Variant report

Variant	nsv831287
Chromosome Location	chr8:36430788-36605374
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	ATF1	chr8:36459712-36459951	K562	blood:	n/a	n/a
2	BACH1	chr8:36431428-36431693	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:36431421-36431659	K562	blood:	n/a	n/a
4	BATF	chr8:36523177-36523383	GM12878	blood:	n/a	chr8:36523276-36523287
5	CBX3	chr8:36431374-36431727	K562	blood:	n/a	n/a
6	CBX3	chr8:36431412-36431638	K562	blood:	n/a	n/a
7	CEBPB	chr8:36431351-36431722	MCF-7	breast:	n/a	n/a
8	CEBPB	chr8:36431405-36431681	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:36559225-36559414	HepG2	liver:	n/a	chr8:36559317-36559334 chr8:36559320-36559333 chr8:36559320-36559331
10	CEBPB	chr8:36433802-36433995	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:36431373-36431719	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr8:36447073-36447285	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:36431375-36431729	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr8:36573842-36574075	A549	lung:	n/a	n/a
15	CEBPB	chr8:36431426-36431638	A549	lung:	n/a	n/a
16	CEBPB	chr8:36431399-36431727	K562	blood:	n/a	n/a
17	CEBPB	chr8:36573870-36573979	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr8:36583575-36583811	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:36596325-36596345	GM13976	blood:	n/a	n/a
20	CTCF	chr8:36485579-36485763	K562	blood:	n/a	n/a
21	CTCF	chr8:36583980-36584130	GM12875	blood:	n/a	n/a
22	CTCF	chr8:36521540-36521690	NB4	blood:	n/a	n/a
23	CTCF	chr8:36504440-36504466	LNCaP	prostate:	n/a	n/a
24	CTCF	chr8:36471680-36471830	GM12867	blood:	n/a	n/a
25	CTCF	chr8:36480800-36480950	GM12871	blood:	n/a	n/a
26	CTCF	chr8:36436409-36436435	Lung_OC	lung:	n/a	n/a
27	CTCF	chr8:36554340-36554490	HRE	kidney:	n/a	n/a
28	CTCF	chr8:36593544-36593620	GM13977	blood:	n/a	n/a
29	E2F4	chr8:36438659-36438690	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr8:36533459-36533603	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr8:36517505-36517583	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr8:36433762-36434074	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr8:36461256-36461383	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr8:36441190-36441374	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr8:36450708-36450857	MCF10A-Er-Src	breast:	n/a	n/a
36	EP300	chr8:36583531-36583860	H1-hESC	embryonic stem cell:	n/a	n/a
37	EP300	chr8:36433563-36434173	ECC-1	luminal epithelium:	n/a	n/a
38	EP300	chr8:36523189-36523402	GM12878	blood:	n/a	n/a
39	EP300	chr8:36523169-36523371	GM12878	blood:	n/a	n/a
40	FOS	chr8:36431213-36431741	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr8:36549017-36549304	MCF10A-Er-Src	breast:	n/a	chr8:36549143-36549153 chr8:36549143-36549153 chr8:36549143-36549153
42	FOS	chr8:36514919-36515053	MCF10A-Er-Src	breast:	n/a	chr8:36514972-36514982 chr8:36514974-36514981 chr8:36514972-36514982 chr8:36514973-36514981 chr8:36514973-36514981 chr8:36514972-36514982 chr8:36514972-36514982
43	FOS	chr8:36433642-36434180	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr8:36461581-36461742	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr8:36431244-36431741	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr8:36430856-36430992	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:36433630-36434169	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr8:36514919-36515124	MCF10A-Er-Src	breast:	n/a	chr8:36514972-36514982 chr8:36514974-36514981 chr8:36514972-36514982 chr8:36514973-36514981 chr8:36514973-36514981 chr8:36515068-36515077 chr8:36514972-36514982 chr8:36514972-36514982
49	FOS	chr8:36433631-36434116	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:36514915-36515036	MCF10A-Er-Src	breast:	n/a	chr8:36514972-36514982 chr8:36514974-36514981 chr8:36514972-36514982 chr8:36514973-36514981 chr8:36514973-36514981 chr8:36514972-36514982 chr8:36514972-36514982

