Variant report

Variant	esv3448470
Chromosome Location	chr4:79898340-80026510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:495)
CpG islands
(count:367)
Chromatin interactive
region (count:25)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79963365-79963515	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:79946392-79946697	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:79963283-79963590	K562	blood:	n/a	n/a
4	ARID3A	chr4:80014814-80014884	K562	blood:	n/a	n/a
5	BACH1	chr4:80004620-80004896	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:79948958-79949016	K562	blood:	n/a	n/a
7	BATF	chr4:79999738-79999918	GM12878	blood:	n/a	n/a
8	BCL3	chr4:79911031-79911378	GM12878	blood:	n/a	n/a
9	BCL3	chr4:79911005-79911426	GM12878	blood:	n/a	n/a
10	BCL3	chr4:79967225-79967466	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:79965203-79965499	K562	blood:	n/a	n/a
12	BHLHE40	chr4:79942496-79942781	K562	blood:	n/a	n/a
13	BHLHE40	chr4:79957101-79957286	K562	blood:	n/a	n/a
14	BHLHE40	chr4:80004667-80004763	K562	blood:	n/a	n/a
15	BRCA1	chr4:79953683-79953684	GM12878	blood:	n/a	n/a
16	BRCA1	chr4:79948836-79948905	Hela-S3	cervix:	n/a	n/a
17	CCNT2	chr4:79971124-79971266	K562	blood:	n/a	n/a
18	CEBPB	chr4:79930362-79930569	IMR90	lung:	n/a	chr4:79930435-79930446
19	CEBPB	chr4:79915916-79916116	HepG2	liver:	n/a	chr4:79916027-79916038
20	CEBPB	chr4:79955753-79956067	IMR90	lung:	n/a	chr4:79955886-79955895 chr4:79955884-79955897 chr4:79955886-79955895 chr4:79955885-79955896 chr4:79955886-79955895 chr4:79955886-79955895
21	CEBPB	chr4:79937418-79937696	K562	blood:	n/a	chr4:79937460-79937471
22	CEBPB	chr4:79930306-79930596	HepG2	liver:	n/a	chr4:79930435-79930446
23	CEBPB	chr4:79955791-79955991	H1-hESC	embryonic stem cell:	n/a	chr4:79955886-79955895 chr4:79955884-79955897 chr4:79955886-79955895 chr4:79955885-79955896 chr4:79955886-79955895 chr4:79955886-79955895
24	CEBPB	chr4:79955786-79956057	HepG2	liver:	n/a	chr4:79955886-79955895 chr4:79955884-79955897 chr4:79955886-79955895 chr4:79955885-79955896 chr4:79955886-79955895 chr4:79955886-79955895
25	CEBPB	chr4:79912570-79912726	IMR90	lung:	n/a	chr4:79912597-79912608
26	CEBPB	chr4:80014734-80014979	K562	blood:	n/a	n/a
27	CEBPB	chr4:79955815-79956054	A549	lung:	n/a	chr4:79955886-79955895 chr4:79955884-79955897 chr4:79955886-79955895 chr4:79955885-79955896 chr4:79955886-79955895 chr4:79955886-79955895
28	CEBPB	chr4:79928638-79928682	K562	blood:	n/a	n/a
29	CEBPB	chr4:79915906-79916070	K562	blood:	n/a	chr4:79916027-79916038
30	CEBPB	chr4:79955326-79956031	K562	blood:	n/a	chr4:79955886-79955895 chr4:79955884-79955897 chr4:79955556-79955564 chr4:79955886-79955895 chr4:79955885-79955896 chr4:79955455-79955468 chr4:79955886-79955895 chr4:79955886-79955895
31	CEBPB	chr4:79912476-79912676	HepG2	liver:	n/a	chr4:79912597-79912608
32	CEBPB	chr4:79937299-79937630	HepG2	liver:	n/a	chr4:79937460-79937471
33	CTCF	chr4:79922188-79922227	GM20000	blood:	n/a	n/a
34	CTCF	chr4:79963380-79963530	K562	blood:	n/a	n/a
35	CTCF	chr4:79963380-79963530	HPF	lung:	n/a	n/a
36	CTCF	chr4:79963248-79963597	IMR90	lung:	n/a	n/a
37	CTCF	chr4:79959200-79959228	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr4:79924760-79924910	HCT-116	colon:	n/a	n/a
39	CTCF	chr4:80000520-80000670	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr4:79963320-79963470	GM12872	blood:	n/a	n/a
41	CTCF	chr4:79963340-79963490	AG10803	skin:	n/a	n/a
42	CTCF	chr4:79963400-79963550	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr4:79963309-79963545	K562	blood:	n/a	n/a
44	CTCF	chr4:79963340-79963490	AG09319	gingival:	n/a	n/a
45	CTCF	chr4:79963333-79963511	GM13977	blood:	n/a	n/a
46	CTCF	chr4:79963420-79963570	NHLF	lung:	n/a	n/a
47	CTCF	chr4:79963340-79963490	HMF	breast:	n/a	n/a
48	CTCF	chr4:79932990-79933041	LNCaP	prostate:	n/a	n/a
49	CTCF	chr4:79963320-79963470	HRE	kidney:	n/a	n/a
50	CTCF	chr4:79963396-79963501	GM19240	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80004287-80004337	SKMC	muscle:	n/a
2	chr4:80004287-80004337	SKMC	muscle:	n/a
3	chr4:79971432-79971482	ovcar-3	ovarian:	n/a
