Variant report

Variant	nsv1005069
Chromosome Location	chr2:12161023-12242734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1444)
CpG islands
(count:305)
Chromatin interactive
region (count:28)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1444 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:12214078-12214735	K562	blood:	n/a	n/a
2	ARID3A	chr2:12190510-12190853	K562	blood:	n/a	n/a
3	ARID3A	chr2:12224320-12224487	K562	blood:	n/a	n/a
4	ARID3A	chr2:12200260-12200798	K562	blood:	n/a	n/a
5	ARID3A	chr2:12215220-12215309	K562	blood:	n/a	n/a
6	ARID3A	chr2:12199810-12200006	K562	blood:	n/a	n/a
7	ATF1	chr2:12214190-12214878	K562	blood:	n/a	n/a
8	ATF1	chr2:12224211-12224502	K562	blood:	n/a	n/a
9	ATF1	chr2:12190507-12190860	K562	blood:	n/a	n/a
10	ATF2	chr2:12172549-12173049	GM12878	blood:	n/a	n/a
11	ATF2	chr2:12216889-12217266	GM12878	blood:	n/a	n/a
12	ATF2	chr2:12211462-12211854	GM12878	blood:	n/a	n/a
13	ATF2	chr2:12172424-12173014	GM12878	blood:	n/a	n/a
14	ATF2	chr2:12197329-12198127	GM12878	blood:	n/a	n/a
15	ATF2	chr2:12185775-12186473	GM12878	blood:	n/a	n/a
16	ATF2	chr2:12174320-12175009	GM12878	blood:	n/a	n/a
17	ATF2	chr2:12184828-12185404	GM12878	blood:	n/a	n/a
18	ATF2	chr2:12185827-12186453	GM12878	blood:	n/a	n/a
19	ATF2	chr2:12211397-12211889	GM12878	blood:	n/a	n/a
20	ATF2	chr2:12214201-12214689	GM12878	blood:	n/a	n/a
21	ATF3	chr2:12200022-12200450	K562	blood:	n/a	n/a
22	ATF3	chr2:12214161-12214796	K562	blood:	n/a	chr2:12214471-12214491
23	BACH1	chr2:12197730-12197944	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr2:12215757-12216021	GM12878	blood:	n/a	n/a
25	BATF	chr2:12185988-12186297	GM12878	blood:	n/a	n/a
26	BATF	chr2:12216963-12217290	GM12878	blood:	n/a	n/a
27	BATF	chr2:12197554-12197870	GM12878	blood:	n/a	n/a
28	BATF	chr2:12215793-12215994	GM12878	blood:	n/a	n/a
29	BATF	chr2:12214284-12214640	GM12878	blood:	n/a	chr2:12214480-12214493
30	BATF	chr2:12185846-12186367	GM12878	blood:	n/a	n/a
31	BATF	chr2:12172595-12172856	GM12878	blood:	n/a	n/a
32	BATF	chr2:12190537-12190844	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:12223232-12223426	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr2:12197485-12197956	GM12878	blood:	n/a	chr2:12197932-12197941
35	BCL11A	chr2:12214363-12214649	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:12197592-12197896	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:12185952-12186265	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:12214269-12214720	GM12878	blood:	n/a	chr2:12214307-12214314
39	BCL11A	chr2:12211422-12211829	GM12878	blood:	n/a	chr2:12211643-12211652
40	BCL11A	chr2:12211508-12211807	GM12878	blood:	n/a	chr2:12211643-12211652
41	BCL3	chr2:12228185-12228478	GM12878	blood:	n/a	n/a
42	BCL3	chr2:12197564-12197985	GM12878	blood:	n/a	chr2:12197932-12197941
43	BCL3	chr2:12237953-12238250	GM12878	blood:	n/a	n/a
44	BCLAF1	chr2:12197493-12198087	GM12878	blood:	n/a	chr2:12197932-12197941
45	BCLAF1	chr2:12172416-12173028	GM12878	blood:	n/a	n/a
46	BCLAF1	chr2:12214128-12214778	K562	blood:	n/a	chr2:12214307-12214314
47	BCLAF1	chr2:12190397-12190921	GM12878	blood:	n/a	n/a
48	BCLAF1	chr2:12184910-12185348	GM12878	blood:	n/a	n/a
49	BCLAF1	chr2:12185792-12186643	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:12184965-12185291	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:12223636-12223686	MCF10A-Er-Src	breast:	n/a
2	chr2:12163118-12163168	HCF	heart:	n/a
3	chr2:12223636-12223686	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:12237012-12237062	HMEC	breast:	n/a
5	chr2:12237012-12237062	SK-N-SH_RA	brain:	n/a
6	chr2:12237012-12237062	HEEpiC	esophagus:	n/a
7	chr2:12163619-12163669	LNCaP	prostate:	n/a
8	chr2:12173618-12173668	GM12892	blood:	n/a
9	chr2:12237012-12237062	Hepatocyte	liver:	n/a
10	chr2:12163118-12163168	Jurkat	blood:	n/a
11	chr2:12237012-12237062	HCM	heart:	n/a
12	chr2:12173618-12173668	Hela-S3	cervix:	n/a
13	chr2:12223636-12223686	BE2_C	brain:	n/a
14	chr2:12173618-12173668	IMR90	lung:	fetal
15	chr2:12223636-12223686	NHBE	bronchial:	n/a
