Variant report

Variant	nsv1008963
Chromosome Location	chr4:107282656-107384924
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	ARID3A	chr4:107286679-107287176	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:107365773-107366027	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:107290661-107290836	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:107290660-107290984	K562	blood:	n/a	n/a
5	ARID3A	chr4:107343316-107343362	HepG2	liver:	n/a	n/a
6	ATF1	chr4:107286804-107287045	K562	blood:	n/a	n/a
7	BACH1	chr4:107361305-107361442	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:107312398-107312411	K562	blood:	n/a	n/a
9	CBX3	chr4:107290594-107290983	HCT-116	colon:	n/a	n/a
10	CBX3	chr4:107316829-107317067	K562	blood:	n/a	n/a
11	CBX3	chr4:107316724-107317113	HCT-116	colon:	n/a	n/a
12	CEBPB	chr4:107284841-107285124	HepG2	liver:	n/a	chr4:107284975-107284986
13	CEBPB	chr4:107286736-107287044	A549	lung:	n/a	n/a
14	CEBPB	chr4:107286629-107287076	A549	lung:	n/a	n/a
15	CEBPB	chr4:107331713-107332073	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:107286660-107287035	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:107310928-107311171	HepG2	liver:	n/a	chr4:107311071-107311082
18	CEBPB	chr4:107310940-107311195	IMR90	lung:	n/a	chr4:107311071-107311082
19	CEBPB	chr4:107286676-107287128	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:107286725-107286997	K562	blood:	n/a	n/a
21	CEBPB	chr4:107286746-107286915	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:107315696-107315897	HepG2	liver:	n/a	chr4:107315784-107315795
23	CEBPB	chr4:107333890-107334181	HepG2	liver:	n/a	chr4:107334015-107334024 chr4:107334070-107334081 chr4:107334013-107334024 chr4:107334015-107334026 chr4:107333986-107333997
24	CEBPB	chr4:107286712-107286929	K562	blood:	n/a	n/a
25	CEBPB	chr4:107381521-107381694	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:107286666-107287092	HCT-116	colon:	n/a	n/a
27	CEBPB	chr4:107286651-107287616	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:107286677-107287016	A549	lung:	n/a	n/a
29	CEBPB	chr4:107286569-107287188	HCT-116	colon:	n/a	n/a
30	CEBPB	chr4:107286709-107287076	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:107333894-107334165	A549	lung:	n/a	chr4:107334015-107334024 chr4:107334070-107334081 chr4:107334013-107334024 chr4:107334015-107334026 chr4:107333986-107333997
32	CHD2	chr4:107310623-107310901	K562	blood:	n/a	n/a
33	CTCF	chr4:107290720-107290870	GM12868	blood:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
34	CTCF	chr4:107290720-107290870	HRPEpiC	eye:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
35	CTCF	chr4:107290740-107290890	BE2_C	brain:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
36	CTCF	chr4:107290530-107291051	HCT-116	colon:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
37	CTCF	chr4:107290720-107290870	GM12865	blood:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
38	CTCF	chr4:107290740-107290890	SAEC	small airway:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
39	CTCF	chr4:107290539-107291170	SK-N-SH	brain:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
40	CTCF	chr4:107290597-107291089	IMR90	lung:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
41	CTCF	chr4:107290764-107290830	MCF-7	breast:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
42	CTCF	chr4:107290720-107290870	AG04450	lung:	n/a	chr4:107290803-107290816 chr4:107290804-107290813 chr4:107290800-107290818
43	CTCF	chr4:107290400-107290550	NHEK	skin:	n/a	n/a
44	CTCF	chr4:107290670-107290947	HUVEC	blood vessel:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
45	CTCF	chr4:107290700-107290850	GM12871	blood:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
46	CTCF	chr4:107290652-107290953	Medullo	brain:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
47	CTCF	chr4:107290720-107290870	HUVEC	blood vessel:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
48	CTCF	chr4:107290700-107290850	HMF	breast:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
49	CTCF	chr4:107290587-107291044	HepG2	liver:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818
50	CTCF	chr4:107290720-107290870	A549	lung:	n/a	chr4:107290804-107290813 chr4:107290803-107290816 chr4:107290800-107290818

