Variant report

Variant	nsv584028
Chromosome Location	chr2:186851224-186965143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:329)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:186855637-186856004	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:186933182-186933390	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:186853506-186853842	HepG2	liver:	n/a	n/a
4	BACH1	chr2:186917756-186918018	H1-hESC	embryonic stem cell:	n/a	chr2:186917846-186917860
5	BACH1	chr2:186855743-186855846	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr2:186896017-186896505	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:186929279-186929572	GM12878	blood:	n/a	n/a
8	CCNT2	chr2:186905250-186905377	K562	blood:	n/a	n/a
9	CEBPB	chr2:186918854-186919223	HepG2	liver:	n/a	chr2:186919035-186919044 chr2:186919033-186919044 chr2:186919034-186919045
10	CEBPB	chr2:186923368-186923898	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:186881616-186881820	HepG2	liver:	n/a	chr2:186881764-186881775
12	CEBPB	chr2:186954617-186954851	HepG2	liver:	n/a	chr2:186954740-186954751
13	CEBPB	chr2:186863446-186863745	Hela-S3	cervix:	n/a	chr2:186863590-186863601
14	CEBPB	chr2:186888229-186888431	HepG2	liver:	n/a	chr2:186888282-186888293 chr2:186888300-186888311
15	CEBPB	chr2:186863427-186863776	IMR90	lung:	n/a	chr2:186863590-186863601
16	CEBPB	chr2:186918858-186919191	IMR90	lung:	n/a	chr2:186919035-186919044 chr2:186919033-186919044 chr2:186919034-186919045
17	CEBPB	chr2:186888225-186888463	A549	lung:	n/a	chr2:186888282-186888293 chr2:186888300-186888311
18	CEBPB	chr2:186881632-186881878	A549	lung:	n/a	chr2:186881764-186881775
19	CEBPB	chr2:186906365-186906557	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:186861384-186861537	HepG2	liver:	n/a	chr2:186861485-186861496
21	CEBPB	chr2:186853669-186853919	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:186886764-186886992	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:186863413-186863783	HepG2	liver:	n/a	chr2:186863590-186863601
24	CEBPB	chr2:186886854-186887053	A549	lung:	n/a	n/a
25	CEBPB	chr2:186863425-186863774	A549	lung:	n/a	chr2:186863590-186863601
26	CHD2	chr2:186896175-186896280	GM12878	blood:	n/a	n/a
27	CHD2	chr2:186874059-186874362	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr2:186954242-186954328	HepG2	liver:	n/a	n/a
29	CTCF	chr2:186853842-186853864	GM10248	blood:	n/a	n/a
30	CTCF	chr2:186954213-186954310	MCF-7	breast:	n/a	n/a
31	CTCF	chr2:186955790-186955928	GM10248	blood:	n/a	n/a
32	CTCF	chr2:186955769-186955930	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr2:186954180-186954330	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:186900997-186901046	GM20000	blood:	n/a	n/a
35	CTCF	chr2:186879091-186879144	GM20000	blood:	n/a	n/a
36	CTCF	chr2:186954240-186954390	HepG2	liver:	n/a	n/a
37	CTCF	chr2:186954160-186954310	HepG2	liver:	n/a	n/a
38	CTCF	chr2:186954200-186954350	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:186954256-186954300	Hela-S3	cervix:	n/a	n/a
40	E2F4	chr2:186925532-186925809	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr2:186882003-186882348	GM12878	blood:	n/a	chr2:186882148-186882159
42	ELK1	chr2:186863325-186863345	GM12878	blood:	n/a	n/a
43	EP300	chr2:186896190-186896390	GM12878	blood:	n/a	n/a
44	EP300	chr2:186932992-186933462	HepG2	liver:	n/a	n/a
45	EP300	chr2:186909269-186910028	SK-N-SH_RA	brain:	n/a	chr2:186909574-186909583 chr2:186909777-186909786 chr2:186909776-186909785
46	EP300	chr2:186897190-186897194	GM12878	blood:	n/a	n/a
47	EP300	chr2:186925220-186926095	SK-N-SH_RA	brain:	n/a	chr2:186925889-186925903
48	EP300	chr2:186932207-186934119	SK-N-SH	brain:	n/a	chr2:186932821-186932835 chr2:186933640-186933654 chr2:186932819-186932833 chr2:186934089-186934103 chr2:186932820-186932834 chr2:186932818-186932832
49	EP300	chr2:186925215-186926066	SK-N-SH_RA	brain:	n/a	chr2:186925889-186925903
50	EP300	chr2:186932878-186933921	SK-N-SH_RA	brain:	n/a	chr2:186933640-186933654

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186924071-186924121	AG04449	skin:	fetal
2	chr2:186924071-186924121	HRPEpiC	eye:	n/a
3	chr2:186924071-186924121	ProgFib	skin:	n/a
4	chr2:186924071-186924121	HRCEpiC	kidney:	n/a
5	chr2:186924071-186924121	HCM	heart:	n/a
6	chr2:186924071-186924121	SK-N-SH_RA	brain:	n/a
7	chr2:186924071-186924121	HCT-116	colon:	n/a
8	chr2:186924071-186924121	GM12891	blood:	n/a
