Variant report

Variant	nsv1029818
Chromosome Location	chr4:188208634-188424431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:670)
CpG islands
(count:611)
Chromatin interactive
region (count:16)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
2	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
3	CBX3	chr4:188301159-188301792	HCT-116	colon:	n/a	n/a
4	CEBPB	chr4:188406167-188406450	A549	lung:	n/a	n/a
5	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
6	CEBPB	chr4:188337469-188337769	A549	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
7	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
8	CEBPB	chr4:188317722-188317931	HepG2	liver:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
9	CEBPB	chr4:188234147-188234350	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:188301323-188301523	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:188263083-188263269	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:188253347-188253499	Hela-S3	cervix:	n/a	chr4:188253450-188253461
13	CEBPB	chr4:188295952-188296114	HepG2	liver:	n/a	chr4:188296003-188296014 chr4:188296003-188296016
14	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:188213364-188213403	K562	blood:	n/a	n/a
16	CEBPB	chr4:188301254-188301599	MCF-7	breast:	n/a	n/a
17	CEBPB	chr4:188301252-188301594	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
20	CEBPB	chr4:188349162-188349196	H1-hESC	embryonic stem cell:	n/a	chr4:188349183-188349194
21	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
22	CEBPB	chr4:188253393-188253593	HepG2	liver:	n/a	chr4:188253450-188253461
23	CEBPB	chr4:188254417-188254534	K562	blood:	n/a	n/a
24	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
25	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
26	CEBPB	chr4:188337488-188337650	K562	blood:	n/a	chr4:188337610-188337621
27	CEBPB	chr4:188223685-188224011	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:188309832-188310058	IMR90	lung:	n/a	chr4:188309977-188309986
29	CEBPB	chr4:188254254-188254599	IMR90	lung:	n/a	chr4:188254404-188254415
30	CEBPB	chr4:188254264-188254489	HepG2	liver:	n/a	chr4:188254404-188254415
31	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
32	CEBPB	chr4:188301254-188301597	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
34	CEBPB	chr4:188254340-188254476	A549	lung:	n/a	chr4:188254404-188254415
35	CEBPB	chr4:188337419-188337771	IMR90	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
36	CTCF	chr4:188337973-188338107	HepG2	liver:	n/a	n/a
37	CTCF	chr4:188301380-188301530	HRE	kidney:	n/a	n/a
38	CTCF	chr4:188249940-188250090	GM12864	blood:	n/a	n/a
39	CTCF	chr4:188301300-188301450	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr4:188301340-188301490	HEK293	kidney:	n/a	n/a
41	CTCF	chr4:188301300-188301450	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr4:188301301-188301509	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:188301320-188301470	AG10803	skin:	n/a	n/a
44	CTCF	chr4:188301320-188301470	AG04449	skin:	n/a	n/a
45	CTCF	chr4:188337940-188338090	GM12873	blood:	n/a	n/a
46	CTCF	chr4:188301340-188301490	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr4:188301282-188301522	Gliobla	brain:	n/a	n/a
48	CTCF	chr4:188301300-188301450	AG09319	gingival:	n/a	n/a
49	CTCF	chr4:188338000-188338150	HCT-116	colon:	n/a	n/a
50	CTCF	chr4:188301400-188301550	WI-38	lung:	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	chr4:188401038-188401088	SKMC	muscle:	n/a
2	chr4:188401038-188401088	SKMC	muscle:	n/a
3	chr4:188256765-188256815	SAEC	small airway:	n/a
4	chr4:188223108-188223158	BJ	skin:	n/a
5	chr4:188256708-188256758	SK-N-SH	brain:	n/a
6	chr4:188423066-188423116	HCM	heart:	n/a
7	chr4:188256708-188256758	MCF10A-Er-Src	breast:	n/a
8	chr4:188256765-188256815	T-47D	breast:	n/a
9	chr4:188223108-188223158	LNCaP	prostate:	n/a
10	chr4:188398437-188398487	AG09319	gingival:	n/a
11	chr4:188256637-188256687	PFSK-1	brain:	n/a
12	chr4:188398437-188398487	SAEC	small airway:	n/a
13	chr4:188398437-188398487	HCM	heart:	n/a
14	chr4:188230390-188230440	AG10803	skin:	n/a
15	chr4:188314314-188314364	Hela-S3	cervix:	n/a
16	chr4:188423066-188423116	GM12891	blood:	n/a
17	chr4:188401038-188401088	MCF-7	breast:	n/a
18	chr4:188401038-188401088	NHBE	bronchial:	n/a
19	chr4:188230390-188230440	SK-N-SH	brain:	n/a
20	chr4:188256637-188256687	HCPEpiC	choroid plexus:	n/a
21	chr4:188230390-188230440	Jurkat	blood:	n/a
22	chr4:188314314-188314364	HCT-116	colon:	n/a
23	chr4:188391387-188391437	HRE	kidney:	n/a
24	chr4:188256765-188256815	MCF10A-Er-Src	breast:	n/a
25	chr4:188256708-188256758	AoSMC	blood vessel:	n/a
26	chr4:188314314-188314364	AG04449	skin:	fetal
27	chr4:188398437-188398487	Jurkat	blood:	n/a
28	chr4:188398437-188398487	Caco-2	colon:	n/a
29	chr4:188398437-188398487	MCF10A-Er-Src	breast:	n/a
30	chr4:188256637-188256687	Hela-S3	cervix:	n/a
31	chr4:188398437-188398487	ProgFib	skin:	n/a
32	chr4:188256637-188256687	GM12891	blood:	n/a
33	chr4:188391387-188391437	HEK293	kidney:	embryo
34	chr4:188230390-188230440	NB4	blood:	n/a
35	chr4:188401038-188401088	IMR90	lung:	fetal
36	chr4:188223108-188223158	IMR90	lung:	fetal
37	chr4:188223108-188223158	HL-60	blood:	n/a
38	chr4:188391387-188391437	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:188314314-188314364	HNPCEpiC	eye:	n/a
40	chr4:188314314-188314364	HMEC	breast:	n/a
41	chr4:188401038-188401088	GM12878	blood:	n/a
42	chr4:188256708-188256758	IMR90	lung:	fetal
