Variant report

Variant	nsv899130
Chromosome Location	chr12:59895548-59970631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:114)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:114 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr12:59928231-59928552	GM12878	blood:	n/a	n/a
2	BCL3	chr12:59928674-59929037	GM12878	blood:	n/a	n/a
3	BCL3	chr12:59928657-59928995	GM12878	blood:	n/a	n/a
4	BRCA1	chr12:59964033-59964223	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr12:59940309-59940328	GM12878	blood:	n/a	n/a
6	CEBPB	chr12:59928811-59928850	A549	lung:	n/a	n/a
7	CEBPB	chr12:59953596-59953714	HepG2	liver:	n/a	chr12:59953660-59953671
8	CEBPB	chr12:59948816-59949027	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr12:59964032-59964226	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:59902238-59902539	HepG2	liver:	n/a	chr12:59902391-59902402
11	CEBPB	chr12:59902264-59902475	H1-hESC	embryonic stem cell:	n/a	chr12:59902391-59902402
12	CEBPB	chr12:59963959-59964357	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr12:59964027-59964339	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr12:59912346-59912416	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr12:59896880-59897030	HFF-Myc	foreskin:	n/a	n/a
16	CTCF	chr12:59912300-59912450	GM12864	blood:	n/a	n/a
17	CTCF	chr12:59912340-59912490	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:59923861-59923887	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr12:59904302-59904358	GM13976	blood:	n/a	n/a
20	E2F4	chr12:59963992-59964192	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr12:59920453-59920597	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr12:59901335-59901530	MCF10A-Er-Src	breast:	n/a	n/a
23	EBF1	chr12:59905442-59905671	GM12878	blood:	n/a	n/a
24	EP300	chr12:59963997-59964350	Hela-S3	cervix:	n/a	n/a
25	FOS	chr12:59913042-59913232	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr12:59963884-59964376	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr12:59963890-59964369	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr12:59912932-59913159	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr12:59963897-59964370	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr12:59913043-59913202	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr12:59963892-59964366	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr12:59913014-59913214	MCF10A-Er-Src	breast:	n/a	n/a
33	FOXA1	chr12:59942809-59943016	T-47D	breast:	n/a	n/a
34	FOXA1	chr12:59942803-59943136	HepG2	liver:	n/a	n/a
35	GATA3	chr12:59968181-59968638	MCF-7	breast:	n/a	n/a
36	GTF2F1	chr12:59964063-59964326	Hela-S3	cervix:	n/a	n/a
37	IRF1	chr12:59908010-59908036	K562	blood:	n/a	n/a
38	IRF1	chr12:59922062-59922098	K562	blood:	n/a	n/a
39	JUN	chr12:59963957-59964336	Hela-S3	cervix:	n/a	n/a
40	JUND	chr12:59963936-59964372	Hela-S3	cervix:	n/a	n/a
41	MAFF	chr12:59899476-59899676	HepG2	liver:	n/a	chr12:59899535-59899553
42	MAFF	chr12:59959051-59959148	HepG2	liver:	n/a	n/a
43	MAFF	chr12:59899372-59899615	K562	blood:	n/a	chr12:59899535-59899553
44	MAFK	chr12:59961468-59961610	HepG2	liver:	n/a	n/a
45	MAFK	chr12:59899406-59899688	HepG2	liver:	n/a	chr12:59899536-59899551
46	MAFK	chr12:59959043-59959092	HepG2	liver:	n/a	n/a
47	MAFK	chr12:59961362-59961658	HepG2	liver:	n/a	n/a
48	MAFK	chr12:59899395-59899701	HepG2	liver:	n/a	chr12:59899536-59899551
49	MAFK	chr12:59961435-59961635	IMR90	lung:	n/a	n/a
50	MAFK	chr12:59899461-59899667	IMR90	lung:	n/a	chr12:59899536-59899551

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:59924853-59924903	HL-60	blood:	n/a
2	chr12:59924853-59924903	HL-60	blood:	n/a
3	chr12:59924853-59924903	GM12891	blood:	n/a
4	chr12:59925323-59925373	HEEpiC	esophagus:	n/a
5	chr12:59925323-59925373	SK-N-SH	brain:	n/a
6	chr12:59925037-59925087	HAEpiC	amniotic membrane:	n/a
7	chr12:59925323-59925373	NH-A	brain:	n/a
8	chr12:59925323-59925373	BE2_C	brain:	n/a
9	chr12:59924853-59924903	GM19239	blood:	n/a
10	chr12:59925037-59925087	CMK	blood:	n/a
11	chr12:59925037-59925087	HepG2	liver:	n/a
12	chr12:59925323-59925373	AG04450	lung:	fetal
13	chr12:59925037-59925087	AG10803	skin:	n/a
14	chr12:59925037-59925087	MCF10A-Er-Src	breast:	n/a
15	chr12:59925037-59925087	Hepatocyte	liver:	n/a
16	chr12:59925037-59925087	GM12892	blood:	n/a
17	chr12:59924853-59924903	AG09309	skin:	n/a
18	chr12:59925037-59925087	PrEC	prostate:	n/a
19	chr12:59924853-59924903	NH-A	brain:	n/a
20	chr12:59925037-59925087	NHBE	bronchial:	n/a
21	chr12:59924853-59924903	AG04449	skin:	fetal
22	chr12:59925323-59925373	HRPEpiC	eye:	n/a
23	chr12:59924853-59924903	NHBE	bronchial:	n/a
24	chr12:59925323-59925373	GM12892	blood:	n/a
25	chr12:59925037-59925087	T-47D	breast:	n/a
26	chr12:59924853-59924903	HNPCEpiC	eye:	n/a
27	chr12:59924853-59924903	RPTEC	kidney:	n/a
28	chr12:59925323-59925373	HRCEpiC	kidney:	n/a
29	chr12:59925037-59925087	HMEC	breast:	n/a