9	chr2:186924071-186924121	HepG2	liver:	n/a
10	chr2:186924071-186924121	U87	brain:	n/a
11	chr2:186924071-186924121	AG09319	gingival:	n/a
12	chr2:186924071-186924121	AG09309	skin:	n/a
13	chr2:186924071-186924121	BE2_C	brain:	n/a
14	chr2:186924071-186924121	CMK	blood:	n/a
15	chr2:186924071-186924121	AoSMC	blood vessel:	n/a
16	chr2:186924071-186924121	PFSK-1	brain:	n/a
17	chr2:186924071-186924121	ECC-1	luminal epithelium:	n/a
18	chr2:186924071-186924121	HUVEC	blood vessel:	n/a
19	chr2:186924071-186924121	HNPCEpiC	eye:	n/a
20	chr2:186924071-186924121	T-47D	breast:	n/a
21	chr2:186924071-186924121	MCF-7	breast:	n/a
22	chr2:186924071-186924121	SK-N-SH	brain:	n/a
23	chr2:186924071-186924121	GM19239	blood:	n/a
24	chr2:186924071-186924121	HCF	heart:	n/a
25	chr2:186924071-186924121	AG10803	skin:	n/a
26	chr2:186924071-186924121	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:186924071-186924121	IMR90	lung:	fetal
28	chr2:186924071-186924121	NT2-D1	testis:	n/a
29	chr2:186924071-186924121	MCF10A-Er-Src	breast:	n/a
30	chr2:186924071-186924121	Hela-S3	cervix:	n/a
31	chr2:186924071-186924121	GM06990	blood:	n/a
32	chr2:186924071-186924121	AG04450	lung:	fetal
33	chr2:186924071-186924121	GM12892	blood:	n/a
34	chr2:186924071-186924121	SKMC	muscle:	n/a
35	chr2:186924071-186924121	RPTEC	kidney:	n/a
36	chr2:186924071-186924121	HEK293	kidney:	embryo
37	chr2:186924071-186924121	HEEpiC	esophagus:	n/a
38	chr2:186924071-186924121	HAEpiC	amniotic membrane:	n/a
39	chr2:186924071-186924121	BJ	skin:	n/a
40	chr2:186924071-186924121	Hepatocyte	liver:	n/a
41	chr2:186924071-186924121	NHDF-neo	bronchial:	n/a
42	chr2:186924071-186924121	NB4	blood:	n/a
43	chr2:186924071-186924121	HCPEpiC	choroid plexus:	n/a
44	chr2:186924071-186924121	ovcar-3	ovarian:	n/a
45	chr2:186924071-186924121	A549	lung:	n/a
46	chr2:186924071-186924121	SK-N-MC	brain:	n/a
47	chr2:186924071-186924121	Jurkat	blood:	n/a
48	chr2:186924071-186924121	SAEC	small airway:	n/a
49	chr2:186924071-186924121	HIPEpiC	eye:	n/a
50	chr2:186924071-186924121	Caco-2	colon:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:
2	chr2:186943617..186946004-chr2:186946269..186949362,3	K562	blood:
3	chr2:186882755..186884529-chr2:186886544..186888768,2	K562	blood:
4	chr2:186898326..186901023-chr2:187349730..187351831,2	K562	blood:
5	chr2:186882755..186884529-chr2:186886544..186888768,2	K562	blood:
6	chr2:186851763..186854059-chr2:186854208..186855953,2	MCF-7	breast:
7	chr2:186861297..186864828-chr2:186866334..186869154,3	K562	blood:
8	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
9	chr2:186905396..186906984-chr2:186927102..186929134,2	K562	blood:
10	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:
11	chr17:57913762..57915412-chr2:186861621..186864023,2	MCF-7	breast:
12	chr2:186861297..186864828-chr2:186866334..186869154,3	K562	blood:
13	chr2:186948418..186950441-chr2:187047439..187049579,2	K562	blood:
14	chr2:186851763..186854059-chr2:186854208..186855953,2	MCF-7	breast:
15	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
16	chr2:186905396..186906984-chr2:186927102..186929134,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-3	chr2:186898261-186898529	NR_110218
2	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877.2
3	lnc-ZSWIM2-3	chr2:186904227-186904282	NONHSAT075981
4	lnc-FSIP2-4	chr2:186947780-186951158	NONHSAT075984
5	lnc-ZSWIM2-3	chr2:186898222-186898531	NONHSAT075981
6	lnc-ZSWIM2-3	chr2:186897872-186898529	ENSG00000237877
7	lnc-FSIP2-4	chr2:186964372-186965726	NONHSAT075984
8	lnc-FSIP2-3	chr2:186963163-186964146	NONHSAT075986
9	lnc-ZSWIM2-3	chr2:186951028-186951044	NR_110218
10	lnc-ZSWIM2-3	chr2:186903058-186903162	NONHSAT075981
11	lnc-ZSWIM2-3	chr2:186946057-186946143	NONHSAT075981
12	lnc-ZSWIM2-3	chr2:186904227-186904282	NR_110218
13	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
14	lnc-ZSWIM2-3	chr2:186897618-186898529	ENSG00000237877.2
15	lnc-ZSWIM2-3	chr2:186947881-186947948	NR_110218
16	lnc-ZSWIM2-3	chr2:186946057-186946143	NR_110218
17	lnc-ZSWIM2-3	chr2:186947881-186947950	ENSG00000237877
18	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877.2
19	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877
20	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
21	lnc-ZSWIM2-3	chr2:186904227-186904282	ENSG00000237877
22	lnc-ZSWIM2-3	chr2:186903058-186903159	ENSG00000237877
23	lnc-ZSWIM2-3	chr2:186903058-186903162	NR_110218
