Variant report

Variant	nsv582029
Chromosome Location	chr2:55159043-55204498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:644)
CpG islands
(count:489)
Chromatin interactive
region (count:35)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55182863-55183388	K562	blood:	n/a	n/a
2	ATF1	chr2:55195656-55195927	K562	blood:	n/a	n/a
3	ATF1	chr2:55182754-55183462	K562	blood:	n/a	n/a
4	ATF2	chr2:55172506-55172897	GM12878	blood:	n/a	n/a
5	ATF2	chr2:55204104-55204774	GM12878	blood:	n/a	n/a
6	BACH1	chr2:55183346-55183717	K562	blood:	n/a	n/a
7	BCL11A	chr2:55181832-55182095	GM12878	blood:	n/a	n/a
8	BCLAF1	chr2:55204196-55204809	GM12878	blood:	n/a	chr2:55204561-55204570
9	BHLHE40	chr2:55182728-55183103	K562	blood:	n/a	n/a
10	BHLHE40	chr2:55195633-55196013	K562	blood:	n/a	n/a
11	BHLHE40	chr2:55179662-55180007	K562	blood:	n/a	n/a
12	BHLHE40	chr2:55172574-55172896	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:55172717-55172864	K562	blood:	n/a	n/a
14	BHLHE40	chr2:55184558-55184788	K562	blood:	n/a	n/a
15	BHLHE40	chr2:55172677-55173209	HepG2	liver:	n/a	n/a
16	CBX3	chr2:55164908-55165283	K562	blood:	n/a	n/a
17	CBX3	chr2:55182164-55183405	K562	blood:	n/a	n/a
18	CCNT2	chr2:55196054-55197980	K562	blood:	n/a	n/a
19	CCNT2	chr2:55198637-55198837	K562	blood:	n/a	n/a
20	CCNT2	chr2:55194332-55194391	K562	blood:	n/a	n/a
21	CCNT2	chr2:55183331-55183529	K562	blood:	n/a	n/a
22	CCNT2	chr2:55179668-55179922	K562	blood:	n/a	n/a
23	CCNT2	chr2:55182754-55183017	K562	blood:	n/a	n/a
24	CCNT2	chr2:55202736-55204004	K562	blood:	n/a	n/a
25	CCNT2	chr2:55199276-55199412	K562	blood:	n/a	n/a
26	CEBPB	chr2:55182573-55182663	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:55172677-55173194	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:55182524-55182777	A549	lung:	n/a	n/a
29	CEBPB	chr2:55173918-55174077	A549	lung:	n/a	n/a
30	CEBPB	chr2:55169728-55169999	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:55182452-55182804	K562	blood:	n/a	n/a
32	CEBPB	chr2:55172594-55173269	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:55190661-55191013	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:55172900-55173370	MCF-7	breast:	n/a	n/a
35	CEBPB	chr2:55169784-55169984	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:55190712-55190940	K562	blood:	n/a	n/a
37	CEBPB	chr2:55182518-55182725	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:55183447-55183604	K562	blood:	n/a	n/a
39	CEBPB	chr2:55169827-55170029	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:55173945-55174112	HepG2	liver:	n/a	n/a
41	CEBPD	chr2:55182756-55183138	K562	blood:	n/a	n/a
42	CHD2	chr2:55172755-55172825	GM12878	blood:	n/a	n/a
43	CHD2	chr2:55182877-55182941	K562	blood:	n/a	n/a
44	CHD2	chr2:55184587-55184676	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr2:55181160-55181310	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr2:55192146-55192425	IMR90	lung:	n/a	n/a
47	CTCF	chr2:55200049-55200266	T-47D	breast:	n/a	n/a
48	CTCF	chr2:55191560-55191710	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr2:55179629-55179783	K562	blood:	n/a	n/a
50	CTCF	chr2:55194340-55194490	HCPEpiC	choroid plexus:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55199843-55199893	GM19239	blood:	n/a
2	chr2:55199843-55199893	GM19239	blood:	n/a
3	chr2:55197707-55197757	LNCaP	prostate:	n/a
4	chr2:55200201-55200251	MCF-7	breast:	n/a
5	chr2:55197220-55197270	HAEpiC	amniotic membrane:	n/a
6	chr2:55174473-55174523	AG10803	skin:	n/a
7	chr2:55203963-55204013	HRE	kidney:	n/a
8	chr2:55199843-55199893	ovcar-3	ovarian:	n/a
9	chr2:55174473-55174523	Jurkat	blood:	n/a
10	chr2:55203963-55204013	AG09309	skin:	n/a
11	chr2:55203963-55204013	CMK	blood:	n/a
12	chr2:55197220-55197270	A549	lung:	n/a
13	chr2:55203963-55204013	SK-N-MC	brain:	n/a
14	chr2:55200201-55200251	HCM	heart:	n/a
15	chr2:55197707-55197757	ProgFib	skin:	n/a
16	chr2:55172992-55173042	HCT-116	colon:	n/a
17	chr2:55199843-55199893	U87	brain:	n/a
18	chr2:55200201-55200251	CMK	blood:	n/a
19	chr2:55203963-55204013	H1-hESC	embryonic stem cell:	embryo
20	chr2:55203963-55204013	PANC-1	pancreas:	n/a
21	chr2:55172992-55173042	AG09309	skin:	n/a
22	chr2:55203963-55204013	GM12892	blood:	n/a
23	chr2:55197220-55197270	AG09309	skin:	n/a
24	chr2:55199843-55199893	ProgFib	skin:	n/a
