Variant report

Variant	nsv1016996
Chromosome Location	chr8:86524837-86553130
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:73)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:73 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
2	CEBPB	chr8:86541828-86542028	HepG2	liver:	n/a	chr8:86541944-86541955
3	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
4	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
5	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
6	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
7	CEBPB	chr8:86548074-86548266	HepG2	liver:	n/a	chr8:86548177-86548194
8	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
9	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
10	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
11	CTCF	chr8:86544750-86544836	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr8:86541400-86541550	HA-sp	spinal cord:	n/a	n/a
13	E2F4	chr8:86547943-86548263	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr8:86528535-86528749	MCF10A-Er-Src	breast:	n/a	n/a
15	EBF1	chr8:86548212-86548420	GM12878	blood:	n/a	chr8:86548316-86548326
16	EP300	chr8:86530109-86530133	K562	blood:	n/a	n/a
17	FOS	chr8:86547861-86548371	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
18	FOS	chr8:86544592-86544996	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr8:86544590-86544994	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr8:86544555-86544966	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr8:86526559-86526927	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr8:86547443-86547509	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr8:86547885-86548430	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
24	FOS	chr8:86544593-86544999	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr8:86526691-86526802	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:86547867-86548278	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
27	FOS	chr8:86547900-86548453	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
28	FOS	chr8:86526689-86526696	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL1	chr8:86544544-86545033	HCT-116	colon:	n/a	n/a
30	FOSL1	chr8:86544543-86545175	HCT-116	colon:	n/a	n/a
31	FOSL2	chr8:86544559-86545076	MCF-7	breast:	n/a	n/a
32	GATA2	chr8:86529877-86530241	K562	blood:	n/a	n/a
33	MAFK	chr8:86538870-86539018	HepG2	liver:	n/a	chr8:86538977-86538992 chr8:86538977-86538993 chr8:86538976-86538990
34	MAFK	chr8:86538877-86539018	HepG2	liver:	n/a	chr8:86538977-86538992 chr8:86538977-86538993 chr8:86538976-86538990
35	MYC	chr8:86547904-86548391	MCF10A-Er-Src	breast:	n/a	chr8:86548153-86548162
36	MYC	chr8:86544659-86544959	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr8:86528059-86528066	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr8:86544592-86545063	MCF10A-Er-Src	breast:	n/a	n/a
39	MYC	chr8:86529973-86530139	K562	blood:	n/a	n/a
40	MYC	chr8:86547373-86547579	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr8:86547787-86548498	MCF10A-Er-Src	breast:	n/a	chr8:86548153-86548162
42	MYC	chr8:86529678-86529707	K562	blood:	n/a	n/a
43	NR2F2	chr8:86544558-86545085	MCF-7	breast:	n/a	n/a
44	NR3C1	chr8:86526550-86526723	ECC-1	luminal epithelium:	n/a	n/a
45	NR3C1	chr8:86526556-86526765	ECC-1	luminal epithelium:	n/a	n/a
46	POLR2A	chr8:86542579-86542676	MCF-7	breast:	n/a	n/a
47	POLR2A	chr8:86527217-86527260	GM12878	blood:	n/a	n/a
48	POLR2A	chr8:86548007-86548207	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr8:86544639-86544919	HCT-116	colon:	n/a	n/a
50	POLR2A	chr8:86526669-86526725	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86551492-86551542	GM19239	blood:	n/a
2	chr8:86551492-86551542	CMK	blood:	n/a
3	chr8:86551492-86551542	HepG2	liver:	n/a
4	chr8:86551492-86551542	GM06990	blood:	n/a
5	chr8:86551492-86551542	SAEC	small airway:	n/a
6	chr8:86551492-86551542	GM12891	blood:	n/a
7	chr8:86551492-86551542	MCF10A-Er-Src	breast:	n/a
8	chr8:86551492-86551542	HNPCEpiC	eye:	n/a
9	chr8:86551492-86551542	ECC-1	luminal epithelium:	n/a
10	chr8:86551492-86551542	AG04450	lung:	fetal
11	chr8:86551492-86551542	IMR90	lung:	fetal
12	chr8:86551492-86551542	AG04449	skin:	fetal
13	chr8:86551492-86551542	PrEC	prostate:	n/a
14	chr8:86551492-86551542	AG10803	skin:	n/a
15	chr8:86551492-86551542	GM12878	blood:	n/a
16	chr8:86551492-86551542	HIPEpiC	eye:	n/a
17	chr8:86551492-86551542	Jurkat	blood:	n/a
18	chr8:86551492-86551542	SK-N-SH	brain:	n/a
19	chr8:86551492-86551542	LNCaP	prostate:	n/a
20	chr8:86551492-86551542	K562	blood:	n/a
21	chr8:86551492-86551542	PANC-1	pancreas:	n/a
22	chr8:86551492-86551542	SK-N-MC	brain:	n/a
23	chr8:86551492-86551542	NHBE	bronchial:	n/a
24	chr8:86551492-86551542	HCF	heart:	n/a
