Variant report

Variant	esv2764124
Chromosome Location	chr10:27593427-27712416
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	chr10:27629946-27630482	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27672857-27673169	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:27649547-27649808	K562	blood:	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	chr10:27643692-27643988	GM12878	blood:	n/a	n/a
7	BATF	chr10:27649564-27649764	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	chr10:27649567-27649799	K562	blood:	n/a	n/a
13	BHLHE40	chr10:27646116-27646388	K562	blood:	n/a	chr10:27646219-27646232 chr10:27646221-27646230 chr10:27646222-27646231 chr10:27646221-27646230
14	BHLHE40	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
15	BHLHE40	chr10:27649517-27649830	GM12878	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	chr10:27681617-27681837	K562	blood:	n/a	n/a
19	CBX3	chr10:27681602-27681815	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	chr10:27624329-27624377	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
24	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
25	CEBPB	chr10:27604158-27604375	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:27609087-27609339	K562	blood:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
27	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
28	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
29	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
31	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
32	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
33	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
34	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr10:27634311-27634682	A549	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
36	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860
37	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
39	CEBPB	chr10:27634350-27634708	IMR90	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
40	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
41	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:27634266-27634780	HepG2	liver:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
43	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
44	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
45	CEBPB	chr10:27595659-27596012	Hela-S3	cervix:	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
46	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
47	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
48	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
49	CEBPB	chr10:27601941-27601990	K562	blood:	n/a	chr10:27601959-27601970
50	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27703362-27703412	Jurkat	blood:	n/a
2	chr10:27703362-27703412	HCPEpiC	choroid plexus:	n/a
3	chr10:27703362-27703412	Jurkat	blood:	n/a
4	chr10:27703362-27703412	HCPEpiC	choroid plexus:	n/a
5	chr10:27702309-27702359	HepG2	liver:	n/a
6	chr10:27609310-27609360	GM12892	blood:	n/a
7	chr10:27633745-27633795	AG10803	skin:	n/a
8	chr10:27703377-27703427	NT2-D1	testis:	n/a
9	chr10:27609310-27609360	BE2_C	brain:	n/a
10	chr10:27703289-27703339	GM12878	blood:	n/a
11	chr10:27633745-27633795	MCF10A-Er-Src	breast:	n/a
12	chr10:27703336-27703386	HL-60	blood:	n/a
13	chr10:27702774-27702824	HCPEpiC	choroid plexus:	n/a
14	chr10:27702774-27702824	GM06990	blood:	n/a
15	chr10:27608703-27608753	BE2_C	brain:	n/a
16	chr10:27703336-27703386	H1-hESC	embryonic stem cell:	embryo
17	chr10:27639136-27639186	NT2-D1	testis:	n/a
18	chr10:27609286-27609336	H1-hESC	embryonic stem cell:	embryo
19	chr10:27703362-27703412	SAEC	small airway:	n/a
20	chr10:27634719-27634769	Caco-2	colon:	n/a
21	chr10:27703547-27703597	NH-A	brain:	n/a
22	chr10:27607960-27608010	HRPEpiC	eye:	n/a
23	chr10:27609286-27609336	HepG2	liver:	n/a
24	chr10:27639156-27639206	HRPEpiC	eye:	n/a
25	chr10:27703289-27703339	AG04449	skin:	fetal
26	chr10:27607960-27608010	HRCEpiC	kidney:	n/a
27	chr10:27705739-27705789	RPTEC	kidney:	n/a
28	chr10:27607960-27608010	MCF-7	breast:	n/a
29	chr10:27609333-27609383	MCF-7	breast:	n/a
30	chr10:27609333-27609383	ProgFib	skin:	n/a
31	chr10:27703547-27703597	RPTEC	kidney:	n/a
32	chr10:27703362-27703412	HEK293	kidney:	embryo
33	chr10:27703329-27703379	AG09309	skin:	n/a
34	chr10:27609310-27609360	GM12891	blood:	n/a
35	chr10:27705739-27705789	HAEpiC	amniotic membrane:	n/a
36	chr10:27703547-27703597	PANC-1	pancreas:	n/a
37	chr10:27608719-27608769	HEEpiC	esophagus:	n/a
38	chr10:27633745-27633795	PFSK-1	brain:	n/a
39	chr10:27702528-27702578	PFSK-1	brain:	n/a
40	chr10:27608719-27608769	NB4	blood:	n/a
41	chr10:27702774-27702824	HCM	heart:	n/a
42	chr10:27639136-27639186	GM06990	blood:	n/a
43	chr10:27609333-27609383	NHBE	bronchial:	n/a
44	chr10:27704592-27704642	NHDF-neo	bronchial:	n/a
45	chr10:27703336-27703386	Caco-2	colon:	n/a
46	chr10:27698606-27698656	Hela-S3	cervix:	n/a
47	chr10:27608719-27608769	GM19239	blood:	n/a
48	chr10:27609163-27609213	ProgFib	skin:	n/a
49	chr10:27704762-27704812	HCT-116	colon:	n/a
50	chr10:27703336-27703386	HRE	kidney:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACBD5-2	chr10:27596292-27596344	XLOC_008759
2	lnc-ACBD5-2	chr10:27596292-27596343	XLOC_008759
3	lnc-PTCHD3-2	chr10:27636298-27636725	l_277_chr10:27627368-27636725_testes
4	lnc-MASTL-2	chr10:27633668-27633846	ENSG00000260151.1
5	lnc-ACBD5-2	chr10:27594769-27595233	XLOC_008759
6	lnc-MASTL-2	chr10:27632365-27633580	ENSG00000260151.1
7	lnc-ACBD5-2	chr10:27595041-27595233	XLOC_008759
8	lnc-PTCHD3-2	chr10:27634694-27635239	l_277_chr10:27627368-27636725_testes
9	lnc-PTCHD3-1	chr10:27667067-27667291	NONHSAT011904
10	lnc-PTCHD3-2	chr10:27627369-27627692	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
ENSG00000213770	chromatin interactions
ENSG00000148459	chromatin interactions
ENSG00000136758	chromatin interactions
ENSG00000107897	chromatin interactions
ENSG00000099246	chromatin interactions
ENSG00000182077	chromatin interactions
ENSG00000120539	chromatin interactions
ENSG00000262412	chromatin interactions
SYPL1	miRNA target sites
PLAG1	miRNA target sites

