Variant report

Variant	nsv894971
Chromosome Location	chr10:25403234-25522280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:716)
CpG islands
(count:1773)
Chromatin interactive
region (count:20)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:25406696-25407027	K562	blood:	n/a	n/a
2	ATF1	chr10:25431525-25431673	K562	blood:	n/a	n/a
3	ATF1	chr10:25406738-25407087	K562	blood:	n/a	n/a
4	BACH1	chr10:25458727-25458927	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:25500358-25500446	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:25463336-25463625	K562	blood:	n/a	n/a
7	BACH1	chr10:25407028-25407185	K562	blood:	n/a	n/a
8	BACH1	chr10:25480141-25480448	K562	blood:	n/a	n/a
9	BACH1	chr10:25480123-25480456	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:25464776-25465136	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:25463233-25463835	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:25464157-25464315	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr10:25463540-25463727	K562	blood:	n/a	n/a
14	BHLHE40	chr10:25406706-25407126	K562	blood:	n/a	n/a
15	BHLHE40	chr10:25408207-25408351	K562	blood:	n/a	n/a
16	CBX3	chr10:25463376-25463764	K562	blood:	n/a	n/a
17	CEBPB	chr10:25487764-25488019	K562	blood:	n/a	n/a
18	CEBPB	chr10:25426882-25427094	A549	lung:	n/a	chr10:25426933-25426944
19	CEBPB	chr10:25430827-25431042	HepG2	liver:	n/a	chr10:25430915-25430926
20	CEBPB	chr10:25504201-25504527	HepG2	liver:	n/a	chr10:25504371-25504382
21	CEBPB	chr10:25426798-25427095	HepG2	liver:	n/a	chr10:25426933-25426944
22	CEBPB	chr10:25487690-25487896	A549	lung:	n/a	n/a
23	CEBPB	chr10:25426815-25427062	IMR90	lung:	n/a	chr10:25426933-25426944
24	CEBPB	chr10:25413363-25413417	K562	blood:	n/a	n/a
25	CEBPB	chr10:25469182-25469316	HepG2	liver:	n/a	chr10:25469261-25469272
26	CEBPB	chr10:25504311-25504511	K562	blood:	n/a	chr10:25504371-25504382
27	CEBPB	chr10:25504218-25504513	IMR90	lung:	n/a	chr10:25504371-25504382
28	CEBPB	chr10:25441695-25441706	K562	blood:	n/a	n/a
29	CEBPB	chr10:25522122-25522346	A549	lung:	n/a	chr10:25522233-25522244 chr10:25522235-25522244
30	CEBPB	chr10:25504195-25504515	A549	lung:	n/a	chr10:25504371-25504382
31	CEBPB	chr10:25413337-25413526	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:25522157-25522350	HepG2	liver:	n/a	chr10:25522233-25522244 chr10:25522235-25522244
33	CEBPB	chr10:25426826-25427085	K562	blood:	n/a	chr10:25426933-25426944
34	CEBPB	chr10:25431745-25431818	A549	lung:	n/a	n/a
35	CHD1	chr10:25463486-25464265	H1-hESC	embryonic stem cell:	n/a	chr10:25463853-25463863
36	CHD2	chr10:25463553-25463660	GM12878	blood:	n/a	n/a
37	CHD2	chr10:25464013-25464093	HepG2	liver:	n/a	n/a
38	CHD2	chr10:25463344-25463982	H1-hESC	embryonic stem cell:	n/a	chr10:25463853-25463863
39	CHD2	chr10:25425368-25425482	GM12878	blood:	n/a	n/a
40	CHD2	chr10:25463511-25463740	K562	blood:	n/a	n/a
41	CHD2	chr10:25463468-25463656	HepG2	liver:	n/a	n/a
42	CREB1	chr10:25463455-25463656	A549	lung:	n/a	n/a
43	CREB1	chr10:25463328-25464096	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr10:25431341-25431746	K562	blood:	n/a	n/a
45	CREB1	chr10:25463307-25463876	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr10:25463289-25463754	A549	lung:	n/a	n/a
47	CTBP2	chr10:25463326-25464241	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr10:25516100-25516250	HPF	lung:	n/a	chr10:25516200-25516218 chr10:25516201-25516217 chr10:25516195-25516216
49	CTCF	chr10:25516100-25516250	MCF-7	breast:	n/a	chr10:25516200-25516218 chr10:25516201-25516217 chr10:25516195-25516216
50	CTCF	chr10:25516076-25516388	HUVEC	blood vessel:	n/a	chr10:25516200-25516218 chr10:25516201-25516217 chr10:25516195-25516216

(count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:25460855-25460905	HEK293	kidney:	embryo
2	chr10:25464132-25464182	HUVEC	blood vessel:	n/a
3	chr10:25460855-25460905	GM12891	blood:	n/a
4	chr10:25460855-25460905	AG10803	skin:	n/a
5	chr10:25460855-25460905	HEK293	kidney:	embryo
6	chr10:25464132-25464182	HUVEC	blood vessel:	n/a
7	chr10:25460855-25460905	GM12891	blood:	n/a
8	chr10:25460855-25460905	AG10803	skin:	n/a
9	chr10:25464425-25464475	CMK	blood:	n/a
10	chr10:25466027-25466077	HRE	kidney:	n/a
11	chr10:25507161-25507211	AoSMC	blood vessel:	n/a
12	chr10:25464165-25464215	HepG2	liver:	n/a
