Variant report

Variant	nsv1017006
Chromosome Location	chr5:179064433-179086482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:317)
CpG islands
(count:550)
Chromatin interactive
region (count:19)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:179085535-179085713	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:179085577-179085757	K562	blood:	n/a	n/a
3	BCL11A	chr5:179084946-179085204	GM12878	blood:	n/a	chr5:179085108-179085117
4	BHLHE40	chr5:179075505-179075756	K562	blood:	n/a	n/a
5	BHLHE40	chr5:179085609-179085785	K562	blood:	n/a	n/a
6	BHLHE40	chr5:179075535-179075759	HepG2	liver:	n/a	n/a
7	CBX3	chr5:179084502-179085318	K562	blood:	n/a	n/a
8	CBX3	chr5:179085381-179086051	K562	blood:	n/a	n/a
9	CBX3	chr5:179084818-179085122	K562	blood:	n/a	n/a
10	CEBPB	chr5:179085604-179085804	A549	lung:	n/a	chr5:179085684-179085695
11	CEBPB	chr5:179085557-179085864	K562	blood:	n/a	chr5:179085684-179085695
12	CEBPB	chr5:179085475-179085861	K562	blood:	n/a	chr5:179085684-179085695
13	CEBPB	chr5:179085594-179085813	Hela-S3	cervix:	n/a	chr5:179085684-179085695
14	CEBPB	chr5:179085604-179085844	H1-hESC	embryonic stem cell:	n/a	chr5:179085684-179085695
15	CEBPB	chr5:179085595-179085795	HepG2	liver:	n/a	chr5:179085684-179085695
16	CEBPB	chr5:179085541-179085892	IMR90	lung:	n/a	chr5:179085684-179085695
17	CTCF	chr5:179084576-179084754	GM12891	blood:	n/a	n/a
18	CTCF	chr5:179085327-179085331	GM19240	blood:	n/a	n/a
19	CTCF	chr5:179084640-179084790	GM06990	blood:	n/a	n/a
20	CTCF	chr5:179084720-179084870	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr5:179084704-179085330	A549	lung:	n/a	n/a
22	CTCF	chr5:179084747-179085147	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:179084842-179085261	Lung_OC	lung:	n/a	n/a
24	CTCF	chr5:179084764-179085244	K562	blood:	n/a	n/a
25	CTCF	chr5:179084822-179085385	GM10266	blood:	n/a	n/a
26	CTCF	chr5:179084640-179084790	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr5:179084680-179084830	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr5:179084824-179085150	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:179084810-179085373	GM12891	blood:	n/a	n/a
30	CTCF	chr5:179084700-179084850	WI-38	lung:	n/a	n/a
31	CTCF	chr5:179084757-179085135	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:179084595-179085181	GM12892	blood:	n/a	n/a
33	CTCF	chr5:179084731-179084738	LNCaP	prostate:	n/a	n/a
34	CTCF	chr5:179085149-179085152	GM13976	blood:	n/a	n/a
35	CTCF	chr5:179084772-179085189	LNCaP	prostate:	n/a	n/a
36	CTCF	chr5:179078140-179078290	NHDF-neo	bronchial:	n/a	chr5:179078192-179078210
37	CTCF	chr5:179084748-179085204	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr5:179085264-179085268	Lung_OC	lung:	n/a	n/a
39	CTCF	chr5:179074854-179074891	GM10266	blood:	n/a	n/a
40	CTCF	chr5:179084483-179084559	GM19239	blood:	n/a	n/a
41	CTCF	chr5:179084811-179085148	GM13976	blood:	n/a	n/a
42	CTCF	chr5:179084700-179084850	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr5:179084839-179085139	K562	blood:	n/a	n/a
44	CTCF	chr5:179084705-179085213	GM19240	blood:	n/a	n/a
45	CTCF	chr5:179084737-179084744	GM10266	blood:	n/a	n/a
46	CTCF	chr5:179080382-179080430	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:179084858-179085158	LNCaP	prostate:	n/a	n/a
48	CTCF	chr5:179084640-179084790	GM12878	blood:	n/a	n/a
49	CTCF	chr5:179084836-179085162	GM13977	blood:	n/a	n/a
50	CTCF	chr5:179084858-179085122	MCF-7	breast:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179085626-179085676	AG09319	gingival:	n/a
2	chr5:179085626-179085676	AG09319	gingival:	n/a
3	chr5:179069308-179069358	ProgFib	skin:	n/a
4	chr5:179071901-179071951	SK-N-MC	brain:	n/a
5	chr5:179071901-179071951	RPTEC	kidney:	n/a
6	chr5:179072247-179072297	T-47D	breast:	n/a
7	chr5:179072791-179072841	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:179071604-179071654	HepG2	liver:	n/a
9	chr5:179072791-179072841	HEK293	kidney:	embryo
10	chr5:179071901-179071951	NHDF-neo	bronchial:	n/a
11	chr5:179085626-179085676	BE2_C	brain:	n/a
12	chr5:179075765-179075815	NH-A	brain:	n/a
13	chr5:179075765-179075815	H1-hESC	embryonic stem cell:	embryo
14	chr5:179072247-179072297	HCT-116	colon:	n/a
15	chr5:179075765-179075815	HUVEC	blood vessel:	n/a
