Variant report

Variant	nsv829946
Chromosome Location	chr4:59913771-60083867
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	BATF	chr4:60020461-60020690	GM12878	blood:	n/a	n/a
2	BATF	chr4:60000562-60000764	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:60038697-60038728	K562	blood:	n/a	n/a
4	CEBPB	chr4:59930191-59930393	A549	lung:	n/a	chr4:59930311-59930322
5	CEBPB	chr4:59991891-59992280	ECC-1	luminal epithelium:	n/a	chr4:59992073-59992082 chr4:59992073-59992082 chr4:59992071-59992084 chr4:59992073-59992082 chr4:59992071-59992082
6	CEBPB	chr4:60027052-60027396	A549	lung:	n/a	chr4:60027214-60027225
7	CEBPB	chr4:59981855-59982124	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:59930192-59930433	HepG2	liver:	n/a	chr4:59930311-59930322
9	CEBPB	chr4:60019549-60019772	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:59926151-59926570	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr4:59923518-59923902	A549	lung:	n/a	n/a
12	CEBPB	chr4:59991966-59992249	K562	blood:	n/a	chr4:59992073-59992082 chr4:59992073-59992082 chr4:59992071-59992084 chr4:59992073-59992082 chr4:59992071-59992082
13	CEBPB	chr4:60066746-60067053	HepG2	liver:	n/a	chr4:60066902-60066915 chr4:60066902-60066913 chr4:60066904-60066915
14	CEBPB	chr4:59923602-59923884	MCF-7	breast:	n/a	n/a
15	CEBPB	chr4:59991895-59992254	IMR90	lung:	n/a	chr4:59992073-59992082 chr4:59992073-59992082 chr4:59992071-59992084 chr4:59992073-59992082 chr4:59992071-59992082
16	CEBPB	chr4:59988882-59989190	HepG2	liver:	n/a	chr4:59989020-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989022-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989020-59989031
17	CEBPB	chr4:59967897-59967945	A549	lung:	n/a	n/a
18	CEBPB	chr4:59923445-59923978	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:59963157-59963401	HepG2	liver:	n/a	chr4:59963289-59963300
20	CEBPB	chr4:59923489-59923985	A549	lung:	n/a	n/a
21	CEBPB	chr4:59981851-59982147	A549	lung:	n/a	n/a
22	CEBPB	chr4:59926170-59926547	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr4:59923562-59923867	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:59988954-59989151	H1-hESC	embryonic stem cell:	n/a	chr4:59989020-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989022-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989020-59989031
25	CEBPB	chr4:60027082-60027356	K562	blood:	n/a	chr4:60027214-60027225
26	CEBPB	chr4:59991889-59992240	A549	lung:	n/a	chr4:59992073-59992082 chr4:59992073-59992082 chr4:59992071-59992084 chr4:59992073-59992082 chr4:59992071-59992082
27	CEBPB	chr4:60066644-60067058	MCF-7	breast:	n/a	chr4:60066902-60066915 chr4:60066902-60066913 chr4:60066904-60066915
28	CEBPB	chr4:60069680-60069873	HepG2	liver:	n/a	chr4:60069699-60069710
29	CEBPB	chr4:60027038-60027403	HepG2	liver:	n/a	chr4:60027214-60027225
30	CEBPB	chr4:59987825-59987886	H1-hESC	embryonic stem cell:	n/a	chr4:59987850-59987863 chr4:59987850-59987861
31	CEBPB	chr4:59963316-59963362	K562	blood:	n/a	n/a
32	CEBPB	chr4:59968474-59968675	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:59991899-59992256	HepG2	liver:	n/a	chr4:59992073-59992082 chr4:59992073-59992082 chr4:59992071-59992084 chr4:59992073-59992082 chr4:59992071-59992082
34	CEBPB	chr4:59981873-59982140	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:59963185-59963406	A549	lung:	n/a	chr4:59963289-59963300
36	CEBPB	chr4:59991901-59992246	H1-hESC	embryonic stem cell:	n/a	chr4:59992073-59992082 chr4:59992073-59992082 chr4:59992071-59992084 chr4:59992073-59992082 chr4:59992071-59992082
37	CEBPB	chr4:59957078-59957161	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:60069581-60069860	A549	lung:	n/a	chr4:60069699-60069710
39	CEBPB	chr4:59988912-59989167	A549	lung:	n/a	chr4:59989020-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989022-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989020-59989031
40	CEBPB	chr4:59991903-59992218	Hela-S3	cervix:	n/a	chr4:59992073-59992082 chr4:59992073-59992082 chr4:59992071-59992084 chr4:59992073-59992082 chr4:59992071-59992082
41	CEBPB	chr4:60066672-60067062	MCF-7	breast:	n/a	chr4:60066902-60066915 chr4:60066902-60066913 chr4:60066904-60066915
42	CEBPB	chr4:59925618-59926106	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr4:60027045-60027342	IMR90	lung:	n/a	chr4:60027214-60027225
44	CEBPB	chr4:60027115-60027368	H1-hESC	embryonic stem cell:	n/a	chr4:60027214-60027225
45	CEBPB	chr4:59988870-59989208	IMR90	lung:	n/a	chr4:59989020-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989022-59989033 chr4:59989022-59989031 chr4:59989022-59989031 chr4:59989020-59989031
46	CHD1	chr4:59983408-59983429	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:60026840-60026990	GM12874	blood:	n/a	n/a
48	CTCF	chr4:60026960-60027110	GM12870	blood:	n/a	n/a
49	CTCF	chr4:59960300-59960450	GM12875	blood:	n/a	chr4:59960397-59960415 chr4:59960336-59960344 chr4:59960399-59960420
50	CTCF	chr4:60048438-60048483	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:60001000-60001050	AG04450	lung:	fetal
2	chr4:60001000-60001050	MCF-7	breast:	n/a
3	chr4:60001000-60001050	SKMC	muscle:	n/a
4	chr4:60001000-60001050	H1-hESC	embryonic stem cell:	embryo
5	chr4:60001000-60001050	PFSK-1	brain:	n/a
6	chr4:60001000-60001050	HCT-116	colon:	n/a
7	chr4:60001000-60001050	HRPEpiC	eye:	n/a
8	chr4:60001000-60001050	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:60001000-60001050	GM12892	blood:	n/a
10	chr4:60001000-60001050	PrEC	prostate:	n/a
11	chr4:60001000-60001050	K562	blood:	n/a
12	chr4:60001000-60001050	BE2_C	brain:	n/a
