Variant report

Variant	nsv557125
Chromosome Location	chr12:4748410-4764137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:795)
Chromatin interactive
region (count:18)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 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	chr12:4757999-4758491	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:4757972-4758620	GM12878	blood:	n/a	n/a
4	ATF2	chr12:4758070-4758634	GM12878	blood:	n/a	n/a
5	BCLAF1	chr12:4757913-4758630	GM12878	blood:	n/a	chr12:4758114-4758123
6	BCLAF1	chr12:4757941-4758505	GM12878	blood:	n/a	chr12:4758114-4758123
7	BHLHE40	chr12:4758013-4758504	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:4757362-4757603	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:4757761-4758471	K562	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	chr12:4759955-4760222	HepG2	liver:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
13	CEBPB	chr12:4757830-4757894	K562	blood:	n/a	n/a
14	CEBPB	chr12:4758026-4758412	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:4760017-4760288	K562	blood:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
16	CEBPB	chr12:4751163-4751331	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:4759436-4759663	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:4751161-4751189	K562	blood:	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	chr12:4758021-4758466	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr12:4758078-4758446	GM12878	blood:	n/a	n/a
23	CHD2	chr12:4757737-4757887	K562	blood:	n/a	n/a
24	CHD2	chr12:4757626-4758623	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr12:4758193-4758446	HepG2	liver:	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	chr12:4762380-4762530	Caco-2	colon:	n/a	n/a
31	CTCF	chr12:4757748-4757758	K562	blood:	n/a	n/a
32	CTCF	chr12:4762380-4762530	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr12:4750293-4750337	Fibrobl	skin:	n/a	n/a
34	CTCF	chr12:4762360-4762510	AG04450	lung:	n/a	n/a
35	CTCF	chr12:4758740-4758890	Caco-2	colon:	n/a	n/a
36	CTCF	chr12:4762400-4762550	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr12:4762460-4762610	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr12:4762420-4762570	HVMF	connective:	n/a	n/a
39	CTCF	chr12:4757980-4758130	NHLF	lung:	n/a	n/a
40	CTCF	chr12:4758165-4758206	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr12:4758195-4758285	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr12:4762460-4762610	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr12:4757660-4757810	A549	lung:	n/a	n/a
