Variant report

Variant	esv3373301
Chromosome Location	chr3:120273762-120421260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2949)
CpG islands
(count:1586)
Chromatin interactive
region (count:120)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2949 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:120398704-120399834	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:120341880-120342626	K562	blood:	n/a	n/a
3	ARID3A	chr3:120397371-120397759	K562	blood:	n/a	n/a
4	ARID3A	chr3:120315223-120315711	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:120289620-120289635	K562	blood:	n/a	n/a
6	ARID3A	chr3:120286520-120286919	K562	blood:	n/a	n/a
7	ARID3A	chr3:120412122-120412644	K562	blood:	n/a	n/a
8	ARID3A	chr3:120397095-120398170	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:120277752-120278783	K562	blood:	n/a	n/a
10	ARID3A	chr3:120408267-120408467	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:120412044-120412859	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:120341925-120342194	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:120361160-120361681	K562	blood:	n/a	n/a
14	ARID3A	chr3:120277800-120278127	HepG2	liver:	n/a	n/a
15	ARID3A	chr3:120286609-120286883	HepG2	liver:	n/a	n/a
16	ARID3A	chr3:120400140-120401452	HepG2	liver:	n/a	n/a
17	ARID3A	chr3:120355804-120356098	HepG2	liver:	n/a	n/a
18	ATF1	chr3:120278366-120278738	K562	blood:	n/a	n/a
19	ATF1	chr3:120341939-120342590	K562	blood:	n/a	n/a
20	ATF1	chr3:120361289-120361740	K562	blood:	n/a	n/a
21	ATF2	chr3:120277610-120278800	H1-hESC	embryonic stem cell:	n/a	chr3:120277975-120277982
22	ATF2	chr3:120315211-120315749	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr3:120277558-120278824	H1-hESC	embryonic stem cell:	n/a	chr3:120277975-120277982
24	ATF2	chr3:120277668-120278277	GM12878	blood:	n/a	chr3:120277975-120277982
25	ATF2	chr3:120277550-120278232	GM12878	blood:	n/a	chr3:120277975-120277982
26	ATF3	chr3:120342207-120342618	K562	blood:	n/a	n/a
27	ATF3	chr3:120396973-120397863	A549	lung:	n/a	n/a
28	ATF3	chr3:120361365-120361638	K562	blood:	n/a	n/a
29	BACH1	chr3:120412283-120412723	H1-hESC	embryonic stem cell:	n/a	chr3:120412451-120412465
30	BACH1	chr3:120397374-120397741	K562	blood:	n/a	n/a
31	BACH1	chr3:120361325-120361606	K562	blood:	n/a	n/a
32	BACH1	chr3:120396925-120397974	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr3:120315133-120315150	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr3:120406979-120407286	GM12878	blood:	n/a	n/a
35	BATF	chr3:120335758-120335938	GM12878	blood:	n/a	chr3:120335884-120335895
36	BATF	chr3:120287543-120287747	GM12878	blood:	n/a	chr3:120287672-120287682 chr3:120287671-120287682
37	BATF	chr3:120407049-120407309	GM12878	blood:	n/a	n/a
38	BCL3	chr3:120400733-120401353	A549	lung:	n/a	n/a
39	BCL3	chr3:120379910-120380704	A549	lung:	n/a	n/a
40	BCL3	chr3:120396921-120397963	A549	lung:	n/a	n/a
41	BCLAF1	chr3:120277677-120278152	GM12878	blood:	n/a	n/a
42	BCLAF1	chr3:120315060-120315764	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:120277704-120278743	K562	blood:	n/a	chr3:120277913-120277929
44	BHLHE40	chr3:120361066-120361718	K562	blood:	n/a	n/a
45	BHLHE40	chr3:120290680-120290871	K562	blood:	n/a	n/a
46	BHLHE40	chr3:120315267-120315701	K562	blood:	n/a	n/a
47	BHLHE40	chr3:120323356-120323556	K562	blood:	n/a	n/a
48	BHLHE40	chr3:120341739-120341939	K562	blood:	n/a	n/a
49	BHLHE40	chr3:120278023-120278532	A549	lung:	n/a	n/a
50	BHLHE40	chr3:120320547-120320565	K562	blood:	n/a	n/a

(count:1586 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:120412084-120412134	ProgFib	skin:	n/a
2	chr3:120314841-120314891	HAEpiC	amniotic membrane:	n/a
3	chr3:120367020-120367070	BE2_C	brain:	n/a
4	chr3:120408071-120408121	HRPEpiC	eye:	n/a
5	chr3:120318272-120318322	AG09319	gingival:	n/a
6	chr3:120397653-120397703	GM12878	blood:	n/a
7	chr3:120314864-120314914	T-47D	breast:	n/a
8	chr3:120277758-120277808	IMR90	lung:	fetal
9	chr3:120287165-120287215	BJ	skin:	n/a
10	chr3:120315176-120315226	ECC-1	luminal epithelium:	n/a
11	chr3:120367020-120367070	HIPEpiC	eye:	n/a
12	chr3:120369337-120369387	GM06990	blood:	n/a
13	chr3:120412084-120412134	SK-N-MC	brain:	n/a
14	chr3:120315127-120315177	NHDF-neo	bronchial:	n/a
15	chr3:120318272-120318322	HRE	kidney:	n/a
16	chr3:120315618-120315668	H1-hESC	embryonic stem cell:	embryo
17	chr3:120277827-120277877	AG10803	skin:	n/a
18	chr3:120412084-120412134	HepG2	liver:	n/a
19	chr3:120314864-120314914	CMK	blood:	n/a
20	chr3:120401058-120401108	SK-N-SH	brain:	n/a
21	chr3:120401095-120401145	AG04450	lung:	fetal
