Variant report

Variant	nsv894978
Chromosome Location	chr10:27185286-27239820
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	chr10:27215887-27216043	HepG2	liver:	n/a	n/a
2	BACH1	chr10:27207852-27207903	K562	blood:	n/a	n/a
3	BATF	chr10:27200819-27201093	GM12878	blood:	n/a	n/a
4	BCL11A	chr10:27200770-27201068	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:27200762-27201086	GM12878	blood:	n/a	n/a
6	BCLAF1	chr10:27200699-27201097	GM12878	blood:	n/a	n/a
7	BCLAF1	chr10:27200661-27201146	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:27200766-27201161	GM12878	blood:	n/a	n/a
9	CCNT2	chr10:27220310-27220518	K562	blood:	n/a	n/a
10	CEBPB	chr10:27198637-27199010	IMR90	lung:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
11	CEBPB	chr10:27208346-27208628	A549	lung:	n/a	chr10:27208444-27208455
12	CEBPB	chr10:27208377-27208567	H1-hESC	embryonic stem cell:	n/a	chr10:27208444-27208455
13	CEBPB	chr10:27215822-27216090	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:27208315-27208632	K562	blood:	n/a	chr10:27208444-27208455
15	CEBPB	chr10:27226988-27227113	A549	lung:	n/a	n/a
16	CEBPB	chr10:27198634-27199009	K562	blood:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
17	CEBPB	chr10:27198632-27199003	HepG2	liver:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
18	CEBPB	chr10:27198705-27198983	Hela-S3	cervix:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
19	CEBPB	chr10:27215887-27216002	IMR90	lung:	n/a	n/a
20	CEBPB	chr10:27198729-27199004	H1-hESC	embryonic stem cell:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
21	CEBPB	chr10:27215866-27216067	K562	blood:	n/a	n/a
22	CEBPB	chr10:27215861-27216075	A549	lung:	n/a	n/a
23	CEBPB	chr10:27208411-27208571	Hela-S3	cervix:	n/a	chr10:27208444-27208455
24	CEBPB	chr10:27208338-27208624	IMR90	lung:	n/a	chr10:27208444-27208455
25	CEBPB	chr10:27198644-27199087	A549	lung:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
26	CEBPB	chr10:27198663-27198985	K562	blood:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
27	CEBPB	chr10:27208365-27208582	HepG2	liver:	n/a	chr10:27208444-27208455
28	CEBPB	chr10:27214768-27214801	HepG2	liver:	n/a	chr10:27214774-27214785
29	CHD1	chr10:27228380-27228580	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr10:27220233-27220239	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr10:27220360-27220395	GM12878	blood:	n/a	n/a
32	CTCF	chr10:27228220-27228370	GM12864	blood:	n/a	n/a
33	CTCF	chr10:27220360-27220510	Caco-2	colon:	n/a	n/a
34	CTCF	chr10:27200843-27200873	GM12878	blood:	n/a	n/a
35	CTCF	chr10:27228340-27228490	GM12870	blood:	n/a	n/a
36	CTCF	chr10:27226080-27226230	GM12872	blood:	n/a	n/a
37	CTCF	chr10:27220324-27220375	GM12891	blood:	n/a	n/a
38	CTCF	chr10:27220320-27220470	Caco-2	colon:	n/a	n/a
39	CTCF	chr10:27230432-27230583	MCF-7	breast:	n/a	n/a
40	CTCF	chr10:27226069-27226163	MCF-7	breast:	n/a	n/a
41	CTCF	chr10:27225900-27226050	GM12872	blood:	n/a	n/a
42	CTCF	chr10:27226020-27226170	GM12875	blood:	n/a	n/a
43	CTCF	chr10:27215467-27215483	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:27226076-27226183	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:27226098-27226178	GM12878	blood:	n/a	n/a
46	CTCF	chr10:27232892-27233042	HepG2	liver:	n/a	n/a
47	CTCF	chr10:27232950-27233007	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr10:27218367-27218443	ProgFib	skin:	n/a	n/a
49	CTCF	chr10:27221214-27221303	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr10:27228740-27228890	GM12866	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27235627-27235677	RPTEC	kidney:	n/a
2	chr10:27230738-27230788	AoSMC	blood vessel:	n/a
3	chr10:27220441-27220491	AG04449	skin:	fetal
4	chr10:27235598-27235648	AoSMC	blood vessel:	n/a
5	chr10:27231223-27231273	Jurkat	blood:	n/a
6	chr10:27230738-27230788	HepG2	liver:	n/a
7	chr10:27235514-27235564	SKMC	muscle:	n/a
8	chr10:27230955-27231005	PrEC	prostate:	n/a
9	chr10:27231882-27231932	PANC-1	pancreas:	n/a
10	chr10:27220234-27220284	T-47D	breast:	n/a
11	chr10:27194523-27194573	HCF	heart:	n/a
12	chr10:27231882-27231932	U87	brain:	n/a
13	chr10:27235598-27235648	HL-60	blood:	n/a
14	chr10:27235598-27235648	HMEC	breast:	n/a
15	chr10:27232252-27232302	PANC-1	pancreas:	n/a
16	chr10:27235627-27235677	HIPEpiC	eye:	n/a
17	chr10:27220234-27220284	HMEC	breast:	n/a
18	chr10:27220441-27220491	A549	lung:	n/a
19	chr10:27194523-27194573	NHBE	bronchial:	n/a
20	chr10:27220441-27220491	HL-60	blood:	n/a
21	chr10:27235514-27235564	Caco-2	colon:	n/a
22	chr10:27231882-27231932	HMEC	breast:	n/a
23	chr10:27230738-27230788	BJ	skin:	n/a
24	chr10:27194523-27194573	A549	lung:	n/a
25	chr10:27194523-27194573	HCT-116	colon:	n/a
26	chr10:27235514-27235564	AoSMC	blood vessel:	n/a
27	chr10:27232252-27232302	SAEC	small airway:	n/a
28	chr10:27235627-27235677	ProgFib	skin:	n/a
29	chr10:27231223-27231273	AG04450	lung:	fetal
30	chr10:27235514-27235564	BJ	skin:	n/a
