Variant report

Variant	nsv899394
Chromosome Location	chr12:85702371-85796968
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	ARID3A	chr12:85704287-85704562	HepG2	liver:	n/a	n/a
2	BRCA1	chr12:85725088-85725176	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr12:85763290-85763939	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:85722457-85722786	A549	lung:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722735-85722752 chr12:85722610-85722619
5	CEBPB	chr12:85766923-85767123	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr12:85766898-85767160	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:85766861-85767198	HepG2	liver:	n/a	n/a
8	CEBPB	chr12:85776529-85776577	A549	lung:	n/a	n/a
9	CEBPB	chr12:85722468-85722799	HepG2	liver:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722735-85722752 chr12:85722610-85722619
10	CEBPB	chr12:85766874-85767185	A549	lung:	n/a	n/a
11	CEBPB	chr12:85722452-85722751	K562	blood:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722610-85722619
12	CEBPB	chr12:85722443-85722800	IMR90	lung:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722735-85722752 chr12:85722610-85722619
13	CEBPB	chr12:85722482-85722750	H1-hESC	embryonic stem cell:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722610-85722619
14	CEBPB	chr12:85718358-85718597	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:85766849-85767176	IMR90	lung:	n/a	n/a
16	CHD2	chr12:85759437-85759734	K562	blood:	n/a	n/a
17	CTCF	chr12:85788680-85788830	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr12:85704420-85704570	SAEC	small airway:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
19	CTCF	chr12:85704353-85704593	HUVEC	blood vessel:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
20	CTCF	chr12:85788640-85788790	HEK293	kidney:	n/a	n/a
21	CTCF	chr12:85704340-85704490	GM12864	blood:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
22	CTCF	chr12:85704462-85704551	HepG2	liver:	n/a	n/a
23	CTCF	chr12:85704073-85704149	GM10266	blood:	n/a	n/a
24	CTCF	chr12:85716520-85716670	HCPEpiC	choroid plexus:	n/a	chr12:85716616-85716637
25	CTCF	chr12:85704420-85704570	GM12869	blood:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
26	CTCF	chr12:85704740-85704890	BE2_C	brain:	n/a	n/a
27	CTCF	chr12:85704000-85704150	GM12873	blood:	n/a	n/a
28	CTCF	chr12:85704320-85704470	A549	lung:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
29	CTCF	chr12:85704340-85704490	NHDF-neo	bronchial:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
30	CTCF	chr12:85704420-85704570	HRE	kidney:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
31	CTCF	chr12:85703940-85704090	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr12:85704453-85704560	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:85704620-85704770	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr12:85704440-85704590	GM12867	blood:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
35	CTCF	chr12:85703920-85704070	BE2_C	brain:	n/a	n/a
36	CTCF	chr12:85704421-85704524	K562	blood:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
37	CTCF	chr12:85788700-85788850	BE2_C	brain:	n/a	n/a
38	CTCF	chr12:85722100-85722250	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr12:85704420-85704570	HCFaa	heart:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
40	CTCF	chr12:85704320-85704621	A549	lung:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
41	CTCF	chr12:85704640-85704790	HRE	kidney:	n/a	n/a
42	CTCF	chr12:85704340-85704490	HRE	kidney:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
43	CTCF	chr12:85704420-85704570	WERI-Rb-1	eye:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
44	CTCF	chr12:85704413-85704568	Hela-S3	cervix:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
45	CTCF	chr12:85703980-85704130	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr12:85704200-85704350	GM12865	blood:	n/a	n/a
47	CTCF	chr12:85704640-85704790	GM12873	blood:	n/a	n/a
48	CTCF	chr12:85704360-85704510	Caco-2	colon:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
49	CTCF	chr12:85704340-85704490	HAc	cerebellar:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
50	CTCF	chr12:85703960-85704110	AG09319	gingival:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85745803..85747917-chr12:85750722..85752952,2	MCF-7	breast:
2	chr12:85712831..85715377-chr12:85729265..85730997,2	MCF-7	breast:
3	chr12:85703964..85704769-chr12:85788512..85789218,4	MCF-7	breast:
4	chr12:85704116..85704872-chr12:85842034..85842872,2	MCF-7	breast:
5	chr12:85767120..85767969-chr12:85795392..85796211,2	MCF-7	breast:
6	chr12:85704213..85704892-chr12:85788326..85789139,2	MCF-7	breast:
7	chr12:85745803..85747917-chr12:85750722..85752952,2	MCF-7	breast:
8	chr12:85767120..85767969-chr12:85795392..85796211,2	MCF-7	breast:
9	chr12:85470147..85471061-chr12:85788737..85789303,2	MCF-7	breast:
10	chr12:85712831..85715377-chr12:85729265..85730997,2	MCF-7	breast:
11	chr12:85703964..85704769-chr12:85788512..85789218,4	MCF-7	breast:
12	chr12:85704213..85704892-chr12:85788326..85789139,2	MCF-7	breast:
13	chr12:85713980..85716222-chr12:85718443..85721765,3	MCF-7	breast:
14	chr12:85735992..85737956-chr12:85742669..85744404,2	MCF-7	breast:
15	chr12:85735992..85737956-chr12:85742669..85744404,2	MCF-7	breast:
16	chr12:85713980..85716222-chr12:85718443..85721765,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALX1-1	chr12:85712736-85712757	ENSG00000258815
2	lnc-ALX1-2	chr12:85763589-85763622	XLOC_009820
3	lnc-ALX1-2	chr12:85793175-85793388	NONHSAT029751
4	lnc-ALX1-1	chr12:85712733-85712757	NONHSAT029749
5	lnc-ALX1-2	chr12:85793271-85793388	XLOC_009820
6	lnc-ALX1-2	chr12:85763588-85763622	NONHSAT029751
7	lnc-ALX1-1	chr12:85711838-85711893	ENSG00000258815
8	lnc-ALX1-1	chr12:85736216-85736970	NONHSAT029749
9	lnc-ALX1-1	chr12:85736250-85736690	ENSG00000258815
10	lnc-ALX1-2	chr12:85759621-85759721	NONHSAT029750
11	lnc-ALX1-1	chr12:85733174-85733276	NONHSAT029749
12	lnc-ALX1-2	chr12:85793271-85793388	NONHSAT029750