44	CTCF	chr12:4762420-4762570	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr12:4762380-4762530	HMEC	breast:	n/a	n/a
46	CTCF	chr12:4762440-4762590	AG04449	skin:	n/a	n/a
47	CTCF	chr12:4758079-4758321	K562	blood:	n/a	n/a
48	CTCF	chr12:4762500-4762650	HEK293	kidney:	n/a	n/a
49	CTCF	chr12:4757436-4757457	GM10266	blood:	n/a	n/a
50	CTCF	chr12:4762460-4762610	RPTEC	kidney:	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	chr12:4757728-4757778	LNCaP	prostate:	n/a
2	chr12:4758496-4758546	HNPCEpiC	eye:	n/a
3	chr12:4757728-4757778	LNCaP	prostate:	n/a
4	chr12:4758496-4758546	HNPCEpiC	eye:	n/a
5	chr12:4757759-4757809	AG10803	skin:	n/a
6	chr12:4758272-4758322	HL-60	blood:	n/a
7	chr12:4762206-4762256	GM19239	blood:	n/a
8	chr12:4758424-4758474	MCF-7	breast:	n/a
9	chr12:4758250-4758300	K562	blood:	n/a
10	chr12:4755479-4755529	HL-60	blood:	n/a
11	chr12:4758201-4758251	PFSK-1	brain:	n/a
12	chr12:4758217-4758267	NT2-D1	testis:	n/a
13	chr12:4757728-4757778	SK-N-SH_RA	brain:	n/a
14	chr12:4758424-4758474	ECC-1	luminal epithelium:	n/a
15	chr12:4755555-4755605	SK-N-MC	brain:	n/a
16	chr12:4757759-4757809	HIPEpiC	eye:	n/a
17	chr12:4754247-4754297	SK-N-MC	brain:	n/a
18	chr12:4758201-4758251	NT2-D1	testis:	n/a
19	chr12:4758496-4758546	ProgFib	skin:	n/a
20	chr12:4762206-4762256	SK-N-SH_RA	brain:	n/a
21	chr12:4758496-4758546	T-47D	breast:	n/a
22	chr12:4758250-4758300	HEEpiC	esophagus:	n/a
23	chr12:4754247-4754297	NH-A	brain:	n/a
24	chr12:4758272-4758322	LNCaP	prostate:	n/a
25	chr12:4758272-4758322	HCPEpiC	choroid plexus:	n/a
26	chr12:4754247-4754297	GM19239	blood:	n/a
27	chr12:4762206-4762256	CMK	blood:	n/a
28	chr12:4754247-4754297	BE2_C	brain:	n/a
29	chr12:4758250-4758300	MCF-7	breast:	n/a
30	chr12:4758201-4758251	ovcar-3	ovarian:	n/a
31	chr12:4757728-4757778	NB4	blood:	n/a
32	chr12:4757728-4757778	HepG2	liver:	n/a
33	chr12:4758217-4758267	Hepatocyte	liver:	n/a
34	chr12:4754247-4754297	NHBE	bronchial:	n/a
35	chr12:4755479-4755529	Hela-S3	cervix:	n/a
36	chr12:4758201-4758251	Caco-2	colon:	n/a
37	chr12:4758272-4758322	NB4	blood:	n/a
38	chr12:4757728-4757778	PANC-1	pancreas:	n/a
39	chr12:4758272-4758322	NHBE	bronchial:	n/a
40	chr12:4754247-4754297	SKMC	muscle:	n/a
41	chr12:4758217-4758267	HEK293	kidney:	embryo
42	chr12:4757717-4757767	Caco-2	colon:	n/a
43	chr12:4762206-4762256	HAEpiC	amniotic membrane:	n/a
44	chr12:4755479-4755529	HRPEpiC	eye:	n/a
45	chr12:4754247-4754297	AG10803	skin:	n/a
46	chr12:4757759-4757809	SK-N-MC	brain:	n/a
47	chr12:4757728-4757778	GM12892	blood:	n/a
48	chr12:4754247-4754297	HUVEC	blood vessel:	n/a
49	chr12:4755479-4755529	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:4758424-4758474	HL-60	blood:	n/a

