Variant report

Variant	nsv1016306
Chromosome Location	chr8:36423652-36480301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

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	chr8:36431421-36431659	K562	blood:	n/a	n/a
3	BACH1	chr8:36431428-36431693	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr8:36431412-36431638	K562	blood:	n/a	n/a
5	CBX3	chr8:36431374-36431727	K562	blood:	n/a	n/a
6	CEBPB	chr8:36431399-36431727	K562	blood:	n/a	n/a
7	CEBPB	chr8:36431426-36431638	A549	lung:	n/a	n/a
8	CEBPB	chr8:36431405-36431681	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:36431375-36431729	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr8:36431373-36431719	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:36447073-36447285	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:36431351-36431722	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:36433802-36433995	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr8:36436409-36436435	Lung_OC	lung:	n/a	n/a
15	CTCF	chr8:36429600-36429750	NHEK	skin:	n/a	n/a
16	CTCF	chr8:36471680-36471830	GM12867	blood:	n/a	n/a
17	E2F4	chr8:36438659-36438690	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr8:36450708-36450857	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr8:36441190-36441374	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr8:36461256-36461383	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr8:36433762-36434074	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr8:36433563-36434173	ECC-1	luminal epithelium:	n/a	n/a
23	FOS	chr8:36433719-36434134	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr8:36426319-36426696	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
25	FOS	chr8:36433630-36434169	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:36433631-36434116	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr8:36426309-36426767	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
28	FOS	chr8:36431244-36431741	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr8:36426300-36426700	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
30	FOS	chr8:36430856-36430992	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:36431238-36431768	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr8:36431249-36431741	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:36426300-36426726	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
34	FOS	chr8:36431213-36431741	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:36433642-36434180	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:36461581-36461742	MCF10A-Er-Src	breast:	n/a	n/a
37	GATA3	chr8:36442439-36442556	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr8:36446198-36446388	SH-SY5Y	brain:	n/a	n/a
39	GTF2F1	chr8:36448848-36448853	K562	blood:	n/a	n/a
40	JUND	chr8:36447059-36447286	HepG2	liver:	n/a	n/a
41	JUND	chr8:36431458-36431720	HepG2	liver:	n/a	chr8:36431573-36431584
42	KAP1	chr8:36431201-36431893	HEK293	kidney:	n/a	n/a
43	KAP1	chr8:36431419-36431699	K562	blood:	n/a	n/a
44	KAP1	chr8:36433757-36434367	U2OS	brain:	n/a	n/a
45	KAP1	chr8:36433702-36434346	HEK293	kidney:	n/a	n/a
46	KAP1	chr8:36431279-36431752	U2OS	brain:	n/a	n/a
47	KAP1	chr8:36426449-36426650	U2OS	brain:	n/a	n/a
48	MAFF	chr8:36437794-36437900	K562	blood:	n/a	chr8:36437802-36437820
49	MAFF	chr8:36463785-36463982	HepG2	liver:	n/a	n/a
50	MAFF	chr8:36431428-36431740	K562	blood:	n/a	chr8:36431566-36431584

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:36427309-36427359	ProgFib	skin:	n/a
2	chr8:36427309-36427359	GM12878	blood:	n/a
3	chr8:36427309-36427359	HRCEpiC	kidney:	n/a
4	chr8:36427309-36427359	HIPEpiC	eye:	n/a
5	chr8:36427309-36427359	NHBE	bronchial:	n/a
6	chr8:36427309-36427359	HCPEpiC	choroid plexus:	n/a
7	chr8:36427309-36427359	HCM	heart:	n/a
8	chr8:36427309-36427359	MCF-7	breast:	n/a
9	chr8:36427309-36427359	AoSMC	blood vessel:	n/a
10	chr8:36427309-36427359	HCF	heart:	n/a
11	chr8:36427309-36427359	AG04450	lung:	fetal
12	chr8:36427309-36427359	AG10803	skin:	n/a
13	chr8:36427309-36427359	PFSK-1	brain:	n/a
14	chr8:36427309-36427359	HepG2	liver:	n/a
15	chr8:36427309-36427359	RPTEC	kidney:	n/a
16	chr8:36427309-36427359	H1-hESC	embryonic stem cell:	embryo
17	chr8:36427309-36427359	GM06990	blood:	n/a
18	chr8:36427309-36427359	HMEC	breast:	n/a
19	chr8:36427309-36427359	PrEC	prostate:	n/a
20	chr8:36427309-36427359	MCF10A-Er-Src	breast:	n/a
21	chr8:36427309-36427359	GM12891	blood:	n/a
22	chr8:36427309-36427359	HEK293	kidney:	embryo
23	chr8:36427309-36427359	Caco-2	colon:	n/a
24	chr8:36427309-36427359	SK-N-SH_RA	brain:	n/a
25	chr8:36427309-36427359	LNCaP	prostate:	n/a
26	chr8:36427309-36427359	BJ	skin:	n/a
27	chr8:36427309-36427359	HL-60	blood:	n/a
28	chr8:36427309-36427359	GM19239	blood:	n/a
29	chr8:36427309-36427359	HNPCEpiC	eye:	n/a
30	chr8:36427309-36427359	HEEpiC	esophagus:	n/a
31	chr8:36427309-36427359	SK-N-MC	brain:	n/a
32	chr8:36427309-36427359	NT2-D1	testis:	n/a
33	chr8:36427309-36427359	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:36427309-36427359	GM12892	blood:	n/a
35	chr8:36427309-36427359	AG09319	gingival:	n/a
36	chr8:36427309-36427359	SKMC	muscle:	n/a
37	chr8:36427309-36427359	Hepatocyte	liver:	n/a
38	chr8:36427309-36427359	HRPEpiC	eye:	n/a
39	chr8:36427309-36427359	ECC-1	luminal epithelium:	n/a
40	chr8:36427309-36427359	U87	brain:	n/a
41	chr8:36427309-36427359	AG04449	skin:	fetal
42	chr8:36427309-36427359	T-47D	breast:	n/a
43	chr8:36427309-36427359	Jurkat	blood:	n/a
44	chr8:36427309-36427359	A549	lung:	n/a
45	chr8:36427309-36427359	ovcar-3	ovarian:	n/a
46	chr8:36427309-36427359	NH-A	brain:	n/a
47	chr8:36427309-36427359	HRE	kidney:	n/a
48	chr8:36427309-36427359	IMR90	lung:	fetal
49	chr8:36427309-36427359	NHDF-neo	bronchial:	n/a
50	chr8:36427309-36427359	K562	blood:	n/a

