Variant report

Variant	nsv882672
Chromosome Location	chr5:105673460-105818481
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	chr5:105735164-105735374	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:105679829-105679900	K562	blood:	n/a	n/a
3	BCL3	chr5:105735041-105735392	A549	lung:	n/a	chr5:105735250-105735259
4	BCL3	chr5:105735051-105735584	A549	lung:	n/a	chr5:105735250-105735259
5	CBX3	chr5:105790354-105791158	HCT-116	colon:	n/a	n/a
6	CBX3	chr5:105733268-105733945	HCT-116	colon:	n/a	n/a
7	CBX3	chr5:105705555-105705987	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:105814124-105814357	A549	lung:	n/a	chr5:105814270-105814281
9	CEBPB	chr5:105799781-105800144	IMR90	lung:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
10	CEBPB	chr5:105718081-105718347	HepG2	liver:	n/a	chr5:105718203-105718214 chr5:105718205-105718214 chr5:105718160-105718173
11	CEBPB	chr5:105755845-105756150	K562	blood:	n/a	n/a
12	CEBPB	chr5:105755861-105756158	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:105799775-105800128	A549	lung:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
14	CEBPB	chr5:105755852-105756151	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr5:105813496-105813814	MCF-7	breast:	n/a	chr5:105813644-105813656
16	CEBPB	chr5:105702740-105703024	HepG2	liver:	n/a	chr5:105702877-105702888
17	CEBPB	chr5:105813435-105813964	MCF-7	breast:	n/a	chr5:105813644-105813656
18	CEBPB	chr5:105799818-105800083	H1-hESC	embryonic stem cell:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
19	CEBPB	chr5:105755813-105756182	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:105770420-105770643	A549	lung:	n/a	chr5:105770535-105770548 chr5:105770535-105770548 chr5:105770534-105770551 chr5:105770536-105770547
21	CEBPB	chr5:105702772-105702972	A549	lung:	n/a	chr5:105702877-105702888
22	CEBPB	chr5:105755831-105756198	A549	lung:	n/a	n/a
23	CEBPB	chr5:105735119-105735451	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:105751117-105751522	IMR90	lung:	n/a	n/a
25	CEBPB	chr5:105739618-105740208	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:105770388-105770650	IMR90	lung:	n/a	chr5:105770535-105770548 chr5:105770535-105770548 chr5:105770534-105770551 chr5:105770536-105770547
27	CEBPB	chr5:105814096-105814440	Hela-S3	cervix:	n/a	chr5:105814270-105814281
28	CEBPB	chr5:105751136-105751473	A549	lung:	n/a	n/a
29	CEBPB	chr5:105743912-105744207	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:105683996-105684271	HepG2	liver:	n/a	chr5:105684127-105684138
31	CEBPB	chr5:105770396-105770623	HepG2	liver:	n/a	chr5:105770535-105770548 chr5:105770535-105770548 chr5:105770534-105770551 chr5:105770536-105770547
32	CEBPB	chr5:105799793-105800150	HepG2	liver:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
33	CEBPB	chr5:105814101-105814422	HepG2	liver:	n/a	chr5:105814270-105814281
34	CEBPB	chr5:105744771-105744988	HepG2	liver:	n/a	chr5:105744829-105744840 chr5:105744827-105744838
35	CEBPB	chr5:105744757-105744935	A549	lung:	n/a	chr5:105744829-105744840 chr5:105744827-105744838
36	CEBPB	chr5:105755825-105756145	HepG2	liver:	n/a	n/a
37	CHD1	chr5:105740276-105740348	GM12878	blood:	n/a	n/a
38	CTCF	chr5:105790480-105790630	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr5:105790520-105790670	HCT-116	colon:	n/a	n/a
40	CTCF	chr5:105790480-105790630	RPTEC	kidney:	n/a	n/a
41	CTCF	chr5:105790445-105790634	A549	lung:	n/a	n/a
42	CTCF	chr5:105790050-105790873	A549	lung:	n/a	n/a
43	CTCF	chr5:105790520-105790670	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:105790460-105790610	AG09309	skin:	n/a	n/a
45	CTCF	chr5:105794874-105794936	GM13976	blood:	n/a	n/a
46	CTCF	chr5:105790500-105790650	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr5:105790520-105790670	GM12870	blood:	n/a	n/a
48	CTCF	chr5:105790520-105790670	BJ	skin:	n/a	n/a
49	CTCF	chr5:105790420-105790570	HFF	foreskin:	n/a	n/a
50	CTCF	chr5:105790540-105790603	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:105791135-105791185	HepG2	liver:	n/a
2	chr5:105753028-105753078	HL-60	blood:	n/a
3	chr5:105753028-105753078	HEEpiC	esophagus:	n/a
4	chr5:105753028-105753078	NH-A	brain:	n/a
5	chr5:105791135-105791185	BJ	skin:	n/a
6	chr5:105753028-105753078	ovcar-3	ovarian:	n/a
7	chr5:105753028-105753078	Jurkat	blood:	n/a
8	chr5:105791135-105791185	H1-hESC	embryonic stem cell:	embryo
9	chr5:105753028-105753078	AG09319	gingival:	n/a
10	chr5:105791135-105791185	HCF	heart:	n/a
11	chr5:105753028-105753078	NB4	blood:	n/a
12	chr5:105791135-105791185	SAEC	small airway:	n/a
13	chr5:105753028-105753078	AG04450	lung:	fetal
14	chr5:105753028-105753078	GM19239	blood:	n/a
15	chr5:105753028-105753078	HAEpiC	amniotic membrane:	n/a
16	chr5:105753028-105753078	HMEC	breast:	n/a
17	chr5:105753028-105753078	H1-hESC	embryonic stem cell:	embryo
18	chr5:105753028-105753078	HRCEpiC	kidney:	n/a
19	chr5:105791135-105791185	ProgFib	skin:	n/a
20	chr5:105753028-105753078	T-47D	breast:	n/a
21	chr5:105791135-105791185	NB4	blood:	n/a
22	chr5:105753028-105753078	NHBE	bronchial:	n/a
23	chr5:105791135-105791185	PFSK-1	brain:	n/a