43	chr4:188314314-188314364	LNCaP	prostate:	n/a
44	chr4:188401038-188401088	Jurkat	blood:	n/a
45	chr4:188423066-188423116	ECC-1	luminal epithelium:	n/a
46	chr4:188391387-188391437	HCF	heart:	n/a
47	chr4:188423066-188423116	U87	brain:	n/a
48	chr4:188256637-188256687	HUVEC	blood vessel:	n/a
49	chr4:188391387-188391437	AG04450	lung:	fetal
50	chr4:188391387-188391437	HIPEpiC	eye:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
2	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
3	chr4:188278385..188280812-chr4:188281318..188282901,2	K562	blood:
4	chr4:188343831..188346613-chr4:188349550..188352474,2	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	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
9	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
10	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
11	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
12	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
13	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
14	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
15	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
16	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAT1-3	chr4:188225237-188225621	XLOC_004217
2	lnc-ZFP42-13	chr4:188228509-188228694	NONHSAT099691
3	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
4	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
5	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
6	lnc-ZFP42-13	chr4:188237423-188237596	NONHSAT099691
7	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
8	lnc-FAT1-3	chr4:188225792-188226855	XLOC_004217
9	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
10	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
11	lnc-ZFP42-4	chr4:188344049-188344151	XLOC_003828
12	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
13	lnc-ZFP42-5	chr4:188334718-188334865	ENSG00000250620
14	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
15	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
16	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
17	lnc-ZFP42-4	chr4:188351216-188351539	XLOC_003828
18	lnc-FAT1-3	chr4:188230336-188230836	XLOC_004217
19	lnc-FAT1-3	chr4:188228260-188228423	XLOC_004217
20	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
21	lnc-ZFP42-6	chr4:188291802-188291929	XLOC_003826
22	lnc-ZFP42-6	chr4:188292838-188293075	XLOC_003826
23	lnc-ZFP42-6	chr4:188292449-188292580	XLOC_003826
24	lnc-ZFP42-13	chr4:188251486-188251546	NONHSAT099691
25	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
26	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
27	lnc-ZFP42-13	chr4:188252448-188253478	NONHSAT099691
28	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620

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: 6452 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6452 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547652464	chr4:188208672-188208673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566968573	chr4:188208674-188208675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112425625	chr4:188208698-188208699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188143595	chr4:188208699-188208700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569247488	chr4:188208718-188208719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373345501	chr4:188208796-188208797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181297540	chr4:188208800-188208801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115447274	chr4:188208836-188208837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559618820	chr4:188208871-188208872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9998520	chr4:188208906-188208907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534125510	chr4:188208988-188208989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147721644	chr4:188208999-188209000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189007560	chr4:188209012-188209013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576489803	chr4:188209044-188209045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539536257	chr4:188209113-188209114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181703840	chr4:188209151-188209152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575969032	chr4:188209163-188209164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533485093	chr4:188209164-188209165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9998820	chr4:188209182-188209183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs561954174	chr4:188209220-188209221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs36006072	chr4:188209226-188209227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572416841	chr4:188209245-188209246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541177932	chr4:188209292-188209293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564280362	chr4:188209322-188209323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35672947	chr4:188209373-188209374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532464307	chr4:188209397-188209398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187209999	chr4:188209456-188209457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138399868	chr4:188209462-188209463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531724926	chr4:188209474-188209475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548227243	