Variant report

Variant	nsv584020
Chromosome Location	chr2:186475590-186661567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:919)
CpG islands
(count:490)
Chromatin interactive
region (count:25)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:186603689-186603907	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:186510210-186510829	HepG2	liver:	n/a	n/a
3	ATF1	chr2:186586784-186586978	K562	blood:	n/a	n/a
4	ATF2	chr2:186509544-186509954	GM12878	blood:	n/a	n/a
5	ATF2	chr2:186603621-186603950	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:186603605-186603967	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:186603273-186603956	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:186509574-186509959	GM12878	blood:	n/a	n/a
9	BATF	chr2:186650918-186651197	GM12878	blood:	n/a	chr2:186651050-186651061
10	BATF	chr2:186650911-186651150	GM12878	blood:	n/a	chr2:186651050-186651061
11	BCLAF1	chr2:186509649-186509904	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:186591465-186591564	HepG2	liver:	n/a	n/a
13	BHLHE40	chr2:186603836-186603843	K562	blood:	n/a	n/a
14	BHLHE40	chr2:186603670-186603870	GM12878	blood:	n/a	n/a
15	BRCA1	chr2:186603755-186603918	HepG2	liver:	n/a	n/a
16	BRCA1	chr2:186603628-186603971	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr2:186554778-186555281	HCT-116	colon:	n/a	n/a
18	CBX3	chr2:186603562-186604004	K562	blood:	n/a	n/a
19	CBX3	chr2:186554740-186555339	HCT-116	colon:	n/a	n/a
20	CCNT2	chr2:186603668-186603984	K562	blood:	n/a	n/a
21	CCNT2	chr2:186508599-186508741	K562	blood:	n/a	n/a
22	CEBPB	chr2:186535082-186535227	HepG2	liver:	n/a	chr2:186535119-186535130
23	CEBPB	chr2:186510221-186510640	HepG2	liver:	n/a	chr2:186510394-186510405
24	CEBPB	chr2:186533482-186533800	HepG2	liver:	n/a	chr2:186533645-186533656
25	CEBPB	chr2:186523553-186523803	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:186533506-186533791	A549	lung:	n/a	chr2:186533645-186533656
27	CEBPB	chr2:186608484-186608783	HepG2	liver:	n/a	chr2:186608617-186608628
28	CEBPB	chr2:186510245-186510608	HepG2	liver:	n/a	chr2:186510394-186510405
29	CEBPB	chr2:186587425-186587627	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:186510298-186510570	HepG2	liver:	n/a	chr2:186510394-186510405
31	CEBPB	chr2:186478620-186478884	HepG2	liver:	n/a	chr2:186478732-186478743
32	CEBPB	chr2:186478710-186478888	A549	lung:	n/a	chr2:186478732-186478743
33	CEBPB	chr2:186544754-186544870	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr2:186603510-186603988	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:186510299-186510509	HepG2	liver:	n/a	chr2:186510394-186510405
36	CEBPB	chr2:186530680-186530902	HepG2	liver:	n/a	chr2:186530798-186530809
37	CEBPB	chr2:186533467-186533798	Hela-S3	cervix:	n/a	chr2:186533645-186533656
38	CEBPB	chr2:186533508-186533786	H1-hESC	embryonic stem cell:	n/a	chr2:186533645-186533656
39	CEBPB	chr2:186533543-186533809	IMR90	lung:	n/a	chr2:186533645-186533656
40	CEBPD	chr2:186510309-186510546	HepG2	liver:	n/a	chr2:186510394-186510405
41	CHD1	chr2:186602941-186603000	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr2:186651270-186651353	GM12878	blood:	n/a	n/a
43	CHD1	chr2:186603604-186603839	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr2:186603687-186603854	HepG2	liver:	n/a	n/a
45	CHD2	chr2:186562832-186562938	HepG2	liver:	n/a	n/a
46	CHD2	chr2:186510399-186510485	HepG2	liver:	n/a	n/a
47	CHD2	chr2:186651414-186651424	GM12878	blood:	n/a	n/a
48	CHD2	chr2:186603319-186604114	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr2:186603505-186604060	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTBP2	chr2:186603108-186603953	H1-hESC	embryonic stem cell:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186603639-186603689	BE2_C	brain:	n/a
2	chr2:186603639-186603689	MCF10A-Er-Src	breast:	n/a
3	chr2:186603639-186603689	BE2_C	brain:	n/a
4	chr2:186603639-186603689	MCF10A-Er-Src	breast:	n/a
5	chr2:186603981-186604031	HNPCEpiC	eye:	n/a
6	chr2:186610279-186610329	K562	blood:	n/a
7	chr2:186603398-186603448	SKMC	muscle:	n/a
8	chr2:186603398-186603448	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:186603561-186603611	HEEpiC	esophagus:	n/a
10	chr2:186603639-186603689	HRPEpiC	eye:	n/a
11	chr2:186609566-186609616	HMEC	breast:	n/a
12	chr2:186603441-186603491	HepG2	liver:	n/a
13	chr2:186603398-186603448	HCPEpiC	choroid plexus:	n/a
14	chr2:186609566-186609616	IMR90	lung:	fetal
15	chr2:186603398-186603448	HCF	heart:	n/a
16	chr2:186603981-186604031	MCF-7	breast:	n/a
17	chr2:186601802-186601852	AG09309	skin:	n/a
18	chr2:186603398-186603448	ProgFib	skin:	n/a
19	chr2:186609566-186609616	HNPCEpiC	eye:	n/a