13	chr10:25464513-25464563	SK-N-SH	brain:	n/a
14	chr10:25466027-25466077	SK-N-MC	brain:	n/a
15	chr10:25464132-25464182	T-47D	breast:	n/a
16	chr10:25465242-25465292	HRPEpiC	eye:	n/a
17	chr10:25464196-25464246	NHBE	bronchial:	n/a
18	chr10:25464513-25464563	HEK293	kidney:	embryo
19	chr10:25465219-25465269	HEK293	kidney:	embryo
20	chr10:25464513-25464563	AG04450	lung:	fetal
21	chr10:25464719-25464769	HMEC	breast:	n/a
22	chr10:25465242-25465292	NH-A	brain:	n/a
23	chr10:25464321-25464371	BE2_C	brain:	n/a
24	chr10:25465503-25465553	HMEC	breast:	n/a
25	chr10:25464184-25464234	Hela-S3	cervix:	n/a
26	chr10:25507202-25507252	Jurkat	blood:	n/a
27	chr10:25465352-25465402	HCT-116	colon:	n/a
28	chr10:25465242-25465292	H1-hESC	embryonic stem cell:	embryo
29	chr10:25468899-25468949	GM06990	blood:	n/a
30	chr10:25464059-25464109	HCF	heart:	n/a
31	chr10:25507202-25507252	SK-N-SH	brain:	n/a
32	chr10:25464139-25464189	MCF-7	breast:	n/a
33	chr10:25464513-25464563	AoSMC	blood vessel:	n/a
34	chr10:25464321-25464371	H1-hESC	embryonic stem cell:	embryo
35	chr10:25460855-25460905	Jurkat	blood:	n/a
36	chr10:25464719-25464769	AG04450	lung:	fetal
37	chr10:25466027-25466077	GM12892	blood:	n/a
38	chr10:25507202-25507252	HRPEpiC	eye:	n/a
39	chr10:25507099-25507149	GM19239	blood:	n/a
40	chr10:25464719-25464769	MCF-7	breast:	n/a
41	chr10:25507099-25507149	HEEpiC	esophagus:	n/a
42	chr10:25464259-25464309	MCF10A-Er-Src	breast:	n/a
43	chr10:25464059-25464109	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:25464825-25464875	PrEC	prostate:	n/a
45	chr10:25507161-25507211	HCF	heart:	n/a
46	chr10:25464165-25464215	HL-60	blood:	n/a
47	chr10:25464139-25464189	HNPCEpiC	eye:	n/a
48	chr10:25464165-25464215	SAEC	small airway:	n/a
49	chr10:25465171-25465221	HCM	heart:	n/a
50	chr10:25464425-25464475	AG09309	skin:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:25434811..25436877-chr10:25455243..25456764,2	K562	blood:
2	chr10:25453554..25455418-chr10:25457570..25459204,2	K562	blood:
3	chr10:25310933..25313238-chr10:25417653..25419899,2	K562	blood:
4	chr10:25453803..25455950-chr10:25458060..25461045,2	MCF-7	breast:
5	chr10:25453803..25455950-chr10:25458060..25461045,2	MCF-7	breast:
6	chr10:25464792..25468231-chr10:25470120..25472618,3	MCF-7	breast:
7	chr10:25402201..25402709-chr10:25515764..25516442,2	K562	blood:
8	chr10:25515615..25516464-chr10:25970963..25971954,2	MCF-7	breast:
9	chr10:25465245..25465751-chr10:25516063..25516582,2	MCF-7	breast:
10	chr10:25401768..25402729-chr10:25515637..25516664,8	MCF-7	breast:
11	chr10:25397970..25400027-chr10:25519164..25521863,2	MCF-7	breast:
12	chr10:25453554..25455418-chr10:25457570..25459204,2	K562	blood:
13	chr10:25495466..25497442-chr10:25499395..25501311,2	K562	blood:
14	chr10:25465245..25465751-chr10:25516063..25516582,2	MCF-7	breast:
15	chr10:25495466..25497442-chr10:25499395..25501311,2	K562	blood:
16	chr10:25401789..25402714-chr10:25514128..25515278,3	MCF-7	breast:
17	chr10:25434811..25436877-chr10:25455243..25456764,2	K562	blood:
18	chr10:25441415..25443400-chr10:25463188..25465016,2	K562	blood:
19	chr10:25495942..25497943-chr10:25499696..25501311,2	K562	blood:
20	chr10:25495942..25497943-chr10:25499696..25501311,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR158-3	chr10:25446227-25446292	NONHSAT011800
2	lnc-ENKUR-4	chr10:25461178-25464289	NONHSAT011802
3	lnc-GPR158-1	chr10:25415180-25415427	ENSG00000231422.2
4	lnc-GPR158-1	chr10:25448580-25450165	ENSG00000231422.2
5	lnc-GPR158-1	chr10:25405541-25405634	ENSG00000231422.2
6	lnc-GPR158-1	chr10:25447298-25447427	NONHSAT011799
7	lnc-GPR158-1	chr10:25415180-25415427	NONHSAT011799
8	lnc-GPR158-1	chr10:25406221-25406342	NONHSAT011799
9	lnc-GPR158-3	chr10:25441993-25442621	NONHSAT011800
10	lnc-ENKUR-5	chr10:25504611-25505211	refGeneNc_2728_NR_027333
11	lnc-GPR158-1	chr10:25414652-25414834	ENSG00000231422.2
12	lnc-GPR158-3	chr10:25445547-25445640	NONHSAT011800
13	lnc-GPR158-1	chr10:25447298-25447427	ENSG00000231422.2
14	lnc-GPR158-1	chr10:25413230-25413320	NONHSAT011799
15	lnc-GPR158-1	chr10:25406221-25406286	XLOC_008414
16	lnc-GPR158-1	chr10:25414755-25414834	NONHSAT011799
17	lnc-ENKUR-5	chr10:25487007-25488838	refGeneNc_2728_NR_027333
18	lnc-GPR158-1	chr10:25406221-25406342	ENSG00000231422.2
19	lnc-GPR158-1	chr10:25448580-25450162	NONHSAT011799