24	lnc-ZSWIM2-3	chr2:186947881-186947951	NONHSAT075981
25	lnc-ZSWIM2-3	chr2:186897623-186897908	NONHSAT075981
26	lnc-FSIP2-4	chr2:186923254-186923714	NONHSAT075984
27	lnc-ZSWIM2-3	chr2:186898258-186898529	ENSG00000237877
28	lnc-FSIP2-4	chr2:186946053-186946143	NONHSAT075984
29	lnc-FSIP2-2	chr2:186953806-186955337	NONHSAT075985
30	lnc-FSIP2-4	chr2:186932840-186933840	NONHSAT075984

No data

Variant related genes	Relation type
ENSG00000237877	TF binding region
ENSG00000237877	CpG island
ENSG00000237877	chromatin interactions
ENSG00000065548	chromatin interactions
ENSG00000062716	chromatin interactions

Extended variants
information (count: 3018 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:3018 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7601385	chr2:186851224-186851225	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560803247	chr2:186851233-186851234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575929072	chr2:186851335-186851336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543364286	chr2:186851339-186851340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543352597	chr2:186851395-186851396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182224041	chr2:186851410-186851411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552801356	chr2:186851417-186851418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184920334	chr2:186851452-186851453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559200234	chr2:186851469-186851470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573852055	chr2:186851483-186851484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530265583	chr2:186851492-186851493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369732615	chr2:186851511-186851512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541457867	chr2:186851544-186851545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559768922	chr2:186851575-186851576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552932074	chr2:186851609-186851610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570830765	chr2:186851737-186851738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147103530	chr2:186851756-186851757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369071022	chr2:186851818-186851819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566317883	chr2:186851874-186851875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534722294	chr2:186852026-186852027	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs553392599	chr2:186852091-186852092	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs139906662	chr2:186852138-186852139	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs535992450	chr2:186852152-186852153	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs373248111	chr2:186852194-186852195	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs575869091	chr2:186852205-186852206	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs535321479	chr2:186852210-186852211	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs13410615	chr2:186852213-186852214	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs190169143	chr2:186852237-186852238	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs540671288	chr2:186852263-186852264	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs182436305	chr2:186852315-186852316	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs16827364	chr2:186852316-186852317	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs141794173	chr2:186852378-186852379	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs188483504	chr2:186852399-186852400	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs531150564	chr2:186852428-186852429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552868772	chr2:186852463-186852464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561208304	chr2:186852579-186852580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114920264	chr2:186852611-186852612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571066848	chr2:186852658-186852659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533493769	chr2:186852740-186852741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146330545	chr2:186852799-186852800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546675520	chr2:186852845-186852846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568482979	