31	chr10:27230738-27230788	NB4	blood:	n/a
32	chr10:27230955-27231005	AG09309	skin:	n/a
33	chr10:27194523-27194573	T-47D	breast:	n/a
34	chr10:27194523-27194573	GM06990	blood:	n/a
35	chr10:27230955-27231005	ECC-1	luminal epithelium:	n/a
36	chr10:27231882-27231932	AG04450	lung:	fetal
37	chr10:27235627-27235677	NT2-D1	testis:	n/a
38	chr10:27220234-27220284	CMK	blood:	n/a
39	chr10:27231882-27231932	HCPEpiC	choroid plexus:	n/a
40	chr10:27230955-27231005	PANC-1	pancreas:	n/a
41	chr10:27220234-27220284	IMR90	lung:	fetal
42	chr10:27235598-27235648	MCF10A-Er-Src	breast:	n/a
43	chr10:27231882-27231932	SKMC	muscle:	n/a
44	chr10:27235627-27235677	K562	blood:	n/a
45	chr10:27235598-27235648	SK-N-MC	brain:	n/a
46	chr10:27220441-27220491	HNPCEpiC	eye:	n/a
47	chr10:27194523-27194573	Caco-2	colon:	n/a
48	chr10:27235514-27235564	PrEC	prostate:	n/a
49	chr10:27235514-27235564	PANC-1	pancreas:	n/a
50	chr10:27230738-27230788	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27228167..27230462-chr10:27233630..27235621,2	MCF-7	breast:
2	chr10:27200392..27202294-chr10:27208159..27210444,2	MCF-7	breast:
3	chr10:27228167..27230462-chr10:27233630..27235621,2	MCF-7	breast:
4	chr10:27200392..27202294-chr10:27208159..27210444,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDSS1-2	chr10:27195824-27196025	XLOC_008422
2	lnc-PDSS1-2	chr10:27198340-27198867	XLOC_008422

Variant related genes	Relation type
LINC00202-1	TF binding region
LINC00614	TF binding region
LINC00202-1	CpG island
LINC00614	CpG island

Extended variants
information (count: 1962 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1962 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2505956	chr10:27185286-27185287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140867233	chr10:27185324-27185325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371501396	chr10:27185326-27185327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577115243	chr10:27185341-27185342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572585330	chr10:27185393-27185394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2505955	chr10:27185423-27185424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557939609	chr10:27185515-27185516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578058656	chr10:27185516-27185517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150144282	chr10:27185547-27185548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138637306	chr10:27185580-27185581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572881342	chr10:27185604-27185605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35232288	chr10:27185620-27185621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529149631	chr10:27185637-27185638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369351971	chr10:27185638-27185639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559487480	chr10:27185650-27185651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528303497	chr10:27185702-27185703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145688182	chr10:27185705-27185706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541795913	chr10:27185729-27185730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571220930	chr10:27185752-27185753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76976001	chr10:27185759-27185760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550590779	chr10:27185779-27185780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114882357	chr10:27185797-27185798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184577810	chr10:27185845-27185846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138254825	chr10:27185848-27185849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149557578	chr10:27185861-27185862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375101360	chr10:27185867-27185868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534869319	chr10:27185913-27185914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144220149	chr10:27185946-27185947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530870308	chr10:27185956-27185957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537196500	chr10:27185970-27185971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374128827	chr10:27186060-27186061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75454375	chr10:27186086-27186087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542495698	chr10:27186107-27186108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559358471	chr10:27186112-27186113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367823577	chr10:27186120-27186121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186550602	chr10:27186122-27186123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141555074	chr10:27186123-27186124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565094369	