Variant report

Variant	nsv879838
Chromosome Location	chr4:118681261-118753062
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:219)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:219 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:118724917-118725250	IMR90	lung:	n/a	chr4:118725141-118725152 chr4:118725142-118725153 chr4:118725141-118725154
2	CEBPB	chr4:118698909-118699357	ECC-1	luminal epithelium:	n/a	chr4:118699065-118699076
3	CEBPB	chr4:118724936-118725263	A549	lung:	n/a	chr4:118725141-118725152 chr4:118725142-118725153 chr4:118725141-118725154
4	CEBPB	chr4:118724947-118725285	HepG2	liver:	n/a	chr4:118725141-118725152 chr4:118725142-118725153 chr4:118725141-118725154
5	CEBPB	chr4:118698957-118699307	ECC-1	luminal epithelium:	n/a	chr4:118699065-118699076
6	CREB1	chr4:118689878-118690070	GM12878	blood:	n/a	n/a
7	CTCF	chr4:118693200-118693350	HepG2	liver:	n/a	n/a
8	CTCF	chr4:118693052-118693497	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr4:118693224-118693297	MCF-7	breast:	n/a	n/a
10	CTCF	chr4:118693160-118693310	NHEK	skin:	n/a	n/a
11	CTCF	chr4:118704580-118704730	HCT-116	colon:	n/a	n/a
12	CTCF	chr4:118693000-118693270	HCT-116	colon:	n/a	n/a
13	CTCF	chr4:118692957-118693001	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr4:118693133-118693406	GM12878	blood:	n/a	n/a
15	CTCF	chr4:118692931-118693433	HCT-116	colon:	n/a	n/a
16	CTCF	chr4:118693200-118693350	HMEC	breast:	n/a	n/a
17	CTCF	chr4:118692900-118693050	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr4:118692934-118693059	Gliobla	brain:	n/a	n/a
19	CTCF	chr4:118693020-118693170	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr4:118692940-118693090	GM12864	blood:	n/a	n/a
21	CTCF	chr4:118692880-118693030	GM12874	blood:	n/a	n/a
22	CTCF	chr4:118693160-118693310	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr4:118693140-118693290	HAc	cerebellar:	n/a	n/a
24	CTCF	chr4:118692860-118693010	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr4:118693080-118693230	GM12864	blood:	n/a	n/a
26	CTCF	chr4:118692880-118693030	GM12871	blood:	n/a	n/a
27	CTCF	chr4:118693180-118693330	HMEC	breast:	n/a	n/a
28	CTCF	chr4:118718089-118718161	K562	blood:	n/a	n/a
29	CTCF	chr4:118693140-118693290	A549	lung:	n/a	n/a
30	CTCF	chr4:118692934-118693027	NHEK	skin:	n/a	n/a
31	CTCF	chr4:118693234-118693286	HepG2	liver:	n/a	n/a
32	CTCF	chr4:118693060-118693210	HL-60	blood:	n/a	n/a
33	CTCF	chr4:118692920-118693070	GM12872	blood:	n/a	n/a
34	CTCF	chr4:118692887-118693027	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:118692940-118693090	GM12865	blood:	n/a	n/a
36	CTCF	chr4:118692860-118693010	NB4	blood:	n/a	n/a
37	CTCF	chr4:118685380-118685530	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr4:118692900-118693050	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr4:118692940-118693090	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr4:118692920-118693070	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr4:118693140-118693290	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr4:118692900-118693050	GM12875	blood:	n/a	n/a
43	CTCF	chr4:118692947-118693011	GM19238	blood:	n/a	n/a
44	CTCF	chr4:118693140-118693290	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr4:118692900-118693050	AG04450	lung:	n/a	n/a
46	CTCF	chr4:118692880-118693030	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:118745675-118745766	Fibrobl	skin:	n/a	n/a
48	CTCF	chr4:118693215-118693311	LNCaP	prostate:	n/a	n/a
49	CTCF	chr4:118752640-118752790	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:118692880-118693030	GM12875	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:118736876-118736926	PFSK-1	brain:	n/a
2	chr4:118736876-118736926	AG04449	skin:	fetal
3	chr4:118736876-118736926	K562	blood:	n/a
4	chr4:118736876-118736926	HL-60	blood:	n/a
5	chr4:118736876-118736926	SK-N-SH_RA	brain:	n/a
6	chr4:118736876-118736926	AoSMC	blood vessel:	n/a
7	chr4:118736876-118736926	RPTEC	kidney:	n/a
8	chr4:118736876-118736926	SK-N-MC	brain:	n/a
9	chr4:118736876-118736926	GM06990	blood:	n/a
10	chr4:118736876-118736926	HepG2	liver:	n/a
11	chr4:118736876-118736926	HIPEpiC	eye:	n/a
12	chr4:118736876-118736926	IMR90	lung:	fetal
13	chr4:118736876-118736926	U87	brain:	n/a
14	chr4:118736876-118736926	NH-A	brain:	n/a
15	chr4:118736876-118736926	Caco-2	colon:	n/a
16	chr4:118736876-118736926	NHDF-neo	bronchial:	n/a
17	chr4:118736876-118736926	NHBE	bronchial:	n/a
18	chr4:118736876-118736926	A549	lung:	n/a
19	chr4:118736876-118736926	GM12878	blood:	n/a
20	chr4:118736876-118736926	MCF-7	breast:	n/a
21	chr4:118736876-118736926	HCT-116	colon:	n/a
22	chr4:118736876-118736926	SK-N-SH	brain:	n/a
23	chr4:118736876-118736926	BJ	skin:	n/a
24	chr4:118736876-118736926	NT2-D1	testis:	n/a
25	chr4:118736876-118736926	HEK293	kidney:	embryo
26	chr4:118736876-118736926	AG09319	gingival:	n/a
27	chr4:118736876-118736926	NB4	blood:	n/a
28	chr4:118736876-118736926	HPAEpiC	pulmonary alveolar:	n/a
29	chr4:118736876-118736926	ProgFib	skin:	n/a
30	chr4:118736876-118736926	BE2_C	brain:	n/a
31	chr4:118736876-118736926	GM19239	blood:	n/a
32	chr4:118736876-118736926	CMK	blood:	n/a
33	chr4:118736876-118736926	HRCEpiC	kidney:	n/a
34	chr4:118736876-118736926	ovcar-3	ovarian:	n/a
