Variant report

Variant	nsv525385
Chromosome Location	chr4:110395146-110466413
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:144)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:144 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:110401131-110401202	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:110416852-110416872	K562	blood:	n/a	n/a
3	BHLHE40	chr4:110416711-110417011	K562	blood:	n/a	n/a
4	CEBPB	chr4:110433705-110433951	HepG2	liver:	n/a	chr4:110433866-110433877
5	CEBPB	chr4:110416574-110416948	K562	blood:	n/a	n/a
6	CEBPB	chr4:110416716-110416944	K562	blood:	n/a	n/a
7	CEBPB	chr4:110433799-110433905	K562	blood:	n/a	chr4:110433866-110433877
8	CEBPB	chr4:110442730-110442774	K562	blood:	n/a	n/a
9	CEBPB	chr4:110432843-110432992	K562	blood:	n/a	n/a
10	CEBPB	chr4:110418021-110418324	HepG2	liver:	n/a	chr4:110418137-110418148
11	CEBPB	chr4:110433740-110433917	IMR90	lung:	n/a	chr4:110433866-110433877
12	CEBPB	chr4:110432770-110433093	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:110432750-110433005	MCF-7	breast:	n/a	n/a
14	CEBPD	chr4:110416611-110417129	K562	blood:	n/a	n/a
15	CEBPD	chr4:110416591-110417025	K562	blood:	n/a	n/a
16	CTCF	chr4:110436353-110436453	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr4:110442658-110442705	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:110452660-110452810	MCF-7	breast:	n/a	chr4:110452785-110452803 chr4:110452780-110452801
19	CTCF	chr4:110464480-110464630	HAc	cerebellar:	n/a	n/a
20	CTCF	chr4:110405234-110405269	Lung_OC	lung:	n/a	n/a
21	CTCF	chr4:110442633-110442712	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:110426804-110426907	IMR90	lung:	n/a	n/a
23	CTCF	chr4:110442600-110442750	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:110463581-110463626	LNCaP	prostate:	n/a	n/a
25	CTCF	chr4:110452640-110452910	HMF	breast:	n/a	chr4:110452785-110452803 chr4:110452780-110452801
26	E2F4	chr4:110426580-110426772	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr4:110411838-110412038	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr4:110431803-110431962	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr4:110418861-110419026	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr4:110440893-110441093	MCF10A-Er-Src	breast:	n/a	n/a
31	EP300	chr4:110445122-110445137	K562	blood:	n/a	n/a
32	EP300	chr4:110416763-110417006	K562	blood:	n/a	n/a
33	FOXA1	chr4:110432666-110432815	T-47D	breast:	n/a	n/a
34	GATA1	chr4:110416379-110417180	K562	blood:	n/a	n/a
35	GATA1	chr4:110415092-110417190	PBDE	blood:	n/a	chr4:110415313-110415320 chr4:110415309-110415325 chr4:110415311-110415323 chr4:110415313-110415320 chr4:110415306-110415327 chr4:110415312-110415322 chr4:110415313-110415320 chr4:110415313-110415322
36	GATA2	chr4:110416641-110416963	K562	blood:	n/a	n/a
37	GATA2	chr4:110432691-110433213	SH-SY5Y	brain:	n/a	chr4:110432847-110432863 chr4:110432847-110432863 chr4:110432845-110432866
38	GATA3	chr4:110437830-110438418	SK-N-SH	brain:	n/a	chr4:110438038-110438047
39	GATA3	chr4:110432543-110433150	SK-N-SH	brain:	n/a	chr4:110432847-110432863 chr4:110432847-110432863 chr4:110432845-110432866
40	GATA3	chr4:110411361-110411528	SH-SY5Y	brain:	n/a	chr4:110411408-110411418 chr4:110411408-110411417
41	GATA3	chr4:110432658-110432956	T-47D	breast:	n/a	chr4:110432847-110432863 chr4:110432847-110432863 chr4:110432845-110432866
42	GATA3	chr4:110432637-110433269	SK-N-SH	brain:	n/a	chr4:110432847-110432863 chr4:110432847-110432863 chr4:110432845-110432866
43	GATA3	chr4:110432821-110433250	SH-SY5Y	brain:	n/a	chr4:110432847-110432863 chr4:110432847-110432863 chr4:110432845-110432866
44	GATA3	chr4:110437773-110438385	SK-N-SH	brain:	n/a	chr4:110438038-110438047
45	GATA3	chr4:110433035-110433310	T-47D	breast:	n/a	n/a
46	GATA3	chr4:110432975-110433231	T-47D	breast:	n/a	n/a
47	JUN	chr4:110461426-110461625	K562	blood:	n/a	n/a
48	JUND	chr4:110416767-110416943	K562	blood:	n/a	n/a
49	KAP1	chr4:110411471-110411820	K562	blood:	n/a	n/a
50	MAFK	chr4:110427707-110427895	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110460898-110460948	SKMC	muscle:	n/a
2	chr4:110460898-110460948	ovcar-3	ovarian:	n/a
3	chr4:110460898-110460948	HEK293	kidney:	embryo
4	chr4:110460898-110460948	T-47D	breast:	n/a
5	chr4:110460898-110460948	AG10803	skin:	n/a
6	chr4:110460898-110460948	HCM	heart:	n/a
7	chr4:110460898-110460948	SAEC	small airway:	n/a
8	chr4:110460898-110460948	AG09319	gingival:	n/a