20	lnc-GPR158-1	chr10:25405541-25405634	XLOC_008414
21	lnc-GPR158-1	chr10:25405541-25405634	NONHSAT011799

No data

Variant related genes	Relation type
GPR158-AS1	TF binding region
GPR158	TF binding region
GPR158-AS1	CpG island
GPR158	CpG island
ENSG00000231422	chromatin interactions
ENSG00000233642	chromatin interactions
ENSG00000151025	chromatin interactions
PPP2R2A	miRNA target sites
TRIM32	miRNA target sites

Extended variants
information (count: 2524 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:2524 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1952131	chr10:25403234-25403235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs76818051	chr10:25403240-25403241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537408654	chr10:25403241-25403242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377387435	chr10:25403242-25403243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77063056	chr10:25403330-25403331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181717940	chr10:25403333-25403334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530913079	chr10:25403335-25403336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114671121	chr10:25403342-25403343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560475402	chr10:25403375-25403376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556974085	chr10:25403433-25403434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577097561	chr10:25403447-25403448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543887225	chr10:25403473-25403474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546048353	chr10:25403502-25403503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11014402	chr10:25403548-25403549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374571191	chr10:25403568-25403569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184091370	chr10:25403570-25403571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112667901	chr10:25403573-25403574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550657881	chr10:25403577-25403578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188824527	chr10:25403588-25403589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112693463	chr10:25403628-25403629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151088437	chr10:25403642-25403643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546876048	chr10:25403650-25403651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12244051	chr10:25403651-25403652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111475578	chr10:25403652-25403653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538822415	chr10:25403658-25403659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11014403	chr10:25403665-25403666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112332946	chr10:25403699-25403700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568818622	chr10:25403704-25403705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537950291	chr10:25403705-25403706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554416371	chr10:25403744-25403745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574474914	chr10:25403752-25403753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185960124	chr10:25403771-25403772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192166858	chr10:25403789-25403790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577232497	chr10:25403824-25403825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182177848	chr10:25403856-25403857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562710375	chr10:25403857-25403858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575600689	chr10:25403937-25403938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544685257	chr10:25403965-25403966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561261430	chr10:25404022-25404023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530018270	chr10:25404028-25404029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560052694	chr10:25404043-25404044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546613239	chr10:25404048-25404049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138575808	chr10:25404063-25404064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186402413	