Variant report

Variant	nsv1014203
Chromosome Location	chr2:187413781-187477586
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1460)
CpG islands
(count:1039)
Chromatin interactive
region (count:90)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1460 , 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	chr2:187454204-187454949	K562	blood:	n/a	n/a
2	ARID3A	chr2:187470764-187470765	K562	blood:	n/a	n/a
3	ARID3A	chr2:187457057-187457358	K562	blood:	n/a	n/a
4	ARID3A	chr2:187455413-187456439	K562	blood:	n/a	n/a
5	ARID3A	chr2:187435446-187435766	K562	blood:	n/a	n/a
6	ARID3A	chr2:187455308-187455463	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:187458734-187458821	K562	blood:	n/a	n/a
8	ARID3A	chr2:187459831-187460249	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:187435476-187435712	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:187455669-187455948	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:187460039-187460181	K562	blood:	n/a	n/a
12	ARID3A	chr2:187433395-187433608	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:187440116-187440425	HepG2	liver:	n/a	n/a
14	ARID3A	chr2:187439988-187440337	K562	blood:	n/a	n/a
15	ARID3A	chr2:187453822-187455000	HepG2	liver:	n/a	n/a
16	ATF1	chr2:187440091-187440380	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	chr2:187457248-187457496	K562	blood:	n/a	n/a
20	ATF1	chr2:187448429-187448519	K562	blood:	n/a	n/a
21	ATF2	chr2:187454327-187455096	GM12878	blood:	n/a	n/a
22	ATF2	chr2:187455592-187456193	GM12878	blood:	n/a	n/a
23	ATF2	chr2:187455606-187456121	GM12878	blood:	n/a	n/a
24	ATF3	chr2:187440034-187440499	A549	lung:	n/a	n/a
25	ATF3	chr2:187440042-187440463	A549	lung:	n/a	n/a
26	ATF3	chr2:187435281-187435823	A549	lung:	n/a	n/a
27	ATF3	chr2:187454457-187455018	A549	lung:	n/a	chr2:187454494-187454503 chr2:187454488-187454497 chr2:187454853-187454862
28	ATF3	chr2:187437336-187437825	A549	lung:	n/a	n/a
29	ATF3	chr2:187437337-187437912	A549	lung:	n/a	n/a
30	ATF3	chr2:187439981-187440385	K562	blood:	n/a	n/a
31	ATF3	chr2:187455591-187456251	K562	blood:	n/a	chr2:187456091-187456104
32	BACH1	chr2:187454279-187455557	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr2:187440095-187440379	K562	blood:	n/a	chr2:187440259-187440273
34	BACH1	chr2:187460264-187460377	K562	blood:	n/a	n/a
35	BACH1	chr2:187440191-187440429	H1-hESC	embryonic stem cell:	n/a	chr2:187440259-187440273
36	BCL3	chr2:187454178-187454855	A549	lung:	n/a	chr2:187454493-187454502 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454810-187454819 chr2:187454741-187454750
37	BCL3	chr2:187454079-187454806	A549	lung:	n/a	chr2:187454493-187454502 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454741-187454750
38	BCL3	chr2:187439771-187440588	A549	lung:	n/a	n/a
39	BCL3	chr2:187437330-187438000	A549	lung:	n/a	n/a
40	BCL3	chr2:187437319-187437942	A549	lung:	n/a	n/a
41	BCL3	chr2:187435240-187435917	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	chr2:187453816-187456219	K562	blood:	n/a	chr2:187454843-187454859 chr2:187454565-187454581
45	BHLHE40	chr2:187459323-187459328	K562	blood:	n/a	n/a
46	BHLHE40	chr2:187454355-187454931	GM12878	blood:	n/a	chr2:187454843-187454859 chr2:187454565-187454581
47	BHLHE40	chr2:187455259-187455403	GM12878	blood:	n/a	n/a
48	BRCA1	chr2:187454402-187454601	GM12878	blood:	n/a	n/a
49	BRCA1	chr2:187440976-187441206	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr2:187454490-187454930	HepG2	liver:	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	chr2:187464902-187464952	HUVEC	blood vessel:	n/a
2	chr2:187454414-187454464	SK-N-SH_RA	brain:	n/a
3	chr2:187464902-187464952	HUVEC	blood vessel:	n/a
4	chr2:187454414-187454464	SK-N-SH_RA	brain:	n/a
5	chr2:187464902-187464952	NB4	blood:	n/a
6	chr2:187454863-187454913	H1-hESC	embryonic stem cell:	embryo
7	chr2:187464581-187464631	Hela-S3	cervix:	n/a
8	chr2:187464902-187464952	A549	lung:	n/a
9	chr2:187454551-187454601	LNCaP	prostate:	n/a
10	chr2:187464902-187464952	NHDF-neo	bronchial:	n/a
11	chr2:187464902-187464952	HRPEpiC	eye:	n/a
12	chr2:187455488-187455538	K562	blood:	n/a
13	chr2:187455298-187455348	PFSK-1	brain:	n/a
14	chr2:187454863-187454913	GM12892	blood:	n/a
15	chr2:187454259-187454309	HUVEC	blood vessel:	n/a
16	chr2:187458732-187458782	ovcar-3	ovarian:	n/a
17	chr2:187455488-187455538	HMEC	breast:	n/a
18	chr2:187454863-187454913	HRE	kidney:	n/a
