Variant report

Variant	esv1834151
Chromosome Location	chr10:96925446-96992955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1597)
CpG islands
(count:1038)
Chromatin interactive
region (count:26)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1597 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:96968456-96968849	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:96941575-96941858	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:96968566-96968766	K562	blood:	n/a	n/a
4	ARID3A	chr10:96937886-96938999	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:96943386-96943426	K562	blood:	n/a	n/a
6	ATF2	chr10:96955730-96956135	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr10:96989260-96990956	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr10:96943372-96943658	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr10:96943280-96943679	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr10:96943278-96943673	GM12878	blood:	n/a	n/a
11	ATF2	chr10:96989170-96991319	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr10:96989222-96989972	A549	lung:	n/a	n/a
13	ATF3	chr10:96990627-96990956	GM12878	blood:	n/a	n/a
14	ATF3	chr10:96943347-96943798	A549	lung:	n/a	n/a
15	BACH1	chr10:96989434-96990974	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr10:96943380-96943878	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:96991400-96991618	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr10:96974644-96974850	GM12878	blood:	n/a	n/a
19	BCL3	chr10:96990626-96991073	GM12878	blood:	n/a	n/a
20	BCL3	chr10:96943282-96944065	A549	lung:	n/a	chr10:96943335-96943344 chr10:96943340-96943353 chr10:96943317-96943330 chr10:96943334-96943347 chr10:96943337-96943350
21	BCL3	chr10:96989110-96989992	A549	lung:	n/a	n/a
22	BCL3	chr10:96943398-96943752	GM12878	blood:	n/a	n/a
23	BCL3	chr10:96989196-96989903	A549	lung:	n/a	n/a
24	BCLAF1	chr10:96943300-96943894	GM12878	blood:	n/a	chr10:96943335-96943344 chr10:96943340-96943353 chr10:96943317-96943330 chr10:96943334-96943347 chr10:96943337-96943350
25	BCLAF1	chr10:96990333-96991038	GM12878	blood:	n/a	n/a
26	BCLAF1	chr10:96942994-96943820	GM12878	blood:	n/a	chr10:96943335-96943344 chr10:96943340-96943353 chr10:96943317-96943330 chr10:96943334-96943347 chr10:96943337-96943350
27	BHLHE40	chr10:96943258-96943763	GM12878	blood:	n/a	chr10:96943258-96943274 chr10:96943337-96943353 chr10:96943336-96943352 chr10:96943328-96943344
28	BHLHE40	chr10:96943199-96943888	K562	blood:	n/a	chr10:96943258-96943274 chr10:96943337-96943353 chr10:96943336-96943352 chr10:96943328-96943344
29	BRCA1	chr10:96943494-96943557	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr10:96939156-96939188	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr10:96989389-96989480	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr10:96989234-96989937	HCT-116	colon:	n/a	n/a
33	CBX3	chr10:96943302-96943679	K562	blood:	n/a	n/a
34	CBX3	chr10:96989210-96990027	HCT-116	colon:	n/a	n/a
35	CBX3	chr10:96943192-96943895	HCT-116	colon:	n/a	n/a
36	CCNT2	chr10:96943236-96943897	K562	blood:	n/a	n/a
37	CCNT2	chr10:96989467-96989708	K562	blood:	n/a	n/a
38	CEBPB	chr10:96968435-96968770	A549	lung:	n/a	n/a
39	CEBPB	chr10:96938610-96938955	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:96974669-96975038	IMR90	lung:	n/a	n/a
41	CEBPB	chr10:96938648-96938912	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:96989510-96990292	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr10:96990689-96991023	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr10:96989392-96989679	K562	blood:	n/a	n/a
45	CEBPB	chr10:96989366-96989891	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr10:96943068-96943674	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr10:96989325-96989847	MCF-7	breast:	n/a	n/a
48	CEBPB	chr10:96989184-96989972	A549	lung:	n/a	n/a
49	CEBPB	chr10:96980708-96981289	A549	lung:	n/a	n/a
50	CEBPB	chr10:96989302-96989818	A549	lung:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96943130-96943180	K562	blood:	n/a
2	chr10:96943130-96943180	K562	blood:	n/a
3	chr10:96990543-96990593	BE2_C	brain:	n/a
4	chr10:96954252-96954302	BE2_C	brain:	n/a
5	chr10:96991431-96991481	AG09309	skin:	n/a
6	chr10:96953953-96954003	Hela-S3	cervix:	n/a
7	chr10:96953447-96953497	PFSK-1	brain:	n/a
8	chr10:96943842-96943892	AG04450	lung:	fetal
