Variant report

Variant	nsv1036683
Chromosome Location	chr10:25337592-25398119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1018)
CpG islands
(count:244)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1018 , 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	chr10:25371398-25372030	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:25349037-25349247	K562	blood:	n/a	n/a
3	ARID3A	chr10:25351365-25351716	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:25369916-25370267	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:25369889-25370231	K562	blood:	n/a	n/a
6	ARID3A	chr10:25349028-25349245	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:25391463-25391574	K562	blood:	n/a	n/a
8	ARID3A	chr10:25350560-25351729	K562	blood:	n/a	n/a
9	ARID3A	chr10:25367422-25368533	HepG2	liver:	n/a	n/a
10	ATF1	chr10:25365656-25366064	K562	blood:	n/a	n/a
11	ATF1	chr10:25350728-25351739	K562	blood:	n/a	n/a
12	ATF1	chr10:25357320-25357627	K562	blood:	n/a	n/a
13	ATF2	chr10:25357189-25357600	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr10:25349000-25349280	K562	blood:	n/a	n/a
15	ATF3	chr10:25351381-25351746	K562	blood:	n/a	n/a
16	ATF3	chr10:25351288-25351785	K562	blood:	n/a	n/a
17	ATF3	chr10:25348898-25349344	K562	blood:	n/a	n/a
18	BACH1	chr10:25350626-25351684	K562	blood:	n/a	n/a
19	BACH1	chr10:25370118-25370135	K562	blood:	n/a	n/a
20	BATF	chr10:25352365-25352714	GM12878	blood:	n/a	chr10:25352563-25352574
21	BATF	chr10:25357156-25357476	GM12878	blood:	n/a	chr10:25357432-25357445 chr10:25357318-25357327
22	BHLHE40	chr10:25350527-25351837	K562	blood:	n/a	n/a
23	BHLHE40	chr10:25369836-25370202	GM12878	blood:	n/a	n/a
24	BHLHE40	chr10:25351356-25351683	A549	lung:	n/a	n/a
25	BHLHE40	chr10:25365610-25366191	K562	blood:	n/a	n/a
26	BHLHE40	chr10:25392671-25393053	K562	blood:	n/a	n/a
27	BHLHE40	chr10:25351006-25351743	HepG2	liver:	n/a	n/a
28	BHLHE40	chr10:25349186-25349285	K562	blood:	n/a	n/a
29	BHLHE40	chr10:25369837-25370263	K562	blood:	n/a	n/a
30	BRCA1	chr10:25348995-25349471	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr10:25383526-25383825	K562	blood:	n/a	n/a
32	CBX3	chr10:25383573-25383835	K562	blood:	n/a	n/a
33	CBX3	chr10:25369779-25370295	K562	blood:	n/a	n/a
34	CBX3	chr10:25339262-25339650	K562	blood:	n/a	n/a
35	CBX3	chr10:25350677-25351934	K562	blood:	n/a	n/a
36	CBX3	chr10:25351123-25351936	HCT-116	colon:	n/a	n/a
37	CCNT2	chr10:25351359-25351787	K562	blood:	n/a	chr10:25351586-25351606
38	CCNT2	chr10:25350662-25351072	K562	blood:	n/a	n/a
39	CCNT2	chr10:25370016-25370363	K562	blood:	n/a	n/a
40	CEBPB	chr10:25367651-25368348	A549	lung:	n/a	n/a
41	CEBPB	chr10:25348039-25348208	K562	blood:	n/a	chr10:25348117-25348128
42	CEBPB	chr10:25365353-25365516	A549	lung:	n/a	n/a
43	CEBPB	chr10:25349121-25349211	H1-hESC	embryonic stem cell:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
44	CEBPB	chr10:25341122-25341163	A549	lung:	n/a	chr10:25341132-25341143
45	CEBPB	chr10:25349024-25349224	K562	blood:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
46	CEBPB	chr10:25348952-25349364	IMR90	lung:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
47	CEBPB	chr10:25374607-25375054	A549	lung:	n/a	chr10:25375031-25375040 chr10:25374829-25374840 chr10:25375029-25375042 chr10:25375029-25375040 chr10:25375030-25375041 chr10:25375029-25375042
48	CEBPB	chr10:25350742-25351940	K562	blood:	n/a	n/a
49	CEBPB	chr10:25347934-25348298	K562	blood:	n/a	chr10:25348117-25348128
50	CEBPB	chr10:25348965-25349369	K562	blood:	n/a	chr10:25349162-25349173 chr10:25349161-25349174

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:25396009-25396059	GM12892	blood:	n/a
2	chr10:25396009-25396059	HRPEpiC	eye:	n/a
3	chr10:25371488-25371538	AoSMC	blood vessel:	n/a
4	chr10:25396009-25396059	U87	brain:	n/a
5	chr10:25396009-25396059	T-47D	breast:	n/a
6	chr10:25396009-25396059	GM12891	blood:	n/a
7	chr10:25371488-25371538	NT2-D1	testis:	n/a
8	chr10:25396009-25396059	PFSK-1	brain:	n/a
9	chr10:25396009-25396059	HUVEC	blood vessel:	n/a
10	chr10:25357368-25357418	MCF-7	breast:	n/a
11	chr10:25371488-25371538	IMR90	lung:	fetal
12	chr10:25396009-25396059	NHDF-neo	bronchial:	n/a
13	chr10:25357368-25357418	AG04450	lung:	fetal
14	chr10:25357368-25357418	PFSK-1	brain:	n/a
15	chr10:25350802-25350852	HNPCEpiC	eye:	n/a
16	chr10:25357368-25357418	HMEC	breast:	n/a
17	chr10:25357368-25357418	HepG2	liver:	n/a
18	chr10:25350802-25350852	PrEC	prostate:	n/a
