Variant report

Variant	nsv899203
Chromosome Location	chr12:64054917-64139771
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	chr12:64106394-64106647	GM12878	blood:	n/a	n/a
2	BATF	chr12:64106436-64106667	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	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
6	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
7	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
8	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
9	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
10	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
11	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
12	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
13	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
15	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
17	CTCF	chr12:64066450-64066570	GM20000	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
18	CTCF	chr12:64066460-64066610	GM12865	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
19	CTCF	chr12:64090705-64090726	GM13977	blood:	n/a	n/a
20	CTCF	chr12:64066166-64066272	GM13976	blood:	n/a	n/a
21	CTCF	chr12:64071657-64071729	GM10248	blood:	n/a	n/a
22	CTCF	chr12:64061800-64061950	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr12:64098081-64098115	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:64066236-64066690	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
25	CTCF	chr12:64066420-64066570	HMF	breast:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
26	CTCF	chr12:64098059-64098164	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:64066440-64066572	GM10266	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
28	CTCF	chr12:64066462-64066580	HUVEC	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
29	CTCF	chr12:64066390-64066622	K562	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
30	CTCF	chr12:64066420-64066570	AG04449	skin:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
31	CTCF	chr12:64066957-64067048	GM20000	blood:	n/a	n/a
32	CTCF	chr12:64061980-64062130	AG04449	skin:	n/a	n/a
33	CTCF	chr12:64066420-64066570	Caco-2	colon:	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	chr12:64066200-64066350	HMEC	breast:	n/a	n/a
36	CTCF	chr12:64066414-64066627	Kidney_OC	kidney:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
37	CTCF	chr12:64068059-64068087	GM10248	blood:	n/a	n/a
38	CTCF	chr12:64066246-64066780	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
39	CTCF	chr12:64066366-64066629	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
40	CTCF	chr12:64055759-64055817	GM13977	blood:	n/a	n/a
41	CTCF	chr12:64061920-64062070	A549	lung:	n/a	n/a
42	CTCF	chr12:64069142-64069249	GM10248	blood:	n/a	n/a
43	CTCF	chr12:64066420-64066570	HPAF	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
44	CTCF	chr12:64058427-64058493	GM13977	blood:	n/a	n/a
45	CTCF	chr12:64061980-64062130	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr12:64137907-64137954	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr12:64061900-64062050	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr12:64066490-64066597	GM13976	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
49	CTCF	chr12:64066451-64066624	GM13977	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
50	CTCF	chr12:64066396-64066696	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64062564-64062614	GM12892	blood:	n/a
2	chr12:64062564-64062614	GM12892	blood:	n/a
3	chr12:64062526-64062576	HAEpiC	amniotic membrane:	n/a
4	chr12:64062498-64062548	SKMC	muscle:	n/a
5	chr12:64062542-64062592	NH-A	brain:	n/a
6	chr12:64062221-64062271	A549	lung:	n/a
7	chr12:64063071-64063121	SAEC	small airway:	n/a
8	chr12:64062505-64062555	PrEC	prostate:	n/a
9	chr12:64062542-64062592	MCF-7	breast:	n/a
10	chr12:64062221-64062271	BJ	skin:	n/a
11	chr12:64062724-64062774	AG10803	skin:	n/a
12	chr12:64062564-64062614	GM06990	blood:	n/a
13	chr12:64062384-64062434	IMR90	lung:	fetal
14	chr12:64062526-64062576	ovcar-3	ovarian:	n/a
15	chr12:64080144-64080194	SAEC	small airway:	n/a
16	chr12:64062505-64062555	Hela-S3	cervix:	n/a
17	chr12:64062498-64062548	BE2_C	brain:	n/a
18	chr12:64062384-64062434	H1-hESC	embryonic stem cell:	embryo
19	chr12:64062544-64062594	HEK293	kidney:	embryo
20	chr12:64062564-64062614	Hepatocyte	liver:	n/a
21	chr12:64062384-64062434	AG09309	skin:	n/a
22	chr12:64080622-64080672	GM12892	blood:	n/a
23	chr12:64080144-64080194	AG09309	skin:	n/a
24	chr12:64062564-64062614	ProgFib	skin:	n/a
25	chr12:64062498-64062548	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:64062542-64062592	RPTEC	kidney:	n/a
27	chr12:64062724-64062774	HUVEC	blood vessel:	n/a
28	chr12:64062542-64062592	HIPEpiC	eye:	n/a
29	chr12:64062542-64062592	GM06990	blood:	n/a
30	chr12:64062724-64062774	Hepatocyte	liver:	n/a
31	chr12:64062544-64062594	Hepatocyte	liver:	n/a
32	chr12:64062221-64062271	SK-N-SH	brain:	n/a
33	chr12:64062221-64062271	GM19239	blood:	n/a
34	chr12:64080622-64080672	AG04449	skin:	fetal
35	chr12:64080144-64080194	HRPEpiC	eye:	n/a
36	chr12:64062498-64062548	ECC-1	luminal epithelium:	n/a
37	chr12:64062564-64062614	HCT-116	colon:	n/a
38	chr12:64062384-64062434	HCT-116	colon:	n/a
39	chr12:64062221-64062271	T-47D	breast:	n/a
40	chr12:64062505-64062555	GM12878	blood:	n/a
41	chr12:64062505-64062555	K562	blood:	n/a
42	chr12:64062542-64062592	AG04450	lung:	fetal
43	chr12:64062526-64062576	HMEC	breast:	n/a
44	chr12:64080144-64080194	HUVEC	blood vessel:	n/a
45	chr12:64062564-64062614	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:64062544-64062594	MCF10A-Er-Src	breast:	n/a
47	chr12:64062526-64062576	AG04450	lung:	fetal
48	chr12:64062384-64062434	HRCEpiC	kidney:	n/a
49	chr12:64062498-64062548	NH-A	brain:	n/a
50	chr12:64080622-64080672	SAEC	small airway:	n/a

