Variant report

Variant	esv2759146
Chromosome Location	chr3:46419634-46444794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:713)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:46441675-46442336	K562	blood:	n/a	n/a
2	ARID3A	chr3:46443029-46443434	K562	blood:	n/a	n/a
3	ARID3A	chr3:46435037-46435340	K562	blood:	n/a	n/a
4	ATF1	chr3:46441097-46442116	K562	blood:	n/a	n/a
5	ATF1	chr3:46427708-46428088	K562	blood:	n/a	n/a
6	ATF1	chr3:46436618-46437128	K562	blood:	n/a	n/a
7	ATF1	chr3:46435062-46435435	K562	blood:	n/a	n/a
8	ATF3	chr3:46441658-46442063	K562	blood:	n/a	n/a
9	BACH1	chr3:46441806-46441966	K562	blood:	n/a	n/a
10	BACH1	chr3:46420259-46420467	K562	blood:	n/a	n/a
11	BACH1	chr3:46436732-46436785	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:46420270-46420476	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr3:46437682-46437883	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:46427743-46427991	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:46419872-46420221	K562	blood:	n/a	n/a
16	BHLHE40	chr3:46435111-46435367	HepG2	liver:	n/a	n/a
17	BHLHE40	chr3:46427646-46428121	K562	blood:	n/a	n/a
18	BHLHE40	chr3:46437674-46438000	K562	blood:	n/a	chr3:46437839-46437848
19	BHLHE40	chr3:46442891-46443148	K562	blood:	n/a	n/a
20	BHLHE40	chr3:46437645-46438047	GM12878	blood:	n/a	chr3:46437839-46437848
21	BHLHE40	chr3:46436634-46437083	K562	blood:	n/a	n/a
22	BHLHE40	chr3:46425430-46425434	K562	blood:	n/a	n/a
23	BHLHE40	chr3:46423525-46423558	K562	blood:	n/a	n/a
24	BHLHE40	chr3:46435037-46435494	K562	blood:	n/a	n/a
25	BHLHE40	chr3:46440709-46441336	K562	blood:	n/a	n/a
26	BHLHE40	chr3:46441636-46442092	K562	blood:	n/a	n/a
27	BRCA1	chr3:46427773-46427972	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:46435600-46435602	HepG2	liver:	n/a	n/a
29	CBX3	chr3:46429309-46429676	K562	blood:	n/a	n/a
30	CCNT2	chr3:46427769-46428163	K562	blood:	n/a	n/a
31	CCNT2	chr3:46441642-46442276	K562	blood:	n/a	n/a
32	CEBPB	chr3:46436900-46437226	K562	blood:	n/a	chr3:46437073-46437084
33	CEBPB	chr3:46435048-46435378	HepG2	liver:	n/a	chr3:46435207-46435218
34	CEBPB	chr3:46434650-46435609	Hela-S3	cervix:	n/a	chr3:46435207-46435218
35	CEBPB	chr3:46427708-46427885	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr3:46436885-46437263	IMR90	lung:	n/a	chr3:46437073-46437084
37	CEBPB	chr3:46436945-46437192	A549	lung:	n/a	chr3:46437073-46437084
38	CEBPB	chr3:46436917-46437195	K562	blood:	n/a	chr3:46437073-46437084
39	CEBPB	chr3:46436945-46437194	Hela-S3	cervix:	n/a	chr3:46437073-46437084
40	CEBPB	chr3:46442897-46443138	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:46435014-46435450	K562	blood:	n/a	chr3:46435207-46435218
42	CEBPB	chr3:46435056-46435391	ECC-1	luminal epithelium:	n/a	chr3:46435207-46435218
43	CEBPB	chr3:46436920-46437258	HepG2	liver:	n/a	chr3:46437073-46437084
44	CEBPB	chr3:46441875-46442094	K562	blood:	n/a	n/a
45	CEBPB	chr3:46435026-46435400	IMR90	lung:	n/a	chr3:46435207-46435218
46	CEBPB	chr3:46435123-46435275	HepG2	liver:	n/a	chr3:46435207-46435218
47	CEBPB	chr3:46442904-46443136	K562	blood:	n/a	n/a
48	CEBPB	chr3:46435022-46435405	H1-hESC	embryonic stem cell:	n/a	chr3:46435207-46435218
49	CEBPB	chr3:46435012-46435363	K562	blood:	n/a	chr3:46435207-46435218
50	CEBPB	chr3:46435029-46435398	ECC-1	luminal epithelium:	n/a	chr3:46435207-46435218