35	chr4:118736876-118736926	HRE	kidney:	n/a
36	chr4:118736876-118736926	SAEC	small airway:	n/a
37	chr4:118736876-118736926	HAEpiC	amniotic membrane:	n/a
38	chr4:118736876-118736926	HUVEC	blood vessel:	n/a
39	chr4:118736876-118736926	PANC-1	pancreas:	n/a
40	chr4:118736876-118736926	MCF10A-Er-Src	breast:	n/a
41	chr4:118736876-118736926	HEEpiC	esophagus:	n/a
42	chr4:118736876-118736926	SKMC	muscle:	n/a
43	chr4:118736876-118736926	PrEC	prostate:	n/a
44	chr4:118736876-118736926	HCF	heart:	n/a
45	chr4:118736876-118736926	AG09309	skin:	n/a
46	chr4:118736876-118736926	HNPCEpiC	eye:	n/a
47	chr4:118736876-118736926	H1-hESC	embryonic stem cell:	embryo
48	chr4:118736876-118736926	Hela-S3	cervix:	n/a
49	chr4:118736876-118736926	Jurkat	blood:	n/a
50	chr4:118736876-118736926	AG04450	lung:	fetal

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	4:118706981-118715929..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo
2	chr4:118746718..118748894-chr4:118754229..118756238,2	K562	blood:
3	4:118320200-118324249..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo
4	4:118320200-118324249..4:118735152-118737645	GM12878	blood:
5	chr4:118667596..118669692-chr4:118697119..118700111,2	K562	blood:
6	4:118559839-118566258..4:118706981-118715929	Hela-S3	cervix:
7	4:118319405-118319911..4:118687551-118689447	H1-hESC	embryonic stem cell:	embryo
8	chr4:118740653..118742964-chr4:118748170..118749888,2	K562	blood:
9	4:118357351-118360885..4:118687551-118689447	H1-hESC	embryonic stem cell:	embryo
10	chr4:118740653..118742964-chr4:118748170..118749888,2	K562	blood:
11	4:118667424-118683756..4:118706981-118715929	Hela-S3	cervix:
12	4:118454469-118464115..4:118706981-118715929	H1-hESC	embryonic stem cell:	embryo
13	4:118387398-118387878..4:118667424-118683756	Hela-S3	cervix:
14	chr4:118692914..118693777-chr4:118955037..118955632,2	MCF-7	breast:
15	chr16:2201497..2202322-chr4:118720038..118720674,2	HCT-116	colon:
16	4:118291537-118294071..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo
17	4:118667424-118683756..4:118706981-118715929	Hela-S3	cervix:
18	chr4:118745601..118747892-chr4:118762895..118764468,2	K562	blood:
19	4:118414019-118416561..4:118706981-118715929	Hela-S3	cervix:
20	4:118706981-118715929..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
ENSG00000229565	TF binding region
ENSG00000229565	CpG island
ENSG00000164100	chromatin interactions
ENSG00000167964	chromatin interactions
ENSG00000229565	chromatin interactions

Extended variants
information (count: 1917 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1917 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13135259	chr4:118691409-118691410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183949815	chr4:118691431-118691432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187926329	chr4:118691438-118691439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532234219	chr4:118691474-118691475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552446913	chr4:118691504-118691505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17869337	chr4:118691574-118691575	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528385217	chr4:118691590-118691591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548430772	chr4:118691609-118691610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs17867476	chr4:118691644-118691645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192853806	chr4:118691663-118691664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34697848	chr4:118691700-118691701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537077132	chr4:118691705-118691706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550546848	chr4:118691746-118691747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184829471	chr4:118691768-118691769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548695854	chr4:118691771-118691772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558077495	chr4:118691776-118691777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190069717	chr4:118691821-118691822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573348611	chr4:118691824-118691825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535792220	chr4:118691837-118691838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6848529	chr4:118691839-118691840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12640843	chr4:118691842-118691843	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs28945385	chr4:118691887-118691888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577015451	chr4:118691891-118691892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376114729	chr4:118691901-118691902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545872886	chr4:118691920-118691921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574005611	chr4:118691934-118691935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542778739	chr4:118691988-118691989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs17869686	chr4:118691995-118691996	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548059870	chr4:118692006-118692007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs17866875	chr4:118692007-118692008	