Variant report

Variant	nsv559162
Chromosome Location	chr12:63899548-64129108
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	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
3	BATF	chr12:64106394-64106647	GM12878	blood:	n/a	n/a
4	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:63945192-63945476	K562	blood:	n/a	n/a
6	BHLHE40	chr12:64062203-64062590	GM12878	blood:	n/a	chr12:64062378-64062391
7	BHLHE40	chr12:64062231-64062577	A549	lung:	n/a	chr12:64062378-64062391
8	BRCA1	chr12:63978333-63978494	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:63916532-63916622	A549	lung:	n/a	chr12:63916575-63916586
10	CEBPB	chr12:63951128-63951259	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
12	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
13	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
15	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
16	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
18	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
19	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
20	CEBPB	chr12:63916557-63916595	HepG2	liver:	n/a	chr12:63916575-63916586
21	CEBPB	chr12:63978276-63978475	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
23	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
25	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
26	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
27	CHD2	chr12:63945273-63945559	K562	blood:	n/a	n/a
28	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
30	CTCF	chr12:64066389-64066659	K562	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
31	CTCF	chr12:64098059-64098164	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:64062584-64062688	GM10248	blood:	n/a	n/a
33	CTCF	chr12:64066414-64066647	Medullo	brain:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
34	CTCF	chr12:64066436-64066626	Pancreas_OC	pancreas:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
35	CTCF	chr12:64066440-64066590	GM12873	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
36	CTCF	chr12:63998896-63998962	ProgFib	skin:	n/a	n/a
37	CTCF	chr12:64066459-64066608	Lung_OC	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
38	CTCF	chr12:63910400-63910550	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:63988418-63988424	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:64066390-64066622	K562	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
41	CTCF	chr12:64062020-64062170	AG10803	skin:	n/a	n/a
42	CTCF	chr12:64061920-64062070	A549	lung:	n/a	n/a
43	CTCF	chr12:64061900-64062050	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr12:63996819-63996903	GM10248	blood:	n/a	n/a
45	CTCF	chr12:63988399-63988434	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:64066420-64066570	AG09319	gingival:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
47	CTCF	chr12:64066220-64066370	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr12:63918980-63919130	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr12:64066200-64066350	HMEC	breast:	n/a	n/a
50	CTCF	chr12:64068059-64068087	GM10248	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64062526-64062576	NHBE	bronchial:	n/a
2	chr12:64062544-64062594	NT2-D1	testis:	n/a
3	chr12:64062544-64062594	HCT-116	colon:	n/a
4	chr12:64080622-64080672	GM06990	blood:	n/a
5	chr12:64062498-64062548	RPTEC	kidney:	n/a
6	chr12:64062526-64062576	HMEC	breast:	n/a
7	chr12:64062724-64062774	RPTEC	kidney:	n/a
8	chr12:64062384-64062434	Hela-S3	cervix:	n/a
9	chr12:64062564-64062614	Hepatocyte	liver:	n/a
10	chr12:64062564-64062614	ovcar-3	ovarian:	n/a
11	chr12:63998373-63998423	SAEC	small airway:	n/a
12	chr12:64062564-64062614	GM12891	blood:	n/a
13	chr12:64063071-64063121	K562	blood:	n/a
14	chr12:64080622-64080672	ProgFib	skin:	n/a
15	chr12:64062221-64062271	Caco-2	colon:	n/a
16	chr12:64062542-64062592	SK-N-SH_RA	brain:	n/a
17	chr12:64062544-64062594	AG04450	lung:	fetal
18	chr12:64062542-64062592	HRPEpiC	eye:	n/a
19	chr12:64080622-64080672	GM12892	blood:	n/a
20	chr12:64062498-64062548	AG09309	skin:	n/a
21	chr12:64062544-64062594	GM06990	blood:	n/a
22	chr12:64063071-64063121	ovcar-3	ovarian:	n/a
23	chr12:63998373-63998423	HUVEC	blood vessel:	n/a
24	chr12:64062526-64062576	SKMC	muscle:	n/a
25	chr12:64062564-64062614	Caco-2	colon:	n/a
26	chr12:64062498-64062548	GM12891	blood:	n/a
27	chr12:64063071-64063121	A549	lung:	n/a
28	chr12:64062724-64062774	Caco-2	colon:	n/a
29	chr12:64063071-64063121	HEEpiC	esophagus:	n/a
30	chr12:64062526-64062576	U87	brain:	n/a
31	chr12:64062542-64062592	HepG2	liver:	n/a
32	chr12:64062384-64062434	NB4	blood:	n/a
33	chr12:64062221-64062271	HCT-116	colon:	n/a
34	chr12:64063071-64063121	NHBE	bronchial:	n/a
35	chr12:64062505-64062555	RPTEC	kidney:	n/a
36	chr12:64062384-64062434	RPTEC	kidney:	n/a
37	chr12:64062564-64062614	H1-hESC	embryonic stem cell:	embryo
38	chr12:64062542-64062592	AG04450	lung:	fetal
39	chr12:64062564-64062614	GM12878	blood:	n/a
40	chr12:64062221-64062271	HEEpiC	esophagus:	n/a
41	chr12:64062526-64062576	SK-N-MC	brain:	n/a
42	chr12:64080144-64080194	U87	brain:	n/a
43	chr12:64062221-64062271	GM06990	blood:	n/a
44	chr12:63998373-63998423	HEEpiC	esophagus:	n/a
45	chr12:64062542-64062592	GM12892	blood:	n/a
46	chr12:64080622-64080672	HCPEpiC	choroid plexus:	n/a
47	chr12:64062724-64062774	HMEC	breast:	n/a
48	chr12:64062498-64062548	ECC-1	luminal epithelium:	n/a
49	chr12:64062526-64062576	NT2-D1	testis:	n/a
50	chr12:64080144-64080194	HCT-116	colon:	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	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:
4	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
5	chr12:64116942..64118463-chr7:35277697..35279270,2	MCF-7	breast:
6	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:
7	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
8	chr12:64088585..64090481-chr12:64171623..64173907,2	MCF-7	breast:
9	chr12:63978668..63979594-chr20:52240028..52240873,2	MCF-7	breast:

