Variant report

Variant	nsv550279
Chromosome Location	chr10:27652398-27705855
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	BCL3	chr10:27672617-27673252	A549	lung:	n/a	n/a
3	BHLHE40	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
4	BRCA1	chr10:27672817-27673127	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr10:27681602-27681815	K562	blood:	n/a	n/a
6	CBX3	chr10:27681617-27681837	K562	blood:	n/a	n/a
7	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860
8	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
9	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
10	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
12	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
13	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
14	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
15	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860
16	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
17	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
18	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
19	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
20	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:27672803-27673162	MCF-7	breast:	n/a	n/a
22	CEBPB	chr10:27655035-27655235	HepG2	liver:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
23	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
24	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
25	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
26	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr10:27660335-27660679	K562	blood:	n/a	n/a
28	CHD2	chr10:27672857-27673148	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr10:27658860-27659010	GM12873	blood:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
30	CTCF	chr10:27658880-27659030	MCF-7	breast:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
31	CTCF	chr10:27658900-27659050	HMEC	breast:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
32	CTCF	chr10:27658880-27659030	HCPEpiC	choroid plexus:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
33	CTCF	chr10:27658920-27659070	HBMEC	blood vessel:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
34	CTCF	chr10:27658900-27659050	WI-38	lung:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
35	CTCF	chr10:27682322-27682358	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr10:27658900-27659050	HMF	breast:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
37	CTCF	chr10:27658880-27659030	K562	blood:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
38	CTCF	chr10:27702500-27702650	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr10:27681748-27681861	Lung_OC	lung:	n/a	n/a
40	CTCF	chr10:27658874-27659005	Spleen_OC	spleen:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
41	CTCF	chr10:27658900-27659050	HCM	heart:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
42	CTCF	chr10:27668200-27668273	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr10:27658940-27659090	HMF	breast:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
44	CTCF	chr10:27658860-27659010	AG09309	skin:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
45	CTCF	chr10:27658780-27658930	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr10:27658860-27659010	HRPEpiC	eye:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
47	CTCF	chr10:27658900-27659050	HPAF	blood vessel:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
48	CTCF	chr10:27658860-27659010	NHDF-neo	bronchial:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
49	CTCF	chr10:27658897-27659037	K562	blood:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
50	CTCF	chr10:27658820-27658970	GM12873	blood:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27698606-27698656	NT2-D1	testis:	n/a
2	chr10:27703289-27703339	GM19239	blood:	n/a
3	chr10:27698606-27698656	SKMC	muscle:	n/a
4	chr10:27704762-27704812	PFSK-1	brain:	n/a
5	chr10:27703377-27703427	CMK	blood:	n/a
6	chr10:27702528-27702578	HNPCEpiC	eye:	n/a
7	chr10:27702309-27702359	NHDF-neo	bronchial:	n/a
8	chr10:27703547-27703597	SK-N-MC	brain:	n/a
9	chr10:27698606-27698656	ECC-1	luminal epithelium:	n/a
10	chr10:27698606-27698656	HIPEpiC	eye:	n/a
11	chr10:27704592-27704642	Hepatocyte	liver:	n/a
12	chr10:27703336-27703386	NHBE	bronchial:	n/a
13	chr10:27703547-27703597	CMK	blood:	n/a
14	chr10:27702309-27702359	H1-hESC	embryonic stem cell:	embryo
15	chr10:27703289-27703339	K562	blood:	n/a
16	chr10:27705739-27705789	HUVEC	blood vessel:	n/a
17	chr10:27704762-27704812	GM12878	blood:	n/a
18	chr10:27703329-27703379	HL-60	blood:	n/a
19	chr10:27702309-27702359	PFSK-1	brain:	n/a
20	chr10:27704592-27704642	AG09319	gingival:	n/a
21	chr10:27705739-27705789	HAEpiC	amniotic membrane:	n/a
22	chr10:27702774-27702824	SAEC	small airway:	n/a
23	chr10:27703329-27703379	HEEpiC	esophagus:	n/a
24	chr10:27703377-27703427	Hela-S3	cervix:	n/a
25	chr10:27702309-27702359	RPTEC	kidney:	n/a
26	chr10:27703289-27703339	H1-hESC	embryonic stem cell:	embryo
27	chr10:27702309-27702359	GM12892	blood:	n/a
28	chr10:27703336-27703386	U87	brain:	n/a
29	chr10:27703329-27703379	AG09309	skin:	n/a
30	chr10:27703362-27703412	HL-60	blood:	n/a
31	chr10:27698606-27698656	HRPEpiC	eye:	n/a
32	chr10:27703247-27703297	HL-60	blood:	n/a
33	chr10:27702774-27702824	AG09309	skin:	n/a
34	chr10:27702309-27702359	ovcar-3	ovarian:	n/a
35	chr10:27698606-27698656	PFSK-1	brain:	n/a
36	chr10:27704592-27704642	MCF10A-Er-Src	breast:	n/a
37	chr10:27703336-27703386	SK-N-SH_RA	brain:	n/a
38	chr10:27704592-27704642	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:27702528-27702578	HCF	heart:	n/a
40	chr10:27703289-27703339	AG04450	lung:	fetal
41	chr10:27704592-27704642	A549	lung:	n/a
42	chr10:27703329-27703379	NHBE	bronchial:	n/a
43	chr10:27698606-27698656	GM12892	blood:	n/a
44	chr10:27703547-27703597	U87	brain:	n/a
45	chr10:27702528-27702578	NT2-D1	testis:	n/a
46	chr10:27704592-27704642	AG09309	skin:	n/a
47	chr10:27703547-27703597	HEEpiC	esophagus:	n/a
48	chr10:27703377-27703427	HMEC	breast:	n/a
49	chr10:27703486-27703536	HPAEpiC	pulmonary alveolar:	n/a
50	chr10:27703247-27703297	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
2	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
3	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
4	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
5	chr10:27694442..27697083-chr10:27703247..27705702,3	K562	blood:
6	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
7	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
8	chr10:27659175..27661663-chr10:27792060..27794224,2	MCF-7	breast:
9	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
10	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTCHD3-1	chr10:27667067-27667291	NONHSAT011904

