Variant report

Variant	nsv5521
Chromosome Location	chr10:986842-1031352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:580)
CpG islands
(count:976)
Chromatin interactive
region (count:114)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:1030018-1030553	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:1019922-1020290	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:1016027-1017475	HepG2	liver:	n/a	n/a
4	ATF2	chr10:1020013-1020380	GM12878	blood:	n/a	n/a
5	ATF2	chr10:1019961-1020367	GM12878	blood:	n/a	n/a
6	ATF3	chr10:1015490-1015684	K562	blood:	n/a	n/a
7	ATF3	chr10:1009570-1009894	K562	blood:	n/a	n/a
8	BACH1	chr10:1020093-1020177	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr10:1019992-1020322	GM12878	blood:	n/a	n/a
10	BATF	chr10:989748-990049	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:1020141-1020398	GM12878	blood:	n/a	chr10:1020236-1020245
12	BCL11A	chr10:1019946-1020339	GM12878	blood:	n/a	chr10:1019984-1019992 chr10:1020236-1020245
13	BCL3	chr10:1020022-1020432	GM12878	blood:	n/a	chr10:1020236-1020245
14	BHLHE40	chr10:1016187-1017356	HepG2	liver:	n/a	n/a
15	BHLHE40	chr10:990467-990813	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:990466-990731	K562	blood:	n/a	n/a
17	BHLHE40	chr10:1017670-1017832	K562	blood:	n/a	n/a
18	BHLHE40	chr10:995462-995623	K562	blood:	n/a	n/a
19	BHLHE40	chr10:1017618-1017989	HepG2	liver:	n/a	n/a
20	BHLHE40	chr10:1014440-1014729	K562	blood:	n/a	n/a
21	BHLHE40	chr10:1019571-1020585	GM12878	blood:	n/a	n/a
22	BHLHE40	chr10:1018772-1019068	GM12878	blood:	n/a	chr10:1019006-1019022
23	BHLHE40	chr10:1019884-1020287	HepG2	liver:	n/a	n/a
24	BRCA1	chr10:1029872-1030642	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr10:1020112-1020312	HepG2	liver:	n/a	n/a
26	CBX3	chr10:1026389-1026851	K562	blood:	n/a	n/a
27	CBX3	chr10:1024696-1025263	HCT-116	colon:	n/a	n/a
28	CBX3	chr10:1024732-1025187	K562	blood:	n/a	n/a
29	CBX3	chr10:1024697-1025191	K562	blood:	n/a	n/a
30	CBX3	chr10:1026443-1026801	K562	blood:	n/a	n/a
31	CBX3	chr10:1024671-1025246	HCT-116	colon:	n/a	n/a
32	CBX3	chr10:1009608-1009907	K562	blood:	n/a	n/a
33	CCNT2	chr10:1001902-1001966	K562	blood:	n/a	n/a
34	CEBPB	chr10:1009582-1009891	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:1022271-1023005	IMR90	lung:	n/a	chr10:1022451-1022462
36	CEBPB	chr10:1016084-1017587	MCF-7	breast:	n/a	chr10:1016926-1016937
37	CEBPB	chr10:1029958-1030627	IMR90	lung:	n/a	chr10:1030146-1030157
38	CEBPB	chr10:1029864-1030796	MCF-7	breast:	n/a	chr10:1030146-1030157
39	CEBPB	chr10:1015920-1017737	MCF-7	breast:	n/a	chr10:1016926-1016937
40	CEBPB	chr10:1015570-1015980	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr10:1008410-1008587	K562	blood:	n/a	chr10:1008536-1008547
42	CEBPB	chr10:1008351-1008707	K562	blood:	n/a	chr10:1008536-1008547
43	CEBPB	chr10:1015414-1016074	MCF-7	breast:	n/a	n/a
44	CEBPB	chr10:1017079-1017515	A549	lung:	n/a	n/a
45	CEBPB	chr10:1009588-1009955	K562	blood:	n/a	chr10:1009916-1009928 chr10:1009914-1009931
46	CEBPB	chr10:1016207-1016515	A549	lung:	n/a	n/a
47	CEBPB	chr10:1008355-1008715	IMR90	lung:	n/a	chr10:1008536-1008547
48	CEBPB	chr10:1016171-1017539	Hela-S3	cervix:	n/a	chr10:1016926-1016937
49	CEBPB	chr10:1008287-1008738	MCF-7	breast:	n/a	chr10:1008536-1008547
50	CEBPB	chr10:1015462-1015789	K562	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:1011142-1011192	RPTEC	kidney:	n/a
2	chr10:994943-994993	H1-hESC	embryonic stem cell:	embryo
3	chr10:995290-995340	HRE	kidney:	n/a
4	chr10:995290-995340	AG04449	skin:	fetal
5	chr10:1011248-1011298	PrEC	prostate:	n/a
6	chr10:1019787-1019837	GM12892	blood:	n/a
7	chr10:995290-995340	LNCaP	prostate:	n/a
8	chr10:1011248-1011298	Hela-S3	cervix:	n/a
9	chr10:1021712-1021762	NHBE	bronchial:	n/a
10	chr10:1025639-1025689	HCT-116	colon:	n/a
11	chr10:1019161-1019211	NHDF-neo	bronchial:	n/a
12	chr10:1011381-1011431	HPAEpiC	pulmonary alveolar:	n/a
13	chr10:1011142-1011192	MCF10A-Er-Src	breast:	n/a
14	chr10:1000300-1000350	AoSMC	blood vessel:	n/a
15	chr10:994943-994993	GM12878	blood:	n/a
16	chr10:1011381-1011431	AG04449	skin:	fetal
17	chr10:1021712-1021762	HMEC	breast:	n/a
18	chr10:994943-994993	HepG2	liver:	n/a
19	chr10:1019787-1019837	HEK293	kidney:	embryo
20	chr10:994943-994993	AG09319	gingival:	n/a
21	chr10:1019787-1019837	NHDF-neo	bronchial:	n/a
