Variant report

Variant	nsv536661
Chromosome Location	chr3:98286588-98315764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1218)
CpG islands
(count:977)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1218 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:98293783-98294317	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:98302584-98303309	K562	blood:	n/a	n/a
3	ARID3A	chr3:98312443-98312835	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:98303816-98304523	K562	blood:	n/a	n/a
5	ARID3A	chr3:98312425-98312859	K562	blood:	n/a	n/a
6	ATF1	chr3:98312428-98312843	K562	blood:	n/a	n/a
7	ATF1	chr3:98302561-98303000	K562	blood:	n/a	n/a
8	ATF2	chr3:98292032-98292547	GM12878	blood:	n/a	n/a
9	ATF2	chr3:98286327-98287069	GM12878	blood:	n/a	n/a
10	ATF2	chr3:98291848-98292665	GM12878	blood:	n/a	n/a
11	ATF2	chr3:98286226-98286856	GM12878	blood:	n/a	n/a
12	ATF2	chr3:98312225-98312860	GM12878	blood:	n/a	n/a
13	ATF2	chr3:98312342-98312911	GM12878	blood:	n/a	n/a
14	ATF3	chr3:98304192-98304405	K562	blood:	n/a	n/a
15	ATF3	chr3:98304182-98304503	K562	blood:	n/a	n/a
16	BACH1	chr3:98312399-98312894	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr3:98304373-98304490	K562	blood:	n/a	n/a
18	BATF	chr3:98293055-98293341	GM12878	blood:	n/a	n/a
19	BATF	chr3:98286493-98286818	GM12878	blood:	n/a	n/a
20	BATF	chr3:98286504-98286803	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:98286428-98286973	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:98286514-98286775	GM12878	blood:	n/a	n/a
23	BCL3	chr3:98286499-98286903	GM12878	blood:	n/a	n/a
24	BCLAF1	chr3:98286357-98287114	GM12878	blood:	n/a	n/a
25	BCLAF1	chr3:98312104-98313017	GM12878	blood:	n/a	chr3:98312521-98312529
26	BCLAF1	chr3:98291833-98292582	GM12878	blood:	n/a	chr3:98292275-98292284
27	BCLAF1	chr3:98312163-98312906	GM12878	blood:	n/a	chr3:98312521-98312529
28	BHLHE40	chr3:98313478-98313710	K562	blood:	n/a	n/a
29	BHLHE40	chr3:98312369-98313008	K562	blood:	n/a	n/a
30	BHLHE40	chr3:98302466-98303116	K562	blood:	n/a	n/a
31	BHLHE40	chr3:98292079-98292534	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:98312301-98312931	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:98304180-98304466	K562	blood:	n/a	n/a
34	BHLHE40	chr3:98311877-98312920	HepG2	liver:	n/a	n/a
35	BRCA1	chr3:98300500-98300535	GM12878	blood:	n/a	n/a
36	BRCA1	chr3:98312497-98312697	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr3:98312411-98312542	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr3:98312335-98312460	HepG2	liver:	n/a	n/a
39	CBX3	chr3:98312550-98312789	K562	blood:	n/a	n/a
40	CBX3	chr3:98312357-98312875	K562	blood:	n/a	n/a
41	CBX3	chr3:98304000-98304800	HCT-116	colon:	n/a	n/a
42	CCNT2	chr3:98302376-98303004	K562	blood:	n/a	chr3:98302829-98302849
43	CCNT2	chr3:98304108-98304412	K562	blood:	n/a	n/a
44	CCNT2	chr3:98311854-98312917	K562	blood:	n/a	n/a
45	CEBPB	chr3:98311856-98312168	K562	blood:	n/a	n/a
46	CEBPB	chr3:98293890-98294239	HepG2	liver:	n/a	chr3:98294185-98294198
47	CEBPB	chr3:98311889-98312130	A549	lung:	n/a	n/a
48	CEBPB	chr3:98312483-98312642	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr3:98311440-98311608	K562	blood:	n/a	chr3:98311557-98311570
50	CEBPB	chr3:98293931-98294196	HepG2	liver:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:98312544-98312594	HIPEpiC	eye:	n/a
2	chr3:98312544-98312594	HIPEpiC	eye:	n/a
3	chr3:98299487-98299537	SKMC	muscle:	n/a
4	chr3:98311910-98311960	H1-hESC	embryonic stem cell:	embryo
5	chr3:98312544-98312594	Jurkat	blood:	n/a
6	chr3:98313516-98313566	GM19239	blood:	n/a
7	chr3:98312354-98312404	AG09319	gingival:	n/a
8	chr3:98312547-98312597	HNPCEpiC	eye:	n/a
9	chr3:98299487-98299537	NH-A	brain:	n/a
10	chr3:98312534-98312584	AG10803	skin:	n/a
11	chr3:98299487-98299537	SAEC	small airway:	n/a
12	chr3:98312544-98312594	HL-60	blood:	n/a
13	chr3:98312971-98313021	GM12878	blood:	n/a
14	chr3:98312651-98312701	H1-hESC	embryonic stem cell:	embryo
15	chr3:98311063-98311113	NHBE	bronchial:	n/a
16	chr3:98312023-98312073	SKMC	muscle:	n/a
17	chr3:98299487-98299537	HEEpiC	esophagus:	n/a
18	chr3:98308022-98308072	HL-60	blood:	n/a
19	chr3:98312680-98312730	HCF	heart:	n/a
20	chr3:98311910-98311960	LNCaP	prostate:	n/a
21	chr3:98313516-98313566	CMK	blood:	n/a