13	chr4:60001000-60001050	Jurkat	blood:	n/a
14	chr4:60001000-60001050	CMK	blood:	n/a
15	chr4:60001000-60001050	HRCEpiC	kidney:	n/a
16	chr4:60001000-60001050	IMR90	lung:	fetal
17	chr4:60001000-60001050	SK-N-MC	brain:	n/a
18	chr4:60001000-60001050	LNCaP	prostate:	n/a
19	chr4:60001000-60001050	ovcar-3	ovarian:	n/a
20	chr4:60001000-60001050	HUVEC	blood vessel:	n/a
21	chr4:60001000-60001050	HCPEpiC	choroid plexus:	n/a
22	chr4:60001000-60001050	MCF10A-Er-Src	breast:	n/a
23	chr4:60001000-60001050	HepG2	liver:	n/a
24	chr4:60001000-60001050	HIPEpiC	eye:	n/a
25	chr4:60001000-60001050	Hela-S3	cervix:	n/a
26	chr4:60001000-60001050	AG09309	skin:	n/a
27	chr4:60001000-60001050	Caco-2	colon:	n/a
28	chr4:60001000-60001050	ProgFib	skin:	n/a
29	chr4:60001000-60001050	AG04449	skin:	fetal
30	chr4:60001000-60001050	Hepatocyte	liver:	n/a
31	chr4:60001000-60001050	SAEC	small airway:	n/a
32	chr4:60001000-60001050	HCF	heart:	n/a
33	chr4:60001000-60001050	ECC-1	luminal epithelium:	n/a
34	chr4:60001000-60001050	HRE	kidney:	n/a
35	chr4:60001000-60001050	NB4	blood:	n/a
36	chr4:60001000-60001050	AG10803	skin:	n/a
37	chr4:60001000-60001050	T-47D	breast:	n/a
38	chr4:60001000-60001050	A549	lung:	n/a
39	chr4:60001000-60001050	NT2-D1	testis:	n/a
40	chr4:60001000-60001050	HEK293	kidney:	embryo
41	chr4:60001000-60001050	GM12891	blood:	n/a
42	chr4:60001000-60001050	SK-N-SH	brain:	n/a
43	chr4:60001000-60001050	HCM	heart:	n/a
44	chr4:60001000-60001050	NH-A	brain:	n/a
45	chr4:60001000-60001050	AoSMC	blood vessel:	n/a
46	chr4:60001000-60001050	NHBE	bronchial:	n/a
47	chr4:60001000-60001050	RPTEC	kidney:	n/a
48	chr4:60001000-60001050	SK-N-SH_RA	brain:	n/a
49	chr4:60001000-60001050	BJ	skin:	n/a
50	chr4:60001000-60001050	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:60079114..60081147-chr4:60084061..60086552,2	MCF-7	breast:
2	chr4:59952219..59954148-chr4:59969899..59971579,2	K562	blood:
3	chr4:59915929..59917798-chr4:59918941..59921861,2	MCF-7	breast:
4	chr4:60043552..60045132-chr4:60047786..60049460,2	K562	blood:
5	chr4:59952219..59954148-chr4:59969899..59971579,2	K562	blood:
6	chr4:60043552..60045132-chr4:60047786..60049460,2	K562	blood:
7	chr4:59915929..59917798-chr4:59918941..59921861,2	MCF-7	breast:
8	chr4:59909700..59911681-chr4:59912339..59914598,2	MCF-7	breast:
9	chr4:59959700..59961456-chr4:59961992..59964536,2	MCF-7	breast:
10	chr4:59959700..59961456-chr4:59961992..59964536,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPHN3-7	chr4:60041591-60041864	XLOC_003552
2	lnc-IGFBP7-6	chr4:59940898-59940974	ENSG00000250375
3	lnc-IGFBP7-6	chr4:59940898-59940960	XLOC_003963
4	lnc-IGFBP7-6	chr4:59913667-59913853	XLOC_003963
5	lnc-IGFBP7-6	chr4:59913667-59913853	ENSG00000250375
6	lnc-LPHN3-7	chr4:60018552-60018604	XLOC_003552

Variant related genes	Relation type
ENSG00000250375	TF binding region
ENSG00000249111	TF binding region
ENSG00000250375	CpG island
ENSG00000249111	CpG island
TTC30A	miRNA target sites
HELZ	miRNA target sites

Extended variants
information (count: 1987 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28753828	chr4:59916428-59916429	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183543167	chr4:59916430-59916431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77627551	chr4:59916434-59916435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142786730	chr4:59916438-59916439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541512719	chr4:59916453-59916454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368198723	chr4:59916454-59916455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563326828	chr4:59916474-59916475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530401007	chr4:59916487-59916488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35144580	chr4:59916621-59916622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs73194845	chr4:59916633-59916634	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs2036098	chr4:59916674-59916675	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs73194846	chr4:59916736-59916737	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs6812746	chr4:59916771-59916772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543911162	chr4:59925814-59925815	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs577389670	chr4:59925826-59925827	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs113889450	chr4:59925915-59925916	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs111742480	chr4:59925916-59925917	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs560172628	chr4:59925962-59925963	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs2333730	chr4:59926051-59926052	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs111392869	chr4:59926061-59926062	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561118432	chr4:59926063-59926064	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115026205	chr4:59926110-59926111	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201943557	chr4:59926120-59926121	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369835698	chr4:59926121-59926122	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs199502947	chr4:59926124-59926125	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3034271	chr4:59926125-59926126	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138678177	chr4:59926156-59926157	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2088196	chr4:59926182-59926183	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532716696	chr4:59926183-59926184	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551507854	