19	chr2:187464902-187464952	HepG2	liver:	n/a
20	chr2:187454299-187454349	NH-A	brain:	n/a
21	chr2:187454747-187454797	AG09309	skin:	n/a
22	chr2:187464581-187464631	NHBE	bronchial:	n/a
23	chr2:187454551-187454601	GM12891	blood:	n/a
24	chr2:187464581-187464631	HepG2	liver:	n/a
25	chr2:187451704-187451754	HNPCEpiC	eye:	n/a
26	chr2:187464581-187464631	SKMC	muscle:	n/a
27	chr2:187474432-187474482	Hela-S3	cervix:	n/a
28	chr2:187454863-187454913	A549	lung:	n/a
29	chr2:187454299-187454349	AoSMC	blood vessel:	n/a
30	chr2:187454747-187454797	NHBE	bronchial:	n/a
31	chr2:187454299-187454349	Hela-S3	cervix:	n/a
32	chr2:187454414-187454464	SK-N-SH	brain:	n/a
33	chr2:187464068-187464118	Jurkat	blood:	n/a
34	chr2:187454590-187454640	HCF	heart:	n/a
35	chr2:187454590-187454640	Hela-S3	cervix:	n/a
36	chr2:187454414-187454464	HMEC	breast:	n/a
37	chr2:187454259-187454309	HNPCEpiC	eye:	n/a
38	chr2:187454863-187454913	AoSMC	blood vessel:	n/a
39	chr2:187455298-187455348	HEEpiC	esophagus:	n/a
40	chr2:187451704-187451754	NHDF-neo	bronchial:	n/a
41	chr2:187463618-187463668	K562	blood:	n/a
42	chr2:187474432-187474482	GM12891	blood:	n/a
43	chr2:187454299-187454349	AG09309	skin:	n/a
44	chr2:187451704-187451754	A549	lung:	n/a
45	chr2:187454299-187454349	AG04450	lung:	fetal
46	chr2:187454747-187454797	HAEpiC	amniotic membrane:	n/a
47	chr2:187454414-187454464	PANC-1	pancreas:	n/a
48	chr2:187463618-187463668	HUVEC	blood vessel:	n/a
49	chr2:187454747-187454797	AG09319	gingival:	n/a
50	chr2:187463618-187463668	NH-A	brain:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:187408437..187410562-chr2:187417781..187420649,2	K562	blood:
2	chr2:187370485..187373217-chr2:187453776..187456177,3	MCF-7	breast:
3	chr2:187412931..187415408-chr2:187415614..187417884,2	K562	blood:
4	chr2:187437479..187442784-chr2:187443924..187447436,6	MCF-7	breast:
5	chr2:187397253..187399860-chr2:187417880..187419525,2	MCF-7	breast:
6	chr2:187370870..187374778-chr2:187436583..187438876,3	MCF-7	breast:
7	chr2:187416465..187418037-chr2:187440678..187443102,2	MCF-7	breast:
8	chr2:187370609..187373386-chr2:187454442..187456199,2	MCF-7	breast:
9	chr2:187451176..187453820-chr2:187556844..187559816,2	K562	blood:
10	chr2:187419131..187421753-chr2:187453589..187456403,3	MCF-7	breast:
11	chr2:187408692..187413087-chr2:187413826..187419706,7	MCF-7	breast:
12	chr2:187470424..187473004-chr2:187473894..187476819,4	K562	blood:
13	chr2:187442776..187446488-chr2:187447901..187451766,4	MCF-7	breast:
14	chr2:187454467..187456170-chr2:187472478..187474784,2	MCF-7	breast:
15	chr2:187368789..187369555-chr2:187454140..187454681,2	MCF-7	breast:
16	chr2:187454667..187455243-chr2:187466759..187467666,2	MCF-7	breast:
17	chr2:187350319..187353074-chr2:187452754..187457832,8	K562	blood:
18	chr2:187348960..187352767-chr2:187423783..187427050,3	K562	blood:
19	chr2:187435611..187437376-chr2:187439116..187441984,2	MCF-7	breast:
20	chr2:187433203..187436265-chr2:187453472..187457114,4	K562	blood:
21	chr2:187470425..187472217-chr2:187482022..187483885,2	MCF-7	breast:
22	chr2:187470424..187473004-chr2:187473894..187476819,4	K562	blood:
23	chr2:187414472..187416121-chr2:187454340..187456107,2	MCF-7	breast:
24	chr2:187412946..187417035-chr2:187453622..187456860,4	MCF-7	breast:
25	chr2:187435611..187437376-chr2:187439116..187441984,2	MCF-7	breast:
26	chr2:187438845..187441409-chr2:187470852..187472926,2	K562	blood:
27	chr2:187352327..187355103-chr2:187460869..187462881,2	K562	blood:
28	chr2:187418262..187420744-chr2:187454965..187457537,2	MCF-7	breast:
29	chr2:187412931..187415408-chr2:187415614..187417884,2	K562	blood:
30	chr2:187367976..187370185-chr2:187454691..187457440,2	MCF-7	breast:
31	chr2:187470424..187473004-chr2:187473894..187475620,2	K562	blood:
32	chr2:187350081..187352556-chr2:187433116..187434911,2	MCF-7	breast:
33	chr2:187350070..187352270-chr2:187452591..187455868,3	MCF-7	breast:
34	chr2:187349672..187352615-chr2:187454696..187458504,4	K562	blood:
35	chr2:183901739..183903655-chr2:187454012..187455892,2	MCF-7	breast:
36	chr2:187465660..187469278-chr2:187474543..187476426,3	K562	blood:
37	chr2:187438412..187440075-chr2:187442178..187444992,2	K562	blood:
38	chr2:187473255..187475524-chr2:187477074..187478666,2	K562	blood:
39	chr2:187459735..187462088-chr2:187466877..187468680,2	MCF-7	breast:
40	chr2:187473139..187475194-chr2:187476719..187478486,2	MCF-7	breast:
41	chr2:187359427..187362374-chr2:187449290..187451810,2	K562	blood:
42	chr2:187442776..187446488-chr2:187447901..187451766,4	MCF-7	breast:
43	chr2:187360313..187361827-chr2:187456108..187458564,2	K562	blood:
44	chr2:187410468..187412799-chr2:187439579..187442121,2	MCF-7	breast:
45	chr2:187433275..187435459-chr2:187454415..187456337,2	MCF-7	breast:
46	chr2:187470424..187473004-chr2:187473894..187475620,2	K562	blood:
47	chr2:187438845..187441409-chr2:187470852..187472926,2	K562	blood:
48	chr2:187418262..187420744-chr2:187454965..187457537,2	MCF-7	breast:
49	chr2:187349398..187350973-chr2:187420308..187421923,2	K562	blood:
50	chr2:187458884..187460611-chr2:187482455..187484231,2	K562	blood:

No data

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

Extended variants
information (count: 2152 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2152 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533634727	chr2:187413835-187413836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551486466	chr2:187413925-187413926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs117461301	chr2:187413950-187413951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565076210	chr2:187413963-187413964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569812198	chr2:187413964-187413965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183524465	chr2:187413965-187413966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549101628	chr2:187413990-187413991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567400456	chr2:187413992-187413993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs535312401	chr2:187414006-187414007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11695304	chr2:187414013-187414014	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs145488782	chr2:187414016-187414017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547145107	chr2:187414053-187414054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539674906	chr2:187414100-187414101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557482514	chr2:187414133-187414134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572828881	chr2:187414156-187414157	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541134241	chr2:187414205-187414206	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372259583	chr2:187414249-187414250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540210106	chr2:187414276-187414277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs10931250	chr2:187414282-187414283	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs573769883	chr2:187414284-187414285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561380759	chr2:187414321-187414322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563050080	chr2:187414336-187414337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533477447	chr2:187414364-187414365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545650679	chr2:187414385-187414386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188071986	chr2:187414418-187414419	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs137929198	chr2:187414431-187414432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540396659	chr2:187414437-187414438	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs80246001	chr2:187414614-187414615	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567464056	chr2:187414687-187414688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531656512	chr2:187414689-187414690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185037328	chr2:187414696-187414697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs550366349	chr2:187414722-187414723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145230129	chr2:187414750-187414751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188264848	chr2:187414769-187414770	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35616078	chr2:187414792-187414793	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs376101524	chr2:187414829-187414830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532870467	chr2:187414836-187414837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550977704	chr2:187414882-187414883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566647475	chr2:187414893-187414894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530270473	