Variant report

Variant	nsv894970
Chromosome Location	chr10:25385858-25522280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1020)
CpG islands
(count:1831)
Chromatin interactive
region (count:27)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:25402075-25402439	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:25391463-25391574	K562	blood:	n/a	n/a
3	ARID3A	chr10:25406696-25407027	K562	blood:	n/a	n/a
4	ATF1	chr10:25406738-25407087	K562	blood:	n/a	n/a
5	ATF1	chr10:25431525-25431673	K562	blood:	n/a	n/a
6	BACH1	chr10:25463336-25463625	K562	blood:	n/a	n/a
7	BACH1	chr10:25480141-25480448	K562	blood:	n/a	n/a
8	BACH1	chr10:25464157-25464315	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:25464776-25465136	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:25458727-25458927	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:25480123-25480456	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:25500358-25500446	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:25463233-25463835	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr10:25407028-25407185	K562	blood:	n/a	n/a
15	BHLHE40	chr10:25392671-25393053	K562	blood:	n/a	n/a
16	BHLHE40	chr10:25406706-25407126	K562	blood:	n/a	n/a
17	BHLHE40	chr10:25408207-25408351	K562	blood:	n/a	n/a
18	BHLHE40	chr10:25402169-25402386	K562	blood:	n/a	n/a
19	BHLHE40	chr10:25463540-25463727	K562	blood:	n/a	n/a
20	CBX3	chr10:25463376-25463764	K562	blood:	n/a	n/a
21	CBX3	chr10:25402089-25402362	K562	blood:	n/a	n/a
22	CEBPB	chr10:25504218-25504513	IMR90	lung:	n/a	chr10:25504371-25504382
23	CEBPB	chr10:25426815-25427062	IMR90	lung:	n/a	chr10:25426933-25426944
24	CEBPB	chr10:25487764-25488019	K562	blood:	n/a	n/a
25	CEBPB	chr10:25426798-25427095	HepG2	liver:	n/a	chr10:25426933-25426944
26	CEBPB	chr10:25426882-25427094	A549	lung:	n/a	chr10:25426933-25426944
27	CEBPB	chr10:25402739-25402978	HepG2	liver:	n/a	n/a
28	CEBPB	chr10:25413337-25413526	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:25504201-25504527	HepG2	liver:	n/a	chr10:25504371-25504382
30	CEBPB	chr10:25504195-25504515	A549	lung:	n/a	chr10:25504371-25504382
31	CEBPB	chr10:25504311-25504511	K562	blood:	n/a	chr10:25504371-25504382
32	CEBPB	chr10:25413363-25413417	K562	blood:	n/a	n/a
33	CEBPB	chr10:25441695-25441706	K562	blood:	n/a	n/a
34	CEBPB	chr10:25522157-25522350	HepG2	liver:	n/a	chr10:25522233-25522244 chr10:25522235-25522244
35	CEBPB	chr10:25426826-25427085	K562	blood:	n/a	chr10:25426933-25426944
36	CEBPB	chr10:25430827-25431042	HepG2	liver:	n/a	chr10:25430915-25430926
37	CEBPB	chr10:25431745-25431818	A549	lung:	n/a	n/a
38	CEBPB	chr10:25487690-25487896	A549	lung:	n/a	n/a
39	CEBPB	chr10:25522122-25522346	A549	lung:	n/a	chr10:25522233-25522244 chr10:25522235-25522244
40	CEBPB	chr10:25469182-25469316	HepG2	liver:	n/a	chr10:25469261-25469272
41	CHD1	chr10:25463486-25464265	H1-hESC	embryonic stem cell:	n/a	chr10:25463853-25463863
42	CHD2	chr10:25464013-25464093	HepG2	liver:	n/a	n/a
43	CHD2	chr10:25463553-25463660	GM12878	blood:	n/a	n/a
44	CHD2	chr10:25425368-25425482	GM12878	blood:	n/a	n/a
45	CHD2	chr10:25463511-25463740	K562	blood:	n/a	n/a
46	CHD2	chr10:25463468-25463656	HepG2	liver:	n/a	n/a
47	CHD2	chr10:25463344-25463982	H1-hESC	embryonic stem cell:	n/a	chr10:25463853-25463863
48	CREB1	chr10:25463307-25463876	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr10:25463289-25463754	A549	lung:	n/a	n/a
50	CREB1	chr10:25431341-25431746	K562	blood:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:25465350-25465400	HAEpiC	amniotic membrane:	n/a
2	chr10:25465350-25465400	HAEpiC	amniotic membrane:	n/a
3	chr10:25464196-25464246	ECC-1	luminal epithelium:	n/a
4	chr10:25464132-25464182	AG09319	gingival:	n/a
5	chr10:25464008-25464058	SAEC	small airway:	n/a
6	chr10:25464184-25464234	GM06990	blood:	n/a
7	chr10:25464825-25464875	A549	lung:	n/a
8	chr10:25507202-25507252	Jurkat	blood:	n/a
9	chr10:25464059-25464109	Jurkat	blood:	n/a
10	chr10:25464008-25464058	T-47D	breast:	n/a
11	chr10:25507202-25507252	ECC-1	luminal epithelium:	n/a
12	chr10:25465263-25465313	U87	brain:	n/a
13	chr10:25507202-25507252	HCT-116	colon:	n/a
14	chr10:25464513-25464563	HCT-116	colon:	n/a
15	chr10:25465350-25465400	Jurkat	blood:	n/a
16	chr10:25464418-25464468	AG04450	lung:	fetal
17	chr10:25464321-25464371	IMR90	lung:	fetal
18	chr10:25464425-25464475	SK-N-MC	brain:	n/a
19	chr10:25464165-25464215	T-47D	breast:	n/a
