Variant report

Variant	nsv899200
Chromosome Location	chr12:64001180-64139771
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	chr12:64106436-64106667	GM12878	blood:	n/a	n/a
2	BATF	chr12:64106394-64106647	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:64062231-64062577	A549	lung:	n/a	chr12:64062378-64062391
4	BHLHE40	chr12:64062203-64062590	GM12878	blood:	n/a	chr12:64062378-64062391
5	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
8	CEBPB	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
9	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
11	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
12	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
13	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
14	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
15	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
16	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
17	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
18	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
19	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
21	CTCF	chr12:64066366-64066629	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
22	CTCF	chr12:64069142-64069249	GM10248	blood:	n/a	n/a
23	CTCF	chr12:64066420-64066570	AG09319	gingival:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
24	CTCF	chr12:64066540-64066690	AG10803	skin:	n/a	n/a
25	CTCF	chr12:64066389-64066659	K562	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
26	CTCF	chr12:64068876-64068931	Lung_OC	lung:	n/a	chr12:64068923-64068931
27	CTCF	chr12:64071657-64071729	GM10248	blood:	n/a	n/a
28	CTCF	chr12:64116405-64116484	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:64066200-64066350	AG09309	skin:	n/a	n/a
30	CTCF	chr12:64098081-64098115	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:64037457-64037530	GM13977	blood:	n/a	n/a
32	CTCF	chr12:64068059-64068087	GM10248	blood:	n/a	n/a
33	CTCF	chr12:64066420-64066570	HRE	kidney:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
34	CTCF	chr12:64066200-64066350	HMEC	breast:	n/a	n/a
35	CTCF	chr12:64066440-64066590	HCFaa	heart:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
36	CTCF	chr12:64066246-64066780	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
37	CTCF	chr12:64066420-64066570	HMEC	breast:	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	chr12:64066462-64066580	HUVEC	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
40	CTCF	chr12:64066180-64066330	RPTEC	kidney:	n/a	n/a
41	CTCF	chr12:64090705-64090726	GM13977	blood:	n/a	n/a
42	CTCF	chr12:64066451-64066624	GM13977	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
43	CTCF	chr12:64066440-64066590	AG10803	skin:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
44	CTCF	chr12:64066420-64066570	HPAF	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
45	CTCF	chr12:64068528-64068580	GM10248	blood:	n/a	n/a
46	CTCF	chr12:64066440-64066590	GM12873	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
47	CTCF	chr12:64066164-64066278	GM10248	blood:	n/a	n/a
48	CTCF	chr12:64066490-64066597	GM13976	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
49	CTCF	chr12:64066440-64066590	HPAF	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
50	CTCF	chr12:64066393-64066610	HCT-116	colon:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64062544-64062594	MCF-7	breast:	n/a
2	chr12:64062544-64062594	MCF-7	breast:	n/a
3	chr12:64062724-64062774	AG09319	gingival:	n/a
4	chr12:64080622-64080672	PANC-1	pancreas:	n/a
5	chr12:64062384-64062434	HRE	kidney:	n/a
6	chr12:64062221-64062271	A549	lung:	n/a
7	chr12:64063071-64063121	HMEC	breast:	n/a
8	chr12:64080144-64080194	GM06990	blood:	n/a
9	chr12:64062564-64062614	H1-hESC	embryonic stem cell:	embryo
10	chr12:64062564-64062614	SK-N-SH_RA	brain:	n/a
11	chr12:64062505-64062555	AG04450	lung:	fetal
12	chr12:64062505-64062555	Hepatocyte	liver:	n/a
13	chr12:64062505-64062555	U87	brain:	n/a
14	chr12:64080144-64080194	Caco-2	colon:	n/a
15	chr12:64080144-64080194	GM12891	blood:	n/a
16	chr12:64080622-64080672	RPTEC	kidney:	n/a
17	chr12:64062505-64062555	ovcar-3	ovarian:	n/a
18	chr12:64062526-64062576	NHDF-neo	bronchial:	n/a
19	chr12:64062505-64062555	BE2_C	brain:	n/a
20	chr12:64062724-64062774	HUVEC	blood vessel:	n/a
21	chr12:64062724-64062774	HCM	heart:	n/a
22	chr12:64062498-64062548	GM06990	blood:	n/a
23	chr12:64062221-64062271	HCF	heart:	n/a
24	chr12:64062384-64062434	HCPEpiC	choroid plexus:	n/a
25	chr12:64062564-64062614	HCM	heart:	n/a
26	chr12:64063071-64063121	NHDF-neo	bronchial:	n/a
27	chr12:64062564-64062614	U87	brain:	n/a
28	chr12:64062544-64062594	HCPEpiC	choroid plexus:	n/a
29	chr12:64080622-64080672	HRPEpiC	eye:	n/a
30	chr12:64062564-64062614	HCF	heart:	n/a
31	chr12:64062544-64062594	HEEpiC	esophagus:	n/a
32	chr12:64062505-64062555	CMK	blood:	n/a
33	chr12:64062498-64062548	SK-N-SH	brain:	n/a
34	chr12:64080144-64080194	HNPCEpiC	eye:	n/a
35	chr12:64062724-64062774	AG10803	skin:	n/a
36	chr12:64062526-64062576	HAEpiC	amniotic membrane:	n/a
37	chr12:64062724-64062774	HAEpiC	amniotic membrane:	n/a
38	chr12:64062498-64062548	Hepatocyte	liver:	n/a
39	chr12:64062384-64062434	SKMC	muscle:	n/a
40	chr12:64063071-64063121	GM12891	blood:	n/a
41	chr12:64062221-64062271	GM12891	blood:	n/a
42	chr12:64062498-64062548	ProgFib	skin:	n/a
43	chr12:64062544-64062594	PFSK-1	brain:	n/a
44	chr12:64062498-64062548	HepG2	liver:	n/a
45	chr12:64062544-64062594	AG09319	gingival:	n/a
46	chr12:64062724-64062774	GM19239	blood:	n/a
47	chr12:64080622-64080672	K562	blood:	n/a
48	chr12:64062505-64062555	AG09319	gingival:	n/a
49	chr12:64062564-64062614	SAEC	small airway:	n/a
50	chr12:64062498-64062548	MCF-7	breast:	n/a

