Variant report

Variant	nsv829883
Chromosome Location	chr4:22666326-22842517
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	chr4:22692275-22692679	HepG2	liver:	n/a	n/a
2	ATF1	chr4:22719632-22719730	K562	blood:	n/a	n/a
3	BACH1	chr4:22698950-22698993	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:22744976-22745283	GM12878	blood:	n/a	n/a
5	BATF	chr4:22708980-22709529	GM12878	blood:	n/a	n/a
6	BATF	chr4:22731779-22732025	GM12878	blood:	n/a	chr4:22731857-22731868
7	BATF	chr4:22672653-22672907	GM12878	blood:	n/a	chr4:22672831-22672841
8	BATF	chr4:22709049-22709228	GM12878	blood:	n/a	n/a
9	BATF	chr4:22746279-22746633	GM12878	blood:	n/a	n/a
10	BATF	chr4:22705564-22705832	GM12878	blood:	n/a	chr4:22705743-22705756
11	BCL11A	chr4:22765892-22766128	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:22741560-22741796	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:22765924-22766113	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:22745050-22745270	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:22746313-22746715	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:22743318-22743737	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:22741747-22741819	K562	blood:	n/a	chr4:22741783-22741792 chr4:22741782-22741791 chr4:22741782-22741791 chr4:22741776-22741797
18	BHLHE40	chr4:22780143-22780359	K562	blood:	n/a	n/a
19	BHLHE40	chr4:22709041-22709436	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:22741537-22742094	GM12878	blood:	n/a	chr4:22741783-22741792 chr4:22741782-22741791 chr4:22741782-22741791 chr4:22741776-22741797
21	BHLHE40	chr4:22741686-22741886	HepG2	liver:	n/a	chr4:22741783-22741792 chr4:22741782-22741791 chr4:22741782-22741791 chr4:22741776-22741797
22	BRCA1	chr4:22821352-22821365	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:22692460-22692801	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:22694471-22694622	HepG2	liver:	n/a	chr4:22694555-22694568
25	CEBPB	chr4:22787439-22787639	A549	lung:	n/a	chr4:22787537-22787548 chr4:22787537-22787550
26	CEBPB	chr4:22681282-22681502	HepG2	liver:	n/a	chr4:22681416-22681428
27	CEBPB	chr4:22787429-22787701	HepG2	liver:	n/a	chr4:22787537-22787548 chr4:22787537-22787550
28	CEBPB	chr4:22692487-22692735	A549	lung:	n/a	n/a
29	CEBPB	chr4:22831953-22832235	HepG2	liver:	n/a	chr4:22832095-22832108 chr4:22832096-22832107 chr4:22832095-22832106 chr4:22832095-22832106
30	CEBPB	chr4:22787430-22787647	IMR90	lung:	n/a	chr4:22787537-22787548 chr4:22787537-22787550
31	CEBPB	chr4:22707381-22707588	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:22754513-22754516	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr4:22746272-22746774	GM12878	blood:	n/a	n/a
34	CHD1	chr4:22745106-22745865	GM12878	blood:	n/a	n/a
35	CHD2	chr4:22780120-22780516	K562	blood:	n/a	n/a
36	CHD2	chr4:22746260-22746643	GM12878	blood:	n/a	n/a
37	CHD2	chr4:22741606-22741903	GM12878	blood:	n/a	n/a
38	CHD2	chr4:22813122-22813145	HepG2	liver:	n/a	n/a
39	CTCF	chr4:22694660-22694810	RPTEC	kidney:	n/a	n/a
40	CTCF	chr4:22692420-22692570	GM12865	blood:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
41	CTCF	chr4:22692460-22692610	HRE	kidney:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
42	CTCF	chr4:22692333-22692678	A549	lung:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
43	CTCF	chr4:22692298-22692781	GM12878	blood:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
44	CTCF	chr4:22692420-22692570	BJ	skin:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
45	CTCF	chr4:22692434-22692607	A549	lung:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
46	CTCF	chr4:22692420-22692570	HFF-Myc	foreskin:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
47	CTCF	chr4:22692401-22692432	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr4:22694620-22694770	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:22692440-22692590	GM12871	blood:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548
50	CTCF	chr4:22692440-22692590	HAc	cerebellar:	n/a	chr4:22692525-22692546 chr4:22692531-22692547 chr4:22692530-22692548

