Variant report

Variant	nsv879533
Chromosome Location	chr4:89832532-89917135
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	chr4:89888308-89888316	K562	blood:	n/a	n/a
2	ARID3A	chr4:89890408-89890619	HepG2	liver:	n/a	n/a
3	BATF	chr4:89833021-89833268	GM12878	blood:	n/a	n/a
4	BATF	chr4:89885593-89885832	GM12878	blood:	n/a	chr4:89885728-89885739 chr4:89885705-89885716 chr4:89885750-89885761
5	BATF	chr4:89885594-89885893	GM12878	blood:	n/a	chr4:89885728-89885739 chr4:89885705-89885716 chr4:89885750-89885761
6	BCL11A	chr4:89885573-89885913	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:89885729-89885765	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:89859235-89859579	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr4:89870777-89870963	K562	blood:	n/a	n/a
10	CEBPB	chr4:89870275-89870582	A549	lung:	n/a	chr4:89870413-89870424
11	CEBPB	chr4:89885043-89885391	MCF-7	breast:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
12	CEBPB	chr4:89870364-89870564	H1-hESC	embryonic stem cell:	n/a	chr4:89870413-89870424
13	CEBPB	chr4:89885069-89885448	IMR90	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
14	CEBPB	chr4:89885067-89885456	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
15	CEBPB	chr4:89870249-89870592	K562	blood:	n/a	chr4:89870413-89870424
16	CEBPB	chr4:89897290-89897569	K562	blood:	n/a	chr4:89897421-89897432
17	CEBPB	chr4:89885137-89885375	H1-hESC	embryonic stem cell:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
18	CEBPB	chr4:89906512-89906919	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:89881808-89882115	H1-hESC	embryonic stem cell:	n/a	chr4:89881983-89881994 chr4:89881983-89881994
20	CEBPB	chr4:89884978-89885499	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
21	CEBPB	chr4:89885035-89885463	MCF-7	breast:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
22	CEBPB	chr4:89870278-89870601	HepG2	liver:	n/a	chr4:89870413-89870424
23	CEBPB	chr4:89915542-89915723	A549	lung:	n/a	n/a
24	CEBPB	chr4:89861072-89861198	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:89897274-89897580	HepG2	liver:	n/a	chr4:89897421-89897432
26	CEBPB	chr4:89897320-89897571	A549	lung:	n/a	chr4:89897421-89897432
27	CEBPB	chr4:89832391-89832757	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:89874722-89874868	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:89912413-89912613	IMR90	lung:	n/a	chr4:89912539-89912550
30	CEBPB	chr4:89874716-89874832	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:89885074-89885441	A549	lung:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
32	CEBPB	chr4:89912424-89912629	HepG2	liver:	n/a	chr4:89912539-89912550
33	CEBPB	chr4:89906601-89906833	A549	lung:	n/a	n/a
34	CEBPB	chr4:89859282-89859714	IMR90	lung:	n/a	chr4:89859523-89859535 chr4:89859464-89859477
35	CEBPB	chr4:89859267-89859714	Hela-S3	cervix:	n/a	chr4:89859523-89859535 chr4:89859464-89859477
36	CEBPB	chr4:89873417-89873576	HepG2	liver:	n/a	chr4:89873529-89873540
37	CEBPB	chr4:89906528-89906906	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr4:89885095-89885403	K562	blood:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
39	CEBPB	chr4:89874632-89874836	K562	blood:	n/a	n/a
40	CEBPB	chr4:89915490-89915738	MCF-7	breast:	n/a	n/a
41	CEBPB	chr4:89858357-89858612	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:89881959-89882394	Hela-S3	cervix:	n/a	chr4:89881983-89881994 chr4:89881983-89881994
43	CEBPB	chr4:89885060-89885416	Hela-S3	cervix:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
44	CEBPB	chr4:89912425-89912616	H1-hESC	embryonic stem cell:	n/a	chr4:89912539-89912550
45	CEBPB	chr4:89832405-89832770	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:89889271-89889545	MCF-7	breast:	n/a	n/a
47	CEBPB	chr4:89885166-89885321	HepG2	liver:	n/a	chr4:89885253-89885266 chr4:89885253-89885264 chr4:89885253-89885264 chr4:89885254-89885265
