Variant report

Variant	nsv980219
Chromosome Location	chr4:74603561-74618789
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	chr4:74606903-74607111	K562	blood:	n/a	n/a
2	ARID3A	chr4:74605518-74606658	K562	blood:	n/a	n/a
3	ARID3A	chr4:74606096-74606251	HepG2	liver:	n/a	n/a
4	ATF1	chr4:74606052-74606521	K562	blood:	n/a	n/a
5	ATF3	chr4:74605945-74606350	K562	blood:	n/a	n/a
6	BATF	chr4:74616901-74617286	GM12878	blood:	n/a	n/a
7	BATF	chr4:74616879-74617266	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:74616914-74617238	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:74617265-74617327	K562	blood:	n/a	n/a
10	BHLHE40	chr4:74605828-74605927	K562	blood:	n/a	n/a
11	BHLHE40	chr4:74606185-74606529	K562	blood:	n/a	n/a
12	CBX3	chr4:74605924-74606567	HCT-116	colon:	n/a	n/a
13	CCNT2	chr4:74607868-74608009	K562	blood:	n/a	n/a
14	CCNT2	chr4:74606166-74606425	K562	blood:	n/a	n/a
15	CEBPB	chr4:74606876-74607023	K562	blood:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984
16	CEBPB	chr4:74618134-74618508	K562	blood:	n/a	chr4:74618239-74618252 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618308-74618321
17	CEBPB	chr4:74606007-74606251	K562	blood:	n/a	n/a
18	CEBPB	chr4:74618184-74618417	H1-hESC	embryonic stem cell:	n/a	chr4:74618239-74618252 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618308-74618321
19	CEBPB	chr4:74605951-74606541	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:74606780-74607127	A549	lung:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984
21	CEBPB	chr4:74606714-74607260	A549	lung:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606755-74606768
22	CEBPB	chr4:74606801-74607154	K562	blood:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984
23	CEBPB	chr4:74618154-74618547	A549	lung:	n/a	chr4:74618239-74618252 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618308-74618321
24	CEBPB	chr4:74618230-74618460	Hela-S3	cervix:	n/a	chr4:74618239-74618252 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618308-74618321
25	CEBPB	chr4:74618150-74618496	HepG2	liver:	n/a	chr4:74618239-74618252 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618308-74618321
26	CEBPB	chr4:74618148-74618493	IMR90	lung:	n/a	chr4:74618239-74618252 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618308-74618321
27	CEBPB	chr4:74605867-74606600	HCT-116	colon:	n/a	n/a
28	CEBPB	chr4:74606806-74607168	Hela-S3	cervix:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984
29	CEBPB	chr4:74606005-74606408	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:74606768-74607223	K562	blood:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984
31	CEBPB	chr4:74606802-74607151	IMR90	lung:	n/a	chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606982 chr4:74606971-74606984 chr4:74606972-74606983
32	CEBPB	chr4:74605972-74606374	A549	lung:	n/a	n/a
33	CEBPB	chr4:74606816-74607118	HepG2	liver:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984
34	CEBPB	chr4:74605902-74606453	A549	lung:	n/a	n/a
35	CEBPB	chr4:74618170-74618493	A549	lung:	n/a	chr4:74618239-74618252 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618310-74618319 chr4:74618308-74618321
36	CEBPB	chr4:74605853-74606635	HCT-116	colon:	n/a	n/a
37	CEBPB	chr4:74605997-74606381	A549	lung:	n/a	n/a
38	CEBPB	chr4:74606803-74607134	A549	lung:	n/a	chr4:74606971-74606982 chr4:74606972-74606983 chr4:74606971-74606984 chr4:74606971-74606984 chr4:74606971-74606984
39	CEBPB	chr4:74605144-74605360	K562	blood:	n/a	n/a
40	CHD1	chr4:74606208-74606259	GM12878	blood:	n/a	n/a
41	CHD2	chr4:74616948-74617301	GM12878	blood:	n/a	n/a
42	CHD2	chr4:74610034-74610160	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr4:74606175-74606481	A549	lung:	n/a	n/a
44	CUX1	chr4:74606148-74606512	K562	blood:	n/a	n/a
45	CUX1	chr4:74606725-74607338	K562	blood:	n/a	n/a