16	chr5:179082448-179082498	Hela-S3	cervix:	n/a
17	chr5:179083592-179083642	HUVEC	blood vessel:	n/a
18	chr5:179072791-179072841	A549	lung:	n/a
19	chr5:179085626-179085676	HNPCEpiC	eye:	n/a
20	chr5:179069308-179069358	H1-hESC	embryonic stem cell:	embryo
21	chr5:179082448-179082498	LNCaP	prostate:	n/a
22	chr5:179071901-179071951	NH-A	brain:	n/a
23	chr5:179085626-179085676	MCF-7	breast:	n/a
24	chr5:179071604-179071654	ECC-1	luminal epithelium:	n/a
25	chr5:179069308-179069358	HEK293	kidney:	embryo
26	chr5:179082448-179082498	NT2-D1	testis:	n/a
27	chr5:179083592-179083642	HEEpiC	esophagus:	n/a
28	chr5:179075765-179075815	PFSK-1	brain:	n/a
29	chr5:179082448-179082498	HAEpiC	amniotic membrane:	n/a
30	chr5:179069308-179069358	GM12892	blood:	n/a
31	chr5:179071901-179071951	HEEpiC	esophagus:	n/a
32	chr5:179072791-179072841	Hepatocyte	liver:	n/a
33	chr5:179072791-179072841	CMK	blood:	n/a
34	chr5:179071901-179071951	HUVEC	blood vessel:	n/a
35	chr5:179071901-179071951	ProgFib	skin:	n/a
36	chr5:179071901-179071951	SK-N-SH_RA	brain:	n/a
37	chr5:179069308-179069358	GM12891	blood:	n/a
38	chr5:179069308-179069358	BJ	skin:	n/a
39	chr5:179072791-179072841	HCF	heart:	n/a
40	chr5:179082448-179082498	RPTEC	kidney:	n/a
41	chr5:179071604-179071654	H1-hESC	embryonic stem cell:	embryo
42	chr5:179072247-179072297	AoSMC	blood vessel:	n/a
43	chr5:179069308-179069358	HCPEpiC	choroid plexus:	n/a
44	chr5:179071901-179071951	HRCEpiC	kidney:	n/a
45	chr5:179083592-179083642	PFSK-1	brain:	n/a
46	chr5:179071901-179071951	HPAEpiC	pulmonary alveolar:	n/a
47	chr5:179082448-179082498	HEK293	kidney:	embryo
48	chr5:179072247-179072297	NT2-D1	testis:	n/a
49	chr5:179083592-179083642	HIPEpiC	eye:	n/a
50	chr5:179075765-179075815	BE2_C	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179065572..179067135-chr5:179078949..179080962,2	K562	blood:
2	chr5:179048487..179050192-chr5:179084037..179087067,3	K562	blood:
3	chr5:179065572..179067135-chr5:179078949..179080962,2	K562	blood:
4	chr5:179049252..179052008-chr5:179078855..179080395,2	K562	blood:
5	chr5:179085578..179087269-chr5:179124562..179126084,2	MCF-7	breast:
6	chr5:179048380..179051829-chr5:179074872..179077735,3	K562	blood:
7	chr5:179048357..179051414-chr5:179069051..179070806,3	K562	blood:
8	chr5:179050028..179052097-chr5:179080349..179082018,2	MCF-7	breast:
9	chr5:179048537..179052008-chr5:179078753..179080980,4	K562	blood:
10	chr5:179085719..179088021-chr5:179125069..179127270,2	K562	blood:
11	chr5:178976725..178979261-chr5:179073948..179076733,2	MCF-7	breast:
12	chr5:179049010..179052109-chr5:179075423..179078137,6	MCF-7	breast:
13	chr5:179064378..179067657-chr5:179095247..179097749,4	K562	blood:
14	chr5:179047959..179050192-chr5:179084037..179087067,3	K562	blood:
15	chr5:179085589..179087601-chr5:179105143..179107865,2	MCF-7	breast:
16	chr5:179048484..179051740-chr5:179086105..179090360,4	MCF-7	breast:
17	chr5:179049252..179051807-chr5:179078099..179079783,3	MCF-7	breast:
18	chr5:179048281..179049857-chr5:179068285..179070728,2	K562	blood:
19	chr5:179085577..179087271-chr5:179159837..179161552,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf60-1	chr5:179070431-179070491	NONHSAT105607
2	lnc-C5orf60-1	chr5:179071332-179071842	NONHSAT105608
3	lnc-C5orf60-1	chr5:179071946-179072008	NONHSAT105608
4	lnc-C5orf60-1	chr5:179068545-179070211	NONHSAT105606
5	lnc-AC136604.1-1	chr5:179084763-179085098	XLOC_004677
6	lnc-AC136604.1-1	chr5:179085266-179085482	XLOC_004677
7	lnc-AC136604.1-1	chr5:179085237-179085482	XLOC_004677
8	lnc-C5orf60-1	chr5:179069896-179070211	NONHSAT105607
9	lnc-C5orf60-1	chr5:179071946-179072008	NONHSAT105607
10	lnc-C5orf60-1	chr5:179070431-179072008	NONHSAT105606
11	lnc-AC136604.1-1	chr5:179085079-179085482	XLOC_004677
12	lnc-C5orf60-1	chr5:179071030-179071087	NONHSAT105607
13	lnc-AC136604.1-1	chr5:179085390-179085482	XLOC_004677

No data

Variant related genes	Relation type
ENSG00000250999	TF binding region
C5orf60	TF binding region
ENSG00000228259	TF binding region
HNRNPH1	TF binding region
ENSG00000250999	CpG island
C5orf60	CpG island
ENSG00000228259	CpG island
HNRNPH1	CpG island
ENSG00000169045	chromatin interactions
ENSG00000176783	chromatin interactions