20	chr2:186603441-186603491	HRCEpiC	kidney:	n/a
21	chr2:186603639-186603689	HAEpiC	amniotic membrane:	n/a
22	chr2:186603981-186604031	ECC-1	luminal epithelium:	n/a
23	chr2:186603981-186604031	AG09319	gingival:	n/a
24	chr2:186603561-186603611	HEK293	kidney:	embryo
25	chr2:186603441-186603491	AG04450	lung:	fetal
26	chr2:186603981-186604031	MCF10A-Er-Src	breast:	n/a
27	chr2:186603441-186603491	HCT-116	colon:	n/a
28	chr2:186603441-186603491	IMR90	lung:	fetal
29	chr2:186601802-186601852	A549	lung:	n/a
30	chr2:186610279-186610329	Caco-2	colon:	n/a
31	chr2:186601802-186601852	NHDF-neo	bronchial:	n/a
32	chr2:186603441-186603491	GM12891	blood:	n/a
33	chr2:186603441-186603491	H1-hESC	embryonic stem cell:	embryo
34	chr2:186603398-186603448	HRE	kidney:	n/a
35	chr2:186610279-186610329	T-47D	breast:	n/a
36	chr2:186610279-186610329	HRE	kidney:	n/a
37	chr2:186609566-186609616	LNCaP	prostate:	n/a
38	chr2:186610279-186610329	HCT-116	colon:	n/a
39	chr2:186610279-186610329	HepG2	liver:	n/a
40	chr2:186603561-186603611	GM19239	blood:	n/a
41	chr2:186610279-186610329	HL-60	blood:	n/a
42	chr2:186603398-186603448	U87	brain:	n/a
43	chr2:186601802-186601852	HMEC	breast:	n/a
44	chr2:186603441-186603491	HNPCEpiC	eye:	n/a
45	chr2:186603398-186603448	SK-N-SH	brain:	n/a
46	chr2:186603639-186603689	HIPEpiC	eye:	n/a
47	chr2:186609566-186609616	AG09309	skin:	n/a
48	chr2:186610279-186610329	SK-N-MC	brain:	n/a
49	chr2:186603398-186603448	HEK293	kidney:	embryo
50	chr2:186603441-186603491	HL-60	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186614301..186616575-chr2:186619081..186620745,2	MCF-7	breast:
2	chr2:186594845..186596919-chr2:186599054..186601841,2	K562	blood:
3	chr2:186598239..186601001-chr2:186602437..186604775,2	K562	blood:
4	chr2:186657715..186659336-chr2:186665984..186667594,2	K562	blood:
5	chr2:186650871..186652540-chr2:186657235..186659322,2	K562	blood:
6	chr2:186608726..186611279-chr2:186612824..186614382,2	MCF-7	breast:
7	chr2:186493592..186494450-chr2:186603275..186603898,3	MCF-7	breast:
8	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:
9	chr2:186650871..186652540-chr2:186657235..186659322,2	K562	blood:
10	chr2:186597190..186601859-chr2:186602437..186604775,4	K562	blood:
11	chr2:186588408..186592015-chr2:186593924..186596626,4	K562	blood:
12	chr2:186492938..186493701-chr2:186603922..186604721,2	MCF-7	breast:
13	chr2:186532536..186534671-chr2:186536499..186538385,2	K562	blood:
14	chr2:186540633..186542551-chr2:186567883..186570534,2	MCF-7	breast:
15	chr2:186594845..186596919-chr2:186599054..186601841,2	K562	blood:
16	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:
17	chr2:186493563..186494107-chr2:187121512..187122407,2	MCF-7	breast:
18	chr2:186532536..186534671-chr2:186536499..186538385,2	K562	blood:
19	chr14:42041047..42041943-chr2:186615944..186616587,2	MCF-7	breast:
20	chr2:186588408..186592015-chr2:186593924..186596626,4	K562	blood:
21	chr2:186540633..186542551-chr2:186567883..186570534,2	MCF-7	breast:
22	chr2:186603293..186603807-chr8:145027949..145028449,2	MCF-7	breast:
23	chr2:186603383..186603935-chr8:145027949..145028449,2	MCF-7	breast:
24	chr2:186614301..186616575-chr2:186619081..186620745,2	MCF-7	breast:
25	chr16:88876629..88878732-chr2:186490716..186492785,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-6	chr2:186600789-186600864	ENSG00000226747
2	lnc-ZSWIM2-5	chr2:186652747-186652936	ENSG00000231646.1
3	lnc-ZSWIM2-5	chr2:186653493-186653670	ENSG00000231646.1
4	lnc-ZSWIM2-6	chr2:186594009-186594164	NONHSAT075967
5	lnc-ZSWIM2-6	chr2:186600789-186600930	NONHSAT075967
6	lnc-ZSWIM2-6	chr2:186600789-186600859	ENSG00000226747
7	lnc-ZSWIM2-6	chr2:186600789-186600864	NR_110214
8	lnc-ZSWIM2-6	chr2:186603634-186603820	NR_110214
9	lnc-ZSWIM2-14	chr2:186611303-186611407	l_2006_chr2:186606630-186611407_prostate
10	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110216
11	lnc-ZSWIM2-6	chr2:186603297-186603448	ENSG00000226747
12	lnc-ZSWIM2-5	chr2:186648418-186648857	ENSG00000231646.1
13	lnc-ZSWIM2-6	chr2:186584939-186585447	ENSG00000226747
14	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110217
15	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110214
16	lnc-ZSWIM2-6	chr2:186594056-186594164	ENSG00000226747
17	lnc-ZSWIM2-6	chr2:186584601-186585447	ENSG00000226747
18	lnc-ZSWIM2-6	chr2:186594056-186594164	ENSG00000226747
19	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110217
20	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110215
21	lnc-ZSWIM2-6	chr2:186602913-186602980	ENSG00000226747
22	lnc-ZSWIM2-6	chr2:186600789-186600859	NR_110215
23	lnc-ZSWIM2-6	chr2:186603297-186603446	NR_110216
24	lnc-ZSWIM2-6	chr2:186603297-186603446	NR_110215
