Variant report

Variant	nsv462511
Chromosome Location	chr5:167275087-167324809
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	BACH1	chr5:167317090-167317307	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr5:167280520-167280865	IMR90	lung:	n/a	chr5:167280701-167280714
3	CEBPB	chr5:167276984-167277355	K562	blood:	n/a	chr5:167276984-167276995
4	CEBPB	chr5:167300606-167300648	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:167305352-167305552	Hela-S3	cervix:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
6	CEBPB	chr5:167305271-167305612	HepG2	liver:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
7	CEBPB	chr5:167305294-167305513	K562	blood:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
8	CEBPB	chr5:167301479-167301615	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:167305274-167305556	A549	lung:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
10	CEBPB	chr5:167305386-167305522	H1-hESC	embryonic stem cell:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
11	CEBPB	chr5:167305255-167305579	IMR90	lung:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
12	CEBPB	chr5:167276830-167277382	HepG2	liver:	n/a	chr5:167276984-167276995
13	CEBPB	chr5:167276912-167277055	Hela-S3	cervix:	n/a	chr5:167276984-167276995
14	CEBPB	chr5:167276840-167277402	IMR90	lung:	n/a	chr5:167276984-167276995
15	CEBPB	chr5:167276851-167277372	A549	lung:	n/a	chr5:167276984-167276995
16	CTCF	chr5:167315440-167315590	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr5:167315440-167315590	HFF	foreskin:	n/a	n/a
18	CTCF	chr5:167315440-167315590	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr5:167315497-167315557	Gliobla	brain:	n/a	n/a
20	CTCF	chr5:167323380-167323530	Caco-2	colon:	n/a	n/a
21	CTCF	chr5:167315460-167315610	Caco-2	colon:	n/a	n/a
22	CTCF	chr5:167323420-167323570	HFF	foreskin:	n/a	n/a
23	CTCF	chr5:167323460-167323610	AG10803	skin:	n/a	n/a
24	CTCF	chr5:167315380-167315530	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr5:167323380-167323530	HAc	cerebellar:	n/a	n/a
26	CTCF	chr5:167315400-167315550	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr5:167323420-167323570	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr5:167315440-167315590	HMF	breast:	n/a	n/a
29	CTCF	chr5:167315400-167315550	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr5:167323100-167323250	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr5:167315460-167315610	A549	lung:	n/a	n/a
32	CTCF	chr5:167315480-167315630	HCM	heart:	n/a	n/a
33	CTCF	chr5:167315340-167315490	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr5:167315440-167315590	BJ	skin:	n/a	n/a
35	CTCF	chr5:167323460-167323610	AG09309	skin:	n/a	n/a
36	CTCF	chr5:167315508-167315554	NHEK	skin:	n/a	n/a
37	CTCF	chr5:167315420-167315570	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr5:167323460-167323610	AG04449	skin:	n/a	n/a
39	CTCF	chr5:167315488-167315596	HepG2	liver:	n/a	n/a
40	CTCF	chr5:167315540-167315690	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr5:167315400-167315550	HMF	breast:	n/a	n/a
42	CTCF	chr5:167315380-167315530	HRE	kidney:	n/a	n/a
43	CTCF	chr5:167288380-167288530	HMF	breast:	n/a	n/a
44	CTCF	chr5:167315440-167315590	HMEC	breast:	n/a	n/a
45	CTCF	chr5:167315440-167315590	RPTEC	kidney:	n/a	n/a
46	CTCF	chr5:167315420-167315570	RPTEC	kidney:	n/a	n/a
47	CTCF	chr5:167298120-167298270	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr5:167315400-167315550	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr5:167315440-167315590	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr5:167315420-167315570	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:167285540-167285590	SAEC	small airway:	n/a
2	chr5:167282267-167282317	HPAEpiC	pulmonary alveolar:	n/a
3	chr5:167282267-167282317	BJ	skin:	n/a
4	chr5:167285540-167285590	SKMC	muscle:	n/a
5	chr5:167315790-167315840	MCF10A-Er-Src	breast:	n/a
6	chr5:167284031-167284081	HCPEpiC	choroid plexus:	n/a
7	chr5:167284031-167284081	T-47D	breast:	n/a
8	chr5:167285540-167285590	ProgFib	skin:	n/a
9	chr5:167282267-167282317	PrEC	prostate:	n/a
10	chr5:167315790-167315840	Hepatocyte	liver:	n/a
11	chr5:167288661-167288711	HL-60	blood:	n/a
12	chr5:167284031-167284081	PrEC	prostate:	n/a
13	chr5:167285561-167285611	ECC-1	luminal epithelium:	n/a
14	chr5:167282267-167282317	A549	lung:	n/a
15	chr5:167315790-167315840	PrEC	prostate:	n/a
16	chr5:167285540-167285590	HCPEpiC	choroid plexus:	n/a
17	chr5:167315790-167315840	HL-60	blood:	n/a
18	chr5:167315790-167315840	SKMC	muscle:	n/a
19	chr5:167285561-167285611	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:167282267-167282317	PANC-1	pancreas:	n/a
21	chr5:167284031-167284081	K562	blood:	n/a
22	chr5:167288661-167288711	ovcar-3	ovarian:	n/a
23	chr5:167284031-167284081	MCF10A-Er-Src	breast:	n/a
24	chr5:167285540-167285590	LNCaP	prostate:	n/a
25	chr5:167288661-167288711	HCF	heart:	n/a
26	chr5:167315790-167315840	AG04450	lung:	fetal
27	chr5:167285561-167285611	BJ	skin:	n/a
28	chr5:167288661-167288711	BJ	skin:	n/a
29	chr5:167284031-167284081	HCT-116	colon:	n/a
30	chr5:167285540-167285590	GM19239	blood:	n/a
31	chr5:167288661-167288711	HMEC	breast:	n/a
32	chr5:167285561-167285611	AG09319	gingival:	n/a
33	chr5:167288661-167288711	ECC-1	luminal epithelium:	n/a
34	chr5:167285561-167285611	ovcar-3	ovarian:	n/a
35	chr5:167285561-167285611	HEEpiC	esophagus:	n/a
36	chr5:167285561-167285611	LNCaP	prostate:	n/a
37	chr5:167284031-167284081	NHDF-neo	bronchial:	n/a
38	chr5:167282267-167282317	HEK293	kidney:	embryo
39	chr5:167284031-167284081	GM19239	blood:	n/a
40	chr5:167285561-167285611	K562	blood:	n/a
41	chr5:167285561-167285611	PrEC	prostate:	n/a
42	chr5:167285561-167285611	AG10803	skin:	n/a
43	chr5:167285561-167285611	MCF-7	breast:	n/a
44	chr5:167282267-167282317	GM12892	blood:	n/a
45	chr5:167288661-167288711	HEEpiC	esophagus:	n/a
46	chr5:167282267-167282317	Hepatocyte	liver:	n/a
47	chr5:167282267-167282317	HNPCEpiC	eye:	n/a
48	chr5:167284031-167284081	HAEpiC	amniotic membrane:	n/a
49	chr5:167284031-167284081	MCF-7	breast:	n/a
50	chr5:167284031-167284081	GM12878	blood:	n/a

