Variant report

Variant	nsv829971
Chromosome Location	chr4:73709753-73880451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:963)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:73752425-73752685	K562	blood:	n/a	n/a
2	ATF1	chr4:73712224-73712696	K562	blood:	n/a	n/a
3	ATF1	chr4:73767404-73767588	K562	blood:	n/a	n/a
4	ATF1	chr4:73837388-73837623	K562	blood:	n/a	n/a
5	ATF1	chr4:73840470-73840819	K562	blood:	n/a	n/a
6	ATF2	chr4:73871938-73872434	GM12878	blood:	n/a	n/a
7	BACH1	chr4:73712297-73712431	K562	blood:	n/a	n/a
8	BACH1	chr4:73712142-73712521	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr4:73808865-73809094	GM12878	blood:	n/a	n/a
10	BCL3	chr4:73724003-73724516	A549	lung:	n/a	chr4:73724231-73724240
11	BCL3	chr4:73723988-73724466	A549	lung:	n/a	chr4:73724231-73724240
12	BCL3	chr4:73840888-73841347	A549	lung:	n/a	n/a
13	BHLHE40	chr4:73872045-73873022	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:73712187-73712424	K562	blood:	n/a	n/a
15	BHLHE40	chr4:73840485-73840793	K562	blood:	n/a	n/a
16	BHLHE40	chr4:73762452-73762533	HepG2	liver:	n/a	n/a
17	CBX3	chr4:73712113-73712633	K562	blood:	n/a	n/a
18	CCNT2	chr4:73840566-73840741	K562	blood:	n/a	n/a
19	CEBPB	chr4:73762219-73762561	A549	lung:	n/a	chr4:73762377-73762388
20	CEBPB	chr4:73762289-73762431	K562	blood:	n/a	chr4:73762377-73762388
21	CEBPB	chr4:73762258-73762526	MCF-7	breast:	n/a	chr4:73762377-73762388
22	CEBPB	chr4:73742284-73742565	A549	lung:	n/a	chr4:73742449-73742458 chr4:73742448-73742459 chr4:73742447-73742458
23	CEBPB	chr4:73831662-73831942	A549	lung:	n/a	n/a
24	CEBPB	chr4:73762245-73762497	K562	blood:	n/a	chr4:73762377-73762388
25	CEBPB	chr4:73712261-73712507	K562	blood:	n/a	n/a
26	CEBPB	chr4:73842859-73843086	HepG2	liver:	n/a	chr4:73842981-73842994 chr4:73842983-73842994 chr4:73842983-73842992
27	CEBPB	chr4:73762197-73762568	K562	blood:	n/a	chr4:73762377-73762388
28	CEBPB	chr4:73762103-73762757	IMR90	lung:	n/a	chr4:73762377-73762388
29	CEBPB	chr4:73724190-73724392	A549	lung:	n/a	n/a
30	CEBPB	chr4:73785644-73786024	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:73724075-73724451	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:73802083-73802411	IMR90	lung:	n/a	chr4:73802240-73802251
33	CEBPB	chr4:73742282-73742587	IMR90	lung:	n/a	chr4:73742449-73742458 chr4:73742448-73742459 chr4:73742447-73742458
34	CEBPB	chr4:73762185-73762537	Hela-S3	cervix:	n/a	chr4:73762377-73762388
35	CEBPB	chr4:73841069-73841460	A549	lung:	n/a	chr4:73841147-73841160 chr4:73841272-73841285
36	CEBPB	chr4:73764984-73765195	HepG2	liver:	n/a	chr4:73765102-73765113
37	CEBPB	chr4:73764926-73765280	HepG2	liver:	n/a	chr4:73765102-73765113
38	CEBPB	chr4:73762122-73762685	A549	lung:	n/a	chr4:73762377-73762388
39	CEBPB	chr4:73762204-73762563	A549	lung:	n/a	chr4:73762377-73762388
40	CEBPB	chr4:73802111-73802367	A549	lung:	n/a	chr4:73802240-73802251
41	CEBPB	chr4:73842870-73843093	IMR90	lung:	n/a	chr4:73842981-73842994 chr4:73842983-73842994 chr4:73842983-73842992
42	CEBPB	chr4:73811012-73811300	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:73802153-73802382	H1-hESC	embryonic stem cell:	n/a	chr4:73802240-73802251
44	CEBPB	chr4:73831647-73831941	K562	blood:	n/a	n/a
45	CEBPB	chr4:73762241-73762494	HepG2	liver:	n/a	chr4:73762377-73762388
46	CEBPB	chr4:73785725-73785876	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:73762194-73762732	H1-hESC	embryonic stem cell:	n/a	chr4:73762377-73762388
48	CEBPB	chr4:73762094-73762621	HepG2	liver:	n/a	chr4:73762377-73762388
49	CEBPB	chr4:73802075-73802401	HepG2	liver:	n/a	chr4:73802240-73802251
50	CEBPB	chr4:73724141-73724399	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:73753087-73753137	AoSMC	blood vessel:	n/a
2	chr4:73753087-73753137	AG09309	skin:	n/a
3	chr4:73753087-73753137	Hepatocyte	liver:	n/a
4	chr4:73753087-73753137	HepG2	liver:	n/a
5	chr4:73753087-73753137	HRPEpiC	eye:	n/a
6	chr4:73753087-73753137	Jurkat	blood:	n/a
7	chr4:73753087-73753137	SAEC	small airway:	n/a
8	chr4:73753087-73753137	HAEpiC	amniotic membrane:	n/a
9	chr4:73753087-73753137	SK-N-SH	brain:	n/a
10	chr4:73753087-73753137	GM12878	blood:	n/a
11	chr4:73753087-73753137	HCT-116	colon:	n/a
12	chr4:73753087-73753137	HRCEpiC	kidney:	n/a
13	chr4:73753087-73753137	NB4	blood:	n/a
14	chr4:73753087-73753137	ovcar-3	ovarian:	n/a
15	chr4:73753087-73753137	HMEC	breast:	n/a
16	chr4:73753087-73753137	GM12892	blood:	n/a
17	chr4:73753087-73753137	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:73753087-73753137	HIPEpiC	eye:	n/a
19	chr4:73753087-73753137	BJ	skin:	n/a
20	chr4:73753087-73753137	SK-N-SH_RA	brain:	n/a
21	chr4:73753087-73753137	NT2-D1	testis:	n/a
22	chr4:73753087-73753137	AG04449	skin:	fetal
23	chr4:73753087-73753137	LNCaP	prostate:	n/a
24	chr4:73753087-73753137	MCF10A-Er-Src	breast:	n/a
25	chr4:73753087-73753137	GM06990	blood:	n/a
26	chr4:73753087-73753137	GM12891	blood:	n/a
27	chr4:73753087-73753137	HRE	kidney:	n/a
28	chr4:73753087-73753137	Hela-S3	cervix:	n/a
29	chr4:73753087-73753137	HUVEC	blood vessel:	n/a
30	chr4:73753087-73753137	Caco-2	colon:	n/a
31	chr4:73753087-73753137	T-47D	breast:	n/a
32	chr4:73753087-73753137	HNPCEpiC	eye:	n/a
33	chr4:73753087-73753137	K562	blood:	n/a
