Variant report

Variant	nsv1047450
Chromosome Location	chr12:63988788-64136645
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	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
2	BATF	chr12:64106394-64106647	GM12878	blood:	n/a	n/a
3	BATF	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
4	BATF	chr12:64106436-64106667	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:64062231-64062577	A549	lung:	n/a	chr12:64062378-64062391
6	BHLHE40	chr12:64062203-64062590	GM12878	blood:	n/a	chr12:64062378-64062391
7	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
8	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
9	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
10	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
12	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
13	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
14	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
15	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
16	CEBPB	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
17	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
18	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
19	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
20	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
21	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
23	CTCF	chr12:64066420-64066570	HMF	breast:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
24	CTCF	chr12:64061900-64062050	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr12:64066166-64066272	GM13976	blood:	n/a	n/a
26	CTCF	chr12:64055759-64055817	GM13977	blood:	n/a	n/a
27	CTCF	chr12:64062780-64062930	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr12:64068528-64068580	GM10248	blood:	n/a	n/a
29	CTCF	chr12:64066540-64066690	AG10803	skin:	n/a	n/a
30	CTCF	chr12:63989475-63989500	GM13977	blood:	n/a	n/a
31	CTCF	chr12:64066436-64066626	Pancreas_OC	pancreas:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
32	CTCF	chr12:64066420-64066570	Caco-2	colon:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
33	CTCF	chr12:64066460-64066610	GM12865	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
34	CTCF	chr12:64066417-64066643	GM10248	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
35	CTCF	chr12:64066420-64066570	AG09319	gingival:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
36	CTCF	chr12:64041876-64041933	Medullo	brain:	n/a	n/a
37	CTCF	chr12:64066440-64066590	GM12873	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
38	CTCF	chr12:64066450-64066601	LNCaP	prostate:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
39	CTCF	chr12:64066451-64066624	GM13977	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
40	CTCF	chr12:64061980-64062130	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr12:64066438-64066625	LNCaP	prostate:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
42	CTCF	chr12:64069142-64069249	GM10248	blood:	n/a	n/a
43	CTCF	chr12:64066440-64066590	HPAF	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
44	CTCF	chr12:64098059-64098164	MCF-7	breast:	n/a	n/a
45	CTCF	chr12:64037457-64037530	GM13977	blood:	n/a	n/a
46	CTCF	chr12:64066420-64066570	HL-60	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
47	CTCF	chr12:64066440-64066590	NHDF-neo	bronchial:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
48	CTCF	chr12:64066440-64066590	AG10803	skin:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
49	CTCF	chr12:64066200-64066350	HMEC	breast:	n/a	n/a
50	CTCF	chr12:64131155-64131239	Medullo	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64062564-64062614	LNCaP	prostate:	n/a
2	chr12:63998373-63998423	HNPCEpiC	eye:	n/a
3	chr12:64062221-64062271	HRPEpiC	eye:	n/a
4	chr12:64062564-64062614	LNCaP	prostate:	n/a
5	chr12:63998373-63998423	HNPCEpiC	eye:	n/a
6	chr12:64062221-64062271	HRPEpiC	eye:	n/a
7	chr12:64062384-64062434	AG09309	skin:	n/a
8	chr12:64080144-64080194	NH-A	brain:	n/a
9	chr12:64062384-64062434	H1-hESC	embryonic stem cell:	embryo
10	chr12:64062564-64062614	SK-N-SH_RA	brain:	n/a
11	chr12:63998373-63998423	GM06990	blood:	n/a
12	chr12:64062498-64062548	Hepatocyte	liver:	n/a
13	chr12:64062526-64062576	AG10803	skin:	n/a
14	chr12:64063071-64063121	Jurkat	blood:	n/a
15	chr12:64063071-64063121	BE2_C	brain:	n/a
16	chr12:64062221-64062271	Hela-S3	cervix:	n/a
17	chr12:64062505-64062555	SK-N-MC	brain:	n/a
18	chr12:64062221-64062271	AG04450	lung:	fetal
19	chr12:64063071-64063121	HCM	heart:	n/a
20	chr12:64080144-64080194	AoSMC	blood vessel:	n/a
21	chr12:64080144-64080194	HCF	heart:	n/a
22	chr12:64063071-64063121	PANC-1	pancreas:	n/a
23	chr12:64062221-64062271	HAEpiC	amniotic membrane:	n/a
24	chr12:64062544-64062594	Caco-2	colon:	n/a
25	chr12:63998373-63998423	HAEpiC	amniotic membrane:	n/a
26	chr12:64080144-64080194	HIPEpiC	eye:	n/a
27	chr12:64062542-64062592	ovcar-3	ovarian:	n/a
28	chr12:64062498-64062548	NH-A	brain:	n/a
29	chr12:64080144-64080194	Hela-S3	cervix:	n/a
30	chr12:64080622-64080672	H1-hESC	embryonic stem cell:	embryo
31	chr12:63998373-63998423	BJ	skin:	n/a
32	chr12:64063071-64063121	T-47D	breast:	n/a
33	chr12:64062544-64062594	PFSK-1	brain:	n/a
34	chr12:64062498-64062548	LNCaP	prostate:	n/a
35	chr12:63998373-63998423	T-47D	breast:	n/a
36	chr12:64062542-64062592	Hela-S3	cervix:	n/a
37	chr12:64062564-64062614	SAEC	small airway:	n/a
38	chr12:64062724-64062774	CMK	blood:	n/a
39	chr12:64062498-64062548	A549	lung:	n/a
40	chr12:64063071-64063121	AoSMC	blood vessel:	n/a
41	chr12:64062505-64062555	PANC-1	pancreas:	n/a
42	chr12:64062542-64062592	HUVEC	blood vessel:	n/a
43	chr12:64062384-64062434	HCT-116	colon:	n/a
44	chr12:64062564-64062614	AG04449	skin:	fetal
45	chr12:64062564-64062614	GM12891	blood:	n/a
46	chr12:64062542-64062592	BJ	skin:	n/a
47	chr12:64062724-64062774	BJ	skin:	n/a
48	chr12:64062505-64062555	MCF10A-Er-Src	breast:	n/a
49	chr12:64080622-64080672	BE2_C	brain:	n/a
50	chr12:64062384-64062434	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
2	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
3	chr12:64130174..64132619-chr12:64170875..64173477,2	MCF-7	breast:
4	chr12:64088585..64090481-chr12:64171623..64173907,2	MCF-7	breast:
5	chr12:64116942..64118463-chr7:35277697..35279270,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPY19L2-1	chr12:64017568-64017604	ENSG00000249753.2

