Variant report

Variant	nsv596448
Chromosome Location	chr4:188201350-188411479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:637)
CpG islands
(count:611)
Chromatin interactive
region (count:15)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
2	CBX3	chr4:188301159-188301792	HCT-116	colon:	n/a	n/a
3	CEBPB	chr4:188337469-188337769	A549	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
4	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
5	CEBPB	chr4:188317722-188317931	HepG2	liver:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
6	CEBPB	chr4:188234147-188234350	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:188301323-188301523	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:188301252-188301594	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:188349162-188349196	H1-hESC	embryonic stem cell:	n/a	chr4:188349183-188349194
11	CEBPB	chr4:188254340-188254476	A549	lung:	n/a	chr4:188254404-188254415
12	CEBPB	chr4:188223685-188224011	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:188301254-188301599	MCF-7	breast:	n/a	n/a
14	CEBPB	chr4:188337419-188337771	IMR90	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
15	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
16	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
17	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
18	CEBPB	chr4:188254417-188254534	K562	blood:	n/a	n/a
19	CEBPB	chr4:188213364-188213403	K562	blood:	n/a	n/a
20	CEBPB	chr4:188406167-188406450	A549	lung:	n/a	n/a
21	CEBPB	chr4:188254254-188254599	IMR90	lung:	n/a	chr4:188254404-188254415
22	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
23	CEBPB	chr4:188309832-188310058	IMR90	lung:	n/a	chr4:188309977-188309986
24	CEBPB	chr4:188301254-188301597	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:188254264-188254489	HepG2	liver:	n/a	chr4:188254404-188254415
26	CEBPB	chr4:188263083-188263269	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:188253393-188253593	HepG2	liver:	n/a	chr4:188253450-188253461
28	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:188337488-188337650	K562	blood:	n/a	chr4:188337610-188337621
30	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
31	CEBPB	chr4:188295952-188296114	HepG2	liver:	n/a	chr4:188296003-188296014 chr4:188296003-188296016
32	CEBPB	chr4:188253347-188253499	Hela-S3	cervix:	n/a	chr4:188253450-188253461
33	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
34	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
35	CTCF	chr4:188331560-188331645	GM10266	blood:	n/a	n/a
36	CTCF	chr4:188338004-188338041	NHEK	skin:	n/a	n/a
37	CTCF	chr4:188243984-188244028	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:188301340-188301490	HepG2	liver:	n/a	n/a
39	CTCF	chr4:188301300-188301450	HVMF	connective:	n/a	n/a
40	CTCF	chr4:188301286-188301618	K562	blood:	n/a	n/a
41	CTCF	chr4:188228280-188228430	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr4:188301300-188301450	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr4:188338100-188338250	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr4:188301347-188301449	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr4:188301380-188301530	A549	lung:	n/a	n/a
46	CTCF	chr4:188338040-188338190	HRE	kidney:	n/a	n/a
47	CTCF	chr4:188301360-188301510	HMF	breast:	n/a	n/a
48	CTCF	chr4:188301340-188301490	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:188301280-188301430	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr4:188243900-188244050	HepG2	liver:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188208070-188208120	NB4	blood:	n/a
2	chr4:188208070-188208120	NB4	blood:	n/a
3	chr4:188314314-188314364	NH-A	brain:	n/a
4	chr4:188208070-188208120	MCF-7	breast:	n/a
5	chr4:188256637-188256687	HCPEpiC	choroid plexus:	n/a
6	chr4:188256708-188256758	NB4	blood:	n/a
7	chr4:188391387-188391437	HEEpiC	esophagus:	n/a
8	chr4:188223108-188223158	SK-N-MC	brain:	n/a
9	chr4:188223108-188223158	SK-N-SH_RA	brain:	n/a
10	chr4:188208070-188208120	PrEC	prostate:	n/a
11	chr4:188398437-188398487	RPTEC	kidney:	n/a
12	chr4:188230390-188230440	HCF	heart:	n/a
13	chr4:188230390-188230440	U87	brain:	n/a
14	chr4:188256637-188256687	AG10803	skin:	n/a
15	chr4:188391387-188391437	HRE	kidney:	n/a
16	chr4:188401038-188401088	HRE	kidney:	n/a
17	chr4:188208070-188208120	RPTEC	kidney:	n/a
18	chr4:188208070-188208120	HMEC	breast:	n/a
19	chr4:188256708-188256758	HIPEpiC	eye:	n/a
20	chr4:188256708-188256758	AG09309	skin:	n/a
21	chr4:188391387-188391437	HAEpiC	amniotic membrane:	n/a
22	chr4:188230390-188230440	HCM	heart:	n/a
23	chr4:188223108-188223158	HCPEpiC	choroid plexus:	n/a
24	chr4:188256708-188256758	MCF10A-Er-Src	breast:	n/a
25	chr4:188256765-188256815	HAEpiC	amniotic membrane:	n/a
26	chr4:188314314-188314364	AG04449	skin:	fetal
27	chr4:188256637-188256687	HRPEpiC	eye:	n/a
28	chr4:188391387-188391437	HUVEC	blood vessel:	n/a
29	chr4:188401038-188401088	K562	blood:	n/a
30	chr4:188314314-188314364	SK-N-SH	brain:	n/a
31	chr4:188256637-188256687	HepG2	liver:	n/a
32	chr4:188230390-188230440	AG04450	lung:	fetal
33	chr4:188208070-188208120	ovcar-3	ovarian:	n/a
34	chr4:188391387-188391437	Jurkat	blood:	n/a
35	chr4:188398437-188398487	NHDF-neo	bronchial:	n/a
36	chr4:188398437-188398487	BJ	skin:	n/a
37	chr4:188391387-188391437	CMK	blood:	n/a
38	chr4:188256765-188256815	AG10803	skin:	n/a
39	chr4:188401038-188401088	GM12892	blood:	n/a
40	chr4:188256708-188256758	MCF-7	breast:	n/a
41	chr4:188256765-188256815	NH-A	brain:	n/a
42	chr4:188256708-188256758	HCPEpiC	choroid plexus:	n/a
43	chr4:188208070-188208120	HRCEpiC	kidney:	n/a
44	chr4:188398437-188398487	BE2_C	brain:	n/a
45	chr4:188256765-188256815	SKMC	muscle:	n/a
46	chr4:188256708-188256758	HCF	heart:	n/a
47	chr4:188256708-188256758	NH-A	brain:	n/a
48	chr4:188256708-188256758	AG04449	skin:	fetal
49	chr4:188223108-188223158	BJ	skin:	n/a
50	chr4:188208070-188208120	AG04450	lung:	fetal