4	chr4:79971432-79971482	NHBE	bronchial:	n/a
5	chr4:79971177-79971227	Hepatocyte	liver:	n/a
6	chr4:79971432-79971482	AoSMC	blood vessel:	n/a
7	chr4:80004287-80004337	U87	brain:	n/a
8	chr4:79971462-79971512	Hela-S3	cervix:	n/a
9	chr4:79971408-79971458	CMK	blood:	n/a
10	chr4:79971408-79971458	SK-N-MC	brain:	n/a
11	chr4:79971432-79971482	HEEpiC	esophagus:	n/a
12	chr4:79971235-79971285	AG10803	skin:	n/a
13	chr4:79971408-79971458	T-47D	breast:	n/a
14	chr4:79971235-79971285	MCF10A-Er-Src	breast:	n/a
15	chr4:80004287-80004337	A549	lung:	n/a
16	chr4:79971235-79971285	HEEpiC	esophagus:	n/a
17	chr4:79971462-79971512	HRCEpiC	kidney:	n/a
18	chr4:79971462-79971512	PFSK-1	brain:	n/a
19	chr4:79971462-79971512	NHDF-neo	bronchial:	n/a
20	chr4:79971177-79971227	NB4	blood:	n/a
21	chr4:79971235-79971285	Caco-2	colon:	n/a
22	chr4:79971432-79971482	SKMC	muscle:	n/a
23	chr4:79971432-79971482	HL-60	blood:	n/a
24	chr4:79971432-79971482	HUVEC	blood vessel:	n/a
25	chr4:79971432-79971482	HCM	heart:	n/a
26	chr4:79971235-79971285	A549	lung:	n/a
27	chr4:80004287-80004337	HL-60	blood:	n/a
28	chr4:79971177-79971227	ovcar-3	ovarian:	n/a
29	chr4:79971462-79971512	GM12891	blood:	n/a
30	chr4:79971432-79971482	HMEC	breast:	n/a
31	chr4:79971235-79971285	RPTEC	kidney:	n/a
32	chr4:79971408-79971458	SKMC	muscle:	n/a
33	chr4:79971462-79971512	Caco-2	colon:	n/a
34	chr4:79971408-79971458	IMR90	lung:	fetal
35	chr4:79971177-79971227	A549	lung:	n/a
36	chr4:79971432-79971482	AG09319	gingival:	n/a
37	chr4:79971462-79971512	HRE	kidney:	n/a
38	chr4:79971177-79971227	AG09309	skin:	n/a
39	chr4:80004287-80004337	HRCEpiC	kidney:	n/a
40	chr4:79971432-79971482	HRE	kidney:	n/a
41	chr4:79971462-79971512	HL-60	blood:	n/a
42	chr4:79971408-79971458	AG09309	skin:	n/a
43	chr4:80004287-80004337	AG09319	gingival:	n/a
44	chr4:79971235-79971285	HepG2	liver:	n/a
45	chr4:79971177-79971227	H1-hESC	embryonic stem cell:	embryo
46	chr4:79971432-79971482	NHDF-neo	bronchial:	n/a
47	chr4:79971177-79971227	GM19239	blood:	n/a
48	chr4:79971462-79971512	Jurkat	blood:	n/a
49	chr4:79971408-79971458	ovcar-3	ovarian:	n/a
50	chr4:79971177-79971227	HUVEC	blood vessel:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:79906212..79908512-chr4:79912830..79915570,2	K562	blood:
2	chr4:79964140..79964963-chr4:80497048..80497852,2	MCF-7	breast:
3	chr4:79906212..79908512-chr4:79912830..79915570,2	K562	blood:
4	chr4:79943664..79946142-chr9:83452129..83453630,2	MCF-7	breast:
5	chr4:79944609..79947579-chr4:79951684..79954668,2	K562	blood:
6	chr4:80002356..80003863-chr4:80013961..80016777,2	K562	blood:
7	chr4:79963329..79963907-chr4:80497328..80498247,2	K562	blood:
8	chr4:79962952..79963679-chr4:81105091..81105941,3	MCF-7	breast:
9	chr4:80008962..80011213-chrX:125885071..125887806,2	MCF-7	breast:
10	chr4:79963103..79964922-chr4:79966258..79968873,2	K562	blood:
11	chr4:79963382..79963898-chr4:80312179..80313004,2	K562	blood:
12	chr4:79962355..79964603-chr4:79966690..79968873,2	K562	blood:
13	chr4:79998907..80000572-chr4:80006530..80008071,2	K562	blood:
14	chr4:79998907..80000572-chr4:80006530..80008071,2	K562	blood:
15	chr4:80002356..80003863-chr4:80013961..80016777,2	K562	blood:
16	chr4:79963103..79964922-chr4:79966258..79968873,2	K562	blood:
17	chr4:79962355..79964603-chr4:79966690..79968873,2	K562	blood:
18	chr4:79875322..79875845-chr4:79962992..79963610,2	MCF-7	breast:
19	chr4:79963314..79963869-chr4:80218868..80219372,2	K562	blood:
20	chr4:79963311..79963867-chr4:80497354..80497886,2	MCF-7	breast:
21	chr4:79959121..79962093-chr4:79967361..79969057,2	K562	blood:
22	chr4:79959717..79962130-chr4:79962284..79964886,2	K562	blood:
23	chr4:79944609..79947579-chr4:79951684..79954668,2	K562	blood:
24	chr4:79959121..79962093-chr4:79967361..79969057,2	K562	blood:
25	chr4:79959717..79962130-chr4:79962284..79964886,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMP2K-1	chr4:80007244-80007416	NONHSAT097101
2	lnc-BMP2K-1	chr4:80007250-80007416	NONHSAT097098
3	lnc-BMP2K-1	chr4:80007250-80007416	ENSG00000249307.1
4	lnc-BMP2K-1	chr4:80007244-80007416	NONHSAT097102
5	lnc-BMP2K-1	chr4:80007250-80007416	ENSG00000249307.1
