Variant report

Variant	nsv1006289
Chromosome Location	chr3:133137664-133186808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1509)
CpG islands
(count:549)
Chromatin interactive
region (count:67)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1509 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:133174992-133175157	K562	blood:	n/a	n/a
2	ARID3A	chr3:133162962-133163067	K562	blood:	n/a	n/a
3	ARID3A	chr3:133156704-133157073	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:133176357-133176641	K562	blood:	n/a	n/a
5	ARID3A	chr3:133176380-133176641	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:133171646-133172197	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:133162975-133163294	HepG2	liver:	n/a	n/a
8	ATF1	chr3:133174836-133175307	K562	blood:	n/a	n/a
9	ATF2	chr3:133167079-133168028	GM12878	blood:	n/a	n/a
10	ATF2	chr3:133185291-133186134	GM12878	blood:	n/a	n/a
11	ATF2	chr3:133142398-133142693	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr3:133166990-133168141	GM12878	blood:	n/a	n/a
13	ATF3	chr3:133162944-133163357	A549	lung:	n/a	n/a
14	BACH1	chr3:133163108-133163230	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:133163169-133163196	K562	blood:	n/a	n/a
16	BATF	chr3:133167212-133168049	GM12878	blood:	n/a	n/a
17	BATF	chr3:133168910-133169128	GM12878	blood:	n/a	n/a
18	BATF	chr3:133161396-133161659	GM12878	blood:	n/a	n/a
19	BATF	chr3:133167292-133167760	GM12878	blood:	n/a	n/a
20	BATF	chr3:133183505-133183734	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:133166638-133166892	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:133167273-133167755	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:133167185-133167791	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:133174907-133175106	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:133174789-133175134	GM12878	blood:	n/a	n/a
26	BCL3	chr3:133162874-133163354	A549	lung:	n/a	n/a
27	BCL3	chr3:133167225-133167767	GM12878	blood:	n/a	n/a
28	BCL3	chr3:133162950-133163348	A549	lung:	n/a	n/a
29	BCLAF1	chr3:133167158-133167928	GM12878	blood:	n/a	n/a
30	BCLAF1	chr3:133160617-133161181	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:133167280-133167988	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:133183407-133183825	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:133174829-133175279	K562	blood:	n/a	n/a
34	BHLHE40	chr3:133144019-133144340	HepG2	liver:	n/a	chr3:133144178-133144199 chr3:133144184-133144193 chr3:133144183-133144192 chr3:133144184-133144193 chr3:133144182-133144195
35	BHLHE40	chr3:133143874-133144338	GM12878	blood:	n/a	chr3:133144178-133144199 chr3:133144184-133144193 chr3:133144183-133144192 chr3:133144184-133144193 chr3:133144182-133144195
36	BHLHE40	chr3:133166690-133168104	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:133160780-133160957	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:133142501-133142692	HepG2	liver:	n/a	n/a
39	BHLHE40	chr3:133144084-133144338	K562	blood:	n/a	chr3:133144178-133144199 chr3:133144184-133144193 chr3:133144183-133144192 chr3:133144184-133144193 chr3:133144182-133144195
40	BHLHE40	chr3:133174998-133175027	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:133185370-133185738	GM12878	blood:	n/a	n/a
42	CBX3	chr3:133176267-133176824	HCT-116	colon:	n/a	n/a
43	CBX3	chr3:133176216-133176765	HCT-116	colon:	n/a	n/a
44	CCNT2	chr3:133174832-133175254	K562	blood:	n/a	n/a
45	CEBPB	chr3:133174858-133175271	K562	blood:	n/a	chr3:133175107-133175120 chr3:133175107-133175118
46	CEBPB	chr3:133156910-133157182	A549	lung:	n/a	n/a
47	CEBPB	chr3:133180044-133180474	MCF-7	breast:	n/a	n/a
48	CEBPB	chr3:133162967-133163321	A549	lung:	n/a	n/a
49	CEBPB	chr3:133163028-133163510	IMR90	lung:	n/a	chr3:133163427-133163435
50	CEBPB	chr3:133142431-133142732	H1-hESC	embryonic stem cell:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133160722-133160772	HEEpiC	esophagus:	n/a
2	chr3:133174674-133174724	H1-hESC	embryonic stem cell:	embryo
3	chr3:133174674-133174724	A549	lung:	n/a
4	chr3:133174649-133174699	HUVEC	blood vessel:	n/a
5	chr3:133160722-133160772	SK-N-MC	brain:	n/a
6	chr3:133160722-133160772	MCF10A-Er-Src	breast:	n/a
7	chr3:133174674-133174724	GM06990	blood:	n/a
8	chr3:133174926-133174976	Caco-2	colon:	n/a
9	chr3:133174674-133174724	NHDF-neo	bronchial:	n/a
10	chr3:133174687-133174737	SAEC	small airway:	n/a
11	chr3:133175241-133175291	AG04449	skin:	fetal
12	chr3:133182835-133182885	BE2_C	brain:	n/a
13	chr3:133180261-133180311	NH-A	brain:	n/a
14	chr3:133174687-133174737	AoSMC	blood vessel:	n/a
15	chr3:133180261-133180311	HAEpiC	amniotic membrane:	n/a
16	chr3:133175241-133175291	BE2_C	brain:	n/a
17	chr3:133174649-133174699	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:133175241-133175291	AG04450	lung:	fetal
