Variant report

Variant	esv3338822
Chromosome Location	chr10:116579462-116583960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:659)
CpG islands
(count:610)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:116582532-116582797	HepG2	liver:	n/a	n/a
2	BACH1	chr10:116581091-116581507	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr10:116581320-116581682	GM12878	blood:	n/a	chr10:116581564-116581577
4	BCLAF1	chr10:116581091-116581650	GM12878	blood:	n/a	chr10:116581564-116581577
5	BHLHE40	chr10:116581215-116581604	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:116581237-116581877	K562	blood:	n/a	chr10:116581809-116581825 chr10:116581749-116581765 chr10:116581760-116581776 chr10:116581763-116581779
7	BRCA1	chr10:116581416-116581586	HepG2	liver:	n/a	n/a
8	BRCA1	chr10:116580611-116580929	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr10:116579101-116579527	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr10:116581162-116581461	K562	blood:	n/a	n/a
11	CCNT2	chr10:116581247-116582165	K562	blood:	n/a	n/a
12	CEBPB	chr10:116582497-116583034	A549	lung:	n/a	n/a
13	CEBPB	chr10:116582256-116582736	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:116582219-116582907	K562	blood:	n/a	n/a
15	CEBPB	chr10:116579078-116579518	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr10:116582627-116582869	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:116581544-116581570	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:116582520-116583228	MCF-7	breast:	n/a	n/a
19	CEBPB	chr10:116581096-116581668	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr10:116582180-116582938	IMR90	lung:	n/a	n/a
21	CEBPB	chr10:116580521-116580887	Hela-S3	cervix:	n/a	chr10:116580606-116580617
22	CEBPB	chr10:116582606-116582939	A549	lung:	n/a	n/a
23	CEBPB	chr10:116582208-116583193	Hela-S3	cervix:	n/a	n/a
24	CHD1	chr10:116581639-116582386	H1-hESC	embryonic stem cell:	n/a	chr10:116581716-116581726
25	CHD1	chr10:116580993-116583316	IMR90	lung:	n/a	chr10:116581716-116581726
26	CHD1	chr10:116581223-116583093	GM12878	blood:	n/a	chr10:116581716-116581726
27	CHD2	chr10:116581263-116581463	K562	blood:	n/a	n/a
28	CHD2	chr10:116581215-116581806	Hela-S3	cervix:	n/a	chr10:116581716-116581726
29	CHD2	chr10:116581136-116581770	GM12878	blood:	n/a	chr10:116581716-116581726
30	CHD2	chr10:116581616-116581803	HepG2	liver:	n/a	chr10:116581716-116581726
31	CHD2	chr10:116582464-116582656	GM12878	blood:	n/a	n/a
32	CREB1	chr10:116581276-116581700	A549	lung:	n/a	n/a
33	CTBP2	chr10:116581441-116582211	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr10:116581331-116581618	MCF-7	breast:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
35	CTCF	chr10:116581400-116581550	AG09319	gingival:	n/a	n/a
36	CTCF	chr10:116581166-116581754	K562	blood:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
37	CTCF	chr10:116581800-116581801	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:116581380-116581530	HAc	cerebellar:	n/a	n/a
39	CTCF	chr10:116581320-116581470	GM06990	blood:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
40	CTCF	chr10:116581285-116581670	Fibrobl	skin:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
41	CTCF	chr10:116581240-116581390	HPF	lung:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
42	CTCF	chr10:116581420-116581570	GM12869	blood:	n/a	n/a
43	CTCF	chr10:116581460-116581610	GM12874	blood:	n/a	n/a
44	CTCF	chr10:116581180-116581330	BE2_C	brain:	n/a	n/a
45	CTCF	chr10:116581400-116581550	Caco-2	colon:	n/a	n/a
46	CTCF	chr10:116581440-116581590	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr10:116581220-116581370	HRPEpiC	eye:	n/a	chr10:116581357-116581370