20	chr10:25464259-25464309	HCT-116	colon:	n/a
21	chr10:25465503-25465553	HL-60	blood:	n/a
22	chr10:25464719-25464769	BE2_C	brain:	n/a
23	chr10:25464059-25464109	ovcar-3	ovarian:	n/a
24	chr10:25464513-25464563	HepG2	liver:	n/a
25	chr10:25464008-25464058	Hela-S3	cervix:	n/a
26	chr10:25507202-25507252	LNCaP	prostate:	n/a
27	chr10:25465242-25465292	U87	brain:	n/a
28	chr10:25464165-25464215	HUVEC	blood vessel:	n/a
29	chr10:25464321-25464371	PANC-1	pancreas:	n/a
30	chr10:25464719-25464769	GM06990	blood:	n/a
31	chr10:25396009-25396059	AG09309	skin:	n/a
32	chr10:25464196-25464246	LNCaP	prostate:	n/a
33	chr10:25464418-25464468	AoSMC	blood vessel:	n/a
34	chr10:25507202-25507252	HRCEpiC	kidney:	n/a
35	chr10:25507099-25507149	HRCEpiC	kidney:	n/a
36	chr10:25464418-25464468	BE2_C	brain:	n/a
37	chr10:25468899-25468949	Jurkat	blood:	n/a
38	chr10:25507099-25507149	HCPEpiC	choroid plexus:	n/a
39	chr10:25507202-25507252	HMEC	breast:	n/a
40	chr10:25464196-25464246	GM19239	blood:	n/a
41	chr10:25464719-25464769	AG09319	gingival:	n/a
42	chr10:25465171-25465221	NT2-D1	testis:	n/a
43	chr10:25507161-25507211	U87	brain:	n/a
44	chr10:25466027-25466077	HRE	kidney:	n/a
45	chr10:25463757-25463807	NB4	blood:	n/a
46	chr10:25465219-25465269	GM12878	blood:	n/a
47	chr10:25464259-25464309	GM12891	blood:	n/a
48	chr10:25465430-25465480	HMEC	breast:	n/a
49	chr10:25464321-25464371	HIPEpiC	eye:	n/a
50	chr10:25464196-25464246	Hepatocyte	liver:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:25384858..25387044-chr10:25387748..25390557,2	K562	blood:
2	chr10:25495466..25497442-chr10:25499395..25501311,2	K562	blood:
3	chr10:25434811..25436877-chr10:25455243..25456764,2	K562	blood:
4	chr10:25011194..25013594-chr10:25390011..25392696,2	K562	blood:
5	chr10:25401768..25402729-chr10:25515637..25516664,8	MCF-7	breast:
6	chr10:25441415..25443400-chr10:25463188..25465016,2	K562	blood:
7	chr10:25402201..25402709-chr10:25515764..25516442,2	K562	blood:
8	chr10:25465245..25465751-chr10:25516063..25516582,2	MCF-7	breast:
9	chr10:25402163..25402736-chr10:25722736..25723649,2	MCF-7	breast:
10	chr10:25453803..25455950-chr10:25458060..25461045,2	MCF-7	breast:
11	chr10:25402201..25402709-chr10:25515764..25516442,2	K562	blood:
12	chr10:25401789..25402714-chr10:25514128..25515278,3	MCF-7	breast:
13	chr10:25453554..25455418-chr10:25457570..25459204,2	K562	blood:
14	chr10:25434811..25436877-chr10:25455243..25456764,2	K562	blood:
15	chr10:25453803..25455950-chr10:25458060..25461045,2	MCF-7	breast:
16	chr10:25495942..25497943-chr10:25499696..25501311,2	K562	blood:
17	chr10:25465245..25465751-chr10:25516063..25516582,2	MCF-7	breast:
18	chr10:25515615..25516464-chr10:25970963..25971954,2	MCF-7	breast:
19	chr10:25464792..25468231-chr10:25470120..25472618,3	MCF-7	breast:
20	chr10:25384858..25387044-chr10:25387748..25390557,2	K562	blood:
21	chr10:25350226..25351753-chr10:25385209..25386887,2	K562	blood:
22	chr10:25397970..25400027-chr10:25519164..25521863,2	MCF-7	breast:
23	chr10:25453554..25455418-chr10:25457570..25459204,2	K562	blood:
24	chr10:25495466..25497442-chr10:25499395..25501311,2	K562	blood:
25	chr10:25495942..25497943-chr10:25499696..25501311,2	K562	blood:
26	chr10:25397970..25400027-chr10:25519164..25521863,2	MCF-7	breast:
27	chr10:25310933..25313238-chr10:25417653..25419899,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR158-1	chr10:25447298-25447427	ENSG00000231422.2
2	lnc-ENKUR-5	chr10:25487007-25488838	refGeneNc_2728_NR_027333
3	lnc-GPR158-1	chr10:25405541-25405634	NONHSAT011799
4	lnc-GPR158-3	chr10:25441993-25442621	NONHSAT011800
5	lnc-GPR158-3	chr10:25445547-25445640	NONHSAT011800
6	lnc-GPR158-1	chr10:25405541-25405634	XLOC_008414
7	lnc-GPR158-1	chr10:25447298-25447427	NONHSAT011799
8	lnc-GPR158-1	chr10:25415180-25415427	NONHSAT011799
9	lnc-ENKUR-5	chr10:25504611-25505211	refGeneNc_2728_NR_027333
10	lnc-GPR158-1	chr10:25405541-25405634	ENSG00000231422.2
11	lnc-GPR158-1	chr10:25406221-25406342	ENSG00000231422.2
12	lnc-GPR158-1	chr10:25414652-25414834	ENSG00000231422.2
13	lnc-GPR158-1	chr10:25401987-25402615	ENSG00000231422.2
14	lnc-GPR158-1	chr10:25401987-25402615	XLOC_008414
15	lnc-GPR158-1	chr10:25406221-25406342	NONHSAT011799
16	lnc-GPR158-1	chr10:25413230-25413320	NONHSAT011799
17	lnc-GPR158-1	chr10:25414755-25414834	NONHSAT011799
18	lnc-ENKUR-4	chr10:25461178-25464289	NONHSAT011802
19	lnc-GPR158-1	chr10:25401987-25402615	NONHSAT011799
20	lnc-GPR158-1	chr10:25406221-25406286	XLOC_008414