19	chr3:133180261-133180311	RPTEC	kidney:	n/a
20	chr3:133182835-133182885	SKMC	muscle:	n/a
21	chr3:133175241-133175291	U87	brain:	n/a
22	chr3:133174926-133174976	HMEC	breast:	n/a
23	chr3:133182835-133182885	SK-N-SH_RA	brain:	n/a
24	chr3:133182835-133182885	SK-N-SH	brain:	n/a
25	chr3:133175241-133175291	HEEpiC	esophagus:	n/a
26	chr3:133180261-133180311	U87	brain:	n/a
27	chr3:133174926-133174976	NT2-D1	testis:	n/a
28	chr3:133180261-133180311	AG04450	lung:	fetal
29	chr3:133174926-133174976	Hepatocyte	liver:	n/a
30	chr3:133180261-133180311	AoSMC	blood vessel:	n/a
31	chr3:133174674-133174724	AG04449	skin:	fetal
32	chr3:133174674-133174724	Caco-2	colon:	n/a
33	chr3:133174687-133174737	NT2-D1	testis:	n/a
34	chr3:133174926-133174976	AG09319	gingival:	n/a
35	chr3:133174649-133174699	HCF	heart:	n/a
36	chr3:133182835-133182885	HCF	heart:	n/a
37	chr3:133174687-133174737	HEK293	kidney:	embryo
38	chr3:133142442-133142492	NH-A	brain:	n/a
39	chr3:133160722-133160772	AG04450	lung:	fetal
40	chr3:133174687-133174737	AG04450	lung:	fetal
41	chr3:133174674-133174724	MCF-7	breast:	n/a
42	chr3:133174687-133174737	AG09319	gingival:	n/a
43	chr3:133142442-133142492	IMR90	lung:	fetal
44	chr3:133160722-133160772	GM12878	blood:	n/a
45	chr3:133174687-133174737	GM12891	blood:	n/a
46	chr3:133174687-133174737	GM12878	blood:	n/a
47	chr3:133182835-133182885	HepG2	liver:	n/a
48	chr3:133174649-133174699	HCPEpiC	choroid plexus:	n/a
49	chr3:133174674-133174724	AG09319	gingival:	n/a
50	chr3:133160722-133160772	GM12892	blood:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:133175597..133178522-chr3:133290456..133293347,3	MCF-7	breast:
2	chr3:133162579..133164484-chr3:133291508..133294173,3	MCF-7	breast:
3	chr3:133166486..133169051-chr3:133181517..133184490,2	MCF-7	breast:
4	chr3:133105226..133106115-chr3:133142183..133142702,2	MCF-7	breast:
5	chr3:133167229..133167755-chr3:133175434..133175991,2	MCF-7	breast:
6	chr3:133164640..133168534-chr3:133291750..133294077,5	MCF-7	breast:
7	chr3:133157939..133159842-chr3:133161653..133163728,2	MCF-7	breast:
8	chr3:133157614..133159681-chr3:133160592..133163349,2	MCF-7	breast:
9	chr3:133143999..133146404-chr3:133171252..133173491,2	MCF-7	breast:
10	chr3:133162011..133163962-chr3:133171581..133174008,3	MCF-7	breast:
11	chr3:133182278..133184590-chr3:133188280..133190685,2	MCF-7	breast:
12	chr3:133179034..133181660-chr3:133249507..133251496,2	MCF-7	breast:
13	chr3:132759801..132760742-chr3:133142128..133143076,4	K562	blood:
14	chr3:133162582..133163499-chr3:133297110..133297716,3	MCF-7	breast:
15	chr3:133143999..133146404-chr3:133171252..133173491,2	MCF-7	breast:
16	chr3:133146085..133148197-chr3:133291906..133294267,2	MCF-7	breast:
17	chr3:133178497..133180168-chr3:133538134..133540708,2	MCF-7	breast:
18	chr3:133169681..133172224-chr3:133173356..133176269,2	K562	blood:
19	chr3:132439632..132442220-chr3:133141166..133143810,2	K562	blood:
20	chr3:133173610..133177245-chr3:133178784..133182075,5	MCF-7	breast:
21	chr3:133179746..133182359-chr3:133292415..133294343,2	K562	blood:
22	chr3:133161498..133163430-chr3:133177580..133180492,2	MCF-7	breast:
23	chr3:132759750..132760749-chr3:133142099..133143085,7	MCF-7	breast:
24	chr3:133180327..133181853-chr3:133181928..133184881,2	MCF-7	breast:
25	chr3:132450051..132450561-chr3:133142135..133143010,2	MCF-7	breast:
26	chr3:133157614..133159681-chr3:133160592..133163349,2	MCF-7	breast:
27	chr3:133180154..133181710-chr3:133287523..133290190,2	MCF-7	breast:
28	chr3:133161498..133163430-chr3:133177580..133180492,2	MCF-7	breast:
29	chr3:132440764..132443232-chr3:133142306..133144547,2	MCF-7	breast:
30	chr3:133103081..133103646-chr3:133142086..133142975,2	MCF-7	breast:
31	chr3:133153374..133155623-chr3:133178756..133181568,2	MCF-7	breast:
32	chr3:133162344..133164568-chr3:133170486..133172340,2	MCF-7	breast:
33	chr3:133169398..133190840-chr3:133288286..133298861,41	MCF-7	breast:
34	chr3:133103700..133105206-chr3:133145260..133147537,2	MCF-7	breast:
35	chr3:133105415..133106537-chr3:133142074..133142947,6	MCF-7	breast:
36	chr3:133162655..133165073-chr3:133302328..133304905,2	MCF-7	breast:
37	chr3:133162344..133164568-chr3:133170486..133172340,2	MCF-7	breast:
38	chr3:133165936..133167701-chr3:133170915..133173583,2	MCF-7	breast:
39	chr3:132254793..132255497-chr3:133142223..133143012,2	MCF-7	breast:
40	chr3:133182317..133184120-chr3:133296724..133299109,2	MCF-7	breast:
41	chr3:133155354..133158074-chr3:133292278..133293875,2	MCF-7	breast:
42	chr3:133180327..133181853-chr3:133181928..133184881,2	MCF-7	breast:
43	chr3:133170213..133174135-chr3:133291301..133294544,7	MCF-7	breast:
44	chr3:133153374..133155623-chr3:133178756..133181568,2	MCF-7	breast:
45	chr3:133165936..133167701-chr3:133170915..133173583,2	MCF-7	breast:
46	chr3:132445024..132445748-chr3:133142162..133143068,3	MCF-7	breast:
47	chr3:133167608..133169678-chr3:133177159..133179764,2	MCF-7	breast:
48	chr3:133182951..133184510-chr3:133300267..133301904,2	K562	blood:
49	chr3:133180499..133182281-chr3:133188502..133190705,2	MCF-7	breast:
50	chr3:133162011..133163962-chr3:133171581..133174008,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOPBP1-1	chr3:133164249-133164419	ENSG00000249993.1
2	lnc-TOPBP1-1	chr3:133174589-133174620	ENSG00000249993.1
3	lnc-TOPBP1-1	chr3:133174173-133174307	ENSG00000249993.1
4	lnc-TOPBP1-1	chr3:133148113-133148553	ENSG00000249993.1
5	lnc-TOPBP1-1	chr3:133167625-133167739	ENSG00000249993.1

No data

Variant related genes	Relation type
BFSP2-AS1	TF binding region
BFSP2	TF binding region
BFSP2-AS1	CpG island
BFSP2	CpG island
ENSG00000144867	chromatin interactions
ENSG00000091527	chromatin interactions
ENSG00000249993	chromatin interactions
ENSG00000113971	chromatin interactions
ENSG00000170819	chromatin interactions
ENSG00000248724	chromatin interactions
ENSG00000144868	chromatin interactions

Extended variants
information (count: 2071 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2071 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6806169	chr3:133137664-133137665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542233950	chr3:133137682-133137683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562111558	chr3:133137686-133137687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533784464	chr3:133137687-133137688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368497059	chr3:133137718-133137719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185259815	chr3:133137730-133137731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564621537	chr3:133137748-133137749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62280907	chr3:133137757-133137758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189966978	chr3:133137768-133137769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146521960	chr3:133137799-133137800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183369360	chr3:133137826-133137827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139951195	chr3:133137855-133137856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189229288	chr3:133137882-133137883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149667637	chr3:133137910-133137911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547782293	chr3:133137945-133137946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191383596	chr3:133137947-133137948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375058801	chr3:133137958-133137959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536660887	chr3:133137990-133137991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12489349	chr3:133138036-133138037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs12489328	chr3:133138112-133138113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs183746678	chr3:133138135-133138136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187837290	chr3:133138148-133138149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375215544	chr3:133138160-133138161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145484874	chr3:133138162-133138163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148821449	chr3:133138167-133138168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562048734	chr3:133138195-133138196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575675697	chr3:133138255-133138256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575643688	chr3:133138298-133138299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191606765	chr3:133138303-133138304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184090099	chr3:133138311-133138312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12492831	chr3:133138339-133138340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs564441144	chr3:133138348-133138349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560763163	chr3:133138350-133138351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117540821	chr3:133138384-133138385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73863532	chr3:133138480-133138481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569213811	chr3:133138523-133138524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369783847	chr3:133138524-133138525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376035908	chr3:133138527-133138528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77641780	chr3:133138546-133138547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550568536	