Variant report

Variant	nsv469466
Chromosome Location	chr12:72830441-72885554
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	ATF1	chr12:72859758-72860020	K562	blood:	n/a	n/a
2	BHLHE40	chr12:72860123-72860173	K562	blood:	n/a	n/a
3	CCNT2	chr12:72859542-72860056	K562	blood:	n/a	chr12:72859908-72859928
4	CEBPB	chr12:72845517-72845779	IMR90	lung:	n/a	chr12:72845664-72845675
5	CEBPB	chr12:72841878-72842216	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr12:72841932-72842202	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:72841906-72842264	IMR90	lung:	n/a	n/a
8	CEBPB	chr12:72845564-72845780	HepG2	liver:	n/a	chr12:72845664-72845675
9	CEBPB	chr12:72841939-72842199	A549	lung:	n/a	n/a
10	CEBPB	chr12:72841922-72842245	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:72845631-72845823	A549	lung:	n/a	chr12:72845664-72845675
12	CEBPB	chr12:72841994-72842182	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr12:72866355-72866399	MCF-7	breast:	n/a	n/a
14	CTCF	chr12:72866260-72866372	GM12878	blood:	n/a	n/a
15	CTCF	chr12:72866200-72866350	BJ	skin:	n/a	n/a
16	CTCF	chr12:72860120-72860270	HepG2	liver:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
17	CTCF	chr12:72866191-72866470	GM12878	blood:	n/a	n/a
18	CTCF	chr12:72866360-72866510	GM12873	blood:	n/a	n/a
19	CTCF	chr12:72860217-72860285	Gliobla	brain:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
20	CTCF	chr12:72866305-72866366	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr12:72866260-72866410	AG04449	skin:	n/a	n/a
22	CTCF	chr12:72860140-72860290	HepG2	liver:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
23	CTCF	chr12:72866264-72866381	GM13977	blood:	n/a	n/a
24	CTCF	chr12:72866280-72866430	HL-60	blood:	n/a	n/a
25	CTCF	chr12:72866289-72866384	K562	blood:	n/a	n/a
26	CTCF	chr12:72866240-72866390	GM12872	blood:	n/a	n/a
27	CTCF	chr12:72866328-72866367	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:72860094-72860485	MCF-7	breast:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
29	CTCF	chr12:72860248-72860271	Pancreas_OC	pancreas:	n/a	chr12:72860253-72860269 chr12:72860252-72860270
30	CTCF	chr12:72866300-72866450	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr12:72866280-72866430	HPF	lung:	n/a	n/a
32	CTCF	chr12:72866240-72866390	AG10803	skin:	n/a	n/a
33	CTCF	chr12:72866273-72866415	Gliobla	brain:	n/a	n/a
34	CTCF	chr12:72866260-72866410	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr12:72860220-72860370	MCF-7	breast:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
36	CTCF	chr12:72866217-72866472	IMR90	lung:	n/a	n/a
37	CTCF	chr12:72866260-72866410	HMEC	breast:	n/a	n/a
38	CTCF	chr12:72860246-72860260	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:72860200-72860350	Caco-2	colon:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
40	CTCF	chr12:72866220-72866370	HRE	kidney:	n/a	n/a
41	CTCF	chr12:72866320-72866470	GM12872	blood:	n/a	n/a
42	CTCF	chr12:72866260-72866410	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr12:72860149-72860332	MCF-7	breast:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
44	CTCF	chr12:72860218-72860294	MCF-7	breast:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270
45	CTCF	chr12:72866298-72866343	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr12:72866240-72866390	RPTEC	kidney:	n/a	n/a
47	CTCF	chr12:72866240-72866390	HFF	foreskin:	n/a	n/a
48	CTCF	chr12:72866160-72866310	HVMF	connective:	n/a	n/a
49	CTCF	chr12:72866220-72866370	GM12875	blood:	n/a	n/a
50	CTCF	chr12:72860221-72860274	MCF-7	breast:	n/a	chr12:72860247-72860268 chr12:72860253-72860269 chr12:72860252-72860270

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:72836959-72837009	HCT-116	colon:	n/a
2	chr12:72836959-72837009	HAEpiC	amniotic membrane:	n/a
3	chr12:72875216-72875266	LNCaP	prostate:	n/a
4	chr12:72875216-72875266	BJ	skin:	n/a
5	chr12:72875216-72875266	SKMC	muscle:	n/a
6	chr12:72836959-72837009	BE2_C	brain:	n/a
7	chr12:72836959-72837009	SKMC	muscle:	n/a
8	chr12:72865218-72865268	PANC-1	pancreas:	n/a
9	chr12:72865218-72865268	NHBE	bronchial:	n/a
10	chr12:72865218-72865268	HCT-116	colon:	n/a
11	chr12:72875216-72875266	SK-N-MC	brain:	n/a
12	chr12:72865218-72865268	AG10803	skin:	n/a
13	chr12:72875216-72875266	HepG2	liver:	n/a
14	chr12:72865218-72865268	HAEpiC	amniotic membrane:	n/a
15	chr12:72865218-72865268	BE2_C	brain:	n/a
16	chr12:72836959-72837009	SAEC	small airway:	n/a
17	chr12:72865218-72865268	MCF10A-Er-Src	breast:	n/a
18	chr12:72865218-72865268	ovcar-3	ovarian:	n/a
19	chr12:72836959-72837009	HMEC	breast:	n/a
20	chr12:72865218-72865268	HRCEpiC	kidney:	n/a
21	chr12:72865218-72865268	ECC-1	luminal epithelium:	n/a
22	chr12:72875216-72875266	GM19239	blood:	n/a
23	chr12:72875216-72875266	AG04450	lung:	fetal
24	chr12:72865218-72865268	Jurkat	blood:	n/a
25	chr12:72865218-72865268	GM19239	blood:	n/a
26	chr12:72836959-72837009	IMR90	lung:	fetal
27	chr12:72836959-72837009	PFSK-1	brain:	n/a