No.	Distal block	Cell Line	Cell type
1	chr4:107290301..107292526-chr4:107422827..107424058,19	MCF-7	breast:
2	chr4:107287024..107287560-chr5:153670760..153671260,2	Hela-S3	cervix:
3	chr4:107303398..107305509-chr4:107317461..107319625,2	K562	blood:
4	chr4:107235080..107237825-chr4:107304121..107307055,2	K562	blood:
5	chr4:107275880..107279456-chr4:107281523..107285039,4	K562	blood:
6	chr4:107349397..107350031-chr4:107362531..107363489,2	MCF-7	breast:
7	chr4:107290770..107291311-chr4:107424769..107425646,2	MCF-7	breast:
8	chr4:107335618..107338970-chr4:107353446..107357718,3	K562	blood:
9	chr4:107288668..107290808-chr4:107293759..107296062,2	K562	blood:
10	chr4:107303398..107305509-chr4:107317461..107319625,2	K562	blood:
11	chr4:107349397..107350031-chr4:107362531..107363489,2	MCF-7	breast:
12	chr4:107290348..107291609-chr4:107422851..107424531,10	MCF-7	breast:
13	chr4:107288668..107290808-chr4:107293759..107296062,2	K562	blood:
14	chr4:107335618..107338970-chr4:107353446..107357718,3	K562	blood:
15	chr4:107288592..107289255-chr4:107423410..107423938,2	MCF-7	breast:
16	chr4:107290453..107290976-chr4:107421149..107422009,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AIMP1-1	chr4:107370168-107370249	XLOC_003636
2	lnc-AIMP1-1	chr4:107378159-107378478	XLOC_003636
3	lnc-AIMP1-1	chr4:107370168-107370249	XLOC_003636
4	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636
5	lnc-AIMP1-1	chr4:107354683-107354911	XLOC_003636
6	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636
7	lnc-AIMP1-1	chr4:107354868-107354911	XLOC_003636
8	lnc-AIMP1-1	chr4:107378159-107378384	XLOC_003636
9	lnc-AIMP1-1	chr4:107374383-107374556	XLOC_003636
10	lnc-AIMP1-1	chr4:107354683-107354929	XLOC_003636
11	lnc-AIMP1-1	chr4:107354710-107354732	XLOC_003636
12	lnc-AIMP1-1	chr4:107374383-107374605	XLOC_003636
13	lnc-AIMP1-1	chr4:107374383-107374556	XLOC_003636
14	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636
15	lnc-AIMP1-1	chr4:107370168-107370244	XLOC_003636
16	lnc-AIMP1-1	chr4:107378159-107378384	XLOC_003636
17	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636
18	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636
19	lnc-AIMP1-1	chr4:107354683-107354929	XLOC_003636
20	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636
21	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636
22	lnc-AIMP1-1	chr4:107354683-107354929	XLOC_003636
23	lnc-AIMP1-1	chr4:107354683-107354911	XLOC_003636
24	lnc-AIMP1-1	chr4:107354781-107354911	XLOC_003636
25	lnc-AIMP1-1	chr4:107355769-107355858	XLOC_003636

Variant related genes	Relation type
ENSG00000222333	TF binding region
ENSG00000249613	TF binding region
GIMD1	TF binding region
ENSG00000249613	chromatin interactions
ENSG00000145348	chromatin interactions
ENSG00000164022	chromatin interactions
ENSG00000222333	chromatin interactions
RAB6A	miRNA target sites
NFAT5	miRNA target sites
RAB5C	miRNA target sites
BMPR2	miRNA target sites
NFATC1	miRNA target sites
RAB5B	miRNA target sites
UHRF1	miRNA target sites