25	chr8:86551492-86551542	U87	brain:	n/a
26	chr8:86551492-86551542	H1-hESC	embryonic stem cell:	embryo
27	chr8:86551492-86551542	Hela-S3	cervix:	n/a
28	chr8:86551492-86551542	NB4	blood:	n/a
29	chr8:86551492-86551542	HCM	heart:	n/a
30	chr8:86551492-86551542	Hepatocyte	liver:	n/a
31	chr8:86551492-86551542	SK-N-SH_RA	brain:	n/a
32	chr8:86551492-86551542	ovcar-3	ovarian:	n/a
33	chr8:86551492-86551542	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:86551492-86551542	HAEpiC	amniotic membrane:	n/a
35	chr8:86551492-86551542	HCT-116	colon:	n/a
36	chr8:86551492-86551542	HRE	kidney:	n/a
37	chr8:86551492-86551542	HEK293	kidney:	embryo
38	chr8:86551492-86551542	AG09319	gingival:	n/a
39	chr8:86551492-86551542	BJ	skin:	n/a
40	chr8:86551492-86551542	GM12892	blood:	n/a
41	chr8:86551492-86551542	RPTEC	kidney:	n/a
42	chr8:86551492-86551542	SKMC	muscle:	n/a
43	chr8:86551492-86551542	HMEC	breast:	n/a
44	chr8:86551492-86551542	MCF-7	breast:	n/a
45	chr8:86551492-86551542	ProgFib	skin:	n/a
46	chr8:86551492-86551542	HCPEpiC	choroid plexus:	n/a
47	chr8:86551492-86551542	Caco-2	colon:	n/a
48	chr8:86551492-86551542	NHDF-neo	bronchial:	n/a
49	chr8:86551492-86551542	HRCEpiC	kidney:	n/a
50	chr8:86551492-86551542	HEEpiC	esophagus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
2	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
3	chr8:86374283..86376503-chr8:86538225..86540669,2	MCF-7	breast:
4	chr22:21257752..21260264-chr8:86546631..86548915,2	MCF-7	breast:
5	chr8:86375424..86377352-chr8:86545353..86547430,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253680	TF binding region
ENSG00000253680	CpG island
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 675 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192813054	chr8:86524843-86524844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370593826	chr8:86524878-86524879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551979394	chr8:86524880-86524881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571621539	chr8:86524977-86524978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79815016	chr8:86524999-86525000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113881194	chr8:86525010-86525011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556896831	chr8:86525019-86525020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35415407	chr8:86525026-86525027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573702801	chr8:86525029-86525030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373752133	chr8:86525037-86525038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533268607	chr8:86525095-86525096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536295312	chr8:86525123-86525124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571680297	chr8:86525146-86525147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377681023	chr8:86525211-86525212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150470797	chr8:86525218-86525219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138551520	chr8:86525261-86525262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565112536	chr8:86525318-86525319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199998301	chr8:86525322-86525323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575207410	chr8:86525361-86525362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143958792	chr8:86525422-86525423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539018059	chr8:86525452-86525453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138579812	chr8:86525483-86525484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs72464136	chr8:86525484-86525485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6150684	chr8:86525498-86525499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561010056	chr8:86525512-86525513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529703144	chr8:86525530-86525531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554193807	chr8:86525534-86525535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546652186	chr8:86525541-86525542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111746127	chr8:86525731-86525732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9942742	chr8:86525764-86525765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115832500	chr8:86525850-86525851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112438833	chr8:86525901-86525902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34012058	chr8:86525973-86525974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs28373224	chr8:86525978-86525979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571821533	