34	chr4:73753087-73753137	HCM	heart:	n/a
35	chr4:73753087-73753137	RPTEC	kidney:	n/a
36	chr4:73753087-73753137	ProgFib	skin:	n/a
37	chr4:73753087-73753137	AG09319	gingival:	n/a
38	chr4:73753087-73753137	MCF-7	breast:	n/a
39	chr4:73753087-73753137	PANC-1	pancreas:	n/a
40	chr4:73753087-73753137	NHBE	bronchial:	n/a
41	chr4:73753087-73753137	SK-N-MC	brain:	n/a
42	chr4:73753087-73753137	IMR90	lung:	fetal
43	chr4:73753087-73753137	HEEpiC	esophagus:	n/a
44	chr4:73753087-73753137	HEK293	kidney:	embryo
45	chr4:73753087-73753137	H1-hESC	embryonic stem cell:	embryo
46	chr4:73753087-73753137	HL-60	blood:	n/a
47	chr4:73753087-73753137	NH-A	brain:	n/a
48	chr4:73753087-73753137	PFSK-1	brain:	n/a
49	chr4:73753087-73753137	HCPEpiC	choroid plexus:	n/a
50	chr4:73753087-73753137	U87	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:73876629..73878196-chr4:73883041..73885471,2	K562	blood:
2	chr4:73832060..73834957-chr4:73837760..73840547,2	K562	blood:
3	chr4:73862823..73864524-chr4:73868675..73870631,2	K562	blood:
4	chr4:73865080..73867115-chr4:73870729..73873090,2	K562	blood:
5	chr4:73862823..73864524-chr4:73868675..73870631,2	K562	blood:
6	chr4:73568023..73568623-chr4:73752188..73753038,2	MCF-7	breast:
7	chr4:73864020..73867115-chr4:73870729..73873090,3	K562	blood:
8	chr4:73800834..73803291-chr4:73816440..73818270,2	K562	blood:
9	chr4:73865080..73867115-chr4:73870729..73873090,2	K562	blood:
10	chr4:73864020..73867115-chr4:73870729..73873090,3	K562	blood:
11	chr4:73872915..73876082-chr4:73876162..73879588,3	K562	blood:
12	chr4:73834694..73836763-chr4:73837867..73839908,2	MCF-7	breast:
13	chr4:73834694..73836763-chr4:73837867..73839908,2	MCF-7	breast:
14	chr4:73567647..73568539-chr4:73774935..73775763,2	MCF-7	breast:
15	chr4:73370699..73371400-chr4:73774972..73775771,2	MCF-7	breast:
16	chr4:73832060..73834957-chr4:73837760..73840547,2	K562	blood:
17	chr4:73711557..73713794-chr4:73715010..73716796,2	K562	blood:
18	chr4:73431201..73433969-chr4:73767436..73769841,2	K562	blood:
19	chr4:73800834..73803291-chr4:73816440..73818270,2	K562	blood:
20	chr4:73226037..73227750-chr4:73750692..73753662,2	K562	blood:
21	chr4:73872915..73876082-chr4:73876162..73879588,3	K562	blood:
22	chr4:73711557..73713794-chr4:73715010..73716796,2	K562	blood:
23	chr4:73192107..73193147-chr4:73752130..73753066,3	K562	blood:

No data

Variant related genes	Relation type
RNU4ATAC9P	TF binding region
RNU4ATAC9P	CpG island
ENSG00000156140	chromatin interactions

Extended variants
information (count: 4797 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4797 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186062492	chr4:73709798-73709799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7689873	chr4:73709809-73709810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs576283040	chr4:73709815-73709816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566128833	chr4:73709856-73709857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543722105	chr4:73709919-73709920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72661006	chr4:73709923-73709924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573871631	chr4:73709953-73709954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541174216	chr4:73709960-73709961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192256311	chr4:73709962-73709963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542270311	chr4:73710046-73710047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146779013	chr4:73710069-73710070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2194931	chr4:73710078-73710079	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs563271257	chr4:73710089-73710090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140530683	chr4:73710190-73710191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369978966	chr4:73710285-73710286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573305546	chr4:73710286-73710287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549256828	chr4:73710309-73710310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs221592	chr4:73710343-73710344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs564962160	chr4:73710372-73710373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532383053	chr4:73710398-73710399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76336041	chr4:73710399-73710400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571668180	chr4:73710419-73710420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539097599	chr4:73710438-73710439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557108260	chr4:73710543-73710544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569262611	chr4:73710558-73710559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116320682	chr4:73710563-73710564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555697614	chr4:73710591-73710592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369691681	chr4:73710598-73710599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1461516	chr4:73710603-73710604	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541239156	chr4:73710612-73710613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115548293	