Variant report

Variant	nsv466840
Chromosome Location	chr10:27581845-27705855
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	chr10:27672857-27673169	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27649547-27649808	K562	blood:	n/a	n/a
3	ARID3A	chr10:27629946-27630482	HepG2	liver:	n/a	n/a
4	ATF1	chr10:27649531-27649804	K562	blood:	n/a	n/a
5	BATF	chr10:27633841-27634192	GM12878	blood:	n/a	n/a
6	BATF	chr10:27649564-27649764	GM12878	blood:	n/a	n/a
7	BATF	chr10:27643692-27643988	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:27643724-27643987	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:27643658-27644039	GM12878	blood:	n/a	n/a
10	BCL3	chr10:27672617-27673252	A549	lung:	n/a	n/a
11	BCLAF1	chr10:27643572-27643923	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:27646116-27646388	K562	blood:	n/a	chr10:27646219-27646232 chr10:27646221-27646230 chr10:27646222-27646231 chr10:27646221-27646230
13	BHLHE40	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
14	BHLHE40	chr10:27649517-27649830	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:27649567-27649799	K562	blood:	n/a	n/a
16	BHLHE40	chr10:27633890-27634818	GM12878	blood:	n/a	n/a
17	BRCA1	chr10:27672817-27673127	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr10:27681602-27681815	K562	blood:	n/a	n/a
19	CBX3	chr10:27681617-27681837	K562	blood:	n/a	n/a
20	CCNT2	chr10:27639061-27639239	K562	blood:	n/a	n/a
21	CCNT2	chr10:27649596-27649806	K562	blood:	n/a	n/a
22	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
23	CEBPB	chr10:27595662-27596001	A549	lung:	n/a	chr10:27595825-27595834 chr10:27595785-27595798 chr10:27595820-27595837 chr10:27595825-27595836 chr10:27595825-27595834 chr10:27595823-27595836 chr10:27595825-27595834 chr10:27595823-27595834 chr10:27595825-27595834
24	CEBPB	chr10:27608518-27609427	Hela-S3	cervix:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
25	CEBPB	chr10:27595703-27595979	K562	blood:	n/a	chr10:27595825-27595834 chr10:27595785-27595798 chr10:27595820-27595837 chr10:27595825-27595836 chr10:27595825-27595834 chr10:27595823-27595836 chr10:27595825-27595834 chr10:27595823-27595834 chr10:27595825-27595834
26	CEBPB	chr10:27595659-27596017	IMR90	lung:	n/a	chr10:27595825-27595834 chr10:27595785-27595798 chr10:27595820-27595837 chr10:27595825-27595836 chr10:27595825-27595834 chr10:27595823-27595836 chr10:27595825-27595834 chr10:27595823-27595834 chr10:27595825-27595834
27	CEBPB	chr10:27609087-27609339	K562	blood:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
28	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
29	CEBPB	chr10:27595642-27596019	HepG2	liver:	n/a	chr10:27595825-27595834 chr10:27595785-27595798 chr10:27595820-27595837 chr10:27595825-27595836 chr10:27595825-27595834 chr10:27595823-27595836 chr10:27595825-27595834 chr10:27595823-27595834 chr10:27595825-27595834
30	CEBPB	chr10:27600676-27600841	K562	blood:	n/a	n/a
31	CEBPB	chr10:27595735-27595977	MCF-7	breast:	n/a	chr10:27595825-27595834 chr10:27595785-27595798 chr10:27595820-27595837 chr10:27595825-27595836 chr10:27595825-27595834 chr10:27595823-27595836 chr10:27595825-27595834 chr10:27595823-27595834 chr10:27595825-27595834
32	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
33	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
34	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
35	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860
36	CEBPB	chr10:27634311-27634682	A549	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
37	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
39	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr10:27634350-27634708	IMR90	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
41	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
42	CEBPB	chr10:27609114-27609279	H1-hESC	embryonic stem cell:	n/a	chr10:27609201-27609212 chr10:27609124-27609137
43	CEBPB	chr10:27595705-27596018	ECC-1	luminal epithelium:	n/a	chr10:27595825-27595834 chr10:27595785-27595798 chr10:27595820-27595837 chr10:27595825-27595836 chr10:27595825-27595834 chr10:27595823-27595836 chr10:27595825-27595834 chr10:27595823-27595834 chr10:27595825-27595834
44	CEBPB	chr10:27604158-27604375	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr10:27634283-27634772	Hela-S3	cervix:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
46	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
47	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
48	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
49	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
