Variant report

Variant	nsv1052676
Chromosome Location	chr12:85466799-85556788
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	CBX3	chr12:85486417-85486899	HCT-116	colon:	n/a	n/a
2	CEBPB	chr12:85536096-85536348	A549	lung:	n/a	chr12:85536185-85536196
3	CEBPB	chr12:85551145-85551452	A549	lung:	n/a	n/a
4	CEBPB	chr12:85536088-85536377	HepG2	liver:	n/a	chr12:85536185-85536196
5	CTCF	chr12:85549580-85549850	HA-sp	spinal cord:	n/a	n/a
6	CTCF	chr12:85549700-85549850	BJ	skin:	n/a	n/a
7	CTCF	chr12:85549702-85549805	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr12:85470541-85470652	SK-N-SH_RA	brain:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
9	CTCF	chr12:85470520-85470670	GM12873	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
10	CTCF	chr12:85470460-85470610	A549	lung:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
11	CTCF	chr12:85470500-85470650	HCM	heart:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
12	CTCF	chr12:85470500-85470650	HRPEpiC	eye:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
13	CTCF	chr12:85470520-85470670	AoAF	blood vessel:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
14	CTCF	chr12:85549620-85549770	Caco-2	colon:	n/a	n/a
15	CTCF	chr12:85550560-85550710	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:85470535-85470705	HepG2	liver:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
17	CTCF	chr12:85549675-85549845	LNCaP	prostate:	n/a	n/a
18	CTCF	chr12:85550360-85550510	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:85549680-85549830	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr12:85549540-85549690	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr12:85549702-85549813	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:85470973-85470986	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr12:85549780-85549930	A549	lung:	n/a	n/a
24	CTCF	chr12:85470520-85470670	BJ	skin:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
25	CTCF	chr12:85470520-85470670	HA-sp	spinal cord:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
26	CTCF	chr12:85470900-85471050	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr12:85549720-85549870	HMF	breast:	n/a	n/a
28	CTCF	chr12:85470520-85470670	Caco-2	colon:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
29	CTCF	chr12:85470440-85470590	GM12864	blood:	n/a	chr12:85470580-85470588
30	CTCF	chr12:85470507-85470688	GM10266	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
31	CTCF	chr12:85470920-85471070	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr12:85549680-85549830	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr12:85549720-85549870	HPF	lung:	n/a	n/a
34	CTCF	chr12:85470456-85470726	Medullo	brain:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
35	CTCF	chr12:85470480-85470630	NHDF-neo	bronchial:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
36	CTCF	chr12:85470500-85470650	GM12864	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
37	CTCF	chr12:85470520-85470670	BE2_C	brain:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
38	CTCF	chr12:85470260-85470410	A549	lung:	n/a	n/a
39	CTCF	chr12:85470540-85470690	GM12865	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
40	CTCF	chr12:85470520-85470670	GM12878	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
41	CTCF	chr12:85470480-85470630	AG09309	skin:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
42	CTCF	chr12:85549760-85549789	HepG2	liver:	n/a	n/a
43	CTCF	chr12:85470520-85470670	GM12865	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
