Variant report

Variant	nsv3806
Chromosome Location	chr3:47488784-47518133
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:877)
CpG islands
(count:856)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:47517138-47517674	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:47517354-47517603	K562	blood:	n/a	n/a
3	ATF2	chr3:47507614-47508065	GM12878	blood:	n/a	n/a
4	ATF2	chr3:47507646-47508096	GM12878	blood:	n/a	n/a
5	ATF3	chr3:47507677-47508053	K562	blood:	n/a	n/a
6	ATF3	chr3:47517311-47517751	K562	blood:	n/a	n/a
7	ATF3	chr3:47517372-47517729	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr3:47517415-47517649	HepG2	liver:	n/a	n/a
9	BACH1	chr3:47516646-47517645	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr3:47507653-47508018	GM12878	blood:	n/a	chr3:47507886-47507897
11	BATF	chr3:47507655-47508077	GM12878	blood:	n/a	chr3:47507886-47507897
12	BCL3	chr3:47517118-47517699	GM12878	blood:	n/a	chr3:47517469-47517482
13	BCLAF1	chr3:47516917-47517729	GM12878	blood:	n/a	chr3:47517469-47517482 chr3:47517068-47517081
14	BHLHE40	chr3:47503981-47504181	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:47517330-47517633	HepG2	liver:	n/a	n/a
16	BHLHE40	chr3:47516660-47518282	K562	blood:	n/a	chr3:47517065-47517081 chr3:47517150-47517166
17	BHLHE40	chr3:47507730-47508046	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:47516732-47517905	HepG2	liver:	n/a	chr3:47517065-47517081 chr3:47517150-47517166
19	BHLHE40	chr3:47517201-47517635	HepG2	liver:	n/a	n/a
20	BHLHE40	chr3:47517279-47517694	A549	lung:	n/a	n/a
21	BHLHE40	chr3:47516766-47517868	GM12878	blood:	n/a	chr3:47517065-47517081 chr3:47517150-47517166
22	BRCA1	chr3:47517365-47517733	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr3:47517414-47517633	HepG2	liver:	n/a	n/a
24	BRCA1	chr3:47516605-47517112	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr3:47501227-47501565	K562	blood:	n/a	n/a
26	CBX3	chr3:47517359-47517925	K562	blood:	n/a	n/a
27	CBX3	chr3:47516556-47518151	K562	blood:	n/a	n/a
28	CBX3	chr3:47501183-47501569	K562	blood:	n/a	n/a
29	CCNT2	chr3:47516491-47517751	K562	blood:	n/a	chr3:47517097-47517106
30	CEBPB	chr3:47509022-47509077	A549	lung:	n/a	chr3:47509045-47509056
31	CEBPB	chr3:47497333-47497728	IMR90	lung:	n/a	chr3:47497524-47497535
32	CEBPB	chr3:47517163-47517680	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:47508892-47509223	K562	blood:	n/a	chr3:47509045-47509056
34	CEBPB	chr3:47497178-47497755	HCT-116	colon:	n/a	chr3:47497524-47497535
35	CEBPB	chr3:47497325-47497822	HCT-116	colon:	n/a	chr3:47497524-47497535
36	CEBPB	chr3:47497132-47497882	A549	lung:	n/a	chr3:47497524-47497535
37	CEBPB	chr3:47497299-47497715	K562	blood:	n/a	chr3:47497524-47497535
38	CEBPB	chr3:47497393-47497629	HepG2	liver:	n/a	chr3:47497524-47497535
39	CEBPB	chr3:47507481-47507603	HepG2	liver:	n/a	chr3:47507573-47507584
40	CEBPB	chr3:47507407-47507943	Hela-S3	cervix:	n/a	chr3:47507573-47507584
41	CEBPB	chr3:47507498-47507678	IMR90	lung:	n/a	chr3:47507573-47507584
42	CEBPB	chr3:47497330-47497741	A549	lung:	n/a	chr3:47497524-47497535
43	CEBPB	chr3:47507423-47507702	K562	blood:	n/a	chr3:47507573-47507584
44	CEBPB	chr3:47497266-47497730	ECC-1	luminal epithelium:	n/a	chr3:47497524-47497535
45	CEBPB	chr3:47497310-47497670	ECC-1	luminal epithelium:	n/a	chr3:47497524-47497535
46	CEBPB	chr3:47500887-47501068	HepG2	liver:	n/a	chr3:47500927-47500938
47	CEBPB	chr3:47497315-47497697	A549	lung:	n/a	chr3:47497524-47497535
48	CEBPB	chr3:47497250-47497710	MCF-7	breast:	n/a	chr3:47497524-47497535
49	CEBPB	chr3:47497372-47497788	HepG2	liver:	n/a	chr3:47497524-47497535
50	CEBPB	chr3:47497391-47497683	HepG2	liver:	n/a	chr3:47497524-47497535

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47517624-47517674	BJ	skin:	n/a
2	chr3:47517504-47517554	GM19239	blood:	n/a
3	chr3:47517624-47517674	BJ	skin:	n/a
4	chr3:47517504-47517554	GM19239	blood:	n/a
5	chr3:47517500-47517550	RPTEC	kidney:	n/a
6	chr3:47517624-47517674	HCPEpiC	choroid plexus:	n/a
7	chr3:47517781-47517831	HepG2	liver:	n/a
8	chr3:47517624-47517674	HEK293	kidney:	embryo
9	chr3:47517263-47517313	MCF10A-Er-Src	breast:	n/a