chr8:86525984-86525985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376213396	chr8:86525990-86525991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537105211	chr8:86526026-86526027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550659067	chr8:86526035-86526036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567463924	chr8:86526040-86526041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536231317	chr8:86526042-86526043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552980272	chr8:86526054-86526055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79682555	chr8:86526058-86526059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375398189	chr8:86526124-86526125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538930348	chr8:86526169-86526170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191627989	chr8:86526176-86526177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575391397	chr8:86526177-86526178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183734658	chr8:86526320-86526321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146713876	chr8:86526404-86526405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56698727	chr8:86526443-86526444	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs13258194	chr8:86526490-86526491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86524000-86526000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr8:86524000-86528200	Enhancers	Adipose Nuclei	Adipose
3	chr8:86524600-86525400	Enhancers	Right Atrium	heart
4	chr8:86524600-86526000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr8:86525000-86525200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:86525400-86526600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:86526000-86526800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr8:86526000-86527200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:86526000-86527200	Enhancers	Liver	Liver
10	chr8:86526000-86527400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr8:86526000-86527800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr8:86526400-86527000	Enhancers	Brain Hippocampus Middle	brain
13	chr8:86526400-86527800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:86526400-86528000	Enhancers	Brain Anterior Caudate	brain
15	chr8:86526400-86528000	Enhancers	Brain Substantia Nigra	brain
16	chr8:86526600-86527200	Enhancers	HMEC	breast
17	chr8:86526600-86527400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:86526800-86527200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:86527000-86528400	Weak transcription	Brain Hippocampus Middle	brain
20	chr8:86528400-86528600	Enhancers	Brain Hippocampus Middle	brain
21	chr8:86538000-86539800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:86538200-86539800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:86538400-86539400	Enhancers	Brain Hippocampus Middle	brain
24	chr8:86538600-86538800	Enhancers	Brain Cingulate Gyrus	brain
25	chr8:86538800-86539000	Enhancers	Fetal Lung	lung
26	chr8:86539200-86541400	Weak transcription	Fetal Lung	lung
27	chr8:86539400-86539600	Enhancers	Brain Cingulate Gyrus	brain
28	chr8:86539800-86544000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:86541400-86544400	Enhancers	Fetal Lung	lung
30	chr8:86543400-86544400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:86543400-86544600	Enhancers	Brain Anterior Caudate	brain
32	chr8:86543600-86543800	Enhancers	Brain Hippocampus Middle	brain
33	chr8:86543600-86544400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:86543600-86544600	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr8:86543600-86547000	Enhancers	NHEK	skin
36	chr8:86544000-86544600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:86544000-86545400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:86544000-86545600	Enhancers	HMEC	breast
39	chr8:86544200-86544600	Active TSS	Hela-S3	cervix
40	chr8:86544200-86545200	Active TSS	Duodenum Mucosa	Duodenum
41	chr8:86544400-86545200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:86544400-86545200	Enhancers	Fetal Intestine Large	intestine
43	chr8:86544800-86545000	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr8:86544800-86545400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr8:86545000-86545400	Enhancers	Fetal Intestine Small	intestine
46	chr8:86545200-86545800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:86545400-86546600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:86545400-86546800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr8:86545600-86547000	Weak transcription	HMEC	breast
50	chr8:86545800-86546800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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