Variant report

Variant	nsv1040280
Chromosome Location	chr10:90962032-90979093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:90976794-90977083	K562	blood:	n/a	n/a
2	ARID3A	chr10:90977504-90977801	HepG2	liver:	n/a	n/a
3	ATF1	chr10:90962713-90962913	K562	blood:	n/a	n/a
4	ATF2	chr10:90967074-90967622	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr10:90967890-90968348	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:90977557-90977558	K562	blood:	n/a	n/a
7	BACH1	chr10:90966612-90967905	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr10:90973091-90973291	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:90973134-90973341	K562	blood:	n/a	n/a
10	BHLHE40	chr10:90978376-90978456	K562	blood:	n/a	n/a
11	BHLHE40	chr10:90976770-90976990	GM12878	blood:	n/a	n/a
12	CEBPB	chr10:90964348-90964494	A549	lung:	n/a	chr10:90964352-90964365
13	CEBPB	chr10:90967011-90967556	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:90964249-90964402	IMR90	lung:	n/a	chr10:90964352-90964365
15	CEBPB	chr10:90967911-90968202	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr10:90970809-90971128	IMR90	lung:	n/a	n/a
17	CEBPB	chr10:90967078-90967537	A549	lung:	n/a	n/a
18	CEBPB	chr10:90967242-90967532	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:90970901-90971092	Hela-S3	cervix:	n/a	n/a
20	CHD1	chr10:90967727-90968083	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr10:90972921-90973427	IMR90	lung:	n/a	n/a
22	CHD2	chr10:90967594-90967794	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr10:90966262-90966896	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr10:90966214-90967345	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTBP2	chr10:90967588-90968408	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr10:90976800-90976950	GM06990	blood:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
27	CTCF	chr10:90976797-90977032	Pancreas_OC	pancreas:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
28	CTCF	chr10:90973083-90973244	GM10248	blood:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
29	CTCF	chr10:90973103-90973224	NHEK	skin:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
30	CTCF	chr10:90976840-90976990	NHDF-neo	bronchial:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
31	CTCF	chr10:90977463-90977763	HUVEC	blood vessel:	n/a	chr10:90977617-90977630 chr10:90977617-90977630 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90977610-90977631
32	CTCF	chr10:90977476-90977691	A549	lung:	n/a	chr10:90977617-90977630 chr10:90977617-90977630 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90977610-90977631
33	CTCF	chr10:90977520-90977670	HCM	heart:	n/a	chr10:90977617-90977630 chr10:90977617-90977630 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90977610-90977631
34	CTCF	chr10:90976840-90976990	HRPEpiC	eye:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
35	CTCF	chr10:90977580-90977730	GM12864	blood:	n/a	chr10:90977617-90977630 chr10:90977617-90977630 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90977610-90977631
36	CTCF	chr10:90973031-90973283	HepG2	liver:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
37	CTCF	chr10:90977520-90977670	WI-38	lung:	n/a	chr10:90977617-90977630 chr10:90977617-90977630 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90977610-90977631
38	CTCF	chr10:90973043-90973289	A549	lung:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
39	CTCF	chr10:90973100-90973250	HRE	kidney:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
40	CTCF	chr10:90977416-90977761	ECC-1	luminal epithelium:	n/a	chr10:90977617-90977630 chr10:90977617-90977630 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90977610-90977631
41	CTCF	chr10:90976814-90977018	GM10266	blood:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
42	CTCF	chr10:90973080-90973230	BE2_C	brain:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
43	CTCF	chr10:90973062-90973273	K562	blood:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
44	CTCF	chr10:90977520-90977670	HCT-116	colon:	n/a	chr10:90977617-90977630 chr10:90977617-90977630 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90977610-90977631
45	CTCF	chr10:90976800-90976950	HA-sp	spinal cord:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
46	CTCF	chr10:90966740-90966890	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr10:90976583-90977857	SK-N-SH	brain:	n/a	chr10:90976913-90976929 chr10:90977617-90977630 chr10:90976914-90976935 chr10:90977617-90977630 chr10:90976915-90976928 chr10:90977615-90977633 chr10:90977616-90977632 chr10:90976912-90976930 chr10:90976915-90976928 chr10:90977610-90977631
48	CTCF	chr10:90968100-90968250	HRE	kidney:	n/a	n/a
49	CTCF	chr10:90976780-90976930	HRE	kidney:	n/a	chr10:90976913-90976929 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
50	CTCF	chr10:90976780-90976930	HMEC	breast:	n/a	chr10:90976913-90976929 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90967700-90967750	GM06990	blood:	n/a
2	chr10:90967700-90967750	GM06990	blood:	n/a
3	chr10:90967189-90967239	HMEC	breast:	n/a
4	chr10:90971685-90971735	AG10803	skin:	n/a
5	chr10:90973635-90973685	T-47D	breast:	n/a
6	chr10:90967113-90967163	NB4	blood:	n/a
7	chr10:90964806-90964856	ovcar-3	ovarian:	n/a
8	chr10:90967918-90967968	AG09309	skin:	n/a
9	chr10:90967918-90967968	BE2_C	brain:	n/a
10	chr10:90964806-90964856	Jurkat	blood:	n/a
11	chr10:90966807-90966857	PFSK-1	brain:	n/a
12	chr10:90967189-90967239	HRE	kidney:	n/a
13	chr10:90967233-90967283	T-47D	breast:	n/a
