Variant report

Variant	nsv559202
Chromosome Location	chr12:64710719-64749372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:64712262-64712769	GM12878	blood:	n/a	n/a
2	BACH1	chr12:64712590-64712766	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:64712340-64712614	GM12878	blood:	n/a	n/a
4	BCL3	chr12:64712274-64712660	GM12878	blood:	n/a	n/a
5	CBX3	chr12:64744981-64745512	HCT-116	colon:	n/a	n/a
6	CEBPB	chr12:64712453-64712762	HepG2	liver:	n/a	chr12:64712583-64712594
7	CEBPB	chr12:64712529-64712729	A549	lung:	n/a	chr12:64712583-64712594
8	CEBPB	chr12:64712252-64712856	GM12878	blood:	n/a	chr12:64712583-64712594
9	CEBPB	chr12:64712489-64712660	HepG2	liver:	n/a	chr12:64712583-64712594
10	CEBPB	chr12:64729192-64729509	HepG2	liver:	n/a	chr12:64729338-64729349
11	CEBPB	chr12:64712408-64712997	H1-hESC	embryonic stem cell:	n/a	chr12:64712583-64712594
12	CEBPB	chr12:64729258-64729483	A549	lung:	n/a	chr12:64729338-64729349
13	CEBPB	chr12:64729206-64729522	K562	blood:	n/a	chr12:64729338-64729349
14	CEBPB	chr12:64729269-64729465	Hela-S3	cervix:	n/a	chr12:64729338-64729349
15	CEBPB	chr12:64712467-64712749	MCF-7	breast:	n/a	chr12:64712583-64712594
16	CEBPB	chr12:64727046-64727134	A549	lung:	n/a	chr12:64727099-64727110
17	CEBPB	chr12:64729216-64729506	IMR90	lung:	n/a	chr12:64729338-64729349
18	CEBPB	chr12:64729182-64729509	MCF-7	breast:	n/a	chr12:64729338-64729349
19	CHD1	chr12:64712522-64712712	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr12:64712442-64712747	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr12:64746080-64746230	GM12872	blood:	n/a	n/a
22	CTCF	chr12:64712591-64712705	K562	blood:	n/a	n/a
23	CTCF	chr12:64746040-64746190	GM12875	blood:	n/a	n/a
24	CTCF	chr12:64746140-64746290	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr12:64712540-64712690	HEK293	kidney:	n/a	n/a
26	CTCF	chr12:64746013-64746250	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr12:64746060-64746210	GM12878	blood:	n/a	n/a
28	CTCF	chr12:64745940-64746090	NB4	blood:	n/a	n/a
29	CTCF	chr12:64712620-64712770	AG10803	skin:	n/a	n/a
30	CTCF	chr12:64712560-64712710	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:64712520-64712670	RPTEC	kidney:	n/a	n/a
32	CTCF	chr12:64712564-64712728	GM19240	blood:	n/a	n/a
33	CTCF	chr12:64712600-64712750	NB4	blood:	n/a	n/a
34	CTCF	chr12:64712621-64712724	HepG2	liver:	n/a	n/a
35	CTCF	chr12:64746060-64746210	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr12:64746040-64746190	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr12:64746109-64746153	ProgFib	skin:	n/a	n/a
38	CTCF	chr12:64712591-64712718	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr12:64712620-64712770	HepG2	liver:	n/a	n/a
40	CTCF	chr12:64745797-64745874	K562	blood:	n/a	n/a
41	CTCF	chr12:64712584-64712733	GM12891	blood:	n/a	n/a
42	CTCF	chr12:64746060-64746210	HEK293	kidney:	n/a	n/a
43	CTCF	chr12:64746100-64746250	BE2_C	brain:	n/a	n/a
44	CTCF	chr12:64712443-64712753	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr12:64746100-64746250	A549	lung:	n/a	n/a
46	CTCF	chr12:64746040-64746190	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr12:64712580-64712730	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr12:64746048-64746289	K562	blood:	n/a	n/a
49	CTCF	chr12:64712585-64712726	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:64746079-64746208	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64713903-64713953	AG09309	skin:	n/a
2	chr12:64713903-64713953	SKMC	muscle:	n/a
3	chr12:64713903-64713953	Caco-2	colon:	n/a
4	chr12:64713903-64713953	HMEC	breast:	n/a
5	chr12:64713903-64713953	Hepatocyte	liver:	n/a
6	chr12:64713903-64713953	PFSK-1	brain:	n/a
7	chr12:64713903-64713953	GM12878	blood:	n/a
8	chr12:64713903-64713953	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:64713903-64713953	HRCEpiC	kidney:	n/a
10	chr12:64713903-64713953	BE2_C	brain:	n/a
11	chr12:64713903-64713953	GM06990	blood:	n/a
12	chr12:64713903-64713953	K562	blood:	n/a
13	chr12:64713903-64713953	ovcar-3	ovarian:	n/a
14	chr12:64713903-64713953	AG04450	lung:	fetal
15	chr12:64713903-64713953	NHDF-neo	bronchial:	n/a
16	chr12:64713903-64713953	MCF10A-Er-Src	breast:	n/a
17	chr12:64713903-64713953	AG04449	skin:	fetal
18	chr12:64713903-64713953	HCT-116	colon:	n/a
19	chr12:64713903-64713953	HepG2	liver:	n/a
20	chr12:64713903-64713953	HCPEpiC	choroid plexus:	n/a
21	chr12:64713903-64713953	NH-A	brain:	n/a
22	chr12:64713903-64713953	GM12892	blood:	n/a
23	chr12:64713903-64713953	SK-N-MC	brain:	n/a
24	chr12:64713903-64713953	A549	lung:	n/a
25	chr12:64713903-64713953	Jurkat	blood:	n/a
26	chr12:64713903-64713953	HAEpiC	amniotic membrane:	n/a
27	chr12:64713903-64713953	PrEC	prostate:	n/a
28	chr12:64713903-64713953	AG09319	gingival:	n/a
29	chr12:64713903-64713953	PANC-1	pancreas:	n/a
30	chr12:64713903-64713953	SK-N-SH	brain:	n/a
31	chr12:64713903-64713953	RPTEC	kidney:	n/a
32	chr12:64713903-64713953	BJ	skin:	n/a
33	chr12:64713903-64713953	HIPEpiC	eye:	n/a
34	chr12:64713903-64713953	HRE	kidney:	n/a
35	chr12:64713903-64713953	U87	brain:	n/a
36	chr12:64713903-64713953	NHBE	bronchial:	n/a
37	chr12:64713903-64713953	NT2-D1	testis:	n/a