46	CUX1	chr4:74616969-74617235	GM12878	blood:	n/a	n/a
47	EBF1	chr4:74616967-74617257	GM12878	blood:	n/a	n/a
48	ELF1	chr4:74605978-74606481	K562	blood:	n/a	n/a
49	ELF1	chr4:74605926-74606689	HCT-116	colon:	n/a	n/a
50	ELF1	chr4:74606129-74606596	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74606465-74606515	HCPEpiC	choroid plexus:	n/a
2	chr4:74608458-74608508	HEEpiC	esophagus:	n/a
3	chr4:74608458-74608508	HEK293	kidney:	embryo
4	chr4:74606465-74606515	NB4	blood:	n/a
5	chr4:74606465-74606515	AG10803	skin:	n/a
6	chr4:74608458-74608508	SK-N-SH_RA	brain:	n/a
7	chr4:74606465-74606515	U87	brain:	n/a
8	chr4:74606465-74606515	SKMC	muscle:	n/a
9	chr4:74606465-74606515	CMK	blood:	n/a
10	chr4:74608458-74608508	AG04450	lung:	fetal
11	chr4:74606465-74606515	SK-N-MC	brain:	n/a
12	chr4:74608458-74608508	H1-hESC	embryonic stem cell:	embryo
13	chr4:74606465-74606515	ProgFib	skin:	n/a
14	chr4:74608458-74608508	AG09319	gingival:	n/a
15	chr4:74608458-74608508	ovcar-3	ovarian:	n/a
16	chr4:74608458-74608508	PFSK-1	brain:	n/a
17	chr4:74608458-74608508	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:74608458-74608508	HMEC	breast:	n/a
19	chr4:74606465-74606515	AG04450	lung:	fetal
20	chr4:74608458-74608508	SAEC	small airway:	n/a
21	chr4:74608458-74608508	NHBE	bronchial:	n/a
22	chr4:74608458-74608508	CMK	blood:	n/a
23	chr4:74608458-74608508	Jurkat	blood:	n/a
24	chr4:74606465-74606515	BJ	skin:	n/a
25	chr4:74608458-74608508	T-47D	breast:	n/a
26	chr4:74606465-74606515	Hepatocyte	liver:	n/a
27	chr4:74608458-74608508	ProgFib	skin:	n/a
28	chr4:74608458-74608508	HRE	kidney:	n/a
29	chr4:74606465-74606515	Hela-S3	cervix:	n/a
30	chr4:74608458-74608508	HCF	heart:	n/a
31	chr4:74606465-74606515	MCF10A-Er-Src	breast:	n/a
32	chr4:74606465-74606515	H1-hESC	embryonic stem cell:	embryo
33	chr4:74608458-74608508	HUVEC	blood vessel:	n/a
34	chr4:74608458-74608508	AoSMC	blood vessel:	n/a
35	chr4:74608458-74608508	SK-N-MC	brain:	n/a
36	chr4:74606465-74606515	GM06990	blood:	n/a
37	chr4:74608458-74608508	BE2_C	brain:	n/a
38	chr4:74608458-74608508	LNCaP	prostate:	n/a
39	chr4:74606465-74606515	LNCaP	prostate:	n/a
40	chr4:74608458-74608508	Caco-2	colon:	n/a
41	chr4:74606465-74606515	HCT-116	colon:	n/a
42	chr4:74606465-74606515	IMR90	lung:	fetal
43	chr4:74606465-74606515	HepG2	liver:	n/a
44	chr4:74606465-74606515	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:74606465-74606515	HRE	kidney:	n/a
46	chr4:74608458-74608508	HCT-116	colon:	n/a
47	chr4:74608458-74608508	HIPEpiC	eye:	n/a
48	chr4:74608458-74608508	A549	lung:	n/a
49	chr4:74608458-74608508	NH-A	brain:	n/a
50	chr4:74606465-74606515	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:74609331..74611384-chr4:74617018..74619785,2	K562	blood:
2	chr4:74613677..74615255-chr4:74615539..74617498,2	MCF-7	breast:
3	chr4:74613677..74615255-chr4:74615539..74617498,2	MCF-7	breast:
4	chr4:74606241..74607772-chr4:74611875..74613764,2	K562	blood:
5	chr4:74613405..74615443-chr4:74615480..74619617,3	K562	blood:
6	chr4:74609331..74611384-chr4:74617018..74619785,2	K562	blood:
7	chr4:74616774..74619634-chr4:74626803..74629633,2	K562	blood:
8	chr4:74613567..74615922-chr4:74616921..74619617,2	K562	blood:
9	chr4:74613441..74615334-chr4:74623016..74625012,2	K562	blood:
10	chr4:74123296..74125010-chr4:74605307..74607860,2	K562	blood:
11	chr4:74615686..74617847-chr4:74622511..74624521,2	K562	blood:
12	chr4:74613567..74615922-chr4:74616921..74619617,2	K562	blood:
13	chr4:74606241..74607909-chr4:74611875..74614295,2	K562	blood:
14	chr4:74613405..74615443-chr4:74615480..74619617,3	K562	blood:
15	chr4:74612735..74615091-chr4:74635829..74638388,2	K562	blood:
16	chr11:45873444..45876329-chr4:74608235..74610589,2	MCF-7	breast:
17	chr4:74616341..74618099-chr4:74619715..74622030,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CXCL6-1	chr4:74608856-74609068	NONHSAT096868

