Variant report

Variant	nsv1045119
Chromosome Location	chr10:766867-855251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1496)
CpG islands
(count:4029)
Chromatin interactive
region (count:67)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1496 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:834600-835039	HepG2	liver:	n/a	chr10:834754-834770
2	ARID3A	chr10:840593-840806	HepG2	liver:	n/a	n/a
3	ATF1	chr10:813001-813370	K562	blood:	n/a	n/a
4	ATF3	chr10:835269-835673	A549	lung:	n/a	n/a
5	BACH1	chr10:830736-831092	H1-hESC	embryonic stem cell:	n/a	chr10:830863-830877
6	BACH1	chr10:834956-835728	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:835339-835594	K562	blood:	n/a	n/a
8	BCL11A	chr10:769301-769535	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:811979-812582	GM12878	blood:	n/a	n/a
10	BCL3	chr10:848783-849025	GM12878	blood:	n/a	n/a
11	BCL3	chr10:850410-851109	K562	blood:	n/a	n/a
12	BCL3	chr10:837478-837818	GM12878	blood:	n/a	n/a
13	BCL3	chr10:812586-812912	GM12878	blood:	n/a	n/a
14	BCL3	chr10:835049-835724	A549	lung:	n/a	chr10:835215-835224 chr10:835319-835332 chr10:835073-835082 chr10:835063-835076
15	BCL3	chr10:837596-837974	GM12878	blood:	n/a	n/a
16	BCL3	chr10:851319-851820	GM12878	blood:	n/a	n/a
17	BCL3	chr10:850707-851034	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:834752-835119	HepG2	liver:	n/a	n/a
19	BHLHE40	chr10:769085-769382	K562	blood:	n/a	n/a
20	BHLHE40	chr10:834946-835733	K562	blood:	n/a	n/a
21	BHLHE40	chr10:836004-836159	K562	blood:	n/a	chr10:836014-836023 chr10:836008-836029 chr10:836014-836023 chr10:836015-836024 chr10:836012-836025
22	BHLHE40	chr10:850930-850986	K562	blood:	n/a	n/a
23	BHLHE40	chr10:769894-770344	K562	blood:	n/a	n/a
24	BRCA1	chr10:835479-835555	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr10:835352-835677	K562	blood:	n/a	n/a
26	CBX3	chr10:835027-835220	K562	blood:	n/a	n/a
27	CBX3	chr10:769860-770105	K562	blood:	n/a	n/a
28	CBX3	chr10:806640-806884	K562	blood:	n/a	n/a
29	CBX3	chr10:835409-835597	K562	blood:	n/a	n/a
30	CBX3	chr10:834865-835275	K562	blood:	n/a	n/a
31	CCNT2	chr10:851115-851936	K562	blood:	n/a	n/a
32	CCNT2	chr10:834870-835771	K562	blood:	n/a	chr10:835329-835338 chr10:835323-835332
33	CCNT2	chr10:849052-849379	K562	blood:	n/a	n/a
34	CCNT2	chr10:850177-850516	K562	blood:	n/a	n/a
35	CEBPB	chr10:799626-799733	HepG2	liver:	n/a	n/a
36	CEBPB	chr10:830409-830580	IMR90	lung:	n/a	n/a
37	CEBPB	chr10:799560-799705	K562	blood:	n/a	n/a
38	CEBPB	chr10:834826-835077	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:776514-776865	HepG2	liver:	n/a	chr10:776667-776678
40	CEBPB	chr10:830359-830527	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:776582-776736	Hela-S3	cervix:	n/a	chr10:776667-776678
42	CEBPB	chr10:776542-776771	H1-hESC	embryonic stem cell:	n/a	chr10:776667-776678
43	CEBPB	chr10:776512-776828	A549	lung:	n/a	chr10:776667-776678
44	CEBPB	chr10:830989-831276	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPD	chr10:834761-835165	HepG2	liver:	n/a	n/a
46	CHD1	chr10:830362-831385	IMR90	lung:	n/a	chr10:830616-830626
47	CHD2	chr10:831058-831106	HepG2	liver:	n/a	n/a
48	CHD2	chr10:835478-835819	HepG2	liver:	n/a	n/a
49	CHD2	chr10:834813-835213	HepG2	liver:	n/a	n/a
50	CHD2	chr10:834975-835659	H1-hESC	embryonic stem cell:	n/a	n/a