19	chr10:25371488-25371538	HCF	heart:	n/a
20	chr10:25396009-25396059	BJ	skin:	n/a
21	chr10:25371488-25371538	NB4	blood:	n/a
22	chr10:25371488-25371538	SK-N-SH_RA	brain:	n/a
23	chr10:25357368-25357418	HCM	heart:	n/a
24	chr10:25350802-25350852	A549	lung:	n/a
25	chr10:25396009-25396059	HCM	heart:	n/a
26	chr10:25350802-25350852	SK-N-SH_RA	brain:	n/a
27	chr10:25350802-25350852	BJ	skin:	n/a
28	chr10:25350802-25350852	GM06990	blood:	n/a
29	chr10:25371488-25371538	ECC-1	luminal epithelium:	n/a
30	chr10:25350802-25350852	HCM	heart:	n/a
31	chr10:25357368-25357418	HRCEpiC	kidney:	n/a
32	chr10:25371488-25371538	HPAEpiC	pulmonary alveolar:	n/a
33	chr10:25350802-25350852	AoSMC	blood vessel:	n/a
34	chr10:25396009-25396059	SK-N-MC	brain:	n/a
35	chr10:25371488-25371538	HL-60	blood:	n/a
36	chr10:25357368-25357418	NB4	blood:	n/a
37	chr10:25357368-25357418	NHDF-neo	bronchial:	n/a
38	chr10:25396009-25396059	HCF	heart:	n/a
39	chr10:25357368-25357418	BJ	skin:	n/a
40	chr10:25357368-25357418	LNCaP	prostate:	n/a
41	chr10:25357368-25357418	GM06990	blood:	n/a
42	chr10:25357368-25357418	HNPCEpiC	eye:	n/a
43	chr10:25396009-25396059	ECC-1	luminal epithelium:	n/a
44	chr10:25371488-25371538	NH-A	brain:	n/a
45	chr10:25396009-25396059	AG09319	gingival:	n/a
46	chr10:25396009-25396059	SAEC	small airway:	n/a
47	chr10:25357368-25357418	GM12892	blood:	n/a
48	chr10:25357368-25357418	NH-A	brain:	n/a
49	chr10:25396009-25396059	K562	blood:	n/a
50	chr10:25357368-25357418	HEEpiC	esophagus:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:25350226..25351753-chr10:25385209..25386887,2	K562	blood:
2	chr10:25315173..25316027-chr10:25369505..25370579,6	MCF-7	breast:
3	chr10:25079435..25081057-chr10:25368417..25370064,2	K562	blood:
4	chr10:25344134..25348116-chr10:25349607..25352644,3	MCF-7	breast:
5	chr10:25239858..25242854-chr10:25350195..25352504,2	K562	blood:
6	chr10:25304278..25309002-chr10:25368191..25372754,5	K562	blood:
7	chr10:25345062..25348953-chr10:25349936..25353027,4	K562	blood:
8	chr10:25369667..25370602-chr10:25971300..25972009,2	MCF-7	breast:
9	chr10:25303827..25307969-chr10:25351029..25354599,5	K562	blood:
10	chr10:25304955..25307281-chr10:25348708..25354586,7	MCF-7	breast:
11	chr10:25303695..25307800-chr10:25367762..25370827,4	K562	blood:
12	chr10:25306319..25307953-chr10:25346499..25349389,2	MCF-7	breast:
13	chr10:25306123..25307821-chr10:25350955..25353147,2	MCF-7	breast:
14	chr10:25338585..25341464-chr10:25343228..25345616,2	K562	blood:
15	chr10:25303584..25305418-chr10:25364552..25366194,2	MCF-7	breast:
16	chr10:25356543..25358700-chr10:25359934..25363281,3	K562	blood:
17	chr10:25344134..25348116-chr10:25349607..25352644,3	MCF-7	breast:
18	chr10:25175280..25178160-chr10:25364501..25366305,2	K562	blood:
19	chr10:25239725..25241588-chr10:25374362..25376183,2	K562	blood:
20	chr10:25303827..25307133-chr10:25349437..25354097,8	K562	blood:
21	chr10:25349510..25351855-chr10:25352161..25354821,2	MCF-7	breast:
22	chr10:25362224..25363937-chr10:25363978..25365901,2	K562	blood:
23	chr10:25397970..25400027-chr10:25519164..25521863,2	MCF-7	breast:
24	chr10:25334592..25336921-chr10:25350299..25353033,2	K562	blood:
25	chr10:25304592..25306407-chr10:25373363..25375162,2	MCF-7	breast:
26	chr10:25343578..25346366-chr10:25349000..25351556,3	MCF-7	breast:
27	chr10:25341537..25343849-chr10:25349173..25350705,2	K562	blood:
28	chr10:25305403..25308444-chr10:25369519..25373361,4	MCF-7	breast:
29	chr10:24854730..24857189-chr10:25359782..25362279,2	K562	blood:
30	chr10:25343371..25346299-chr10:25346762..25349074,2	K562	blood:
31	chr10:25011013..25013160-chr10:25345003..25347658,2	K562	blood:
32	chr10:25340489..25343849-chr10:25349173..25351054,3	K562	blood:
33	chr10:25338585..25341464-chr10:25343228..25345616,2	K562	blood:
34	chr10:25340489..25343849-chr10:25349173..25351054,3	K562	blood:
35	chr10:25016699..25017443-chr10:25369664..25370556,4	K562	blood:
36	chr10:25315371..25316092-chr10:25369588..25370596,3	K562	blood:
37	chr10:25372240..25374997-chr10:25377094..25379582,2	K562	blood:
38	chr10:25331770..25334410-chr10:25337603..25339717,2	MCF-7	breast:
39	chr10:24906446..24907157-chr10:25369477..25370117,2	MCF-7	breast:
40	chr10:25357593..25359343-chr10:25368933..25370472,2	K562	blood:
41	chr10:25344528..25346562-chr10:25350767..25353027,3	K562	blood:
42	chr10:25343578..25346366-chr10:25349000..25351556,3	MCF-7	breast:
43	chr10:25374556..25376666-chr10:25584263..25586779,2	K562	blood:
44	chr10:25304583..25307026-chr10:25335686..25338076,2	MCF-7	breast:
45	chr10:25304800..25307444-chr10:25366624..25371121,4	MCF-7	breast:
46	chr10:25344528..25346562-chr10:25350767..25353027,3	K562	blood:
47	chr10:25384858..25387044-chr10:25387748..25390557,2	K562	blood:
48	chr10:25384858..25387044-chr10:25387748..25390557,2	K562	blood:
49	chr10:24931513..24932500-chr10:25369531..25370644,4	K562	blood:
50	chr10:25372240..25374997-chr10:25377094..25379582,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000231422	TF binding region
ENSG00000266069	TF binding region
ENSG00000231422	CpG island
ENSG00000266069	CpG island
ENSG00000107863	chromatin interactions
ENSG00000099256	chromatin interactions
ENSG00000151023	chromatin interactions
ENSG00000185875	chromatin interactions
ENSG00000273107	chromatin interactions

Extended variants
information (count: 2073 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:2073 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543773510	chr10:25337622-25337623	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs1158057	chr10:25337669-25337670	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575401087	chr10:25337689-25337690	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543819164	chr10:25337692-25337693	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563305490	chr10:25337695-25337696	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569721761	chr10:25337760-25337761	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573828339	chr10:25337764-25337765	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs34318277	chr10:25337789-25337790	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs397809739	chr10:25337798-25337799	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs397750279	chr10:25337799-25337800	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs142216025	chr10:25337882-25337883	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190430569	chr10:25337936-25337937	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs144698033	chr10:25337961-25337962	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs183551498	chr10:25337966-25337967	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188247547	chr10:25338000-25338001	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531085587	chr10:25338062-25338063	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550611692	chr10:25338107-25338108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192785073	chr10:25338162-25338163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182632764	chr10:25338166-25338167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75568941	chr10:25338186-25338187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147912262	chr10:25338188-25338189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141664730	chr10:25338228-25338229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558436805	chr10:25338240-25338241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575509456	chr10:25338261-25338262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537730580	chr10:25338269-25338270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556964232	chr10:25338277-25338278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114615272	chr10:25338285-25338286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34707180	chr10:25338335-25338336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4749001	chr10:25338445-25338446	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs559429017	chr10:25338490-25338491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573211062	chr10:25338492-25338493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545606081	chr10:25338521-25338522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565302401	chr10:25338526-25338527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531270866	chr10:25338562-25338563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544900919	chr10:25338594-25338595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55910423	chr10:25338599-25338600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546673677	chr10:25338645-25338646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113157305	chr10:25338648-25338649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553241253	chr10:25338649-25338650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138149250	