Variant report

Variant	esv2756956
Chromosome Location	chr2:187416599-187492742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1486)
CpG islands
(count:1039)
Chromatin interactive
region (count:110)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1486 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:187470764-187470765	K562	blood:	n/a	n/a
2	ARID3A	chr2:187453822-187455000	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:187455308-187455463	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:187435446-187435766	K562	blood:	n/a	n/a
5	ARID3A	chr2:187458734-187458821	K562	blood:	n/a	n/a
6	ARID3A	chr2:187435476-187435712	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:187459831-187460249	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:187440116-187440425	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:187454204-187454949	K562	blood:	n/a	n/a
10	ARID3A	chr2:187457057-187457358	K562	blood:	n/a	n/a
11	ARID3A	chr2:187439988-187440337	K562	blood:	n/a	n/a
12	ARID3A	chr2:187433395-187433608	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:187455413-187456439	K562	blood:	n/a	n/a
14	ARID3A	chr2:187460039-187460181	K562	blood:	n/a	n/a
15	ARID3A	chr2:187455669-187455948	HepG2	liver:	n/a	n/a
16	ATF1	chr2:187457248-187457496	K562	blood:	n/a	n/a
17	ATF1	chr2:187419867-187420160	K562	blood:	n/a	n/a
18	ATF1	chr2:187455439-187456452	K562	blood:	n/a	n/a
19	ATF1	chr2:187440091-187440380	K562	blood:	n/a	n/a
20	ATF1	chr2:187448429-187448519	K562	blood:	n/a	n/a
21	ATF2	chr2:187455606-187456121	GM12878	blood:	n/a	n/a
22	ATF2	chr2:187454327-187455096	GM12878	blood:	n/a	n/a
23	ATF2	chr2:187455592-187456193	GM12878	blood:	n/a	n/a
24	ATF3	chr2:187437336-187437825	A549	lung:	n/a	n/a
25	ATF3	chr2:187437337-187437912	A549	lung:	n/a	n/a
26	ATF3	chr2:187455591-187456251	K562	blood:	n/a	chr2:187456091-187456104
27	ATF3	chr2:187454457-187455018	A549	lung:	n/a	chr2:187454494-187454503 chr2:187454488-187454497 chr2:187454853-187454862
28	ATF3	chr2:187440034-187440499	A549	lung:	n/a	n/a
29	ATF3	chr2:187435281-187435823	A549	lung:	n/a	n/a
30	ATF3	chr2:187440042-187440463	A549	lung:	n/a	n/a
31	ATF3	chr2:187439981-187440385	K562	blood:	n/a	n/a
32	BACH1	chr2:187460264-187460377	K562	blood:	n/a	n/a
33	BACH1	chr2:187440095-187440379	K562	blood:	n/a	chr2:187440259-187440273
34	BACH1	chr2:187440191-187440429	H1-hESC	embryonic stem cell:	n/a	chr2:187440259-187440273
35	BACH1	chr2:187454279-187455557	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL3	chr2:187454079-187454806	A549	lung:	n/a	chr2:187454493-187454502 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454741-187454750
37	BCL3	chr2:187437330-187438000	A549	lung:	n/a	n/a
38	BCL3	chr2:187437319-187437942	A549	lung:	n/a	n/a
39	BCL3	chr2:187454178-187454855	A549	lung:	n/a	chr2:187454493-187454502 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454810-187454819 chr2:187454741-187454750
40	BCL3	chr2:187435240-187435917	A549	lung:	n/a	n/a
41	BCL3	chr2:187439771-187440588	A549	lung:	n/a	n/a
42	BCLAF1	chr2:187454202-187455109	GM12878	blood:	n/a	chr2:187454493-187454502 chr2:187455010-187455019 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454810-187454819 chr2:187454741-187454750
43	BCLAF1	chr2:187454331-187455179	GM12878	blood:	n/a	chr2:187454493-187454502 chr2:187455010-187455019 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454810-187454819 chr2:187454741-187454750
44	BHLHE40	chr2:187455259-187455403	GM12878	blood:	n/a	n/a
45	BHLHE40	chr2:187454355-187454931	GM12878	blood:	n/a	chr2:187454843-187454859 chr2:187454565-187454581
46	BHLHE40	chr2:187459323-187459328	K562	blood:	n/a	n/a
47	BHLHE40	chr2:187453816-187456219	K562	blood:	n/a	chr2:187454843-187454859 chr2:187454565-187454581
48	BRCA1	chr2:187454402-187454601	GM12878	blood:	n/a	n/a
49	BRCA1	chr2:187454490-187454930	HepG2	liver:	n/a	n/a
50	BRCA1	chr2:187440976-187441206	Hela-S3	cervix:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:187451704-187451754	NB4	blood:	n/a
2	chr2:187454414-187454464	HMEC	breast:	n/a
3	chr2:187451704-187451754	NB4	blood:	n/a
4	chr2:187454414-187454464	HMEC	breast:	n/a
5	chr2:187454747-187454797	Jurkat	blood:	n/a
6	chr2:187464581-187464631	NT2-D1	testis:	n/a
7	chr2:187464902-187464952	ECC-1	luminal epithelium:	n/a
8	chr2:187454863-187454913	HCPEpiC	choroid plexus:	n/a
9	chr2:187463618-187463668	BE2_C	brain:	n/a
10	chr2:187474432-187474482	HNPCEpiC	eye:	n/a
11	chr2:187455298-187455348	K562	blood:	n/a
12	chr2:187464068-187464118	HCM	heart:	n/a
13	chr2:187474432-187474482	A549	lung:	n/a