22	chr3:98299487-98299537	IMR90	lung:	fetal
23	chr3:98312534-98312584	SK-N-SH_RA	brain:	n/a
24	chr3:98312544-98312594	CMK	blood:	n/a
25	chr3:98299487-98299537	Caco-2	colon:	n/a
26	chr3:98312473-98312523	HMEC	breast:	n/a
27	chr3:98312534-98312584	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:98311910-98311960	HMEC	breast:	n/a
29	chr3:98312544-98312594	NH-A	brain:	n/a
30	chr3:98299487-98299537	AG04449	skin:	fetal
31	chr3:98312547-98312597	PrEC	prostate:	n/a
32	chr3:98312354-98312404	GM12878	blood:	n/a
33	chr3:98312547-98312597	Hepatocyte	liver:	n/a
34	chr3:98299487-98299537	AG09309	skin:	n/a
35	chr3:98312680-98312730	T-47D	breast:	n/a
36	chr3:98312473-98312523	HIPEpiC	eye:	n/a
37	chr3:98308022-98308072	AG09309	skin:	n/a
38	chr3:98311910-98311960	RPTEC	kidney:	n/a
39	chr3:98312651-98312701	PFSK-1	brain:	n/a
40	chr3:98308022-98308072	T-47D	breast:	n/a
41	chr3:98312515-98312565	NHDF-neo	bronchial:	n/a
42	chr3:98313516-98313566	ProgFib	skin:	n/a
43	chr3:98313516-98313566	H1-hESC	embryonic stem cell:	embryo
44	chr3:98312515-98312565	Hepatocyte	liver:	n/a
45	chr3:98312354-98312404	HNPCEpiC	eye:	n/a
46	chr3:98312680-98312730	MCF-7	breast:	n/a
47	chr3:98312354-98312404	NH-A	brain:	n/a
48	chr3:98312971-98313021	NB4	blood:	n/a
49	chr3:98313398-98313448	GM06990	blood:	n/a
50	chr3:98313516-98313566	HRE	kidney:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:98307277..98308985-chr3:98312690..98314425,2	K562	blood:
2	chr3:97689639..97691921-chr3:98303800..98305616,2	K562	blood:
3	chr20:46129382..46132079-chr3:98291150..98293500,2	MCF-7	breast:
4	chr3:98310880..98314109-chr3:98314173..98316859,5	K562	blood:
5	chr3:98287743..98290049-chr3:98291155..98295348,3	K562	blood:
6	chr3:98303079..98305719-chr3:98311231..98314146,3	K562	blood:
7	chr3:98303079..98305719-chr3:98311231..98314146,3	K562	blood:
8	chr3:98311227..98312951-chr3:98314970..98316859,2	K562	blood:
9	chr3:98292600..98294311-chr3:98296464..98299165,2	K562	blood:
10	chr3:98300331..98302518-chr3:98312399..98314281,2	K562	blood:
11	chr3:98306181..98309113-chr3:98310458..98312557,3	K562	blood:
12	chr3:98287743..98290049-chr3:98291155..98295348,3	K562	blood:
13	chr3:98315529..98316439-chr3:98531389..98532230,2	MCF-7	breast:
14	chr3:98289153..98292045-chr3:98293949..98295528,2	K562	blood:
15	chr3:98292600..98294311-chr3:98296464..98299165,2	K562	blood:
16	chr3:98303079..98306972-chr3:98311108..98314146,5	K562	blood:
17	chr3:98236014..98237762-chr3:98314366..98316058,2	K562	blood:
18	chr3:98306990..98308896-chr3:98311622..98313547,2	MCF-7	breast:
19	chr3:98314191..98315885-chr3:98317245..98319751,3	K562	blood:
20	chr3:98289153..98292045-chr3:98293949..98295528,2	K562	blood:
21	chr3:98282871..98285029-chr3:98286675..98289199,2	K562	blood:
22	chr3:98078662..98079479-chr3:98306722..98307655,3	MCF-7	breast:
23	chr3:98302949..98305459-chr3:98308547..98310946,2	K562	blood:
24	chr3:98293731..98295757-chr3:98296962..98298884,2	MCF-7	breast:
25	chr3:98303079..98306972-chr3:98311108..98314146,5	K562	blood:
26	chr3:98311356..98313726-chr3:98530079..98532585,2	MCF-7	breast:
27	chr3:98293731..98295757-chr3:98296962..98298884,2	MCF-7	breast:
28	chr3:98241309..98243234-chr3:98301701..98304609,2	K562	blood:
29	chr3:97757965..97758653-chr3:98306720..98307286,2	MCF-7	breast:
30	chr16:68344315..68345025-chr3:98311977..98312615,2	HCT-116	colon:
31	chr3:98315462..98316376-chr3:98520278..98520831,2	MCF-7	breast:
32	chr3:98307277..98308985-chr3:98312690..98314425,2	K562	blood:
33	chr3:98240168..98242320-chr3:98310651..98312763,2	K562	blood:
34	chr3:98175989..98176774-chr3:98306461..98307236,2	MCF-7	breast:
35	chr3:98257605..98258242-chr3:98291111..98291831,2	K562	blood:
36	chr3:98315543..98316397-chr3:98531264..98532318,3	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CPOX	hsa-miR-124-3p	chr3:98299425-98299443
2	CPOX	hsa-miR-30c-5p	chr3:98299277-98299299
3	CPOX	hsa-miR-361-5p	chr3:98298773-98298792
4	CPOX	hsa-miR-361-5p	chr3:98298779-98298773
5	CPOX	hsa-miR-30a-5p	chr3:98299277-98299298

Variant related genes	Relation type
CPOX	TF binding region
CPOX	CpG island
ENSG00000080822	chromatin interactions
ENSG00000170854	chromatin interactions
ENSG00000057019	chromatin interactions
