Variant report

Variant	nsv1042428
Chromosome Location	chr10:90962252-90977164
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	ATF1	chr10:90962713-90962913	K562	blood:	n/a	n/a
3	ATF2	chr10:90967890-90968348	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:90967074-90967622	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:90966612-90967905	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr10:90973091-90973291	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:90976770-90976990	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:90973134-90973341	K562	blood:	n/a	n/a
9	CEBPB	chr10:90970901-90971092	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr10:90967242-90967532	HepG2	liver:	n/a	n/a
11	CEBPB	chr10:90964348-90964494	A549	lung:	n/a	chr10:90964352-90964365
12	CEBPB	chr10:90967078-90967537	A549	lung:	n/a	n/a
13	CEBPB	chr10:90970809-90971128	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:90964249-90964402	IMR90	lung:	n/a	chr10:90964352-90964365
15	CEBPB	chr10:90967011-90967556	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:90967911-90968202	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr10:90972921-90973427	IMR90	lung:	n/a	n/a
18	CHD1	chr10:90967727-90968083	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr10:90967594-90967794	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr10:90966262-90966896	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr10:90967588-90968408	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr10:90966214-90967345	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr10:90973080-90973230	WERI-Rb-1	eye:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
24	CTCF	chr10:90976785-90976952	SK-N-SH_RA	brain:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
25	CTCF	chr10:90966801-90966896	NHEK	skin:	n/a	n/a
26	CTCF	chr10:90973100-90973250	Caco-2	colon:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
27	CTCF	chr10:90976780-90976930	BE2_C	brain:	n/a	chr10:90976913-90976929 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
28	CTCF	chr10:90976820-90976970	HMF	breast:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
29	CTCF	chr10:90973080-90973230	BJ	skin:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
30	CTCF	chr10:90976784-90977049	ECC-1	luminal epithelium:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
31	CTCF	chr10:90973120-90973270	GM12875	blood:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
32	CTCF	chr10:90973100-90973250	K562	blood:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
33	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
34	CTCF	chr10:90973047-90973277	Hela-S3	cervix:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
35	CTCF	chr10:90973120-90973270	WERI-Rb-1	eye:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
36	CTCF	chr10:90976860-90977010	AG04450	lung:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
37	CTCF	chr10:90973042-90973316	ECC-1	luminal epithelium:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
38	CTCF	chr10:90976820-90976970	AG10803	skin:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
39	CTCF	chr10:90973053-90973281	Lung_OC	lung:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
40	CTCF	chr10:90976740-90976890	RPTEC	kidney:	n/a	n/a
41	CTCF	chr10:90973100-90973250	AG04450	lung:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
42	CTCF	chr10:90976720-90977836	IMR90	lung:	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
43	CTCF	chr10:90976786-90977098	HUVEC	blood vessel:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
44	CTCF	chr10:90966820-90966970	HRE	kidney:	n/a	n/a
45	CTCF	chr10:90976840-90976990	GM12872	blood:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
46	CTCF	chr10:90966820-90966970	GM12864	blood:	n/a	n/a
47	CTCF	chr10:90976840-90976990	AoAF	blood vessel:	n/a	chr10:90976913-90976929 chr10:90976914-90976935 chr10:90976915-90976928 chr10:90976912-90976930 chr10:90976915-90976928
48	CTCF	chr10:90973100-90973250	GM12871	blood:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
49	CTCF	chr10:90973080-90973230	AG04449	skin:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169
50	CTCF	chr10:90973100-90973250	HEEpiC	esophagus:	n/a	chr10:90973155-90973168 chr10:90973153-90973171 chr10:90973154-90973170 chr10:90973148-90973169

