Variant report

Variant	nsv735
Chromosome Location	chr12:59799232-59882716
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	BHLHE40	chr12:59801689-59801776	GM12878	blood:	n/a	chr12:59801704-59801713
2	BRCA1	chr12:59855963-59855973	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr12:59842558-59842653	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:59847276-59847462	A549	lung:	n/a	chr12:59847298-59847311 chr12:59847298-59847311 chr12:59847299-59847310
5	CEBPB	chr12:59825882-59826190	IMR90	lung:	n/a	chr12:59826011-59826022
6	CEBPB	chr12:59850774-59851014	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:59847192-59847470	IMR90	lung:	n/a	chr12:59847298-59847311 chr12:59847298-59847311 chr12:59847299-59847310
8	CEBPB	chr12:59847295-59847317	Hela-S3	cervix:	n/a	chr12:59847298-59847311 chr12:59847298-59847311 chr12:59847299-59847310
9	CEBPB	chr12:59822731-59822996	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:59822764-59822936	MCF-7	breast:	n/a	n/a
11	CEBPB	chr12:59850796-59851001	A549	lung:	n/a	n/a
12	CEBPB	chr12:59819669-59819744	Hela-S3	cervix:	n/a	chr12:59819695-59819708 chr12:59819695-59819708 chr12:59819695-59819706 chr12:59819695-59819706
13	CEBPB	chr12:59825871-59826185	HepG2	liver:	n/a	chr12:59826011-59826022
14	CEBPB	chr12:59819626-59819840	IMR90	lung:	n/a	chr12:59819780-59819789 chr12:59819695-59819708 chr12:59819695-59819708 chr12:59819778-59819789 chr12:59819695-59819706 chr12:59819695-59819706
15	CEBPB	chr12:59825866-59826194	Hela-S3	cervix:	n/a	chr12:59826011-59826022
16	CEBPB	chr12:59867348-59867510	A549	lung:	n/a	n/a
17	CEBPB	chr12:59833740-59833840	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:59846095-59846499	IMR90	lung:	n/a	chr12:59846293-59846306 chr12:59846293-59846304
19	CEBPB	chr12:59825934-59826167	A549	lung:	n/a	chr12:59826011-59826022
20	CEBPB	chr12:59805257-59805515	A549	lung:	n/a	chr12:59805398-59805411 chr12:59805398-59805411 chr12:59805398-59805409 chr12:59805398-59805409
21	CEBPB	chr12:59847220-59847370	H1-hESC	embryonic stem cell:	n/a	chr12:59847298-59847311 chr12:59847298-59847311 chr12:59847299-59847310
22	CEBPB	chr12:59847202-59847445	HepG2	liver:	n/a	chr12:59847298-59847311 chr12:59847298-59847311 chr12:59847299-59847310
23	CTCF	chr12:59825040-59825190	Caco-2	colon:	n/a	n/a
24	CTCF	chr12:59838840-59838990	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr12:59838795-59838949	GM20000	blood:	n/a	n/a
26	CTCF	chr12:59825120-59825270	AG04449	skin:	n/a	chr12:59825231-59825247 chr12:59825230-59825248 chr12:59825232-59825253
27	CTCF	chr12:59838860-59839010	NHEK	skin:	n/a	n/a
28	CTCF	chr12:59838783-59839013	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr12:59825200-59825350	BJ	skin:	n/a	chr12:59825231-59825247 chr12:59825230-59825248 chr12:59825232-59825253
30	CTCF	chr12:59838800-59838950	HPF	lung:	n/a	n/a
31	CTCF	chr12:59838832-59838994	LNCaP	prostate:	n/a	n/a
32	CTCF	chr12:59825148-59825271	GM13977	blood:	n/a	chr12:59825231-59825247 chr12:59825230-59825248 chr12:59825232-59825253
33	CTCF	chr12:59825148-59825300	H1-hESC	embryonic stem cell:	n/a	chr12:59825231-59825247 chr12:59825230-59825248 chr12:59825232-59825253
34	CTCF	chr12:59805760-59805910	RPTEC	kidney:	n/a	n/a
35	CTCF	chr12:59825120-59825270	AG09309	skin:	n/a	chr12:59825231-59825247 chr12:59825230-59825248 chr12:59825232-59825253
36	CTCF	chr12:59825160-59825310	AG10803	skin:	n/a	chr12:59825231-59825247 chr12:59825230-59825248 chr12:59825232-59825253
37	CTCF	chr12:59866799-59866844	Medullo	brain:	n/a	n/a
38	CTCF	chr12:59810320-59810470	GM12878	blood:	n/a	n/a
39	CTCF	chr12:59838808-59838961	Gliobla	brain:	n/a	n/a
40	CTCF	chr12:59838800-59838950	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:59838880-59839030	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr12:59838800-59838950	HMF	breast:	n/a	n/a
43	CTCF	chr12:59851140-59851290	BJ	skin:	n/a	n/a
44	CTCF	chr12:59838740-59838890	HL-60	blood:	n/a	n/a
45	CTCF	chr12:59838800-59838950	BE2_C	brain:	n/a	n/a
46	CTCF	chr12:59838840-59838990	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:59838841-59838962	GM19240	blood:	n/a	n/a
48	CTCF	chr12:59825120-59825270	Hela-S3	cervix:	n/a	chr12:59825231-59825247 chr12:59825230-59825248 chr12:59825232-59825253
49	CTCF	chr12:59838880-59839030	NHEK	skin:	n/a	n/a
50	CTCF	chr12:59838640-59838790	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:59845805-59845855	ECC-1	luminal epithelium:	n/a
2	chr12:59845805-59845855	LNCaP	prostate:	n/a
3	chr12:59845805-59845855	PFSK-1	brain:	n/a
4	chr12:59845805-59845855	NH-A	brain:	n/a
5	chr12:59845805-59845855	BE2_C	brain:	n/a
6	chr12:59845805-59845855	T-47D	breast:	n/a
7	chr12:59845805-59845855	GM19239	blood:	n/a
8	chr12:59845805-59845855	Jurkat	blood:	n/a
9	chr12:59845805-59845855	Caco-2	colon:	n/a
10	chr12:59845805-59845855	MCF-7	breast:	n/a
11	chr12:59845805-59845855	SK-N-SH	brain:	n/a
12	chr12:59845805-59845855	GM12891	blood:	n/a
13	chr12:59845805-59845855	HepG2	liver:	n/a
14	chr12:59845805-59845855	HAEpiC	amniotic membrane:	n/a
15	chr12:59845805-59845855	AoSMC	blood vessel:	n/a
16	chr12:59845805-59845855	HCM	heart:	n/a
17	chr12:59845805-59845855	CMK	blood:	n/a
18	chr12:59845805-59845855	BJ	skin:	n/a
19	chr12:59845805-59845855	MCF10A-Er-Src	breast:	n/a
20	chr12:59845805-59845855	NHBE	bronchial:	n/a
21	chr12:59845805-59845855	NT2-D1	testis:	n/a
22	chr12:59845805-59845855	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:59845805-59845855	ProgFib	skin:	n/a