38	chr12:64713903-64713953	HRPEpiC	eye:	n/a
39	chr12:64713903-64713953	GM19239	blood:	n/a
40	chr12:64713903-64713953	ProgFib	skin:	n/a
41	chr12:64713903-64713953	GM12891	blood:	n/a
42	chr12:64713903-64713953	AoSMC	blood vessel:	n/a
43	chr12:64713903-64713953	ECC-1	luminal epithelium:	n/a
44	chr12:64713903-64713953	T-47D	breast:	n/a
45	chr12:64713903-64713953	HL-60	blood:	n/a
46	chr12:64713903-64713953	SAEC	small airway:	n/a
47	chr12:64713903-64713953	H1-hESC	embryonic stem cell:	embryo
48	chr12:64713903-64713953	AG10803	skin:	n/a
49	chr12:64713903-64713953	HCF	heart:	n/a
50	chr12:64713903-64713953	HNPCEpiC	eye:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:64726392..64729160-chr12:64798471..64802447,3	K562	blood:
2	chr12:64709338..64711273-chr12:64798098..64800969,2	K562	blood:
3	chr12:64715951..64718419-chr12:64728633..64731253,2	MCF-7	breast:
4	chr12:64719649..64721244-chr12:64724934..64726490,2	K562	blood:
5	chr12:64713435..64716211-chr12:64716690..64718444,2	K562	blood:
6	chr12:64721969..64724483-chr12:64728009..64729540,2	K562	blood:
7	chr12:64700521..64702909-chr12:64717073..64718593,2	MCF-7	breast:
8	chr12:64719649..64721244-chr12:64724934..64726490,2	K562	blood:
9	chr12:64713435..64716211-chr12:64716690..64718444,2	K562	blood:
10	chr12:64721969..64724483-chr12:64728009..64729540,2	K562	blood:
11	chr12:64715656..64718159-chr12:64726296..64727850,2	K562	blood:
12	chr12:64707395..64710674-chr12:64712585..64715820,4	MCF-7	breast:
13	chr12:64715951..64718419-chr12:64728633..64731253,2	MCF-7	breast:
14	chr12:64719649..64721355-chr12:64724218..64726490,3	K562	blood:
15	chr12:64715656..64718210-chr12:64724024..64727796,3	K562	blood:
16	chr12:64715656..64718159-chr12:64726296..64727850,2	K562	blood:
17	chr12:64715656..64718210-chr12:64724024..64727796,3	K562	blood:
18	chr12:64719649..64721355-chr12:64724218..64726490,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XPOT-4	chr12:64746097-64746181	NONHSAT029140

No data

Variant related genes	Relation type
RPS11P6	TF binding region
ENSG00000256293	TF binding region
RPS11P6	CpG island
ENSG00000256293	CpG island
ENSG00000184575	chromatin interactions

Extended variants
information (count: 1396 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12308116	chr12:64710719-64710720	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535717090	chr12:64710764-64710765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557708931	chr12:64710823-64710824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555627129	chr12:64710846-64710847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs10784403	chr12:64710999-64711000	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs183565651	chr12:64711017-64711018	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs138094732	chr12:64711028-64711029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368151449	chr12:64711182-64711183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112263666	chr12:64711267-64711268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs188346028	chr12:64711306-64711307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539992316	chr12:64711338-64711339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143657393	chr12:64711397-64711398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181852111	chr12:64711409-64711410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10878147	chr12:64711424-64711425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs143934137	chr12:64711443-64711444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531578902	chr12:64711450-64711451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551513539	chr12:64711471-64711472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570860232	chr12:64711489-64711490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533439719	chr12:64711516-64711517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553798929	chr12:64711546-64711547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146517095	chr12:64711557-64711558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566563550	chr12:64711583-64711584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535433380	chr12:64711601-64711602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549311996	chr12:64711614-64711615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569195576	chr12:64711641-64711642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367794637	chr12:64711702-64711703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541164803	chr12:64711757-64711758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7133188	chr12:64711766-64711767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs186066949	chr12:64711794-64711795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139274148	chr12:64711808-64711809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112479211	chr12:64711840-64711841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377646703	chr12:64711841-64711842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397935516	chr12:64711846-64711847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370566050	