Variant report

Variant	nsv890906
Chromosome Location	chr8:53408434-53491159
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	chr8:53490305-53490673	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:53490268-53490616	K562	blood:	n/a	n/a
3	BACH1	chr8:53476807-53478567	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:53474425-53474625	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr8:53408672-53409049	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:53408740-53408939	K562	blood:	n/a	n/a
7	BHLHE40	chr8:53408743-53409081	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:53490163-53490169	K562	blood:	n/a	n/a
9	CBX3	chr8:53459232-53459585	K562	blood:	n/a	n/a
10	CCNT2	chr8:53436081-53436281	K562	blood:	n/a	n/a
11	CEBPB	chr8:53408624-53409176	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr8:53482192-53482440	A549	lung:	n/a	chr8:53482355-53482366
13	CEBPB	chr8:53473666-53473994	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:53409023-53409724	HepG2	liver:	n/a	chr8:53409580-53409589
15	CEBPB	chr8:53484150-53484340	HepG2	liver:	n/a	chr8:53484205-53484216
16	CEBPB	chr8:53482232-53482516	HepG2	liver:	n/a	chr8:53482355-53482366
17	CEBPB	chr8:53473588-53474038	A549	lung:	n/a	n/a
18	CEBPB	chr8:53409458-53409730	Hela-S3	cervix:	n/a	chr8:53409580-53409589
19	CEBPB	chr8:53475278-53475403	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:53473671-53473965	K562	blood:	n/a	n/a
21	CEBPB	chr8:53473626-53474007	IMR90	lung:	n/a	n/a
22	CEBPB	chr8:53473661-53473959	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:53475202-53475451	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:53473645-53474169	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:53473675-53474000	A549	lung:	n/a	n/a
26	CHD1	chr8:53478215-53478807	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr8:53490413-53490437	GM12878	blood:	n/a	n/a
28	CHD1	chr8:53474867-53474966	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr8:53476833-53478582	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:53415860-53416010	GM12870	blood:	n/a	chr8:53415943-53415961 chr8:53415944-53415960
31	CTCF	chr8:53490378-53490547	GM13976	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
32	CTCF	chr8:53415860-53416010	GM12867	blood:	n/a	chr8:53415943-53415961 chr8:53415944-53415960
33	CTCF	chr8:53436240-53436390	A549	lung:	n/a	n/a
34	CTCF	chr8:53436000-53436150	NHLF	lung:	n/a	n/a
35	CTCF	chr8:53409146-53409150	ProgFib	skin:	n/a	n/a
36	CTCF	chr8:53490139-53490175	A549	lung:	n/a	n/a
37	CTCF	chr8:53490360-53490510	GM06990	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
38	CTCF	chr8:53415840-53415990	GM12864	blood:	n/a	chr8:53415943-53415961 chr8:53415944-53415960
39	CTCF	chr8:53490060-53490210	GM06990	blood:	n/a	n/a
40	CTCF	chr8:53408820-53408970	GM12878	blood:	n/a	chr8:53408901-53408911 chr8:53408900-53408913 chr8:53408893-53408914 chr8:53408900-53408913 chr8:53408898-53408916 chr8:53408899-53408915
41	CTCF	chr8:53408698-53409198	K562	blood:	n/a	chr8:53408901-53408911 chr8:53408900-53408913 chr8:53408893-53408914 chr8:53408900-53408913 chr8:53408898-53408916 chr8:53408899-53408915
42	CTCF	chr8:53490337-53490590	K562	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
43	CTCF	chr8:53415876-53416010	HUVEC	blood vessel:	n/a	chr8:53415943-53415961 chr8:53415944-53415960
44	CTCF	chr8:53415540-53415690	HCT-116	colon:	n/a	n/a
45	CTCF	chr8:53490357-53490577	Pancreas_OC	pancreas:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
46	CTCF	chr8:53408420-53408570	HMEC	breast:	n/a	n/a
47	CTCF	chr8:53490360-53490510	K562	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
48	CTCF	chr8:53432285-53432320	GM10248	blood:	n/a	n/a
49	CTCF	chr8:53409180-53409330	GM12871	blood:	n/a	n/a
50	CTCF	chr8:53412660-53412810	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53478053-53478103	PFSK-1	brain:	n/a
2	chr8:53478053-53478103	PFSK-1	brain:	n/a
3	chr8:53485704-53485754	GM12891	blood:	n/a
4	chr8:53477218-53477268	HRPEpiC	eye:	n/a
5	chr8:53477881-53477931	CMK	blood:	n/a
6	chr8:53485670-53485720	AG09309	skin:	n/a
7	chr8:53452398-53452448	AoSMC	blood vessel:	n/a
8	chr8:53452398-53452448	GM06990	blood:	n/a
9	chr8:53452398-53452448	A549	lung:	n/a
10	chr8:53450729-53450779	ovcar-3	ovarian:	n/a
11	chr8:53478102-53478152	SKMC	muscle:	n/a
12	chr8:53478454-53478504	HPAEpiC	pulmonary alveolar:	n/a
13	chr8:53490251-53490301	HRCEpiC	kidney:	n/a
14	chr8:53477264-53477314	HEK293	kidney:	embryo
15	chr8:53478706-53478756	HUVEC	blood vessel:	n/a
16	chr8:53477264-53477314	U87	brain:	n/a
17	chr8:53477881-53477931	MCF10A-Er-Src	breast:	n/a
18	chr8:53476865-53476915	AG04450	lung:	fetal
19	chr8:53477218-53477268	PANC-1	pancreas:	n/a
20	chr8:53476865-53476915	HIPEpiC	eye:	n/a
21	chr8:53485670-53485720	SK-N-SH_RA	brain:	n/a
22	chr8:53478102-53478152	BE2_C	brain:	n/a
23	chr8:53478624-53478674	NT2-D1	testis:	n/a
24	chr8:53474887-53474937	HCT-116	colon:	n/a