48	CTCF	chr10:116581460-116581610	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr10:116581440-116581590	GM12878	blood:	n/a	n/a
50	CTCF	chr10:116581440-116581590	HEK293	kidney:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116582469-116582519	NHDF-neo	bronchial:	n/a
2	chr10:116581305-116581355	AoSMC	blood vessel:	n/a
3	chr10:116581183-116581233	AG10803	skin:	n/a
4	chr10:116582469-116582519	H1-hESC	embryonic stem cell:	embryo
5	chr10:116581344-116581394	HL-60	blood:	n/a
6	chr10:116581344-116581394	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:116582469-116582519	HMEC	breast:	n/a
8	chr10:116581344-116581394	LNCaP	prostate:	n/a
9	chr10:116581183-116581233	GM06990	blood:	n/a
10	chr10:116581829-116581879	PFSK-1	brain:	n/a
11	chr10:116581305-116581355	PANC-1	pancreas:	n/a
12	chr10:116581344-116581394	AG04450	lung:	fetal
13	chr10:116581112-116581162	HL-60	blood:	n/a
14	chr10:116581344-116581394	K562	blood:	n/a
15	chr10:116582297-116582347	MCF-7	breast:	n/a
16	chr10:116582469-116582519	U87	brain:	n/a
17	chr10:116581112-116581162	GM19239	blood:	n/a
18	chr10:116582297-116582347	SKMC	muscle:	n/a
19	chr10:116581305-116581355	HCPEpiC	choroid plexus:	n/a
20	chr10:116581808-116581858	HCPEpiC	choroid plexus:	n/a
21	chr10:116581248-116581298	NHDF-neo	bronchial:	n/a
22	chr10:116581829-116581879	Hela-S3	cervix:	n/a
23	chr10:116581112-116581162	AG04449	skin:	fetal
24	chr10:116581183-116581233	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:116581808-116581858	SK-N-SH	brain:	n/a
26	chr10:116581183-116581233	SKMC	muscle:	n/a
27	chr10:116581305-116581355	MCF-7	breast:	n/a
28	chr10:116581808-116581858	PANC-1	pancreas:	n/a
29	chr10:116581112-116581162	SKMC	muscle:	n/a
30	chr10:116581248-116581298	NB4	blood:	n/a
31	chr10:116581358-116581408	HMEC	breast:	n/a
32	chr10:116581344-116581394	T-47D	breast:	n/a
33	chr10:116581344-116581394	AG10803	skin:	n/a
34	chr10:116581344-116581394	NHDF-neo	bronchial:	n/a
35	chr10:116581183-116581233	MCF10A-Er-Src	breast:	n/a
36	chr10:116581808-116581858	Hela-S3	cervix:	n/a
37	chr10:116581183-116581233	HCT-116	colon:	n/a
38	chr10:116581183-116581233	ECC-1	luminal epithelium:	n/a
39	chr10:116581808-116581858	NHDF-neo	bronchial:	n/a
40	chr10:116581248-116581298	HepG2	liver:	n/a
41	chr10:116581829-116581879	AoSMC	blood vessel:	n/a
42	chr10:116581344-116581394	MCF10A-Er-Src	breast:	n/a
43	chr10:116581829-116581879	NB4	blood:	n/a
44	chr10:116581358-116581408	ovcar-3	ovarian:	n/a
45	chr10:116582297-116582347	T-47D	breast:	n/a
46	chr10:116582469-116582519	Jurkat	blood:	n/a
47	chr10:116581183-116581233	SAEC	small airway:	n/a
48	chr10:116582297-116582347	AG04450	lung:	fetal
49	chr10:116581358-116581408	HCPEpiC	choroid plexus:	n/a
50	chr10:116581358-116581408	GM12878	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:116577691..116581134-chr10:116581459..116583772,3	MCF-7	breast:
2	chr10:116579148..116581126-chr10:116581176..116582786,3	MCF-7	breast:
3	chr10:116296905..116298827-chr10:116577093..116580051,2	MCF-7	breast:
4	chr10:116581424..116582241-chr6:24720620..24721196,2	Hela-S3	cervix:
5	chr10:116567584..116574580-chr10:116575101..116583231,11	MCF-7	breast:
6	chr10:116575494..116578184-chr10:116579422..116580946,2	K562	blood:
7	chr10:116580811..116581705-chr8:27631902..27632494,2	Hela-S3	cervix:
8	chr10:116581616..116582495-chr7:115851052..115851797,2	Hela-S3	cervix:
9	chr10:116564843..116568193-chr10:116577870..116580490,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABLIM1-1	chr10:116581032-116581425	NONHSAT016464