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs17861254	chr4:118692068-118692069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530707630	chr4:118692116-118692117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550610123	chr4:118692131-118692132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181554379	chr4:118692137-118692138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28945123	chr4:118692152-118692153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572815283	chr4:118692935-118692936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186191763	chr4:118692967-118692968	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs1459538	chr4:118692970-118692971	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1459539	chr4:118693007-118693008	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs190871079	chr4:118693047-118693048	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563011695	chr4:118693052-118693053	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564171810	chr4:118693084-118693085	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150110088	chr4:118693116-118693117	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533179885	chr4:118693203-118693204	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs552530867	chr4:118693328-118693329	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs10011404	chr4:118693329-118693330	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs181153066	chr4:118693334-118693335	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529324876	chr4:118693346-118693347	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs549601452	chr4:118693364-118693365	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560451949	chr4:118693365-118693366	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118691400-118691800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:118691800-118692200	Enhancers	Liver	Liver
3	chr4:118691800-118692200	Enhancers	Brain Anterior Caudate	brain
4	chr4:118693000-118693600	Enhancers	Placenta Amnion	Placenta Amnion
5	chr4:118693000-118694000	Enhancers	Dnd41	blood
6	chr4:118693400-118694000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:118693400-118694600	Enhancers	Gastric	stomach
8	chr4:118693800-118694800	Enhancers	Stomach Mucosa	stomach
9	chr4:118694000-118694600	Enhancers	Fetal Muscle Trunk	muscle
10	chr4:118694600-118705000	Weak transcription	Gastric	stomach
11	chr4:118694800-118698600	Weak transcription	Stomach Mucosa	stomach
12	chr4:118698600-118699200	Enhancers	Stomach Mucosa	stomach
13	chr4:118698600-118699600	Enhancers	NH-A	brain
14	chr4:118700600-118701000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:118701000-118704600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:118704600-118705600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:118704800-118705400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:118704800-118705600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr4:118705000-118705200	Enhancers	Gastric	stomach
20	chr4:118705000-118705400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:118705000-118705400	Enhancers	Fetal Stomach	stomach
22	chr4:118705000-118705600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr4:118705600-118707600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:118705600-118714800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr4:118706400-118707800	Enhancers	Dnd41	blood
26	chr4:118707600-118708400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:118708400-118708600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:118711000-118711800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:118711200-118712000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr4:118711200-118712000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr4:118711400-118711800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:118711400-118712000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:118711400-118712000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr4:118711400-118712200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:118712200-118719800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:118713400-118714400	Enhancers	Stomach Mucosa	stomach
37	chr4:118714400-118714800	Weak transcription	Stomach Mucosa	stomach
38	chr4:118714600-118715600	Enhancers	Fetal Lung	lung
39	chr4:118714600-118715800	Enhancers	Dnd41	blood
40	chr4:118714600-118715800	Enhancers	NHEK	skin
41	chr4:118714600-118716400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:118714800-118715600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:118714800-118715800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr4:118714800-118716000	Enhancers	HMEC	breast
45	chr4:118714800-118716400	Enhancers	Stomach Mucosa	stomach
46	chr4:118715000-118715600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:118715200-118715600	Enhancers	Fetal Heart	heart
48	chr4:118715200-118716000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:118715400-118716000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:118715800-118717800	Weak transcription	Dnd41	blood

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