Variant report

Variant	nsv825566
Chromosome Location	chr10:112830014-112871333
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	ATF1	chr10:112847022-112847322	K562	blood:	n/a	n/a
2	ATF2	chr10:112835928-112836256	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr10:112836293-112836298	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr10:112835859-112836195	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:112836018-112836051	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:112858646-112858648	K562	blood:	n/a	n/a
7	BHLHE40	chr10:112847051-112847524	K562	blood:	n/a	n/a
8	BRCA1	chr10:112837094-112837268	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr10:112847112-112847562	K562	blood:	n/a	n/a
10	CEBPB	chr10:112844871-112844959	Hela-S3	cervix:	n/a	chr10:112844920-112844933 chr10:112844921-112844932
11	CEBPB	chr10:112844781-112845083	A549	lung:	n/a	chr10:112844920-112844933 chr10:112844921-112844932
12	CEBPB	chr10:112844757-112845052	K562	blood:	n/a	chr10:112844920-112844933 chr10:112844921-112844932
13	CEBPB	chr10:112844844-112845002	IMR90	lung:	n/a	chr10:112844920-112844933 chr10:112844921-112844932
14	CEBPB	chr10:112844765-112844954	H1-hESC	embryonic stem cell:	n/a	chr10:112844920-112844933 chr10:112844921-112844932
15	CEBPB	chr10:112839602-112839860	HepG2	liver:	n/a	n/a
16	CEBPB	chr10:112844745-112845090	HepG2	liver:	n/a	chr10:112844920-112844933 chr10:112844921-112844932
17	CEBPB	chr10:112835911-112836210	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr10:112866822-112866833	HepG2	liver:	n/a	n/a
19	CHD1	chr10:112836738-112836921	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr10:112836615-112837339	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr10:112835906-112836229	A549	lung:	n/a	n/a
22	CREB1	chr10:112837851-112838588	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr10:112835669-112837158	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr10:112858620-112858770	HMEC	breast:	n/a	n/a
25	CTCF	chr10:112858640-112858790	GM12872	blood:	n/a	n/a
26	CTCF	chr10:112835940-112836090	GM12870	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
27	CTCF	chr10:112858580-112858730	NHEK	skin:	n/a	n/a
28	CTCF	chr10:112836460-112836610	SK-N-SH_RA	brain:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
29	CTCF	chr10:112836260-112836410	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr10:112866920-112867070	HepG2	liver:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
31	CTCF	chr10:112835906-112836222	NHEK	skin:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
32	CTCF	chr10:112835940-112836090	K562	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
33	CTCF	chr10:112866890-112866948	Gliobla	brain:	n/a	n/a
34	CTCF	chr10:112858650-112858732	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr10:112835889-112836181	SK-N-SH_RA	brain:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
36	CTCF	chr10:112836440-112836590	RPTEC	kidney:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
37	CTCF	chr10:112835980-112836130	GM12865	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
38	CTCF	chr10:112866840-112866990	Hela-S3	cervix:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
39	CTCF	chr10:112835875-112836241	GM19240	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
40	CTCF	chr10:112835960-112836110	HPAF	blood vessel:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
41	CTCF	chr10:112835980-112836130	HCM	heart:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
42	CTCF	chr10:112836420-112836570	HRPEpiC	eye:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
43	CTCF	chr10:112835960-112836110	GM12865	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
44	CTCF	chr10:112836302-112836370	A549	lung:	n/a	n/a
45	CTCF	chr10:112835960-112836110	HCM	heart:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
46	CTCF	chr10:112866889-112866935	GM10248	blood:	n/a	n/a
47	CTCF	chr10:112836440-112836590	HFF	foreskin:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
48	CTCF	chr10:112835960-112836110	A549	lung:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
49	CTCF	chr10:112835980-112836130	HBMEC	blood vessel:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
50	CTCF	chr10:112858560-112858710	AG04449	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:112836780-112836830	RPTEC	kidney:	n/a
2	chr10:112837537-112837587	HRCEpiC	kidney:	n/a
3	chr10:112836785-112836835	Caco-2	colon:	n/a
4	chr10:112836681-112836731	LNCaP	prostate:	n/a
5	chr10:112839302-112839352	HUVEC	blood vessel:	n/a
6	chr10:112836785-112836835	HMEC	breast:	n/a
7	chr10:112835859-112835909	HRE	kidney:	n/a
8	chr10:112839446-112839496	SK-N-SH_RA	brain:	n/a
9	chr10:112837240-112837290	PANC-1	pancreas:	n/a
10	chr10:112839446-112839496	SKMC	muscle:	n/a
11	chr10:112835859-112835909	ProgFib	skin:	n/a
12	chr10:112836724-112836774	SK-N-SH_RA	brain:	n/a
13	chr10:112836780-112836830	HEK293	kidney:	embryo
14	chr10:112832758-112832808	GM19239	blood:	n/a
15	chr10:112838983-112839033	AG09309	skin:	n/a
16	chr10:112837240-112837290	Hepatocyte	liver:	n/a
17	chr10:112864820-112864870	ovcar-3	ovarian:	n/a
18	chr10:112832758-112832808	HNPCEpiC	eye:	n/a
19	chr10:112836681-112836731	BJ	skin:	n/a
20	chr10:112836785-112836835	ECC-1	luminal epithelium:	n/a
21	chr10:112836609-112836659	GM12891	blood:	n/a
22	chr10:112836609-112836659	HRPEpiC	eye:	n/a
23	chr10:112834861-112834911	ECC-1	luminal epithelium:	n/a
24	chr10:112836681-112836731	NT2-D1	testis:	n/a