25	chr2:55197220-55197270	AoSMC	blood vessel:	n/a
26	chr2:55197707-55197757	NH-A	brain:	n/a
27	chr2:55172992-55173042	HepG2	liver:	n/a
28	chr2:55172992-55173042	Caco-2	colon:	n/a
29	chr2:55199843-55199893	GM06990	blood:	n/a
30	chr2:55174473-55174523	HEEpiC	esophagus:	n/a
31	chr2:55197707-55197757	HCM	heart:	n/a
32	chr2:55203963-55204013	NHDF-neo	bronchial:	n/a
33	chr2:55197220-55197270	MCF10A-Er-Src	breast:	n/a
34	chr2:55197220-55197270	SK-N-SH_RA	brain:	n/a
35	chr2:55203963-55204013	HAEpiC	amniotic membrane:	n/a
36	chr2:55197707-55197757	HRCEpiC	kidney:	n/a
37	chr2:55183957-55184007	SAEC	small airway:	n/a
38	chr2:55197707-55197757	NT2-D1	testis:	n/a
39	chr2:55197220-55197270	NH-A	brain:	n/a
40	chr2:55172992-55173042	HIPEpiC	eye:	n/a
41	chr2:55183957-55184007	AG09309	skin:	n/a
42	chr2:55199843-55199893	H1-hESC	embryonic stem cell:	embryo
43	chr2:55200201-55200251	HNPCEpiC	eye:	n/a
44	chr2:55174473-55174523	Hela-S3	cervix:	n/a
45	chr2:55200201-55200251	HCPEpiC	choroid plexus:	n/a
46	chr2:55174473-55174523	A549	lung:	n/a
47	chr2:55174473-55174523	U87	brain:	n/a
48	chr2:55199843-55199893	NHDF-neo	bronchial:	n/a
49	chr2:55197707-55197757	A549	lung:	n/a
50	chr2:55183957-55184007	LNCaP	prostate:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:90568357..90570526-chr2:55172089..55173609,2	MCF-7	breast:
2	chr2:55140902..55143790-chr2:55162996..55164852,2	K562	blood:
3	chr2:55204435..55209089-chr2:55274911..55278052,4	MCF-7	breast:
4	chr2:55164941..55167851-chr2:55169428..55172697,4	K562	blood:
5	chr2:39442463..39443026-chr2:55172640..55173316,2	MCF-7	breast:
6	chr2:55198988..55201900-chr2:55213351..55214997,2	MCF-7	breast:
7	chr2:55198243..55200430-chr2:55275521..55278393,2	MCF-7	breast:
8	chr2:55152934..55155386-chr2:55163705..55166391,2	K562	blood:
9	chr2:55164082..55167109-chr2:55181433..55184478,3	K562	blood:
10	chr2:55171297..55173305-chr2:55180645..55183398,2	K562	blood:
11	chr2:55176432..55179496-chr2:55180651..55183314,3	MCF-7	breast:
12	chr2:55154430..55157005-chr2:55162762..55165481,2	MCF-7	breast:
13	chr2:55130491..55133378-chr2:55191719..55193881,2	MCF-7	breast:
14	chr2:55184760..55187706-chr2:55190562..55193036,2	MCF-7	breast:
15	chr2:55164082..55168413-chr2:55180367..55184478,5	K562	blood:
16	chr2:55155736..55157540-chr2:55159036..55160806,2	K562	blood:
17	chr2:55192020..55193773-chr2:55201950..55203496,2	K562	blood:
18	chr2:55183331..55185244-chr2:55275914..55277791,2	MCF-7	breast:
19	chr2:55197790..55202065-chr2:55203128..55206918,7	K562	blood:
20	chr2:55195869..55197384-chr2:55197903..55200472,2	K562	blood:
21	chr2:55164082..55167109-chr2:55181433..55184478,3	K562	blood:
22	chr2:55186295..55188752-chr2:55197497..55200388,2	K562	blood:
23	chr2:55183507..55185896-chr2:55194020..55195726,2	MCF-7	breast:
24	chr2:55199321..55201590-chr2:55202195..55204669,2	MCF-7	breast:
25	chr2:55174500..55176023-chr2:55178242..55180647,2	MCF-7	breast:
26	chr2:55190781..55193657-chr2:55198367..55200199,2	K562	blood:
27	chr2:55180338..55182211-chr2:55203492..55207061,3	MCF-7	breast:
28	chr2:55145921..55147506-chr2:55166901..55168744,2	K562	blood:
29	chr2:55192020..55193773-chr2:55201950..55203496,2	K562	blood:
30	chr2:55164941..55167851-chr2:55169428..55172697,4	K562	blood:
31	chr2:55182667..55184271-chr2:55275610..55277952,2	MCF-7	breast:
32	chr2:55195869..55197384-chr2:55197903..55200472,2	K562	blood:
33	chr2:55186380..55189336-chr2:55191001..55193632,2	K562	blood:
34	chr2:55122602..55124737-chr2:55161405..55163876,2	K562	blood:
35	chr2:55181556..55184216-chr2:55338582..55340390,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf63-3	chr2:55199932-55200334	NONHSAT070753
2	lnc-C2orf63-3	chr2:55199933-55200334	NONHSAT070754
3	lnc-C2orf63-4	chr2:55199695-55199912	NONHSAT070752
4	lnc-RTN4-1	chr2:55196736-55198803	ENSG00000248316
5	lnc-EML6-2	chr2:55198874-55199157	NONHSAT070751
6	lnc-EML6-2	chr2:55197791-55198009	NONHSAT070751
7	lnc-C2orf63-3	chr2:55200699-55200757	NONHSAT070754
8	lnc-C2orf63-3	chr2:55200699-55201155	NONHSAT070753
9	lnc-C2orf63-3	chr2:55200957-55201327	NONHSAT070754
10	lnc-RTN4-1	chr2:55198860-55199154	ENSG00000248316

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RTN4	hsa-miR-101-3p	chr2:55199778-55199798
2	RTN4	hsa-miR-16-5p	chr2:55200087-55200081
3	RTN4	hsa-miR-21-5p	chr2:55200085-55200106
