Variant report

Variant	nsv879658
Chromosome Location	chr4:100123776-100131163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:93)
CpG islands
(count:184)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:93 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:100126236-100127065	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:100126305-100126657	HepG2	liver:	n/a	chr4:100126486-100126497
3	CEBPB	chr4:100126297-100127136	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126486-100126497 chr4:100126944-100126955 chr4:100126888-100126900
4	CEBPB	chr4:100125068-100125268	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:100128577-100128913	H1-hESC	embryonic stem cell:	n/a	chr4:100128748-100128759
6	CEBPB	chr4:100126335-100126686	MCF-7	breast:	n/a	chr4:100126486-100126497
7	CEBPB	chr4:100126313-100127116	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126486-100126497 chr4:100126944-100126955 chr4:100126888-100126900
8	CEBPB	chr4:100128570-100128804	HepG2	liver:	n/a	chr4:100128748-100128759
9	CEBPB	chr4:100125099-100125246	K562	blood:	n/a	n/a
10	CEBPB	chr4:100125021-100125340	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:100126351-100126650	H1-hESC	embryonic stem cell:	n/a	chr4:100126486-100126497
12	CEBPB	chr4:100126778-100127013	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126944-100126955 chr4:100126888-100126900
13	CEBPB	chr4:100128569-100128934	IMR90	lung:	n/a	chr4:100128748-100128759
14	CEBPB	chr4:100123717-100123973	IMR90	lung:	n/a	chr4:100123756-100123767 chr4:100123756-100123767
15	CEBPB	chr4:100126333-100127073	IMR90	lung:	n/a	chr4:100126944-100126955 chr4:100126486-100126497 chr4:100126944-100126955 chr4:100126888-100126900
16	CEBPB	chr4:100128587-100128935	HepG2	liver:	n/a	chr4:100128748-100128759
17	CEBPB	chr4:100126828-100127018	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126944-100126955 chr4:100126888-100126900
18	CEBPB	chr4:100125038-100125274	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:100126346-100126581	HepG2	liver:	n/a	chr4:100126486-100126497
20	CEBPB	chr4:100128604-100128837	K562	blood:	n/a	chr4:100128748-100128759
21	CEBPB	chr4:100128629-100128898	A549	lung:	n/a	chr4:100128748-100128759
22	CTCF	chr4:100124980-100125130	BJ	skin:	n/a	n/a
23	CTCF	chr4:100126260-100126410	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr4:100126340-100126490	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:100126320-100126470	GM12878	blood:	n/a	n/a
26	CTCF	chr4:100126320-100126470	HCFaa	heart:	n/a	n/a
27	CTCF	chr4:100126380-100126530	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr4:100126360-100126510	AG04449	skin:	n/a	n/a
29	CTCF	chr4:100126260-100126410	HMF	breast:	n/a	n/a
30	CTCF	chr4:100126240-100126390	HFF	foreskin:	n/a	n/a
31	CTCF	chr4:100126300-100126450	AG10803	skin:	n/a	n/a
32	CTCF	chr4:100126320-100126470	HEK293	kidney:	n/a	n/a
33	CTCF	chr4:100126340-100126490	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr4:100126360-100126510	AG04450	lung:	n/a	n/a
35	CTCF	chr4:100126320-100126470	HMF	breast:	n/a	n/a
36	CTCF	chr4:100126300-100126450	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr4:100126340-100126490	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr4:100126320-100126470	NHLF	lung:	n/a	n/a