chr4:59926202-59926203	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566526241	chr4:59926203-59926204	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533647007	chr4:59926204-59926205	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549002173	chr4:59926205-59926206	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149327120	chr4:59926230-59926231	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115496600	chr4:59926235-59926236	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112464340	chr4:59926252-59926253	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2088195	chr4:59926261-59926262	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577425461	chr4:59926315-59926316	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147442491	chr4:59926316-59926317	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553550493	chr4:59926324-59926325	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561409585	chr4:59926326-59926327	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542742538	chr4:59926345-59926346	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561364911	chr4:59926352-59926353	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192425646	chr4:59926366-59926367	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2088194	chr4:59926419-59926420	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs565079631	chr4:59926428-59926429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532754104	chr4:59926431-59926432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540267609	chr4:59926443-59926444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73194867	chr4:59926487-59926488	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs527414878	chr4:59926520-59926521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	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
Multiple myeloma	16616336	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
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:59916400-59916800	Enhancers	HMEC	breast
2	chr4:59925800-59926200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:59925800-59926400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:59926000-59926400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:59926400-59927000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:59928800-59929400	Enhancers	Fetal Heart	heart
7	chr4:59929000-59930400	Enhancers	Placenta Amnion	Placenta Amnion
8	chr4:59934400-59935400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:59952200-59952600	Enhancers	Brain Hippocampus Middle	brain
10	chr4:59952600-59953000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:59957000-59957200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:59957000-59958000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:59957000-59958200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:59957200-59957400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:59957200-59957600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:59957200-59957600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:59957200-59957800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:59957200-59958000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr4:59957200-59958200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:59957400-59958000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:59957800-59958200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr4:59963600-59964200	Active TSS	A549	lung
23	chr4:59975800-59977600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:59977600-59977800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:59985000-59986200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr4:59985000-59987200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:59985400-59987000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr4:59986000-59986400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:59986200-59987000	Enhancers	A549	lung
30	chr4:59986200-59988200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:59986400-59986800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr4:59986400-59987200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:59986800-59987000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:59986800-59987000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:59987000-59988200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr4:59987000-59991000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr4:59987200-59988200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr4:59987200-59990800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:59988200-59988400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:59988200-59988400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:59988200-59988600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:59990800-59991200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:59991000-59991200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:59991200-59992200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:59992200-59993800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:59992200-59995000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:59993600-59994000	Enhancers	Placenta Amnion	Placenta Amnion
48	chr4:59994000-59995000	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr4:59995000-59995200	Enhancers	Placenta Amnion	Placenta Amnion
50	chr4:59999800-60002000	Enhancers	HUES48 Cell Line	embryonic stem cell

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