chr10:25404069-25404070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112353367	chr10:25404079-25404080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111831475	chr10:25404083-25404084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201512293	chr10:25404127-25404128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190409323	chr10:25404137-25404138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552449737	chr10:25404139-25404140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368537177	chr10:25404151-25404152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Breast cancer	17133270	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
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25392400-25414200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:25395000-25405000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr10:25397400-25404800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr10:25398200-25404600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr10:25400400-25403400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr10:25401800-25403400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:25401800-25403400	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr10:25402000-25403400	Enhancers	Stomach Mucosa	stomach
9	chr10:25402000-25403400	Enhancers	HMEC	breast
10	chr10:25402200-25403600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr10:25402600-25403400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr10:25402600-25403400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr10:25402600-25403400	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr10:25402600-25403600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:25402600-25404600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr10:25402600-25404600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr10:25402600-25409600	Weak transcription	Pancreas	Pancrea
18	chr10:25402800-25404800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr10:25402800-25405400	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr10:25403000-25403400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:25403000-25403400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr10:25403000-25403600	Enhancers	Brain Substantia Nigra	brain
23	chr10:25403000-25404800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:25403200-25404800	Weak transcription	A549	lung
25	chr10:25403200-25405800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr10:25403200-25406400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr10:25403400-25404400	Weak transcription	Stomach Mucosa	stomach
28	chr10:25403400-25405800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr10:25403400-25406200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr10:25403400-25406800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr10:25404600-25404800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr10:25404600-25404800	Enhancers	Stomach Mucosa	stomach
33	chr10:25404600-25406200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr10:25404600-25406200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr10:25404800-25405200	Enhancers	K562	blood
36	chr10:25404800-25405800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr10:25404800-25406000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr10:25404800-25406200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr10:25405000-25405200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr10:25405000-25405200	Enhancers	A549	lung
41	chr10:25405200-25405600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr10:25405200-25406600	Weak transcription	K562	blood
43	chr10:25405400-25406000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr10:25405600-25406000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr10:25405600-25406800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr10:25405800-25406000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr10:25405800-25407600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr10:25406000-25411600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr10:25406200-25407000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr10:25406400-25408400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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