Variant related genes	Relation type
ENSG00000255583	TF binding region
DPY19L2	TF binding region
ENSG00000257005	TF binding region
ENSG00000255583	CpG island
DPY19L2	CpG island
ENSG00000257005	CpG island
ENSG00000118600	chromatin interactions

Extended variants
information (count: 3896 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3896 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372728756	chr12:63988846-63988847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115684922	chr12:63988854-63988855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538826906	chr12:63988912-63988913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558607208	chr12:63988939-63988940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571994338	chr12:63988988-63988989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190174509	chr12:63989247-63989248	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576435428	chr12:63989329-63989330	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11504146	chr12:63989394-63989395	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs181839178	chr12:63989396-63989397	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542793978	chr12:63989445-63989446	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145054112	chr12:63989452-63989453	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557657903	chr12:63989473-63989474	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531836135	chr12:63989479-63989480	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147131692	chr12:63989530-63989531	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565441621	chr12:63989584-63989585	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528012118	chr12:63989587-63989588	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548064870	chr12:63989588-63989589	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11832069	chr12:63989604-63989605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540484642	chr12:63989666-63989667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142129607	chr12:63989672-63989673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2971502	chr12:63989693-63989694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549659706	chr12:63989697-63989698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560213845	chr12:63989755-63989756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2971501	chr12:63989807-63989808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373778933	chr12:63989808-63989809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144086460	chr12:63989813-63989814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376959422	chr12:63989826-63989827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188411390	chr12:63989829-63989830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2659961	chr12:63989844-63989845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2659962	chr12:63989879-63989880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558346698	chr12:63989881-63989882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181223350	chr12:63989922-63989923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534611359	chr12:63989971-63989972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554433361	chr12:63990048-63990049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573996663	chr12:63990069-63990070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2971500	chr12:63990087-63990088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151168792	chr12:63990089-63990090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556413653	chr12:63990104-63990105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140341451	chr12:63990126-63990127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61935054	chr12:63990131-63990132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565480665	chr12:63990145-63990146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527848721	chr12:63990146-63990147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117690890	chr12:63990153-63990154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374965499	chr12:63990164-63990165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369109588	chr12:63990189-63990190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111854011	chr12:63990214-63990215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374736678	chr12:63990245-63990246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190955952	chr12:63990261-63990262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182364211	chr12:63990329-63990330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187361096	chr12:63990364-63990365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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	17899364	CNVD
Colorectal cancer	16272173	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
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	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
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63962000-64027800	Weak transcription	Ovary	ovary
2	chr12:63965400-63998800	Weak transcription	Left Ventricle	heart
3	chr12:63971800-63989200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:63986200-63999200	Weak transcription	Fetal Heart	heart
5	chr12:63988400-63989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:63989600-63990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:63990400-63990800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:63990800-63997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:63997200-63997800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:63997800-64012400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:63998800-63999200	Enhancers	Left Ventricle	heart
12	chr12:63999000-63999200	Enhancers	Colon Smooth Muscle	Colon
13	chr12:63999200-63999400	Enhancers	Fetal Heart	heart
14	chr12:63999200-64008600	Weak transcription	Left Ventricle	heart
15	chr12:63999400-63999600	Weak transcription	Fetal Heart	heart
16	chr12:64008200-64009000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:64008600-64008800	Enhancers	Left Ventricle	heart
18	chr12:64008600-64009000	Enhancers	NHDF-Ad	bronchial
19	chr12:64008800-64009400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr12:64009000-64009800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:64009800-64010000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:64012400-64012800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:64012800-64027400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:64019400-64059000	Weak transcription	Left Ventricle	heart
25	chr12:64020200-64022600	Weak transcription	Right Ventricle	heart
26	chr12:64021800-64022400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:64022400-64027800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:64027400-64031000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:64027600-64037400	Weak transcription	Fetal Heart	heart
30	chr12:64027800-64028600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:64027800-64028600	Strong transcription	Ovary	ovary
32	chr12:64028000-64029800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr12:64028200-64028600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:64028600-64029000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:64028600-64029600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:64028600-64030000	Weak transcription	Ovary	ovary
37	chr12:64032000-64032600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:64032600-64037200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:64037200-64037600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:64037200-64037800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:64037200-64037800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:64037200-64037800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:64037400-64038600	Enhancers	Fetal Heart	heart
44	chr12:64037800-64047800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr12:64037800-64048000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:64042600-64043000	Enhancers	NH-A	brain
47	chr12:64042600-64043200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr12:64042800-64043400	Enhancers	Osteobl	bone
49	chr12:64043000-64043400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr12:64043200-64043600	Weak transcription	Muscle Satellite Cultured Cells	--

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