chr4:188209500-188209501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568370920	chr4:188209526-188209527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534231110	chr4:188209580-188209581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs72721162	chr4:188209652-188209653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs571048400	chr4:188209667-188209668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1462080	chr4:188209692-188209693	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs13126851	chr4:188209701-188209702	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs192457761	chr4:188209723-188209724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149634165	chr4:188209743-188209744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555406112	chr4:188209745-188209746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572326918	chr4:188209766-188209767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs13126675	chr4:188209788-188209789	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs13126689	chr4:188209801-188209802	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs182079735	chr4:188209802-188209803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13126500	chr4:188209814-188209815	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs563561286	chr4:188209826-188209827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562997287	chr4:188209881-188209882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185423020	chr4:188209917-188209918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs56070525	chr4:188209918-188209919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561765584	chr4:188209965-188209966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558029423	chr4:188209979-188209980	Weak transcription Enhancers	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:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188205000-188210200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr4:188205000-188210200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr4:188205000-188210400	Weak transcription	Osteobl	bone
4	chr4:188207800-188209600	Weak transcription	Fetal Intestine Large	intestine
5	chr4:188208200-188210400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:188208600-188210200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:188209600-188211000	Enhancers	Fetal Intestine Large	intestine
8	chr4:188210200-188210400	Enhancers	Muscle Satellite Cultured Cells	--
9	chr4:188210200-188210600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:188210200-188211000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:188210200-188211000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:188210200-188211000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:188210400-188210600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr4:188210400-188210600	Enhancers	Osteobl	bone
15	chr4:188210400-188210800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:188210400-188211000	Enhancers	NHEK	skin
17	chr4:188210600-188210800	Enhancers	Muscle Satellite Cultured Cells	--
18	chr4:188210600-188212200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr4:188210800-188211000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
20	chr4:188210800-188216200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:188211000-188211600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr4:188211000-188215400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr4:188211000-188215600	Weak transcription	NHEK	skin
24	chr4:188211600-188216000	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr4:188212200-188212600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:188212600-188217200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:188215200-188216400	Enhancers	Fetal Lung	lung
28	chr4:188215400-188215600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:188215400-188215600	Enhancers	Fetal Stomach	stomach
30	chr4:188215400-188216600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:188215600-188216200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr4:188215600-188216600	Enhancers	NHEK	skin
33	chr4:188216000-188216400	Enhancers	Muscle Satellite Cultured Cells	--
34	chr4:188216200-188216400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:188216200-188216400	Enhancers	Fetal Stomach	stomach
36	chr4:188216200-188216600	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr4:188216200-188216600	Enhancers	HMEC	breast
38	chr4:188216200-188216800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:188216400-188223000	Weak transcription	Fetal Lung	lung
40	chr4:188216800-188217400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:188217200-188217400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr4:188217200-188217800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:188217200-188217800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:188217400-188218000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:188217800-188230400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:188218000-188218600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:188218600-188227600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:188218600-188234000	Weak transcription	Aorta	Aorta
49	chr4:188219600-188219800	Enhancers	Fetal Kidney	kidney
50	chr4:188219800-188223600	Weak transcription	Fetal Kidney	kidney

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