14	chr10:90967189-90967239	H1-hESC	embryonic stem cell:	embryo
15	chr10:90966807-90966857	GM06990	blood:	n/a
16	chr10:90967052-90967102	HRPEpiC	eye:	n/a
17	chr10:90967157-90967207	HRE	kidney:	n/a
18	chr10:90967233-90967283	GM19239	blood:	n/a
19	chr10:90973635-90973685	HAEpiC	amniotic membrane:	n/a
20	chr10:90967113-90967163	GM12878	blood:	n/a
21	chr10:90967894-90967944	NHBE	bronchial:	n/a
22	chr10:90966807-90966857	BJ	skin:	n/a
23	chr10:90966221-90966271	SK-N-SH_RA	brain:	n/a
24	chr10:90966524-90966574	HCM	heart:	n/a
25	chr10:90971685-90971735	ovcar-3	ovarian:	n/a
26	chr10:90973635-90973685	MCF-7	breast:	n/a
27	chr10:90967700-90967750	AG04450	lung:	fetal
28	chr10:90967165-90967215	HEK293	kidney:	embryo
29	chr10:90967160-90967210	SK-N-SH_RA	brain:	n/a
30	chr10:90967612-90967662	HEEpiC	esophagus:	n/a
31	chr10:90966807-90966857	AG10803	skin:	n/a
32	chr10:90966221-90966271	ovcar-3	ovarian:	n/a
33	chr10:90967700-90967750	A549	lung:	n/a
34	chr10:90967896-90967946	PANC-1	pancreas:	n/a
35	chr10:90967165-90967215	GM19239	blood:	n/a
36	chr10:90967894-90967944	AG04449	skin:	fetal
37	chr10:90967052-90967102	HEEpiC	esophagus:	n/a
38	chr10:90966221-90966271	GM06990	blood:	n/a
39	chr10:90967918-90967968	NHBE	bronchial:	n/a
40	chr10:90967700-90967750	PANC-1	pancreas:	n/a
41	chr10:90967189-90967239	HAEpiC	amniotic membrane:	n/a
42	chr10:90967233-90967283	ECC-1	luminal epithelium:	n/a
43	chr10:90967700-90967750	HUVEC	blood vessel:	n/a
44	chr10:90967918-90967968	AG09319	gingival:	n/a
45	chr10:90967896-90967946	AG04449	skin:	fetal
46	chr10:90971685-90971735	K562	blood:	n/a
47	chr10:90967918-90967968	MCF10A-Er-Src	breast:	n/a
48	chr10:90964806-90964856	GM12891	blood:	n/a
49	chr10:90967165-90967215	U87	brain:	n/a
50	chr10:90967052-90967102	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:90694758..90695380-chr10:90973136..90973942,2	MCF-7	breast:
2	chr10:90694072..90695760-chr10:90972688..90973953,5	K562	blood:
3	chr10:90976747..90977329-chr10:91148741..91149345,3	MCF-7	breast:
4	chr10:90595067..90595903-chr10:90977181..90977798,2	MCF-7	breast:
5	chr10:90790531..90793137-chr10:90969474..90972044,2	MCF-7	breast:
6	chr10:90791836..90792785-chr10:90972789..90973327,2	K562	blood:
7	chr10:90789320..90789878-chr10:90977149..90978105,4	MCF-7	breast:
8	chr10:90789103..90790276-chr10:90972621..90973980,11	MCF-7	breast:
9	chr10:90694766..90695788-chr10:90977194..90977863,3	MCF-7	breast:
10	chr10:90789744..90790664-chr10:90976871..90977665,2	K562	blood:
11	chr10:90789732..90790480-chr10:90976549..90977068,2	MCF-7	breast:
12	chr10:90976929..90977851-chr3:181501046..181501546,2	K562	blood:
13	chr10:90977663..90978549-chr16:17305673..17306359,2	MCF-7	breast:
14	chr10:90976826..90977367-chr10:91323303..91323918,2	MCF-7	breast:
15	chr10:90694469..90695004-chr10:90977172..90978110,2	MCF-7	breast:
16	chr10:90789343..90790605-chr10:90972311..90973617,4	MCF-7	breast:

Variant related genes	Relation type
CH25H	TF binding region
CH25H	CpG island

Extended variants
information (count: 704 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115082909	chr10:90962041-90962042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536622324	chr10:90962050-90962051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566614898	chr10:90962051-90962052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs578180458	chr10:90962078-90962079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556196908	chr10:90962135-90962136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545593633	chr10:90962171-90962172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560434078	chr10:90962197-90962198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144680710	chr10:90962229-90962230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138503713	chr10:90962239-90962240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561352200	chr10:90962260-90962261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575103376	chr10:90962270-90962271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74622033	chr10:90962344-90962345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549901361	chr10:90962371-90962372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544905799	chr10:90962375-90962376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141112679	chr10:90962376-90962377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141160735	chr10:90962439-90962440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150788919	chr10:90962454-90962455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192323526	chr10:90962471-90962472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565506150	chr10:90962482-90962483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574630661	chr10:90962534-90962535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554795166	chr10:90962538-90962539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78904889	chr10:90962562-90962563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547912071	chr10:90962593-90962594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117112441	chr10:90962680-90962681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537090532	chr10:90962718-90962719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558228444	chr10:90962726-90962727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73368289	chr10:90962736-90962737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs538934701	chr10:90962751-90962752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554420273	