16	chr2:12237012-12237062	GM12892	blood:	n/a
17	chr2:12163619-12163669	BJ	skin:	n/a
18	chr2:12163118-12163168	RPTEC	kidney:	n/a
19	chr2:12173618-12173668	HIPEpiC	eye:	n/a
20	chr2:12237012-12237062	HNPCEpiC	eye:	n/a
21	chr2:12223636-12223686	Hepatocyte	liver:	n/a
22	chr2:12163619-12163669	RPTEC	kidney:	n/a
23	chr2:12237012-12237062	AG04450	lung:	fetal
24	chr2:12163118-12163168	AoSMC	blood vessel:	n/a
25	chr2:12237012-12237062	GM19239	blood:	n/a
26	chr2:12173618-12173668	T-47D	breast:	n/a
27	chr2:12163619-12163669	HAEpiC	amniotic membrane:	n/a
28	chr2:12163118-12163168	SK-N-MC	brain:	n/a
29	chr2:12173618-12173668	Jurkat	blood:	n/a
30	chr2:12163619-12163669	AoSMC	blood vessel:	n/a
31	chr2:12163619-12163669	PrEC	prostate:	n/a
32	chr2:12223636-12223686	HAEpiC	amniotic membrane:	n/a
33	chr2:12223636-12223686	HepG2	liver:	n/a
34	chr2:12237012-12237062	GM12878	blood:	n/a
35	chr2:12173618-12173668	GM12878	blood:	n/a
36	chr2:12237012-12237062	AoSMC	blood vessel:	n/a
37	chr2:12163619-12163669	T-47D	breast:	n/a
38	chr2:12173618-12173668	GM06990	blood:	n/a
39	chr2:12163118-12163168	HAEpiC	amniotic membrane:	n/a
40	chr2:12237012-12237062	ProgFib	skin:	n/a
41	chr2:12163619-12163669	NH-A	brain:	n/a
42	chr2:12223636-12223686	Jurkat	blood:	n/a
43	chr2:12223636-12223686	SK-N-SH	brain:	n/a
44	chr2:12163619-12163669	BE2_C	brain:	n/a
45	chr2:12163619-12163669	H1-hESC	embryonic stem cell:	embryo
46	chr2:12223636-12223686	AG04449	skin:	fetal
47	chr2:12163118-12163168	NHBE	bronchial:	n/a
48	chr2:12223636-12223686	LNCaP	prostate:	n/a
49	chr2:12223636-12223686	HIPEpiC	eye:	n/a
50	chr2:12163619-12163669	GM12891	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:12180693..12182626-chr2:12190865..12193405,2	K562	blood:
2	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
3	chr2:12240589..12242524-chr2:12244995..12247436,2	K562	blood:
4	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
5	chr2:12200110..12202419-chr2:12206699..12209506,2	K562	blood:
6	chr2:12176844..12179370-chr2:12184810..12186635,2	MCF-7	breast:
7	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
8	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
9	chr2:12142937..12145403-chr2:12173680..12175523,2	K562	blood:
10	chr2:12194778..12196811-chr2:12221641..12223390,2	K562	blood:
11	chr2:12003714..12004353-chr2:12188666..12189311,2	MCF-7	breast:
12	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
13	chr2:12180693..12182626-chr2:12190865..12193405,2	K562	blood:
14	chr2:12003510..12004337-chr2:12188494..12189188,2	MCF-7	breast:
15	chr2:12233977..12235737-chr2:12241751..12243264,2	K562	blood:
16	chr2:12155340..12157815-chr2:12177536..12179462,2	MCF-7	breast:
17	chr2:12202416..12205140-chr2:12205945..12209401,3	K562	blood:
18	chr2:12200110..12202419-chr2:12206699..12209506,2	K562	blood:
19	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
20	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
21	chr2:12176844..12179370-chr2:12184810..12186635,2	MCF-7	breast:
22	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
23	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
24	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
25	chr2:12202416..12205140-chr2:12205945..12209401,3	K562	blood:
26	chr2:12194778..12196811-chr2:12221641..12223390,2	K562	blood:
27	chr2:12219592..12223181-chr2:12244088..12246187,3	K562	blood:
28	chr2:12233977..12235737-chr2:12241751..12243264,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GREB1-10	chr2:12188883-12189125	NONHSAT069216
2	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069196
3	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069210
4	lnc-GREB1-10	chr2:12164161-12164261	NONHSAT069216
5	lnc-GREB1-10	chr2:12164395-12164528	NONHSAT069209
6	lnc-LPIN1-1	chr2:12223575-12223743	NR_110198
7	lnc-LPIN1-1	chr2:12223575-12223744	ENSG00000224184
8	lnc-GREB1-10	chr2:12164395-12164528	NONHSAT069216
9	lnc-GREB1-10	chr2:12188883-12189162	NONHSAT069209

No data

Variant related genes	Relation type
ENSG00000238503	TF binding region
