Variant report

Variant	nsv6155
Chromosome Location	chr8:36407646-36452741
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	chr8:36417098-36417187	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	CBX3	chr8:36431374-36431727	K562	blood:	n/a	n/a
5	CBX3	chr8:36431412-36431638	K562	blood:	n/a	n/a
6	CEBPB	chr8:36447073-36447285	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:36431351-36431722	MCF-7	breast:	n/a	n/a
8	CEBPB	chr8:36433802-36433995	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:36431405-36431681	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr8:36431426-36431638	A549	lung:	n/a	n/a
11	CEBPB	chr8:36431375-36431729	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr8:36431373-36431719	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:36431399-36431727	K562	blood:	n/a	n/a
14	CEBPD	chr8:36416869-36417294	K562	blood:	n/a	n/a
15	CHD2	chr8:36408477-36408479	GM12878	blood:	n/a	n/a
16	CTCF	chr8:36436409-36436435	Lung_OC	lung:	n/a	n/a
17	CTCF	chr8:36429600-36429750	NHEK	skin:	n/a	n/a
18	E2F4	chr8:36450708-36450857	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr8:36438659-36438690	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr8:36441190-36441374	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr8:36433762-36434074	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr8:36416836-36417253	K562	blood:	n/a	chr8:36416853-36416867
23	EP300	chr8:36433563-36434173	ECC-1	luminal epithelium:	n/a	n/a
24	FOS	chr8:36426309-36426767	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
25	FOS	chr8:36433719-36434134	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:36426300-36426726	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
27	FOS	chr8:36408238-36408538	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr8:36408343-36408721	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr8:36430856-36430992	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr8:36431249-36431741	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:36426319-36426696	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
32	FOS	chr8:36433631-36434116	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:36408367-36408533	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:36408315-36408604	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:36433630-36434169	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:36431213-36431741	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr8:36431238-36431768	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr8:36431244-36431741	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:36433642-36434180	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:36426300-36426700	MCF10A-Er-Src	breast:	n/a	chr8:36426506-36426513 chr8:36426505-36426513 chr8:36426505-36426513
41	GATA2	chr8:36416848-36417179	K562	blood:	n/a	chr8:36417110-36417117 chr8:36417108-36417120 chr8:36417107-36417117 chr8:36417109-36417119 chr8:36416867-36416878 chr8:36417110-36417119
42	GATA3	chr8:36423190-36423469	SH-SY5Y	brain:	n/a	chr8:36423278-36423285 chr8:36423271-36423292 chr8:36423274-36423290 chr8:36423278-36423285 chr8:36423278-36423285
43	GATA3	chr8:36418842-36419382	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr8:36446198-36446388	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr8:36442439-36442556	SH-SY5Y	brain:	n/a	n/a
46	GTF2F1	chr8:36448848-36448853	K562	blood:	n/a	n/a
47	JUND	chr8:36431458-36431720	HepG2	liver:	n/a	chr8:36431573-36431584
48	JUND	chr8:36408258-36408513	HepG2	liver:	n/a	chr8:36408336-36408347
49	JUND	chr8:36416947-36417098	K562	blood:	n/a	n/a
50	JUND	chr8:36447059-36447286	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:36427309-36427359	AG04450	lung:	fetal
2	chr8:36427309-36427359	HCF	heart:	n/a
3	chr8:36427309-36427359	ECC-1	luminal epithelium:	n/a
4	chr8:36427309-36427359	HRE	kidney:	n/a
5	chr8:36427309-36427359	HUVEC	blood vessel:	n/a
6	chr8:36427309-36427359	GM06990	blood:	n/a
7	chr8:36427309-36427359	Caco-2	colon:	n/a
8	chr8:36427309-36427359	HEEpiC	esophagus:	n/a
9	chr8:36427309-36427359	A549	lung:	n/a
10	chr8:36427309-36427359	HEK293	kidney:	embryo
11	chr8:36427309-36427359	CMK	blood:	n/a
12	chr8:36427309-36427359	NHBE	bronchial:	n/a
13	chr8:36427309-36427359	NB4	blood:	n/a
14	chr8:36427309-36427359	SK-N-SH_RA	brain:	n/a
15	chr8:36427309-36427359	PrEC	prostate:	n/a
16	chr8:36427309-36427359	MCF-7	breast:	n/a
17	chr8:36427309-36427359	PFSK-1	brain:	n/a
18	chr8:36427309-36427359	HRPEpiC	eye:	n/a
19	chr8:36427309-36427359	HCT-116	colon:	n/a
20	chr8:36427309-36427359	NT2-D1	testis:	n/a
21	chr8:36427309-36427359	ovcar-3	ovarian:	n/a
22	chr8:36427309-36427359	HRCEpiC	kidney:	n/a
23	chr8:36427309-36427359	U87	brain:	n/a
24	chr8:36427309-36427359	GM19239	blood:	n/a
25	chr8:36427309-36427359	HNPCEpiC	eye:	n/a
26	chr8:36427309-36427359	HCPEpiC	choroid plexus:	n/a
27	chr8:36427309-36427359	GM12891	blood:	n/a
28	chr8:36427309-36427359	AG09319	gingival:	n/a
29	chr8:36427309-36427359	SK-N-SH	brain:	n/a
30	chr8:36427309-36427359	H1-hESC	embryonic stem cell:	embryo
31	chr8:36427309-36427359	AG04449	skin:	fetal
32	chr8:36427309-36427359	NH-A	brain:	n/a
33	chr8:36427309-36427359	PANC-1	pancreas:	n/a
34	chr8:36427309-36427359	K562	blood:	n/a
35	chr8:36427309-36427359	HIPEpiC	eye:	n/a
36	chr8:36427309-36427359	RPTEC	kidney:	n/a
37	chr8:36427309-36427359	MCF10A-Er-Src	breast:	n/a
38	chr8:36427309-36427359	T-47D	breast:	n/a
39	chr8:36427309-36427359	GM12878	blood:	n/a
40	chr8:36427309-36427359	AoSMC	blood vessel:	n/a
41	chr8:36427309-36427359	Hepatocyte	liver:	n/a
42	chr8:36427309-36427359	NHDF-neo	bronchial:	n/a
43	chr8:36427309-36427359	HMEC	breast:	n/a
44	chr8:36427309-36427359	HAEpiC	amniotic membrane:	n/a
45	chr8:36427309-36427359	GM12892	blood:	n/a
46	chr8:36427309-36427359	AG09309	skin:	n/a
47	chr8:36427309-36427359	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:36427309-36427359	SAEC	small airway:	n/a
49	chr8:36427309-36427359	ProgFib	skin:	n/a
50	chr8:36427309-36427359	IMR90	lung:	fetal