9	chr10:96988478-96988528	CMK	blood:	n/a
10	chr10:96943563-96943613	GM12892	blood:	n/a
11	chr10:96943842-96943892	GM12891	blood:	n/a
12	chr10:96990700-96990750	GM06990	blood:	n/a
13	chr10:96943842-96943892	NHDF-neo	bronchial:	n/a
14	chr10:96990858-96990908	SK-N-SH_RA	brain:	n/a
15	chr10:96991431-96991481	NT2-D1	testis:	n/a
16	chr10:96990543-96990593	LNCaP	prostate:	n/a
17	chr10:96991431-96991481	GM06990	blood:	n/a
18	chr10:96946522-96946572	H1-hESC	embryonic stem cell:	embryo
19	chr10:96943130-96943180	MCF10A-Er-Src	breast:	n/a
20	chr10:96990543-96990593	AG10803	skin:	n/a
21	chr10:96943130-96943180	HCT-116	colon:	n/a
22	chr10:96954252-96954302	SAEC	small airway:	n/a
23	chr10:96943196-96943246	HRE	kidney:	n/a
24	chr10:96991505-96991555	LNCaP	prostate:	n/a
25	chr10:96991431-96991481	HUVEC	blood vessel:	n/a
26	chr10:96954252-96954302	Hela-S3	cervix:	n/a
27	chr10:96943196-96943246	HCF	heart:	n/a
28	chr10:96991505-96991555	GM19239	blood:	n/a
29	chr10:96989650-96989700	HRPEpiC	eye:	n/a
30	chr10:96991461-96991511	GM12891	blood:	n/a
31	chr10:96954252-96954302	HUVEC	blood vessel:	n/a
32	chr10:96943563-96943613	PANC-1	pancreas:	n/a
33	chr10:96943196-96943246	HAEpiC	amniotic membrane:	n/a
34	chr10:96991461-96991511	Hepatocyte	liver:	n/a
35	chr10:96953447-96953497	NT2-D1	testis:	n/a
36	chr10:96954252-96954302	HRE	kidney:	n/a
37	chr10:96954252-96954302	GM06990	blood:	n/a
38	chr10:96990858-96990908	SK-N-MC	brain:	n/a
39	chr10:96991505-96991555	BJ	skin:	n/a
40	chr10:96988478-96988528	HNPCEpiC	eye:	n/a
41	chr10:96943842-96943892	CMK	blood:	n/a
42	chr10:96943196-96943246	T-47D	breast:	n/a
43	chr10:96988478-96988528	SAEC	small airway:	n/a
44	chr10:96953447-96953497	AoSMC	blood vessel:	n/a
45	chr10:96943130-96943180	Hela-S3	cervix:	n/a
46	chr10:96990858-96990908	HUVEC	blood vessel:	n/a
47	chr10:96991505-96991555	HCM	heart:	n/a
48	chr10:96943130-96943180	HCM	heart:	n/a
49	chr10:96990543-96990593	HAEpiC	amniotic membrane:	n/a
50	chr10:96943196-96943246	AG09319	gingival:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:96980306..96982138-chr10:96989812..96992321,2	MCF-7	breast:
2	chr10:96941976..96944883-chr10:96989765..96992078,3	MCF-7	breast:
3	chr10:96943335..96943883-chr10:96990715..96991433,2	MCF-7	breast:
4	chr10:96988601..96990244-chr10:96996425..96998002,2	K562	blood:
5	chr10:96944739..96947695-chr10:96950554..96953637,4	MCF-7	breast:
6	chr10:96989099..96991002-chr10:97047738..97051859,4	MCF-7	breast:
7	chr10:96983483..96986000-chr10:96988928..96992913,3	MCF-7	breast:
8	chr10:96930488..96932812-chr10:96939629..96941375,2	K562	blood:
9	chr10:96983667..96985290-chr10:96987249..96989514,2	MCF-7	breast:
10	chr10:96983667..96985290-chr10:96987249..96989514,2	MCF-7	breast:
11	chr10:96942861..96945609-chr10:96947623..96949502,2	K562	blood:
12	chr10:96985157..96986698-chr10:96990407..96993016,2	MCF-7	breast:
13	chr10:96941976..96944883-chr10:96989765..96992078,3	MCF-7	breast:
14	chr10:96943146..96943822-chr10:96960689..96961635,2	MCF-7	breast:
15	chr10:96968177..96969122-chr10:97002506..97003338,4	MCF-7	breast:
16	chr10:96983644..96985637-chr10:96989361..96991556,3	K562	blood:
17	chr10:96944739..96947695-chr10:96950554..96953637,4	MCF-7	breast:
18	chr10:96975681..96977490-chr10:97052151..97054934,2	K562	blood:
19	chr10:96930488..96932812-chr10:96939629..96941375,2	K562	blood:
20	chr10:96951132..96952713-chr10:96952994..96955144,2	K562	blood:
21	chr10:96389607..96390553-chr10:96935620..96936165,2	MCF-7	breast:
22	chr10:96950676..96951601-chr12:66448498..66449065,2	MCF-7	breast:
23	chr10:96389495..96390471-chr10:96935594..96936525,3	MCF-7	breast:
24	chr10:96961108..96962057-chr10:97002638..97003736,3	MCF-7	breast:
25	chr10:96977704..96978224-chr3:16493125..16493645,2	MCF-7	breast:
26	chr10:96943335..96943883-chr10:96990715..96991433,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDLIM1-1	chr10:96988595-96988626	NONHSAT015754
2	lnc-PDLIM1-1	chr10:96988095-96988183	NONHSAT015752
3	lnc-PDLIM1-1	chr10:96985248-96985468	NONHSAT015752
4	lnc-PDLIM1-2	chr10:96928138-96928182	ENSG00000231829.2
5	lnc-PDLIM1-3	chr10:96976459-96978173	ucscGeneNc_uc001kkg_1
6	lnc-PDLIM1-3	chr10:96980413-96980891	ucscGeneNc_uc001kkg_1
7	lnc-PDLIM1-1	chr10:96990423-96990901	NONHSAT015753
8	lnc-PDLIM1-1	chr10:96986469-96988183	NONHSAT015753
9	lnc-PDLIM1-1	chr10:96990423-96990825	NONHSAT015754