10	chr3:47514673-47514723	HIPEpiC	eye:	n/a
11	chr3:47516975-47517025	Hela-S3	cervix:	n/a
12	chr3:47517263-47517313	ECC-1	luminal epithelium:	n/a
13	chr3:47517690-47517740	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:47517504-47517554	HEEpiC	esophagus:	n/a
15	chr3:47517263-47517313	K562	blood:	n/a
16	chr3:47517624-47517674	AG04449	skin:	fetal
17	chr3:47516975-47517025	SK-N-MC	brain:	n/a
18	chr3:47517690-47517740	BJ	skin:	n/a
19	chr3:47517624-47517674	HepG2	liver:	n/a
20	chr3:47516702-47516752	AG04450	lung:	fetal
21	chr3:47517621-47517671	Caco-2	colon:	n/a
22	chr3:47517819-47517869	NHDF-neo	bronchial:	n/a
23	chr3:47517781-47517831	HAEpiC	amniotic membrane:	n/a
24	chr3:47517690-47517740	SAEC	small airway:	n/a
25	chr3:47517510-47517560	ECC-1	luminal epithelium:	n/a
26	chr3:47517807-47517857	SK-N-SH	brain:	n/a
27	chr3:47517504-47517554	ovcar-3	ovarian:	n/a
28	chr3:47514673-47514723	AG09319	gingival:	n/a
29	chr3:47516975-47517025	AoSMC	blood vessel:	n/a
30	chr3:47517001-47517051	CMK	blood:	n/a
31	chr3:47517807-47517857	NT2-D1	testis:	n/a
32	chr3:47517624-47517674	RPTEC	kidney:	n/a
33	chr3:47517621-47517671	HEK293	kidney:	embryo
34	chr3:47517001-47517051	HRCEpiC	kidney:	n/a
35	chr3:47517690-47517740	HNPCEpiC	eye:	n/a
36	chr3:47517819-47517869	AG04450	lung:	fetal
37	chr3:47517621-47517671	AG09309	skin:	n/a
38	chr3:47517807-47517857	A549	lung:	n/a
39	chr3:47517819-47517869	MCF10A-Er-Src	breast:	n/a
40	chr3:47516975-47517025	AG10803	skin:	n/a
41	chr3:47516975-47517025	HMEC	breast:	n/a
42	chr3:47517781-47517831	ECC-1	luminal epithelium:	n/a
43	chr3:47517001-47517051	HL-60	blood:	n/a
44	chr3:47517781-47517831	ProgFib	skin:	n/a
45	chr3:47517500-47517550	HCT-116	colon:	n/a
46	chr3:47517504-47517554	NB4	blood:	n/a
47	chr3:47517819-47517869	AoSMC	blood vessel:	n/a
48	chr3:47517510-47517560	AG04450	lung:	fetal
49	chr3:47516702-47516752	PrEC	prostate:	n/a
50	chr3:47516975-47517025	U87	brain:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:47515959..47519018-chr3:47554813..47558530,7	K562	blood:
2	chr3:47494708..47496702-chr3:47497942..47500024,2	K562	blood:
3	chr3:47462059..47463174-chr3:47516921..47518022,7	K562	blood:
4	chr3:47496728..47499027-chr3:47502700..47504481,2	K562	blood:
5	chr3:47421212..47424258-chr3:47516702..47519185,3	K562	blood:
6	chr3:47516853..47519140-chr3:47552540..47554804,2	K562	blood:
7	chr3:47510437..47514442-chr3:47515301..47518815,8	K562	blood:
8	chr3:47490582..47492929-chr3:47496391..47498138,2	MCF-7	breast:
9	chr3:47462473..47463111-chr3:47517060..47518005,2	MCF-7	breast:
10	chr3:47495443..47497442-chr3:47500032..47502167,2	K562	blood:
11	chr3:47496728..47499027-chr3:47502700..47504481,2	K562	blood:
12	chr3:47506187..47509677-chr3:47510013..47512919,3	K562	blood:
13	chr3:47462559..47463377-chr3:47517045..47517970,3	MCF-7	breast:
14	chr3:47515849..47519127-chr3:47552237..47555413,3	MCF-7	breast:
15	chr3:47505383..47508183-chr3:47513358..47515947,2	K562	blood:
16	chr3:47490125..47492275-chr3:47492500..47495080,2	K562	blood:
17	chr3:47490582..47492929-chr3:47496391..47498138,2	MCF-7	breast:
18	chr3:47494708..47496702-chr3:47497942..47500024,2	K562	blood:
19	chr3:47484894..47485414-chr3:47514547..47515158,2	MCF-7	breast:
20	chr3:47500348..47503625-chr3:47514780..47518707,3	K562	blood:
21	chr3:47421161..47424382-chr3:47515710..47518539,3	MCF-7	breast:
22	chr3:47497462..47499073-chr3:47553005..47555711,2	MCF-7	breast:
23	chr3:47490214..47492275-chr3:47492500..47494353,2	K562	blood:
24	chr3:47463570..47464475-chr3:47516993..47518028,5	MCF-7	breast:
25	chr3:47501641..47506010-chr3:47514476..47518567,5	K562	blood:
26	chr3:47483730..47486562-chr3:47497535..47500120,2	MCF-7	breast:
27	chr3:47495443..47497442-chr3:47500032..47502167,2	K562	blood:
28	chr3:47473187..47475541-chr3:47495094..47496706,2	K562	blood:
29	chr3:47517000..47518898-chr3:47553503..47555286,3	MCF-7	breast:
30	chr3:47490125..47492275-chr3:47492500..47495080,2	K562	blood:
31	chr3:47514858..47522453-chr3:47552535..47558710,16	K562	blood:
32	chr3:47513969..47516839-chr3:47829270..47830805,2	K562	blood:
33	chr3:47490214..47492275-chr3:47492500..47494353,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238350	TF binding region
SCAP	TF binding region
ENSG00000238350	CpG island
SCAP	CpG island
ENSG00000114650	chromatin interactions
ENSG00000163832	chromatin interactions
ENSG00000076201	chromatin interactions
ENSG00000260236	chromatin interactions
ENSG00000238350	chromatin interactions

Extended variants
information (count: 948 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117610268	chr3:47488788-47488789	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs564415888	chr3:47488877-47488878	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs371809207	chr3:47488878-47488879	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563807434	chr3:47488908-47488909	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs9867204	chr3:47488954-47488955	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs528963104	chr3:47489014-47489015	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs550676601	chr3:47489023-47489024	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs568506498	chr3:47489085-47489086	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs543837785	chr3:47489091-47489092	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs551616921	chr3:47489093-47489094	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs377031065	chr3:47489103-47489104	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs367788810	chr3:47489140-47489141	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534097234	chr3:47489157-47489158	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562474785	chr3:47489160-47489161	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369739992	chr3:47489166-47489167	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189119290	chr3:47489185-47489186	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58248669	chr3:47489189-47489190	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs59995300	chr3:47489194-47489195	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537932521	chr3:47489200-47489201	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556664669	chr3:47489245-47489246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372725830	chr3:47489251-47489252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138180647	chr3:47489291-47489292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539047580	chr3:47489325-47489326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529832053	chr3:47489340-47489341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192800046	chr3:47489351-47489352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573198025	chr3:47489363-47489364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143648811	chr3:47489409-47489410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185548472	chr3:47489450-47489451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548270125	chr3:47489451-47489452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573823528	chr3:47489464-47489465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112933622	chr3:47489485-47489486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142490430	chr3:47489493-47489494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113945636	chr3:47489507-47489508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56132307	chr3:47489521-47489522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545577065	chr3:47489522-47489523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568778060	chr3:47489523-47489524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374556340	chr3:47489581-47489582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560672392	chr3:47489583-47489584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562253115	chr3:47489630-47489631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12054363	chr3:47489634-47489635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527887770	chr3:47489656-47489657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12054364	chr3:47489699-47489700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190450586	chr3:47489717-47489718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181905406	