Variant report

Variant	nsv523422
Chromosome Location	chr12:85939419-85995733
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	chr12:85943398-85943797	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:85943425-85943748	A549	lung:	n/a	n/a
3	CEBPB	chr12:85957585-85957738	Hela-S3	cervix:	n/a	chr12:85957676-85957689 chr12:85957676-85957689 chr12:85957676-85957687 chr12:85957676-85957689 chr12:85957676-85957687
4	CEBPB	chr12:85981944-85982144	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr12:85948894-85949140	A549	lung:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
6	CEBPB	chr12:85942503-85942765	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr12:85948898-85949146	HepG2	liver:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
8	CEBPB	chr12:85981876-85982197	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:85942408-85942794	A549	lung:	n/a	chr12:85942416-85942428
10	CEBPB	chr12:85978878-85979088	A549	lung:	n/a	chr12:85978973-85978986 chr12:85978973-85978984 chr12:85978975-85978984 chr12:85978974-85978985 chr12:85978973-85978986 chr12:85978975-85978984 chr12:85978975-85978984 chr12:85978973-85978986 chr12:85978975-85978984
11	CEBPB	chr12:85978809-85979116	HepG2	liver:	n/a	chr12:85978973-85978986 chr12:85978973-85978984 chr12:85978975-85978984 chr12:85978974-85978985 chr12:85978973-85978986 chr12:85978975-85978984 chr12:85978975-85978984 chr12:85978973-85978986 chr12:85978975-85978984
12	CEBPB	chr12:85966835-85967062	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:85942491-85942784	A549	lung:	n/a	n/a
14	CEBPB	chr12:85942473-85942800	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:85943405-85943769	HepG2	liver:	n/a	n/a
16	CTCF	chr12:85969580-85969730	SK-N-SH_RA	brain:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
17	CTCF	chr12:85969560-85969710	GM12865	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
18	CTCF	chr12:85969600-85969750	AG09309	skin:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
19	CTCF	chr12:85969300-85969450	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr12:85969600-85969750	HMF	breast:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
21	CTCF	chr12:85969572-85969802	GM13976	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
22	CTCF	chr12:85969580-85969730	HRE	kidney:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
23	CTCF	chr12:85969546-85969785	LNCaP	prostate:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
24	CTCF	chr12:85969560-85969710	GM12801	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
25	CTCF	chr12:85969220-85969370	HEK293	kidney:	n/a	n/a
26	CTCF	chr12:85969580-85969730	A549	lung:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
27	CTCF	chr12:85969600-85969750	GM12874	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
28	CTCF	chr12:85969599-85969738	MCF-7	breast:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
29	CTCF	chr12:85969560-85969710	HEK293	kidney:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
30	CTCF	chr12:85969538-85969787	Kidney_OC	kidney:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
31	CTCF	chr12:85969519-85969819	GM12878	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
32	CTCF	chr12:85969600-85969750	GM12866	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
33	CTCF	chr12:85969560-85969710	HepG2	liver:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
34	CTCF	chr12:85969580-85969730	GM06990	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
35	CTCF	chr12:85969508-85969804	Gliobla	brain:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
36	CTCF	chr12:85969200-85969350	NB4	blood:	n/a	n/a
37	CTCF	chr12:85969518-85969823	HUVEC	blood vessel:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
38	CTCF	chr12:85969560-85969710	AG09319	gingival:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
39	CTCF	chr12:85969620-85969770	HCT-116	colon:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
40	CTCF	chr12:85969528-85969783	ProgFib	skin:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
