Variant report

Variant	nsv430150
Chromosome Location	chr10:27602959-27701920
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1086)
CpG islands
(count:732)
Chromatin interactive
region (count:23)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr10:27649547-27649808	K562	blood:	n/a	n/a
3	ARID3A	chr10:27672857-27673169	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	chr10:27643692-27643988	GM12878	blood:	n/a	n/a
7	BATF	chr10:27649564-27649764	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:27643658-27644039	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:27643724-27643987	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	chr10:27649517-27649830	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:27672558-27673044	HepG2	liver:	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	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
23	CEBPB	chr10:27634311-27634682	A549	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
24	CEBPB	chr10:27634266-27634780	HepG2	liver:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
25	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
26	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
27	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
28	CEBPB	chr10:27655035-27655235	HepG2	liver:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
29	CEBPB	chr10:27672803-27673162	MCF-7	breast:	n/a	n/a
30	CEBPB	chr10:27634283-27634772	Hela-S3	cervix:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
31	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
32	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
33	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
35	CEBPB	chr10:27608939-27609321	ECC-1	luminal epithelium:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
36	CEBPB	chr10:27609114-27609279	H1-hESC	embryonic stem cell:	n/a	chr10:27609201-27609212 chr10:27609124-27609137
37	CEBPB	chr10:27634350-27634708	IMR90	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
38	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
39	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
40	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
41	CEBPB	chr10:27604158-27604375	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:27624329-27624377	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686
44	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
45	CEBPB	chr10:27608518-27609427	Hela-S3	cervix:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
46	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
47	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
48	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
50	CEBPB	chr10:27609087-27609339	K562	blood:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27607960-27608010	HL-60	blood:	n/a
2	chr10:27609310-27609360	Caco-2	colon:	n/a
3	chr10:27698606-27698656	BJ	skin:	n/a
4	chr10:27609333-27609383	GM12892	blood:	n/a
5	chr10:27633745-27633795	AG04449	skin:	fetal
6	chr10:27609163-27609213	HRPEpiC	eye:	n/a
7	chr10:27609310-27609360	HRCEpiC	kidney:	n/a
8	chr10:27698606-27698656	NHBE	bronchial:	n/a
9	chr10:27639136-27639186	ECC-1	luminal epithelium:	n/a
10	chr10:27639156-27639206	PrEC	prostate:	n/a
11	chr10:27698606-27698656	ProgFib	skin:	n/a
12	chr10:27639136-27639186	CMK	blood:	n/a
13	chr10:27608703-27608753	AoSMC	blood vessel:	n/a
14	chr10:27608703-27608753	AG10803	skin:	n/a
15	chr10:27633745-27633795	MCF-7	breast:	n/a
16	chr10:27639156-27639206	PANC-1	pancreas:	n/a
17	chr10:27609310-27609360	IMR90	lung:	fetal
18	chr10:27609286-27609336	BJ	skin:	n/a
19	chr10:27639136-27639186	NHBE	bronchial:	n/a
20	chr10:27609286-27609336	AG04450	lung:	fetal
21	chr10:27609310-27609360	AoSMC	blood vessel:	n/a
22	chr10:27639156-27639206	T-47D	breast:	n/a
23	chr10:27607960-27608010	ECC-1	luminal epithelium:	n/a
24	chr10:27633745-27633795	RPTEC	kidney:	n/a
25	chr10:27607960-27608010	HMEC	breast:	n/a
26	chr10:27609163-27609213	PrEC	prostate:	n/a
27	chr10:27698606-27698656	AoSMC	blood vessel:	n/a
28	chr10:27633745-27633795	Hepatocyte	liver:	n/a
29	chr10:27609310-27609360	ECC-1	luminal epithelium:	n/a
30	chr10:27609333-27609383	Caco-2	colon:	n/a
31	chr10:27608719-27608769	H1-hESC	embryonic stem cell:	embryo
32	chr10:27607960-27608010	HIPEpiC	eye:	n/a
33	chr10:27608719-27608769	NB4	blood:	n/a
34	chr10:27608719-27608769	AG09319	gingival:	n/a
35	chr10:27607960-27608010	NHDF-neo	bronchial:	n/a
36	chr10:27608719-27608769	SK-N-SH_RA	brain:	n/a
37	chr10:27634719-27634769	HCPEpiC	choroid plexus:	n/a
38	chr10:27608703-27608753	ProgFib	skin:	n/a
39	chr10:27608703-27608753	HCM	heart:	n/a
40	chr10:27609286-27609336	NB4	blood:	n/a
41	chr10:27633745-27633795	SAEC	small airway:	n/a
42	chr10:27639136-27639186	HRPEpiC	eye:	n/a
43	chr10:27609310-27609360	GM12892	blood:	n/a
44	chr10:27608719-27608769	Hepatocyte	liver:	n/a
45	chr10:27634719-27634769	HRPEpiC	eye:	n/a
46	chr10:27607960-27608010	HCM	heart:	n/a
47	chr10:27634719-27634769	MCF-7	breast:	n/a
48	chr10:27609333-27609383	U87	brain:	n/a
49	chr10:27609333-27609383	HRPEpiC	eye:	n/a
50	chr10:27608719-27608769	HMEC	breast:	n/a

