Variant report

Variant	esv1841988
Chromosome Location	chr8:49093467-49156411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:202)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:49133982-49134145	K562	blood:	n/a	n/a
2	CEBPB	chr8:49129092-49129370	MCF-7	breast:	n/a	chr8:49129155-49129166
3	CEBPB	chr8:49108003-49108200	A549	lung:	n/a	chr8:49108057-49108068
4	CEBPB	chr8:49110259-49110440	H1-hESC	embryonic stem cell:	n/a	chr8:49110304-49110315
5	CEBPB	chr8:49129083-49129343	A549	lung:	n/a	chr8:49129155-49129166
6	CEBPB	chr8:49110146-49110437	Hela-S3	cervix:	n/a	chr8:49110304-49110315
7	CEBPB	chr8:49097598-49097841	IMR90	lung:	n/a	chr8:49097705-49097716
8	CEBPB	chr8:49107893-49108163	K562	blood:	n/a	chr8:49108057-49108068
9	CEBPB	chr8:49110216-49110455	IMR90	lung:	n/a	chr8:49110304-49110315
10	CEBPB	chr8:49107898-49108243	HepG2	liver:	n/a	chr8:49108057-49108068
11	CEBPB	chr8:49097614-49097814	K562	blood:	n/a	chr8:49097705-49097716
12	CEBPB	chr8:49155386-49155461	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:49155353-49155988	HepG2	liver:	n/a	chr8:49155838-49155849
14	CEBPB	chr8:49114843-49115066	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:49129013-49129409	MCF-7	breast:	n/a	chr8:49129155-49129166
16	CEBPB	chr8:49097610-49097855	HepG2	liver:	n/a	chr8:49097705-49097716
17	CEBPB	chr8:49155736-49155989	A549	lung:	n/a	chr8:49155838-49155849
18	CEBPB	chr8:49107927-49108224	IMR90	lung:	n/a	chr8:49108057-49108068
19	CEBPB	chr8:49155702-49155992	IMR90	lung:	n/a	chr8:49155838-49155849
20	CEBPB	chr8:49129041-49129344	HepG2	liver:	n/a	chr8:49129155-49129166
21	CEBPB	chr8:49110163-49110451	A549	lung:	n/a	chr8:49110304-49110315
22	CEBPB	chr8:49155317-49155514	A549	lung:	n/a	n/a
23	CEBPB	chr8:49115430-49115669	HepG2	liver:	n/a	chr8:49115567-49115578
24	CEBPB	chr8:49129124-49129241	K562	blood:	n/a	chr8:49129155-49129166
25	CEBPB	chr8:49155716-49155972	Hela-S3	cervix:	n/a	chr8:49155838-49155849
26	CEBPB	chr8:49110133-49110487	HepG2	liver:	n/a	chr8:49110304-49110315
27	CEBPB	chr8:49114803-49114839	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr8:49131450-49131692	HepG2	liver:	n/a	chr8:49131552-49131563
29	CEBPB	chr8:49129149-49129230	IMR90	lung:	n/a	chr8:49129155-49129166
30	CEBPB	chr8:49097693-49097731	A549	lung:	n/a	chr8:49097705-49097716
31	CEBPB	chr8:49110168-49110450	K562	blood:	n/a	chr8:49110304-49110315
32	CTCF	chr8:49112020-49112170	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr8:49138555-49138725	A549	lung:	n/a	n/a
34	CTCF	chr8:49138580-49138735	HepG2	liver:	n/a	n/a
35	CTCF	chr8:49138624-49138681	GM12878	blood:	n/a	n/a
36	CTCF	chr8:49104015-49104077	Fibrobl	skin:	n/a	n/a
37	CTCF	chr8:49103960-49104110	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr8:49104000-49104150	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:49138619-49138689	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:49140154-49140202	Lung_OC	lung:	n/a	n/a
