Variant report

Variant	nsv1019332
Chromosome Location	chr5:116888074-117248632
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	chr5:116926161-116926311	K562	blood:	n/a	n/a
2	BACH1	chr5:117188782-117188783	K562	blood:	n/a	n/a
3	BATF	chr5:117036830-117037055	GM12878	blood:	n/a	chr5:117036937-117036948
4	BHLHE40	chr5:116985952-116985981	A549	lung:	n/a	n/a
5	BRCA1	chr5:117225271-117225273	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:117192690-117192791	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr5:117049291-117049655	K562	blood:	n/a	n/a
8	CBX3	chr5:117049153-117049707	HCT-116	colon:	n/a	n/a
9	CBX3	chr5:117049274-117049666	K562	blood:	n/a	n/a
10	CBX3	chr5:117049184-117049819	HCT-116	colon:	n/a	n/a
11	CCNT2	chr5:117173830-117173997	K562	blood:	n/a	n/a
12	CEBPB	chr5:117168511-117168821	IMR90	lung:	n/a	chr5:117168641-117168652
13	CEBPB	chr5:116924426-116924707	ECC-1	luminal epithelium:	n/a	chr5:116924496-116924507
14	CEBPB	chr5:117026047-117026258	A549	lung:	n/a	chr5:117026085-117026098
15	CEBPB	chr5:117172356-117172719	HepG2	liver:	n/a	chr5:117172536-117172547
16	CEBPB	chr5:117139138-117139638	IMR90	lung:	n/a	n/a
17	CEBPB	chr5:117168507-117168774	A549	lung:	n/a	chr5:117168641-117168652
18	CEBPB	chr5:116924370-116924687	K562	blood:	n/a	chr5:116924496-116924507
19	CEBPB	chr5:117168502-117168804	HepG2	liver:	n/a	chr5:117168641-117168652
20	CEBPB	chr5:116924316-116924672	A549	lung:	n/a	chr5:116924496-116924507
21	CEBPB	chr5:117172935-117173233	HepG2	liver:	n/a	chr5:117173066-117173079 chr5:117173067-117173078
22	CEBPB	chr5:117172354-117172704	A549	lung:	n/a	chr5:117172536-117172547
23	CEBPB	chr5:116924315-116924924	HepG2	liver:	n/a	chr5:116924496-116924507
24	CEBPB	chr5:117000930-117001227	HepG2	liver:	n/a	chr5:117001080-117001093 chr5:117001081-117001092 chr5:117001080-117001093 chr5:117001080-117001091 chr5:117001080-117001093
25	CEBPB	chr5:117001005-117001104	K562	blood:	n/a	chr5:117001080-117001093 chr5:117001081-117001092 chr5:117001080-117001093 chr5:117001080-117001091 chr5:117001080-117001093
26	CEBPB	chr5:116924271-116924784	MCF-7	breast:	n/a	chr5:116924496-116924507
27	CEBPB	chr5:117225285-117225673	IMR90	lung:	n/a	n/a
28	CEBPB	chr5:116924325-116924666	Hela-S3	cervix:	n/a	chr5:116924496-116924507
29	CEBPB	chr5:117238164-117238250	A549	lung:	n/a	n/a
30	CEBPB	chr5:117172423-117172650	H1-hESC	embryonic stem cell:	n/a	chr5:117172536-117172547
31	CEBPB	chr5:117172347-117172719	IMR90	lung:	n/a	chr5:117172536-117172547
32	CEBPB	chr5:117000984-117001177	H1-hESC	embryonic stem cell:	n/a	chr5:117001080-117001093 chr5:117001081-117001092 chr5:117001080-117001093 chr5:117001080-117001091 chr5:117001080-117001093
33	CEBPB	chr5:117228871-117229261	IMR90	lung:	n/a	n/a
34	CEBPB	chr5:117067971-117068479	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr5:116924343-116924581	H1-hESC	embryonic stem cell:	n/a	chr5:116924496-116924507
36	CEBPB	chr5:117122720-117122726	K562	blood:	n/a	n/a
37	CEBPB	chr5:116924258-116924716	MCF-7	breast:	n/a	chr5:116924496-116924507
38	CEBPB	chr5:116924319-116924948	IMR90	lung:	n/a	chr5:116924496-116924507
39	CEBPZ	chr5:117049337-117049629	HepG2	liver:	n/a	n/a
40	CHD2	chr5:117027526-117027566	GM12878	blood:	n/a	n/a
41	CTCF	chr5:117124217-117124730	MCF-7	breast:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
42	CTCF	chr5:116926820-116926970	GM12872	blood:	n/a	chr5:116926831-116926847 chr5:116926832-116926853 chr5:116926830-116926848
43	CTCF	chr5:116926657-116927005	IMR90	lung:	n/a	chr5:116926831-116926847 chr5:116926832-116926853 chr5:116926830-116926848
44	CTCF	chr5:117124365-117124750	HCT-116	colon:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
45	CTCF	chr5:116926760-116926910	GM12868	blood:	n/a	chr5:116926831-116926847 chr5:116926832-116926853 chr5:116926830-116926848
46	CTCF	chr5:116926767-116926911	HUVEC	blood vessel:	n/a	chr5:116926831-116926847 chr5:116926832-116926853 chr5:116926830-116926848
47	CTCF	chr5:116926760-116926910	HVMF	connective:	n/a	chr5:116926831-116926847 chr5:116926832-116926853 chr5:116926830-116926848
48	CTCF	chr5:116926780-116926930	GM12872	blood:	n/a	chr5:116926831-116926847 chr5:116926832-116926853 chr5:116926830-116926848
49	CTCF	chr5:117124401-117124562	LNCaP	prostate:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