chr3:133138548-133138549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12489467	chr3:133138552-133138553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570439137	chr3:133138569-133138570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539548238	chr3:133138604-133138605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552888857	chr3:133138678-133138679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566713748	chr3:133138702-133138703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368941069	chr3:133138726-133138727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535655726	chr3:133138732-133138733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34673573	chr3:133138766-133138767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575630723	chr3:133138775-133138776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554891623	chr3:133138788-133138789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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	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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Hailey-hailey disease	17597066	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133124600-133138400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr3:133133000-133140600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:133138400-133140600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:133138600-133140600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:133139400-133139800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:133141800-133143000	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr3:133141800-133143000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr3:133142000-133142200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
9	chr3:133142000-133142200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
10	chr3:133142000-133142400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr3:133142000-133142400	Enhancers	Osteobl	bone
12	chr3:133142200-133142800	Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr3:133142200-133144600	Enhancers	Primary B cells from peripheral blood	blood
14	chr3:133142400-133142600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr3:133142400-133142800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr3:133142400-133142800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr3:133142400-133142800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:133142400-133142800	Enhancers	Fetal Muscle Trunk	muscle
19	chr3:133142400-133142800	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr3:133142400-133142800	Enhancers	Placenta	Placenta
21	chr3:133142400-133142800	Flanking Active TSS	Osteobl	bone
22	chr3:133142600-133142800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr3:133142600-133142800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:133142600-133142800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:133142600-133142800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
26	chr3:133142600-133142800	Enhancers	Liver	Liver
27	chr3:133142600-133142800	Flanking Active TSS	Brain Anterior Caudate	brain
28	chr3:133142600-133142800	Enhancers	Esophagus	oesophagus
29	chr3:133142600-133142800	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr3:133142600-133143000	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr3:133142600-133143000	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr3:133142600-133143000	Enhancers	Fetal Brain Male	brain
33	chr3:133142600-133143000	Enhancers	Fetal Thymus	thymus
34	chr3:133142600-133143000	Bivalent Enhancer	Thymus	Thymus
35	chr3:133142600-133143000	Enhancers	HSMMtube	muscle
36	chr3:133142600-133144200	Enhancers	GM12878-XiMat	blood
37	chr3:133142800-133143200	Enhancers	Primary B cells from cord blood	blood
38	chr3:133142800-133143800	Weak transcription	Liver	Liver
39	chr3:133142800-133145200	Weak transcription	Osteobl	bone
40	chr3:133142800-133147000	Weak transcription	Placenta	Placenta
41	chr3:133142800-133147200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:133142800-133147400	Weak transcription	Esophagus	oesophagus
43	chr3:133142800-133151800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:133142800-133154000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr3:133143000-133145200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:133143000-133145400	Weak transcription	HSMMtube	muscle
47	chr3:133143000-133145800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr3:133143400-133145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:133143800-133144800	Enhancers	Liver	Liver
50	chr3:133144200-133144600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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