No data

Variant related genes	Relation type
FAM160B1	TF binding region
FAM160B1	CpG island
ENSG00000112308	chromatin interactions
ENSG00000171320	chromatin interactions
ENSG00000151553	chromatin interactions
ENSG00000215760	chromatin interactions

Extended variants
information (count: 153 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:153 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186756985	chr10:116579531-116579532	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs574482697	chr10:116579594-116579595	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs117240742	chr10:116579643-116579644	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs142913608	chr10:116579645-116579646	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs532100809	chr10:116579655-116579656	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs575684421	chr10:116579708-116579709	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs545949156	chr10:116579775-116579776	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs564150892	chr10:116579825-116579826	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs548052450	chr10:116579897-116579898	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs528343432	chr10:116579898-116579899	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs556781017	chr10:116579905-116579906	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs371674192	chr10:116579909-116579910	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs374986328	chr10:116579967-116579968	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs114354427	chr10:116580084-116580085	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs562000775	chr10:116580109-116580110	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368737493	chr10:116580134-116580135	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs201773637	chr10:116580136-116580137	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs550621891	chr10:116580153-116580154	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568956971	chr10:116580154-116580155	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532900419	chr10:116580176-116580177	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs558792630	chr10:116580183-116580184	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7079314	chr10:116580195-116580196	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs7079435	chr10:116580197-116580198	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201856194	chr10:116580217-116580218	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377321872	chr10:116580219-116580220	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs60016739	chr10:116580220-116580221	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570960085	chr10:116580250-116580251	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs140393204	chr10:116580256-116580257	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566031110	chr10:116580258-116580259	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201877586	chr10:116580260-116580261	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs111825981	chr10:116580269-116580270	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs139383277	chr10:116580275-116580276	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs10450383	chr10:116580335-116580336	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs564480231	chr10:116580344-116580345	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs535443595	chr10:116580351-116580352	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs146614082	chr10:116580352-116580353	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs575667224	chr10:116580414-116580415	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs545986793	chr10:116580425-116580426	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs34316384	chr10:116580436-116580437	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs71474800	chr10:116580439-116580440	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572940309	chr10:116580446-116580447	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs79746221	chr10:116580454-116580455	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs76772047	chr10:116580455-116580456	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs397845451	chr10:116580457-116580458	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370680315	chr10:116580458-116580459	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs12218933	chr10:116580459-116580460	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573464353	chr10:116580479-116580480	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540775235	chr10:116580505-116580506	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs561940307	chr10:116580525-116580526	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs529237487	chr10:116580529-116580530	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116569800-116580600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr10:116571000-116580600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr10:116572200-116580600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:116572200-116580800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr10:116576000-116581000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr10:116576000-116581000	Weak transcription	NHDF-Ad	bronchial
7	chr10:116576200-116579600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:116576200-116581000	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr10:116576400-116579600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:116578800-116580600	Enhancers	Hela-S3	cervix
11	chr10:116579000-116579600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:116579000-116579600	Enhancers	GM12878-XiMat	blood
13	chr10:116579000-116580600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr10:116579000-116580600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:116579200-116580600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr10:116579400-116579800	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr10:116579400-116579800	Flanking Active TSS	Osteobl	bone
18	chr10:116579400-116580600	Weak transcription	A549	lung
19	chr10:116579400-116580600	Weak transcription	NH-A	brain
20	chr10:116579400-116581000	Enhancers	Liver	Liver
21	chr10:116579400-116583600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr10:116579600-116579800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:116579600-116579800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr10:116579600-116580000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr10:116579600-116580600	Weak transcription	GM12878-XiMat	blood
26	chr10:116579600-116581000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr10:116579800-116580000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr10:116579800-116580000	Active TSS	Osteobl	bone
29	chr10:116579800-116580600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr10:116579800-116580600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr10:116579800-116580800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr10:116579800-116583600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr10:116580000-116580200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr10:116580000-116580200	Enhancers	Fetal Brain Male	brain
35	chr10:116580000-116580200	Flanking Active TSS	Osteobl	bone
36	chr10:116580000-116580600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr10:116580000-116580600	Enhancers	Adipose Nuclei	Adipose
38	chr10:116580200-116580600	Active TSS	Osteobl	bone
39	chr10:116580200-116582200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr10:116580400-116580600	Enhancers	Dnd41	blood
41	chr10:116580400-116580600	Enhancers	HUVEC	blood vessel
42	chr10:116580400-116580600	Enhancers	NHEK	skin
43	chr10:116580400-116581000	Enhancers	Primary T cells fromperipheralblood	blood
44	chr10:116580400-116581200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr10:116580600-116580800	Enhancers	Primary T cells from cord blood	blood
46	chr10:116580600-116580800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr10:116580600-116580800	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr10:116580600-116580800	Enhancers	Stomach Mucosa	stomach
49	chr10:116580600-116580800	Flanking Active TSS	A549	lung
50	chr10:116580600-116580800	Flanking Active TSS	Hela-S3	cervix

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