chr3:47489736-47489737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560381751	chr3:47489765-47489766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527964267	chr3:47489768-47489769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549679099	chr3:47489785-47489786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139566246	chr3:47489802-47489803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9683033	chr3:47489820-47489821	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs149172776	chr3:47489845-47489846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47474600-47489600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:47476600-47514200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:47481400-47496000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:47481400-47500600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:47481800-47492600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr3:47482200-47488800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr3:47484000-47507800	Weak transcription	Primary B cells from cord blood	blood
8	chr3:47484000-47511200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr3:47484200-47511200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr3:47484400-47492600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr3:47484400-47497200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr3:47484600-47490000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr3:47484600-47494200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr3:47484600-47497400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr3:47484600-47500600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr3:47484600-47514000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr3:47484600-47514200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr3:47484600-47514200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr3:47484600-47514200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr3:47484600-47514800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr3:47484800-47504400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr3:47484800-47504600	Weak transcription	Primary T cells from cord blood	blood
23	chr3:47484800-47514800	Weak transcription	Thymus	Thymus
24	chr3:47485000-47514800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr3:47485200-47502600	Weak transcription	K562	blood
26	chr3:47485400-47489400	Weak transcription	GM12878-XiMat	blood
27	chr3:47485400-47490800	Weak transcription	Fetal Lung	lung
28	chr3:47485400-47493000	Weak transcription	Spleen	Spleen
29	chr3:47485400-47494200	Weak transcription	Ovary	ovary
30	chr3:47485400-47503200	Weak transcription	Gastric	stomach
31	chr3:47485600-47493200	Weak transcription	Esophagus	oesophagus
32	chr3:47485600-47494000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr3:47485800-47493600	Weak transcription	Fetal Heart	heart
34	chr3:47486000-47490800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr3:47486000-47492200	Weak transcription	Psoas Muscle	Psoas
36	chr3:47486000-47494200	Weak transcription	Left Ventricle	heart
37	chr3:47486000-47497200	Weak transcription	A549	lung
38	chr3:47486000-47497400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr3:47486000-47500200	Weak transcription	Fetal Intestine Large	intestine
40	chr3:47486000-47500400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:47486000-47504600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr3:47486000-47516000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:47486000-47516000	Weak transcription	Small Intestine	intestine
44	chr3:47486000-47516000	Weak transcription	HSMM	muscle
45	chr3:47486200-47497200	Weak transcription	Hela-S3	cervix
46	chr3:47486200-47502600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr3:47486200-47506000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:47486200-47516000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr3:47486600-47494400	Weak transcription	HepG2	liver
50	chr3:47486600-47500600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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