6	lnc-BMP2K-5	chr4:80010301-80010583	expReg_chr4_4149_+
7	lnc-BMP2K-1	chr4:80007250-80007416	ENSG00000249307.1
8	lnc-BMP2K-1	chr4:80006393-80006501	ENSG00000249307.1

No data

Variant related genes	Relation type
LINC01088	TF binding region
LINC01088	CpG island
ENSG00000152784	chromatin interactions

Extended variants
information (count: 3522 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3522 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570807707	chr4:79898358-79898359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569694857	chr4:79898402-79898403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186958702	chr4:79898511-79898512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552443588	chr4:79898545-79898546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569097513	chr4:79898551-79898552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538151028	chr4:79898589-79898590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139710019	chr4:79898622-79898623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574701724	chr4:79898663-79898664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533858470	chr4:79898680-79898681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553938200	chr4:79898751-79898752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182922216	chr4:79898787-79898788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186117534	chr4:79898837-79898838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545524606	chr4:79898971-79898972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562515095	chr4:79898994-79898995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190973092	chr4:79898999-79899000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542140774	chr4:79899058-79899059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561910012	chr4:79899064-79899065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534860785	chr4:79899071-79899072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182125835	chr4:79899100-79899101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547462207	chr4:79899113-79899114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370468916	chr4:79899145-79899146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564467688	chr4:79899151-79899152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533351634	chr4:79899176-79899177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549866506	chr4:79899192-79899193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570035531	chr4:79899220-79899221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531607380	chr4:79899243-79899244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541222726	chr4:79899260-79899261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553933717	chr4:79899271-79899272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577258804	chr4:79899284-79899285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568240964	chr4:79899312-79899313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77008196	chr4:79899324-79899325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553821469	chr4:79899339-79899340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570414820	chr4:79899343-79899344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539526370	chr4:79899348-79899349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574677503	chr4:79899378-79899379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141352212	chr4:79899390-79899391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143850991	chr4:79899393-79899394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542100398	chr4:79899402-79899403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370817855	chr4:79899458-79899459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555666005	chr4:79899566-79899567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199803321	chr4:79899580-79899581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146845083	chr4:79899676-79899677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564712449	