Variant report

Variant	nsv894717
Chromosome Location	chr10:763714-834736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:546)
CpG islands
(count:3176)
Chromatin interactive
region (count:35)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	ATF1	chr10:813001-813370	K562	blood:	n/a	n/a
3	BACH1	chr10:830736-831092	H1-hESC	embryonic stem cell:	n/a	chr10:830863-830877
4	BCL11A	chr10:769301-769535	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:811979-812582	GM12878	blood:	n/a	n/a
6	BCL3	chr10:812586-812912	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:764330-764448	K562	blood:	n/a	n/a
8	BHLHE40	chr10:769894-770344	K562	blood:	n/a	n/a
9	BHLHE40	chr10:769085-769382	K562	blood:	n/a	n/a
10	CBX3	chr10:806640-806884	K562	blood:	n/a	n/a
11	CBX3	chr10:769860-770105	K562	blood:	n/a	n/a
12	CEBPB	chr10:830359-830527	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:830989-831276	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:776582-776736	Hela-S3	cervix:	n/a	chr10:776667-776678
15	CEBPB	chr10:799560-799705	K562	blood:	n/a	n/a
16	CEBPB	chr10:776514-776865	HepG2	liver:	n/a	chr10:776667-776678
17	CEBPB	chr10:776512-776828	A549	lung:	n/a	chr10:776667-776678
18	CEBPB	chr10:799626-799733	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:776542-776771	H1-hESC	embryonic stem cell:	n/a	chr10:776667-776678
20	CEBPB	chr10:830409-830580	IMR90	lung:	n/a	n/a
21	CHD1	chr10:830362-831385	IMR90	lung:	n/a	chr10:830616-830626
22	CHD2	chr10:764260-764276	K562	blood:	n/a	n/a
23	CHD2	chr10:831058-831106	HepG2	liver:	n/a	n/a
24	CTCF	chr10:830429-830597	H1-hESC	embryonic stem cell:	n/a	chr10:830492-830510
25	CTCF	chr10:824288-824325	GM20000	blood:	n/a	n/a
26	CTCF	chr10:830740-830890	HCT-116	colon:	n/a	n/a
27	CTCF	chr10:830880-831030	HFF-Myc	foreskin:	n/a	chr10:830940-830953
28	CTCF	chr10:830360-831162	MCF-7	breast:	n/a	chr10:830492-830510 chr10:830940-830953 chr10:831098-831111
29	CTCF	chr10:830740-830890	A549	lung:	n/a	n/a
30	CTCF	chr10:830480-830630	HA-sp	spinal cord:	n/a	chr10:830492-830510
31	CTCF	chr10:830800-830950	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:830800-830950	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr10:830450-830573	Fibrobl	skin:	n/a	chr10:830492-830510
34	CTCF	chr10:830420-830570	HepG2	liver:	n/a	chr10:830492-830510
35	CTCF	chr10:830920-831070	HEK293	kidney:	n/a	chr10:830940-830953
36	CTCF	chr10:775310-775349	Lung_OC	lung:	n/a	n/a
37	CTCF	chr10:830860-831010	HCFaa	heart:	n/a	chr10:830940-830953
38	CTCF	chr10:830435-830581	MCF-7	breast:	n/a	chr10:830492-830510
39	CTCF	chr10:830840-830990	HMF	breast:	n/a	chr10:830940-830953
40	CTCF	chr10:830873-830990	HUVEC	blood vessel:	n/a	chr10:830940-830953
41	CTCF	chr10:830434-830577	Pancreas_OC	pancreas:	n/a	chr10:830492-830510
42	CTCF	chr10:769293-769332	GM20000	blood:	n/a	n/a
43	CTCF	chr10:830420-830570	BE2_C	brain:	n/a	chr10:830492-830510
44	CTCF	chr10:830400-830550	Caco-2	colon:	n/a	chr10:830492-830510
45	CTCF	chr10:830820-830970	AG04449	skin:	n/a	chr10:830940-830953
46	CTCF	chr10:830840-830990	HEK293	kidney:	n/a	chr10:830940-830953
47	CTCF	chr10:834640-834790	GM12871	blood:	n/a	n/a
48	CTCF	chr10:830440-830590	SK-N-SH_RA	brain:	n/a	chr10:830492-830510
49	CTCF	chr10:830880-831030	HCPEpiC	choroid plexus:	n/a	chr10:830940-830953
50	CTCF	chr10:830880-831030	NHDF-neo	bronchial:	n/a	chr10:830940-830953

(count:3176 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:769945-769995	HAEpiC	amniotic membrane:	n/a
2	chr10:816999-817049	AG09309	skin:	n/a
3	chr10:766041-766091	HRE	kidney:	n/a
4	chr10:778709-778759	HEK293	kidney:	embryo
5	chr10:769945-769995	HAEpiC	amniotic membrane:	n/a
6	chr10:816999-817049	AG09309	skin:	n/a
7	chr10:766041-766091	HRE	kidney:	n/a
8	chr10:778709-778759	HEK293	kidney:	embryo
9	chr10:778709-778759	HNPCEpiC	eye:	n/a
10	chr10:831779-831829	HMEC	breast:	n/a
11	chr10:778123-778173	RPTEC	kidney:	n/a
12	chr10:778709-778759	GM12891	blood:	n/a
13	chr10:766464-766514	GM12892	blood:	n/a
14	chr10:772969-773019	SAEC	small airway:	n/a
15	chr10:819603-819653	Hepatocyte	liver:	n/a
16	chr10:821395-821445	MCF-7	breast:	n/a
17	chr10:778123-778173	HAEpiC	amniotic membrane:	n/a
18	chr10:823151-823201	RPTEC	kidney:	n/a
19	chr10:778073-778123	GM12891	blood:	n/a
20	chr10:766041-766091	SK-N-SH_RA	brain:	n/a
21	chr10:833127-833177	Caco-2	colon:	n/a
22	chr10:773141-773191	SK-N-SH_RA	brain:	n/a
23	chr10:831779-831829	Hepatocyte	liver:	n/a
24	chr10:834378-834428	AG04450	lung:	fetal
25	chr10:782282-782332	BE2_C	brain:	n/a
26	chr10:821124-821174	A549	lung:	n/a
27	chr10:831947-831997	AG04450	lung:	fetal
28	chr10:772969-773019	HL-60	blood:	n/a
29	chr10:817083-817133	HPAEpiC	pulmonary alveolar:	n/a
30	chr10:833290-833340	AG09319	gingival:	n/a
31	chr10:831835-831885	GM12878	blood:	n/a
32	chr10:766041-766091	GM12892	blood:	n/a
33	chr10:778073-778123	Hela-S3	cervix:	n/a
34	chr10:819603-819653	AoSMC	blood vessel:	n/a
35	chr10:768867-768917	PANC-1	pancreas:	n/a
36	chr10:829420-829470	SKMC	muscle:	n/a
37	chr10:769945-769995	HEK293	kidney:	embryo
38	chr10:778709-778759	HepG2	liver:	n/a