ENSG00000161021	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000225051	chromatin interactions
KRAS	miRNA target sites

Extended variants
information (count: 982 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:982 , 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	rs544649518	chr5:179064444-179064445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72662115	chr5:179064460-179064461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564390466	chr5:179064475-179064476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72662114	chr5:179064479-179064480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72662113	chr5:179064492-179064493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187569636	chr5:179064574-179064575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543961499	chr5:179064585-179064586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548165718	chr5:179064604-179064605	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs116815766	chr5:179064769-179064770	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs529516878	chr5:179064779-179064780	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs375826021	chr5:179064785-179064786	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs191851910	chr5:179064808-179064809	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs368711741	chr5:179064859-179064860	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs183319888	chr5:179064907-179064908	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs139091214	chr5:179065001-179065002	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs569894198	chr5:179065104-179065105	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs372878689	chr5:179065105-179065106	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs549133318	chr5:179065110-179065111	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567327510	chr5:179065119-179065120	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs534543090	chr5:179065120-179065121	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs547178331	chr5:179065121-179065122	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs570683319	chr5:179065145-179065146	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs4700818	chr5:179065148-179065149	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs538205977	chr5:179065223-179065224	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs551951435	chr5:179065227-179065228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs556698086	chr5:179065231-179065232	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs76764213	chr5:179065241-179065242	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs34880542	chr5:179065242-179065243	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs113931453	chr5:179065243-179065244	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs79038895	chr5:179065260-179065261	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs543733919	chr5:179065263-179065264	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs562436391	chr5:179065315-179065316	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs574140692	chr5:179065320-179065321	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs541690646	chr5:179065338-179065339	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs367693207	chr5:179065376-179065377	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs559841596	chr5:179065408-179065409	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs576304712	chr5:179065416-179065417	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs533476954	chr5:179065444-179065445	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535791100	chr5:179065474-179065475	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs149117743	chr5:179065503-179065504	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs144480007	chr5:179065531-179065532	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186204069	chr5:179065544-179065545	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs548992270	chr5:179065601-179065602	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs567593150	chr5:179065640-179065641	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs6601062	chr5:179065642-179065643	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs147846537	chr5:179065643-179065644	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs536905854	chr5:179065664-179065665	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs572356206	chr5:179065680-179065681	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs6860158	chr5:179065684-179065685	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs541398898	chr5:179065701-179065702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	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