(count:23 , 50 per page) page: 1

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

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTCHD3-2	chr10:27634694-27635239	l_277_chr10:27627368-27636725_testes
2	lnc-MASTL-2	chr10:27633668-27633846	ENSG00000260151.1
3	lnc-PTCHD3-2	chr10:27627369-27627692	l_277_chr10:27627368-27636725_testes
4	lnc-PTCHD3-1	chr10:27667067-27667291	NONHSAT011904
5	lnc-PTCHD3-2	chr10:27636298-27636725	l_277_chr10:27627368-27636725_testes
6	lnc-MASTL-2	chr10:27632365-27633580	ENSG00000260151.1

No data

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

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

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

Extended variants
information (count: 2775 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:2775 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143688703	chr10:27602988-27602989	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs567613119	chr10:27603000-27603001	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs1780087	chr10:27603099-27603100	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs536496486	chr10:27603115-27603116	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs185078787	chr10:27603117-27603118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201311378	chr10:27603124-27603125	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs11015692	chr10:27603483-27603484	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs182186115	chr10:27603834-27603835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554979293	chr10:27603838-27603839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187628575	chr10:27603840-27603841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191903333	chr10:27603841-27603842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576965401	chr10:27603860-27603861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545971395	chr10:27603884-27603885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182191493	chr10:27603885-27603886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576068007	chr10:27603907-27603908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541461472	chr10:27603908-27603909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561363486	chr10:27603954-27603955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34460208	chr10:27603989-27603990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372622813	chr10:27603991-27603992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527267044	chr10:27603992-27603993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570901412	chr10:27603998-27603999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377552188	chr10:27604009-27604010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185820781	chr10:27604014-27604015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150278894	chr10:27604019-27604020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559948164	chr10:27604041-27604042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552734343	chr10:27604063-27604064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190134350	chr10:27604089-27604090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182366140	chr10:27604091-27604092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548666571	chr10:27604093-27604094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568485525	chr10:27604108-27604109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186720568	chr10:27604110-27604111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190894517	chr10:27604116-27604117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182511604	chr10:27604117-27604118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539285575	chr10:27604127-27604128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556310607	chr10:27604132-27604133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576124466	chr10:27604134-27604135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545539937	chr10:27604142-27604143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541548040	chr10:27604155-27604156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147515226	chr10:27604167-27604168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2484207	chr10:27604172-27604173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571718768	chr10:27604174-27604175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540615927	chr10:27604175-27604176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1638628	chr10:27604229-27604230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs35034083	chr10:27604237-27604238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189163452	chr10:27604298-27604299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193092309	chr10:27604337-27604338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547162304	chr10:27604357-27604358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184572381	chr10:27604391-27604392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs519092	chr10:27604406-27604407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548701539	chr10:27604426-27604427	Enhancers	n/a	n/a	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:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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

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