Extended variants
information (count: 2358 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2358 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2949626	chr4:107282656-107282657	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547642863	chr4:107282698-107282699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370946729	chr4:107282705-107282706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs17275217	chr4:107282717-107282718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs529238901	chr4:107282767-107282768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549761541	chr4:107282769-107282770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569756729	chr4:107282791-107282792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535467813	chr4:107282796-107282797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150596584	chr4:107282819-107282820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548206320	chr4:107282824-107282825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533716830	chr4:107282841-107282842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139685436	chr4:107282868-107282869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184142498	chr4:107282893-107282894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539587599	chr4:107282930-107282931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556185944	chr4:107282966-107282967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190697878	chr4:107282975-107282976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181801135	chr4:107283028-107283029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113512421	chr4:107283050-107283051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541723999	chr4:107283053-107283054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528646410	chr4:107283076-107283077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77372970	chr4:107283104-107283105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572733450	chr4:107283140-107283141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371667171	chr4:107283147-107283148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541244533	chr4:107283180-107283181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564750782	chr4:107283181-107283182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533242969	chr4:107283214-107283215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73839458	chr4:107283235-107283236	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs536601857	chr4:107283240-107283241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563446935	chr4:107283249-107283250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571906115	chr4:107283259-107283260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549376531	chr4:107283309-107283310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73839459	chr4:107283349-107283350	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs527609315	chr4:107283392-107283393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547270083	chr4:107283431-107283432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570698490	chr4:107283443-107283444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115577778	chr4:107283460-107283461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556246740	chr4:107283490-107283491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149341885	chr4:107283510-107283511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188886612	chr4:107283537-107283538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555369278	chr4:107283548-107283549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34527808	chr4:107283551-107283552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558447476	chr4:107283561-107283562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537659713	chr4:107283564-107283565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572647320	chr4:107283577-107283578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73839460	chr4:107283614-107283615	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs558177602	chr4:107283632-107283633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577770459	chr4:107283660-107283661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576691470	chr4:107283668-107283669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543632096	chr4:107283672-107283673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35814742	chr4:107283737-107283738	Weak transcription Enhancers	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107260800-107285400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr4:107270600-107286200	Weak transcription	HepG2	liver
3	chr4:107270800-107283200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr4:107270800-107290600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr4:107271200-107286400	Weak transcription	Fetal Intestine Large	intestine
6	chr4:107273000-107286600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:107273000-107286600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:107280400-107286400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr4:107280800-107285400	Weak transcription	HSMM	muscle
10	chr4:107280800-107285400	Weak transcription	NHLF	lung
11	chr4:107280800-107285400	Weak transcription	Osteobl	bone
12	chr4:107280800-107285600	Weak transcription	HSMMtube	muscle
13	chr4:107280800-107286200	Weak transcription	NH-A	brain
14	chr4:107281000-107285200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:107281000-107286200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr4:107281200-107285400	Weak transcription	NHDF-Ad	bronchial
17	chr4:107283200-107283800	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr4:107283400-107283800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:107283800-107285400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:107283800-107286600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr4:107285200-107288600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:107285400-107285800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:107285400-107285800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:107285400-107286000	Enhancers	Fetal Muscle Leg	muscle
25	chr4:107285400-107286600	Enhancers	NHDF-Ad	bronchial
26	chr4:107285400-107287800	Enhancers	NHLF	lung
27	chr4:107285400-107287800	Enhancers	Osteobl	bone
28	chr4:107285400-107288400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:107285400-107288400	Enhancers	HSMM	muscle
30	chr4:107285600-107285800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:107285600-107285800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:107285600-107285800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:107285600-107285800	Enhancers	Psoas Muscle	Psoas
34	chr4:107285600-107287600	Enhancers	HSMMtube	muscle
35	chr4:107285600-107287800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:107285800-107286600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:107285800-107286800	Weak transcription	Colon Smooth Muscle	Colon
38	chr4:107285800-107287000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:107285800-107287000	Weak transcription	Psoas Muscle	Psoas
40	chr4:107285800-107288200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:107286000-107287000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:107286200-107287000	Enhancers	NH-A	brain
43	chr4:107286200-107287400	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr4:107286200-107287400	Enhancers	HepG2	liver
45	chr4:107286200-107287600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:107286200-107287800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr4:107286200-107287800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr4:107286200-107287800	Enhancers	HUVEC	blood vessel
49	chr4:107286200-107288800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:107286400-107286600	Enhancers	Fetal Intestine Large	intestine

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