Variant report

Variant	esv3399914
Chromosome Location	chr12:106695772-106696870
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:501)
CpG islands
(count:551)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:106696316-106696541	K562	blood:	n/a	n/a
2	ARID3A	chr12:106696326-106697314	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:106695587-106695892	K562	blood:	n/a	n/a
4	ATF1	chr12:106695456-106695952	K562	blood:	n/a	n/a
5	ATF3	chr12:106695512-106695916	K562	blood:	n/a	n/a
6	BACH1	chr12:106695484-106696089	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:106696326-106697437	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:106695656-106696052	K562	blood:	n/a	n/a
9	BCL3	chr12:106695373-106695811	K562	blood:	n/a	n/a
10	BCL3	chr12:106696167-106696916	A549	lung:	n/a	n/a
11	BCLAF1	chr12:106695503-106695990	K562	blood:	n/a	chr12:106695847-106695856
12	BHLHE40	chr12:106695347-106697430	K562	blood:	n/a	chr12:106696295-106696311 chr12:106695968-106695984
13	BHLHE40	chr12:106695590-106695939	A549	lung:	n/a	n/a
14	BHLHE40	chr12:106695200-106697453	GM12878	blood:	n/a	chr12:106696295-106696311 chr12:106695968-106695984
15	BHLHE40	chr12:106696230-106696604	A549	lung:	n/a	chr12:106696295-106696311
16	BHLHE40	chr12:106695562-106697456	HepG2	liver:	n/a	chr12:106696295-106696311 chr12:106695968-106695984
17	BRCA1	chr12:106696281-106696591	GM12878	blood:	n/a	n/a
18	BRCA1	chr12:106696320-106696870	HepG2	liver:	n/a	n/a
19	BRCA1	chr12:106696275-106696751	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr12:106696262-106696658	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr12:106695450-106695963	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr12:106695314-106696047	K562	blood:	n/a	n/a
23	CBX3	chr12:106695509-106695957	K562	blood:	n/a	n/a
24	CCNT2	chr12:106695379-106697332	K562	blood:	n/a	chr12:106696293-106696302 chr12:106696230-106696239 chr12:106696811-106696831 chr12:106695692-106695712 chr12:106697247-106697256 chr12:106696589-106696598 chr12:106697201-106697210
25	CEBPB	chr12:106695382-106695980	K562	blood:	n/a	n/a
26	CEBPB	chr12:106695805-106695925	A549	lung:	n/a	n/a
27	CEBPB	chr12:106695317-106695969	K562	blood:	n/a	n/a
28	CEBPD	chr12:106696170-106696707	HepG2	liver:	n/a	n/a
29	CEBPD	chr12:106695448-106696001	K562	blood:	n/a	n/a
30	CEBPD	chr12:106695401-106696095	K562	blood:	n/a	n/a
31	CHD1	chr12:106695382-106697216	GM12878	blood:	n/a	chr12:106696734-106696744 chr12:106696291-106696301
32	CHD1	chr12:106696212-106697917	IMR90	lung:	n/a	chr12:106696734-106696744 chr12:106696291-106696301
33	CHD1	chr12:106696222-106696950	H1-hESC	embryonic stem cell:	n/a	chr12:106696734-106696744 chr12:106696291-106696301
34	CHD2	chr12:106695380-106697419	Hela-S3	cervix:	n/a	chr12:106696734-106696744 chr12:106696291-106696301
35	CHD2	chr12:106695369-106697498	GM12878	blood:	n/a	chr12:106696734-106696744 chr12:106696291-106696301
36	CHD2	chr12:106696285-106697405	HepG2	liver:	n/a	chr12:106696734-106696744 chr12:106696291-106696301
37	CHD2	chr12:106696269-106696547	K562	blood:	n/a	chr12:106696291-106696301
38	CHD2	chr12:106695453-106695937	K562	blood:	n/a	n/a
39	CREB1	chr12:106695402-106696097	K562	blood:	n/a	n/a
40	CREB1	chr12:106696093-106697496	HepG2	liver:	n/a	n/a
41	CREB1	chr12:106695374-106696110	K562	blood:	n/a	n/a
42	CREB1	chr12:106696066-106696772	GM12878	blood:	n/a	n/a
43	CREB1	chr12:106696163-106696743	A549	lung:	n/a	n/a
44	CTCF	chr12:106695584-106695843	K562	blood:	n/a	n/a
45	CTCF	chr12:106695640-106695790	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr12:106695640-106695790	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:106696860-106697090	GM12870	blood:	n/a	n/a
48	CTCF	chr12:106696381-106696522	GM12878	blood:	n/a	n/a
49	CTCF	chr12:106695700-106695850	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr12:106695700-106695850	HEK293	kidney:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:106695932-106695982	SK-N-SH	brain:	n/a
2	chr12:106696525-106696575	NT2-D1	testis:	n/a
3	chr12:106695932-106695982	SK-N-SH	brain:	n/a
4	chr12:106696525-106696575	NT2-D1	testis:	n/a
5	chr12:106696673-106696723	CMK	blood:	n/a
6	chr12:106695932-106695982	BJ	skin:	n/a
7	chr12:106696452-106696502	SK-N-SH_RA	brain:	n/a
8	chr12:106696452-106696502	HepG2	liver:	n/a
9	chr12:106695998-106696048	RPTEC	kidney:	n/a
10	chr12:106695932-106695982	T-47D	breast:	n/a
11	chr12:106695932-106695982	GM19239	blood:	n/a
12	chr12:106696452-106696502	NHDF-neo	bronchial:	n/a
13	chr12:106696384-106696434	NHBE	bronchial:	n/a
14	chr12:106696452-106696502	GM19239	blood:	n/a
15	chr12:106696384-106696434	Hepatocyte	liver:	n/a
16	chr12:106696527-106696577	PrEC	prostate:	n/a
17	chr12:106696525-106696575	HAEpiC	amniotic membrane:	n/a
18	chr12:106696384-106696434	GM12892	blood:	n/a
19	chr12:106696673-106696723	ECC-1	luminal epithelium:	n/a
20	chr12:106696452-106696502	SK-N-SH	brain:	n/a
21	chr12:106696255-106696305	RPTEC	kidney:	n/a
22	chr12:106696527-106696577	LNCaP	prostate:	n/a