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22818572-22818622	MCF10A-Er-Src	breast:	n/a
2	chr4:22694667-22694717	GM12891	blood:	n/a
3	chr4:22818572-22818622	MCF10A-Er-Src	breast:	n/a
4	chr4:22694667-22694717	GM12891	blood:	n/a
5	chr4:22780415-22780465	HAEpiC	amniotic membrane:	n/a
6	chr4:22744871-22744921	GM12878	blood:	n/a
7	chr4:22694230-22694280	Hepatocyte	liver:	n/a
8	chr4:22780491-22780541	AG10803	skin:	n/a
9	chr4:22694667-22694717	AG09309	skin:	n/a
10	chr4:22780415-22780465	K562	blood:	n/a
11	chr4:22746262-22746312	GM12891	blood:	n/a
12	chr4:22780491-22780541	AG04450	lung:	fetal
13	chr4:22694230-22694280	PANC-1	pancreas:	n/a
14	chr4:22694230-22694280	NHBE	bronchial:	n/a
15	chr4:22694667-22694717	HNPCEpiC	eye:	n/a
16	chr4:22744871-22744921	PrEC	prostate:	n/a
17	chr4:22818572-22818622	SK-N-MC	brain:	n/a
18	chr4:22693739-22693789	CMK	blood:	n/a
19	chr4:22780387-22780437	HCM	heart:	n/a
20	chr4:22694667-22694717	AG09319	gingival:	n/a
21	chr4:22746262-22746312	NHBE	bronchial:	n/a
22	chr4:22694230-22694280	U87	brain:	n/a
23	chr4:22694667-22694717	NB4	blood:	n/a
24	chr4:22818572-22818622	MCF-7	breast:	n/a
25	chr4:22694230-22694280	Jurkat	blood:	n/a
26	chr4:22694667-22694717	GM12892	blood:	n/a
27	chr4:22694667-22694717	SK-N-SH	brain:	n/a
28	chr4:22693739-22693789	U87	brain:	n/a
29	chr4:22818572-22818622	HL-60	blood:	n/a
30	chr4:22780491-22780541	IMR90	lung:	fetal
31	chr4:22780491-22780541	SK-N-SH	brain:	n/a
32	chr4:22693739-22693789	HRE	kidney:	n/a
33	chr4:22694667-22694717	U87	brain:	n/a
34	chr4:22744871-22744921	SK-N-MC	brain:	n/a
35	chr4:22818572-22818622	HCF	heart:	n/a
36	chr4:22694230-22694280	HCF	heart:	n/a
37	chr4:22693739-22693789	ECC-1	luminal epithelium:	n/a
38	chr4:22694230-22694280	HEEpiC	esophagus:	n/a
39	chr4:22780491-22780541	AG09319	gingival:	n/a
40	chr4:22744871-22744921	H1-hESC	embryonic stem cell:	embryo
41	chr4:22693739-22693789	Hepatocyte	liver:	n/a
42	chr4:22693739-22693789	A549	lung:	n/a
43	chr4:22818572-22818622	NHDF-neo	bronchial:	n/a
44	chr4:22693739-22693789	GM06990	blood:	n/a
45	chr4:22818572-22818622	BE2_C	brain:	n/a
46	chr4:22818572-22818622	HCM	heart:	n/a
47	chr4:22694667-22694717	BJ	skin:	n/a
48	chr4:22694667-22694717	NHBE	bronchial:	n/a
49	chr4:22694230-22694280	LNCaP	prostate:	n/a
50	chr4:22780491-22780541	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:22412171..22412954-chr4:22692156..22692748,2	K562	blood:
2	chr4:21791076..21791579-chr4:22691911..22692590,2	K562	blood:
3	chr4:22516555..22518423-chr4:22670641..22673303,2	MCF-7	breast:
4	chr4:22412823..22413341-chr4:22692071..22692819,2	MCF-7	breast:
5	chr4:22687079..22688984-chr4:22690023..22692580,2	MCF-7	breast:
6	chr4:22816382..22818106-chr4:22821091..22824068,2	K562	blood:
7	chr4:22772449..22775297-chr4:22778279..22780984,3	K562	blood:
8	chr4:22684475..22686472-chr4:22689943..22692504,2	K562	blood:
9	chr4:22816382..22818106-chr4:22821091..22824068,2	K562	blood:
10	chr4:22687079..22688984-chr4:22690023..22692580,2	MCF-7	breast:
11	chr4:22796834..22798825-chr4:22803164..22804695,2	K562	blood:
12	chr4:22684475..22686472-chr4:22689943..22692504,2	K562	blood:
13	chr4:22772449..22775297-chr4:22778279..22780984,3	K562	blood:
14	chr4:22796834..22798825-chr4:22803164..22804695,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-12	chr4:22694418-22694509	l_2614_chr4:22608314-22651921_testes
2	lnc-PACRGL-11	chr4:22715715-22715773	NONHSAT095766
3	lnc-SOD3-13	chr4:22825575-22826631	NONHSAT095768
4	lnc-PACRGL-12	chr4:22731041-22731137	l_2614_chr4:22608314-22651921_testes
5	lnc-PACRGL-12	chr4:22666560-22667583	ucscGeneNc_uc003gqr_1
6	lnc-PACRGL-12	chr4:22731328-22732285	l_2614_chr4:22608314-22651921_testes
7	lnc-PACRGL-12	chr4:22733121-22733157	l_2614_chr4:22608314-22651921_testes
8	lnc-SOD3-13	chr4:22823158-22825371	NONHSAT095768
9	lnc-PACRGL-12	chr4:22731272-22731308	l_2614_chr4:22608314-22651921_testes
10	lnc-PACRGL-11	chr4:22716579-22717119	NONHSAT095766
11	lnc-PACRGL-12	chr4:22734103-22734156	l_2614_chr4:22608314-22651921_testes