25	chr8:53478454-53478504	HCPEpiC	choroid plexus:	n/a
26	chr8:53477264-53477314	HCF	heart:	n/a
27	chr8:53478454-53478504	HEEpiC	esophagus:	n/a
28	chr8:53478454-53478504	HRPEpiC	eye:	n/a
29	chr8:53485704-53485754	K562	blood:	n/a
30	chr8:53477218-53477268	SK-N-SH	brain:	n/a
31	chr8:53478624-53478674	HMEC	breast:	n/a
32	chr8:53476943-53476993	AG04450	lung:	fetal
33	chr8:53471884-53471934	U87	brain:	n/a
34	chr8:53478624-53478674	ECC-1	luminal epithelium:	n/a
35	chr8:53477881-53477931	MCF-7	breast:	n/a
36	chr8:53478706-53478756	AG04450	lung:	fetal
37	chr8:53456003-53456053	U87	brain:	n/a
38	chr8:53478706-53478756	SKMC	muscle:	n/a
39	chr8:53476865-53476915	ovcar-3	ovarian:	n/a
40	chr8:53477881-53477931	HRE	kidney:	n/a
41	chr8:53478454-53478504	NHDF-neo	bronchial:	n/a
42	chr8:53485704-53485754	HCF	heart:	n/a
43	chr8:53474030-53474080	AG09319	gingival:	n/a
44	chr8:53456003-53456053	AG04449	skin:	fetal
45	chr8:53477545-53477595	NT2-D1	testis:	n/a
46	chr8:53452398-53452448	GM12891	blood:	n/a
47	chr8:53478074-53478124	HUVEC	blood vessel:	n/a
48	chr8:53478053-53478103	Caco-2	colon:	n/a
49	chr8:53477218-53477268	A549	lung:	n/a
50	chr8:53485670-53485720	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:53408834..53411625-chr8:53415197..53417909,2	MCF-7	breast:
2	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
3	chr8:53490108..53490739-chr8:53649694..53650429,2	MCF-7	breast:
4	chr8:53024718..53025840-chr8:53408415..53409142,5	K562	blood:
5	chr8:53408834..53411625-chr8:53415197..53417909,2	MCF-7	breast:
6	chr8:53396327..53397778-chr8:53408319..53409731,6	MCF-7	breast:
7	chr8:53333125..53334025-chr8:53408456..53409345,8	MCF-7	breast:
8	chr8:53333238..53334019-chr8:53408621..53409292,5	MCF-7	breast:
9	chr8:53333510..53334034-chr8:53408804..53409370,2	K562	blood:

Variant related genes	Relation type
FAM150A	TF binding region
FAM150A	CpG island

Extended variants
information (count: 1962 )
Associated
traits (count: 92 )

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	rs11776276	chr8:53408434-53408435	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs12680116	chr8:53408441-53408442	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs372471632	chr8:53408486-53408487	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs113172896	chr8:53408490-53408491	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs537292559	chr8:53408513-53408514	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs576967369	chr8:53408535-53408536	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs180848143	chr8:53408550-53408551	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs200285847	chr8:53408660-53408661	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs557121715	chr8:53408716-53408717	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs375125116	chr8:53408745-53408746	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs148384251	chr8:53408780-53408781	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs562457148	chr8:53408810-53408811	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs574356637	chr8:53408870-53408871	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs375283575	chr8:53408885-53408886	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs561246094	chr8:53408886-53408887	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs528803044	chr8:53408916-53408917	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs546900805	chr8:53408941-53408942	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs375683358	chr8:53408947-53408948	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs565091087	chr8:53408965-53408966	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs535488517	chr8:53408974-53408975	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs532619446	chr8:53409001-53409002	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs142084924	chr8:53409010-53409011	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs7844059	chr8:53409057-53409058	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs28668576	chr8:53409082-53409083	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs151218866	chr8:53409097-53409098	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs567047867	chr8:53409118-53409119	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs555128025	chr8:53409168-53409169	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs535599891	chr8:53409174-53409175	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs111661607	chr8:53409229-53409230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112163446	chr8:53409280-53409281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140411205	chr8:53409312-53409313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184278444	chr8:53409360-53409361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576933211	chr8:53409375-53409376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537677233	chr8:53409498-53409499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189675136	