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90967157-90967207	T-47D	breast:	n/a
2	chr10:90967165-90967215	GM12891	blood:	n/a
3	chr10:90964806-90964856	HRE	kidney:	n/a
4	chr10:90967896-90967946	HEK293	kidney:	embryo
5	chr10:90966524-90966574	ovcar-3	ovarian:	n/a
6	chr10:90971685-90971735	HRCEpiC	kidney:	n/a
7	chr10:90964806-90964856	NHDF-neo	bronchial:	n/a
8	chr10:90966524-90966574	ProgFib	skin:	n/a
9	chr10:90967700-90967750	HepG2	liver:	n/a
10	chr10:90967165-90967215	HIPEpiC	eye:	n/a
11	chr10:90967052-90967102	ECC-1	luminal epithelium:	n/a
12	chr10:90967896-90967946	Caco-2	colon:	n/a
13	chr10:90967165-90967215	GM06990	blood:	n/a
14	chr10:90967157-90967207	ProgFib	skin:	n/a
15	chr10:90966524-90966574	GM12878	blood:	n/a
16	chr10:90967052-90967102	PANC-1	pancreas:	n/a
17	chr10:90967612-90967662	CMK	blood:	n/a
18	chr10:90966701-90966751	ProgFib	skin:	n/a
19	chr10:90966524-90966574	Hela-S3	cervix:	n/a
20	chr10:90973635-90973685	BJ	skin:	n/a
21	chr10:90967052-90967102	HNPCEpiC	eye:	n/a
22	chr10:90967113-90967163	HPAEpiC	pulmonary alveolar:	n/a
23	chr10:90966524-90966574	SAEC	small airway:	n/a
24	chr10:90967189-90967239	GM06990	blood:	n/a
25	chr10:90966524-90966574	HRE	kidney:	n/a
26	chr10:90967612-90967662	A549	lung:	n/a
27	chr10:90967894-90967944	GM19239	blood:	n/a
28	chr10:90966807-90966857	NH-A	brain:	n/a
29	chr10:90967918-90967968	ovcar-3	ovarian:	n/a
30	chr10:90967157-90967207	Hepatocyte	liver:	n/a
31	chr10:90967113-90967163	ProgFib	skin:	n/a
32	chr10:90967160-90967210	NHDF-neo	bronchial:	n/a
33	chr10:90966701-90966751	MCF10A-Er-Src	breast:	n/a
34	chr10:90967233-90967283	BE2_C	brain:	n/a
35	chr10:90968091-90968141	GM12878	blood:	n/a
36	chr10:90967894-90967944	CMK	blood:	n/a
37	chr10:90967160-90967210	HRE	kidney:	n/a
38	chr10:90966701-90966751	GM19239	blood:	n/a
39	chr10:90967612-90967662	Hela-S3	cervix:	n/a
40	chr10:90967918-90967968	HCF	heart:	n/a
41	chr10:90967918-90967968	HepG2	liver:	n/a
42	chr10:90967233-90967283	Jurkat	blood:	n/a
43	chr10:90967113-90967163	SK-N-SH_RA	brain:	n/a
44	chr10:90966701-90966751	HCM	heart:	n/a
45	chr10:90967233-90967283	MCF-7	breast:	n/a
46	chr10:90971685-90971735	HPAEpiC	pulmonary alveolar:	n/a
47	chr10:90967894-90967944	ECC-1	luminal epithelium:	n/a
48	chr10:90967894-90967944	HNPCEpiC	eye:	n/a
49	chr10:90967113-90967163	Hepatocyte	liver:	n/a
50	chr10:90973635-90973685	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:90789320..90789878-chr10:90977149..90978105,4	MCF-7	breast:
2	chr10:90694758..90695380-chr10:90973136..90973942,2	MCF-7	breast:
3	chr10:90976826..90977367-chr10:91323303..91323918,2	MCF-7	breast:
4	chr10:90790531..90793137-chr10:90969474..90972044,2	MCF-7	breast:
5	chr10:90976929..90977851-chr3:181501046..181501546,2	K562	blood:
6	chr10:90789343..90790605-chr10:90972311..90973617,4	MCF-7	breast:
7	chr10:90789732..90790480-chr10:90976549..90977068,2	MCF-7	breast:
8	chr10:90791836..90792785-chr10:90972789..90973327,2	K562	blood:
9	chr10:90789103..90790276-chr10:90972621..90973980,11	MCF-7	breast:
10	chr10:90694072..90695760-chr10:90972688..90973953,5	K562	blood:
11	chr10:90789744..90790664-chr10:90976871..90977665,2	K562	blood:
12	chr10:90976747..90977329-chr10:91148741..91149345,3	MCF-7	breast:

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

Extended variants
information (count: 621 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561352200	chr10:90962260-90962261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575103376	chr10:90962270-90962271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74622033	chr10:90962344-90962345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549901361	chr10:90962371-90962372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544905799	chr10:90962375-90962376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141112679	chr10:90962376-90962377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141160735	chr10:90962439-90962440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150788919	chr10:90962454-90962455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192323526	chr10:90962471-90962472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565506150	chr10:90962482-90962483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574630661	chr10:90962534-90962535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554795166	chr10:90962538-90962539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78904889	chr10:90962562-90962563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547912071	chr10:90962593-90962594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117112441	chr10:90962680-90962681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537090532	chr10:90962718-90962719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558228444	chr10:90962726-90962727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73368289	chr10:90962736-90962737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs538934701	chr10:90962751-90962752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554420273	chr10:90962779-90962780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373594464	chr10:90962781-90962782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543218753	chr10:90962789-90962790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376141404	chr10:90962837-90962838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115191281	chr10:90962848-90962849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4934456	chr10:90962878-90962879	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs543806795	chr10:90962913-90962914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147203581	chr10:90962932-90962933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532454304	chr10:90962959-90962960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547413110	chr10:90962961-90962962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559203431	chr10:90962995-90962996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541881166	chr10:90963005-90963006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185735678	chr10:90963040-90963041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547973293	chr10:90963116-90963117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574783456	chr10:90963117-90963118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188241577	chr10:90963159-90963160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530477421	chr10:90963169-90963170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193176722	chr10:90963210-90963211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200432946	chr10:90963231-90963232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201522383	chr10:90963232-90963233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184665323	chr10:90963288-90963289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570316493	chr10:90963289-90963290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534595056	chr10:90963327-90963328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554532614	chr10:90963331-90963332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115108425	chr10:90963346-90963347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536884317	chr10:90963371-90963372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555158902	chr10:90963373-90963374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189985912	chr10:90963386-90963387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543519154	chr10:90963405-90963406	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs370209491	chr10:90963409-90963410	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs372147258	chr10:90963415-90963416	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	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:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90961400-90962400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr10:90961600-90962400	Enhancers	Esophagus	oesophagus
3	chr10:90961600-90963000	Weak transcription	NHDF-Ad	bronchial
4	chr10:90961800-90963000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:90962200-90963200	Weak transcription	NHLF	lung
6	chr10:90962400-90963400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr10:90962400-90966200	Weak transcription	Esophagus	oesophagus
8	chr10:90962800-90963000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:90963000-90963200	Enhancers	NHDF-Ad	bronchial
10	chr10:90963000-90963600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:90963000-90964000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:90963200-90963800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:90963200-90963800	Enhancers	NHLF	lung
14	chr10:90963400-90963600	Bivalent/Poised TSS	NHDF-Ad	bronchial
15	chr10:90963400-90963800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr10:90963400-90963800	Bivalent Enhancer	Fetal Thymus	thymus
17	chr10:90963400-90964000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:90963600-90963800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
19	chr10:90963600-90963800	Bivalent Enhancer	Aorta	Aorta
20	chr10:90963800-90964000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr10:90963800-90964000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr10:90963800-90965000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr10:90963800-90965800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr10:90964000-90964400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr10:90964200-90964400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
26	chr10:90964400-90965200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr10:90964600-90965000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
28	chr10:90964800-90967400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr10:90965000-90965400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
30	chr10:90965000-90966800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr10:90965200-90965400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr10:90965200-90965600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr10:90965200-90965800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
34	chr10:90965200-90966400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
35	chr10:90965400-90965600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
36	chr10:90965400-90966200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
37	chr10:90965400-90966200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
38	chr10:90965400-90966200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:90965400-90966200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
40	chr10:90965400-90966200	Bivalent/Poised TSS	Fetal Thymus	thymus
41	chr10:90965400-90966200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
42	chr10:90965400-90966200	Bivalent/Poised TSS	NHDF-Ad	bronchial
43	chr10:90965400-90966800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
44	chr10:90965400-90966800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr10:90965600-90966200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr10:90965600-90968400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
47	chr10:90965800-90966000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
48	chr10:90965800-90966200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr10:90965800-90966400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
50	chr10:90965800-90966400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum

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