Variant report

Variant	esv2422218
Chromosome Location	chr12:31218947-31268752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31226612-31226780	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31227278-31227505	K562	blood:	n/a	n/a
3	ARID3A	chr12:31227121-31227652	HepG2	liver:	n/a	n/a
4	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
5	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
6	ATF1	chr12:31219201-31219422	K562	blood:	n/a	n/a
7	ATF3	chr12:31226662-31226898	K562	blood:	n/a	n/a
8	BACH1	chr12:31226535-31226812	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:31228050-31228506	GM12878	blood:	n/a	chr12:31228339-31228347
10	BATF	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
11	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
12	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
13	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
14	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
16	BCL11A	chr12:31228135-31228506	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:31227413-31227974	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
18	BCL11A	chr12:31226719-31227117	GM12878	blood:	n/a	chr12:31226785-31226794 chr12:31227056-31227065
19	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:31227467-31227641	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
21	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
22	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31219222-31219531	K562	blood:	n/a	n/a
24	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
29	BHLHE40	chr12:31226599-31226889	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
31	BRCA1	chr12:31226630-31226830	GM12878	blood:	n/a	n/a
32	BRCA1	chr12:31226555-31227323	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr12:31224793-31225171	K562	blood:	n/a	n/a
34	CBX3	chr12:31226185-31227769	K562	blood:	n/a	n/a
35	CBX3	chr12:31219097-31219592	K562	blood:	n/a	n/a
36	CEBPB	chr12:31219220-31219425	K562	blood:	n/a	n/a
37	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr12:31226508-31227197	GM12878	blood:	n/a	chr12:31227015-31227027
41	CEBPB	chr12:31226603-31227301	Hela-S3	cervix:	n/a	chr12:31227015-31227027
42	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
43	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
44	CEBPB	chr12:31268138-31268370	H1-hESC	embryonic stem cell:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
45	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
46	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
47	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
48	CEBPD	chr12:31219231-31219589	K562	blood:	n/a	n/a
49	CEBPD	chr12:31226951-31227517	K562	blood:	n/a	n/a
50	CEBPD	chr12:31226472-31226934	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31230936-31230986	Caco-2	colon:	n/a
2	chr12:31256838-31256888	MCF-7	breast:	n/a
3	chr12:31226952-31227002	MCF10A-Er-Src	breast:	n/a
4	chr12:31226952-31227002	SK-N-SH_RA	brain:	n/a
5	chr12:31256838-31256888	BE2_C	brain:	n/a
6	chr12:31226718-31226768	ovcar-3	ovarian:	n/a
7	chr12:31230936-31230986	Caco-2	colon:	n/a
8	chr12:31256838-31256888	MCF-7	breast:	n/a
9	chr12:31226952-31227002	MCF10A-Er-Src	breast:	n/a
10	chr12:31226952-31227002	SK-N-SH_RA	brain:	n/a
11	chr12:31256838-31256888	BE2_C	brain:	n/a
12	chr12:31226718-31226768	ovcar-3	ovarian:	n/a
13	chr12:31233201-31233251	HMEC	breast:	n/a
14	chr12:31224413-31224463	GM12878	blood:	n/a
15	chr12:31257362-31257412	SK-N-MC	brain:	n/a
16	chr12:31241496-31241546	PFSK-1	brain:	n/a
17	chr12:31241496-31241546	IMR90	lung:	fetal
18	chr12:31224413-31224463	HepG2	liver:	n/a
19	chr12:31233201-31233251	HRE	kidney:	n/a
20	chr12:31226441-31226491	HEK293	kidney:	embryo
21	chr12:31226801-31226851	HRPEpiC	eye:	n/a
22	chr12:31257362-31257412	HCT-116	colon:	n/a
23	chr12:31226632-31226682	ECC-1	luminal epithelium:	n/a
24	chr12:31255279-31255329	HUVEC	blood vessel:	n/a
25	chr12:31230936-31230986	BJ	skin:	n/a
26	chr12:31226441-31226491	HCT-116	colon:	n/a
27	chr12:31256838-31256888	T-47D	breast:	n/a
28	chr12:31226714-31226764	GM12891	blood:	n/a
29	chr12:31226441-31226491	HCPEpiC	choroid plexus:	n/a
30	chr12:31226606-31226656	HUVEC	blood vessel:	n/a
31	chr12:31255279-31255329	Jurkat	blood:	n/a
32	chr12:31226714-31226764	K562	blood:	n/a
33	chr12:31226952-31227002	NHBE	bronchial:	n/a
34	chr12:31223310-31223360	K562	blood:	n/a
35	chr12:31230936-31230986	ProgFib	skin:	n/a
36	chr12:31226622-31226672	AG09319	gingival:	n/a
37	chr12:31223310-31223360	NT2-D1	testis:	n/a
38	chr12:31241496-31241546	AG10803	skin:	n/a
39	chr12:31254007-31254057	PFSK-1	brain:	n/a
40	chr12:31241496-31241546	HCPEpiC	choroid plexus:	n/a
41	chr12:31226718-31226768	NHBE	bronchial:	n/a
42	chr12:31226606-31226656	H1-hESC	embryonic stem cell:	embryo
43	chr12:31226441-31226491	HIPEpiC	eye:	n/a
44	chr12:31226952-31227002	HNPCEpiC	eye:	n/a
45	chr12:31226714-31226764	AG04450	lung:	fetal
46	chr12:31254007-31254057	Jurkat	blood:	n/a
47	chr12:31224413-31224463	GM12892	blood:	n/a
48	chr12:31227271-31227321	ECC-1	luminal epithelium:	n/a
49	chr12:31226801-31226851	GM12891	blood:	n/a
50	chr12:31226825-31226875	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:
2	chr12:31226738..31227630-chr20:47894738..47895520,2	Hela-S3	cervix:
3	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:
4	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
2	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
3	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000270926	CpG island
ENSG00000212533	CpG island
DDX11	CpG island
ENSG00000177410	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000111788	chromatin interactions