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

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

Extended variants
information (count: 1460 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1460 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144825507	chr8:36408002-36408003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370969173	chr8:36408028-36408029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552050336	chr8:36408034-36408035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185727748	chr8:36408047-36408048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527390974	chr8:36408065-36408066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs386724471	chr8:36408083-36408084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78798982	chr8:36408085-36408086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147945613	chr8:36408123-36408124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190437119	chr8:36408165-36408166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571234371	chr8:36408176-36408177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140619047	chr8:36408188-36408189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181276137	chr8:36408200-36408201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572957244	chr8:36408207-36408208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534325589	chr8:36408208-36408209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185449132	chr8:36408224-36408225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190934473	chr8:36408261-36408262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544309756	chr8:36408279-36408280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150395120	chr8:36408320-36408321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145171658	chr8:36408329-36408330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11995775	chr8:36408349-36408350	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182638351	chr8:36408368-36408369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527352874	chr8:36408380-36408381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75707683	chr8:36408405-36408406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76117256	chr8:36408406-36408407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77180656	chr8:36408408-36408409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78036718	chr8:36408409-36408410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371693305	chr8:36408419-36408420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575552143	chr8:36408425-36408426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549076212	chr8:36408451-36408452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536210124	chr8:36408520-36408521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188796020	chr8:36408545-36408546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149146697	chr8:36408557-36408558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs16885190	chr8:36408571-36408572	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376875361	chr8:36408582-36408583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77064263	chr8:36408620-36408621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540417625	chr8:36408645-36408646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538551676	chr8:36408760-36408761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547163543	chr8:36408795-36408796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565555975	chr8:36408829-36408830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145048676	chr8:36408845-36408846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138909916	chr8:36408874-36408875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574098663	chr8:36408932-36408933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192183620	chr8:36408933-36408934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556605919	chr8:36408990-36408991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs578238132	chr8:36408997-36408998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183096530	chr8:36409004-36409005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555834990	chr8:36409025-36409026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560633851	chr8:36409042-36409043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187629099	chr8:36409054-36409055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192073525	chr8:36409084-36409085	Enhancers	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:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36408000-36408600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr8:36408400-36409200	Enhancers	Fetal Heart	heart
3	chr8:36409200-36411000	Weak transcription	Fetal Heart	heart
4	chr8:36409800-36411400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:36410800-36411600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:36411000-36412200	Enhancers	Fetal Heart	heart
7	chr8:36411200-36411600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:36411600-36416800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:36414800-36415000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:36415000-36423600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:36416800-36417200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr8:36416800-36417200	Enhancers	Fetal Heart	heart
13	chr8:36416800-36417200	Enhancers	Fetal Muscle Trunk	muscle
14	chr8:36416800-36417800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:36417000-36417400	Enhancers	Duodenum Mucosa	Duodenum
16	chr8:36417800-36423600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:36418200-36419400	Enhancers	Fetal Muscle Leg	muscle
18	chr8:36419400-36424000	Weak transcription	Fetal Muscle Leg	muscle
19	chr8:36423400-36424000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr8:36423600-36423800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:36423600-36424200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:36423600-36424200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr8:36423800-36424000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:36424000-36424400	Enhancers	Fetal Heart	heart
25	chr8:36424000-36424400	Enhancers	Fetal Muscle Leg	muscle
26	chr8:36424000-36426000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr8:36424200-36425600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:36424400-36424600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:36424400-36425600	Weak transcription	Fetal Heart	heart
30	chr8:36424400-36425600	Weak transcription	Fetal Muscle Leg	muscle
31	chr8:36425000-36425200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:36425200-36426200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:36425400-36426000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:36425600-36426600	Enhancers	Fetal Heart	heart
35	chr8:36425600-36427600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:36425600-36428200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr8:36425600-36429600	Enhancers	Brain Germinal Matrix	brain
38	chr8:36425600-36429800	Enhancers	Fetal Muscle Leg	muscle
39	chr8:36425800-36426400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:36426000-36426400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:36426000-36426800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr8:36426000-36427000	Enhancers	Fetal Brain Female	brain
43	chr8:36426000-36427600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr8:36426000-36427800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr8:36426000-36427800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:36426000-36428000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:36426000-36428200	Enhancers	Fetal Kidney	kidney
48	chr8:36426000-36429400	Enhancers	Fetal Brain Male	brain
49	chr8:36426200-36427400	Enhancers	Duodenum Mucosa	Duodenum
50	chr8:36426200-36428200	Enhancers	HUES6 Cell Line	embryonic stem cell

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