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

Variant related genes	Relation type
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: 6232 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6232 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375468151	chr12:63907029-63907030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs118051662	chr12:63907053-63907054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575274529	chr12:63907077-63907078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185807984	chr12:63907082-63907083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536331661	chr12:63907083-63907084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191059323	chr12:63907085-63907086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11609221	chr12:63907112-63907113	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs576554105	chr12:63907186-63907187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540040246	chr12:63907191-63907192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146929267	chr12:63907218-63907219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573623812	chr12:63907226-63907227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117962097	chr12:63907257-63907258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561757363	chr12:63907275-63907276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530766697	chr12:63907289-63907290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183213162	chr12:63907300-63907301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564415385	chr12:63907310-63907311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533607709	chr12:63907323-63907324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529875224	chr12:63907341-63907342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546857253	chr12:63907344-63907345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546810290	chr12:63907347-63907348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138023540	chr12:63907380-63907381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565394273	chr12:63907381-63907382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549654246	chr12:63907382-63907383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368257096	chr12:63907407-63907408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572424292	chr12:63907416-63907417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552165621	chr12:63907421-63907422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557870540	chr12:63907453-63907454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186585680	chr12:63907462-63907463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146006756	chr12:63907465-63907466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148237664	chr12:63907479-63907480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573461965	chr12:63907499-63907500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542516471	chr12:63907515-63907516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556038358	chr12:63907539-63907540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75840716	chr12:63907548-63907549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79626310	chr12:63907557-63907558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200998856	chr12:63907558-63907559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201977760	chr12:63907559-63907560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190595731	chr12:63907568-63907569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183154564	chr12:63907617-63907618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544263116	chr12:63907626-63907627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564630163	chr12:63907639-63907640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10547034	chr12:63907664-63907665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200425735	chr12:63907666-63907667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372350962	chr12:63907667-63907668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533288162	chr12:63907753-63907754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540687156	chr12:63907783-63907784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560674433	chr12:63907786-63907787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150805873	chr12:63909010-63909011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538565035	chr12:63909015-63909016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192585269	chr12:63909025-63909026	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	16620391	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63907000-63907800	Enhancers	Brain Germinal Matrix	brain
2	chr12:63909000-63909200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:63909200-63910000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:63910000-63910200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:63915800-63916800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:63926400-63926600	Enhancers	Right Atrium	heart
7	chr12:63931800-63932000	Enhancers	Fetal Brain Male	brain
8	chr12:63931800-63932400	Enhancers	HSMMtube	muscle
9	chr12:63931800-63933200	Enhancers	Fetal Heart	heart
10	chr12:63932000-63938800	Weak transcription	Fetal Brain Male	brain
11	chr12:63938800-63939200	Enhancers	Fetal Brain Male	brain
12	chr12:63942400-63943800	Enhancers	Fetal Heart	heart
13	chr12:63943800-63969400	Weak transcription	Fetal Heart	heart
14	chr12:63959200-63960800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:63960000-63969200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:63960200-63964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:63960200-63971200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr12:63960800-63967200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:63962000-64027800	Weak transcription	Ovary	ovary
20	chr12:63962600-63964200	Weak transcription	Left Ventricle	heart
21	chr12:63964200-63964600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:63964200-63965400	Strong transcription	Left Ventricle	heart
23	chr12:63964600-63965200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:63964800-63967200	Weak transcription	Pancreas	Pancrea
25	chr12:63965200-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:63965400-63998800	Weak transcription	Left Ventricle	heart
27	chr12:63967200-63967800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:63967800-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:63968600-63969000	Enhancers	Dnd41	blood
30	chr12:63971200-63971600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr12:63971200-63971800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells	blood
33	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:63971800-63989200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr12:63972000-63988400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:63986200-63999200	Weak transcription	Fetal Heart	heart
37	chr12:63988200-63988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr12:63988400-63989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:63989600-63990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:63990400-63990800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:63990800-63997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:63997200-63997800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:63997800-64012400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:63998800-63999200	Enhancers	Left Ventricle	heart
45	chr12:63999000-63999200	Enhancers	Colon Smooth Muscle	Colon
46	chr12:63999200-63999400	Enhancers	Fetal Heart	heart
47	chr12:63999200-64008600	Weak transcription	Left Ventricle	heart
48	chr12:63999400-63999600	Weak transcription	Fetal Heart	heart
49	chr12:64008200-64009000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:64008600-64008800	Enhancers	Left Ventricle	heart

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