chr2:186852913-186852914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs16827365	chr2:186852931-186852932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs545490994	chr2:186852963-186852964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193076264	chr2:186852970-186852971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373147630	chr2:186853005-186853006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76036843	chr2:186853010-186853011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377452605	chr2:186853028-186853029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13425817	chr2:186853033-186853034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs13022014	chr2:186853063-186853064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164919	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186828400-186857400	Weak transcription	Aorta	Aorta
2	chr2:186828800-186867400	Weak transcription	Ovary	ovary
3	chr2:186844600-186852000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr2:186845200-186867400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:186852000-186852400	Active TSS	Muscle Satellite Cultured Cells	--
6	chr2:186852400-186855600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:186853600-186854000	Enhancers	HepG2	liver
8	chr2:186854000-186855600	Weak transcription	HepG2	liver
9	chr2:186854200-186855800	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr2:186854600-186867200	Weak transcription	Left Ventricle	heart
11	chr2:186854800-186857200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr2:186854800-186857400	Weak transcription	Liver	Liver
13	chr2:186855000-186857600	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:186855400-186856000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:186855400-186857600	Weak transcription	Fetal Brain Male	brain
16	chr2:186855600-186856200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr2:186855600-186856200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:186855600-186856400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr2:186855600-186856400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:186855600-186856400	Enhancers	Muscle Satellite Cultured Cells	--
21	chr2:186855600-186856400	Enhancers	HepG2	liver
22	chr2:186855800-186856400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:186855800-186856600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr2:186855800-186856600	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr2:186856000-186856200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr2:186856000-186856400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr2:186856000-186856400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr2:186856200-186856800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
29	chr2:186856200-186857000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:186856600-186867600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr2:186856800-186868800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr2:186857600-186858000	Active TSS	Fetal Brain Male	brain
33	chr2:186867400-186867600	ZNF genes & repeats	Ovary	ovary
34	chr2:186867400-186867800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr2:186867600-186868200	Weak transcription	Ovary	ovary
36	chr2:186867800-186870200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:186868600-186873800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr2:186870600-186871200	Weak transcription	Left Ventricle	heart
39	chr2:186871200-186871400	ZNF genes & repeats	Left Ventricle	heart
40	chr2:186871200-186871600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:186871600-186871800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:186871800-186875800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr2:186873400-186874600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr2:186873600-186874600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr2:186873600-186875000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr2:186873800-186874000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr2:186873800-186874000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr2:186873800-186874200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr2:186874000-186874400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr2:186874000-186874400	ZNF genes & repeats	Aorta	Aorta

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