Extended variants
information (count: 2419 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2419 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556248174	chr12:31218974-31218975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370360678	chr12:31219025-31219026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578015009	chr12:31219043-31219044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545874571	chr12:31219051-31219052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554044379	chr12:31219088-31219089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572266424	chr12:31219150-31219151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4931416	chr12:31219161-31219162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs2543229	chr12:31219172-31219173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561049660	chr12:31219210-31219211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576022814	chr12:31219256-31219257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11051230	chr12:31219292-31219293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543429036	chr12:31219295-31219296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564518705	chr12:31219316-31219317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533482063	chr12:31219338-31219339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551651599	chr12:31219385-31219386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2543231	chr12:31219415-31219416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560357680	chr12:31219437-31219438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527887364	chr12:31219583-31219584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549267805	chr12:31219632-31219633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567762488	chr12:31219665-31219666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537922685	chr12:31219745-31219746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537851037	chr12:31219823-31219824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550226277	chr12:31219832-31219833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571651755	chr12:31219882-31219883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113576670	chr12:31219899-31219900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs61917180	chr12:31219953-31219954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182799046	chr12:31219995-31219996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554111544	chr12:31220016-31220017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2543233	chr12:31220030-31220031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572207390	chr12:31220036-31220037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs397833711	chr12:31220052-31220053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536463529	chr12:31220055-31220056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187891833	chr12:31220077-31220078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2543235	chr12:31220081-31220082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61917181	chr12:31220095-31220096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543138372	chr12:31220149-31220150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192806994	chr12:31220173-31220174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371164969	chr12:31220174-31220175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184308555	chr12:31220206-31220207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576430780	chr12:31220223-31220224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs67285601	chr12:31220246-31220247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189074233	chr12:31220346-31220347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560420817	chr12:31220364-31220365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527943465	chr12:31220365-31220366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376180691	chr12:31220419-31220420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2543236	chr12:31220466-31220467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116991395	chr12:31220487-31220488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370885520	chr12:31220499-31220500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112049169	chr12:31220501-31220502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs2543237	chr12:31220505-31220506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1350 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31189800-31225400	Weak transcription	Fetal Stomach	stomach
2	chr12:31202200-31219400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:31210800-31225200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:31217600-31219200	Weak transcription	K562	blood
5	chr12:31219200-31219600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:31219200-31220000	Enhancers	K562	blood
7	chr12:31219600-31225600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:31220400-31221000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:31220400-31221200	Enhancers	HMEC	breast
10	chr12:31220400-31221200	Enhancers	NHEK	skin
11	chr12:31220800-31221400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:31220800-31221600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr12:31221000-31225600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:31221200-31225400	Weak transcription	HMEC	breast
15	chr12:31221200-31225600	Weak transcription	NHEK	skin
16	chr12:31221400-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr12:31221600-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr12:31225000-31225200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:31225000-31225200	Enhancers	Dnd41	blood
20	chr12:31225200-31225400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr12:31225200-31225400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:31225200-31225400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:31225200-31225400	Active TSS	Fetal Thymus	thymus
24	chr12:31225200-31225400	Active TSS	Hela-S3	cervix
25	chr12:31225200-31225600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr12:31225200-31225600	Enhancers	HepG2	liver
27	chr12:31225200-31225600	Enhancers	K562	blood
28	chr12:31225200-31225800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:31225200-31226200	Flanking Active TSS	Dnd41	blood
30	chr12:31225200-31228000	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr12:31225200-31228400	Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr12:31225200-31228600	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr12:31225400-31225600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:31225400-31225600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:31225400-31225600	Active TSS	iPS-15b Cell Line	embryonic stem cell
36	chr12:31225400-31225600	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr12:31225400-31225600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr12:31225400-31225600	Flanking Active TSS	Brain Germinal Matrix	brain
39	chr12:31225400-31225600	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr12:31225400-31225600	Flanking Active TSS	Fetal Thymus	thymus
41	chr12:31225400-31225600	Enhancers	Pancreas	Pancrea
42	chr12:31225400-31225600	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr12:31225400-31225800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
44	chr12:31225400-31225800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr12:31225400-31225800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr12:31225400-31225800	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr12:31225400-31225800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:31225400-31225800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:31225400-31225800	Flanking Active TSS	GM12878-XiMat	blood
50	chr12:31225400-31225800	Flanking Active TSS	HMEC	breast

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