39	chr10:829333-829383	SKMC	muscle:	n/a
40	chr10:816999-817049	HL-60	blood:	n/a
41	chr10:820835-820885	LNCaP	prostate:	n/a
42	chr10:833127-833177	GM12878	blood:	n/a
43	chr10:768541-768591	U87	brain:	n/a
44	chr10:778123-778173	HIPEpiC	eye:	n/a
45	chr10:830689-830739	NB4	blood:	n/a
46	chr10:768867-768917	HUVEC	blood vessel:	n/a
47	chr10:829463-829513	T-47D	breast:	n/a
48	chr10:831835-831885	LNCaP	prostate:	n/a
49	chr10:834378-834428	HCPEpiC	choroid plexus:	n/a
50	chr10:782282-782332	HMEC	breast:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:817104..818718-chr10:820025..821722,2	MCF-7	breast:
2	chr10:634195..634721-chr10:829974..830911,3	MCF-7	breast:
3	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
4	chr10:829650..833485-chr10:834016..837949,4	MCF-7	breast:
5	chr10:632878..635792-chr10:829676..832349,2	MCF-7	breast:
6	chr10:734426..737338-chr10:832688..834504,2	MCF-7	breast:
7	chr10:783561..786479-chr10:789093..790752,2	MCF-7	breast:
8	chr10:735583..738437-chr10:825634..828452,2	MCF-7	breast:
9	chr10:833990..835898-chr10:1099433..1102164,2	K562	blood:
10	chr10:826973..829590-chr10:832494..835604,4	K562	blood:
11	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
12	chr10:657394..659426-chr10:833405..835908,2	MCF-7	breast:
13	chr10:826973..829121-chr10:832494..834058,2	K562	blood:
14	chr10:826973..829121-chr10:832494..834058,2	K562	blood:
15	chr10:461824..462560-chr10:834643..835579,2	MCF-7	breast:
16	chr10:550299..552878-chr10:830515..832425,2	MCF-7	breast:
17	chr10:831933..833433-chr10:65279794..65281725,2	MCF-7	breast:
18	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:
19	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
20	chr10:735855..737615-chr10:818949..821134,2	MCF-7	breast:
21	chr10:733897..735933-chr10:814143..815828,2	MCF-7	breast:
22	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:
23	chr10:733976..736630-chr10:829821..832143,2	MCF-7	breast:
24	chr10:739318..742202-chr10:834057..836421,2	MCF-7	breast:
25	chr10:733970..741093-chr10:828125..835309,12	MCF-7	breast:
26	chr10:819060..821540-chr10:825309..827354,2	MCF-7	breast:
27	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
28	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:
29	chr10:829650..833485-chr10:834016..837949,4	MCF-7	breast:
30	chr10:826973..829590-chr10:832494..835604,4	K562	blood:
31	chr10:698785..701781-chr10:833421..835495,2	MCF-7	breast:
32	chr10:817104..818718-chr10:820025..821722,2	MCF-7	breast:
33	chr10:823329..824026-chr16:78285555..78286055,2	MCF-7	breast:
34	chr10:819060..821540-chr10:825309..827354,2	MCF-7	breast:
35	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 3449 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3449 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12768599	chr10:763714-763715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs111964640	chr10:763738-763739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112252480	chr10:763746-763747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111759311	chr10:763755-763756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2993894	chr10:763768-763769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2993895	chr10:763769-763770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs71482852	chr10:763775-763776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546355240	chr10:763777-763778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12768655	chr10:763784-763785	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs562974734	chr10:763789-763790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71482851	chr10:763791-763792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113089514	chr10:763808-763809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548745279	chr10:763816-763817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2993896	chr10:763818-763819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111821020	chr10:763825-763826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12779469	chr10:763845-763846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12768840	chr10:763847-763848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12768844	chr10:763854-763855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77136205	chr10:763859-763860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12773324	chr10:763861-763862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113634262	chr10:763878-763879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2993897	chr10:763888-763889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112602444	chr10:763895-763896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369785352	chr10:763915-763916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374036683	chr10:763917-763918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375453415	chr10:763924-763925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369851540	chr10:763929-763930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372735831	chr10:763931-763932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61831377	