10	lnc-PDLIM1-1	chr10:96990423-96990825	NONHSAT015752
11	lnc-PDLIM1-1	chr10:96988000-96988183	ENSG00000234026
12	lnc-PDLIM1-1	chr10:96990423-96990901	ENSG00000234026
13	lnc-PDLIM1-2	chr10:96928138-96928182	XLOC_008910

No data

Variant related genes	Relation type
ENSG00000234026	TF binding region
PAWRP1	TF binding region
C10orf129	TF binding region
ENSG00000231829	TF binding region
ENSG00000234026	CpG island
PAWRP1	CpG island
C10orf129	CpG island
ENSG00000231829	CpG island
ENSG00000234026	chromatin interactions
ENSG00000107438	chromatin interactions
ENSG00000173124	chromatin interactions
ENSG00000225533	chromatin interactions

Extended variants
information (count: 2362 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2362 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560902820	chr10:96926411-96926412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571718446	chr10:96926440-96926441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149483768	chr10:96926479-96926480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543591006	chr10:96926492-96926493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563228169	chr10:96926535-96926536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183584690	chr10:96926553-96926554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551654180	chr10:96926592-96926593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565587952	chr10:96926636-96926637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528011491	chr10:96926751-96926752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112996052	chr10:96926758-96926759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567367714	chr10:96926814-96926815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36187277	chr10:96926857-96926858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536235115	chr10:96926859-96926860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188955182	chr10:96926915-96926916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570001730	chr10:96926918-96926919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7090961	chr10:96926921-96926922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs558436464	chr10:96926926-96926927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572190874	chr10:96926973-96926974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs815267	chr10:96926983-96926984	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554900214	chr10:96927011-96927012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574527785	chr10:96927013-96927014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192448042	chr10:96927056-96927057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs815268	chr10:96927060-96927061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568168300	chr10:96927079-96927080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576829513	chr10:96927112-96927113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552589177	chr10:96927181-96927182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566471270	chr10:96927189-96927190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545867597	chr10:96927190-96927191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182224223	chr10:96927218-96927219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527876048	chr10:96927228-96927229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541363641	chr10:96927250-96927251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561204539	chr10:96927331-96927332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530036860	chr10:96927338-96927339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538509670	chr10:96927362-96927363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186469709	chr10:96927374-96927375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191769681	chr10:96927386-96927387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141000836	chr10:96927388-96927389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536045255	chr10:96927444-96927445	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs117946892	chr10:96927505-96927506	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534803129	chr10:96927545-96927546	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554912307	chr10:96927546-96927547	