24	chr12:59845805-59845855	AG09319	gingival:	n/a
25	chr12:59845805-59845855	A549	lung:	n/a
26	chr12:59845805-59845855	AG10803	skin:	n/a
27	chr12:59845805-59845855	HRPEpiC	eye:	n/a
28	chr12:59845805-59845855	RPTEC	kidney:	n/a
29	chr12:59845805-59845855	PrEC	prostate:	n/a
30	chr12:59845805-59845855	HMEC	breast:	n/a
31	chr12:59845805-59845855	K562	blood:	n/a
32	chr12:59845805-59845855	HUVEC	blood vessel:	n/a
33	chr12:59845805-59845855	HNPCEpiC	eye:	n/a
34	chr12:59845805-59845855	U87	brain:	n/a
35	chr12:59845805-59845855	H1-hESC	embryonic stem cell:	embryo
36	chr12:59845805-59845855	IMR90	lung:	fetal
37	chr12:59845805-59845855	HEEpiC	esophagus:	n/a
38	chr12:59845805-59845855	AG09309	skin:	n/a
39	chr12:59845805-59845855	GM12892	blood:	n/a
40	chr12:59845805-59845855	HL-60	blood:	n/a
41	chr12:59845805-59845855	GM12878	blood:	n/a
42	chr12:59845805-59845855	NHDF-neo	bronchial:	n/a
43	chr12:59845805-59845855	Hela-S3	cervix:	n/a
44	chr12:59845805-59845855	HEK293	kidney:	embryo
45	chr12:59845805-59845855	SK-N-MC	brain:	n/a
46	chr12:59845805-59845855	HRE	kidney:	n/a
47	chr12:59845805-59845855	HRCEpiC	kidney:	n/a
48	chr12:59845805-59845855	PANC-1	pancreas:	n/a
49	chr12:59845805-59845855	SKMC	muscle:	n/a
50	chr12:59845805-59845855	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:59819624..59822247-chr12:59822871..59826193,3	K562	blood:
2	chr12:59846048..59848605-chr12:59989591..59991500,2	MCF-7	breast:
3	chr12:59802183..59802836-chr20:52395505..52396391,2	MCF-7	breast:
4	chr12:59839463..59841278-chr12:59990128..59991816,2	MCF-7	breast:
5	chr12:59838603..59839620-chr12:60174016..60175145,3	MCF-7	breast:
6	chr12:59825209..59825865-chr12:60201866..60202550,2	MCF-7	breast:
7	chr12:59824786..59825486-chr12:60174654..60175192,2	MCF-7	breast:
8	chr12:59507468..59508144-chr12:59801341..59801884,3	MCF-7	breast:
9	chr12:59828775..59830470-chr12:59832141..59834359,2	K562	blood:
10	chr12:59819624..59822247-chr12:59822871..59826193,3	K562	blood:
11	chr12:59828775..59830470-chr12:59832141..59834359,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-272B17.2.1-1	chr12:59804912-59804952	ENSG00000258214
2	lnc-SLC16A7-1	chr12:59833557-59835248	XLOC_009783
3	lnc-SLC16A7-1	chr12:59832093-59832126	XLOC_009783

Variant related genes	Relation type
ENSG00000258214	TF binding region
RNU6-871P	TF binding region
ENSG00000258214	CpG island
RNU6-871P	CpG island
ENSG00000118596	chromatin interactions
KIF1B	miRNA target sites

Extended variants
information (count: 2228 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2228 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541176844	chr12:59799281-59799282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574619403	chr12:59799284-59799285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535571233	chr12:59799439-59799440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556996872	chr12:59799443-59799444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575597765	chr12:59799489-59799490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181684656	chr12:59799503-59799504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs276058	chr12:59799505-59799506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs141188031	chr12:59799531-59799532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540450918	chr12:59799542-59799543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs276057	chr12:59799612-59799613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529062387	chr12:59799616-59799617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550702991	chr12:59799636-59799637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372300364	chr12:59799658-59799659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558899211	chr12:59799713-59799714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564004757	chr12:59799744-59799745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373923927	chr12:59799766-59799767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146931876	chr12:59799873-59799874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571156983	chr12:59799875-59799876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534983377	chr12:59799877-59799878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570631689	chr12:59799906-59799907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117397389	chr12:59799970-59799971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568326470	chr12:59799982-59799983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs172110	chr12:59799997-59799998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs186256450	chr12:59800016-59800017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543445041	chr12:59800069-59800070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79703743	chr12:59800073-59800074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557846607	chr12:59800184-59800185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573164815	chr12:59800185-59800186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71463206	chr12:59800254-59800255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189133538	chr12:59800260-59800261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570070649	chr12:59800266-59800267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527336209	chr12:59800388-59800389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547139139	