9	chr4:110460898-110460948	ProgFib	skin:	n/a
10	chr4:110460898-110460948	IMR90	lung:	fetal
11	chr4:110460898-110460948	AG04450	lung:	fetal
12	chr4:110460898-110460948	NHBE	bronchial:	n/a
13	chr4:110460898-110460948	NHDF-neo	bronchial:	n/a
14	chr4:110460898-110460948	HRCEpiC	kidney:	n/a
15	chr4:110460898-110460948	HepG2	liver:	n/a
16	chr4:110460898-110460948	BJ	skin:	n/a
17	chr4:110460898-110460948	H1-hESC	embryonic stem cell:	embryo
18	chr4:110460898-110460948	SK-N-SH	brain:	n/a
19	chr4:110460898-110460948	SK-N-MC	brain:	n/a
20	chr4:110460898-110460948	AoSMC	blood vessel:	n/a
21	chr4:110460898-110460948	HRE	kidney:	n/a
22	chr4:110460898-110460948	AG04449	skin:	fetal
23	chr4:110460898-110460948	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:110460898-110460948	PFSK-1	brain:	n/a
25	chr4:110460898-110460948	U87	brain:	n/a
26	chr4:110460898-110460948	MCF-7	breast:	n/a
27	chr4:110460898-110460948	CMK	blood:	n/a
28	chr4:110460898-110460948	GM19239	blood:	n/a
29	chr4:110460898-110460948	NH-A	brain:	n/a
30	chr4:110460898-110460948	HIPEpiC	eye:	n/a
31	chr4:110460898-110460948	BE2_C	brain:	n/a
32	chr4:110460898-110460948	Caco-2	colon:	n/a
33	chr4:110460898-110460948	HCT-116	colon:	n/a
34	chr4:110460898-110460948	HRPEpiC	eye:	n/a
35	chr4:110460898-110460948	HNPCEpiC	eye:	n/a
36	chr4:110460898-110460948	HMEC	breast:	n/a
37	chr4:110460898-110460948	Hepatocyte	liver:	n/a
38	chr4:110460898-110460948	RPTEC	kidney:	n/a
39	chr4:110460898-110460948	Jurkat	blood:	n/a
40	chr4:110460898-110460948	MCF10A-Er-Src	breast:	n/a
41	chr4:110460898-110460948	PANC-1	pancreas:	n/a
42	chr4:110460898-110460948	K562	blood:	n/a
43	chr4:110460898-110460948	SK-N-SH_RA	brain:	n/a
44	chr4:110460898-110460948	PrEC	prostate:	n/a
45	chr4:110460898-110460948	HAEpiC	amniotic membrane:	n/a
46	chr4:110460898-110460948	A549	lung:	n/a
47	chr4:110460898-110460948	GM12892	blood:	n/a
48	chr4:110460898-110460948	LNCaP	prostate:	n/a
49	chr4:110460898-110460948	HCF	heart:	n/a
50	chr4:110460898-110460948	GM12878	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:110461566..110463825-chr4:110465703..110468687,3	K562	blood:
2	chr11:118550919..118551712-chr4:110446873..110447532,2	MCF-7	breast:
3	chr4:110406792..110410897-chr4:110414033..110418121,4	MCF-7	breast:
4	chr4:110391073..110393458-chr4:110395121..110397973,3	K562	blood:
5	chr4:110418898..110420639-chr4:110427969..110430594,2	K562	blood:
6	chr4:110422366..110424452-chr4:110425566..110428111,2	K562	blood:
7	chr4:110400854..110403769-chr4:110406464..110409189,2	K562	blood:
8	chr4:110435524..110438522-chr4:110443269..110445686,2	K562	blood:
9	chr4:110381575..110383743-chr4:110417040..110418619,2	MCF-7	breast:
10	chr4:110353206..110355233-chr4:110452632..110454561,2	MCF-7	breast:
11	chr4:110418898..110420639-chr4:110427969..110430594,2	K562	blood:
12	chr4:110400854..110403769-chr4:110406464..110409189,2	K562	blood:
13	chr4:110384184..110389120-chr4:110389509..110396492,10	K562	blood:
14	chr4:110434896..110437050-chr4:110440887..110442437,2	K562	blood:
15	chr4:110434896..110437050-chr4:110440887..110442437,2	K562	blood:
16	chr4:110351897..110354482-chr4:110431012..110433361,3	MCF-7	breast:
17	chr4:110396923..110399404-chr4:110400868..110402670,2	K562	blood:
18	chr4:110456887..110459079-chr4:110460957..110462832,2	K562	blood:
19	chr4:110435524..110438522-chr4:110443269..110445686,2	K562	blood:
20	chr4:110435524..110439030-chr4:110443269..110448028,4	K562	blood:
21	chr4:110435524..110439030-chr4:110443269..110448028,4	K562	blood:
22	chr4:110411951..110414607-chr4:110416539..110418397,2	K562	blood:
23	chr4:110422366..110424452-chr4:110425566..110428111,2	K562	blood:
24	chr4:110452392..110452892-chr5:11840296..11840825,2	MCF-7	breast:
25	chr4:110396923..110399404-chr4:110400868..110402670,2	K562	blood:
26	chr4:110362207..110365023-chr4:110395130..110397808,3	K562	blood:
27	chr4:110456887..110459079-chr4:110460957..110462832,2	K562	blood:
28	chr4:110463063..110464866-chr4:110466518..110468456,2	MCF-7	breast:
29	chr4:110411951..110414607-chr4:110416539..110418397,2	K562	blood:
30	chr4:110387620..110389236-chr4:110394728..110397410,2	K562	blood:
31	chr4:110353208..110355443-chr4:110459517..110461072,2	K562	blood:
32	chr4:110461566..110463825-chr4:110465703..110468687,3	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-576-5p	chr4:110409869-110409890	MIMAT0003241