41	CTCF	chr12:85969340-85969490	GM12869	blood:	n/a	n/a
42	CTCF	chr12:85969554-85969775	GM19239	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
43	CTCF	chr12:85969560-85969710	HPAF	blood vessel:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
44	CTCF	chr12:85969520-85969670	GM12871	blood:	n/a	n/a
45	CTCF	chr12:85969600-85969750	WERI-Rb-1	eye:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
46	CTCF	chr12:85969540-85969690	HCM	heart:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
47	CTCF	chr12:85969569-85969763	GM19240	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
48	CTCF	chr12:85969511-85969820	Hela-S3	cervix:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
49	CTCF	chr12:85969640-85969790	HepG2	liver:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
50	CTCF	chr12:85969015-85970054	SK-N-SH	brain:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85945089-85945139	AG04450	lung:	fetal
2	chr12:85945089-85945139	AG10803	skin:	n/a
3	chr12:85945089-85945139	HRPEpiC	eye:	n/a
4	chr12:85945089-85945139	SK-N-SH_RA	brain:	n/a
5	chr12:85945089-85945139	SKMC	muscle:	n/a
6	chr12:85945089-85945139	GM12891	blood:	n/a
7	chr12:85945089-85945139	HEK293	kidney:	embryo
8	chr12:85945089-85945139	HIPEpiC	eye:	n/a
9	chr12:85945089-85945139	U87	brain:	n/a
10	chr12:85945089-85945139	PANC-1	pancreas:	n/a
11	chr12:85945089-85945139	HCM	heart:	n/a
12	chr12:85945089-85945139	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:85945089-85945139	GM12892	blood:	n/a
14	chr12:85945089-85945139	LNCaP	prostate:	n/a
15	chr12:85945089-85945139	SK-N-SH	brain:	n/a
16	chr12:85945089-85945139	MCF-7	breast:	n/a
17	chr12:85945089-85945139	AoSMC	blood vessel:	n/a
18	chr12:85945089-85945139	ECC-1	luminal epithelium:	n/a
19	chr12:85945089-85945139	Hepatocyte	liver:	n/a
20	chr12:85945089-85945139	SK-N-MC	brain:	n/a
21	chr12:85945089-85945139	HEEpiC	esophagus:	n/a
22	chr12:85945089-85945139	BJ	skin:	n/a
23	chr12:85945089-85945139	GM12878	blood:	n/a
24	chr12:85945089-85945139	HRE	kidney:	n/a
25	chr12:85945089-85945139	A549	lung:	n/a
26	chr12:85945089-85945139	GM06990	blood:	n/a
27	chr12:85945089-85945139	Caco-2	colon:	n/a
28	chr12:85945089-85945139	ProgFib	skin:	n/a
29	chr12:85945089-85945139	HNPCEpiC	eye:	n/a
30	chr12:85945089-85945139	SAEC	small airway:	n/a
31	chr12:85945089-85945139	T-47D	breast:	n/a
32	chr12:85945089-85945139	NHDF-neo	bronchial:	n/a
33	chr12:85945089-85945139	HCT-116	colon:	n/a
34	chr12:85945089-85945139	NH-A	brain:	n/a
35	chr12:85945089-85945139	BE2_C	brain:	n/a
36	chr12:85945089-85945139	HCF	heart:	n/a
37	chr12:85945089-85945139	Jurkat	blood:	n/a
38	chr12:85945089-85945139	HUVEC	blood vessel:	n/a
39	chr12:85945089-85945139	HRCEpiC	kidney:	n/a
40	chr12:85945089-85945139	AG04449	skin:	fetal
41	chr12:85945089-85945139	HAEpiC	amniotic membrane:	n/a
42	chr12:85945089-85945139	NB4	blood:	n/a
43	chr12:85945089-85945139	K562	blood:	n/a
44	chr12:85945089-85945139	HL-60	blood:	n/a
45	chr12:85945089-85945139	HCPEpiC	choroid plexus:	n/a
46	chr12:85945089-85945139	H1-hESC	embryonic stem cell:	embryo
47	chr12:85945089-85945139	MCF10A-Er-Src	breast:	n/a
48	chr12:85945089-85945139	IMR90	lung:	fetal
49	chr12:85945089-85945139	PFSK-1	brain:	n/a
50	chr12:85945089-85945139	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
2	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
3	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
4	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:
5	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
6	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
7	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
8	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
9	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
10	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
11	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
12	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALX1-2	chr12:85988245-85988373	NONHSAT029750