ENSG00000103061	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000248839	chromatin interactions
ENSG00000132600	chromatin interactions
ENSG00000080819	chromatin interactions

Extended variants
information (count: 1190 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1190 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564483522	chr3:98286627-98286628	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs572103114	chr3:98286664-98286665	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs386663761	chr3:98286763-98286764	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs138954264	chr3:98286771-98286772	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs183468177	chr3:98286773-98286774	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs4857097	chr3:98286775-98286776	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs578144328	chr3:98286786-98286787	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs142070855	chr3:98286801-98286802	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs374581931	chr3:98286839-98286840	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs4857098	chr3:98286871-98286872	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371406003	chr3:98286885-98286886	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs35605598	chr3:98286888-98286889	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs188614768	chr3:98286906-98286907	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs111573494	chr3:98286940-98286941	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs527674764	chr3:98286941-98286942	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs55724833	chr3:98286942-98286943	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs397936720	chr3:98286948-98286949	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs150844019	chr3:98286991-98286992	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs548087608	chr3:98287076-98287077	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs139262448	chr3:98287106-98287107	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542563629	chr3:98287107-98287108	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs533391552	chr3:98287113-98287114	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs386663762	chr3:98287175-98287176	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs550195678	chr3:98287239-98287240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs570204696	chr3:98287241-98287242	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs149552029	chr3:98287265-98287266	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs183155736	chr3:98287269-98287270	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs555529449	chr3:98287313-98287314	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs116132321	chr3:98287344-98287345	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs541196226	chr3:98287346-98287347	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs534504047	chr3:98287350-98287351	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs557661190	chr3:98287377-98287378	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs186766174	chr3:98287400-98287401	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs191378704	chr3:98287437-98287438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550280801	chr3:98287446-98287447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183474693	chr3:98287475-98287476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542731848	chr3:98287495-98287496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538153894	chr3:98287499-98287500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76349259	chr3:98287512-98287513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370373073	chr3:98287534-98287535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201217255	chr3:98287595-98287596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552225590	chr3:98287612-98287613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541614510	chr3:98287618-98287619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564814076	chr3:98287634-98287635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551699643	chr3:98287734-98287735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373702488	chr3:98287735-98287736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368401696	chr3:98287748-98287749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533654337	chr3:98287759-98287760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187051687	chr3:98287778-98287779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6793347	chr3:98287817-98287818	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Neurodevelopmental disorder	22521361	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