50	CTCF	chr5:117124340-117124490	NB4	blood:	n/a	chr5:117124461-117124482 chr5:117124466-117124484

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117084231-117084281	HUVEC	blood vessel:	n/a
2	chr5:117098484-117098534	NH-A	brain:	n/a
3	chr5:117002269-117002319	HIPEpiC	eye:	n/a
4	chr5:117098484-117098534	NT2-D1	testis:	n/a
5	chr5:117002269-117002319	AG04449	skin:	fetal
6	chr5:117002269-117002319	NHBE	bronchial:	n/a
7	chr5:117084231-117084281	SAEC	small airway:	n/a
8	chr5:117098484-117098534	HNPCEpiC	eye:	n/a
9	chr5:117002269-117002319	A549	lung:	n/a
10	chr5:117084231-117084281	AG04449	skin:	fetal
11	chr5:117098484-117098534	NHBE	bronchial:	n/a
12	chr5:117098484-117098534	MCF10A-Er-Src	breast:	n/a
13	chr5:117098484-117098534	U87	brain:	n/a
14	chr5:117098484-117098534	NHDF-neo	bronchial:	n/a
15	chr5:117084231-117084281	NHDF-neo	bronchial:	n/a
16	chr5:117098484-117098534	LNCaP	prostate:	n/a
17	chr5:117002269-117002319	SAEC	small airway:	n/a
18	chr5:117098484-117098534	AoSMC	blood vessel:	n/a
19	chr5:117084231-117084281	HMEC	breast:	n/a
20	chr5:117084231-117084281	NB4	blood:	n/a
21	chr5:117002269-117002319	SK-N-SH_RA	brain:	n/a
22	chr5:117002269-117002319	Hepatocyte	liver:	n/a
23	chr5:117098484-117098534	Caco-2	colon:	n/a
24	chr5:117084231-117084281	HCPEpiC	choroid plexus:	n/a
25	chr5:117002269-117002319	PrEC	prostate:	n/a
26	chr5:117084231-117084281	SK-N-MC	brain:	n/a
27	chr5:117084231-117084281	SKMC	muscle:	n/a
28	chr5:117098484-117098534	PrEC	prostate:	n/a
29	chr5:117098484-117098534	AG04449	skin:	fetal
30	chr5:117098484-117098534	A549	lung:	n/a
31	chr5:117098484-117098534	AG09319	gingival:	n/a
32	chr5:117098484-117098534	HRE	kidney:	n/a
33	chr5:117084231-117084281	AG09319	gingival:	n/a
34	chr5:117084231-117084281	GM12891	blood:	n/a
35	chr5:117002269-117002319	SKMC	muscle:	n/a
36	chr5:117098484-117098534	HRCEpiC	kidney:	n/a
37	chr5:117098484-117098534	HCPEpiC	choroid plexus:	n/a
38	chr5:117084231-117084281	HRE	kidney:	n/a
39	chr5:117098484-117098534	GM12891	blood:	n/a
40	chr5:117084231-117084281	BJ	skin:	n/a
41	chr5:117002269-117002319	HCM	heart:	n/a
42	chr5:117002269-117002319	SK-N-MC	brain:	n/a
43	chr5:117084231-117084281	PFSK-1	brain:	n/a
44	chr5:117098484-117098534	RPTEC	kidney:	n/a
45	chr5:117098484-117098534	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:117002269-117002319	HEK293	kidney:	embryo
47	chr5:117084231-117084281	HNPCEpiC	eye:	n/a
48	chr5:117002269-117002319	Jurkat	blood:	n/a
49	chr5:117002269-117002319	HCT-116	colon:	n/a
50	chr5:117002269-117002319	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:117077570..117079876-chr5:117081896..117084183,2	MCF-7	breast:
2	chr5:116929272..116931860-chr5:116932599..116935583,2	MCF-7	breast:
3	chr5:116951542..116953877-chr5:116957366..116959083,2	K562	blood:
4	chr5:117089885..117092759-chr5:117093000..117095939,2	MCF-7	breast:
5	chr5:117050991..117053069-chr5:117068100..117070459,2	MCF-7	breast:
6	chr5:117077570..117079876-chr5:117081896..117084183,2	MCF-7	breast:
7	chr5:116884300..116886423-chr5:116888475..116890420,2	K562	blood:
8	chr5:116929272..116931860-chr5:116932599..116935583,2	MCF-7	breast:
9	chr5:116951542..116953877-chr5:116957366..116959083,2	K562	blood:
10	chr5:117149206..117151782-chr5:117152643..117155518,2	MCF-7	breast:
11	chr5:117125890..117127438-chr5:117130783..117133189,2	MCF-7	breast:
12	chr5:117201656..117203414-chr5:117208664..117210271,2	MCF-7	breast:
13	chr5:117125890..117127438-chr5:117130783..117133189,2	MCF-7	breast:
14	chr5:117089885..117092759-chr5:117093000..117095939,2	MCF-7	breast:
15	chr5:117072184..117074866-chr5:118040239..118042048,2	MCF-7	breast:
16	chr5:117201656..117203414-chr5:117208664..117210271,2	MCF-7	breast:
17	chr5:117005779..117008314-chr5:117034629..117036437,2	K562	blood:
18	chr5:117112749..117115394-chr5:117119190..117122198,3	K562	blood:
19	chr5:117080321..117081196-chr8:117848296..117848880,2	MCF-7	breast:
20	chr5:117149206..117151782-chr5:117152643..117155518,2	MCF-7	breast:
21	chr5:117005684..117008647-chr5:117010420..117012880,2	K562	blood:
22	chr5:117050991..117053069-chr5:117068100..117070459,2	MCF-7	breast:
23	chr5:117005684..117008647-chr5:117010420..117012880,2	K562	blood:
24	chr5:117005779..117008314-chr5:117034629..117036437,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-5	chr5:116891341-116891475	NONHSAT103387