No data

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

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

No data

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

Extended variants
information (count: 994 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534369684	chr8:36423665-36423666	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553292058	chr8:36423684-36423685	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs16885223	chr8:36423707-36423708	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs34645897	chr8:36423752-36423753	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140207781	chr8:36423786-36423787	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76462159	chr8:36423800-36423801	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141368431	chr8:36423826-36423827	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576425139	chr8:36423871-36423872	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543883268	chr8:36423872-36423873	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565261661	chr8:36423915-36423916	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147006886	chr8:36423922-36423923	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372780502	chr8:36423964-36423965	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541036746	chr8:36424010-36424011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554064669	chr8:36424013-36424014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73601422	chr8:36424035-36424036	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs530348844	chr8:36424071-36424072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548341594	chr8:36424086-36424087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147653033	chr8:36424117-36424118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377485308	chr8:36424120-36424121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529395587	chr8:36424136-36424137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545814015	chr8:36424174-36424175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564238348	chr8:36424204-36424205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531042922	chr8:36424241-36424242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576042976	chr8:36424267-36424268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184307132	chr8:36424291-36424292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543473753	chr8:36424340-36424341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570496220	chr8:36424344-36424345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534567420	chr8:36424351-36424352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187015922	chr8:36424384-36424385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568331002	chr8:36424411-36424412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535761543	chr8:36424414-36424415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192718835	chr8:36424484-36424485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575373142	chr8:36424496-36424497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368836851	chr8:36424519-36424520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141912063	chr8:36424524-36424525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184194341	chr8:36424543-36424544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566043051	chr8:36424593-36424594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577271867	chr8:36424605-36424606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150089856	chr8:36424606-36424607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559337937	chr8:36424613-36424614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574529527	chr8:36424630-36424631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138428746	chr8:36424644-36424645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149266129	chr8:36424755-36424756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531126290	chr8:36424768-36424769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552503052	chr8:36424823-36424824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143517282	chr8:36424832-36424833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530186938	chr8:36424833-36424834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138960351	chr8:36424855-36424856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6468369	chr8:36424909-36424910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374885947	chr8:36424928-36424929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36419400-36424000	Weak transcription	Fetal Muscle Leg	muscle
2	chr8:36423400-36424000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr8:36423600-36423800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:36423600-36424200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:36423600-36424200	Enhancers	Placenta Amnion	Placenta Amnion
6	chr8:36423800-36424000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:36424000-36424400	Enhancers	Fetal Heart	heart
8	chr8:36424000-36424400	Enhancers	Fetal Muscle Leg	muscle
9	chr8:36424000-36426000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr8:36424200-36425600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:36424400-36424600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:36424400-36425600	Weak transcription	Fetal Heart	heart
13	chr8:36424400-36425600	Weak transcription	Fetal Muscle Leg	muscle
14	chr8:36425000-36425200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:36425200-36426200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:36425400-36426000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:36425600-36426600	Enhancers	Fetal Heart	heart
18	chr8:36425600-36427600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr8:36425600-36428200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr8:36425600-36429600	Enhancers	Brain Germinal Matrix	brain
21	chr8:36425600-36429800	Enhancers	Fetal Muscle Leg	muscle
22	chr8:36425800-36426400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:36426000-36426400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:36426000-36426800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr8:36426000-36427000	Enhancers	Fetal Brain Female	brain
26	chr8:36426000-36427600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:36426000-36427800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr8:36426000-36427800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr8:36426000-36428000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:36426000-36428200	Enhancers	Fetal Kidney	kidney
31	chr8:36426000-36429400	Enhancers	Fetal Brain Male	brain
32	chr8:36426200-36427400	Enhancers	Duodenum Mucosa	Duodenum
33	chr8:36426200-36428200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr8:36426200-36428200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr8:36426200-36428200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:36426400-36426800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr8:36426400-36426800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:36426400-36427000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:36426400-36427000	Enhancers	HMEC	breast
40	chr8:36426400-36428200	Enhancers	H9 Cell Line	embryonic stem cell
41	chr8:36426400-36428200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr8:36426400-36428200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:36426400-36428400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:36426400-36429600	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr8:36426400-36431200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr8:36426600-36427000	Enhancers	NHEK	skin
47	chr8:36426600-36427800	Weak transcription	Fetal Heart	heart
48	chr8:36426600-36428800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr8:36426800-36427400	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr8:36426800-36428200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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