23	chr12:106696384-106696434	PANC-1	pancreas:	n/a
24	chr12:106696384-106696434	MCF10A-Er-Src	breast:	n/a
25	chr12:106696384-106696434	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:106696255-106696305	GM12892	blood:	n/a
27	chr12:106696673-106696723	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:106695932-106695982	RPTEC	kidney:	n/a
29	chr12:106696673-106696723	MCF-7	breast:	n/a
30	chr12:106696527-106696577	PFSK-1	brain:	n/a
31	chr12:106696525-106696575	SKMC	muscle:	n/a
32	chr12:106696527-106696577	HEK293	kidney:	embryo
33	chr12:106695932-106695982	PrEC	prostate:	n/a
34	chr12:106696527-106696577	GM06990	blood:	n/a
35	chr12:106696452-106696502	ECC-1	luminal epithelium:	n/a
36	chr12:106696452-106696502	HCF	heart:	n/a
37	chr12:106695984-106696034	SKMC	muscle:	n/a
38	chr12:106696673-106696723	HepG2	liver:	n/a
39	chr12:106696527-106696577	HCPEpiC	choroid plexus:	n/a
40	chr12:106695984-106696034	AG10803	skin:	n/a
41	chr12:106696525-106696575	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:106695984-106696034	RPTEC	kidney:	n/a
43	chr12:106696384-106696434	Caco-2	colon:	n/a
44	chr12:106696673-106696723	BJ	skin:	n/a
45	chr12:106696452-106696502	AG04449	skin:	fetal
46	chr12:106695984-106696034	Caco-2	colon:	n/a
47	chr12:106695984-106696034	HAEpiC	amniotic membrane:	n/a
48	chr12:106696525-106696575	HUVEC	blood vessel:	n/a
49	chr12:106696255-106696305	BE2_C	brain:	n/a
50	chr12:106696527-106696577	HCF	heart:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:106695715..106698780-chr12:106751795..106753760,4	K562	blood:
2	chr12:106640063..106644049-chr12:106694395..106698756,11	MCF-7	breast:
3	chr12:106694726..106698780-chr12:106749876..106753760,9	K562	blood:
4	chr12:106693946..106698218-chr12:106750404..106754111,7	MCF-7	breast:
5	chr12:106693434..106696954-chr12:106697519..106701215,4	MCF-7	breast:
6	chr12:106639346..106644112-chr12:106694122..106698214,13	MCF-7	breast:

No data

Variant related genes	Relation type
TCP11L2	TF binding region
TCP11L2	CpG island
ENSG00000166046	chromatin interactions
ENSG00000258355	chromatin interactions
ENSG00000013503	chromatin interactions
ENSG00000136026	chromatin interactions

Extended variants
information (count: 44 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539775995	chr12:106695865-106695866	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs538226384	chr12:106695908-106695909	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs532901694	chr12:106695986-106695987	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs576048528	chr12:106696017-106696018	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs369293756	chr12:106696047-106696048	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs555448486	chr12:106696082-106696083	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs532038025	chr12:106696090-106696091	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs199615546	chr12:106696098-106696099	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs559059036	chr12:106696110-106696111	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs71072666	chr12:106696111-106696112	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs572487257	chr12:106696112-106696113	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs533071776	chr12:106696119-106696120	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs544886455	chr12:106696181-106696182	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs34553566	chr12:106696182-106696183	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs563170657	chr12:106696184-106696185	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs530616491	chr12:106696185-106696186	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs541511271	chr12:106696193-106696194	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs564161291	chr12:106696194-106696195	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs533115952	chr12:106696196-106696197	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs543762815	chr12:106696197-106696198	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs114307783	chr12:106696414-106696415	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs11112933	chr12:106696453-106696454	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549041876	chr12:106696465-106696466	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs373389531	chr12:106696469-106696470	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs565679542	chr12:106696512-106696513	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs10861574	chr12:106696557-106696558	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs34652259	chr12:106696576-106696577	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs201647351	chr12:106696578-106696579	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs570970256	chr12:106696579-106696580	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs539993237	chr12:106696582-106696583	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs71311256	chr12:106696584-106696585	