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
2	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
3	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
4	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
5	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
6	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
7	chr4:188278385..188280812-chr4:188281318..188282901,2	K562	blood:
8	chr4:188278385..188280812-chr4:188281318..188282901,2	K562	blood:
9	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
10	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:
11	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
12	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
13	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
14	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
15	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-13	chr4:188252448-188253478	NONHSAT099691
2	lnc-FAT1-3	chr4:188228260-188228423	XLOC_004217
3	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
4	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
5	lnc-ZFP42-13	chr4:188251486-188251546	NONHSAT099691
6	lnc-ZFP42-5	chr4:188334718-188334865	ENSG00000250620
7	lnc-FAT1-3	chr4:188225792-188226855	XLOC_004217
8	lnc-FAT1-3	chr4:188230336-188230836	XLOC_004217
9	lnc-ZFP42-13	chr4:188237423-188237596	NONHSAT099691
10	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
11	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
12	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
13	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
14	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
15	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
16	lnc-ZFP42-4	chr4:188344049-188344151	XLOC_003828
17	lnc-ZFP42-6	chr4:188291802-188291929	XLOC_003826
18	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
19	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
20	lnc-FAT1-3	chr4:188225237-188225621	XLOC_004217
21	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
22	lnc-ZFP42-6	chr4:188292449-188292580	XLOC_003826
23	lnc-ZFP42-4	chr4:188351216-188351539	XLOC_003828
24	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
25	lnc-ZFP42-6	chr4:188292838-188293075	XLOC_003826
26	lnc-ZFP42-13	chr4:188228509-188228694	NONHSAT099691

No data

Variant related genes	Relation type
ENSG00000251643	TF binding region
ENSG00000250620	TF binding region
ENSG00000250042	TF binding region
ENSG00000250658	TF binding region
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ENSG00000250042	CpG island
ENSG00000250658	CpG island
ENSG00000251643	chromatin interactions