24	chr5:105791135-105791185	PANC-1	pancreas:	n/a
25	chr5:105753028-105753078	ProgFib	skin:	n/a
26	chr5:105753028-105753078	HIPEpiC	eye:	n/a
27	chr5:105791135-105791185	BE2_C	brain:	n/a
28	chr5:105791135-105791185	Caco-2	colon:	n/a
29	chr5:105753028-105753078	AG09309	skin:	n/a
30	chr5:105791135-105791185	MCF10A-Er-Src	breast:	n/a
31	chr5:105753028-105753078	BJ	skin:	n/a
32	chr5:105753028-105753078	SKMC	muscle:	n/a
33	chr5:105791135-105791185	NHDF-neo	bronchial:	n/a
34	chr5:105753028-105753078	PFSK-1	brain:	n/a
35	chr5:105791135-105791185	AG09319	gingival:	n/a
36	chr5:105753028-105753078	NHDF-neo	bronchial:	n/a
37	chr5:105753028-105753078	RPTEC	kidney:	n/a
38	chr5:105753028-105753078	Hepatocyte	liver:	n/a
39	chr5:105753028-105753078	GM12892	blood:	n/a
40	chr5:105753028-105753078	HepG2	liver:	n/a
41	chr5:105791135-105791185	Hela-S3	cervix:	n/a
42	chr5:105753028-105753078	MCF10A-Er-Src	breast:	n/a
43	chr5:105753028-105753078	AG10803	skin:	n/a
44	chr5:105791135-105791185	NH-A	brain:	n/a
45	chr5:105753028-105753078	HCF	heart:	n/a
46	chr5:105753028-105753078	CMK	blood:	n/a
47	chr5:105753028-105753078	HUVEC	blood vessel:	n/a
48	chr5:105791135-105791185	AG10803	skin:	n/a
49	chr5:105753028-105753078	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:105753028-105753078	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:105678713..105680256-chr5:105733390..105735536,2	K562	blood:
2	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
3	chr5:105678713..105680256-chr5:105733390..105735536,2	K562	blood:
4	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
5	chr5:105695067..105695819-chr7:152358250..152358853,2	MCF-7	breast:
6	chr5:105690890..105692893-chr5:105701188..105703588,2	MCF-7	breast:
7	chr5:105690890..105692893-chr5:105701188..105703588,2	MCF-7	breast:
8	chr5:105577079..105577725-chr5:105702519..105703290,2	MCF-7	breast:
9	chr5:105683065..105685836-chr5:105691749..105694214,2	MCF-7	breast:
10	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
11	chr5:105775699..105778002-chr5:105784029..105786359,2	MCF-7	breast:
12	chr5:105775699..105778002-chr5:105784029..105786359,2	MCF-7	breast:
13	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
14	chr5:105683065..105685836-chr5:105691749..105694214,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251204	TF binding region
ENSG00000251204	CpG island

Extended variants
information (count: 2176 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2176 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80283312	chr5:105692613-105692614	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72788914	chr5:105692641-105692642	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569924311	chr5:105692664-105692665	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543251947	chr5:105692679-105692680	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35337868	chr5:105692698-105692699	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565144059	chr5:105692750-105692751	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369649337	chr5:105692760-105692761	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367907618	chr5:105692810-105692811	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs10068397	chr5:105692826-105692827	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs146573534	chr5:105692840-105692841	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs141313950	chr5:105692845-105692846	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373595917	chr5:105692885-105692886	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs557758076	chr5:105692890-105692891	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs571222628	chr5:105692924-105692925	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs66480472	chr5:105693008-105693009	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs551126393	chr5:105693064-105693065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573932480	chr5:105693078-105693079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116437968	chr5:105693113-105693114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186235478	chr5:105693125-105693126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190951149	chr5:105693152-105693153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569659430	chr5:105693196-105693197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143237460	chr5:105693292-105693293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs151259258	chr5:105693333-105693334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564519913	chr5:105693385-105693386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533228343	chr5:105693420-105693421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371161990	chr5:105693521-105693522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543513230	chr5:105693544-105693545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534887306	chr5:105693563-105693564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558960629	chr5:105693693-105693694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78883827	