22	chr3:120401765-120401815	HL-60	blood:	n/a
23	chr3:120412084-120412134	GM12892	blood:	n/a
24	chr3:120315127-120315177	GM12891	blood:	n/a
25	chr3:120315127-120315177	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:120315025-120315075	RPTEC	kidney:	n/a
27	chr3:120315182-120315232	NT2-D1	testis:	n/a
28	chr3:120401095-120401145	BJ	skin:	n/a
29	chr3:120315127-120315177	AG04450	lung:	fetal
30	chr3:120320383-120320433	PFSK-1	brain:	n/a
31	chr3:120401095-120401145	U87	brain:	n/a
32	chr3:120408071-120408121	AG09319	gingival:	n/a
33	chr3:120314841-120314891	HepG2	liver:	n/a
34	chr3:120287165-120287215	AoSMC	blood vessel:	n/a
35	chr3:120315460-120315510	HCT-116	colon:	n/a
36	chr3:120397653-120397703	AG04450	lung:	fetal
37	chr3:120277758-120277808	GM12892	blood:	n/a
38	chr3:120315618-120315668	K562	blood:	n/a
39	chr3:120315182-120315232	HEEpiC	esophagus:	n/a
40	chr3:120315121-120315171	LNCaP	prostate:	n/a
41	chr3:120277827-120277877	HUVEC	blood vessel:	n/a
42	chr3:120277758-120277808	MCF10A-Er-Src	breast:	n/a
43	chr3:120312459-120312509	HCPEpiC	choroid plexus:	n/a
44	chr3:120398684-120398734	IMR90	lung:	fetal
45	chr3:120315182-120315232	HEK293	kidney:	embryo
46	chr3:120397653-120397703	HL-60	blood:	n/a
47	chr3:120314841-120314891	ProgFib	skin:	n/a
48	chr3:120367020-120367070	U87	brain:	n/a
49	chr3:120315121-120315171	AG04450	lung:	fetal
50	chr3:120367020-120367070	HCT-116	colon:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:120361500..120364085-chr3:120460567..120462504,2	K562	blood:
2	chr3:120355160..120357124-chr3:120358970..120361276,2	K562	blood:
3	chr3:120403041..120405585-chr3:120409977..120412139,2	MCF-7	breast:
4	chr3:120365289..120367083-chr3:120384448..120386613,2	MCF-7	breast:
5	chr3:120417863..120420778-chr3:120426396..120428792,2	MCF-7	breast:
6	chr3:120282278..120284804-chr3:120287050..120289696,2	K562	blood:
7	chr3:120321021..120323929-chr3:120363267..120365846,3	MCF-7	breast:
8	chr3:120402292..120405361-chr3:120406380..120408889,3	MCF-7	breast:
9	chr3:120313507..120317684-chr3:120458763..120463692,6	MCF-7	breast:
10	chr3:120304768..120307515-chr3:120314124..120316734,2	MCF-7	breast:
11	chr3:120398352..120401309-chr3:120403225..120407401,5	K562	blood:
12	chr3:120321293..120323169-chr3:120342458..120344360,2	MCF-7	breast:
13	chr3:120354742..120356779-chr3:120359962..120362019,2	MCF-7	breast:
14	chr3:120392048..120394831-chr3:120397080..120399083,3	K562	blood:
15	chr3:120346339..120348392-chr3:120349471..120352368,2	K562	blood:
16	chr3:120322103..120323838-chr3:120326789..120329238,2	MCF-7	breast:
17	chr3:120346339..120348392-chr3:120349471..120352368,2	K562	blood:
18	chr3:120279797..120280809-chr3:120513558..120514502,6	MCF-7	breast:
19	chr3:120135445..120137288-chr3:120277206..120278376,12	MCF-7	breast:
20	chr3:120279821..120280465-chr3:121247825..121248767,2	MCF-7	breast:
21	chr3:120137444..120138878-chr3:120277379..120278358,9	MCF-7	breast:
22	chr3:120411360..120413123-chr3:120418535..120421038,2	K562	blood:
23	chr3:120319897..120322089-chr3:120410422..120413508,3	MCF-7	breast:
24	chr3:120410148..120412083-chr3:120412165..120413730,2	MCF-7	breast:
25	chr3:120303870..120306627-chr3:120311703..120313546,2	MCF-7	breast:
26	chr3:120139429..120140118-chr3:120277415..120278258,3	MCF-7	breast:
27	chr3:120322143..120324149-chr3:120374822..120377400,2	K562	blood:
28	chr3:120342144..120344111-chr3:120512256..120514740,2	K562	blood:
29	chr3:120330377..120333113-chr3:120333439..120336650,4	K562	blood:
30	chr3:120066931..120069030-chr3:120314504..120317461,2	MCF-7	breast:
31	chr3:120322103..120323838-chr3:120326789..120329238,2	MCF-7	breast:
32	chr3:120361046..120363928-chr3:120366924..120370072,3	K562	blood:
33	chr3:120315040..120318401-chr3:120459431..120463263,5	MCF-7	breast:
34	chr3:120321293..120323169-chr3:120342458..120344360,2	MCF-7	breast:
35	chr3:120392048..120394831-chr3:120397080..120399083,3	K562	blood:
36	chr3:120279838..120280352-chr3:120871430..120872100,2	MCF-7	breast:
37	chr3:120285088..120287233-chr3:120289069..120290878,2	K562	blood:
38	chr3:120374684..120377546-chr3:120461627..120463329,2	MCF-7	breast:
39	chr3:120270757..120272549-chr3:120274263..120277082,2	K562	blood:
40	chr3:120396369..120399119-chr3:120400893..120402859,2	K562	blood:
41	chr3:120137423..120138991-chr3:120276678..120279072,31	MCF-7	breast:
42	chr14:104808000..104808682-chr3:120279791..120280680,2	MCF-7	breast:
43	chr3:120284576..120286509-chr3:120313591..120316096,2	K562	blood:
44	chr3:120356918..120358882-chr3:120361496..120363749,2	K562	blood:
45	chr3:120386379..120388030-chr3:120460714..120462361,2	MCF-7	breast:
46	chr3:120320397..120322628-chr6:26044181..26045926,2	MCF-7	breast:
47	chr3:120308415..120311212-chr3:120314390..120316448,2	K562	blood:
48	chr3:120310434..120313277-chr3:120313584..120317454,5	MCF-7	breast:
49	chr3:120136391..120139340-chr3:120276034..120279006,3	MCF-7	breast:
50	chr3:120314901..120316711-chr3:120394884..120396575,2	MCF-7	breast:

No data

Variant related genes	Relation type
HGD	TF binding region
NDUFB4	TF binding region
HGD	CpG island
NDUFB4	CpG island
ENSG00000163428	chromatin interactions
ENSG00000196532	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000065518	chromatin interactions
ENSG00000175697	chromatin interactions
ENSG00000113924	chromatin interactions
ENSG00000153767	chromatin interactions
ENSG00000144840	chromatin interactions
ENSG00000234816	chromatin interactions
ENSG00000240661	chromatin interactions
ENSG00000261360	chromatin interactions

Extended variants
information (count: 5191 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5191 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368077449	chr3:120273763-120273764	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs536449150	chr3:120273799-120273800	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs552851625	chr3:120273854-120273855	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs574931529	chr3:120273874-120273875	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs114842281	chr3:120273879-120273880	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs376765050	chr3:120273902-120273903	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs559318085	chr3:120273944-120273945	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs6770836	chr3:120273968-120273969	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs143075575	chr3:120274010-120274011	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs575744472	chr3:120274031-120274032	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs78156035	chr3:120274103-120274104	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs78160629	chr3:120274106-120274107	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs75375212	chr3:120274107-120274108	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs34048223	chr3:120274117-120274118	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs191904874	chr3:120274122-120274123	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs555093288	chr3:120274136-120274137	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs375074149	chr3:120274179-120274180	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs574793944	chr3:120274195-120274196	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs376527472	chr3:120274206-120274207	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs79269946	chr3:120274220-120274221	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs560281402	chr3:120274262-120274263	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs182949499	chr3:120274263-120274264	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs546119138	chr3:120274264-120274265	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs147460391	chr3:120274277-120274278	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs530573106	chr3:120274298-120274299	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs550259412	chr3:120274327-120274328	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs567362804	chr3:120274432-120274433	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs139822922	chr3:120274560-120274561	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs546837937	chr3:120274604-120274605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10511399	chr3:120274668-120274669	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs538821367	chr3:120274670-120274671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377629253	chr3:120274688-120274689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71327235	chr3:120274689-120274690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35446232	chr3:120274692-120274693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71327236	chr3:120274698-120274699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558934901	chr3:120274739-120274740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372847463	chr3:120274748-120274749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569170905	chr3:120274752-120274753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542058028	