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

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

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

Extended variants
information (count: 3546 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3546 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4044900	chr12:64001180-64001181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570823948	chr12:64001208-64001209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539715886	chr12:64001303-64001304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552696659	chr12:64001381-64001382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142282412	chr12:64001394-64001395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397843543	chr12:64001435-64001436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185081854	chr12:64001439-64001440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555438339	chr12:64001468-64001469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575538810	chr12:64001538-64001539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397834088	chr12:64001539-64001540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188258804	chr12:64001544-64001545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557521874	chr12:64001602-64001603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2202644	chr12:64001613-64001614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs191569851	chr12:64001614-64001615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559525662	chr12:64001634-64001635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528480653	chr12:64001645-64001646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546432718	chr12:64001667-64001668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548419202	chr12:64001672-64001673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7307761	chr12:64001715-64001716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs200928150	chr12:64001752-64001753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183869998	chr12:64001795-64001796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570663956	chr12:64001816-64001817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539752983	chr12:64001841-64001842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547263991	chr12:64001874-64001875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140435744	chr12:64001889-64001890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535410796	chr12:64001941-64001942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2936235	chr12:64002086-64002087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59918642	chr12:64002120-64002121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs182421094	chr12:64002131-64002132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537914644	chr12:64002145-64002146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186537545	chr12:64002222-64002223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2971487	chr12:64002226-64002227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2659937	chr12:64002239-64002240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190421752	chr12:64002244-64002245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2659938	chr12:64002254-64002255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181240259	chr12:64002258-64002259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2971486	chr12:64002297-64002298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79399008	chr12:64002301-64002302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79949407	chr12:64002303-64002304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540203141	chr12:64002315-64002316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560371115	chr12:64002416-64002417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573188846	chr12:64002431-64002432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542222335	chr12:64002504-64002505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561718613	chr12:64002591-64002592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530913786	chr12:64002602-64002603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550620310	chr12:64002611-64002612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2936234	chr12:64002627-64002628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2942662	chr12:64002639-64002640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147074861	chr12:64002651-64002652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542231587	chr12:64002666-64002667	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:436 , 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	chr12:63997800-64012400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:63999200-64008600	Weak transcription	Left Ventricle	heart
4	chr12:64008200-64009000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:64008600-64008800	Enhancers	Left Ventricle	heart
6	chr12:64008600-64009000	Enhancers	NHDF-Ad	bronchial
7	chr12:64008800-64009400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr12:64009000-64009800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:64009800-64010000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:64012400-64012800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:64012800-64027400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:64019400-64059000	Weak transcription	Left Ventricle	heart
13	chr12:64020200-64022600	Weak transcription	Right Ventricle	heart
14	chr12:64021800-64022400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:64022400-64027800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:64027400-64031000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:64027600-64037400	Weak transcription	Fetal Heart	heart
18	chr12:64027800-64028600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:64027800-64028600	Strong transcription	Ovary	ovary
20	chr12:64028000-64029800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:64028200-64028600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr12:64028600-64029000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:64028600-64029600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:64028600-64030000	Weak transcription	Ovary	ovary
25	chr12:64032000-64032600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:64032600-64037200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:64037200-64037600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:64037200-64037800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:64037200-64037800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:64037200-64037800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:64037400-64038600	Enhancers	Fetal Heart	heart
32	chr12:64037800-64047800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr12:64037800-64048000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:64042600-64043000	Enhancers	NH-A	brain
35	chr12:64042600-64043200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr12:64042800-64043400	Enhancers	Osteobl	bone
37	chr12:64043000-64043400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:64043200-64043600	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr12:64043600-64044200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr12:64047800-64048200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:64048000-64048200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:64048200-64048400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:64048200-64048600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr12:64048400-64048600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:64048600-64048800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:64048600-64050200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr12:64048800-64049600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:64049000-64050600	Enhancers	Fetal Heart	heart
49	chr12:64049400-64049800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:64049600-64050200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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