4	RTN4	hsa-miR-148b-3p	chr2:55200146-55200168
5	RTN4	hsa-miR-21-5p	chr2:55199630-55199651
6	RTN4	hsa-miR-34a-5p	chr2:55200115-55200136
7	RTN4	hsa-miR-101-3p	chr2:55199390-55199410
8	RTN4	hsa-miR-132-3p	chr2:55199777-55199797
9	RTN4	hsa-miR-148b-3p	chr2:55199909-55199931
10	RTN4	hsa-miR-30c-5p	chr2:55199468-55199490
11	RTN4	hsa-miR-16-5p	chr2:55200082-55200102
12	RTN4	hsa-miR-33a-5p	chr2:55199371-55199391

Variant related genes	Relation type
RTN4	TF binding region
EML6	TF binding region
RTN4	CpG island
EML6	CpG island
ENSG00000214595	chromatin interactions
ENSG00000115310	chromatin interactions
ITGAV	miRNA target sites
CCDC47	miRNA target sites

Extended variants
information (count: 2453 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2453 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12475185	chr2:55159043-55159044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556061383	chr2:55159097-55159098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs55748000	chr2:55159098-55159099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190672147	chr2:55159116-55159117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141283784	chr2:55159173-55159174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536158465	chr2:55159201-55159202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557478250	chr2:55159202-55159203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150197191	chr2:55159235-55159236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114581533	chr2:55159258-55159259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553868137	chr2:55159273-55159274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs13422342	chr2:55159284-55159285	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs542436893	chr2:55159306-55159307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562398662	chr2:55159319-55159320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575944003	chr2:55159327-55159328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115774144	chr2:55159390-55159391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564318466	chr2:55159394-55159395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544645056	chr2:55159396-55159397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573595890	chr2:55159398-55159399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546761232	chr2:55159410-55159411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560582274	chr2:55159435-55159436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567745710	chr2:55159441-55159442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549600816	chr2:55159444-55159445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138681247	chr2:55159451-55159452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564826138	chr2:55159460-55159461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79948790	chr2:55159484-55159485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552080239	chr2:55159488-55159489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180820996	chr2:55159522-55159523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149431504	chr2:55159553-55159554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533800169	chr2:55159592-55159593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556532673	chr2:55159605-55159606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573406798	chr2:55159616-55159617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536003869	chr2:55159635-55159636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555933975	chr2:55159636-55159637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377061213	chr2:55159642-55159643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143843057	chr2:55159654-55159655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187364310	chr2:55159657-55159658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544950215	chr2:55159683-55159684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561544979	chr2:55159688-55159689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192262293	chr2:55159690-55159691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs80143439	chr2:55159691-55159692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540643859	