chr4:79899692-79899693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533222789	chr4:79899693-79899694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368305240	chr4:79899714-79899715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113323485	chr4:79899716-79899717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113489463	chr4:79899722-79899723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531612357	chr4:79899750-79899751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543916965	chr4:79899751-79899752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563519069	chr4:79899764-79899765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	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
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79897200-79903600	Weak transcription	Aorta	Aorta
2	chr4:79903600-79903800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
3	chr4:79903600-79904000	ZNF genes & repeats	Aorta	Aorta
4	chr4:79903800-79904200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:79904000-79904800	Weak transcription	Aorta	Aorta
6	chr4:79904200-79906200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:79904800-79905000	ZNF genes & repeats	Aorta	Aorta
8	chr4:79905000-79917600	Weak transcription	Aorta	Aorta
9	chr4:79905800-79906800	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr4:79906200-79906800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:79906400-79906800	Bivalent Enhancer	Stomach Mucosa	stomach
12	chr4:79906800-79907400	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr4:79906800-79908600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:79908600-79909400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:79908600-79910400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:79908600-79910400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:79909000-79909400	Enhancers	Primary hematopoietic stem cells	blood
18	chr4:79910200-79910400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:79911200-79911400	Enhancers	Psoas Muscle	Psoas
20	chr4:79911400-79915200	Weak transcription	Psoas Muscle	Psoas
21	chr4:79911600-79913000	Enhancers	Fetal Heart	heart
22	chr4:79912200-79912800	Enhancers	Brain Substantia Nigra	brain
23	chr4:79912800-79913200	Enhancers	Left Ventricle	heart
24	chr4:79917600-79917800	ZNF genes & repeats	Aorta	Aorta
25	chr4:79917800-79923400	Weak transcription	Aorta	Aorta
26	chr4:79922600-79922800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
27	chr4:79924800-79925400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:79934400-79935600	Enhancers	Dnd41	blood
29	chr4:79934600-79935200	Enhancers	Primary hematopoietic stem cells	blood
30	chr4:79934600-79935400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:79935000-79935400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:79935200-79936000	Enhancers	Fetal Heart	heart
33	chr4:79935800-79936800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:79936000-79936600	Weak transcription	Fetal Heart	heart
35	chr4:79936600-79936800	Enhancers	Fetal Heart	heart
36	chr4:79936600-79937000	Enhancers	Brain Substantia Nigra	brain
37	chr4:79936800-79937200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:79937200-79938200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:79938000-79938400	Enhancers	Pancreas	Pancrea
40	chr4:79938200-79942400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:79938400-79943600	Weak transcription	Pancreas	Pancrea
42	chr4:79942200-79943600	Enhancers	NHEK	skin
43	chr4:79942400-79942800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:79942400-79943000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:79942400-79944000	Enhancers	Gastric	stomach
46	chr4:79942600-79943400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:79942800-79947000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:79943200-79943600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:79943800-79944000	Enhancers	Esophagus	oesophagus
50	chr4:79943800-79944000	Enhancers	Pancreas	Pancrea

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