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs11831752	chr12:106696586-106696587	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs569972527	chr12:106696600-106696601	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs535737498	chr12:106696611-106696612	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs555388743	chr12:106696635-106696636	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs572389943	chr12:106696640-106696641	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs534823393	chr12:106696647-106696648	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs77370280	chr12:106696684-106696685	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs534090144	chr12:106696703-106696704	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs116277781	chr12:106696708-106696709	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs77680762	chr12:106696750-106696751	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs563464975	chr12:106696773-106696774	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs116673010	chr12:106696838-106696839	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs542925056	chr12:106696842-106696843	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106689000-106695800	Weak transcription	Lung	lung
2	chr12:106693400-106695800	Weak transcription	Gastric	stomach
3	chr12:106693400-106695800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr12:106694400-106695800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:106694600-106695800	Enhancers	Fetal Heart	heart
6	chr12:106694600-106696000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
7	chr12:106694800-106695800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
8	chr12:106695000-106695800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
9	chr12:106695000-106696000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:106695000-106696000	Flanking Active TSS	Hela-S3	cervix
11	chr12:106695200-106695800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:106695200-106695800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
13	chr12:106695200-106695800	Flanking Active TSS	Rectal Smooth Muscle	rectum
14	chr12:106695200-106695800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr12:106695200-106696000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr12:106695200-106696000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr12:106695200-106696000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr12:106695200-106696000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:106695200-106696000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr12:106695200-106696000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr12:106695200-106696000	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr12:106695200-106696000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr12:106695200-106696000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:106695200-106696000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:106695200-106696000	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr12:106695200-106696000	Flanking Active TSS	Brain Cingulate Gyrus	brain
27	chr12:106695200-106696000	Flanking Active TSS	Duodenum Mucosa	Duodenum
28	chr12:106695200-106696000	Flanking Active TSS	Stomach Mucosa	stomach
29	chr12:106695200-106696000	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr12:106695200-106696000	Flanking Active TSS	GM12878-XiMat	blood
31	chr12:106695200-106696000	Flanking Active TSS	HSMMtube	muscle
32	chr12:106695200-106696000	Flanking Active TSS	NHDF-Ad	bronchial
33	chr12:106695200-106696000	Flanking Active TSS	Osteobl	bone
34	chr12:106695200-106697600	Active TSS	Esophagus	oesophagus
35	chr12:106695400-106695800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:106695400-106695800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr12:106695400-106695800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr12:106695400-106695800	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr12:106695400-106695800	Flanking Active TSS	Primary T cells from cord blood	blood
40	chr12:106695400-106695800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr12:106695400-106695800	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr12:106695400-106695800	Flanking Active TSS	Brain Substantia Nigra	brain
43	chr12:106695400-106695800	Flanking Active TSS	Colon Smooth Muscle	Colon
44	chr12:106695400-106695800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr12:106695400-106695800	Flanking Active TSS	Fetal Brain Female	brain
46	chr12:106695400-106695800	Active TSS	HepG2	liver
47	chr12:106695400-106696000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
48	chr12:106695400-106696000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
49	chr12:106695400-106696000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
50	chr12:106695400-106696000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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