50	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27607960-27608010	PrEC	prostate:	n/a
2	chr10:27634719-27634769	LNCaP	prostate:	n/a
3	chr10:27704762-27704812	IMR90	lung:	fetal
4	chr10:27607960-27608010	MCF-7	breast:	n/a
5	chr10:27607960-27608010	PrEC	prostate:	n/a
6	chr10:27634719-27634769	LNCaP	prostate:	n/a
7	chr10:27704762-27704812	IMR90	lung:	fetal
8	chr10:27607960-27608010	MCF-7	breast:	n/a
9	chr10:27705739-27705789	GM12892	blood:	n/a
10	chr10:27634719-27634769	HIPEpiC	eye:	n/a
11	chr10:27609333-27609383	AG09319	gingival:	n/a
12	chr10:27698606-27698656	SK-N-SH_RA	brain:	n/a
13	chr10:27703247-27703297	HCT-116	colon:	n/a
14	chr10:27702309-27702359	NHDF-neo	bronchial:	n/a
15	chr10:27608703-27608753	AG09309	skin:	n/a
16	chr10:27698606-27698656	HL-60	blood:	n/a
17	chr10:27609333-27609383	CMK	blood:	n/a
18	chr10:27705739-27705789	GM06990	blood:	n/a
19	chr10:27608703-27608753	Hepatocyte	liver:	n/a
20	chr10:27703247-27703297	HCPEpiC	choroid plexus:	n/a
21	chr10:27703247-27703297	HRPEpiC	eye:	n/a
22	chr10:27705739-27705789	HUVEC	blood vessel:	n/a
23	chr10:27703247-27703297	GM19239	blood:	n/a
24	chr10:27609333-27609383	IMR90	lung:	fetal
25	chr10:27607960-27608010	AG09309	skin:	n/a
26	chr10:27704592-27704642	BE2_C	brain:	n/a
27	chr10:27639156-27639206	GM19239	blood:	n/a
28	chr10:27704762-27704812	T-47D	breast:	n/a
29	chr10:27609333-27609383	HAEpiC	amniotic membrane:	n/a
30	chr10:27702309-27702359	HEEpiC	esophagus:	n/a
31	chr10:27703289-27703339	ECC-1	luminal epithelium:	n/a
32	chr10:27702528-27702578	HL-60	blood:	n/a
33	chr10:27609333-27609383	NH-A	brain:	n/a
34	chr10:27705739-27705789	HepG2	liver:	n/a
35	chr10:27703247-27703297	U87	brain:	n/a
36	chr10:27634719-27634769	U87	brain:	n/a
37	chr10:27639156-27639206	HepG2	liver:	n/a
38	chr10:27639156-27639206	SAEC	small airway:	n/a
39	chr10:27609163-27609213	BE2_C	brain:	n/a
40	chr10:27703547-27703597	AG04449	skin:	fetal
41	chr10:27703377-27703427	AoSMC	blood vessel:	n/a
42	chr10:27703362-27703412	HEK293	kidney:	embryo
43	chr10:27703289-27703339	GM19239	blood:	n/a
44	chr10:27639156-27639206	GM12878	blood:	n/a
45	chr10:27703247-27703297	HL-60	blood:	n/a
46	chr10:27698606-27698656	K562	blood:	n/a
47	chr10:27639156-27639206	PFSK-1	brain:	n/a
48	chr10:27608703-27608753	MCF10A-Er-Src	breast:	n/a
49	chr10:27702309-27702359	GM12892	blood:	n/a
50	chr10:27703377-27703427	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
2	chr10:27694442..27697083-chr10:27703247..27705702,3	K562	blood:
3	chr10:26984968..26988044-chr10:27607336..27609040,6	MCF-7	breast:
4	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
5	chr10:27659175..27661663-chr10:27792060..27794224,2	MCF-7	breast:
6	chr10:27609103..27610966-chr10:27614340..27616128,2	K562	blood:
7	chr10:26985474..26987624-chr10:27607358..27610341,4	MCF-7	breast:
8	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
9	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
10	chr10:27527860..27530153-chr10:27647076..27648802,2	MCF-7	breast:
11	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
12	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
13	chr10:27531028..27532588-chr10:27647976..27649755,2	K562	blood:
14	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
15	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
16	chr10:27530380..27532088-chr10:27585866..27587933,2	MCF-7	breast:
17	chr10:27609103..27610966-chr10:27614340..27616128,2	K562	blood:
18	chr10:27441984..27445191-chr10:27642152..27645235,3	MCF-7	breast:
19	chr10:27530526..27532390-chr10:27644695..27646372,2	MCF-7	breast:
20	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
21	chr10:27529763..27532096-chr10:27643724..27645777,2	MCF-7	breast:
22	chr10:27607489..27609150-chr10:27638206..27640628,2	MCF-7	breast:
23	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
24	chr10:26985698..26986799-chr10:27608358..27609419,4	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MASTL-2	chr10:27633668-27633846	ENSG00000260151.1
2	lnc-PTCHD3-1	chr10:27667067-27667291	NONHSAT011904
3	lnc-MASTL-2	chr10:27632365-27633580	ENSG00000260151.1
4	lnc-PTCHD3-2	chr10:27636298-27636725	l_277_chr10:27627368-27636725_testes
5	lnc-ACBD5-2	chr10:27594769-27595233	XLOC_008759
6	lnc-ACBD5-2	chr10:27596292-27596343	XLOC_008759
7	lnc-PTCHD3-2	chr10:27627369-27627692	l_277_chr10:27627368-27636725_testes
8	lnc-ACBD5-2	chr10:27587363-27587686	XLOC_008759
9	lnc-ACBD5-2	chr10:27595041-27595233	XLOC_008759
10	lnc-ACBD5-2	chr10:27596292-27596344	XLOC_008759