41	CTCF	chr8:49104040-49104190	NHEK	skin:	n/a	n/a
42	CTCF	chr8:49138599-49138663	GM19240	blood:	n/a	n/a
43	CTCF	chr8:49117840-49117990	NHLF	lung:	n/a	n/a
44	CTCF	chr8:49104016-49104106	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr8:49103940-49104090	SAEC	small airway:	n/a	n/a
46	CTCF	chr8:49104020-49104170	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr8:49138611-49138691	Fibrobl	skin:	n/a	n/a
48	CTCF	chr8:49104040-49104190	HMEC	breast:	n/a	n/a
49	CTCF	chr8:49104000-49104150	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr8:49103995-49104117	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:49111711-49111761	MCF10A-Er-Src	breast:	n/a
2	chr8:49111711-49111761	HRE	kidney:	n/a
3	chr8:49111711-49111761	A549	lung:	n/a
4	chr8:49111711-49111761	GM06990	blood:	n/a
5	chr8:49111711-49111761	AG09309	skin:	n/a
6	chr8:49111711-49111761	NB4	blood:	n/a
7	chr8:49111711-49111761	HCM	heart:	n/a
8	chr8:49111711-49111761	HEEpiC	esophagus:	n/a
9	chr8:49111711-49111761	Hepatocyte	liver:	n/a
10	chr8:49111711-49111761	HAEpiC	amniotic membrane:	n/a
11	chr8:49111711-49111761	Caco-2	colon:	n/a
12	chr8:49111711-49111761	HNPCEpiC	eye:	n/a
13	chr8:49111711-49111761	AG10803	skin:	n/a
14	chr8:49111711-49111761	HCPEpiC	choroid plexus:	n/a
15	chr8:49111711-49111761	ovcar-3	ovarian:	n/a
16	chr8:49111711-49111761	CMK	blood:	n/a
17	chr8:49111711-49111761	PANC-1	pancreas:	n/a
18	chr8:49111711-49111761	HRCEpiC	kidney:	n/a
19	chr8:49111711-49111761	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:49111711-49111761	HUVEC	blood vessel:	n/a
21	chr8:49111711-49111761	ProgFib	skin:	n/a
22	chr8:49111711-49111761	NT2-D1	testis:	n/a
23	chr8:49111711-49111761	Jurkat	blood:	n/a
24	chr8:49111711-49111761	HepG2	liver:	n/a
25	chr8:49111711-49111761	HCT-116	colon:	n/a
26	chr8:49111711-49111761	Hela-S3	cervix:	n/a
27	chr8:49111711-49111761	U87	brain:	n/a
28	chr8:49111711-49111761	NH-A	brain:	n/a
29	chr8:49111711-49111761	BE2_C	brain:	n/a
30	chr8:49111711-49111761	HL-60	blood:	n/a
31	chr8:49111711-49111761	AoSMC	blood vessel:	n/a
32	chr8:49111711-49111761	GM19239	blood:	n/a
33	chr8:49111711-49111761	PrEC	prostate:	n/a
34	chr8:49111711-49111761	IMR90	lung:	fetal
35	chr8:49111711-49111761	T-47D	breast:	n/a
36	chr8:49111711-49111761	AG04449	skin:	fetal
37	chr8:49111711-49111761	HEK293	kidney:	embryo
38	chr8:49111711-49111761	SK-N-SH	brain:	n/a
39	chr8:49111711-49111761	LNCaP	prostate:	n/a
40	chr8:49111711-49111761	HCF	heart:	n/a
41	chr8:49111711-49111761	GM12892	blood:	n/a
42	chr8:49111711-49111761	HMEC	breast:	n/a
43	chr8:49111711-49111761	SKMC	muscle:	n/a
44	chr8:49111711-49111761	SAEC	small airway:	n/a
45	chr8:49111711-49111761	MCF-7	breast:	n/a
46	chr8:49111711-49111761	NHDF-neo	bronchial:	n/a
47	chr8:49111711-49111761	SK-N-MC	brain:	n/a
48	chr8:49111711-49111761	ECC-1	luminal epithelium:	n/a
49	chr8:49111711-49111761	NHBE	bronchial:	n/a
50	chr8:49111711-49111761	H1-hESC	embryonic stem cell:	embryo