chr10:90962779-90962780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373594464	chr10:90962781-90962782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543218753	chr10:90962789-90962790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376141404	chr10:90962837-90962838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115191281	chr10:90962848-90962849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4934456	chr10:90962878-90962879	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs543806795	chr10:90962913-90962914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147203581	chr10:90962932-90962933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532454304	chr10:90962959-90962960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547413110	chr10:90962961-90962962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559203431	chr10:90962995-90962996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541881166	chr10:90963005-90963006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185735678	chr10:90963040-90963041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547973293	chr10:90963116-90963117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574783456	chr10:90963117-90963118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188241577	chr10:90963159-90963160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530477421	chr10:90963169-90963170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193176722	chr10:90963210-90963211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200432946	chr10:90963231-90963232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201522383	chr10:90963232-90963233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184665323	chr10:90963288-90963289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570316493	chr10:90963289-90963290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90960800-90962200	Enhancers	NHEK	skin
2	chr10:90961000-90962200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr10:90961000-90962200	Enhancers	NHLF	lung
4	chr10:90961200-90962200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr10:90961400-90962200	Enhancers	HMEC	breast
6	chr10:90961400-90962400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr10:90961600-90962200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr10:90961600-90962400	Enhancers	Esophagus	oesophagus
9	chr10:90961600-90963000	Weak transcription	NHDF-Ad	bronchial
10	chr10:90961800-90963000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr10:90962200-90963200	Weak transcription	NHLF	lung
12	chr10:90962400-90963400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr10:90962400-90966200	Weak transcription	Esophagus	oesophagus
14	chr10:90962800-90963000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:90963000-90963200	Enhancers	NHDF-Ad	bronchial
16	chr10:90963000-90963600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:90963000-90964000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:90963200-90963800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr10:90963200-90963800	Enhancers	NHLF	lung
20	chr10:90963400-90963600	Bivalent/Poised TSS	NHDF-Ad	bronchial
21	chr10:90963400-90963800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr10:90963400-90963800	Bivalent Enhancer	Fetal Thymus	thymus
23	chr10:90963400-90964000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:90963600-90963800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
25	chr10:90963600-90963800	Bivalent Enhancer	Aorta	Aorta
26	chr10:90963800-90964000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr10:90963800-90964000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:90963800-90965000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr10:90963800-90965800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr10:90964000-90964400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr10:90964200-90964400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
32	chr10:90964400-90965200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr10:90964600-90965000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
34	chr10:90964800-90967400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr10:90965000-90965400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr10:90965000-90966800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr10:90965200-90965400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
38	chr10:90965200-90965600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr10:90965200-90965800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
40	chr10:90965200-90966400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
41	chr10:90965400-90965600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
42	chr10:90965400-90966200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
43	chr10:90965400-90966200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr10:90965400-90966200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr10:90965400-90966200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
46	chr10:90965400-90966200	Bivalent/Poised TSS	Fetal Thymus	thymus
47	chr10:90965400-90966200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
48	chr10:90965400-90966200	Bivalent/Poised TSS	NHDF-Ad	bronchial
49	chr10:90965400-90966800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
50	chr10:90965400-90966800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell

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