(count:4029 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:778073-778123	A549	lung:	n/a
2	chr10:834428-834478	PFSK-1	brain:	n/a
3	chr10:778709-778759	PrEC	prostate:	n/a
4	chr10:778073-778123	A549	lung:	n/a
5	chr10:834428-834478	PFSK-1	brain:	n/a
6	chr10:778709-778759	PrEC	prostate:	n/a
7	chr10:831835-831885	MCF-7	breast:	n/a
8	chr10:835615-835665	K562	blood:	n/a
9	chr10:835505-835555	ovcar-3	ovarian:	n/a
10	chr10:773141-773191	ECC-1	luminal epithelium:	n/a
11	chr10:851265-851315	MCF-7	breast:	n/a
12	chr10:769945-769995	ovcar-3	ovarian:	n/a
13	chr10:820767-820817	HAEpiC	amniotic membrane:	n/a
14	chr10:850393-850443	SK-N-MC	brain:	n/a
15	chr10:835070-835120	U87	brain:	n/a
16	chr10:851265-851315	HPAEpiC	pulmonary alveolar:	n/a
17	chr10:768867-768917	MCF10A-Er-Src	breast:	n/a
18	chr10:820509-820559	NB4	blood:	n/a
19	chr10:852009-852059	BE2_C	brain:	n/a
20	chr10:823151-823201	SK-N-MC	brain:	n/a
21	chr10:829333-829383	K562	blood:	n/a
22	chr10:833127-833177	K562	blood:	n/a
23	chr10:844186-844236	CMK	blood:	n/a
24	chr10:820206-820256	PANC-1	pancreas:	n/a
25	chr10:853153-853203	ovcar-3	ovarian:	n/a
26	chr10:832765-832815	ECC-1	luminal epithelium:	n/a
27	chr10:816999-817049	PFSK-1	brain:	n/a
28	chr10:853153-853203	ECC-1	luminal epithelium:	n/a
29	chr10:820430-820480	IMR90	lung:	fetal
30	chr10:829333-829383	GM12891	blood:	n/a
31	chr10:778219-778269	LNCaP	prostate:	n/a
32	chr10:768541-768591	SK-N-SH	brain:	n/a
33	chr10:851439-851489	AG09319	gingival:	n/a
34	chr10:829463-829513	HCPEpiC	choroid plexus:	n/a
35	chr10:831835-831885	HRE	kidney:	n/a
36	chr10:820767-820817	ProgFib	skin:	n/a
37	chr10:772323-772373	A549	lung:	n/a
38	chr10:829333-829383	Hepatocyte	liver:	n/a
39	chr10:850393-850443	PANC-1	pancreas:	n/a
40	chr10:817083-817133	NB4	blood:	n/a
41	chr10:775353-775403	BE2_C	brain:	n/a
42	chr10:830689-830739	NH-A	brain:	n/a
43	chr10:851439-851489	U87	brain:	n/a
44	chr10:835505-835555	SKMC	muscle:	n/a
45	chr10:773141-773191	ovcar-3	ovarian:	n/a
46	chr10:820321-820371	Hepatocyte	liver:	n/a
47	chr10:783591-783641	HNPCEpiC	eye:	n/a
48	chr10:853153-853203	NT2-D1	testis:	n/a
49	chr10:853215-853265	HEK293	kidney:	embryo
50	chr10:832765-832815	Jurkat	blood:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:698785..701781-chr10:833421..835495,2	MCF-7	breast:
2	chr10:844752..846844-chr10:853886..856295,2	K562	blood:
3	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
4	chr10:634195..634721-chr10:829974..830911,3	MCF-7	breast:
5	chr10:826973..829590-chr10:832494..835604,4	K562	blood:
6	chr10:739318..742202-chr10:834057..836421,2	MCF-7	breast:
7	chr10:835663..837203-chr10:849697..852402,2	MCF-7	breast:
8	chr10:851680..853848-chr10:854341..855901,2	K562	blood:
9	chr10:823329..824026-chr16:78285555..78286055,2	MCF-7	breast:
10	chr10:849218..853180-chr10:854145..855910,4	K562	blood:
11	chr10:851217..854668-chr10:856285..859147,3	MCF-7	breast:
12	chr10:783561..786479-chr10:789093..790752,2	MCF-7	breast:
13	chr10:849121..851622-chr10:853279..855417,2	K562	blood:
14	chr10:819060..821540-chr10:825309..827354,2	MCF-7	breast:
15	chr10:840517..842192-chr10:842666..844549,2	MCF-7	breast:
16	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:
17	chr10:847643..849814-chr10:851213..852909,2	K562	blood:
18	chr10:734426..737338-chr10:832688..834504,2	MCF-7	breast:
19	chr10:844752..846844-chr10:853886..856295,2	K562	blood:
20	chr10:835224..837627-chr10:1092339..1094785,2	MCF-7	breast:
21	chr10:556675..557469-chr10:840259..840863,3	MCF-7	breast:
22	chr10:461824..462560-chr10:834643..835579,2	MCF-7	breast:
23	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:
24	chr10:633910..634891-chr10:834953..835643,3	MCF-7	breast:
25	chr10:556841..557546-chr10:834923..836004,5	MCF-7	breast:
26	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
27	chr10:456178..457890-chr10:852622..854288,2	MCF-7	breast:
28	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
29	chr10:852322..854745-chr10:858049..860254,2	K562	blood:
30	chr10:840309..840941-chr10:856321..856837,2	MCF-7	breast:
31	chr10:831933..833433-chr10:65279794..65281725,2	MCF-7	breast:
32	chr10:556641..557560-chr10:835088..835885,2	K562	blood:
33	chr10:284740..285439-chr10:835087..835858,2	MCF-7	breast:
34	chr10:851047..854031-chr10:861867..864621,2	K562	blood:
35	chr10:840517..842192-chr10:842666..844549,2	MCF-7	breast:
36	chr10:849218..853180-chr10:854145..855910,4	K562	blood:
37	chr10:556492..557579-chr10:835209..836234,4	MCF-7	breast:
38	chr10:833990..835898-chr10:1099433..1102164,2	K562	blood:
39	chr10:180500..182203-chr10:836766..839418,2	MCF-7	breast:
40	chr10:826973..829590-chr10:832494..835604,4	K562	blood:
41	chr10:550299..552878-chr10:830515..832425,2	MCF-7	breast:
42	chr10:817104..818718-chr10:820025..821722,2	MCF-7	breast:
43	chr10:851680..853848-chr10:854341..855901,2	K562	blood:
44	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:
45	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:
46	chr10:847643..849814-chr10:851213..852909,2	K562	blood:
47	chr10:733970..741093-chr10:828125..835309,12	MCF-7	breast:
48	chr10:461779..462665-chr10:840464..841138,2	MCF-7	breast:
49	chr10:835119..835814-chr10:856015..856751,2	MCF-7	breast:
50	chr10:733897..735933-chr10:814143..815828,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-6	chr10:779932-779973	NONHSAT010872
2	lnc-C10orf108-4	chr10:790517-790898	XLOC_008335
3	lnc-C10orf108-4	chr10:789932-789973	XLOC_008335
4	lnc-C10orf108-6	chr10:780517-780898	NONHSAT010872

