Variant report

Variant	nsv898620
Chromosome Location	chr12:4745313-4771456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:486)
CpG islands
(count:795)
Chromatin interactive
region (count:23)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:4757430-4758315	K562	blood:	n/a	n/a
2	ATF2	chr12:4757972-4758620	GM12878	blood:	n/a	n/a
3	ATF2	chr12:4758070-4758634	GM12878	blood:	n/a	n/a
4	ATF2	chr12:4757999-4758491	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr12:4757941-4758505	GM12878	blood:	n/a	chr12:4758114-4758123
6	BCLAF1	chr12:4757913-4758630	GM12878	blood:	n/a	chr12:4758114-4758123
7	BHLHE40	chr12:4757761-4758471	K562	blood:	n/a	n/a
8	BHLHE40	chr12:4758013-4758504	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:4757362-4757603	GM12878	blood:	n/a	n/a
10	BRCA1	chr12:4757522-4758889	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr12:4757956-4758363	K562	blood:	n/a	n/a
12	CEBPB	chr12:4757830-4757894	K562	blood:	n/a	n/a
13	CEBPB	chr12:4758026-4758412	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:4751161-4751189	K562	blood:	n/a	n/a
15	CEBPB	chr12:4759436-4759663	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:4760017-4760288	K562	blood:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
17	CEBPB	chr12:4759955-4760222	HepG2	liver:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
18	CEBPB	chr12:4751163-4751331	HepG2	liver:	n/a	n/a
19	CEBPD	chr12:4758143-4758473	HepG2	liver:	n/a	n/a
20	CHD1	chr12:4757476-4758871	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr12:4758193-4758446	HepG2	liver:	n/a	n/a
22	CHD2	chr12:4757626-4758623	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr12:4758078-4758446	GM12878	blood:	n/a	n/a
24	CHD2	chr12:4757737-4757887	K562	blood:	n/a	n/a
25	CHD2	chr12:4758021-4758466	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr12:4758078-4758323	A549	lung:	n/a	n/a
27	CREB1	chr12:4757960-4758541	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr12:4758112-4758477	A549	lung:	n/a	n/a
29	CREB1	chr12:4754210-4754564	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr12:4758195-4758285	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr12:4762460-4762610	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr12:4762380-4762530	Caco-2	colon:	n/a	n/a
33	CTCF	chr12:4762460-4762610	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr12:4762400-4762550	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr12:4762380-4762530	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr12:4762420-4762570	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr12:4758165-4758206	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr12:4762420-4762570	HVMF	connective:	n/a	n/a
39	CTCF	chr12:4762500-4762650	AG10803	skin:	n/a	n/a
40	CTCF	chr12:4757980-4758130	NHLF	lung:	n/a	n/a
41	CTCF	chr12:4762440-4762590	AG04449	skin:	n/a	n/a
42	CTCF	chr12:4758740-4758890	Caco-2	colon:	n/a	n/a
43	CTCF	chr12:4762500-4762650	HEK293	kidney:	n/a	n/a
44	CTCF	chr12:4762360-4762510	AG04450	lung:	n/a	n/a
45	CTCF	chr12:4758162-4758291	GM12878	blood:	n/a	n/a
46	CTCF	chr12:4758079-4758321	K562	blood:	n/a	n/a
47	CTCF	chr12:4757436-4757457	GM10266	blood:	n/a	n/a
48	CTCF	chr12:4757660-4757810	A549	lung:	n/a	n/a
49	CTCF	chr12:4762460-4762610	RPTEC	kidney:	n/a	n/a
50	CTCF	chr12:4757748-4757758	K562	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:4758496-4758546	NB4	blood:	n/a
2	chr12:4754247-4754297	NHBE	bronchial:	n/a
3	chr12:4758496-4758546	NB4	blood:	n/a
4	chr12:4754247-4754297	NHBE	bronchial:	n/a
5	chr12:4758217-4758267	SKMC	muscle:	n/a
6	chr12:4755555-4755605	HUVEC	blood vessel:	n/a
7	chr12:4754247-4754297	SKMC	muscle:	n/a
8	chr12:4758496-4758546	HEK293	kidney:	embryo