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46441609-46441659	ovcar-3	ovarian:	n/a
2	chr3:46441609-46441659	SKMC	muscle:	n/a
3	chr3:46441609-46441659	SK-N-MC	brain:	n/a
4	chr3:46441609-46441659	CMK	blood:	n/a
5	chr3:46441609-46441659	HCF	heart:	n/a
6	chr3:46441609-46441659	MCF10A-Er-Src	breast:	n/a
7	chr3:46441609-46441659	GM12891	blood:	n/a
8	chr3:46441609-46441659	HNPCEpiC	eye:	n/a
9	chr3:46441609-46441659	Caco-2	colon:	n/a
10	chr3:46441609-46441659	MCF-7	breast:	n/a
11	chr3:46441609-46441659	HEK293	kidney:	embryo
12	chr3:46441609-46441659	AoSMC	blood vessel:	n/a
13	chr3:46441609-46441659	HRCEpiC	kidney:	n/a
14	chr3:46441609-46441659	HPAEpiC	pulmonary alveolar:	n/a
15	chr3:46441609-46441659	ProgFib	skin:	n/a
16	chr3:46441609-46441659	HRPEpiC	eye:	n/a
17	chr3:46441609-46441659	PFSK-1	brain:	n/a
18	chr3:46441609-46441659	NB4	blood:	n/a
19	chr3:46441609-46441659	AG09319	gingival:	n/a
20	chr3:46441609-46441659	PrEC	prostate:	n/a
21	chr3:46441609-46441659	HCPEpiC	choroid plexus:	n/a
22	chr3:46441609-46441659	SK-N-SH	brain:	n/a
23	chr3:46441609-46441659	SAEC	small airway:	n/a
24	chr3:46441609-46441659	HUVEC	blood vessel:	n/a
25	chr3:46441609-46441659	IMR90	lung:	fetal
26	chr3:46441609-46441659	GM19239	blood:	n/a
27	chr3:46441609-46441659	AG04450	lung:	fetal
28	chr3:46441609-46441659	GM12892	blood:	n/a
29	chr3:46441609-46441659	ECC-1	luminal epithelium:	n/a
30	chr3:46441609-46441659	GM06990	blood:	n/a
31	chr3:46441609-46441659	NH-A	brain:	n/a
32	chr3:46441609-46441659	Jurkat	blood:	n/a
33	chr3:46441609-46441659	AG09309	skin:	n/a
34	chr3:46441609-46441659	BE2_C	brain:	n/a
35	chr3:46441609-46441659	GM12878	blood:	n/a
36	chr3:46441609-46441659	AG04449	skin:	fetal
37	chr3:46441609-46441659	Hela-S3	cervix:	n/a
38	chr3:46441609-46441659	U87	brain:	n/a
39	chr3:46441609-46441659	Hepatocyte	liver:	n/a
40	chr3:46441609-46441659	PANC-1	pancreas:	n/a
41	chr3:46441609-46441659	K562	blood:	n/a
42	chr3:46441609-46441659	HMEC	breast:	n/a
43	chr3:46441609-46441659	T-47D	breast:	n/a
44	chr3:46441609-46441659	A549	lung:	n/a
45	chr3:46441609-46441659	HCT-116	colon:	n/a
46	chr3:46441609-46441659	AG10803	skin:	n/a
47	chr3:46441609-46441659	NT2-D1	testis:	n/a
48	chr3:46441609-46441659	HL-60	blood:	n/a
49	chr3:46441609-46441659	HCM	heart:	n/a
50	chr3:46441609-46441659	BJ	skin:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46130909..46132770-chr3:46427115..46429449,2	K562	blood:
2	chr3:46428873..46431436-chr3:46435878..46437838,2	K562	blood:
3	chr3:46428873..46431436-chr3:46435878..46437838,2	K562	blood:
4	chr3:46436463..46438554-chr3:46441253..46442786,2	K562	blood:
5	chr3:46435342..46437357-chr3:46438783..46441176,2	K562	blood:
6	chr3:46436027..46436544-chr3:46483822..46484338,2	MCF-7	breast:
7	chr3:46427138..46428924-chr3:46441384..46443422,2	K562	blood:
8	chr3:46428487..46432121-chr3:46469362..46472728,3	MCF-7	breast:
9	chr3:46428873..46431704-chr3:46436211..46437838,2	K562	blood:
10	chr3:46441887..46442673-chr3:46529916..46530717,2	K562	blood:
11	chr3:46441114..46442760-chr3:46445695..46448198,2	MCF-7	breast:
12	chr3:46428873..46431704-chr3:46436211..46437838,2	K562	blood:
13	chr3:45979997..45980877-chr3:46419945..46420540,2	K562	blood:
14	chr3:46420928..46423796-chr3:46462092..46464094,2	K562	blood:
15	chr3:46436463..46438554-chr3:46441253..46442786,2	K562	blood:
16	chr3:46414355..46417313-chr3:46422093..46423831,2	K562	blood:
17	chr3:46436362..46436961-chr3:46468661..46469389,2	MCF-7	breast:
18	chr3:46434903..46437048-chr3:46441452..46445081,4	K562	blood:
19	chr3:46433060..46435170-chr3:46436766..46439385,2	K562	blood:
20	chr3:46435342..46437357-chr3:46438783..46441176,2	K562	blood:
21	chr3:46433060..46435170-chr3:46436766..46439385,2	K562	blood:
22	chr3:46436690..46437276-chr3:46483787..46484399,2	MCF-7	breast:
23	chr3:46435557..46438302-chr3:46445017..46447658,3	MCF-7	breast:
24	chr3:46434903..46437048-chr3:46441452..46445081,4	K562	blood:
25	chr3:46427138..46428924-chr3:46441384..46443422,2	K562	blood:
26	chr3:46436315..46436954-chr3:46671328..46672082,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LTF-1	chr3:46434316-46434543	ENSG00000223552.1