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IL8	hsa-miR-124-3p	chr4:74608678-74608696

Variant related genes	Relation type
IL8	TF binding region
IL8	CpG island
ENSG00000169429	chromatin interactions
ENSG00000250220	chromatin interactions
ENSG00000132466	chromatin interactions

Extended variants
information (count: 695 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189369099	chr4:74603596-74603597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147142569	chr4:74603603-74603604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573798300	chr4:74603615-74603616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181078762	chr4:74603616-74603617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377732771	chr4:74603640-74603641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140338689	chr4:74603655-74603656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs36030864	chr4:74603666-74603667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs397786759	chr4:74603676-74603677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2227524	chr4:74603679-74603680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572024570	chr4:74603681-74603682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561428097	chr4:74603714-74603715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528828400	chr4:74603737-74603738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546782124	chr4:74603749-74603750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565171684	chr4:74603771-74603772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532050886	chr4:74603802-74603803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114968108	chr4:74603841-74603842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568793645	chr4:74603849-74603850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199667265	chr4:74603901-74603902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541049382	chr4:74603902-74603903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535872389	chr4:74603912-74603913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548212759	chr4:74603914-74603915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147804704	chr4:74603995-74603996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2227525	chr4:74604043-74604044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2227526	chr4:74604079-74604080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577135326	chr4:74604106-74604107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541865188	chr4:74604110-74604111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557186187	chr4:74604112-74604113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187363375	chr4:74604119-74604120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559375067	chr4:74604189-74604190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368462682	chr4:74604192-74604193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142930739	chr4:74604240-74604241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561375368	chr4:74604248-74604249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189314786	chr4:74604252-74604253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181936753	chr4:74604255-74604256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151077808	chr4:74604281-74604282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs578212714	chr4:74604286-74604287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565102920	chr4:74604335-74604336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532575648	chr4:74604362-74604363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550603353	chr4:74604367-74604368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543975906	chr4:74604371-74604372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562438802	chr4:74604373-74604374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141104105	chr4:74604379-74604380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547859340	chr4:74604384-74604385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529341052	chr4:74604420-74604421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2227527	chr4:74604465-74604466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527558459	chr4:74604486-74604487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552518564	chr4:74604528-74604529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200766750	chr4:74604548-74604549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2227528	chr4:74604550-74604551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397724457	chr4:74604551-74604552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Non-small cell lung cancer	21829676	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Renal cell carcinoma	20952505	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74596400-74605400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:74596400-74606000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:74598000-74605200	Weak transcription	Left Ventricle	heart
4	chr4:74600400-74605400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr4:74600400-74606200	Weak transcription	Primary B cells from cord blood	blood
6	chr4:74600600-74605200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:74600600-74606200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr4:74600800-74605400	Weak transcription	NH-A	brain
9	chr4:74600800-74605800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:74600800-74606200	Weak transcription	HMEC	breast
11	chr4:74601200-74605000	Weak transcription	Hela-S3	cervix
12	chr4:74601200-74605200	Weak transcription	Small Intestine	intestine
13	chr4:74601200-74605200	Weak transcription	NHLF	lung
14	chr4:74601200-74605400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:74601200-74605400	Weak transcription	Adipose Nuclei	Adipose
16	chr4:74601400-74605200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr4:74601400-74605600	Weak transcription	NHEK	skin
18	chr4:74601400-74606000	Weak transcription	Osteobl	bone
19	chr4:74601600-74604400	Weak transcription	K562	blood
20	chr4:74601600-74604800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:74601600-74605400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:74601600-74605400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr4:74601600-74605600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:74601800-74604200	Weak transcription	HUVEC	blood vessel
25	chr4:74601800-74604800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:74602000-74604400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:74602000-74605400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr4:74602200-74605000	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr4:74602400-74605400	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr4:74602400-74605400	Weak transcription	A549	lung
31	chr4:74604200-74604400	Enhancers	HUVEC	blood vessel
32	chr4:74604400-74604800	Weak transcription	HUVEC	blood vessel
33	chr4:74604400-74605400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr4:74604400-74606000	Enhancers	K562	blood
35	chr4:74604800-74605800	Enhancers	HUVEC	blood vessel
36	chr4:74604800-74606200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr4:74604800-74606200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:74605000-74606200	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr4:74605000-74606200	Enhancers	Hela-S3	cervix
40	chr4:74605200-74605400	Enhancers	Left Ventricle	heart
41	chr4:74605200-74605800	Enhancers	NHLF	lung
42	chr4:74605200-74606200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr4:74605200-74606400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:74605400-74605600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:74605400-74605600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:74605400-74605600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:74605400-74605600	Enhancers	Small Intestine	intestine
48	chr4:74605400-74606200	Enhancers	Primary hematopoietic stem cells	blood
49	chr4:74605400-74606200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:74605400-74606200	Weak transcription	Left Ventricle	heart

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