25	lnc-ZSWIM2-5	chr2:186653493-186653670	ENSG00000231646.1
26	lnc-ZSWIM2-6	chr2:186600789-186600864	NR_110216
27	lnc-ZSWIM2-14	chr2:186606631-186606774	l_2006_chr2:186606630-186611407_prostate
28	lnc-ZSWIM2-6	chr2:186594072-186594164	NONHSAT075968
29	lnc-ZSWIM2-6	chr2:186605106-186605206	ENSG00000226747
30	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110214
31	lnc-ZSWIM2-6	chr2:186603634-186603752	ENSG00000226747
32	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110216
33	lnc-ZSWIM2-6	chr2:186603634-186603808	NONHSAT075968
34	lnc-ZSWIM2-6	chr2:186600789-186600864	NONHSAT075968
35	lnc-ZSWIM2-6	chr2:186605106-186605204	NR_110217
36	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110215

No data

Variant related genes	Relation type
ENSG00000212581	TF binding region
FSIP2	TF binding region
ENSG00000226747	TF binding region
ENSG00000212581	CpG island
FSIP2	CpG island
ENSG00000226747	CpG island
ENSG00000226747	chromatin interactions
ENSG00000178209	chromatin interactions
ENSG00000198931	chromatin interactions
ENSG00000188738	chromatin interactions

Extended variants
information (count: 4398 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4398 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2111710	chr2:186475590-186475591	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149159932	chr2:186475605-186475606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565728293	chr2:186475633-186475634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540125048	chr2:186475665-186475666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561933244	chr2:186475708-186475709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573791119	chr2:186475744-186475745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs72910219	chr2:186475762-186475763	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs556323010	chr2:186475774-186475775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533244762	chr2:186475784-186475785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375448967	chr2:186475788-186475789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13387585	chr2:186475794-186475795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13387594	chr2:186475828-186475829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148291120	chr2:186475840-186475841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528010531	chr2:186475867-186475868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549378028	chr2:186475870-186475871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369963906	chr2:186475888-186475889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567925878	chr2:186475908-186475909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199896353	chr2:186475916-186475917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141415403	chr2:186475923-186475924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115904748	chr2:186475935-186475936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190541034	chr2:186475959-186475960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184852277	chr2:186475978-186475979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17206513	chr2:186475997-186475998	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs147103326	chr2:186476022-186476023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566308343	chr2:186476026-186476027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138533391	chr2:186476058-186476059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7608349	chr2:186476111-186476112	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs375230672	chr2:186476116-186476117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147293185	chr2:186476129-186476130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183479810	chr2:186476228-186476229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369408243	chr2:186476292-186476293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188858237	chr2:186476297-186476298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555673070	chr2:186476309-186476310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139917995	chr2:186476340-186476341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372917587	chr2:186476348-186476349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs193218591	chr2:186476381-186476382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527713503	chr2:186476456-186476457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565600088	chr2:186476483-186476484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567548096	chr2:186476558-186476559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77105399	