Extended variants
information (count: 6337 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6337 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4862792	chr4:188201350-188201351	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12645570	chr4:188201393-188201394	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs144214189	chr4:188201437-188201438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568179289	chr4:188201489-188201490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147733911	chr4:188201518-188201519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553170536	chr4:188201534-188201535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573409286	chr4:188201535-188201536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6843554	chr4:188201562-188201563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144968041	chr4:188201563-188201564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190129673	chr4:188201575-188201576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113645618	chr4:188201579-188201580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368922846	chr4:188201582-188201583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148986401	chr4:188201587-188201588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574953566	chr4:188201589-188201590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192039498	chr4:188201600-188201601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6843234	chr4:188201615-188201616	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs532123826	chr4:188201622-188201623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6553054	chr4:188201651-188201652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs562154377	chr4:188201652-188201653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71595144	chr4:188201664-188201665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370983849	chr4:188201665-188201666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184923268	chr4:188201668-188201669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189305596	chr4:188201675-188201676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79697439	chr4:188201688-188201689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368724391	chr4:188201725-188201726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141169458	chr4:188201737-188201738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144981468	chr4:188201776-188201777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566966664	chr4:188201802-188201803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138832947	chr4:188201818-188201819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141831471	chr4:188201836-188201837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575722814	chr4:188201849-188201850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75582961	chr4:188201858-188201859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1903626	chr4:188201898-188201899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs575120280	chr4:188201924-188201925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145589186	chr4:188201967-188201968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560318303	chr4:188201981-188201982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58197727	chr4:188202031-188202032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1903627	chr4:188202037-188202038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs112390180	chr4:188202052-188202053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545510727	chr4:188202136-188202137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149514888	chr4:188202149-188202150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1903628	chr4:188202155-188202156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143923641	chr4:188202201-188202202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574860095	chr4:188202252-188202253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78817927	chr4:188202262-188202263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572181615	chr4:188202263-188202264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547567046	chr4:188202313-188202314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181899735	chr4:188202314-188202315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148221851	chr4:188202361-188202362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552723606	chr4:188202362-188202363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cognitive impairment	21505072	CNVD

Chromatin state (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188198400-188204400	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr4:188198600-188207400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:188198800-188203800	Weak transcription	Fetal Lung	lung
4	chr4:188203400-188203800	Enhancers	Fetal Muscle Leg	muscle
5	chr4:188203400-188207600	Weak transcription	NHLF	lung
6	chr4:188203600-188204000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:188203800-188204200	Weak transcription	Fetal Muscle Leg	muscle
8	chr4:188203800-188204600	Enhancers	Fetal Lung	lung
9	chr4:188203800-188205200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:188204000-188204400	Active TSS	Adipose Nuclei	Adipose
11	chr4:188204000-188204400	Weak transcription	Osteobl	bone
12	chr4:188204200-188204400	Enhancers	HSMMtube	muscle
13	chr4:188204200-188204800	Enhancers	Fetal Muscle Leg	muscle
14	chr4:188204400-188204600	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr4:188204400-188204800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:188204400-188205000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:188204400-188205000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:188204400-188205000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr4:188204400-188205000	Enhancers	Muscle Satellite Cultured Cells	--
20	chr4:188204400-188205000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr4:188204400-188205000	Enhancers	HSMM	muscle
22	chr4:188204400-188205000	Flanking Active TSS	HSMMtube	muscle
23	chr4:188204400-188205000	Enhancers	Osteobl	bone
24	chr4:188204600-188205000	Enhancers	Adipose Nuclei	Adipose
25	chr4:188204600-188207600	Weak transcription	Fetal Lung	lung
26	chr4:188204800-188207000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:188205000-188206200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:188205000-188210200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:188205000-188210200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr4:188205000-188210400	Weak transcription	Osteobl	bone
31	chr4:188206400-188206600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr4:188207400-188207800	Bivalent Enhancer	Fetal Intestine Large	intestine
33	chr4:188207400-188208600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:188207600-188208000	Enhancers	Placenta Amnion	Placenta Amnion
35	chr4:188207600-188208200	Enhancers	NHLF	lung
36	chr4:188207600-188208400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:188207600-188208400	Enhancers	Fetal Kidney	kidney
38	chr4:188207600-188208400	Enhancers	Fetal Lung	lung
39	chr4:188207800-188208000	Enhancers	Ovary	ovary
40	chr4:188207800-188209600	Weak transcription	Fetal Intestine Large	intestine
41	chr4:188208200-188210400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:188208600-188210200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:188209600-188211000	Enhancers	Fetal Intestine Large	intestine
44	chr4:188210200-188210400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr4:188210200-188210600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:188210200-188211000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:188210200-188211000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr4:188210200-188211000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:188210400-188210600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr4:188210400-188210600	Enhancers	Osteobl	bone

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