chr10:25338665-25338666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567169423	chr10:25338671-25338672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370736098	chr10:25338699-25338700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs60646580	chr10:25338730-25338731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370927147	chr10:25338731-25338732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546581004	chr10:25338750-25338751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72780387	chr10:25338751-25338752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs11014362	chr10:25338764-25338765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548906608	chr10:25338781-25338782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186796233	chr10:25338785-25338786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568934496	chr10:25338788-25338789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:42)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25335600-25338000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr10:25336000-25337800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr10:25336000-25337800	Enhancers	HMEC	breast
4	chr10:25336000-25338000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:25336000-25338000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:25336200-25337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:25336200-25337600	Enhancers	Osteobl	bone
8	chr10:25336200-25337800	Enhancers	NHEK	skin
9	chr10:25336200-25338200	Enhancers	Fetal Intestine Small	intestine
10	chr10:25336400-25337600	Enhancers	HSMM	muscle
11	chr10:25336400-25338200	Enhancers	Brain Anterior Caudate	brain
12	chr10:25336600-25338000	Enhancers	HSMMtube	muscle
13	chr10:25337000-25338000	Enhancers	Brain Substantia Nigra	brain
14	chr10:25337000-25338200	Enhancers	Fetal Intestine Large	intestine
15	chr10:25337200-25337600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:25337200-25337600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
17	chr10:25337200-25337800	Enhancers	Ovary	ovary
18	chr10:25337200-25338200	Enhancers	Duodenum Mucosa	Duodenum
19	chr10:25337400-25337600	Enhancers	Fetal Brain Female	brain
20	chr10:25337400-25337600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
21	chr10:25337400-25338200	Enhancers	K562	blood
22	chr10:25337400-25348200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr10:25337600-25337800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr10:25337600-25337800	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr10:25337600-25337800	Bivalent Enhancer	Osteobl	bone
26	chr10:25337600-25348200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:25337800-25338000	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr10:25337800-25338000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr10:25337800-25339400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr10:25338000-25341000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr10:25338200-25338800	Weak transcription	Fetal Intestine Small	intestine
32	chr10:25338200-25340400	Weak transcription	Fetal Intestine Large	intestine
33	chr10:25338200-25348400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr10:25338800-25340800	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chr10:25339000-25339200	Enhancers	Osteobl	bone
36	chr10:25339400-25339600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr10:25340400-25341000	Enhancers	Fetal Intestine Large	intestine
38	chr10:25340800-25341200	Enhancers	Liver	Liver
39	chr10:25340800-25341400	Enhancers	Fetal Intestine Small	intestine
40	chr10:25341000-25345600	Weak transcription	Fetal Intestine Large	intestine
41	chr10:25341200-25345800	Weak transcription	Liver	Liver
42	chr10:25341400-25342000	Genic enhancers	Fetal Intestine Small	intestine
43	chr10:25342000-25345200	Weak transcription	Fetal Intestine Small	intestine
44	chr10:25344800-25345600	Enhancers	K562	blood
45	chr10:25345200-25349400	Enhancers	Fetal Intestine Small	intestine
46	chr10:25345600-25346000	Genic enhancers	K562	blood
47	chr10:25345600-25350600	Enhancers	Fetal Intestine Large	intestine
48	chr10:25345800-25346000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr10:25345800-25347200	Enhancers	Liver	Liver
50	chr10:25346000-25347200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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