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs611416	chr10:96927574-96927575	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs376635561	chr10:96927592-96927593	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537059379	chr10:96927597-96927598	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34011964	chr10:96927612-96927613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556716537	chr10:96927614-96927615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184605645	chr10:96927646-96927647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188196220	chr10:96927666-96927667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545626615	chr10:96927678-96927679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79395738	chr10:96927723-96927724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	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
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96926400-96937400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr10:96927000-96931800	Weak transcription	Aorta	Aorta
3	chr10:96927200-96935400	Weak transcription	Fetal Intestine Small	intestine
4	chr10:96927400-96927600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr10:96927600-96928600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:96928000-96929000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:96928600-96928800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr10:96928600-96928800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr10:96928800-96929000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr10:96928800-96929000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr10:96929000-96932400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:96930200-96932000	Enhancers	Pancreas	Pancrea
13	chr10:96930600-96931400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr10:96931000-96931800	Enhancers	Liver	Liver
15	chr10:96931000-96932000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:96931200-96933000	Enhancers	Gastric	stomach
17	chr10:96931400-96931800	Enhancers	Esophagus	oesophagus
18	chr10:96931400-96932200	Enhancers	HepG2	liver
19	chr10:96931400-96932600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:96931600-96932000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr10:96931800-96937200	Weak transcription	Liver	Liver
22	chr10:96932000-96932400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr10:96932000-96932400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:96932000-96943000	Weak transcription	Pancreas	Pancrea
25	chr10:96932400-96933000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr10:96932400-96933000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr10:96932600-96933000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr10:96932600-96933000	Enhancers	NHEK	skin
29	chr10:96932800-96941400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr10:96935600-96936600	ZNF genes & repeats	Fetal Intestine Small	intestine
31	chr10:96936600-96941400	Weak transcription	Fetal Intestine Small	intestine
32	chr10:96936800-96942400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr10:96937200-96942200	Enhancers	Liver	Liver
34	chr10:96937400-96940000	Enhancers	HepG2	liver
35	chr10:96938400-96939000	Enhancers	Fetal Intestine Large	intestine
36	chr10:96938800-96939200	Enhancers	A549	lung
37	chr10:96939000-96942200	Weak transcription	Fetal Intestine Large	intestine
38	chr10:96939200-96941400	Weak transcription	A549	lung
39	chr10:96940000-96941200	Weak transcription	HepG2	liver
40	chr10:96941200-96941400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr10:96941200-96942000	Enhancers	HepG2	liver
42	chr10:96941400-96941600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr10:96941400-96941600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr10:96941400-96941600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:96941400-96941600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr10:96941400-96941600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr10:96941400-96941800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr10:96941400-96941800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr10:96941400-96941800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:96941400-96942000	Enhancers	Fetal Lung	lung

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