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:36602729-36602779	HCT-116	colon:	n/a
2	chr8:36602729-36602779	PANC-1	pancreas:	n/a
3	chr8:36602729-36602779	BJ	skin:	n/a
4	chr8:36602729-36602779	K562	blood:	n/a
5	chr8:36602729-36602779	Caco-2	colon:	n/a
6	chr8:36602729-36602779	AG10803	skin:	n/a
7	chr8:36602729-36602779	NB4	blood:	n/a
8	chr8:36602729-36602779	NHDF-neo	bronchial:	n/a
9	chr8:36602729-36602779	HCPEpiC	choroid plexus:	n/a
10	chr8:36602729-36602779	HAEpiC	amniotic membrane:	n/a
11	chr8:36602729-36602779	HRE	kidney:	n/a
12	chr8:36602729-36602779	HIPEpiC	eye:	n/a
13	chr8:36602729-36602779	LNCaP	prostate:	n/a
14	chr8:36602729-36602779	HL-60	blood:	n/a
15	chr8:36602729-36602779	HMEC	breast:	n/a
16	chr8:36602729-36602779	Hela-S3	cervix:	n/a
17	chr8:36602729-36602779	AG09319	gingival:	n/a
18	chr8:36602729-36602779	IMR90	lung:	fetal
19	chr8:36602729-36602779	AG09309	skin:	n/a
20	chr8:36602729-36602779	HNPCEpiC	eye:	n/a
21	chr8:36602729-36602779	HEEpiC	esophagus:	n/a
22	chr8:36602729-36602779	H1-hESC	embryonic stem cell:	embryo
23	chr8:36602729-36602779	AG04450	lung:	fetal
24	chr8:36602729-36602779	NH-A	brain:	n/a
25	chr8:36602729-36602779	U87	brain:	n/a
26	chr8:36602729-36602779	AG04449	skin:	fetal
27	chr8:36602729-36602779	PFSK-1	brain:	n/a
28	chr8:36602729-36602779	GM12891	blood:	n/a
29	chr8:36602729-36602779	MCF-7	breast:	n/a
30	chr8:36602729-36602779	PrEC	prostate:	n/a
31	chr8:36602729-36602779	HRPEpiC	eye:	n/a
32	chr8:36602729-36602779	ECC-1	luminal epithelium:	n/a
33	chr8:36602729-36602779	Jurkat	blood:	n/a
34	chr8:36602729-36602779	HRCEpiC	kidney:	n/a
35	chr8:36602729-36602779	NT2-D1	testis:	n/a
36	chr8:36602729-36602779	CMK	blood:	n/a
37	chr8:36602729-36602779	SK-N-SH	brain:	n/a
38	chr8:36602729-36602779	ProgFib	skin:	n/a
39	chr8:36602729-36602779	SK-N-MC	brain:	n/a
40	chr8:36602729-36602779	SK-N-SH_RA	brain:	n/a
41	chr8:36602729-36602779	Hepatocyte	liver:	n/a
42	chr8:36602729-36602779	HUVEC	blood vessel:	n/a
43	chr8:36602729-36602779	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:36602729-36602779	GM19239	blood:	n/a
45	chr8:36602729-36602779	HEK293	kidney:	embryo
46	chr8:36602729-36602779	GM12892	blood:	n/a
47	chr8:36602729-36602779	T-47D	breast:	n/a
48	chr8:36602729-36602779	AoSMC	blood vessel:	n/a
49	chr8:36602729-36602779	HepG2	liver:	n/a
50	chr8:36602729-36602779	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:36532784..36534570-chr8:36538161..36540032,3	K562	blood:
2	chr8:36532784..36534474-chr8:36538409..36540032,2	K562	blood:
3	chr8:36532784..36534474-chr8:36538409..36540032,2	K562	blood:
4	chr8:36532784..36534570-chr8:36538161..36540032,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-419C23.1.1-7	chr8:36438698-36439109	NONHSAT126019
2	lnc-RP11-419C23.1.1-3	chr8:36559339-36559411	ENSG00000253363.1

Variant related genes	Relation type
RPL23P10	TF binding region
RPL23P10	CpG island