Variant related genes	Relation type
GBA3	TF binding region
CDC42P6	TF binding region
GBA3	CpG island
CDC42P6	CpG island
ENSG00000152990	chromatin interactions

Extended variants
information (count: 6820 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6820 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201096379	chr4:22666337-22666338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145203100	chr4:22666367-22666368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs118012164	chr4:22666423-22666424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552860399	chr4:22666454-22666455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571172465	chr4:22666458-22666459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538209824	chr4:22666463-22666464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550172642	chr4:22666468-22666469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376388650	chr4:22666479-22666480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535929626	chr4:22666481-22666482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554015317	chr4:22666485-22666486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs36080428	chr4:22666500-22666501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371070597	chr4:22666529-22666530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539252914	chr4:22666544-22666545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557589929	chr4:22666584-22666585	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs575946215	chr4:22666651-22666652	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs191795243	chr4:22666654-22666655	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs73106153	chr4:22666672-22666673	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs184015707	chr4:22666693-22666694	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs541109062	chr4:22666749-22666750	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs559225825	chr4:22666762-22666763	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs527850574	chr4:22666793-22666794	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs188952016	chr4:22666801-22666802	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs137874187	chr4:22666818-22666819	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs532023429	chr4:22666819-22666820	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs192391647	chr4:22666825-22666826	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs550243242	chr4:22666851-22666852	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs141695956	chr4:22666878-22666879	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs535527349	chr4:22666879-22666880	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs547823445	chr4:22666903-22666904	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs370383161	chr4:22666945-22666946	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs182133178	chr4:22666978-22666979	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs187186117	chr4:22666980-22666981	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs557551167	chr4:22667002-22667003	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs150114012	chr4:22667018-22667019	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs191941584	chr4:22667023-22667024	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs184142150	chr4:22667050-22667051	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs143657175	chr4:22667057-22667058	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs376336491	chr4:22667061-22667062	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs188508129	chr4:22667067-22667068	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs566684041	chr4:22667096-22667097	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs537435560	chr4:22667125-22667126	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs150179040	chr4:22667188-22667189	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs78275722	chr4:22667190-22667191	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs35197621	chr4:22667191-22667192	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs577837108	chr4:22667195-22667196	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs397776016	chr4:22667205-22667206	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs545154994	chr4:22667244-22667245	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs564656298	chr4:22667258-22667259	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs374723200	chr4:22667433-22667434	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs193064074	chr4:22667455-22667456	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22663200-22668000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:22663200-22668600	Weak transcription	Placenta	Placenta
3	chr4:22663200-22674800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:22663800-22668400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:22664000-22668200	Weak transcription	NHEK	skin
6	chr4:22665800-22670000	Weak transcription	Fetal Intestine Small	intestine
7	chr4:22666000-22669200	Weak transcription	Liver	Liver
8	chr4:22668000-22669400	Enhancers	Placenta Amnion	Placenta Amnion
9	chr4:22668000-22670800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr4:22668200-22668800	Enhancers	NHEK	skin
11	chr4:22668400-22668800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:22668600-22669400	Enhancers	Placenta	Placenta
13	chr4:22668800-22669000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:22668800-22669000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:22669000-22669200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:22669000-22669200	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr4:22669000-22669800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:22669000-22669800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:22669000-22670400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:22669000-22670400	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr4:22669000-22670600	Enhancers	Adipose Nuclei	Adipose
22	chr4:22669200-22669400	Enhancers	HSMMtube	muscle
23	chr4:22669200-22669600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:22669200-22669800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr4:22669200-22670000	Enhancers	Primary T cells from cord blood	blood
26	chr4:22669200-22670400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr4:22669200-22670800	Enhancers	Liver	Liver
28	chr4:22669200-22671600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr4:22669200-22673800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr4:22669400-22670200	Weak transcription	HSMMtube	muscle
31	chr4:22669400-22670600	Weak transcription	Placenta	Placenta
32	chr4:22669400-22670600	Enhancers	Osteobl	bone
33	chr4:22669400-22672600	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr4:22669600-22670400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:22669800-22670000	Active TSS	Primary hematopoietic stem cells	blood
36	chr4:22669800-22670000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:22669800-22670200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:22669800-22670200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
39	chr4:22669800-22670600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:22669800-22671800	Enhancers	Primary B cells from cord blood	blood
41	chr4:22670000-22670400	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr4:22670000-22670400	Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr4:22670000-22670400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:22670000-22670600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr4:22670000-22670600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:22670000-22670600	Enhancers	Fetal Intestine Small	intestine
47	chr4:22670000-22670600	Enhancers	Fetal Lung	lung
48	chr4:22670000-22670600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr4:22670000-22670800	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr4:22670000-22671200	Enhancers	Primary hematopoietic stem cells short term culture	blood

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