30	chr12:59925037-59925087	NH-A	brain:	n/a
31	chr12:59925323-59925373	H1-hESC	embryonic stem cell:	embryo
32	chr12:59925037-59925087	LNCaP	prostate:	n/a
33	chr12:59925037-59925087	HEK293	kidney:	embryo
34	chr12:59925037-59925087	U87	brain:	n/a
35	chr12:59924853-59924903	PrEC	prostate:	n/a
36	chr12:59924853-59924903	HCT-116	colon:	n/a
37	chr12:59924853-59924903	HAEpiC	amniotic membrane:	n/a
38	chr12:59925323-59925373	HEK293	kidney:	embryo
39	chr12:59924853-59924903	A549	lung:	n/a
40	chr12:59924853-59924903	HEEpiC	esophagus:	n/a
41	chr12:59924853-59924903	PANC-1	pancreas:	n/a
42	chr12:59925323-59925373	NHDF-neo	bronchial:	n/a
43	chr12:59925323-59925373	GM19239	blood:	n/a
44	chr12:59925323-59925373	ProgFib	skin:	n/a
45	chr12:59925323-59925373	SAEC	small airway:	n/a
46	chr12:59925323-59925373	PANC-1	pancreas:	n/a
47	chr12:59925323-59925373	NHBE	bronchial:	n/a
48	chr12:59925323-59925373	HCM	heart:	n/a
49	chr12:59924853-59924903	HUVEC	blood vessel:	n/a
50	chr12:59925037-59925087	ovcar-3	ovarian:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:59919709..59922642-chr12:59929595..59932355,2	MCF-7	breast:
2	chr12:59970227..59972157-chr12:59989473..59991716,2	MCF-7	breast:
3	chr12:59894898..59897398-chr12:59898807..59901162,2	MCF-7	breast:
4	chr12:59941726..59943985-chr12:59989663..59991635,2	MCF-7	breast:
5	chr12:59914091..59917711-chr12:59989940..59992108,3	MCF-7	breast:
6	chr12:59894898..59897398-chr12:59898807..59901162,2	MCF-7	breast:
7	chr12:59952670..59955367-chr12:59988706..59991381,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000266724	TF binding region
ENSG00000265430	TF binding region
ENSG00000257230	TF binding region
ENSG00000266724	CpG island
ENSG00000265430	CpG island
ENSG00000257230	CpG island
ENSG00000118596	chromatin interactions
ENSG00000265430	chromatin interactions
ENSG00000266724	chromatin interactions

Extended variants
information (count: 1113 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188029	chr12:59895548-59895549	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576250524	chr12:59895575-59895576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568003748	chr12:59895605-59895606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76145921	chr12:59895632-59895633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78313187	chr12:59895633-59895634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536566472	chr12:59895658-59895659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189044013	chr12:59895671-59895672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576745502	chr12:59895678-59895679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544010560	chr12:59895699-59895700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10747845	chr12:59895732-59895733	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181827595	chr12:59895759-59895760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564910553	chr12:59895773-59895774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143886753	chr12:59895775-59895776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559490624	chr12:59895779-59895780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530075877	chr12:59895796-59895797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11173057	chr12:59895818-59895819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184849525	chr12:59895869-59895870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146868555	chr12:59895904-59895905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547628642	chr12:59895906-59895907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551947231	chr12:59895923-59895924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs416700	chr12:59895932-59895933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs144309435	chr12:59895963-59895964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188145992	chr12:59895986-59895987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546649215	chr12:59895988-59895989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567980087	chr12:59896024-59896025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74749473	chr12:59896071-59896072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35083512	chr12:59896075-59896076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555330535	chr12:59896082-59896083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75948736	chr12:59896096-59896097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537682186	chr12:59896125-59896126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559204589	chr12:59896149-59896150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376022090	chr12:59896155-59896156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77160339	chr12:59896211-59896212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566131242	chr12:59896217-59896218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534828281	