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

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

Extended variants
information (count: 1219 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1219 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2942610	chr12:64054917-64054918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545931376	chr12:64054928-64054929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559997843	chr12:64055031-64055032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528663104	chr12:64055073-64055074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113117975	chr12:64055081-64055082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370452561	chr12:64055089-64055090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372966852	chr12:64055106-64055107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151194464	chr12:64055141-64055142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568748023	chr12:64055163-64055164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367589953	chr12:64055176-64055177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145514959	chr12:64055189-64055190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530456810	chr12:64055217-64055218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371693431	chr12:64055218-64055219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146516881	chr12:64055222-64055223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375942892	chr12:64055224-64055225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529589708	chr12:64055230-64055231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201239410	chr12:64055245-64055246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202064990	chr12:64055263-64055264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552030278	chr12:64055269-64055270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539520590	chr12:64055270-64055271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552749867	chr12:64055277-64055278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs496917	chr12:64055345-64055346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112964973	chr12:64055347-64055348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77582486	chr12:64055348-64055349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs398076698	chr12:64055358-64055359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56094111	chr12:64055359-64055360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375264418	chr12:64055360-64055361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145348338	chr12:64055391-64055392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376648492	chr12:64055422-64055423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs55937010	chr12:64055477-64055478	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1827979	chr12:64055539-64055540	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs80109087	chr12:64055561-64055562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575178984	chr12:64055574-64055575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537099260	chr12:64055600-64055601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557329100	chr12:64055610-64055611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571381156	chr12:64055634-64055635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185071798	chr12:64055717-64055718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546293880	chr12:64055724-64055725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549156142	chr12:64055731-64055732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386763706	chr12:64055772-64055773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143149691	chr12:64055773-64055774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562408363	chr12:64055776-64055777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117872144	chr12:64055792-64055793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201890734	chr12:64055832-64055833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571250421	chr12:64055951-64055952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550944645	chr12:64056012-64056013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564116014	chr12:64056058-64056059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371572994	chr12:64056095-64056096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1848170	chr12:64056102-64056103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35189548	chr12:64056116-64056117	Weak transcription Enhancers	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:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64019400-64059000	Weak transcription	Left Ventricle	heart
2	chr12:64050200-64059400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:64050200-64059600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:64050600-64055800	Weak transcription	Fetal Heart	heart
5	chr12:64052600-64060000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:64055800-64056200	Enhancers	Fetal Heart	heart
7	chr12:64056200-64057800	Weak transcription	Fetal Heart	heart
8	chr12:64057200-64057400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:64057400-64058000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:64057800-64058600	Enhancers	Fetal Heart	heart
11	chr12:64058000-64058200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:64058200-64061400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:64058600-64060200	Weak transcription	Fetal Heart	heart
14	chr12:64059000-64059200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr12:64059000-64059200	Enhancers	Left Ventricle	heart
16	chr12:64059000-64059200	Enhancers	Ovary	ovary
17	chr12:64059000-64063600	Active TSS	Fetal Brain Female	brain
18	chr12:64059200-64060000	Weak transcription	Left Ventricle	heart
19	chr12:64059200-64060200	Weak transcription	Ovary	ovary
20	chr12:64059400-64059800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:64059400-64063200	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr12:64059600-64060000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:64059800-64060200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr12:64059800-64060800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:64059800-64062400	Active TSS	Right Atrium	heart
26	chr12:64060000-64060200	Active TSS	Brain Anterior Caudate	brain
27	chr12:64060000-64060200	Active TSS	Brain Germinal Matrix	brain
28	chr12:64060000-64060400	Active TSS	Left Ventricle	heart
29	chr12:64060000-64060400	Active TSS	Right Ventricle	heart
30	chr12:64060000-64060600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:64060000-64060800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr12:64060000-64061200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:64060000-64061400	Enhancers	Fetal Brain Male	brain
34	chr12:64060000-64061800	Active TSS	Adipose Nuclei	Adipose
35	chr12:64060200-64060400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr12:64060200-64060400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:64060200-64060400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:64060200-64060400	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr12:64060200-64060400	Enhancers	Primary T cells from cord blood	blood
40	chr12:64060200-64060400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr12:64060200-64060400	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr12:64060200-64060400	Flanking Active TSS	Brain Germinal Matrix	brain
43	chr12:64060200-64060400	Enhancers	Ovary	ovary
44	chr12:64060200-64060400	Enhancers	Rectal Smooth Muscle	rectum
45	chr12:64060200-64060400	Enhancers	Small Intestine	intestine
46	chr12:64060200-64060400	Enhancers	A549	lung
47	chr12:64060200-64060600	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr12:64060200-64060600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:64060200-64060800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:64060200-64063200	Active TSS	Fetal Heart	heart

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