25	chr10:112836681-112836731	HIPEpiC	eye:	n/a
26	chr10:112836780-112836830	Jurkat	blood:	n/a
27	chr10:112864820-112864870	HepG2	liver:	n/a
28	chr10:112864698-112864748	HCM	heart:	n/a
29	chr10:112837240-112837290	HEK293	kidney:	embryo
30	chr10:112836681-112836731	RPTEC	kidney:	n/a
31	chr10:112836780-112836830	GM12892	blood:	n/a
32	chr10:112832758-112832808	SKMC	muscle:	n/a
33	chr10:112837240-112837290	HAEpiC	amniotic membrane:	n/a
34	chr10:112836724-112836774	ECC-1	luminal epithelium:	n/a
35	chr10:112864698-112864748	GM06990	blood:	n/a
36	chr10:112836609-112836659	CMK	blood:	n/a
37	chr10:112835859-112835909	MCF10A-Er-Src	breast:	n/a
38	chr10:112864820-112864870	HMEC	breast:	n/a
39	chr10:112838078-112838128	HRE	kidney:	n/a
40	chr10:112836724-112836774	HEK293	kidney:	embryo
41	chr10:112836185-112836235	NH-A	brain:	n/a
42	chr10:112836785-112836835	AG04450	lung:	fetal
43	chr10:112835859-112835909	H1-hESC	embryonic stem cell:	embryo
44	chr10:112842008-112842058	CMK	blood:	n/a
45	chr10:112836724-112836774	GM06990	blood:	n/a
46	chr10:112836609-112836659	NH-A	brain:	n/a
47	chr10:112838983-112839033	GM12878	blood:	n/a
48	chr10:112842008-112842058	HUVEC	blood vessel:	n/a
49	chr10:112836609-112836659	HRCEpiC	kidney:	n/a
50	chr10:112834861-112834911	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:112867287..112868074-chr10:113150093..113150654,2	MCF-7	breast:
2	chr10:112835558..112836069-chr10:112858564..112859533,2	MCF-7	breast:
3	chr10:112835905..112836784-chr10:113041082..113041711,3	MCF-7	breast:
4	chr10:112858644..112861642-chr10:112871139..112872875,2	MCF-7	breast:
5	chr10:112835558..112836069-chr10:112858564..112859533,2	MCF-7	breast:
6	chr10:112835556..112836368-chr10:113357671..113358964,3	MCF-7	breast:
7	chr10:112857274..112860234-chr10:112900319..112903397,3	K562	blood:
8	chr10:112677000..112679422-chr10:112861364..112862923,2	MCF-7	breast:
9	chr10:112835831..112836588-chr10:112967176..112967740,2	MCF-7	breast:
10	chr10:112837126..112840004-chr10:112842044..112844644,2	K562	blood:
11	chr10:112854536..112855207-chr10:112867276..112868184,2	MCF-7	breast:
12	chr10:112835910..112836421-chr10:113083278..113083990,2	MCF-7	breast:
13	chr10:112837126..112840004-chr10:112842044..112844644,2	K562	blood:
14	chr10:112854536..112855207-chr10:112867276..112868184,2	MCF-7	breast:
15	chr10:112858644..112861642-chr10:112871139..112872875,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADRA2A-3	chr10:112864714-112865006	NONHSAT016385

Variant related genes	Relation type
ADRA2A	TF binding region
ENSG00000213247	TF binding region
ADRA2A	CpG island
ENSG00000213247	CpG island
ENSG00000214413	chromatin interactions
ENSG00000108061	chromatin interactions

Extended variants
information (count: 1610 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564672527	chr10:112830027-112830028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539303612	chr10:112830042-112830043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367842089	chr10:112830092-112830093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558212643	chr10:112830108-112830109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532056833	chr10:112830194-112830195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370760375	chr10:112830338-112830339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77188019	chr10:112830352-112830353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56165476	chr10:112830353-112830354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397936631	chr10:112830365-112830366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560960316	chr10:112830388-112830389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573706410	chr10:112830418-112830419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544493999	chr10:112830458-112830459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188939061	chr10:112830467-112830468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149960670	chr10:112830471-112830472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201344829	chr10:112830502-112830503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181384198	chr10:112830555-112830556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528147542	chr10:112830565-112830566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540326445	chr10:112830570-112830571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561630248	chr10:112830581-112830582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144977770	chr10:112830587-112830588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550892747	chr10:112830601-112830602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148676871	chr10:112830609-112830610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533271242	chr10:112830653-112830654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12765301	chr10:112830680-112830681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568973370	chr10:112830681-112830682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs478849	chr10:112830724-112830725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186613915	chr10:112830727-112830728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs478931	chr10:112830754-112830755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573593528	chr10:112830771-112830772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566660005	chr10:112830777-112830778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533993527	