14	chr2:187464581-187464631	T-47D	breast:	n/a
15	chr2:187474432-187474482	Jurkat	blood:	n/a
16	chr2:187454414-187454464	GM06990	blood:	n/a
17	chr2:187454299-187454349	SKMC	muscle:	n/a
18	chr2:187454551-187454601	BE2_C	brain:	n/a
19	chr2:187454590-187454640	CMK	blood:	n/a
20	chr2:187454590-187454640	MCF-7	breast:	n/a
21	chr2:187454259-187454309	LNCaP	prostate:	n/a
22	chr2:187454259-187454309	GM19239	blood:	n/a
23	chr2:187451704-187451754	AG09319	gingival:	n/a
24	chr2:187463618-187463668	HRCEpiC	kidney:	n/a
25	chr2:187454747-187454797	HCT-116	colon:	n/a
26	chr2:187463618-187463668	IMR90	lung:	fetal
27	chr2:187463618-187463668	A549	lung:	n/a
28	chr2:187464068-187464118	A549	lung:	n/a
29	chr2:187454299-187454349	NB4	blood:	n/a
30	chr2:187454863-187454913	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:187451704-187451754	AG09309	skin:	n/a
32	chr2:187454863-187454913	BE2_C	brain:	n/a
33	chr2:187454259-187454309	T-47D	breast:	n/a
34	chr2:187464902-187464952	HRPEpiC	eye:	n/a
35	chr2:187464581-187464631	HCT-116	colon:	n/a
36	chr2:187464902-187464952	HEEpiC	esophagus:	n/a
37	chr2:187455488-187455538	NHBE	bronchial:	n/a
38	chr2:187454259-187454309	HEK293	kidney:	embryo
39	chr2:187464068-187464118	HIPEpiC	eye:	n/a
40	chr2:187455488-187455538	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:187454613-187454663	AG09309	skin:	n/a
42	chr2:187464068-187464118	AoSMC	blood vessel:	n/a
43	chr2:187458732-187458782	T-47D	breast:	n/a
44	chr2:187454259-187454309	AG10803	skin:	n/a
45	chr2:187458732-187458782	GM06990	blood:	n/a
46	chr2:187454259-187454309	Hepatocyte	liver:	n/a
47	chr2:187454299-187454349	BE2_C	brain:	n/a
48	chr2:187454747-187454797	MCF-7	breast:	n/a
49	chr2:187454299-187454349	HRE	kidney:	n/a
50	chr2:187474432-187474482	BE2_C	brain:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:187475649..187479205-chr2:187480222..187482215,3	MCF-7	breast:
2	chr2:187410468..187412799-chr2:187439579..187442121,2	MCF-7	breast:
3	chr2:187380709..187383265-chr2:187491364..187493572,2	K562	blood:
4	chr2:187438759..187442258-chr2:187444014..187446139,4	MCF-7	breast:
5	chr2:187473194..187474789-chr2:187497969..187500920,2	K562	blood:
6	chr2:187470425..187472217-chr2:187482022..187483885,2	MCF-7	breast:
7	chr2:187350920..187353075-chr2:187470374..187472407,2	K562	blood:
8	chr2:187433203..187436265-chr2:187453472..187457114,4	K562	blood:
9	chr2:187438412..187440075-chr2:187442178..187444992,2	K562	blood:
10	chr2:187406067..187412442-chr2:187438004..187442761,8	MCF-7	breast:
11	chr2:187458884..187460611-chr2:187482455..187484231,2	K562	blood:
12	chr2:187350081..187352556-chr2:187433116..187434911,2	MCF-7	breast:
13	chr2:187454467..187456170-chr2:187472478..187474784,2	MCF-7	breast:
14	chr2:187416465..187418037-chr2:187440678..187443102,2	MCF-7	breast:
15	chr2:187437479..187442784-chr2:187443924..187447436,6	MCF-7	breast:
16	chr2:187488598..187492559-chr2:187493903..187496422,4	K562	blood:
17	chr2:187487385..187490996-chr2:187491673..187498174,5	K562	blood:
18	chr2:187365220..187368794-chr2:187491092..187495037,4	K562	blood:
19	chr2:187473139..187475194-chr2:187476719..187478486,2	MCF-7	breast:
20	chr2:187407559..187410721-chr2:187423895..187426771,4	MCF-7	breast:
21	chr2:187350028..187353171-chr2:187452977..187457092,6	MCF-7	breast:
22	chr2:187377349..187379042-chr2:187478698..187480439,2	MCF-7	breast:
23	chr2:187414378..187416859-chr2:187424448..187427803,3	K562	blood:
24	chr2:187420574..187422329-chr2:187424400..187426246,2	K562	blood:
25	chr2:187470424..187473004-chr2:187473894..187476819,4	K562	blood:
26	chr2:187481172..187483246-chr2:187487628..187489917,2	MCF-7	breast:
27	chr2:187411689..187413817-chr2:187434858..187437606,2	MCF-7	breast:
28	chr2:187412931..187415408-chr2:187415614..187417884,2	K562	blood:
29	chr2:187482291..187484673-chr2:187487622..187489404,2	K562	blood:
30	chr2:187465200..187467213-chr2:187503920..187506563,2	K562	blood:
31	chr2:187480029..187482174-chr2:187486614..187488319,2	MCF-7	breast:
32	chr2:187482291..187484673-chr2:187487622..187489404,2	K562	blood:
33	chr2:187480029..187482174-chr2:187486614..187488319,2	MCF-7	breast:
34	chr2:187396369..187398023-chr2:187440810..187442748,2	MCF-7	breast:
35	chr2:187359427..187362374-chr2:187449290..187451810,2	K562	blood:
36	chr2:187454844..187457492-chr2:187557694..187560224,2	K562	blood:
37	chr2:187420574..187422329-chr2:187424400..187426246,2	K562	blood:
38	chr2:187416465..187418037-chr2:187440678..187443102,2	MCF-7	breast:
39	chr2:187475649..187479205-chr2:187480222..187482215,3	MCF-7	breast:
40	chr2:187348960..187352767-chr2:187423783..187427050,3	K562	blood:
41	chr2:187470424..187473004-chr2:187473894..187476819,4	K562	blood:
42	chr2:187360313..187361827-chr2:187456108..187458564,2	K562	blood:
43	chr2:187442776..187446488-chr2:187447901..187451766,4	MCF-7	breast:
44	chr2:187466949..187471073-chr2:187471987..187477288,6	MCF-7	breast:
45	chr2:187433275..187435459-chr2:187454415..187456337,2	MCF-7	breast:
46	chr2:187406154..187410015-chr2:187435632..187441776,6	MCF-7	breast:
47	chr2:187458884..187460611-chr2:187482455..187484231,2	K562	blood:
48	chr2:187432930..187434820-chr2:187437011..187439461,2	MCF-7	breast:
49	chr2:187481172..187483246-chr2:187487628..187489917,2	MCF-7	breast:
50	chr2:187459735..187462088-chr2:187466877..187468680,2	MCF-7	breast:

No data

Variant related genes	Relation type
ITGAV	TF binding region
ITGAV	CpG island
ENSG00000227227	chromatin interactions
ENSG00000213953	chromatin interactions
ENSG00000138448	chromatin interactions
ENSG00000061676	chromatin interactions
ENSG00000224323	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000144369	chromatin interactions
ENSG00000268846	chromatin interactions
ENSG00000065548	chromatin interactions

Extended variants
information (count: 2606 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2606 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12693453	chr2:187416599-187416600	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551556414	chr2:187416600-187416601	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542605851	chr2:187416662-187416663	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560361832	chr2:187416677-187416678	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114987154	chr2:187416729-187416730	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370903093	chr2:187416790-187416791	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186689785	chr2:187416805-187416806	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532839808	chr2:187416819-187416820	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189653744	chr2:187416830-187416831	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs116928146	chr2:187416856-187416857	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571328860	chr2:187416928-187416929	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs538311039	chr2:187416946-187416947	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554368748	chr2:187416954-187416955	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs554662299	chr2:187416970-187416971	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572975785	chr2:187416978-187416979	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572273745	chr2:187417037-187417038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116375850	chr2:187417057-187417058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116814829	chr2:187417058-187417059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140687288	chr2:187417083-187417084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543100323	chr2:187417114-187417115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143018667	chr2:187417128-187417129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558631765	chr2:187417287-187417288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367991177	chr2:187417293-187417294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552855327	chr2:187417384-187417385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376408797	chr2:187417399-187417400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571120321	chr2:187417403-187417404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370801474	chr2:187417404-187417405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559868593	chr2:187417443-187417444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79515868	chr2:187417454-187417455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542841512	chr2:187417457-187417458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199760674	chr2:187417487-187417488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61154251	chr2:187417527-187417528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546660825	chr2:187417531-187417532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565174593	chr2:187417541-187417542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62197706	chr2:187417561-187417562	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531466418	chr2:187417640-187417641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367718090	