28	chr12:72875216-72875266	HRE	kidney:	n/a
29	chr12:72875216-72875266	GM06990	blood:	n/a
30	chr12:72875216-72875266	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:72836959-72837009	HepG2	liver:	n/a
32	chr12:72836959-72837009	T-47D	breast:	n/a
33	chr12:72875216-72875266	NT2-D1	testis:	n/a
34	chr12:72865218-72865268	AG09309	skin:	n/a
35	chr12:72875216-72875266	HCF	heart:	n/a
36	chr12:72865218-72865268	HL-60	blood:	n/a
37	chr12:72875216-72875266	PFSK-1	brain:	n/a
38	chr12:72865218-72865268	NHDF-neo	bronchial:	n/a
39	chr12:72875216-72875266	HMEC	breast:	n/a
40	chr12:72875216-72875266	K562	blood:	n/a
41	chr12:72836959-72837009	HEEpiC	esophagus:	n/a
42	chr12:72836959-72837009	AG04450	lung:	fetal
43	chr12:72836959-72837009	GM12891	blood:	n/a
44	chr12:72875216-72875266	Hepatocyte	liver:	n/a
45	chr12:72865218-72865268	U87	brain:	n/a
46	chr12:72875216-72875266	BE2_C	brain:	n/a
47	chr12:72865218-72865268	BJ	skin:	n/a
48	chr12:72875216-72875266	IMR90	lung:	fetal
49	chr12:72836959-72837009	HL-60	blood:	n/a
50	chr12:72875216-72875266	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr12:72739895..72740811-chr12:72859977..72860672,3	MCF-7	breast:
2	chr12:72850617..72852264-chr12:72855112..72856860,2	K562	blood:
3	chr12:72870843..72872636-chr12:72873336..72875663,2	K562	blood:
4	chr12:72831510..72833718-chr12:72835329..72838097,2	K562	blood:
5	chr12:72850617..72852264-chr12:72855112..72856860,2	K562	blood:
6	chr12:72879336..72881093-chr12:72890527..72893144,2	MCF-7	breast:
7	chr12:72831510..72833718-chr12:72835329..72838097,2	K562	blood:
8	chr12:72870843..72872636-chr12:72873336..72875663,2	K562	blood:

Variant related genes	Relation type
ENSG00000257287	TF binding region
ENSG00000257287	CpG island

Extended variants
information (count: 1915 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1915 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17111159	chr12:72830441-72830442	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149194540	chr12:72830486-72830487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181960658	chr12:72830487-72830488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543856544	chr12:72830526-72830527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556460472	chr12:72830563-72830564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143389660	chr12:72830611-72830612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529025051	chr12:72830678-72830679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547316209	chr12:72830694-72830695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369426148	chr12:72830696-72830697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372066156	chr12:72830698-72830699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532804575	chr12:72830718-72830719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551087659	chr12:72830739-72830740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534821033	chr12:72830750-72830751	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12318484	chr12:72830808-72830809	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs151338396	chr12:72830837-72830838	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs549030588	chr12:72830847-72830848	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs11829737	chr12:72830912-72830913	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186209829	chr12:72830920-72830921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554542677	chr12:72830941-72830942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566370865	chr12:72830966-72830967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140434854	chr12:72831028-72831029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190684123	chr12:72831039-72831040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12311565	chr12:72831049-72831050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543687207	chr12:72831061-72831062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12311567	chr12:72831074-72831075	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145656791	chr12:72831135-72831136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12311646	chr12:72831177-72831178	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545959274	chr12:72831208-72831209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111516730	chr12:72831292-72831293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371113079	chr12:72831311-72831312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187941864	chr12:72831369-72831370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533061495	chr12:72831405-72831406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545248370	chr12:72831410-72831411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372411295	chr12:72831463-72831464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375563148	chr12:72831481-72831482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530500194	