hsa-miR-576-3p	chr4:110409908-110409929	MIMAT0004796

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SEC24B	hsa-miR-30a-5p	chr4:110461239-110461260
2	SEC24B	hsa-miR-186-5p	chr4:110461153-110461177

Variant related genes	Relation type
MIR576	TF binding region
MIR576	CpG island
ENSG00000138802	chromatin interactions
ENSG00000207988	chromatin interactions
ENSG00000247950	chromatin interactions
RPL13A	Mature miRNA region
PNMA2	Mature miRNA region

Extended variants
information (count: 2535 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2535 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10516556	chr4:110395146-110395147	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541330489	chr4:110395197-110395198	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186966771	chr4:110395198-110395199	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371136630	chr4:110395224-110395225	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577713667	chr4:110395241-110395242	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367676596	chr4:110395266-110395267	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551480973	chr4:110395280-110395281	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35404930	chr4:110395297-110395298	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192054551	chr4:110395361-110395362	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10516557	chr4:110395406-110395407	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs542435027	chr4:110395458-110395459	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558754715	chr4:110395498-110395499	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562136844	chr4:110395531-110395532	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114974764	chr4:110395532-110395533	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575522308	chr4:110395546-110395547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183995653	chr4:110395553-110395554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs71594186	chr4:110395580-110395581	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555395230	chr4:110395581-110395582	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570765150	chr4:110395592-110395593	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533179713	chr4:110395623-110395624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546798755	chr4:110395625-110395626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368139371	chr4:110395725-110395726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543892246	chr4:110395737-110395738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570168827	chr4:110395738-110395739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535556439	chr4:110395779-110395780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555583377	chr4:110395790-110395791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185381608	chr4:110395800-110395801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149329985	chr4:110395823-110395824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558104929	chr4:110395826-110395827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577972819	chr4:110395860-110395861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574677901	chr4:110395861-110395862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144582796	chr4:110395866-110395867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189740427	chr4:110395873-110395874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559357344	chr4:110395874-110395875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139552379	chr4:110395876-110395877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541199797	chr4:110395912-110395913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564458078	chr4:110395945-110395946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541033902	chr4:110395972-110395973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78262578	chr4:110396045-110396046	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550179089	chr4:110396055-110396056	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182707600	chr4:110396090-110396091	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529430128	chr4:110396102-110396103	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541738609	chr4:110396125-110396126	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187315533	chr4:110396149-110396150	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112861575	chr4:110396150-110396151	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534827646	chr4:110396152-110396153	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557195517	chr4:110396163-110396164	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192905961	chr4:110396205-110396206	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559888520	chr4:110396221-110396222	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77784076	chr4:110396223-110396224	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	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