chr2:187417706-187417707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533792061	chr2:187417709-187417710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544936645	chr2:187417711-187417712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571130526	chr2:187417749-187417750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576687527	chr2:187417760-187417761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547126699	chr2:187417766-187417767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565432148	chr2:187417860-187417861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11888813	chr2:187417979-187417980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573717341	chr2:187418007-187418008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371673687	chr2:187418015-187418016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142922534	chr2:187418019-187418020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570329223	chr2:187418044-187418045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113388251	chr2:187418062-187418063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182253855	chr2:187418092-187418093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187411600-187420000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr2:187412000-187419400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:187412200-187416600	Weak transcription	HSMMtube	muscle
4	chr2:187414400-187426400	Weak transcription	Aorta	Aorta
5	chr2:187415800-187417000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:187416000-187416800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr2:187416200-187416800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:187416200-187417200	Enhancers	NH-A	brain
9	chr2:187416400-187416800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:187416400-187416800	Enhancers	HSMM	muscle
11	chr2:187416400-187416800	Enhancers	NHDF-Ad	bronchial
12	chr2:187416400-187416800	Flanking Active TSS	Osteobl	bone
13	chr2:187416400-187417600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:187416600-187417200	Enhancers	HSMMtube	muscle
15	chr2:187416800-187417200	Enhancers	Osteobl	bone
16	chr2:187416800-187418800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr2:187416800-187419000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:187416800-187423400	Weak transcription	NHDF-Ad	bronchial
19	chr2:187417000-187418800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:187417200-187419000	Weak transcription	NH-A	brain
21	chr2:187417200-187419000	Weak transcription	Osteobl	bone
22	chr2:187417600-187419000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:187418800-187420400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:187419000-187419400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:187419000-187419600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:187419000-187420000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:187419000-187420200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:187419000-187420800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:187419000-187420800	Enhancers	NH-A	brain
30	chr2:187419000-187420800	Enhancers	Osteobl	bone
31	chr2:187419200-187419400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr2:187419200-187419800	Enhancers	A549	lung
33	chr2:187419200-187420000	Enhancers	Hela-S3	cervix
34	chr2:187419200-187420200	Enhancers	NHEK	skin
35	chr2:187419400-187419800	Enhancers	Stomach Smooth Muscle	stomach
36	chr2:187419400-187420000	Enhancers	Placenta Amnion	Placenta Amnion
37	chr2:187419400-187420200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:187419400-187420400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:187419600-187420000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr2:187419600-187420000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr2:187419600-187420200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:187419600-187420200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:187419600-187420400	Enhancers	K562	blood
44	chr2:187419600-187420600	Enhancers	HUVEC	blood vessel
45	chr2:187419600-187420800	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr2:187419800-187420400	Flanking Active TSS	A549	lung
47	chr2:187419800-187420600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr2:187420000-187423200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:187420000-187426000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr2:187420200-187420800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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