Extended variants
information (count: 2568 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:2568 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116120497	chr8:36430889-36430890	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs568989805	chr8:36430890-36430891	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs570099642	chr8:36430931-36430932	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs566894238	chr8:36430939-36430940	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs534415031	chr8:36430944-36430945	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs77062343	chr8:36430951-36430952	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs375135339	chr8:36430959-36430960	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs73601438	chr8:36430998-36430999	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs138461937	chr8:36431014-36431015	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs116019850	chr8:36431034-36431035	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs553205056	chr8:36431074-36431075	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs368561811	chr8:36431092-36431093	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs575055131	chr8:36431100-36431101	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs149634527	chr8:36431102-36431103	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs144408774	chr8:36431106-36431107	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs574259584	chr8:36431108-36431109	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs199635548	chr8:36431117-36431118	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs558193736	chr8:36431136-36431137	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs531165919	chr8:36431157-36431158	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs115979662	chr8:36431186-36431187	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs564207051	chr8:36431189-36431190	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs186446746	chr8:36431242-36431243	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs190920285	chr8:36431300-36431301	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs568315249	chr8:36431302-36431303	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs73601439	chr8:36431306-36431307	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550885156	chr8:36431335-36431336	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs544704333	chr8:36431343-36431344	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs568936572	chr8:36431390-36431391	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562089329	chr8:36431396-36431397	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs148714722	chr8:36431399-36431400	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs574038607	chr8:36431400-36431401	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs141438541	chr8:36431427-36431428	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78213061	chr8:36431428-36431429	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147470482	chr8:36431446-36431447	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183082208	chr8:36431465-36431466	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377167094	chr8:36431489-36431490	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574813464	chr8:36431527-36431528	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542139340	chr8:36431530-36431531	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557685139	chr8:36431538-36431539	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575737382	chr8:36431568-36431569	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78142032	chr8:36431619-36431620	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541547135	chr8:36431620-36431621	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs76183482	chr8:36431719-36431720	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs75144840	chr8:36431725-36431726	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs186909727	chr8:36431772-36431773	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs79650996	chr8:36431806-36431807	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528910186	chr8:36431812-36431813	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs13255381	chr8:36431827-36431828	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs13255390	chr8:36431831-36431832	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs191752831	chr8:36431852-36431853	ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	19651600	CNVD
abnormal development	18461090	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	16620391	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Rhabdomyosarcoma	16790082	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36426400-36431200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:36427000-36430800	Weak transcription	NHEK	skin
3	chr8:36428200-36430800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:36428400-36431200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:36428400-36431400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr8:36429800-36431200	Weak transcription	Adipose Nuclei	Adipose
7	chr8:36430600-36432000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
8	chr8:36430600-36432200	Enhancers	HMEC	breast
9	chr8:36430600-36433800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:36430800-36431200	Enhancers	NHEK	skin
11	chr8:36430800-36434600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:36431200-36431400	Flanking Active TSS	NHEK	skin
13	chr8:36431200-36431800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:36431200-36432000	ZNF genes & repeats	Adipose Nuclei	Adipose
15	chr8:36431200-36432400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
16	chr8:36431400-36431600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr8:36431400-36431600	Enhancers	NHEK	skin
18	chr8:36431600-36432000	Flanking Active TSS	NHEK	skin
19	chr8:36432000-36432200	Enhancers	NHEK	skin
20	chr8:36432200-36432600	ZNF genes & repeats	NHEK	skin
21	chr8:36432400-36440800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr8:36432600-36434600	Enhancers	NHEK	skin
23	chr8:36432600-36434800	Enhancers	Fetal Muscle Leg	muscle
24	chr8:36432800-36433400	Weak transcription	HMEC	breast
25	chr8:36433200-36434000	Enhancers	Fetal Muscle Trunk	muscle
26	chr8:36433400-36433800	Enhancers	Esophagus	oesophagus
27	chr8:36433400-36434400	Enhancers	HMEC	breast
28	chr8:36437200-36437800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:36437200-36438000	Enhancers	Fetal Heart	heart
30	chr8:36438000-36438800	Weak transcription	Fetal Heart	heart
31	chr8:36438800-36439000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:36438800-36439000	Enhancers	Fetal Heart	heart
33	chr8:36439000-36440200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:36439000-36440800	Weak transcription	Fetal Heart	heart
35	chr8:36440000-36440800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:36440000-36442000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr8:36440200-36440600	Enhancers	NHEK	skin
38	chr8:36440200-36441000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:36440200-36441000	Enhancers	Fetal Brain Female	brain
40	chr8:36440200-36441400	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr8:36440200-36442200	Enhancers	Adipose Nuclei	Adipose
42	chr8:36440800-36441000	Enhancers	Fetal Heart	heart
43	chr8:36440800-36441200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr8:36440800-36441200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:36441400-36446000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr8:36442000-36445800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:36445200-36445800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr8:36445800-36446600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr8:36446000-36446800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr8:36457000-36457600	Enhancers	Small Intestine	intestine

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