chr2:186476617-186476618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534968463	chr2:186476646-186476647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561464377	chr2:186476809-186476810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532000759	chr2:186476821-186476822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114945906	chr2:186476825-186476826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571839311	chr2:186476865-186476866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10207584	chr2:186476941-186476942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182705658	chr2:186476967-186476968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553099265	chr2:186476977-186476978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187779738	chr2:186476986-186476987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191927394	chr2:186476988-186476989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Autism	18522746	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
Ependymoma	20639864	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186473600-186483400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:186475000-186476200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:186475800-186476000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:186483400-186483800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:186483400-186483800	Enhancers	Fetal Heart	heart
6	chr2:186483400-186484000	Enhancers	HMEC	breast
7	chr2:186483600-186483800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:186483600-186484000	Enhancers	NHEK	skin
9	chr2:186483800-186490400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:186485000-186485400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:186485400-186485800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:186485400-186490600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:186485800-186489800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:186487200-186487800	Enhancers	Brain Germinal Matrix	brain
15	chr2:186489800-186490400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:186490400-186490600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:186490600-186490800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:186498200-186498600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr2:186498200-186498800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr2:186498200-186498800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:186498400-186498800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr2:186498600-186503000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr2:186498800-186502400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr2:186498800-186503000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:186502400-186503800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:186502400-186504200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr2:186502600-186503200	Enhancers	Brain Germinal Matrix	brain
28	chr2:186502600-186503800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:186502800-186503400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr2:186502800-186503400	Enhancers	Fetal Brain Female	brain
31	chr2:186503000-186503400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:186503000-186503400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:186503000-186503800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:186503800-186508200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:186504200-186509000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr2:186504800-186505400	Enhancers	Fetal Stomach	stomach
37	chr2:186505400-186508400	Weak transcription	Fetal Stomach	stomach
38	chr2:186507000-186507200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:186507000-186510400	Enhancers	Fetal Intestine Small	intestine
40	chr2:186507000-186511000	Enhancers	Fetal Intestine Large	intestine
41	chr2:186507200-186508400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:186507600-186511200	Enhancers	HepG2	liver
43	chr2:186508200-186509000	Enhancers	Ovary	ovary
44	chr2:186508200-186510000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:186508400-186509200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:186508400-186509200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:186508400-186509200	Enhancers	Fetal Stomach	stomach
48	chr2:186509000-186509600	Weak transcription	Ovary	ovary
49	chr2:186509000-186510000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr2:186509600-186509800	Enhancers	Ovary	ovary

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