Extended variants
information (count: 3107 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:3107 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548455223	chr10:27594785-27594786	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs141988515	chr10:27594831-27594832	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs16927394	chr10:27594896-27594897	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs190655549	chr10:27594967-27594968	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs117305258	chr10:27594968-27594969	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs182777297	chr10:27594973-27594974	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs528442157	chr10:27595017-27595018	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs188881493	chr10:27595086-27595087	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs375947000	chr10:27595092-27595093	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs571159404	chr10:27595106-27595107	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs193248331	chr10:27595114-27595115	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs552231908	chr10:27596324-27596325	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs7090358	chr10:27596328-27596329	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs564654494	chr10:27600646-27600647	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs578085184	chr10:27600649-27600650	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs543917160	chr10:27600659-27600660	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs563584453	chr10:27600669-27600670	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs559585016	chr10:27600744-27600745	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs372740726	chr10:27600777-27600778	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528496570	chr10:27600788-27600789	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs548954467	chr10:27600797-27600798	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs548176382	chr10:27600850-27600851	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs191428622	chr10:27600876-27600877	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs144353671	chr10:27600897-27600898	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs374673044	chr10:27600908-27600909	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568256121	chr10:27600924-27600925	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs77672877	chr10:27600937-27600938	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs61849720	chr10:27600954-27600955	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs183564342	chr10:27600961-27600962	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs546685080	chr10:27601617-27601618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566495931	chr10:27601620-27601621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12247140	chr10:27601629-27601630	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs191077424	chr10:27601683-27601684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138993705	chr10:27601695-27601696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11015691	chr10:27601717-27601718	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs534644088	chr10:27601723-27601724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373164478	chr10:27601735-27601736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182209237	chr10:27601745-27601746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542725405	chr10:27601763-27601764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114304284	chr10:27601857-27601858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186856478	chr10:27601870-27601871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544994324	chr10:27601880-27601881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191707197	chr10:27601949-27601950	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs530694956	chr10:27601953-27601954	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs112092534	chr10:27601976-27601977	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200353527	chr10:27601999-27602000	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs34400888	chr10:27602000-27602001	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201033919	chr10:27602009-27602010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs186485745	chr10:27602690-27602691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs543172255	chr10:27602691-27602692	Inactive region	TF binding region	1 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:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27600600-27601000	Active TSS	Placenta	Placenta
2	chr10:27601600-27602000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:27601800-27602000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr10:27603800-27605000	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr10:27605000-27608000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr10:27608000-27608200	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr10:27608000-27608200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
8	chr10:27608000-27608400	Enhancers	GM12878-XiMat	blood
9	chr10:27608000-27608400	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr10:27608000-27608600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr10:27608000-27608600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
12	chr10:27608200-27608400	Enhancers	Primary B cells from cord blood	blood
13	chr10:27608200-27608400	Enhancers	Primary hematopoietic stem cells	blood
14	chr10:27608200-27608400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr10:27608200-27608400	Bivalent Enhancer	Brain Hippocampus Middle	brain
16	chr10:27608200-27608600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr10:27608200-27608600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr10:27608200-27608600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr10:27608200-27608600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr10:27608200-27608600	Enhancers	Fetal Intestine Large	intestine
21	chr10:27608200-27608600	Enhancers	Left Ventricle	heart
22	chr10:27608200-27608600	Enhancers	Right Ventricle	heart
23	chr10:27608200-27608800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr10:27608200-27609200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:27608200-27609200	Enhancers	Primary B cells from peripheral blood	blood
26	chr10:27608200-27609200	Enhancers	Fetal Brain Male	brain
27	chr10:27608200-27609400	Enhancers	Esophagus	oesophagus
28	chr10:27608200-27609800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:27608400-27608600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
30	chr10:27608400-27608600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr10:27608400-27608600	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr10:27608400-27608600	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr10:27608400-27608600	Enhancers	Fetal Muscle Trunk	muscle
34	chr10:27608400-27608600	Enhancers	Hela-S3	cervix
35	chr10:27608400-27608600	Enhancers	HMEC	breast
36	chr10:27608400-27608800	Enhancers	Stomach Mucosa	stomach
37	chr10:27608400-27609000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
38	chr10:27608400-27609000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr10:27608400-27609000	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr10:27608400-27609000	Active TSS	Fetal Kidney	kidney
41	chr10:27608400-27609000	Flanking Active TSS	GM12878-XiMat	blood
42	chr10:27608400-27609200	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr10:27608400-27609200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
44	chr10:27608400-27609200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr10:27608400-27609200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr10:27608400-27609200	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr10:27608400-27609200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr10:27608400-27609200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
49	chr10:27608400-27609200	Active TSS	A549	lung
50	chr10:27608400-27609200	Flanking Active TSS	HUVEC	blood vessel

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