21	lnc-GPR158-3	chr10:25446227-25446292	NONHSAT011800
22	lnc-GPR158-1	chr10:25448580-25450165	ENSG00000231422.2
23	lnc-GPR158-1	chr10:25415180-25415427	ENSG00000231422.2
24	lnc-GPR158-1	chr10:25448580-25450162	NONHSAT011799

No data

Variant related genes	Relation type
ENSG00000231422	TF binding region
GPR158-AS1	TF binding region
GPR158	TF binding region
ENSG00000231422	CpG island
GPR158-AS1	CpG island
GPR158	CpG island
ENSG00000231422	chromatin interactions
ENSG00000233642	chromatin interactions
ENSG00000151025	chromatin interactions
ENSG00000107863	chromatin interactions
EGFR	miRNA target sites
PPP2R2A	miRNA target sites
TRIM32	miRNA target sites

Extended variants
information (count: 3119 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:3119 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1388925	chr10:25385858-25385859	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533544989	chr10:25385904-25385905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550241158	chr10:25385939-25385940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72782209	chr10:25385940-25385941	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs143554989	chr10:25385956-25385957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549001131	chr10:25385989-25385990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544484277	chr10:25386049-25386050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565640551	chr10:25386056-25386057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191806348	chr10:25386070-25386071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557806837	chr10:25386087-25386088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577791061	chr10:25386114-25386115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537237327	chr10:25386258-25386259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556880550	chr10:25386306-25386307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573597292	chr10:25386314-25386315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs57542069	chr10:25386340-25386341	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs558403627	chr10:25386371-25386372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561761445	chr10:25386372-25386373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572373774	chr10:25386390-25386391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574617351	chr10:25386460-25386461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541192050	chr10:25386477-25386478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79684016	chr10:25386498-25386499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs55881837	chr10:25386539-25386540	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550393406	chr10:25386576-25386577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573137539	chr10:25386603-25386604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148327255	chr10:25386626-25386627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs56140300	chr10:25386672-25386673	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146301973	chr10:25386704-25386705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376640835	chr10:25386714-25386715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549666082	chr10:25386726-25386727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs55788231	chr10:25386730-25386731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs78719221	chr10:25386748-25386749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551224790	chr10:25386807-25386808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531143707	chr10:25386865-25386866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571312945	chr10:25386909-25386910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536897319	chr10:25386912-25386913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556743449	chr10:25386927-25386928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573464314	chr10:25386934-25386935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536160827	chr10:25386936-25386937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552824170	chr10:25386972-25386973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572380403	chr10:25386991-25386992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75441232	chr10:25387009-25387010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139388585	