chr10:763948-763949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112846469	chr10:763965-763966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372151226	chr10:763969-763970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377572743	chr10:763978-763979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370804299	chr10:763994-763995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374655603	chr10:763999-764000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367658567	chr10:764001-764002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113884451	chr10:764018-764019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371495698	chr10:764028-764029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553378877	chr10:764031-764032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577450023	chr10:764038-764039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71482849	chr10:764055-764056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113573915	chr10:764088-764089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551493715	chr10:764105-764106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575815	chr10:764109-764110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112022887	chr10:764118-764119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113218884	chr10:764134-764135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7095323	chr10:764139-764140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7068068	chr10:764141-764142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71489280	chr10:764158-764159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563091756	chr10:764192-764193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12784894	chr10:764195-764196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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

Chromatin state (count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr10:764200-764400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
4	chr10:764200-764600	Bivalent Enhancer	HepG2	liver
5	chr10:764800-772000	Weak transcription	Right Atrium	heart
6	chr10:767800-768400	Weak transcription	Spleen	Spleen
7	chr10:768200-768600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr10:768200-769000	Enhancers	Placenta	Placenta
9	chr10:768400-768600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr10:768400-768600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:768400-768600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:768400-768600	Genic enhancers	Spleen	Spleen
13	chr10:768600-768800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr10:768600-770000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr10:768600-771400	Weak transcription	Spleen	Spleen
16	chr10:769000-771600	Weak transcription	Placenta	Placenta
17	chr10:770000-770200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr10:770000-770200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:770000-770400	Enhancers	Pancreas	Pancrea
20	chr10:770200-771800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:770800-771000	Weak transcription	Esophagus	oesophagus
22	chr10:770800-772200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:771400-771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr10:771400-772200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr10:771400-772200	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr10:771400-772200	Enhancers	Fetal Muscle Trunk	muscle
27	chr10:771400-772200	Enhancers	Fetal Muscle Leg	muscle
28	chr10:771400-772200	Enhancers	Spleen	Spleen
29	chr10:771400-773000	Enhancers	Right Ventricle	heart
30	chr10:771600-771800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr10:771600-772000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr10:771600-772200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:771600-774800	Enhancers	Placenta	Placenta
34	chr10:771800-772200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:771800-772400	Enhancers	Placenta Amnion	Placenta Amnion
36	chr10:772000-772200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr10:772000-772200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr10:772000-772200	Enhancers	Esophagus	oesophagus
39	chr10:772000-773400	Strong transcription	Right Atrium	heart
40	chr10:772200-772600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr10:772400-772800	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr10:772600-773000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr10:772800-773200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr10:772800-773600	Enhancers	Placenta Amnion	Placenta Amnion
45	chr10:773000-775200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:773400-775200	Weak transcription	Right Atrium	heart
47	chr10:774600-774800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr10:774600-774800	Enhancers	Right Ventricle	heart
49	chr10:774600-775400	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr10:774600-775600	Enhancers	Duodenum Mucosa	Duodenum

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