No data

Variant related genes	Relation type
ENSG00000231601	TF binding region
ENSG00000231601	CpG island
ENSG00000015171	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000231601	chromatin interactions
ENSG00000151240	chromatin interactions
ENSG00000107929	chromatin interactions
ENSG00000165476	chromatin interactions
SEC23IP	miRNA target sites
SEC24A	miRNA target sites

Extended variants
information (count: 4185 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4185 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs498690	chr10:766867-766868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531102449	chr10:766887-766888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544553190	chr10:766902-766903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114625873	chr10:766905-766906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7092691	chr10:766909-766910	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs816316	chr10:766995-766996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566931201	chr10:767009-767010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532528806	chr10:767040-767041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544765203	chr10:767063-767064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575650495	chr10:767085-767086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147817400	chr10:767121-767122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192904529	chr10:767165-767166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369172341	chr10:767183-767184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537965008	chr10:767189-767190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184311072	chr10:767195-767196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34694613	chr10:767197-767198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574541591	chr10:767203-767204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141351923	chr10:767228-767229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540115880	chr10:767229-767230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72776414	chr10:767235-767236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs552919426	chr10:767248-767249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572877943	chr10:767261-767262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376684642	chr10:767288-767289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544816352	chr10:767321-767322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs816317	chr10:767329-767330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs2066129	chr10:767343-767344	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188718331	chr10:767357-767358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11253354	chr10:767369-767370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs816318	chr10:767395-767396	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs376137140	chr10:767402-767403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540800658	chr10:767412-767413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560558841	chr10:767427-767428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7475589	chr10:767479-767480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs552340856	chr10:767485-767486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs58516421	chr10:767496-767497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4504989	chr10:767508-767509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs4636581	chr10:767516-767517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs548623914	chr10:767524-767525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561644751	chr10:767536-767537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536186608	chr10:767545-767546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183731440	chr10:767546-767547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189267369	chr10:767553-767554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538831131	chr10:767570-767571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558328764	chr10:767577-767578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575010987	chr10:767592-767593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543779679	chr10:767615-767616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs67676753	chr10:767623-767624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4596995	chr10:767630-767631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574778821	chr10:767637-767638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4414142	chr10:767639-767640	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

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
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	21364760	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1251 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:761000-768200	Weak transcription	Placenta	Placenta
2	chr10:761000-768400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:764800-772000	Weak transcription	Right Atrium	heart
4	chr10:767800-768400	Weak transcription	Spleen	Spleen
5	chr10:768200-768600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:768200-769000	Enhancers	Placenta	Placenta
7	chr10:768400-768600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr10:768400-768600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:768400-768600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr10:768400-768600	Genic enhancers	Spleen	Spleen
11	chr10:768600-768800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:768600-770000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:768600-771400	Weak transcription	Spleen	Spleen
14	chr10:769000-771600	Weak transcription	Placenta	Placenta
15	chr10:770000-770200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:770000-770200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:770000-770400	Enhancers	Pancreas	Pancrea
18	chr10:770200-771800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:770800-771000	Weak transcription	Esophagus	oesophagus
20	chr10:770800-772200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr10:771400-771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr10:771400-772200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:771400-772200	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr10:771400-772200	Enhancers	Fetal Muscle Trunk	muscle
25	chr10:771400-772200	Enhancers	Fetal Muscle Leg	muscle
26	chr10:771400-772200	Enhancers	Spleen	Spleen
27	chr10:771400-773000	Enhancers	Right Ventricle	heart
28	chr10:771600-771800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr10:771600-772000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr10:771600-772200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr10:771600-774800	Enhancers	Placenta	Placenta
32	chr10:771800-772200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr10:771800-772400	Enhancers	Placenta Amnion	Placenta Amnion
34	chr10:772000-772200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:772000-772200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:772000-772200	Enhancers	Esophagus	oesophagus
37	chr10:772000-773400	Strong transcription	Right Atrium	heart
38	chr10:772200-772600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr10:772400-772800	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr10:772600-773000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr10:772800-773200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr10:772800-773600	Enhancers	Placenta Amnion	Placenta Amnion
43	chr10:773000-775200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr10:773400-775200	Weak transcription	Right Atrium	heart
45	chr10:774600-774800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr10:774600-774800	Enhancers	Right Ventricle	heart
47	chr10:774600-775400	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr10:774600-775600	Enhancers	Duodenum Mucosa	Duodenum
49	chr10:775200-775400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr10:775400-775600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum

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