Variant related genes	Relation type
ENSG00000257855	TF binding region
ENSG00000257855	CpG island

Extended variants
information (count: 1428 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11116870	chr12:85939419-85939420	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368352715	chr12:85939563-85939564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201336673	chr12:85939584-85939585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35910844	chr12:85939608-85939609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534644295	chr12:85939656-85939657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377443968	chr12:85939658-85939659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568109121	chr12:85939679-85939680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535445945	chr12:85939721-85939722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182398682	chr12:85939726-85939727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116686382	chr12:85939730-85939731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530083304	chr12:85939809-85939810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142958615	chr12:85939829-85939830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548453625	chr12:85939837-85939838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187182016	chr12:85939866-85939867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138513056	chr12:85939889-85939890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541403231	chr12:85939964-85939965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559320349	chr12:85939979-85939980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141205321	chr12:85940011-85940012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114309726	chr12:85940012-85940013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561134492	chr12:85940022-85940023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150321332	chr12:85940108-85940109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542766375	chr12:85940182-85940183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372350465	chr12:85940353-85940354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199565726	chr12:85940380-85940381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113608343	chr12:85940382-85940383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114983001	chr12:85940397-85940398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192483208	chr12:85940401-85940402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375428337	chr12:85940402-85940403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11116871	chr12:85940413-85940414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs528382080	chr12:85940422-85940423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183930865	chr12:85940439-85940440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568373282	chr12:85940448-85940449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535406604	chr12:85940449-85940450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550617830	chr12:85940459-85940460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568951131	chr12:85940508-85940509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539193569	chr12:85940521-85940522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559098379	chr12:85940536-85940537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34281661	chr12:85940565-85940566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149504810	chr12:85940570-85940571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372732289	chr12:85940616-85940617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201319791	chr12:85940634-85940635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188482923	chr12:85940636-85940637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571032018	chr12:85940706-85940707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559630307	chr12:85940715-85940716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192152091	chr12:85940726-85940727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76416093	chr12:85940739-85940740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563373023	chr12:85940811-85940812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575682723	chr12:85940812-85940813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202079336	chr12:85940858-85940859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73367246	chr12:85940945-85940946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

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
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

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85938200-85939600	Enhancers	Fetal Intestine Small	intestine
2	chr12:85938600-85939800	Enhancers	Fetal Intestine Large	intestine
3	chr12:85938800-85943800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr12:85939000-85944000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:85939000-85944200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr12:85939000-85944200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:85939200-85943600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr12:85939200-85944800	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr12:85939400-85943800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr12:85939600-85942400	Weak transcription	Fetal Intestine Small	intestine
11	chr12:85939800-85940200	Weak transcription	Fetal Intestine Large	intestine
12	chr12:85940200-85940400	Enhancers	Fetal Intestine Large	intestine
13	chr12:85940400-85942000	Weak transcription	Fetal Intestine Large	intestine
14	chr12:85942000-85945600	Enhancers	Fetal Intestine Large	intestine
15	chr12:85942400-85942600	Enhancers	Duodenum Mucosa	Duodenum
16	chr12:85942400-85945600	Enhancers	Fetal Intestine Small	intestine
17	chr12:85942600-85943600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr12:85943600-85943800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:85943600-85944800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:85943600-85945400	Enhancers	Duodenum Mucosa	Duodenum
21	chr12:85943600-85947000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr12:85943800-85944600	Enhancers	H9 Cell Line	embryonic stem cell
23	chr12:85943800-85944600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr12:85943800-85944800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr12:85943800-85945200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:85943800-85946800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:85943800-85947000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr12:85944000-85947000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:85944200-85947000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr12:85944200-85947000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr12:85944200-85947000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:85944400-85945200	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr12:85944600-85945000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr12:85944600-85945200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr12:85944800-85945400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr12:85944800-85946400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:85945200-85946200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:85945200-85947000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr12:85945400-85946800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr12:85945400-85952200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr12:85946200-85946400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:85946400-85946600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr12:85946400-85946800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr12:85946800-85947000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr12:85952200-85952600	Enhancers	Duodenum Mucosa	Duodenum
46	chr12:85952200-85952800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:85952400-85952800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr12:85952400-85952800	Enhancers	Fetal Intestine Small	intestine
49	chr12:85952600-85953000	Enhancers	Osteobl	bone
50	chr12:85952800-85953000	Weak transcription	Fetal Intestine Small	intestine

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