ENSG00000224184	TF binding region
ENSG00000238503	CpG island
ENSG00000224184	CpG island
ENSG00000224184	chromatin interactions

Extended variants
information (count: 3218 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3218 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570634292	chr2:12161042-12161043	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141281409	chr2:12161057-12161058	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561491108	chr2:12161073-12161074	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188136521	chr2:12161089-12161090	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541112727	chr2:12161120-12161121	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539767822	chr2:12161164-12161165	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556076392	chr2:12161201-12161202	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56260961	chr2:12161252-12161253	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191772758	chr2:12161291-12161292	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138172873	chr2:12161295-12161296	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570242468	chr2:12161325-12161326	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13012119	chr2:12161330-12161331	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs373241900	chr2:12161388-12161389	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201666619	chr2:12161435-12161436	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549674872	chr2:12161441-12161442	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143854383	chr2:12161459-12161460	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75811652	chr2:12161492-12161493	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13029543	chr2:12161493-12161494	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs13007105	chr2:12161510-12161511	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs143251714	chr2:12161522-12161523	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77017892	chr2:12161571-12161572	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182980058	chr2:12161616-12161617	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35534522	chr2:12161629-12161630	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187432342	chr2:12161634-12161635	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533446492	chr2:12161677-12161678	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576200353	chr2:12161736-12161737	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543323412	chr2:12161741-12161742	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555661048	chr2:12161754-12161755	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573670583	chr2:12161778-12161779	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541074059	chr2:12161782-12161783	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559395227	chr2:12161821-12161822	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533019475	chr2:12161832-12161833	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545105343	chr2:12161845-12161846	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563704470	chr2:12161876-12161877	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531165879	chr2:12161939-12161940	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192339368	chr2:12161967-12161968	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567657380	chr2:12161975-12161976	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184725100	chr2:12161982-12161983	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546541450	chr2:12162007-12162008	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571315299	chr2:12162049-12162050	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538722301	chr2:12162079-12162080	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10929777	chr2:12162113-12162114	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs558686030	chr2:12162130-12162131	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572578394	chr2:12162158-12162159	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562426303	chr2:12162182-12162183	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148294655	chr2:12162188-12162189	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187858944	chr2:12162189-12162190	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192491509	chr2:12162203-12162204	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534926182	chr2:12162281-12162282	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552972852	chr2:12162287-12162288	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	19270706	CNVD