No data

Variant related genes	Relation type
CCRL2	TF binding region
CCRL2	CpG island

Extended variants
information (count: 975 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11575818	chr3:46419634-46419635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560965940	chr3:46419648-46419649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576089737	chr3:46419708-46419709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543515494	chr3:46419873-46419874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11575817	chr3:46419893-46419894	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533142525	chr3:46419894-46419895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183737084	chr3:46419895-46419896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145437444	chr3:46419905-46419906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527612173	chr3:46420007-46420008	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs187703099	chr3:46420039-46420040	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs193230001	chr3:46420042-46420043	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11575816	chr3:46420104-46420105	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs137988054	chr3:46420106-46420107	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs11575815	chr3:46420170-46420171	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs373374519	chr3:46420216-46420217	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs185435383	chr3:46420237-46420238	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs376478687	chr3:46420242-46420243	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190693252	chr3:46420260-46420261	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs142585098	chr3:46420275-46420276	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs536556191	chr3:46420276-46420277	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs144708264	chr3:46420307-46420308	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs2187672	chr3:46420366-46420367	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs369929672	chr3:46420374-46420375	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576026463	chr3:46420389-46420390	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs374079166	chr3:46420452-46420453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368761476	chr3:46420492-46420493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572076222	chr3:46420520-46420521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565024300	chr3:46420562-46420563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573558563	chr3:46420563-46420564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568705276	chr3:46420578-46420579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71327058	chr3:46420602-46420603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181392199	chr3:46420618-46420619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560098458	chr3:46420646-46420647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371176270	chr3:46420653-46420654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71288006	chr3:46420662-46420663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542576505	chr3:46420686-46420687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527533866	chr3:46420703-46420704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549295144	chr3:46420759-46420760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs71327059	chr3:46420781-46420782	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs3181038	chr3:46420799-46420800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs369744793	chr3:46420803-46420804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549828678	chr3:46420816-46420817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571333893	chr3:46420818-46420819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141006953	chr3:46420859-46420860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547933400	chr3:46420863-46420864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184344303	chr3:46420875-46420876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536900817	chr3:46420902-46420903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541525773	chr3:46420916-46420917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554834257	chr3:46420918-46420919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570049250	chr3:46420938-46420939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46396000-46422000	Weak transcription	Lung	lung
2	chr3:46404400-46422200	Weak transcription	Thymus	Thymus
3	chr3:46404400-46424600	Weak transcription	Spleen	Spleen
4	chr3:46410200-46420000	Weak transcription	Primary B cells from cord blood	blood
5	chr3:46411400-46422000	Weak transcription	Small Intestine	intestine
6	chr3:46414800-46422000	Weak transcription	Esophagus	oesophagus
7	chr3:46417000-46419800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr3:46417000-46422200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr3:46417200-46421600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr3:46417400-46421600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr3:46417400-46422000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr3:46417600-46420000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr3:46417600-46421600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr3:46417600-46421800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr3:46417600-46422000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr3:46417600-46422000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr3:46417600-46422000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:46417600-46422000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr3:46417600-46422000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr3:46417800-46421600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr3:46417800-46421600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr3:46418000-46422000	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr3:46418400-46420000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr3:46418400-46421600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr3:46418400-46421600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr3:46418400-46421800	Weak transcription	Primary T cells from cord blood	blood
27	chr3:46418400-46421800	Weak transcription	Primary hematopoietic stem cells	blood
28	chr3:46418400-46422000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr3:46418400-46422000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr3:46418600-46420000	Weak transcription	Dnd41	blood
31	chr3:46418600-46421600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr3:46418600-46421600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr3:46418800-46420000	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr3:46418800-46420000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr3:46418800-46420000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr3:46418800-46420000	Weak transcription	Fetal Thymus	thymus
37	chr3:46419200-46420200	Weak transcription	Brain Hippocampus Middle	brain
38	chr3:46419400-46420000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr3:46419600-46420000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr3:46419800-46420000	Enhancers	Duodenum Mucosa	Duodenum
41	chr3:46419800-46420000	Enhancers	NHEK	skin
42	chr3:46419800-46420200	Enhancers	Fetal Lung	lung
43	chr3:46419800-46420400	Enhancers	HMEC	breast
44	chr3:46420000-46420200	Enhancers	Primary B cells from cord blood	blood
45	chr3:46420000-46420200	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr3:46420000-46420200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr3:46420000-46420200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr3:46420000-46420200	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr3:46420000-46420200	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr3:46420000-46420200	Enhancers	Stomach Mucosa	stomach

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