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
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179052200-179085400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:179060800-179065200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:179061000-179064600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:179061200-179064800	Weak transcription	NHEK	skin
5	chr5:179061200-179065800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:179062000-179064600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:179064600-179064800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:179064600-179065000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:179064800-179065000	Enhancers	NHEK	skin
10	chr5:179064800-179065600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:179065000-179065800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:179065000-179066600	Weak transcription	NHEK	skin
13	chr5:179065200-179065400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:179065600-179065800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:179065800-179066000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:179065800-179067000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:179065800-179070600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:179066000-179066400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr5:179066400-179066800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr5:179066600-179066800	Enhancers	NHEK	skin
21	chr5:179070000-179070600	Active TSS	Spleen	Spleen
22	chr5:179070200-179071000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr5:179070600-179070800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:179070800-179078000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr5:179071800-179072400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:179075400-179075800	Enhancers	Fetal Muscle Leg	muscle
27	chr5:179075400-179076800	Enhancers	Fetal Muscle Trunk	muscle
28	chr5:179076200-179076600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:179076200-179076800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:179076400-179076600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:179078000-179078200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:179078000-179078400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:179078000-179078400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:179078200-179078400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:179078200-179085400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr5:179078400-179079600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:179078400-179085400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:179084400-179084600	Enhancers	Dnd41	blood
39	chr5:179084600-179084800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:179084600-179084800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:179084600-179085000	Flanking Active TSS	Dnd41	blood
42	chr5:179084600-179085400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:179084600-179085400	Active TSS	Rectal Mucosa Donor 31	rectum
44	chr5:179084600-179085400	Enhancers	HMEC	breast
45	chr5:179084600-179085600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr5:179084600-179085600	Active TSS	Duodenum Mucosa	Duodenum
47	chr5:179084600-179085600	Active TSS	Skeletal Muscle Male	skeletal muscle
48	chr5:179084600-179085600	Active TSS	HepG2	liver
49	chr5:179084600-179086000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr5:179084600-179086200	Active TSS	Fetal Brain Female	brain

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