11	lnc-PTCHD3-2	chr10:27634694-27635239	l_277_chr10:27627368-27636725_testes

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTCHD3	hsa-miR-128-3p	chr10:27687123-27687143

Variant related genes	Relation type
TRIAP1P1	TF binding region
RNU6-452P	TF binding region
PTCHD3	TF binding region
RNU6-666P	TF binding region
FAM210CP	TF binding region
ENSG00000260151	TF binding region
ENSG00000215409	TF binding region
TRIAP1P1	CpG island
RNU6-452P	CpG island
PTCHD3	CpG island
RNU6-666P	CpG island
FAM210CP	CpG island
ENSG00000260151	CpG island
ENSG00000215409	CpG island
ENSG00000182077	chromatin interactions
ENSG00000120539	chromatin interactions
ENSG00000107897	chromatin interactions
ENSG00000136758	chromatin interactions
ENSG00000262412	chromatin interactions
ENSG00000213770	chromatin interactions
ENSG00000099246	chromatin interactions
ENSG00000148459	chromatin interactions
PLAG1	miRNA target sites
SYPL1	miRNA target sites

Extended variants
information (count: 3182 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:3182 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183224670	chr10:27585871-27585872	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs550599691	chr10:27585897-27585898	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567304015	chr10:27585918-27585919	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529968147	chr10:27585921-27585922	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546513052	chr10:27585931-27585932	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs369491068	chr10:27585945-27585946	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376722320	chr10:27585949-27585950	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs546792163	chr10:27585963-27585964	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187596932	chr10:27585977-27585978	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558672226	chr10:27585980-27585981	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568906436	chr10:27586015-27586016	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs9665037	chr10:27586024-27586025	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs554641381	chr10:27586027-27586028	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs574505542	chr10:27586028-27586029	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs9664367	chr10:27586099-27586100	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs377519662	chr10:27586131-27586132	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs374290919	chr10:27586150-27586151	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192010481	chr10:27586159-27586160	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549592729	chr10:27586178-27586179	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147420124	chr10:27586179-27586180	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs367673363	chr10:27586186-27586187	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545321607	chr10:27586201-27586202	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs565464407	chr10:27586206-27586207	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530940604	chr10:27586224-27586225	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569614230	chr10:27586233-27586234	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs2800408	chr10:27586242-27586243	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
27	rs34544855	chr10:27586258-27586259	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576786195	chr10:27586273-27586274	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12415459	chr10:27586289-27586290	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs376245116	chr10:27586305-27586306	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs371057819	chr10:27586343-27586344	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs373122375	chr10:27586349-27586350	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs143606173	chr10:27586382-27586383	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs9665127	chr10:27586399-27586400	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs386742242	chr10:27586417-27586418	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs569019318	chr10:27586418-27586419	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201014528	chr10:27586421-27586422	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149604060	chr10:27586425-27586426	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs370238788	chr10:27586426-27586427	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs145238719	chr10:27586432-27586433	