chr10:112830834-112830835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555481317	chr10:112830856-112830857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367971787	chr10:112830885-112830886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78180279	chr10:112830913-112830914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12249031	chr10:112830922-112830923	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs556422913	chr10:112830934-112830935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs578163360	chr10:112831007-112831008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545707852	chr10:112831034-112831035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562450108	chr10:112831035-112831036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189465264	chr10:112831150-112831151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142336408	chr10:112831173-112831174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530014621	chr10:112831204-112831205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540323714	chr10:112831205-112831206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572959686	chr10:112831213-112831214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532744096	chr10:112831216-112831217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551376476	chr10:112831270-112831271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140649029	chr10:112831271-112831272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368576857	chr10:112831272-112831273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528874405	chr10:112831275-112831276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181223797	chr10:112831322-112831323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myxofibrosarcoma	16751306	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	16616336	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Sezary syndrome	18413736	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:112829800-112835600	Weak transcription	Pancreas	Pancrea
2	chr10:112831400-112831800	Enhancers	Stomach Mucosa	stomach
3	chr10:112831400-112835600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:112831600-112832000	Bivalent Enhancer	Fetal Thymus	thymus
5	chr10:112831600-112832200	Bivalent Enhancer	Fetal Muscle Leg	muscle
6	chr10:112831800-112832800	Enhancers	HSMM	muscle
7	chr10:112832800-112833200	Enhancers	Stomach Mucosa	stomach
8	chr10:112834400-112835400	Enhancers	Fetal Brain Female	brain
9	chr10:112835400-112835600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:112835400-112835600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr10:112835400-112835600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
12	chr10:112835400-112835600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr10:112835400-112835600	Bivalent Enhancer	Brain Hippocampus Middle	brain
14	chr10:112835400-112835600	Active TSS	Brain Inferior Temporal Lobe	brain
15	chr10:112835400-112835600	Enhancers	Ovary	ovary
16	chr10:112835400-112835800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
17	chr10:112835400-112835800	Enhancers	Fetal Brain Male	brain
18	chr10:112835400-112835800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr10:112835400-112836000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
20	chr10:112835400-112836000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr10:112835400-112836000	Flanking Active TSS	Fetal Brain Female	brain
22	chr10:112835400-112836000	Bivalent Enhancer	Fetal Heart	heart
23	chr10:112835400-112837000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr10:112835400-112838000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr10:112835600-112835800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr10:112835600-112835800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr10:112835600-112835800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:112835600-112835800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
29	chr10:112835600-112835800	Bivalent Enhancer	Primary B cells from cord blood	blood
30	chr10:112835600-112835800	Bivalent Enhancer	Primary T cells from cord blood	blood
31	chr10:112835600-112835800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
32	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
33	chr10:112835600-112835800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
34	chr10:112835600-112835800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
35	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:112835600-112835800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr10:112835600-112835800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr10:112835600-112835800	Bivalent Enhancer	Liver	Liver
40	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
41	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
42	chr10:112835600-112835800	Bivalent/Poised TSS	Colonic Mucosa	Colon
43	chr10:112835600-112835800	Bivalent Enhancer	Colon Smooth Muscle	Colon
44	chr10:112835600-112835800	Bivalent Enhancer	Fetal Lung	lung
45	chr10:112835600-112835800	Bivalent Enhancer	Fetal Muscle Leg	muscle
46	chr10:112835600-112835800	Bivalent Enhancer	Fetal Stomach	stomach
47	chr10:112835600-112835800	Flanking Active TSS	Ovary	ovary
48	chr10:112835600-112835800	Enhancers	Pancreas	Pancrea
49	chr10:112835600-112835800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
50	chr10:112835600-112835800	Flanking Active TSS	Right Atrium	heart

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