2	lnc-COMMD10-5	chr5:116912943-116915439	NONHSAT103387
3	lnc-DTWD2-12	chr5:117114521-117115227	NONHSAT103390
4	lnc-DTWD2-13	chr5:117054935-117055640	NONHSAT103389
5	lnc-DMXL1-4	chr5:117066056-117066103	NR_104997
6	lnc-DTWD2-13	chr5:117057573-117057792	NONHSAT103389

Variant related genes	Relation type
RPL7L1P4	TF binding region
ENSG00000251477	TF binding region
RPL7L1P4	CpG island
ENSG00000251477	CpG island
ENSG00000249582	chromatin interactions

Extended variants
information (count: 5666 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:5666 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538194911	chr5:116891357-116891358	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs79776135	chr5:116891411-116891412	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs577815987	chr5:116891473-116891474	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs905853	chr5:116892616-116892617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562530063	chr5:116892643-116892644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114570237	chr5:116892651-116892652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552466189	chr5:116892727-116892728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs265904	chr5:116892740-116892741	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534991544	chr5:116892746-116892747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567922222	chr5:116892757-116892758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181555665	chr5:116892775-116892776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556744068	chr5:116892778-116892779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570145897	chr5:116892789-116892790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371105122	chr5:116892849-116892850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559050017	chr5:116892850-116892851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572472126	chr5:116892868-116892869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375403271	chr5:116892891-116892892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142621440	chr5:116892912-116892913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553795668	chr5:116892920-116892921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146015153	chr5:116892932-116892933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553280683	chr5:116892956-116892957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184489858	chr5:116892994-116892995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542537792	chr5:116893000-116893001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6890211	chr5:116894211-116894212	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541129697	chr5:116894245-116894246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182235509	chr5:116894305-116894306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6871102	chr5:116894306-116894307	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs113211298	chr5:116894307-116894308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs265908	chr5:116894341-116894342	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs534830135	chr5:116894366-116894367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187198900	chr5:116894379-116894380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112585143	chr5:116894388-116894389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532882809	chr5:116894409-116894410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114232525	chr5:116894437-116894438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77927576	chr5:116894495-116894496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144657140	chr5:116894506-116894507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201465764	chr5:116894530-116894531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11313583	chr5:116894558-116894559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539523662	chr5:116894565-116894566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568434638	chr5:116894585-116894586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530951923	chr5:116894589-116894590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140192205	chr5:116894613-116894614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs265909	chr5:116894646-116894647	