chr4:73710622-73710623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577691633	chr4:73710661-73710662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4398492	chr4:73710760-73710761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs34717317	chr4:73710787-73710788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563176348	chr4:73710794-73710795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184089080	chr4:73710802-73710803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377604313	chr4:73710814-73710815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569073141	chr4:73710852-73710853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201919032	chr4:73710858-73710859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377275232	chr4:73710862-73710863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78974636	chr4:73710863-73710864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs33982514	chr4:73710864-73710865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561254117	chr4:73710879-73710880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11723795	chr4:73710903-73710904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs11728884	chr4:73710910-73710911	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs571792994	chr4:73710924-73710925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532534671	chr4:73710963-73710964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145684280	chr4:73710995-73710996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569321339	chr4:73711034-73711035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114801408	chr4:73711060-73711061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:73706600-73711800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:73707000-73712000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:73707200-73711800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:73708000-73710200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:73708000-73710400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:73711600-73711800	Enhancers	K562	blood
7	chr4:73711800-73712000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:73711800-73712200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr4:73711800-73712600	Flanking Active TSS	K562	blood
10	chr4:73711800-73712800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:73711800-73712800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:73711800-73712800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:73711800-73712800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:73712000-73712200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:73712000-73712400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:73712000-73712600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:73712000-73712800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:73712000-73712800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr4:73712000-73712800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr4:73712200-73712600	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr4:73712400-73712800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:73712400-73713000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:73712600-73712800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr4:73712600-73713000	Enhancers	K562	blood
25	chr4:73712800-73713000	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr4:73712800-73713000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:73713400-73713800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:73722800-73724800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:73723600-73723800	Enhancers	HMEC	breast
30	chr4:73723600-73724800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr4:73723600-73724800	Enhancers	Osteobl	bone
32	chr4:73723800-73724200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:73723800-73724200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:73724800-73726200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:73726200-73726800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr4:73727000-73727200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:73732200-73732800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:73732600-73733200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:73740600-73741600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr4:73740800-73741000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr4:73740800-73741600	Enhancers	Aorta	Aorta
42	chr4:73741000-73741200	Enhancers	Ovary	ovary
43	chr4:73741400-73742600	Weak transcription	Ovary	ovary
44	chr4:73741600-73741800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:73742600-73743000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:73742600-73743000	Enhancers	Ovary	ovary
47	chr4:73742800-73743000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:73751200-73752600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr4:73752000-73753200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr4:73752200-73752800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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