Variant related genes	Relation type
ENSG00000258815	TF binding region
ID4	miRNA target sites
KCNK1	miRNA target sites

Extended variants
information (count: 1802 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1802 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1512734	chr12:85702371-85702372	Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs145599985	chr12:85702478-85702479	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs1398446	chr12:85702511-85702512	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs562827751	chr12:85702515-85702516	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs533364982	chr12:85702549-85702550	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs184404377	chr12:85702559-85702560	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs566992526	chr12:85702573-85702574	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs527475485	chr12:85702600-85702601	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570130131	chr12:85702618-85702619	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549135262	chr12:85702652-85702653	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189516802	chr12:85702664-85702665	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534653107	chr12:85702672-85702673	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4761131	chr12:85702717-85702718	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556042762	chr12:85702749-85702750	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570908323	chr12:85702758-85702759	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35286097	chr12:85702776-85702777	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371344634	chr12:85702823-85702824	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553569893	chr12:85702824-85702825	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192972272	chr12:85702889-85702890	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148510540	chr12:85702896-85702897	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142747540	chr12:85702976-85702977	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574291107	chr12:85702999-85703000	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549167899	chr12:85703025-85703026	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs184348635	chr12:85703031-85703032	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs369050714	chr12:85703064-85703065	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs74111962	chr12:85703101-85703102	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146592168	chr12:85703147-85703148	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs527752624	chr12:85703251-85703252	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs189630610	chr12:85703254-85703255	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs180912235	chr12:85703268-85703269	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs200584540	chr12:85703407-85703408	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs386377227	chr12:85703408-85703409	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs75588696	chr12:85703409-85703410	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs374734043	chr12:85703422-85703423	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs7313265	chr12:85703488-85703489	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141295051	chr12:85703496-85703497	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs571240930	chr12:85703497-85703498	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs538224582	chr12:85703543-85703544	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs186292189	chr12:85703587-85703588	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs543261386	chr12:85703628-85703629	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs536302253	chr12:85703638-85703639	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs558410428	chr12:85703665-85703666	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs116353152	chr12:85703693-85703694	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555463702	chr12:85703717-85703718	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs376546713	chr12:85703749-85703750	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs115746964	chr12:85703750-85703751	Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs189556366	chr12:85703867-85703868	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573786019	chr12:85703868-85703869	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578243465	chr12:85703877-85703878	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140077518	chr12:85703984-85703985	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85698400-85703000	Weak transcription	A549	lung
2	chr12:85700000-85702400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:85700400-85703000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:85702000-85703200	Bivalent Enhancer	Fetal Lung	lung
5	chr12:85702200-85702400	Flanking Active TSS	Fetal Kidney	kidney
6	chr12:85702400-85702800	Enhancers	Fetal Kidney	kidney
7	chr12:85702400-85703200	Enhancers	Liver	Liver
8	chr12:85702400-85705200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:85702600-85704000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:85702800-85703000	Weak transcription	Fetal Kidney	kidney
11	chr12:85703000-85703400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:85703000-85703600	Active TSS	A549	lung
13	chr12:85703000-85703800	Active TSS	Fetal Kidney	kidney
14	chr12:85703200-85704200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:85705200-85716200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:85711400-85711800	Enhancers	H1 Cell Line	embryonic stem cell
17	chr12:85711400-85712400	Active TSS	H9 Cell Line	embryonic stem cell
18	chr12:85711400-85712400	Active TSS	Placenta	Placenta
19	chr12:85711400-85712800	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr12:85711800-85712200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:85711800-85712200	Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr12:85711800-85712200	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr12:85711800-85712200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr12:85711800-85712400	Active TSS	H1 Cell Line	embryonic stem cell
25	chr12:85711800-85712400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr12:85711800-85712600	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr12:85711800-85713000	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr12:85712000-85712600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr12:85712000-85712600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:85712000-85712800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:85712200-85712800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr12:85712200-85712800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr12:85712600-85713000	Enhancers	H9 Cell Line	embryonic stem cell
34	chr12:85712800-85713000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr12:85712800-85719200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:85713000-85718200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr12:85716200-85716600	Enhancers	Fetal Lung	lung
38	chr12:85716200-85717200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:85716200-85717200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr12:85716600-85718600	Weak transcription	Fetal Lung	lung
41	chr12:85717400-85717800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr12:85717400-85718400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr12:85717800-85718200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr12:85718000-85718400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr12:85718200-85718800	Enhancers	Gastric	stomach
46	chr12:85718200-85719200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr12:85718200-85719400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr12:85718600-85719400	Enhancers	Fetal Lung	lung
49	chr12:85718600-85719600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:85719200-85719400	Enhancers	HUES64 Cell Line	embryonic stem cell

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