39	CTCF	chr4:100126160-100126310	HPF	lung:	n/a	n/a
40	CTCF	chr4:100126300-100126450	SAEC	small airway:	n/a	n/a
41	CTCF	chr4:100126400-100126550	HPF	lung:	n/a	n/a
42	CTCF	chr4:100126300-100126450	AG04449	skin:	n/a	n/a
43	CTCF	chr4:100126340-100126490	BJ	skin:	n/a	n/a
44	CTCF	chr4:100126380-100126530	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr4:100126180-100126330	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:100126460-100126610	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr4:100126320-100126470	HPF	lung:	n/a	n/a
48	CTCF	chr4:100126320-100126470	HCM	heart:	n/a	n/a
49	CTCF	chr4:100126240-100126390	HepG2	liver:	n/a	n/a
50	CTCF	chr4:100126360-100126510	HPAF	blood vessel:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100128186-100128236	NHBE	bronchial:	n/a
2	chr4:100128186-100128236	NHBE	bronchial:	n/a
3	chr4:100128186-100128236	AG04450	lung:	fetal
4	chr4:100125999-100126049	HepG2	liver:	n/a
5	chr4:100130470-100130520	GM12892	blood:	n/a
6	chr4:100130470-100130520	HRCEpiC	kidney:	n/a
7	chr4:100125999-100126049	AG04450	lung:	fetal
8	chr4:100125999-100126049	HNPCEpiC	eye:	n/a
9	chr4:100130470-100130520	AG04449	skin:	fetal
10	chr4:100125999-100126049	GM12878	blood:	n/a
11	chr4:100125999-100126049	LNCaP	prostate:	n/a
12	chr4:100128186-100128236	PANC-1	pancreas:	n/a
13	chr4:100125999-100126049	SK-N-SH	brain:	n/a
14	chr4:100125999-100126049	AG10803	skin:	n/a
15	chr4:100130470-100130520	PrEC	prostate:	n/a
16	chr4:100125999-100126049	SKMC	muscle:	n/a
17	chr4:100125999-100126049	AG09319	gingival:	n/a
18	chr4:100128186-100128236	HEEpiC	esophagus:	n/a
19	chr4:100130470-100130520	LNCaP	prostate:	n/a
20	chr4:100128186-100128236	H1-hESC	embryonic stem cell:	embryo
21	chr4:100125999-100126049	NHBE	bronchial:	n/a
22	chr4:100128186-100128236	ovcar-3	ovarian:	n/a
23	chr4:100130470-100130520	HNPCEpiC	eye:	n/a
24	chr4:100130470-100130520	HRE	kidney:	n/a
25	chr4:100130470-100130520	Jurkat	blood:	n/a
26	chr4:100125999-100126049	ProgFib	skin:	n/a
27	chr4:100130470-100130520	GM19239	blood:	n/a
28	chr4:100125999-100126049	ovcar-3	ovarian:	n/a
29	chr4:100125999-100126049	NH-A	brain:	n/a
30	chr4:100128186-100128236	HepG2	liver:	n/a
31	chr4:100130470-100130520	Caco-2	colon:	n/a
32	chr4:100130470-100130520	AG10803	skin:	n/a
33	chr4:100128186-100128236	HMEC	breast:	n/a
34	chr4:100125999-100126049	HL-60	blood:	n/a
35	chr4:100125999-100126049	AG09309	skin:	n/a
36	chr4:100125999-100126049	IMR90	lung:	fetal
37	chr4:100128186-100128236	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:100125999-100126049	HCF	heart:	n/a
39	chr4:100128186-100128236	NHDF-neo	bronchial:	n/a
40	chr4:100125999-100126049	ECC-1	luminal epithelium:	n/a
41	chr4:100128186-100128236	GM06990	blood:	n/a
42	chr4:100125999-100126049	SAEC	small airway:	n/a
43	chr4:100125999-100126049	BJ	skin:	n/a
44	chr4:100130470-100130520	H1-hESC	embryonic stem cell:	embryo
45	chr4:100125999-100126049	HMEC	breast:	n/a
46	chr4:100130470-100130520	MCF-7	breast:	n/a
47	chr4:100125999-100126049	SK-N-SH_RA	brain:	n/a
48	chr4:100128186-100128236	HRE	kidney:	n/a
49	chr4:100125999-100126049	HEEpiC	esophagus:	n/a
50	chr4:100130470-100130520	U87	brain:	n/a