chr10:27186133-27186134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530611958	chr10:27186134-27186135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550729484	chr10:27186167-27186168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560844670	chr10:27186168-27186169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529686571	chr10:27186179-27186180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150879078	chr10:27186220-27186221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs16927370	chr10:27186275-27186276	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs140080937	chr10:27186300-27186301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551678454	chr10:27186331-27186332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117994059	chr10:27186357-27186358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74829718	chr10:27186398-27186399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192493245	chr10:27186468-27186469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184857416	chr10:27186469-27186470	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute myeloid leukemia	20824076	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21525872	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27184800-27186200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:27184800-27186400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr10:27185200-27186200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr10:27186200-27186400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr10:27186200-27186600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr10:27186400-27186600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr10:27186400-27187000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr10:27186400-27187000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr10:27186600-27192400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr10:27192400-27193000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr10:27193200-27193400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:27194200-27195000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:27194400-27194800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:27194600-27195000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr10:27195000-27196600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr10:27198600-27199000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr10:27198600-27199400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr10:27198600-27199400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr10:27199000-27199400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr10:27199000-27199400	Enhancers	Osteobl	bone
21	chr10:27199200-27199400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr10:27199200-27199400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr10:27199400-27200800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr10:27199400-27203600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr10:27200000-27201600	Enhancers	GM12878-XiMat	blood
26	chr10:27200600-27201400	Enhancers	Primary B cells from peripheral blood	blood
27	chr10:27200800-27201600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:27201000-27201200	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr10:27202400-27203200	Active TSS	Placenta	Placenta
30	chr10:27203200-27203400	Flanking Active TSS	Placenta	Placenta
31	chr10:27203600-27203800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr10:27203800-27204200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr10:27204200-27204600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr10:27207400-27208000	Enhancers	HSMMtube	muscle
35	chr10:27211800-27212200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:27212000-27212200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr10:27213000-27213200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr10:27217800-27218200	Enhancers	Duodenum Mucosa	Duodenum
39	chr10:27218200-27220000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr10:27218400-27219800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:27218800-27220200	Weak transcription	Fetal Muscle Leg	muscle
42	chr10:27219600-27220000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr10:27219600-27220000	Enhancers	Fetal Intestine Large	intestine
44	chr10:27219600-27220000	Enhancers	HepG2	liver
45	chr10:27219800-27220000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr10:27219800-27220000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr10:27219800-27220000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr10:27219800-27220000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr10:27219800-27220200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr10:27219800-27220400	Active TSS	iPS-18 Cell Line	embryonic stem cell

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