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98273600-98292600	Weak transcription	K562	blood
2	chr3:98280400-98287000	Enhancers	Primary T cells fromperipheralblood	blood
3	chr3:98280600-98286800	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr3:98280600-98287000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr3:98280600-98288000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr3:98280800-98287200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr3:98280800-98288200	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr3:98280800-98288200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr3:98281200-98286600	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr3:98281200-98296200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr3:98281400-98295800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:98282600-98288200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr3:98283000-98292200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr3:98283000-98295200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr3:98283400-98288200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr3:98283600-98295800	Weak transcription	Primary B cells from cord blood	blood
17	chr3:98283800-98286600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr3:98283800-98298400	Weak transcription	Primary B cells from peripheral blood	blood
19	chr3:98284600-98292200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr3:98284600-98292200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr3:98284600-98295800	Weak transcription	Thymus	Thymus
22	chr3:98285000-98286600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr3:98285000-98295800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr3:98285000-98296200	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr3:98285000-98296200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr3:98285000-98296200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:98285000-98303400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr3:98285200-98295200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:98285200-98295800	Weak transcription	Fetal Thymus	thymus
30	chr3:98285800-98286600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr3:98285800-98295200	Weak transcription	Primary T cells from cord blood	blood
32	chr3:98285800-98295200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr3:98285800-98295600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr3:98285800-98295800	Weak transcription	Dnd41	blood
35	chr3:98286400-98286600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr3:98286400-98287400	Flanking Active TSS	GM12878-XiMat	blood
37	chr3:98286600-98286800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:98286600-98287000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr3:98286600-98287000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr3:98286600-98287000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr3:98286600-98287200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr3:98286800-98287200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr3:98286800-98287200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr3:98286800-98304200	Weak transcription	Pancreas	Pancrea
45	chr3:98287000-98288000	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr3:98287000-98295400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr3:98287000-98296000	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr3:98287000-98296000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr3:98287000-98296000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr3:98287200-98287400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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