Variant report

Variant	esv2761010
Chromosome Location	chr12:63831085-64145305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:695)
CpG islands
(count:793)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:63874624-63874684	K562	blood:	n/a	n/a
2	BACH1	chr12:63835477-63835549	K562	blood:	n/a	n/a
3	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
4	BATF	chr12:64106394-64106647	GM12878	blood:	n/a	n/a
5	BATF	chr12:64106436-64106667	GM12878	blood:	n/a	n/a
6	BATF	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:64062231-64062577	A549	lung:	n/a	chr12:64062378-64062391
8	BHLHE40	chr12:63945192-63945476	K562	blood:	n/a	n/a
9	BHLHE40	chr12:64140352-64140455	K562	blood:	n/a	n/a
10	BHLHE40	chr12:64062203-64062590	GM12878	blood:	n/a	chr12:64062378-64062391
11	BRCA1	chr12:63978333-63978494	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:63839788-63839947	H1-hESC	embryonic stem cell:	n/a	chr12:63839911-63839922
13	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
14	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:63978276-63978475	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
17	CEBPB	chr12:63839778-63840018	HepG2	liver:	n/a	chr12:63839911-63839922
18	CEBPB	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
19	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
21	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
22	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
23	CEBPB	chr12:63916557-63916595	HepG2	liver:	n/a	chr12:63916575-63916586
24	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
25	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
26	CEBPB	chr12:63951128-63951259	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:63839798-63840058	IMR90	lung:	n/a	chr12:63839911-63839922
28	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
29	CEBPB	chr12:63916532-63916622	A549	lung:	n/a	chr12:63916575-63916586
30	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
31	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
32	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
33	CHD2	chr12:64140336-64140636	K562	blood:	n/a	n/a
34	CHD2	chr12:63945273-63945559	K562	blood:	n/a	n/a
35	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
37	CTCF	chr12:63858298-63858396	GM20000	blood:	n/a	n/a
38	CTCF	chr12:64098081-64098115	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:64132501-64132565	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr12:63887300-63887450	BE2_C	brain:	n/a	n/a
41	CTCF	chr12:64066420-64066570	HPAF	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
42	CTCF	chr12:64066166-64066272	GM13976	blood:	n/a	n/a
43	CTCF	chr12:63886971-63886980	ProgFib	skin:	n/a	n/a
44	CTCF	chr12:64062040-64062190	BJ	skin:	n/a	n/a
45	CTCF	chr12:63844660-63844810	MCF-7	breast:	n/a	chr12:63844756-63844777 chr12:63844761-63844779
46	CTCF	chr12:64066440-64066590	NHDF-neo	bronchial:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
47	CTCF	chr12:64118215-64118243	GM20000	blood:	n/a	n/a
48	CTCF	chr12:63988399-63988434	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:63887240-63887390	BE2_C	brain:	n/a	n/a
50	CTCF	chr12:64066320-64066570	BJ	skin:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64062542-64062592	AG09319	gingival:	n/a
2	chr12:64062542-64062592	ECC-1	luminal epithelium:	n/a
3	chr12:64062498-64062548	HepG2	liver:	n/a
4	chr12:64062542-64062592	CMK	blood:	n/a
5	chr12:64062498-64062548	HCM	heart:	n/a
6	chr12:64063071-64063121	HIPEpiC	eye:	n/a
7	chr12:64080144-64080194	AoSMC	blood vessel:	n/a
8	chr12:64062505-64062555	HNPCEpiC	eye:	n/a
9	chr12:64062498-64062548	ProgFib	skin:	n/a
10	chr12:64062544-64062594	T-47D	breast:	n/a
11	chr12:64062221-64062271	AG04449	skin:	fetal
12	chr12:64062542-64062592	IMR90	lung:	fetal
13	chr12:64062498-64062548	AG09309	skin:	n/a
14	chr12:64062505-64062555	AG10803	skin:	n/a
15	chr12:64062505-64062555	NHBE	bronchial:	n/a
16	chr12:63998373-63998423	GM12891	blood:	n/a
17	chr12:64063071-64063121	SAEC	small airway:	n/a
18	chr12:64062526-64062576	GM06990	blood:	n/a
19	chr12:64062526-64062576	GM12891	blood:	n/a
20	chr12:64062542-64062592	SAEC	small airway:	n/a
21	chr12:64062505-64062555	ECC-1	luminal epithelium:	n/a
22	chr12:64062221-64062271	BE2_C	brain:	n/a
23	chr12:64063071-64063121	AG04450	lung:	fetal
24	chr12:64062221-64062271	HRCEpiC	kidney:	n/a
25	chr12:64062542-64062592	NT2-D1	testis:	n/a
26	chr12:64062498-64062548	AoSMC	blood vessel:	n/a
27	chr12:64062542-64062592	HEEpiC	esophagus:	n/a
28	chr12:64062544-64062594	HRE	kidney:	n/a
29	chr12:64062564-64062614	GM06990	blood:	n/a
30	chr12:64062542-64062592	U87	brain:	n/a
31	chr12:64062526-64062576	LNCaP	prostate:	n/a
32	chr12:64062505-64062555	PFSK-1	brain:	n/a
33	chr12:64063071-64063121	RPTEC	kidney:	n/a
34	chr12:64062384-64062434	ovcar-3	ovarian:	n/a
35	chr12:64063071-64063121	Jurkat	blood:	n/a
36	chr12:64062542-64062592	SK-N-MC	brain:	n/a
37	chr12:64062724-64062774	AG09309	skin:	n/a
38	chr12:64062564-64062614	GM12891	blood:	n/a
39	chr12:64062544-64062594	SAEC	small airway:	n/a
40	chr12:64063071-64063121	CMK	blood:	n/a
41	chr12:64063071-64063121	NB4	blood:	n/a
42	chr12:64062221-64062271	NT2-D1	testis:	n/a
43	chr12:64062544-64062594	GM12891	blood:	n/a
44	chr12:64062498-64062548	Hepatocyte	liver:	n/a
45	chr12:64062384-64062434	AG04450	lung:	fetal
46	chr12:64062544-64062594	NB4	blood:	n/a
47	chr12:64080622-64080672	AoSMC	blood vessel:	n/a
48	chr12:64062221-64062271	PANC-1	pancreas:	n/a
49	chr12:64062724-64062774	NH-A	brain:	n/a
50	chr12:64062724-64062774	NB4	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
2	chr12:64116942..64118463-chr7:35277697..35279270,2	MCF-7	breast:
3	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
4	chr12:63893978..63896181-chr12:64171241..64172887,2	K562	blood:
5	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
6	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
7	chr12:63978668..63979594-chr20:52240028..52240873,2	MCF-7	breast:
8	chr12:64088585..64090481-chr12:64171623..64173907,2	MCF-7	breast:
9	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:
10	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
11	chr12:64130174..64132619-chr12:64170875..64173477,2	MCF-7	breast:
12	chr12:64144773..64147756-chr12:64148105..64150305,2	K562	blood:
13	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
14	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:

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

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

No data

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: 7390 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:7390 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201324886	chr12:63831113-63831114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536556418	chr12:63831152-63831153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10878046	chr12:63831218-63831219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575968247	chr12:63831247-63831248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544954923	chr12:63831272-63831273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564710239	chr12:63831288-63831289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572133340	chr12:63831289-63831290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61937260	chr12:63831408-63831409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546317720	chr12:63831416-63831417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541123000	chr12:63831417-63831418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200402474	chr12:63831604-63831605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561109445	chr12:63831610-63831611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201140808	chr12:63831700-63831701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199563364	chr12:63831701-63831702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368966747	chr12:63831720-63831721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529875710	chr12:63831725-63831726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561292181	chr12:63831728-63831729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563571525	chr12:63831752-63831753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531627795	chr12:63831753-63831754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192065714	chr12:63831800-63831801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571531887	chr12:63831817-63831818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374019577	chr12:63831841-63831842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527830018	chr12:63831848-63831849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547443931	chr12:63831896-63831897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548376827	chr12:63831961-63831962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377709537	chr12:63831962-63831963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556452295	chr12:63831988-63831989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570361029	chr12:63831989-63831990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538941062	chr12:63832004-63832005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568365505	chr12:63832046-63832047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558569359	chr12:63832050-63832051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530791449	chr12:63832052-63832053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571936156	chr12:63832057-63832058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371171310	chr12:63832058-63832059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183570854	chr12:63832079-63832080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554659766	chr12:63832081-63832082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574708210	chr12:63832112-63832113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543611367	chr12:63832151-63832152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113602390	chr12:63832168-63832169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570474906	chr12:63832175-63832176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74578389	chr12:63832230-63832231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532467204	chr12:63832247-63832248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545778047	chr12:63832253-63832254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186619391	chr12:63832267-63832268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191938030	chr12:63832434-63832435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527630488	chr12:63832436-63832437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547505149	chr12:63832458-63832459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567384389	chr12:63832484-63832485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530118892	chr12:63832537-63832538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141109103	chr12:63832598-63832599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	16620391	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63827800-63834000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:63833800-63834200	Enhancers	Fetal Kidney	kidney
3	chr12:63834000-63834200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:63834000-63834200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:63834000-63834400	Enhancers	Aorta	Aorta
6	chr12:63834400-63836400	Weak transcription	Aorta	Aorta
7	chr12:63839000-63840000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:63839000-63840800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:63839200-63840200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr12:63840000-63840200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:63840000-63844600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:63840200-63851200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr12:63840800-63844600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:63844600-63845400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:63844600-63845400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:63844800-63845400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:63850400-63851000	Enhancers	HSMMtube	muscle
18	chr12:63851200-63853200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr12:63852600-63853600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:63853600-63855000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:63855000-63855400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:63872800-63873600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:63873200-63874400	Enhancers	Adipose Nuclei	Adipose
24	chr12:63873400-63874000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:63873600-63873800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:63873600-63874200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:63873800-63874200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:63873800-63874400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr12:63874000-63874400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr12:63874200-63874400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:63874200-63874400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:63875800-63877200	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr12:63888400-63888600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr12:63888400-63888800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:63888800-63890000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:63888800-63890200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:63889400-63890200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:63889600-63890000	Bivalent Enhancer	Stomach Mucosa	stomach
39	chr12:63889600-63890200	Enhancers	Liver	Liver
40	chr12:63889600-63890200	Flanking Active TSS	A549	lung
41	chr12:63889800-63891000	Enhancers	Dnd41	blood
42	chr12:63890000-63891200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr12:63890200-63890400	Enhancers	A549	lung
44	chr12:63890200-63891000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:63907000-63907800	Enhancers	Brain Germinal Matrix	brain
46	chr12:63909000-63909200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:63909200-63910000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:63910000-63910200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr12:63915800-63916800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:63926400-63926600	Enhancers	Right Atrium	heart

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