-SGMS1-1	chr10:52584231-52584285	ENSG00000229711.1
5	lnc-SGMS1-1	chr10:52583738-52583922	ENSG00000229711.1
6	lnc-ASAH2B-5	chr10:52455352-52455741	NONHSAT013397
7	lnc-A1CF-4	chr10:52562445-52565728	NONHSAT013400

No data

Variant related genes	Relation type
A1CF	TF binding region
PGGT1BP1	TF binding region
ENSG00000226168	TF binding region
ENSG00000229711	TF binding region
ASAH2B	TF binding region
CTSLP4	TF binding region
A1CF	CpG island
PGGT1BP1	CpG island
ENSG00000226168	CpG island
ENSG00000229711	CpG island
ASAH2B	CpG island
CTSLP4	CpG island
ENSG00000204147	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000198964	chromatin interactions

Extended variants
information (count: 4146 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4146 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3011759	chr10:52446582-52446583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs3011760	chr10:52446587-52446588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547386227	chr10:52446598-52446599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11006672	chr10:52446618-52446619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs182636301	chr10:52446624-52446625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11006673	chr10:52446659-52446660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs569828928	chr10:52446680-52446681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10763618	chr10:52446697-52446698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78898715	chr10:52446700-52446701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571546742	chr10:52446702-52446703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138711130	chr10:52446703-52446704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79437657	chr10:52446704-52446705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186682116	chr10:52446712-52446713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534701177	chr10:52446721-52446722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529173589	chr10:52446729-52446730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577756104	chr10:52446734-52446735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11006676	chr10:52446757-52446758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192528825	chr10:52446774-52446775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111451972	chr10:52446778-52446779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531289971	chr10:52446794-52446795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542822414	chr10:52446834-52446835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560019156	chr10:52446835-52446836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12254074	chr10:52446864-52446865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74198236	chr10:52446908-52446909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3011761	chr10:52446919-52446920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs533104438	chr10:52446984-52446985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111959621	chr10:52447032-52447033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184757049	chr10:52447045-52447046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187868621	chr10:52447074-52447075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552777847	chr10:52447084-52447085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548875952	chr10:52447085-52447086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565647347	chr10:52447086-52447087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534595828	chr10:52447102-52447103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557778069	chr10:52447135-52447136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571286335	chr10:52447151-52447152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56363004	chr10:52447163-52447164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs557446066	chr10:52447221-52447222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs193002160	chr10:52447234-52447235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547154079	chr10:52447247-52447248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs118153352	chr10:52447294-52447295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10763619	chr10:52447295-52447296	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs56213111	chr10:52447307-52447308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs397699454	chr10:52447308-52447309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545711450	chr10:52447334-52447335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367584439	chr10:52447342-52447343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564097168	chr10:52447350-52447351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2495531	chr10:52447367-52447368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185202643	chr10:52447397-52447398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543016616	chr10:52447428-52447429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563418827	chr10:52447580-52447581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52435000-52452400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:52438200-52462000	Weak transcription	Spleen	Spleen
3	chr10:52458200-52458600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:52458200-52461200	Weak transcription	Hela-S3	cervix
5	chr10:52459200-52459400	Enhancers	K562	blood
6	chr10:52459400-52460800	Weak transcription	K562	blood
7	chr10:52460800-52461600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr10:52460800-52462400	Enhancers	K562	blood
9	chr10:52461200-52462200	Enhancers	Hela-S3	cervix
10	chr10:52461400-52462200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr10:52461400-52462200	Enhancers	HMEC	breast
12	chr10:52461400-52462200	Enhancers	HUVEC	blood vessel
13	chr10:52461800-52462200	Enhancers	NHEK	skin
14	chr10:52462000-52462200	Enhancers	Spleen	Spleen
15	chr10:52483200-52484200	Enhancers	GM12878-XiMat	blood
16	chr10:52485000-52485600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:52487800-52488000	Bivalent Enhancer	K562	blood
18	chr10:52488000-52488200	Enhancers	K562	blood
19	chr10:52492800-52493000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr10:52493000-52493200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:52493200-52493800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr10:52498200-52498800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr10:52498200-52499000	Enhancers	Primary T cells fromperipheralblood	blood
24	chr10:52498400-52499000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr10:52498600-52499000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr10:52498800-52499000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr10:52498800-52499000	Enhancers	Primary B cells from peripheral blood	blood
28	chr10:52498800-52499000	Enhancers	Primary T cells from cord blood	blood
29	chr10:52498800-52499000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr10:52498800-52499000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr10:52498800-52499000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr10:52498800-52499000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr10:52498800-52499000	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr10:52498800-52499000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr10:52498800-52499000	Bivalent Enhancer	Fetal Muscle Leg	muscle
36	chr10:52498800-52499000	Enhancers	Fetal Stomach	stomach
37	chr10:52498800-52499000	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr10:52498800-52499000	Enhancers	HepG2	liver
39	chr10:52498800-52499200	Enhancers	Gastric	stomach
40	chr10:52498800-52499200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr10:52498800-52499400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr10:52498800-52500600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr10:52498800-52500600	Active TSS	HSMM	muscle
44	chr10:52498800-52500800	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr10:52499000-52499200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr10:52499000-52499200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr10:52499000-52499200	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
48	chr10:52499000-52499200	Enhancers	Primary hematopoietic stem cells	blood
49	chr10:52499000-52499200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr10:52499000-52499200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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