chr12:72831563-72831564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190078711	chr12:72831724-72831725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35641505	chr12:72831762-72831763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138230560	chr12:72831782-72831783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567356905	chr12:72831828-72831829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529555938	chr12:72831845-72831846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541599751	chr12:72831878-72831879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548010270	chr12:72831896-72831897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564533573	chr12:72831906-72831907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368324840	chr12:72831910-72831911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540150411	chr12:72831923-72831924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183045971	chr12:72831937-72831938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187404032	chr12:72832009-72832010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192628692	chr12:72832059-72832060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555621266	chr12:72832090-72832091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Autism	20685689	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:72819200-72830800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:72830800-72831200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:72830800-72831200	Enhancers	HMEC	breast
4	chr12:72831200-72847400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:72832600-72833000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
6	chr12:72833000-72833400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr12:72833400-72834000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr12:72833400-72834600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:72833600-72834000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:72833800-72834000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:72833800-72834000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr12:72834000-72834400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:72834000-72836200	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:72834200-72834400	Weak transcription	Pancreas	Pancrea
15	chr12:72834200-72836200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr12:72834400-72834600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr12:72834400-72834600	Enhancers	Pancreas	Pancrea
18	chr12:72834400-72835000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr12:72834600-72835200	Weak transcription	Pancreas	Pancrea
20	chr12:72834600-72836000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr12:72834600-72836400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr12:72835000-72836800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr12:72835200-72835400	Enhancers	Pancreas	Pancrea
24	chr12:72835200-72836600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr12:72835400-72836400	Weak transcription	Pancreas	Pancrea
26	chr12:72835600-72836200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr12:72836000-72836400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr12:72836200-72836800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr12:72836200-72837400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr12:72836200-72837600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr12:72836200-72838800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr12:72836400-72836600	Enhancers	Pancreas	Pancrea
33	chr12:72836400-72838600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr12:72836400-72839200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr12:72836800-72837400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr12:72836800-72837600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr12:72836800-72837800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr12:72836800-72837800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr12:72836800-72838600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:72837400-72838600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr12:72837400-72838600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr12:72837400-72838800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr12:72837600-72838000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr12:72837600-72838600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr12:72837600-72838800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr12:72837800-72838200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr12:72837800-72838200	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr12:72837800-72838600	Enhancers	Brain Germinal Matrix	brain
49	chr12:72838000-72839400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr12:72838200-72838400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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