chr12:59800456-59800457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544414686	chr12:59800482-59800483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368774755	chr12:59800498-59800499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62734260	chr12:59800509-59800510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532786577	chr12:59800510-59800511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549320185	chr12:59800511-59800512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147615727	chr12:59800512-59800513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532871537	chr12:59800560-59800561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs17122488	chr12:59800581-59800582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs557091551	chr12:59800638-59800639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147562373	chr12:59800713-59800714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546894476	chr12:59800751-59800752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77281948	chr12:59800768-59800769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549644822	chr12:59800810-59800811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529486065	chr12:59800818-59800819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181898148	chr12:59800825-59800826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372474051	chr12:59800878-59800879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs276056	chr12:59800932-59800933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Thoracic aortic aneurysm	21092924	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	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	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
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59797600-59802200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:59797800-59801800	Weak transcription	Brain Hippocampus Middle	brain
3	chr12:59797800-59802000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:59801600-59801800	Enhancers	Pancreas	Pancrea
5	chr12:59801800-59802400	Weak transcription	Pancreas	Pancrea
6	chr12:59801800-59802600	Enhancers	Brain Hippocampus Middle	brain
7	chr12:59802000-59802400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr12:59802200-59802800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:59802400-59802600	Enhancers	Pancreas	Pancrea
10	chr12:59802600-59806000	Weak transcription	Pancreas	Pancrea
11	chr12:59805000-59806000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr12:59805000-59806000	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr12:59805000-59806000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr12:59806000-59808800	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr12:59806000-59808800	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr12:59806000-59809000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr12:59808400-59809600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr12:59808600-59809000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:59808600-59809200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr12:59808800-59809600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr12:59808800-59809600	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr12:59809000-59809400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr12:59818000-59818600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:59819000-59820600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:59820600-59823400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr12:59820800-59822600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:59821000-59822000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:59822000-59822600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr12:59822000-59822600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr12:59822000-59822600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:59822200-59822600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr12:59822400-59822800	Enhancers	Brain Hippocampus Middle	brain
33	chr12:59822600-59822800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr12:59822600-59822800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:59822600-59825600	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:59822600-59827000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr12:59822800-59826400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:59823400-59824200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:59825000-59826000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:59825400-59825600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:59825400-59825800	Enhancers	Fetal Heart	heart
42	chr12:59825400-59826200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr12:59825400-59827400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr12:59825600-59825800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr12:59825600-59826000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr12:59825800-59826200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr12:59826000-59827000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr12:59826200-59826600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:59826400-59827200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:59826600-59827200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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