48	CEBPB	chr4:89832423-89832761	A549	lung:	n/a	n/a
49	CEBPB	chr4:89897265-89897581	IMR90	lung:	n/a	chr4:89897421-89897432
50	CEBPB	chr4:89915577-89915647	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:89884612-89884662	SK-N-SH	brain:	n/a
2	chr4:89884612-89884662	SK-N-SH	brain:	n/a
3	chr4:89884612-89884662	Caco-2	colon:	n/a
4	chr4:89881374-89881424	HCF	heart:	n/a
5	chr4:89881374-89881424	SKMC	muscle:	n/a
6	chr4:89884612-89884662	HUVEC	blood vessel:	n/a
7	chr4:89841012-89841062	HepG2	liver:	n/a
8	chr4:89884612-89884662	SKMC	muscle:	n/a
9	chr4:89841012-89841062	Jurkat	blood:	n/a
10	chr4:89881374-89881424	HEEpiC	esophagus:	n/a
11	chr4:89881374-89881424	HEK293	kidney:	embryo
12	chr4:89841012-89841062	NT2-D1	testis:	n/a
13	chr4:89881374-89881424	HCPEpiC	choroid plexus:	n/a
14	chr4:89881374-89881424	CMK	blood:	n/a
15	chr4:89884612-89884662	ovcar-3	ovarian:	n/a
16	chr4:89841012-89841062	GM19239	blood:	n/a
17	chr4:89884612-89884662	AG04450	lung:	fetal
18	chr4:89884612-89884662	ECC-1	luminal epithelium:	n/a
19	chr4:89841012-89841062	Hela-S3	cervix:	n/a
20	chr4:89881374-89881424	GM06990	blood:	n/a
21	chr4:89841012-89841062	MCF10A-Er-Src	breast:	n/a
22	chr4:89841012-89841062	HCPEpiC	choroid plexus:	n/a
23	chr4:89881374-89881424	MCF-7	breast:	n/a
24	chr4:89884612-89884662	T-47D	breast:	n/a
25	chr4:89881374-89881424	PrEC	prostate:	n/a
26	chr4:89881374-89881424	BJ	skin:	n/a
27	chr4:89884612-89884662	AG09319	gingival:	n/a
28	chr4:89881374-89881424	SK-N-MC	brain:	n/a
29	chr4:89841012-89841062	HL-60	blood:	n/a
30	chr4:89841012-89841062	K562	blood:	n/a
31	chr4:89884612-89884662	Jurkat	blood:	n/a
32	chr4:89884612-89884662	MCF10A-Er-Src	breast:	n/a
33	chr4:89884612-89884662	BE2_C	brain:	n/a
34	chr4:89881374-89881424	GM19239	blood:	n/a
35	chr4:89884612-89884662	HNPCEpiC	eye:	n/a
36	chr4:89884612-89884662	NHDF-neo	bronchial:	n/a
37	chr4:89881374-89881424	GM12891	blood:	n/a
38	chr4:89841012-89841062	NHDF-neo	bronchial:	n/a
39	chr4:89881374-89881424	HMEC	breast:	n/a
40	chr4:89884612-89884662	GM06990	blood:	n/a
41	chr4:89841012-89841062	HMEC	breast:	n/a
42	chr4:89841012-89841062	GM12878	blood:	n/a
43	chr4:89841012-89841062	AoSMC	blood vessel:	n/a
44	chr4:89884612-89884662	PrEC	prostate:	n/a
45	chr4:89881374-89881424	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:89881374-89881424	NH-A	brain:	n/a
47	chr4:89881374-89881424	GM12878	blood:	n/a
48	chr4:89881374-89881424	Hepatocyte	liver:	n/a
49	chr4:89884612-89884662	HMEC	breast:	n/a
50	chr4:89841012-89841062	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:89879550..89882970-chr4:89885286..89887934,3	K562	blood:
2	chr4:89870700..89873807-chr4:89875689..89877845,3	MCF-7	breast:
3	chr4:89879550..89882970-chr4:89885286..89887934,3	K562	blood:
4	chr4:89900502..89902834-chr4:89906493..89908325,2	K562	blood:
5	chr4:89864109..89865635-chr4:89874326..89876576,2	K562	blood:
6	chr4:89853119..89856686-chr4:89857478..89862427,5	K562	blood:
7	chr4:89864109..89865635-chr4:89874326..89876576,2	K562	blood:
8	chr4:89900502..89902834-chr4:89906493..89908325,2	K562	blood:
9	chr4:89883284..89885618-chr4:89895803..89899472,3	K562	blood:
10	chr4:89444433..89447084-chr4:89907641..89909631,2	MCF-7	breast:
11	chr4:89870700..89873807-chr4:89875689..89877845,3	MCF-7	breast:
12	chr4:89883284..89885618-chr4:89895803..89899472,3	K562	blood:
13	chr4:89916625..89919056-chr4:89920360..89922873,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAP1L5-4	chr4:89857465-89857573	NONHSAT097381
2	lnc-TIGD2-6	chr4:89863383-89863489	refGeneNc_1707_NR_002806
3	lnc-TIGD2-6	chr4:89849963-89850439	refGeneNc_1707_NR_002806
4	lnc-TIGD2-6	chr4:89852029-89852191	refGeneNc_1707_NR_002806
5	lnc-TIGD2-6	chr4:89868009-89870277	refGeneNc_1707_NR_002806
6	lnc-TIGD2-6	chr4:89862325-89862518	refGeneNc_1707_NR_002806