chr12:59896228-59896229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553394764	chr12:59896287-59896288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117804044	chr12:59896290-59896291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541796097	chr12:59896291-59896292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180684440	chr12:59896510-59896511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114152934	chr12:59896572-59896573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2132027	chr12:59896589-59896590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114620802	chr12:59896634-59896635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563963616	chr12:59896640-59896641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76606997	chr12:59896689-59896690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377710302	chr12:59896691-59896692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139370495	chr12:59896759-59896760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561800115	chr12:59896760-59896761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528929421	chr12:59896774-59896775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552806258	chr12:59896777-59896778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150023982	chr12:59896806-59896807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59893400-59895600	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr12:59893400-59895800	Enhancers	Primary B cells from cord blood	blood
3	chr12:59893600-59895600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:59893600-59895800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:59894000-59895800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr12:59894400-59895600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:59894400-59895600	Enhancers	HMEC	breast
8	chr12:59895000-59897200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr12:59912400-59921000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr12:59913400-59914000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr12:59913600-59914000	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr12:59913600-59914000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr12:59913600-59914000	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr12:59942000-59943600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr12:59942200-59943800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr12:59942400-59943200	Enhancers	Primary T cells fromperipheralblood	blood
17	chr12:59942400-59943200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr12:59942600-59943000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr12:59942600-59943200	Enhancers	Stomach Mucosa	stomach
20	chr12:59942600-59943400	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr12:59942600-59943600	Enhancers	Esophagus	oesophagus
22	chr12:59942600-59944000	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr12:59943000-59943200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
24	chr12:59943200-59943400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr12:59943200-59943600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr12:59947400-59947600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:59961600-59961800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
28	chr12:59961800-59970600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr12:59962600-59964600	Enhancers	Hela-S3	cervix
30	chr12:59964200-59964600	Enhancers	HMEC	breast
31	chr12:59964200-59964600	Enhancers	NHEK	skin
32	chr12:59964600-59968200	Weak transcription	Hela-S3	cervix
33	chr12:59967600-59968800	Enhancers	Primary T cells from cord blood	blood
34	chr12:59967600-59969000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr12:59968200-59968400	Enhancers	Dnd41	blood
36	chr12:59968200-59969200	Enhancers	Hela-S3	cervix
37	chr12:59968400-59968600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr12:59968400-59969000	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr12:59968600-59970600	Weak transcription	Dnd41	blood
40	chr12:59968800-59969200	Weak transcription	Primary T cells from cord blood	blood
41	chr12:59969000-59970600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr12:59969000-59970800	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr12:59969200-59971800	Enhancers	Primary T cells from cord blood	blood
44	chr12:59969400-59969600	Enhancers	Fetal Thymus	thymus
45	chr12:59969600-59969800	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr12:59969600-59970200	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr12:59969800-59972200	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr12:59970000-59971200	Weak transcription	Fetal Thymus	thymus
49	chr12:59970200-59973400	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr12:59970600-59972000	Enhancers	Dnd41	blood

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