No data

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METAP1-3	chr4:100125514-100125588	ENSG00000246090
2	lnc-METAP1-3	chr4:100125514-100125588	ENSG00000246090
3	lnc-METAP1-3	chr4:100125514-100125584	ENSG00000246090

No data

Variant related genes	Relation type
ADH6	TF binding region
ADH6	CpG island

Extended variants
information (count: 243 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:243 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2000864	chr4:100123776-100123777	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539828301	chr4:100123799-100123800	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551828695	chr4:100123827-100123828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374017764	chr4:100123835-100123836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1130921	chr4:100123877-100123878	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs150003925	chr4:100123921-100123922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192930858	chr4:100123932-100123933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574567666	chr4:100123955-100123956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28720167	chr4:100124047-100124048	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs553435768	chr4:100124119-100124120	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569090921	chr4:100124163-100124164	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28720166	chr4:100124170-100124171	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs545389232	chr4:100124173-100124174	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553079690	chr4:100124174-100124175	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576633024	chr4:100124200-100124201	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543763861	chr4:100124209-100124210	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184370277	chr4:100124308-100124309	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116429331	chr4:100124373-100124374	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187916376	chr4:100124381-100124382	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577558185	chr4:100124514-100124515	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551521624	chr4:100124521-100124522	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533512278	chr4:100124524-100124525	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566317390	chr4:100124543-100124544	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1130919	chr4:100124549-100124550	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551791912	chr4:100124584-100124585	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs28720165	chr4:100124622-100124623	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569961609	chr4:100124692-100124693	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1893883	chr4:100124716-100124717	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs1130918	chr4:100124730-100124731	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1130917	chr4:100124768-100124769	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549821746	chr4:100124802-100124803	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568377974	chr4:100124807-100124808	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192699523	chr4:100124834-100124835	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577090648	chr4:100124972-100124973	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184884270	chr4:100124992-100124993	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189318592	chr4:100125029-100125030	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566964283	chr4:100125043-100125044	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs28720164	chr4:100125087-100125088	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs180812733	chr4:100125119-100125120	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575972458	chr4:100125164-100125165	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546063132	chr4:100125193-100125194	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147697570	chr4:100125326-100125327	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201166785	chr4:100125334-100125335	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376058792	chr4:100125343-100125344	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370424785	chr4:100125361-100125362	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374434273	chr4:100125365-100125366	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200229133	chr4:100125395-100125396	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142327148	chr4:100125419-100125420	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146361551	chr4:100125420-100125421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147839189	chr4:100125528-100125529	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Autism	18414403	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
Hirschsprung''s Disease	21712996	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
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100108400-100141600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:100114200-100126400	Weak transcription	Aorta	Aorta
3	chr4:100115200-100129800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr4:100120200-100124000	Enhancers	HepG2	liver
5	chr4:100120600-100124600	Enhancers	Fetal Intestine Large	intestine
6	chr4:100120600-100127600	Enhancers	Fetal Intestine Small	intestine
7	chr4:100121400-100124200	Enhancers	Liver	Liver
8	chr4:100121600-100126200	Enhancers	Fetal Lung	lung
9	chr4:100122600-100127000	Enhancers	Adipose Nuclei	Adipose
10	chr4:100122800-100124200	Enhancers	Stomach Mucosa	stomach
11	chr4:100122800-100124400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:100123000-100123800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr4:100123000-100124000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:100123000-100124000	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr4:100123000-100125200	Enhancers	NHDF-Ad	bronchial
16	chr4:100123000-100127600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:100123200-100124000	Enhancers	Fetal Kidney	kidney
18	chr4:100123200-100124200	Enhancers	Duodenum Mucosa	Duodenum
19	chr4:100123200-100124400	Enhancers	NHLF	lung
20	chr4:100123400-100123800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:100123400-100124400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr4:100123400-100124400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr4:100123400-100124600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:100123400-100124600	Enhancers	Ovary	ovary
25	chr4:100123400-100124600	Enhancers	Small Intestine	intestine
26	chr4:100123400-100126400	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr4:100123600-100126400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr4:100123800-100124000	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:100123800-100124400	Enhancers	Placenta	Placenta
30	chr4:100123800-100124400	Enhancers	Fetal Stomach	stomach
31	chr4:100123800-100124600	Enhancers	Fetal Muscle Leg	muscle
32	chr4:100123800-100126000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr4:100123800-100128200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:100124000-100124600	Genic enhancers	HepG2	liver
35	chr4:100124000-100126000	Weak transcription	Fetal Kidney	kidney
36	chr4:100124000-100126200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:100124000-100126200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr4:100124000-100126400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:100124200-100124600	Enhancers	Left Ventricle	heart
40	chr4:100124200-100126200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr4:100124200-100126400	Weak transcription	Stomach Mucosa	stomach
42	chr4:100124200-100126600	Genic enhancers	Liver	Liver
43	chr4:100124400-100126200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:100124400-100126200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr4:100124400-100126200	Weak transcription	NHLF	lung
46	chr4:100124400-100126400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:100124600-100125200	Weak transcription	HepG2	liver
48	chr4:100124600-100125800	Weak transcription	Fetal Intestine Large	intestine
49	chr4:100124600-100126000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:100124600-100126000	Weak transcription	Small Intestine	intestine

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