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:49107364..49109537-chr8:49113268..49115382,2	K562	blood:
2	chr8:49125826..49128370-chr8:49128948..49131652,4	K562	blood:
3	chr8:49100007..49102917-chr8:49105924..49108350,3	K562	blood:
4	chr8:49101995..49104424-chr8:49230662..49232530,2	MCF-7	breast:
5	chr8:49107364..49109537-chr8:49113268..49115382,2	K562	blood:
6	chr11:19772450..19772957-chr8:49132973..49133610,2	MCF-7	breast:
7	chr8:49125826..49128370-chr8:49128948..49131652,4	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2V2-2	chr8:49138284-49138605	expReg_chr8_2994_+
2	lnc-PRKDC-2	chr8:49106410-49107187	NONHSAT126472

No data

Variant related genes	Relation type
ENSG00000253843	TF binding region
ENSG00000253843	CpG island
ENSG00000253843	chromatin interactions

Extended variants
information (count: 1768 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1768 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377591744	chr8:49093500-49093501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs3934733	chr8:49093501-49093502	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs11991972	chr8:49093505-49093506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs186755396	chr8:49093534-49093535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555563532	chr8:49093535-49093536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556358092	chr8:49093537-49093538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573861359	chr8:49093539-49093540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs3934734	chr8:49093540-49093541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs560147852	chr8:49093561-49093562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190272866	chr8:49093567-49093568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545777342	chr8:49093609-49093610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201560691	chr8:49093621-49093622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142045408	chr8:49093625-49093626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181148204	chr8:49093654-49093655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550063246	chr8:49093679-49093680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185176065	chr8:49093689-49093690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146364427	chr8:49093709-49093710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189791985	chr8:49093710-49093711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182409134	chr8:49093755-49093756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4072343	chr8:49093831-49093832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs369640709	chr8:49093880-49093881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111326351	chr8:49093894-49093895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575430959	chr8:49093977-49093978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544352630	chr8:49094051-49094052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113872578	chr8:49094053-49094054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115793217	chr8:49094075-49094076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569687165	chr8:49094090-49094091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540981477	chr8:49094102-49094103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537364407	chr8:49094154-49094155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555600597	chr8:49094155-49094156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189090175	chr8:49094164-49094165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535218477	chr8:49094185-49094186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553628330	chr8:49094216-49094217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138447040	chr8:49094241-49094242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191798955	chr8:49094267-49094268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112477706	chr8:49094299-49094300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576064498	chr8:49094303-49094304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77643752	chr8:49094323-49094324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374752541	chr8:49094344-49094345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183841160	chr8:49094360-49094361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529115141	chr8:49094364-49094365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34508599	chr8:49094386-49094387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377483748	chr8:49094391-49094392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559062686	chr8:49094429-49094430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143046991	chr8:49094430-49094431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4380968	chr8:49094576-49094577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs551428068	chr8:49094608-49094609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4397430	chr8:49094641-49094642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs201433615	chr8:49094642-49094643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530768437	chr8:49094671-49094672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
22q11 deletion syndrome	20357662	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49085200-49098400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:49089600-49094000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:49098200-49098800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:49098200-49100400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:49098400-49098800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:49099600-49102400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr8:49100400-49103400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:49100600-49101400	Enhancers	Liver	Liver
9	chr8:49100600-49102200	Enhancers	Fetal Muscle Trunk	muscle
10	chr8:49100600-49102400	Enhancers	Adipose Nuclei	Adipose
11	chr8:49100800-49102200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:49100800-49102200	Enhancers	Fetal Muscle Leg	muscle
13	chr8:49101600-49101800	Enhancers	Ovary	ovary
14	chr8:49101800-49110400	Weak transcription	Ovary	ovary
15	chr8:49102200-49103600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr8:49102200-49103800	Weak transcription	Fetal Muscle Trunk	muscle
17	chr8:49102200-49104200	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:49102400-49103400	Weak transcription	Adipose Nuclei	Adipose
19	chr8:49102400-49104600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr8:49103400-49104200	Enhancers	Adipose Nuclei	Adipose
21	chr8:49103400-49104600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:49103600-49104400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:49103800-49104000	Enhancers	Stomach Smooth Muscle	stomach
24	chr8:49103800-49105000	Enhancers	Fetal Muscle Trunk	muscle
25	chr8:49104200-49104600	Enhancers	Brain Cingulate Gyrus	brain
26	chr8:49104200-49105200	Enhancers	Fetal Muscle Leg	muscle
27	chr8:49104200-49105400	Enhancers	Brain Substantia Nigra	brain
28	chr8:49104200-49115400	Weak transcription	Adipose Nuclei	Adipose
29	chr8:49104400-49104800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:49104400-49105000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:49104400-49105200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr8:49104400-49105200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr8:49104400-49105200	Enhancers	Brain Hippocampus Middle	brain
34	chr8:49104400-49105400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:49104400-49105400	Enhancers	Osteobl	bone
36	chr8:49104600-49104800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:49104600-49104800	Enhancers	Stomach Mucosa	stomach
38	chr8:49104600-49105000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:49104600-49105000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:49104600-49105000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr8:49104600-49105000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr8:49104600-49105000	Flanking Active TSS	Brain Cingulate Gyrus	brain
43	chr8:49104600-49105000	Enhancers	Fetal Stomach	stomach
44	chr8:49104600-49105200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr8:49104600-49105200	Enhancers	HMEC	breast
46	chr8:49104600-49105200	Enhancers	HSMM	muscle
47	chr8:49104600-49105200	Enhancers	NH-A	brain
48	chr8:49104600-49105200	Enhancers	NHEK	skin
49	chr8:49104600-49105200	Enhancers	NHLF	lung
50	chr8:49104600-49105400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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