chr10:25387027-25387028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150071885	chr10:25387029-25387030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145345423	chr10:25387031-25387032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563888621	chr10:25387079-25387080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529482997	chr10:25387093-25387094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374322080	chr10:25387153-25387154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559981255	chr10:25387168-25387169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528117149	chr10:25387190-25387191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551356334	chr10:25387191-25387192	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:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25385000-25386800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:25385200-25386600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:25385400-25386000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr10:25385400-25386000	Enhancers	Brain Substantia Nigra	brain
5	chr10:25385400-25386400	Enhancers	Brain Cingulate Gyrus	brain
6	chr10:25385600-25386000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:25385600-25386000	Enhancers	Brain Anterior Caudate	brain
8	chr10:25385600-25386000	Enhancers	Brain Hippocampus Middle	brain
9	chr10:25386000-25389800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr10:25386000-25390400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr10:25386000-25393400	Weak transcription	Brain Anterior Caudate	brain
12	chr10:25386000-25393400	Weak transcription	Brain Hippocampus Middle	brain
13	chr10:25386000-25393400	Weak transcription	Brain Substantia Nigra	brain
14	chr10:25386200-25386400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr10:25386400-25388800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr10:25386600-25386800	Enhancers	Fetal Brain Male	brain
17	chr10:25386600-25390600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:25386800-25390400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr10:25387200-25390200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr10:25388800-25392800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr10:25388800-25394400	Enhancers	Fetal Brain Male	brain
22	chr10:25388800-25395200	Enhancers	Fetal Brain Female	brain
23	chr10:25389800-25391000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr10:25389800-25392800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr10:25389800-25394600	Enhancers	Brain Germinal Matrix	brain
26	chr10:25390000-25390400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr10:25390000-25390600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr10:25390200-25390600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr10:25390200-25390800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr10:25390200-25390800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr10:25390200-25391000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr10:25390200-25391000	Enhancers	Stomach Mucosa	stomach
33	chr10:25390200-25391400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr10:25390200-25393000	Enhancers	K562	blood
35	chr10:25390400-25390800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr10:25390400-25390800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr10:25390400-25391600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr10:25390400-25391800	Enhancers	Fetal Heart	heart
39	chr10:25390400-25392400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr10:25390600-25391600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr10:25390600-25393600	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr10:25390600-25394600	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr10:25390600-25395000	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr10:25390800-25391600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr10:25390800-25392000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:25390800-25393600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr10:25390800-25393800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr10:25391400-25393600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr10:25391600-25394200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr10:25392000-25392200	Enhancers	H1 Cell Line	embryonic stem cell

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