chr12:64711847-64711848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374088212	chr12:64711848-64711849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376832527	chr12:64711873-64711874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7133521	chr12:64711880-64711881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs542637005	chr12:64711917-64711918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112705947	chr12:64711926-64711927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562780641	chr12:64711927-64711928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571418555	chr12:64711951-64711952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78156406	chr12:64711964-64711965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10459258	chr12:64711982-64711983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs564784523	chr12:64711986-64711987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77584587	chr12:64712002-64712003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs117050557	chr12:64712027-64712028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116107017	chr12:64712028-64712029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560207440	chr12:64712041-64712042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529285269	chr12:64712062-64712063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547979369	chr12:64712066-64712067	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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64698600-64714000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:64706200-64713800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:64706600-64712000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:64710200-64713600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:64712000-64713000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:64712000-64713000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:64712200-64712800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr12:64712200-64712800	Enhancers	Adipose Nuclei	Adipose
9	chr12:64712200-64712800	Enhancers	Osteobl	bone
10	chr12:64712200-64713000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr12:64712200-64713000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:64712200-64713000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:64712200-64713000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr12:64712200-64713200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:64712400-64712800	Enhancers	Brain Anterior Caudate	brain
16	chr12:64712400-64713000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:64712400-64713200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:64712400-64713200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr12:64712400-64713200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr12:64712600-64712800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:64712600-64712800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:64712600-64712800	Enhancers	H9 Cell Line	embryonic stem cell
23	chr12:64712600-64712800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:64712600-64712800	Enhancers	Brain Cingulate Gyrus	brain
25	chr12:64712600-64712800	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr12:64712600-64712800	Enhancers	Brain Substantia Nigra	brain
27	chr12:64712600-64712800	Enhancers	HSMMtube	muscle
28	chr12:64712600-64713000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr12:64712600-64713000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:64712600-64713000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr12:64712600-64713000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr12:64712600-64713000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:64712600-64713000	Enhancers	Brain Angular Gyrus	brain
34	chr12:64712600-64713000	Enhancers	Fetal Lung	lung
35	chr12:64712600-64713000	Enhancers	GM12878-XiMat	blood
36	chr12:64712600-64714800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr12:64712800-64713000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr12:64712800-64713000	Enhancers	HepG2	liver
39	chr12:64712800-64714000	Weak transcription	Brain Anterior Caudate	brain
40	chr12:64712800-64714200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr12:64712800-64714400	Weak transcription	Brain Substantia Nigra	brain
42	chr12:64712800-64714600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr12:64712800-64716200	Weak transcription	HSMMtube	muscle
44	chr12:64712800-64717600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr12:64712800-64717800	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr12:64713000-64713400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr12:64713000-64714000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr12:64713000-64714000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr12:64713000-64714000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr12:64713000-64714200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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