chr5:105693750-105693751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549244709	chr5:105693774-105693775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566215083	chr5:105693775-105693776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184239384	chr5:105693809-105693810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368691792	chr5:105693845-105693846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547856614	chr5:105693860-105693861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563049578	chr5:105693883-105693884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34903745	chr5:105693898-105693899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79325496	chr5:105693938-105693939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187567882	chr5:105693940-105693941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557136650	chr5:105693960-105693961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567449357	chr5:105693966-105693967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536476436	chr5:105693968-105693969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531093085	chr5:105693986-105693987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555634670	chr5:105693993-105693994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372111959	chr5:105693994-105693995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552537147	chr5:105693995-105693996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573018452	chr5:105694005-105694006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545295451	chr5:105694095-105694096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs36069787	chr5:105694173-105694174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535527111	chr5:105699010-105699011	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:105692600-105692800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr5:105692600-105693000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:105692600-105693000	Active TSS	Osteobl	bone
4	chr5:105692800-105693000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:105692800-105694200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:105699000-105700000	Enhancers	HMEC	breast
7	chr5:105699400-105699600	Enhancers	NHEK	skin
8	chr5:105699800-105703000	Weak transcription	NHEK	skin
9	chr5:105700000-105703200	Weak transcription	HMEC	breast
10	chr5:105703000-105703600	Enhancers	NHEK	skin
11	chr5:105703200-105703400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:105703200-105704000	Enhancers	HMEC	breast
13	chr5:105703400-105706800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:105704000-105704200	Active TSS	Gastric	stomach
15	chr5:105710800-105711200	Enhancers	HMEC	breast
16	chr5:105711000-105713000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr5:105711600-105713000	Enhancers	Osteobl	bone
18	chr5:105712000-105712600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr5:105712000-105712800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:105712000-105712800	Enhancers	HUVEC	blood vessel
21	chr5:105712000-105713000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:105712000-105713000	Enhancers	NH-A	brain
23	chr5:105712000-105713000	Enhancers	NHDF-Ad	bronchial
24	chr5:105712200-105712600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:105712200-105712800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:105712200-105713000	Enhancers	NHEK	skin
27	chr5:105712400-105713000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:105712600-105713000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:105712800-105716600	Weak transcription	HUVEC	blood vessel
30	chr5:105713000-105716600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:105713000-105716600	Weak transcription	NH-A	brain
32	chr5:105713000-105716600	Weak transcription	NHEK	skin
33	chr5:105716600-105716800	Enhancers	NHDF-Ad	bronchial
34	chr5:105716600-105717000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr5:105716600-105717000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr5:105716600-105717000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:105716600-105717000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:105716600-105717000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:105716600-105717000	Enhancers	HMEC	breast
40	chr5:105716600-105717000	Enhancers	HUVEC	blood vessel
41	chr5:105716600-105717000	Enhancers	NHEK	skin
42	chr5:105716600-105717200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr5:105716600-105717200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:105716600-105717200	Enhancers	NH-A	brain
45	chr5:105716600-105717600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:105716600-105717600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:105716800-105717000	Flanking Active TSS	NHDF-Ad	bronchial
48	chr5:105716800-105717200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:105716800-105717600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr5:105717000-105717600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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