chr8:53409501-53409502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574492176	chr8:53409508-53409509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1595951	chr8:53411612-53411613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551356449	chr8:53411637-53411638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537082658	chr8:53411659-53411660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192286664	chr8:53411670-53411671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376885649	chr8:53411671-53411672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs57914370	chr8:53411687-53411688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575256209	chr8:53411688-53411689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536045061	chr8:53411705-53411706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184177762	chr8:53411717-53411718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569143052	chr8:53411723-53411724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572682881	chr8:53411768-53411769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545955941	chr8:53411776-53411777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187789593	chr8:53411781-53411782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193218435	chr8:53411798-53411799	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53408200-53408600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:53408200-53408600	Bivalent Enhancer	HepG2	liver
3	chr8:53408400-53408600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
4	chr8:53408400-53408600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
5	chr8:53408400-53408600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr8:53408400-53408600	Bivalent Enhancer	Lung	lung
7	chr8:53408400-53408800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
8	chr8:53408400-53408800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
9	chr8:53408400-53408800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
10	chr8:53408400-53408800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
11	chr8:53408400-53408800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
12	chr8:53408400-53408800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
13	chr8:53408400-53408800	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr8:53408400-53408800	Enhancers	Brain Angular Gyrus	brain
15	chr8:53408400-53408800	Flanking Active TSS	Brain Anterior Caudate	brain
16	chr8:53408400-53408800	Flanking Active TSS	Brain Substantia Nigra	brain
17	chr8:53408400-53408800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
18	chr8:53408400-53408800	Enhancers	HMEC	breast
19	chr8:53408400-53409000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
20	chr8:53408400-53409000	Active TSS	Brain Hippocampus Middle	brain
21	chr8:53408400-53409000	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr8:53408400-53409000	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr8:53408400-53409200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:53408400-53409200	Enhancers	Hela-S3	cervix
25	chr8:53408600-53408800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr8:53408600-53408800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:53408600-53408800	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr8:53408600-53408800	Bivalent/Poised TSS	Primary B cells from cord blood	blood
29	chr8:53408600-53408800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
30	chr8:53408600-53408800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr8:53408600-53408800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:53408600-53408800	Bivalent Enhancer	Liver	Liver
33	chr8:53408600-53408800	Enhancers	Colon Smooth Muscle	Colon
34	chr8:53408600-53408800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
35	chr8:53408600-53408800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr8:53408600-53408800	Bivalent/Poised TSS	Fetal Brain Male	brain
37	chr8:53408600-53408800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
38	chr8:53408600-53408800	Enhancers	Rectal Smooth Muscle	rectum
39	chr8:53408600-53408800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
40	chr8:53408600-53408800	Bivalent Enhancer	Stomach Mucosa	stomach
41	chr8:53408600-53408800	Bivalent/Poised TSS	A549	lung
42	chr8:53408600-53408800	Bivalent Enhancer	Dnd41	blood
43	chr8:53408600-53408800	Flanking Bivalent TSS/Enh	HepG2	liver
44	chr8:53408600-53408800	Enhancers	NH-A	brain
45	chr8:53408600-53409000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:53408600-53409000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
47	chr8:53408600-53409000	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
48	chr8:53408600-53409000	Enhancers	NHEK	skin
49	chr8:53408600-53409200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:53408800-53409000	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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