(count:18 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-234B24.6.1-1	chr12:4757002-4757193	ENSG00000256381
2	lnc-AKAP3-3	chr12:4757620-4758174	NONHSAT025968
3	lnc-AKAP3-3	chr12:4756240-4758165	NONHSAT025970
4	lnc-AKAP3-3	chr12:4757911-4758213	NONHSAT025967
5	lnc-AKAP3-3	chr12:4751152-4751170	NONHSAT025968
6	lnc-AKAP3-3	chr12:4754221-4754358	NONHSAT025967
7	lnc-AKAP3-3	chr12:4751065-4751170	NONHSAT025967
8	lnc-RP11-234B24.6.1-1	chr12:4754662-4755041	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
ENSG00000256381	chromatin interactions
ENSG00000139180	chromatin interactions
ENSG00000115750	chromatin interactions
ENSG00000256799	chromatin interactions
ENSG00000111254	chromatin interactions
ENSG00000255639	chromatin interactions

Extended variants
information (count: 569 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10849112	chr12:4748410-4748411	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573094218	chr12:4748456-4748457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77630338	chr12:4748464-4748465	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115556683	chr12:4748474-4748475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530503526	chr12:4748521-4748522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369195885	chr12:4748530-4748531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370469514	chr12:4748537-4748538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12301141	chr12:4748545-4748546	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs200312740	chr12:4748557-4748558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568439676	chr12:4748573-4748574	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532728817	chr12:4748577-4748578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs77695170	chr12:4748666-4748667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112267822	chr12:4748674-4748675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143193445	chr12:4748677-4748678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185063515	chr12:4748726-4748727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529589960	chr12:4748731-4748732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549540129	chr12:4748747-4748748	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374447241	chr12:4748749-4748750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11063277	chr12:4748767-4748768	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs372266367	chr12:4748790-4748791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538463196	chr12:4748824-4748825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570287647	chr12:4748981-4748982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34820221	chr12:4748999-4749000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs59421885	chr12:4749013-4749014	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs189529646	chr12:4749015-4749016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534188098	chr12:4749064-4749065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182115816	chr12:4749068-4749069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560135012	chr12:4749084-4749085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185782135	chr12:4749102-4749103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181530392	chr12:4749112-4749113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368337210	chr12:4749139-4749140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10849113	chr12:4749140-4749141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs558609943	chr12:4749192-4749193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569197114	chr12:4749203-4749204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544014126	chr12:4749211-4749212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570430129	chr12:4749217-4749218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189409233	chr12:4749218-4749219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113786264	chr12:4749228-4749229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540205224	chr12:4749234-4749235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143918078	chr12:4749248-4749249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146501887	chr12:4749250-4749251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549384186	chr12:4749272-4749273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569575139	chr12:4749288-4749289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs61911370	chr12:4749313-4749314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs552043899	chr12:4749367-4749368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541413689	chr12:4749371-4749372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79986742	chr12:4749375-4749376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115035812	chr12:4749378-4749379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554119125	chr12:4749394-4749395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371633699	chr12:4749395-4749396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Breast cancer	21364760	CNVD

Chromatin state (count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr12:4752800-4754000	Enhancers	GM12878-XiMat	blood
8	chr12:4754000-4754800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:4754000-4755000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:4754000-4756600	Weak transcription	GM12878-XiMat	blood
11	chr12:4754200-4754400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr12:4754200-4754600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:4754200-4754800	Weak transcription	Aorta	Aorta
14	chr12:4754400-4757200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:4754600-4754800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:4754600-4756800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:4754800-4755000	ZNF genes & repeats	Aorta	Aorta
18	chr12:4754800-4757200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:4755000-4757000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:4755000-4757400	Weak transcription	Aorta	Aorta
21	chr12:4756400-4757000	Enhancers	Dnd41	blood
22	chr12:4756400-4757600	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr12:4756600-4756800	Enhancers	GM12878-XiMat	blood
24	chr12:4756600-4757200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr12:4756800-4757000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:4756800-4757000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:4756800-4757000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:4756800-4757000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:4756800-4757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:4756800-4757000	Enhancers	Brain Angular Gyrus	brain
31	chr12:4756800-4757000	Enhancers	Duodenum Mucosa	Duodenum
32	chr12:4756800-4757000	Enhancers	Fetal Intestine Large	intestine
33	chr12:4756800-4757000	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr12:4756800-4757000	Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr12:4756800-4757000	Enhancers	HMEC	breast
36	chr12:4756800-4757000	Enhancers	NHEK	skin
37	chr12:4756800-4757200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr12:4756800-4757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:4756800-4757200	Enhancers	Primary B cells from cord blood	blood
40	chr12:4756800-4757200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr12:4756800-4757200	Enhancers	Fetal Intestine Small	intestine
42	chr12:4756800-4757200	Enhancers	Fetal Kidney	kidney
43	chr12:4756800-4757200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr12:4756800-4757200	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr12:4756800-4757200	Enhancers	HepG2	liver
46	chr12:4756800-4757400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr12:4756800-4757400	Enhancers	Liver	Liver
48	chr12:4756800-4757400	Enhancers	Placenta Amnion	Placenta Amnion
49	chr12:4756800-4757400	Enhancers	Stomach Mucosa	stomach
50	chr12:4756800-4757400	Enhancers	Thymus	Thymus

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