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
PTCHD3	TF binding region
TRIAP1P1	CpG island
PTCHD3	CpG island
ENSG00000182077	chromatin interactions
ENSG00000099246	chromatin interactions

Extended variants
information (count: 1262 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56006323	chr10:27652398-27652399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562489413	chr10:27652415-27652416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146832896	chr10:27652429-27652430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544917293	chr10:27652505-27652506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557236492	chr10:27652510-27652511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184373265	chr10:27652594-27652595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576600583	chr10:27652607-27652608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530327359	chr10:27652688-27652689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575756708	chr10:27652689-27652690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547166941	chr10:27652741-27652742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539364722	chr10:27652787-27652788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140912322	chr10:27652803-27652804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74647836	chr10:27652812-27652813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56243416	chr10:27652814-27652815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs552320584	chr10:27652819-27652820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11015720	chr10:27652828-27652829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs79332721	chr10:27652871-27652872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72029538	chr10:27652898-27652899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386742255	chr10:27652905-27652906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11015721	chr10:27652944-27652945	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567970211	chr10:27652952-27652953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189354787	chr10:27652998-27652999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56249133	chr10:27653012-27653013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553898616	chr10:27653019-27653020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528730406	chr10:27653069-27653070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540613153	chr10:27653088-27653089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144663538	chr10:27653089-27653090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545863205	chr10:27653098-27653099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12266893	chr10:27653133-27653134	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs237563	chr10:27653165-27653166	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs55974129	chr10:27653169-27653170	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs193116788	chr10:27653185-27653186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562252797	chr10:27653259-27653260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs237564	chr10:27653275-27653276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs138413974	chr10:27653279-27653280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560718865	chr10:27653280-27653281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs237565	chr10:27653324-27653325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185831722	chr10:27653339-27653340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12252778	chr10:27653370-27653371	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs531602143	chr10:27653402-27653403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564683262	chr10:27653403-27653404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548150808	chr10:27653430-27653431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189246749	chr10:27653440-27653441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs17828819	chr10:27653549-27653550	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs181712822	chr10:27653552-27653553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533547477	chr10:27653574-27653575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570622214	chr10:27653627-27653628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143619615	chr10:27653638-27653639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556232735	chr10:27653648-27653649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560619365	chr10:27653681-27653682	Weak transcription	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:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27633800-27655400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:27653000-27653200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:27654200-27656600	Enhancers	GM12878-XiMat	blood
4	chr10:27655200-27655600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr10:27659000-27659200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr10:27659000-27659400	Enhancers	Hela-S3	cervix
7	chr10:27659000-27659600	Enhancers	Fetal Brain Female	brain
8	chr10:27659000-27660000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:27659200-27659400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:27659400-27661000	Weak transcription	Hela-S3	cervix
11	chr10:27659600-27660800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:27660000-27660400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:27660400-27661200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr10:27660800-27661800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:27661000-27661800	Enhancers	NHDF-Ad	bronchial
16	chr10:27661000-27663200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr10:27661200-27661400	Enhancers	Hela-S3	cervix
18	chr10:27661200-27661600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:27661200-27661600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr10:27661200-27663200	Enhancers	NHEK	skin
21	chr10:27661200-27663400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr10:27661600-27662600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr10:27661600-27662800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr10:27662600-27662800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr10:27669200-27670600	Enhancers	HepG2	liver
26	chr10:27669400-27671200	Enhancers	Adipose Nuclei	Adipose
27	chr10:27669600-27671000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:27669800-27670000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr10:27669800-27670000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
30	chr10:27670600-27672600	Weak transcription	HepG2	liver
31	chr10:27671000-27672600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr10:27672200-27673600	Enhancers	Hela-S3	cervix
33	chr10:27672600-27672800	Enhancers	Thymus	Thymus
34	chr10:27672600-27672800	Flanking Active TSS	HUVEC	blood vessel
35	chr10:27672600-27673000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:27672600-27673200	Enhancers	HepG2	liver
37	chr10:27672600-27673200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr10:27672600-27673400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:27672600-27673400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr10:27672600-27673400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:27672600-27673400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr10:27672600-27673400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr10:27672600-27673400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr10:27672600-27673400	Enhancers	Lung	lung
45	chr10:27672600-27673400	Flanking Active TSS	A549	lung
46	chr10:27672600-27673400	Enhancers	HMEC	breast
47	chr10:27672600-27673400	Enhancers	NHEK	skin
48	chr10:27672800-27673400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr10:27672800-27673400	Enhancers	Stomach Mucosa	stomach
50	chr10:27672800-27673400	Enhancers	HUVEC	blood vessel

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