9	chr12:4758424-4758474	NH-A	brain:	n/a
10	chr12:4758272-4758322	IMR90	lung:	fetal
11	chr12:4758424-4758474	ECC-1	luminal epithelium:	n/a
12	chr12:4754247-4754297	IMR90	lung:	fetal
13	chr12:4762206-4762256	PANC-1	pancreas:	n/a
14	chr12:4758250-4758300	SKMC	muscle:	n/a
15	chr12:4758250-4758300	NHDF-neo	bronchial:	n/a
16	chr12:4754247-4754297	HCPEpiC	choroid plexus:	n/a
17	chr12:4758217-4758267	NHDF-neo	bronchial:	n/a
18	chr12:4762206-4762256	HCF	heart:	n/a
19	chr12:4758250-4758300	T-47D	breast:	n/a
20	chr12:4758272-4758322	ovcar-3	ovarian:	n/a
21	chr12:4755479-4755529	HCF	heart:	n/a
22	chr12:4757759-4757809	HepG2	liver:	n/a
23	chr12:4757728-4757778	GM12892	blood:	n/a
24	chr12:4754247-4754297	A549	lung:	n/a
25	chr12:4757759-4757809	ovcar-3	ovarian:	n/a
26	chr12:4754247-4754297	T-47D	breast:	n/a
27	chr12:4758272-4758322	Hela-S3	cervix:	n/a
28	chr12:4757728-4757778	AG04450	lung:	fetal
29	chr12:4755555-4755605	AoSMC	blood vessel:	n/a
30	chr12:4758496-4758546	AG09319	gingival:	n/a
31	chr12:4758496-4758546	HCF	heart:	n/a
32	chr12:4758272-4758322	HCPEpiC	choroid plexus:	n/a
33	chr12:4757717-4757767	NHDF-neo	bronchial:	n/a
34	chr12:4755479-4755529	GM12878	blood:	n/a
35	chr12:4755555-4755605	AG09309	skin:	n/a
36	chr12:4758424-4758474	AG09309	skin:	n/a
37	chr12:4758217-4758267	NT2-D1	testis:	n/a
38	chr12:4757717-4757767	PrEC	prostate:	n/a
39	chr12:4758272-4758322	HRPEpiC	eye:	n/a
40	chr12:4758272-4758322	H1-hESC	embryonic stem cell:	embryo
41	chr12:4754247-4754297	GM19239	blood:	n/a
42	chr12:4755555-4755605	U87	brain:	n/a
43	chr12:4758201-4758251	HUVEC	blood vessel:	n/a
44	chr12:4762206-4762256	HCPEpiC	choroid plexus:	n/a
45	chr12:4758272-4758322	NT2-D1	testis:	n/a
46	chr12:4758424-4758474	SK-N-SH_RA	brain:	n/a
47	chr12:4758272-4758322	AG04449	skin:	fetal
48	chr12:4758496-4758546	SK-N-MC	brain:	n/a
49	chr12:4758424-4758474	HepG2	liver:	n/a
50	chr12:4758250-4758300	GM06990	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
2	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
3	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
4	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
5	chr12:4757989..4759732-chr12:4759874..4761785,2	MCF-7	breast:
6	chr12:4758381..4761405-chr12:4778974..4782071,3	K562	blood:
7	chr12:4757537..4758351-chr2:9983167..9983703,2	Hela-S3	cervix:
8	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
9	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
10	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
11	chr12:4758240..4760595-chr12:4768074..4769785,2	K562	blood:
12	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
13	chr12:4744167..4745708-chr12:4746619..4748785,2	K562	blood:
14	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
15	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
16	chr12:4743724..4745923-chr12:4752293..4755038,2	K562	blood:
17	chr12:4743724..4745923-chr12:4752293..4755038,2	K562	blood:
18	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
19	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
20	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
21	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
22	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
23	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKAP3-3	chr12:4757911-4758213	NONHSAT025967
2	lnc-AKAP3-3	chr12:4751152-4751170	NONHSAT025968
3	lnc-AKAP3-3	chr12:4754221-4754358	NONHSAT025967
4	lnc-RP11-234B24.6.1-1	chr12:4754662-4755041	ENSG00000256381
5	lnc-AKAP3-3	chr12:4756240-4758165	NONHSAT025970
6	lnc-AKAP3-3	chr12:4751065-4751170	NONHSAT025967
7	lnc-AKAP3-3	chr12:4757620-4758174	NONHSAT025968
8	lnc-RP11-234B24.6.1-1	chr12:4757002-4757193	ENSG00000256381