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs145657024	chr5:116894654-116894655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558389990	chr5:116894655-116894656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147729902	chr5:116894691-116894692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562627758	chr5:116894741-116894742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534487572	chr5:116894780-116894781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191218008	chr5:116894859-116894860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540386201	chr5:116894906-116894907	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22543975	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116892600-116893000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:116894200-116896800	Enhancers	Liver	Liver
3	chr5:116894600-116895000	Enhancers	Fetal Intestine Small	intestine
4	chr5:116894600-116895200	Enhancers	Fetal Intestine Large	intestine
5	chr5:116895000-116896000	Weak transcription	Fetal Intestine Small	intestine
6	chr5:116896000-116896200	Enhancers	Fetal Intestine Small	intestine
7	chr5:116903400-116905400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:116903600-116905200	Enhancers	NHEK	skin
9	chr5:116903600-116905400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr5:116904400-116904800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr5:116918800-116919200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:116918800-116919400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:116919200-116919400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:116919400-116920200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:116920200-116920400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:116922200-116924000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:116922800-116923200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:116922800-116923400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:116922800-116923400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:116923000-116923800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr5:116923200-116923600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr5:116923200-116923800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr5:116923600-116924200	Enhancers	Placenta	Placenta
24	chr5:116924000-116929200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:116929000-116929600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:116929200-116929600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:116929200-116930200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:116929600-116929800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:116929600-116929800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:116929600-116930000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:116929600-116930000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:116929600-116930000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
33	chr5:116929600-116930000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr5:116929600-116930600	Enhancers	Ovary	ovary
35	chr5:116929800-116930000	Enhancers	Colon Smooth Muscle	Colon
36	chr5:116929800-116930200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:116929800-116930200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:116929800-116930200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr5:116929800-116930200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:116929800-116930200	Enhancers	Adipose Nuclei	Adipose
41	chr5:116929800-116930200	Enhancers	NHDF-Ad	bronchial
42	chr5:116930000-116931200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr5:116930000-116935600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:116930200-116930400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:116932400-116932600	Enhancers	Fetal Intestine Small	intestine
46	chr5:116932600-116933600	Weak transcription	Fetal Intestine Small	intestine
47	chr5:116933600-116934600	Enhancers	Fetal Intestine Small	intestine
48	chr5:116935600-116935800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:116949800-116953600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr5:116953600-116953800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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