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
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110363600-110398400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:110378800-110415800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:110383400-110396000	Strong transcription	Fetal Thymus	thymus
4	chr4:110383400-110397600	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr4:110384800-110399800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr4:110384800-110401000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:110385400-110402800	Weak transcription	Brain Germinal Matrix	brain
8	chr4:110385400-110403000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:110385600-110415800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:110385600-110415800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr4:110385600-110415800	Weak transcription	Esophagus	oesophagus
12	chr4:110385800-110398200	Weak transcription	Fetal Intestine Small	intestine
13	chr4:110385800-110415600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:110385800-110415800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:110385800-110415800	Weak transcription	Colonic Mucosa	Colon
16	chr4:110386000-110395200	Weak transcription	Fetal Kidney	kidney
17	chr4:110386000-110415800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr4:110386200-110415800	Weak transcription	Lung	lung
19	chr4:110386200-110415800	Weak transcription	Spleen	Spleen
20	chr4:110386400-110398400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr4:110386400-110413600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr4:110386400-110415600	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr4:110386400-110415800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr4:110386600-110396000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:110386600-110402400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr4:110386600-110415600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr4:110386800-110398000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr4:110386800-110402400	Weak transcription	Fetal Lung	lung
29	chr4:110386800-110405200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr4:110386800-110415600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:110387000-110402200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr4:110387000-110402200	Weak transcription	Fetal Muscle Trunk	muscle
33	chr4:110387000-110402800	Weak transcription	Brain Angular Gyrus	brain
34	chr4:110387000-110415600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:110387000-110415800	Weak transcription	Fetal Brain Male	brain
36	chr4:110387000-110415800	Weak transcription	Fetal Brain Female	brain
37	chr4:110387000-110416400	Weak transcription	Right Ventricle	heart
38	chr4:110387200-110415600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr4:110387600-110415600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr4:110388000-110403600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:110389200-110396600	Strong transcription	Dnd41	blood
42	chr4:110389200-110398000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:110389400-110398800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:110389400-110402200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr4:110389800-110396200	Strong transcription	Liver	Liver
46	chr4:110390000-110415400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr4:110391000-110395400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr4:110391600-110402000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr4:110391800-110415400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr4:110391800-110415600	Weak transcription	Ovary	ovary

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