No data

Variant related genes	Relation type
NDUFA9	TF binding region
ENSG00000256799	TF binding region
ENSG00000255639	TF binding region
ENSG00000256381	TF binding region
AKAP3	TF binding region
NDUFA9	CpG island
ENSG00000256799	CpG island
ENSG00000255639	CpG island
ENSG00000256381	CpG island
AKAP3	CpG island
ENSG00000111254	chromatin interactions
ENSG00000256799	chromatin interactions
ENSG00000115750	chromatin interactions
ENSG00000139180	chromatin interactions
ENSG00000256381	chromatin interactions
ENSG00000255639	chromatin interactions

Extended variants
information (count: 992 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2267546	chr12:4745313-4745314	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191247176	chr12:4745316-4745317	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs541029317	chr12:4745318-4745319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs561374495	chr12:4745388-4745389	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2267547	chr12:4745429-4745430	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs543645089	chr12:4745460-4745461	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563574650	chr12:4745469-4745470	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs532490203	chr12:4745470-4745471	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs139505443	chr12:4745493-4745494	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141124993	chr12:4745517-4745518	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368937938	chr12:4745541-4745542	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs80082834	chr12:4745555-4745556	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs556129647	chr12:4745595-4745596	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs75241150	chr12:4745619-4745620	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs561212467	chr12:4745677-4745678	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183115141	chr12:4745680-4745681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539001635	chr12:4745749-4745750	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs11610298	chr12:4745769-4745770	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs201727162	chr12:4745790-4745791	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs397737499	chr12:4745791-4745792	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs138732532	chr12:4745843-4745844	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569837265	chr12:4745845-4745846	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs538849900	chr12:4745875-4745876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs550626482	chr12:4745882-4745883	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188393867	chr12:4745883-4745884	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs193203292	chr12:4745889-4745890	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544027906	chr12:4745914-4745915	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569042026	chr12:4745915-4745916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs10774252	chr12:4745942-4745943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs149341314	chr12:4745994-4745995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544122601	chr12:4746002-4746003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11614450	chr12:4746014-4746015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs76393096	chr12:4746018-4746019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143647299	chr12:4746025-4746026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10774253	chr12:4746059-4746060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559376179	chr12:4746060-4746061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138416212	chr12:4746063-4746064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372466414	chr12:4746082-4746083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11608546	chr12:4746092-4746093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562149547	chr12:4746112-4746113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529927479	chr12:4746115-4746116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143910841	chr12:4746148-4746149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569973089	chr12:4746197-4746198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532296567	chr12:4746208-4746209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147309382	chr12:4746256-4746257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565627599	chr12:4746338-4746339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374138621	chr12:4746339-4746340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7137549	chr12:4746358-4746359	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs140873875	chr12:4746359-4746360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548306465	chr12:4746364-4746365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Epilepsy	21858020	CNVD
Colorectal cancer	19359472	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4724200-4756800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr12:4725400-4752200	Weak transcription	Brain Hippocampus Middle	brain
3	chr12:4737600-4757400	Weak transcription	Pancreas	Pancrea
4	chr12:4737800-4757200	Weak transcription	Brain Anterior Caudate	brain
5	chr12:4745400-4757200	Weak transcription	Brain Substantia Nigra	brain
6	chr12:4746600-4757000	Weak transcription	Small Intestine	intestine
7	chr12:4747200-4748200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:4747400-4748200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:4752800-4754000	Enhancers	GM12878-XiMat	blood
10	chr12:4754000-4754800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:4754000-4755000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:4754000-4756600	Weak transcription	GM12878-XiMat	blood
13	chr12:4754200-4754400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr12:4754200-4754600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr12:4754200-4754800	Weak transcription	Aorta	Aorta
16	chr12:4754400-4757200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr12:4754600-4754800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr12:4754600-4756800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr12:4754800-4755000	ZNF genes & repeats	Aorta	Aorta
20	chr12:4754800-4757200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:4755000-4757000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:4755000-4757400	Weak transcription	Aorta	Aorta
23	chr12:4756400-4757000	Enhancers	Dnd41	blood
24	chr12:4756400-4757600	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr12:4756600-4756800	Enhancers	GM12878-XiMat	blood
26	chr12:4756600-4757200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr12:4756800-4757000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:4756800-4757000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:4756800-4757000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:4756800-4757000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:4756800-4757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:4756800-4757000	Enhancers	Brain Angular Gyrus	brain
33	chr12:4756800-4757000	Enhancers	Duodenum Mucosa	Duodenum
34	chr12:4756800-4757000	Enhancers	Fetal Intestine Large	intestine
35	chr12:4756800-4757000	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr12:4756800-4757000	Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr12:4756800-4757000	Enhancers	HMEC	breast
38	chr12:4756800-4757000	Enhancers	NHEK	skin
39	chr12:4756800-4757200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr12:4756800-4757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:4756800-4757200	Enhancers	Primary B cells from cord blood	blood
42	chr12:4756800-4757200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr12:4756800-4757200	Enhancers	Fetal Intestine Small	intestine
44	chr12:4756800-4757200	Enhancers	Fetal Kidney	kidney
45	chr12:4756800-4757200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr12:4756800-4757200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr12:4756800-4757200	Enhancers	HepG2	liver
48	chr12:4756800-4757400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr12:4756800-4757400	Enhancers	Liver	Liver
50	chr12:4756800-4757400	Enhancers	Placenta Amnion	Placenta Amnion

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