Prostate cancer	19258504	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:982 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:12155000-12164000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:12157800-12163000	ZNF genes & repeats	GM12878-XiMat	blood
3	chr2:12160400-12161600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
4	chr2:12160400-12161600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:12160600-12161800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
6	chr2:12160800-12161400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:12160800-12161600	ZNF genes & repeats	Fetal Lung	lung
8	chr2:12160800-12162600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr2:12162600-12164000	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr2:12162800-12163600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr2:12163400-12164600	Enhancers	NHDF-Ad	bronchial
12	chr2:12163600-12164400	Enhancers	Fetal Heart	heart
13	chr2:12163600-12164600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:12163600-12165000	Enhancers	HSMM	muscle
15	chr2:12163600-12165000	Enhancers	HSMMtube	muscle
16	chr2:12163800-12164600	Enhancers	HMEC	breast
17	chr2:12163800-12165000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:12163800-12165000	Enhancers	Osteobl	bone
19	chr2:12164000-12165000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:12164000-12165000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr2:12164000-12165000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr2:12164200-12164600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:12164200-12164600	Enhancers	Colon Smooth Muscle	Colon
24	chr2:12164200-12165000	Enhancers	NH-A	brain
25	chr2:12165800-12166400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:12166200-12166600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:12167400-12167600	Enhancers	K562	blood
28	chr2:12167600-12171800	Weak transcription	K562	blood
29	chr2:12167600-12172400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr2:12171200-12171400	Enhancers	Stomach Mucosa	stomach
31	chr2:12171200-12172400	Enhancers	Primary B cells from cord blood	blood
32	chr2:12171200-12178000	Enhancers	Primary B cells from peripheral blood	blood
33	chr2:12171400-12171600	Enhancers	GM12878-XiMat	blood
34	chr2:12171400-12171800	Flanking Active TSS	Stomach Mucosa	stomach
35	chr2:12171400-12173600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:12171600-12172400	Enhancers	Gastric	stomach
37	chr2:12171600-12172800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:12171600-12173400	Flanking Active TSS	GM12878-XiMat	blood
39	chr2:12171800-12172400	Enhancers	Fetal Heart	heart
40	chr2:12171800-12172400	Enhancers	Stomach Mucosa	stomach
41	chr2:12171800-12172400	Enhancers	K562	blood
42	chr2:12172000-12172400	Enhancers	Brain Cingulate Gyrus	brain
43	chr2:12172000-12172400	Bivalent Enhancer	Fetal Brain Male	brain
44	chr2:12172000-12172400	Enhancers	Left Ventricle	heart
45	chr2:12172000-12173400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr2:12172200-12172400	Enhancers	Fetal Muscle Trunk	muscle
47	chr2:12172200-12172800	Enhancers	Ovary	ovary
48	chr2:12172200-12174000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:12172200-12174000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr2:12172200-12174200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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