22	chr10:1025639-1025689	GM12878	blood:	n/a
23	chr10:1019026-1019076	K562	blood:	n/a
24	chr10:1021712-1021762	HRCEpiC	kidney:	n/a
25	chr10:1022108-1022158	GM12878	blood:	n/a
26	chr10:994943-994993	NT2-D1	testis:	n/a
27	chr10:1019787-1019837	HEEpiC	esophagus:	n/a
28	chr10:1022615-1022665	GM06990	blood:	n/a
29	chr10:1025639-1025689	GM19239	blood:	n/a
30	chr10:995290-995340	Hepatocyte	liver:	n/a
31	chr10:1000300-1000350	PFSK-1	brain:	n/a
32	chr10:1019026-1019076	Hela-S3	cervix:	n/a
33	chr10:1000300-1000350	Jurkat	blood:	n/a
34	chr10:1019026-1019076	MCF-7	breast:	n/a
35	chr10:1011381-1011431	SKMC	muscle:	n/a
36	chr10:1021712-1021762	LNCaP	prostate:	n/a
37	chr10:1019026-1019076	CMK	blood:	n/a
38	chr10:1019787-1019837	NB4	blood:	n/a
39	chr10:1011381-1011431	K562	blood:	n/a
40	chr10:1022615-1022665	HRPEpiC	eye:	n/a
41	chr10:995290-995340	GM06990	blood:	n/a
42	chr10:1019026-1019076	HAEpiC	amniotic membrane:	n/a
43	chr10:1025639-1025689	NH-A	brain:	n/a
44	chr10:995095-995145	BJ	skin:	n/a
45	chr10:1016695-1016745	NHDF-neo	bronchial:	n/a
46	chr10:995290-995340	BE2_C	brain:	n/a
47	chr10:1011248-1011298	ECC-1	luminal epithelium:	n/a
48	chr10:1022108-1022158	HRPEpiC	eye:	n/a
49	chr10:995095-995145	GM12892	blood:	n/a
50	chr10:1016695-1016745	AG09319	gingival:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:978959..981256-chr10:1013885..1016544,2	K562	blood:
2	chr10:975132..982582-chr10:1010670..1022073,17	MCF-7	breast:
3	chr10:1006827..1010625-chr10:1012447..1015815,4	K562	blood:
4	chr10:1015085..1016586-chr10:1048514..1051399,2	MCF-7	breast:
5	chr10:1009125..1012338-chr10:1015177..1017521,3	K562	blood:
6	chr10:1002020..1004924-chr10:1009202..1011501,2	MCF-7	breast:
7	chr10:983720..986820-chr10:989199..992227,3	MCF-7	breast:
8	chr10:1023937..1026356-chr10:1028602..1030529,2	K562	blood:
9	chr10:1000614..1004584-chr10:1019814..1022762,4	K562	blood:
10	chr10:1019010..1021511-chr10:1021947..1027823,6	MCF-7	breast:
11	chr10:1001054..1003663-chr10:1008457..1009991,2	MCF-7	breast:
12	chr10:990098..992111-chr10:1033029..1035814,2	MCF-7	breast:
13	chr10:1000614..1004584-chr10:1019814..1022470,3	K562	blood:
14	chr10:1015119..1019104-chr10:1032459..1035516,7	MCF-7	breast:
15	chr10:1024974..1028277-chr10:1028484..1030664,3	MCF-7	breast:
16	chr10:993234..997786-chr10:1013619..1016483,4	MCF-7	breast:
17	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
18	chr10:1019866..1021574-chr10:1021848..1023502,2	K562	blood:
19	chr10:1019866..1021574-chr10:1021848..1023502,2	K562	blood:
20	chr10:1006112..1009530-chr10:1011286..1014390,5	K562	blood:
21	chr10:1009444..1012343-chr10:1093261..1095095,2	MCF-7	breast:
22	chr10:1010243..1012883-chr10:1030629..1033582,2	K562	blood:
23	chr10:991162..993286-chr10:1002150..1004961,2	K562	blood:
24	chr10:1013251..1015818-chr10:1022738..1024636,2	K562	blood:
25	chr10:1014806..1016425-chr10:1022937..1025172,2	MCF-7	breast:
26	chr10:1028166..1030337-chr10:1039910..1042809,2	MCF-7	breast:
27	chr10:1015043..1019353-chr10:1030351..1034278,6	MCF-7	breast:
28	chr10:976263..979384-chr10:986596..991037,4	MCF-7	breast:
29	chr10:1030029..1032197-chr14:35022504..35024073,2	MCF-7	breast:
30	chr10:1002020..1004924-chr10:1009202..1011501,2	MCF-7	breast:
31	chr10:1017049..1018015-chr10:1034396..1035314,2	MCF-7	breast:
32	chr10:1006827..1010625-chr10:1012447..1015815,4	K562	blood:
33	chr10:1019761..1022243-chr10:1028840..1032476,4	MCF-7	breast:
34	chr10:995726..997603-chr10:1033507..1035656,2	K562	blood:
35	chr10:1018775..1022710-chr10:1032776..1036101,4	K562	blood:
36	chr10:987204..991340-chr10:993290..996064,4	MCF-7	breast:
37	chr10:1005925..1008895-chr10:1011879..1014677,2	MCF-7	breast:
38	chr10:975610..978082-chr10:1008022..1009914,3	K562	blood:
39	chr10:1019821..1022788-chr10:1029841..1033519,4	MCF-7	breast:
40	chr10:1009125..1012338-chr10:1015177..1017521,3	K562	blood:
41	chr10:986549..990201-chr10:1030700..1035554,4	K562	blood:
42	chr10:986490..989100-chr10:1016201..1018491,2	MCF-7	breast:
43	chr10:988532..990709-chr10:1000522..1003406,2	MCF-7	breast:
44	chr10:1011250..1013274-chr10:1018564..1020381,2	K562	blood:
45	chr10:974451..976397-chr10:1027362..1028867,2	MCF-7	breast:
46	chr10:983875..986452-chr10:1011606..1014374,2	K562	blood:
47	chr10:1020473..1022394-chr10:1030542..1032536,2	K562	blood:
48	chr10:1002935..1005856-chr10:1082299..1084442,2	MCF-7	breast:
49	chr10:1019010..1021511-chr10:1021947..1027823,6	MCF-7	breast:
50	chr10:1014659..1017574-chr10:1040488..1045906,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTPBP4-3	chr10:988127-988179	ENSG00000229869.1
2	lnc-GTPBP4-3	chr10:988420-988828	NONHSAT010883
3	lnc-GTPBP4-3	chr10:987882-988179	NONHSAT010883
4	lnc-GTPBP4-3	chr10:988420-988683	ENSG00000229869.1
5	lnc-LARP4B-2	chr10:988075-988179	NONHSAT010884
6	lnc-LARP4B-2	chr10:988421-988583	NONHSAT010884
7	lnc-AL359878.1-1	chr10:999388-1000122	NONHSAT010887
8	lnc-AL359878.1-1	chr10:997609-997718	NONHSAT010887

No data

Variant related genes	Relation type
GTPBP4	TF binding region
GTPBP4	CpG island
ENSG00000067064	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000107929	chromatin interactions
ENSG00000229869	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000205740	chromatin interactions

Extended variants
information (count: 1879 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1879 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563132333	chr10:986876-986877	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs76808619	chr10:986884-986885	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs548491580	chr10:986953-986954	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs188715851	chr10:986970-986971	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs527770573	chr10:986979-986980	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547801566	chr10:987044-987045	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs377576041	chr10:987071-987072	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs570537005	chr10:987108-987109	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs193222073	chr10:987203-987204	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs138757741	chr10:987247-987248	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs72360017	chr10:987248-987249	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs558439534	chr10:987251-987252	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs377664949	chr10:987271-987272	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs11253525	chr10:987274-987275	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183119193	chr10:987276-987277	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs575205496	chr10:987341-987342	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs12250052	chr10:987346-987347	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs574502092	chr10:987347-987348	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs370878420	chr10:987356-987357	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs539975569	chr10:987357-987358	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs111833197	chr10:987399-987400	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs553864894	chr10:987413-987414	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs576913972	chr10:987451-987452	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs374135045	chr10:987453-987454	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs116772519	chr10:987464-987465	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs542379110	chr10:987484-987485	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs531903621	chr10:987503-987504	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs542445483	chr10:987570-987571	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs139231685	chr10:987583-987584	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs10904587	chr10:987613-987614	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs547501254	chr10:987645-987646	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs556230475	chr10:987675-987676	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs564200393	chr10:987683-987684	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs533159491	chr10:987686-987687	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs549763356	chr10:987743-987744	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs187371434	chr10:987804-987805	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs537726385	chr10:987894-987895	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs548436751	chr10:988012-988013	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs568177422	chr10:988024-988025	