chr2:55159727-55159728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373868386	chr2:55159733-55159734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550476096	chr2:55159761-55159762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564007198	chr2:55159854-55159855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572339160	chr2:55159862-55159863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148463523	chr2:55159864-55159865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560522654	chr2:55159881-55159882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529416295	chr2:55159903-55159904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549539413	chr2:55159909-55159910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528954205	chr2:55159953-55159954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55150000-55168400	Weak transcription	Pancreas	Pancrea
2	chr2:55154200-55166600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:55154400-55168000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr2:55154800-55167800	Weak transcription	Brain Angular Gyrus	brain
5	chr2:55156400-55163000	Weak transcription	Esophagus	oesophagus
6	chr2:55159000-55159600	Enhancers	K562	blood
7	chr2:55159600-55160800	Weak transcription	K562	blood
8	chr2:55161000-55161200	Enhancers	K562	blood
9	chr2:55163000-55163200	Enhancers	Esophagus	oesophagus
10	chr2:55163400-55164200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr2:55163400-55164600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr2:55164000-55164400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr2:55164000-55164600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:55165800-55169200	Enhancers	Fetal Muscle Leg	muscle
15	chr2:55166200-55166600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:55166200-55166600	Enhancers	Brain Anterior Caudate	brain
17	chr2:55166200-55167000	Enhancers	Fetal Muscle Trunk	muscle
18	chr2:55166200-55169000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr2:55166200-55172800	Weak transcription	Gastric	stomach
20	chr2:55166600-55166800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:55166600-55167200	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr2:55166600-55167600	Weak transcription	Brain Anterior Caudate	brain
23	chr2:55166800-55167800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:55167000-55168400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr2:55167200-55167600	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr2:55167600-55168400	Enhancers	Brain Anterior Caudate	brain
27	chr2:55167600-55168400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr2:55167600-55169000	Enhancers	HepG2	liver
29	chr2:55167800-55168600	Enhancers	Brain Substantia Nigra	brain
30	chr2:55167800-55169000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:55167800-55169000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:55167800-55169800	Enhancers	Brain Hippocampus Middle	brain
33	chr2:55167800-55170000	Enhancers	Brain Angular Gyrus	brain
34	chr2:55168000-55168600	Enhancers	Brain Cingulate Gyrus	brain
35	chr2:55168000-55169200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:55168000-55169200	Enhancers	HMEC	breast
37	chr2:55168200-55169000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:55168400-55168600	Enhancers	Fetal Muscle Trunk	muscle
39	chr2:55168400-55169000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:55168400-55169000	Flanking Active TSS	Brain Anterior Caudate	brain
41	chr2:55168400-55169000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
42	chr2:55168400-55169000	Enhancers	Pancreas	Pancrea
43	chr2:55168400-55169200	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr2:55168600-55169000	Flanking Active TSS	Brain Cingulate Gyrus	brain
45	chr2:55168600-55169000	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr2:55168600-55172600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:55168800-55169000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:55168800-55170600	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr2:55168800-55170800	Enhancers	Primary T cells fromperipheralblood	blood
50	chr2:55168800-55193400	Weak transcription	Primary B cells from peripheral blood	blood

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