chr3:120274753-120274754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538243696	chr3:120274838-120274839	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554628936	chr3:120274871-120274872	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144600183	chr3:120274946-120274947	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540343496	chr3:120274967-120274968	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553830838	chr3:120274997-120274998	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187579883	chr3:120275012-120275013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550850731	chr3:120275131-120275132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571036156	chr3:120275132-120275133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148464654	chr3:120275161-120275162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142627930	chr3:120275205-120275206	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111232351	chr3:120275206-120275207	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Glioblastoma multiforme	22286061	CNVD
Neurodevelopmental disorder	22521361	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:3054 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120269200-120273800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:120269400-120273800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:120270000-120273800	Weak transcription	Osteobl	bone
4	chr3:120270200-120273800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:120271400-120276200	Weak transcription	Right Ventricle	heart
6	chr3:120271400-120277200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:120272000-120273800	Weak transcription	Right Atrium	heart
8	chr3:120272000-120277000	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:120272600-120273800	Weak transcription	Left Ventricle	heart
10	chr3:120273000-120274400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:120273000-120277000	Enhancers	Colon Smooth Muscle	Colon
12	chr3:120273200-120276800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:120273400-120275200	Enhancers	Rectal Smooth Muscle	rectum
14	chr3:120273400-120275200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr3:120273400-120275200	Enhancers	NHDF-Ad	bronchial
16	chr3:120273400-120275800	Enhancers	Fetal Heart	heart
17	chr3:120273400-120277200	Enhancers	Ovary	ovary
18	chr3:120273600-120273800	Weak transcription	Aorta	Aorta
19	chr3:120273600-120274600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:120273600-120275200	Enhancers	Liver	Liver
21	chr3:120273600-120275800	Enhancers	Adipose Nuclei	Adipose
22	chr3:120273600-120276400	Enhancers	Stomach Smooth Muscle	stomach
23	chr3:120273800-120274000	Enhancers	Aorta	Aorta
24	chr3:120273800-120274000	Enhancers	Left Ventricle	heart
25	chr3:120273800-120274000	Enhancers	Psoas Muscle	Psoas
26	chr3:120273800-120274400	Enhancers	Fetal Muscle Leg	muscle
27	chr3:120273800-120274600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr3:120273800-120274600	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr3:120273800-120275000	Enhancers	Right Atrium	heart
30	chr3:120273800-120275200	Enhancers	Osteobl	bone
31	chr3:120273800-120275600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:120273800-120275800	Enhancers	Pancreas	Pancrea
33	chr3:120273800-120277400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr3:120273800-120277400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr3:120274000-120274400	Weak transcription	Left Ventricle	heart
36	chr3:120274000-120274800	Weak transcription	Psoas Muscle	Psoas
37	chr3:120274000-120277200	Weak transcription	Aorta	Aorta
38	chr3:120274200-120274800	Enhancers	Small Intestine	intestine
39	chr3:120274200-120275000	Enhancers	Gastric	stomach
40	chr3:120274200-120277200	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr3:120274400-120274600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:120274400-120274800	Weak transcription	Fetal Muscle Leg	muscle
43	chr3:120274400-120275000	Enhancers	Left Ventricle	heart
44	chr3:120274400-120275200	Enhancers	NHLF	lung
45	chr3:120274400-120275400	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr3:120274400-120275400	Enhancers	Stomach Mucosa	stomach
47	chr3:120274600-120274800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:120274600-120275200	Enhancers	Fetal Intestine Large	intestine
49	chr3:120274600-120275200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr3:120274600-120275400	Enhancers	Lung	lung

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