Variant related genes	Relation type
ENSG00000221741	TF binding region
TENM2	TF binding region
ENSG00000221741	CpG island
TENM2	CpG island

Extended variants
information (count: 1806 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1806 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4869078	chr5:167275087-167275088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117793700	chr5:167275089-167275090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189626079	chr5:167275113-167275114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182103626	chr5:167275147-167275148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4869079	chr5:167275165-167275166	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs545154561	chr5:167275190-167275191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185809309	chr5:167275201-167275202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528027837	chr5:167275218-167275219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548061464	chr5:167275229-167275230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533682959	chr5:167275237-167275238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4869080	chr5:167275250-167275251	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528860936	chr5:167275279-167275280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143469585	chr5:167275306-167275307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568940010	chr5:167275378-167275379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7700480	chr5:167275434-167275435	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs114063875	chr5:167275456-167275457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7704178	chr5:167275476-167275477	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs73803238	chr5:167275510-167275511	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs554010869	chr5:167275521-167275522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151313688	chr5:167275526-167275527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17069307	chr5:167275532-167275533	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs188888787	chr5:167275546-167275547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6555773	chr5:167275549-167275550	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs112734803	chr5:167275624-167275625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79929796	chr5:167275647-167275648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370970836	chr5:167275656-167275657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375544837	chr5:167275667-167275668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185941295	chr5:167275687-167275688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189913951	chr5:167275824-167275825	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561598891	chr5:167275830-167275831	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181398488	chr5:167275844-167275845	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376940144	chr5:167275915-167275916	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140610047	chr5:167275921-167275922	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561513943	chr5:167275930-167275931	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2909797	chr5:167275949-167275950	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185912088	chr5:167275977-167275978	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191211185	chr5:167275986-167275987	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571493671	chr5:167275990-167275991	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183783309	chr5:167276095-167276096	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs373836961	chr5:167276140-167276141	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs538943573	chr5:167276204-167276205	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567508606	chr5:167276225-167276226	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150446698	chr5:167276292-167276293	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10035896	chr5:167276295-167276296	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs56934789	chr5:167276304-167276305	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7725644	chr5:167276307-167276308	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs558606362	chr5:167276310-167276311	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572575062	chr5:167276367-167276368	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200271056	chr5:167276441-167276442	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs541580687	chr5:167276488-167276489	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Breast cancer	17603634	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167251800-167299000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:167252600-167276000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr5:167266600-167326200	Weak transcription	HMEC	breast
4	chr5:167269000-167278000	Strong transcription	NHEK	skin
5	chr5:167271200-167280000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:167271600-167276000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:167271800-167276200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:167273200-167284400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:167273600-167277000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr5:167275000-167280400	Weak transcription	Fetal Lung	lung
11	chr5:167275200-167280400	Weak transcription	NHDF-Ad	bronchial
12	chr5:167275800-167276600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:167276000-167276600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:167276000-167276600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
15	chr5:167276200-167276400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:167276400-167276800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:167276600-167276800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:167276600-167276800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr5:167276600-167278200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:167276800-167277000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr5:167276800-167277000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:167276800-167277400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:167277000-167277600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:167277000-167278000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr5:167277000-167278400	Enhancers	Osteobl	bone
26	chr5:167277000-167279000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:167277000-167282000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr5:167277200-167279000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:167277400-167279400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:167277600-167278200	Enhancers	NH-A	brain
31	chr5:167277600-167278600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr5:167278000-167278600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr5:167278000-167279400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr5:167278000-167283800	Weak transcription	NHEK	skin
35	chr5:167278200-167278400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:167278200-167280400	Weak transcription	NH-A	brain
37	chr5:167278400-167278600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:167278400-167280400	Weak transcription	Osteobl	bone
39	chr5:167278600-167278800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr5:167278600-167279400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:167279000-167280400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:167279000-167281400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr5:167279400-167280000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:167279400-167280400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:167279400-167281400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr5:167280000-167281400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr5:167280000-167289400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:167280400-167280600	Enhancers	Fetal Lung	lung
49	chr5:167280400-167280800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:167280400-167280800	Enhancers	NH-A	brain

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