chr2:187414913-187414914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569675909	chr2:187414920-187414921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113511124	chr2:187414967-187414968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544294743	chr2:187414979-187414980	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556494450	chr2:187414990-187414991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191526238	chr2:187415013-187415014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144853328	chr2:187415068-187415069	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545251666	chr2:187415076-187415077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530422500	chr2:187415080-187415081	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs71432458	chr2:187415120-187415121	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560887943	chr2:187415198-187415199	Weak transcription	Chromatin interactive region	1 gene(s)	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:1689 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187411600-187420000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr2:187411800-187416400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:187412000-187415600	Weak transcription	NH-A	brain
4	chr2:187412000-187419400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:187412200-187415600	Weak transcription	Osteobl	bone
6	chr2:187412200-187415800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:187412200-187416000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:187412200-187416200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:187412200-187416400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:187412200-187416400	Weak transcription	HSMM	muscle
11	chr2:187412200-187416400	Weak transcription	NHDF-Ad	bronchial
12	chr2:187412200-187416600	Weak transcription	HSMMtube	muscle
13	chr2:187414400-187426400	Weak transcription	Aorta	Aorta
14	chr2:187415600-187415800	Enhancers	NH-A	brain
15	chr2:187415600-187416400	Enhancers	Osteobl	bone
16	chr2:187415800-187416200	Weak transcription	NH-A	brain
17	chr2:187415800-187417000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:187416000-187416800	Enhancers	Muscle Satellite Cultured Cells	--
19	chr2:187416200-187416800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:187416200-187417200	Enhancers	NH-A	brain
21	chr2:187416400-187416800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr2:187416400-187416800	Enhancers	HSMM	muscle
23	chr2:187416400-187416800	Enhancers	NHDF-Ad	bronchial
24	chr2:187416400-187416800	Flanking Active TSS	Osteobl	bone
25	chr2:187416400-187417600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:187416600-187417200	Enhancers	HSMMtube	muscle
27	chr2:187416800-187417200	Enhancers	Osteobl	bone
28	chr2:187416800-187418800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:187416800-187419000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:187416800-187423400	Weak transcription	NHDF-Ad	bronchial
31	chr2:187417000-187418800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:187417200-187419000	Weak transcription	NH-A	brain
33	chr2:187417200-187419000	Weak transcription	Osteobl	bone
34	chr2:187417600-187419000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr2:187418800-187420400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:187419000-187419400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:187419000-187419600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:187419000-187420000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:187419000-187420200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:187419000-187420800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr2:187419000-187420800	Enhancers	NH-A	brain
42	chr2:187419000-187420800	Enhancers	Osteobl	bone
43	chr2:187419200-187419400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr2:187419200-187419800	Enhancers	A549	lung
45	chr2:187419200-187420000	Enhancers	Hela-S3	cervix
46	chr2:187419200-187420200	Enhancers	NHEK	skin
47	chr2:187419400-187419800	Enhancers	Stomach Smooth Muscle	stomach
48	chr2:187419400-187420000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr2:187419400-187420200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:187419400-187420400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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