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs61095916	chr10:27586446-27586447	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs11015655	chr10:27586453-27586454	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs200422348	chr10:27586486-27586487	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568121331	chr10:27586510-27586511	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs533772282	chr10:27586516-27586517	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs553725311	chr10:27586525-27586526	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538673105	chr10:27586526-27586527	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573495806	chr10:27586560-27586561	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs78763040	chr10:27586580-27586581	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192688694	chr10:27586632-27586633	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27586400-27587800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:27586600-27587200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:27586600-27587800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr10:27586800-27587400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr10:27587000-27587400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr10:27587200-27587600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:27587400-27587600	Enhancers	Primary T cells fromperipheralblood	blood
8	chr10:27587400-27587600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr10:27587400-27587600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr10:27587600-27587800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
11	chr10:27587600-27588200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:27600600-27601000	Active TSS	Placenta	Placenta
13	chr10:27601600-27602000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr10:27601800-27602000	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr10:27603800-27605000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr10:27605000-27608000	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr10:27608000-27608200	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr10:27608000-27608200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
19	chr10:27608000-27608400	Enhancers	GM12878-XiMat	blood
20	chr10:27608000-27608400	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr10:27608000-27608600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr10:27608000-27608600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
23	chr10:27608200-27608400	Enhancers	Primary B cells from cord blood	blood
24	chr10:27608200-27608400	Enhancers	Primary hematopoietic stem cells	blood
25	chr10:27608200-27608400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr10:27608200-27608400	Bivalent Enhancer	Brain Hippocampus Middle	brain
27	chr10:27608200-27608600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr10:27608200-27608600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
29	chr10:27608200-27608600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr10:27608200-27608600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:27608200-27608600	Enhancers	Fetal Intestine Large	intestine
32	chr10:27608200-27608600	Enhancers	Left Ventricle	heart
33	chr10:27608200-27608600	Enhancers	Right Ventricle	heart
34	chr10:27608200-27608800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr10:27608200-27609200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr10:27608200-27609200	Enhancers	Primary B cells from peripheral blood	blood
37	chr10:27608200-27609200	Enhancers	Fetal Brain Male	brain
38	chr10:27608200-27609400	Enhancers	Esophagus	oesophagus
39	chr10:27608200-27609800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:27608400-27608600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
41	chr10:27608400-27608600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr10:27608400-27608600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr10:27608400-27608600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr10:27608400-27608600	Enhancers	Fetal Muscle Trunk	muscle
45	chr10:27608400-27608600	Enhancers	Hela-S3	cervix
46	chr10:27608400-27608600	Enhancers	HMEC	breast
47	chr10:27608400-27608800	Enhancers	Stomach Mucosa	stomach
48	chr10:27608400-27609000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr10:27608400-27609000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr10:27608400-27609000	Flanking Active TSS	Primary B cells from cord blood	blood

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