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM13A	hsa-miR-10b-5p	chr4:89911301-89911325

Variant related genes	Relation type
FAM13A	TF binding region
FAM13A	CpG island
ENSG00000145337	chromatin interactions
ENSG00000138641	chromatin interactions
ENSG00000138640	chromatin interactions

Extended variants
information (count: 3201 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3201 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10019681	chr4:89832532-89832533	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375634140	chr4:89832574-89832575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs151243562	chr4:89832623-89832624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572971612	chr4:89832630-89832631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186119582	chr4:89832649-89832650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370552696	chr4:89832759-89832760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7695732	chr4:89832791-89832792	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs76097421	chr4:89832858-89832859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190970754	chr4:89832917-89832918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1458556	chr4:89832957-89832958	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs574011980	chr4:89832959-89832960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10031868	chr4:89833000-89833001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72665823	chr4:89833082-89833083	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs114392243	chr4:89833099-89833100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368542604	chr4:89833118-89833119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562138899	chr4:89833151-89833152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182057402	chr4:89833195-89833196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115066115	chr4:89833215-89833216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569259663	chr4:89833239-89833240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187630931	chr4:89833247-89833248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192896272	chr4:89833297-89833298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79208766	chr4:89833314-89833315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71594866	chr4:89833366-89833367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372999788	chr4:89833372-89833373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183215780	chr4:89833373-89833374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534027222	chr4:89833388-89833389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555186085	chr4:89833410-89833411	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs28494688	chr4:89833417-89833418	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573742520	chr4:89833424-89833425	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76480491	chr4:89833432-89833433	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140459557	chr4:89833488-89833489	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368628045	chr4:89833493-89833494	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188586630	chr4:89833496-89833497	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545033032	chr4:89833503-89833504	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560141493	chr4:89833554-89833555	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192302019	chr4:89833603-89833604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532146860	chr4:89833638-89833639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372413068	chr4:89833663-89833664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62310477	chr4:89833719-89833720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200293403	chr4:89833720-89833721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77766256	chr4:89833725-89833726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs3221956	chr4:89833753-89833754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200803976	chr4:89833754-89833755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542735006	chr4:89833794-89833795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562338164	chr4:89833836-89833837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113560189	chr4:89833889-89833890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529441435	chr4:89833912-89833913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184603930	chr4:89833917-89833918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189274479	chr4:89833927-89833928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376249864	chr4:89833940-89833941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
lymphocytic leukemia	21291569	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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Obesity	20622171	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89820000-89859200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr4:89824600-89834000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr4:89825600-89878400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr4:89826000-89832600	Weak transcription	Adipose Nuclei	Adipose
5	chr4:89826000-89839600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:89826400-89838400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:89826600-89836200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:89827200-89837400	Weak transcription	Fetal Lung	lung
9	chr4:89827200-89847000	Weak transcription	Placenta	Placenta
10	chr4:89827400-89847000	Weak transcription	Ovary	ovary
11	chr4:89828000-89847000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr4:89829200-89839400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:89829400-89835600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:89830200-89833400	Weak transcription	Fetal Intestine Small	intestine
15	chr4:89830200-89833400	Weak transcription	Pancreas	Pancrea
16	chr4:89831200-89833000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:89831600-89833600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr4:89832200-89832800	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr4:89832400-89833400	Weak transcription	Fetal Intestine Large	intestine
20	chr4:89832800-89833000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr4:89832800-89833000	Enhancers	Adipose Nuclei	Adipose
22	chr4:89833400-89833600	Genic enhancers	Fetal Intestine Small	intestine
23	chr4:89833400-89834000	Enhancers	Fetal Intestine Large	intestine
24	chr4:89833600-89833800	Enhancers	Fetal Intestine Small	intestine
25	chr4:89833600-89833800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr4:89833800-89841200	Weak transcription	Fetal Intestine Small	intestine
27	chr4:89836800-89842000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:89838400-89838800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:89838800-89852000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:89839400-89840600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
31	chr4:89839400-89840800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:89839600-89839800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:89839800-89840600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr4:89839800-89840800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:89839800-89841000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr4:89840000-89840400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:89840000-89840600	Enhancers	HMEC	breast
38	chr4:89840000-89840800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chr4:89840800-89862800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:89841000-89842400	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:89841200-89841600	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr4:89841600-89847000	Weak transcription	Fetal Intestine Small	intestine
43	chr4:89843800-89851800	Weak transcription	Pancreas	Pancrea
44	chr4:89845400-89859600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr4:89845400-89866400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr4:89845600-89857600	Weak transcription	Gastric	stomach
47	chr4:89846200-89847000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr4:89846800-89847000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr4:89847000-89847200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
50	chr4:89847000-89847200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung

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