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs113790047	chr10:988041-988042	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs11253526	chr10:988069-988070	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577009194	chr10:988082-988083	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs539479375	chr10:988101-988102	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs191822278	chr10:988106-988107	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs576703146	chr10:988122-988123	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs367844471	chr10:988135-988136	Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs559658654	chr10:988205-988206	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs542180367	chr10:988226-988227	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs562372743	chr10:988245-988246	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs370156822	chr10:988259-988260	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:985200-990200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr10:985400-990000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:985400-990400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr10:985600-989600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr10:985600-989600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:985600-989800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr10:985600-989800	Weak transcription	Spleen	Spleen
8	chr10:985600-990200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr10:985600-990200	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr10:985600-990400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:985800-990000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr10:985800-990200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr10:985800-990200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr10:985800-990200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr10:985800-990200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr10:985800-990400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr10:985800-990400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr10:986800-987000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:989200-989400	Enhancers	GM12878-XiMat	blood
20	chr10:989200-989600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr10:989400-990200	Enhancers	Duodenum Mucosa	Duodenum
22	chr10:989400-990600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr10:989400-990800	Flanking Active TSS	GM12878-XiMat	blood
24	chr10:989400-991000	Enhancers	Primary B cells from peripheral blood	blood
25	chr10:989600-989800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr10:989600-990000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr10:989600-990400	Enhancers	Primary hematopoietic stem cells	blood
28	chr10:989600-990600	Enhancers	Esophagus	oesophagus
29	chr10:989600-990800	Enhancers	Stomach Mucosa	stomach
30	chr10:989600-993400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr10:989800-990200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr10:989800-990200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr10:989800-990400	Bivalent Enhancer	HepG2	liver
34	chr10:989800-990600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr10:989800-990600	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr10:989800-990600	Enhancers	Spleen	Spleen
37	chr10:989800-990600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr10:990000-990200	Enhancers	Adipose Nuclei	Adipose
39	chr10:990000-990400	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr10:990000-990400	Enhancers	NHEK	skin
41	chr10:990000-990800	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr10:990000-990800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr10:990000-990800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr10:990200-990400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:990200-990400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr10:990200-990400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr10:990200-990400	Enhancers	Fetal Muscle Leg	muscle
48	chr10:990200-990400	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr10:990200-990400	Enhancers	HSMM	muscle
50	chr10:990200-990400	Enhancers	HUVEC	blood vessel

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