44	CTCF	chr12:85470520-85470670	HBMEC	blood vessel:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
45	CTCF	chr12:85549662-85549868	A549	lung:	n/a	n/a
46	CTCF	chr12:85470520-85470670	GM12871	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
47	CTCF	chr12:85470480-85470630	MCF-7	breast:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
48	CTCF	chr12:85470400-85470550	GM06990	blood:	n/a	n/a
49	CTCF	chr12:85549660-85549810	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr12:85537065-85537096	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85473162-85473212	LNCaP	prostate:	n/a
2	chr12:85473162-85473212	IMR90	lung:	fetal
3	chr12:85473162-85473212	HCM	heart:	n/a
4	chr12:85473162-85473212	H1-hESC	embryonic stem cell:	embryo
5	chr12:85473162-85473212	HL-60	blood:	n/a
6	chr12:85473162-85473212	GM19239	blood:	n/a
7	chr12:85473162-85473212	HRE	kidney:	n/a
8	chr12:85473162-85473212	CMK	blood:	n/a
9	chr12:85473162-85473212	HRCEpiC	kidney:	n/a
10	chr12:85473162-85473212	BE2_C	brain:	n/a
11	chr12:85473162-85473212	HIPEpiC	eye:	n/a
12	chr12:85473162-85473212	HepG2	liver:	n/a
13	chr12:85473162-85473212	SKMC	muscle:	n/a
14	chr12:85473162-85473212	Caco-2	colon:	n/a
15	chr12:85473162-85473212	AG09309	skin:	n/a
16	chr12:85473162-85473212	HCT-116	colon:	n/a
17	chr12:85473162-85473212	HMEC	breast:	n/a
18	chr12:85473162-85473212	BJ	skin:	n/a
19	chr12:85473162-85473212	HEK293	kidney:	embryo
20	chr12:85473162-85473212	HCF	heart:	n/a
21	chr12:85473162-85473212	HUVEC	blood vessel:	n/a
22	chr12:85473162-85473212	RPTEC	kidney:	n/a
23	chr12:85473162-85473212	HRPEpiC	eye:	n/a
24	chr12:85473162-85473212	AG04449	skin:	fetal
25	chr12:85473162-85473212	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:85473162-85473212	Hepatocyte	liver:	n/a
27	chr12:85473162-85473212	NT2-D1	testis:	n/a
28	chr12:85473162-85473212	GM12892	blood:	n/a
29	chr12:85473162-85473212	SK-N-MC	brain:	n/a
30	chr12:85473162-85473212	ECC-1	luminal epithelium:	n/a
31	chr12:85473162-85473212	SAEC	small airway:	n/a
32	chr12:85473162-85473212	MCF-7	breast:	n/a
33	chr12:85473162-85473212	Jurkat	blood:	n/a
34	chr12:85473162-85473212	NHDF-neo	bronchial:	n/a
35	chr12:85473162-85473212	NHBE	bronchial:	n/a
36	chr12:85473162-85473212	AG10803	skin:	n/a
37	chr12:85473162-85473212	GM12891	blood:	n/a
38	chr12:85473162-85473212	AG04450	lung:	fetal
39	chr12:85473162-85473212	AoSMC	blood vessel:	n/a
40	chr12:85473162-85473212	A549	lung:	n/a
41	chr12:85473162-85473212	ovcar-3	ovarian:	n/a
42	chr12:85473162-85473212	HAEpiC	amniotic membrane:	n/a
43	chr12:85473162-85473212	PrEC	prostate:	n/a
44	chr12:85473162-85473212	U87	brain:	n/a
45	chr12:85473162-85473212	SK-N-SH_RA	brain:	n/a
46	chr12:85473162-85473212	MCF10A-Er-Src	breast:	n/a
47	chr12:85473162-85473212	SK-N-SH	brain:	n/a
48	chr12:85473162-85473212	HEEpiC	esophagus:	n/a
49	chr12:85473162-85473212	NB4	blood:	n/a
50	chr12:85473162-85473212	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85549075..85550214-chr12:85841829..85842800,6	MCF-7	breast:
2	chr12:85500330..85501960-chr12:85504219..85505982,2	K562	blood:
3	chr12:85470481..85471011-chr12:86260831..86261575,2	MCF-7	breast:
4	chr12:85500330..85501960-chr12:85504219..85505982,2	K562	blood:
5	chr12:85496315..85499030-chr12:85506456..85509353,2	K562	blood:
6	chr12:85496315..85499030-chr12:85506456..85509353,2	K562	blood:
7	chr12:85470175..85471007-chr12:86313905..86314467,2	MCF-7	breast:
8	chr12:85549387..85549978-chr12:85835659..85836204,2	MCF-7	breast:
9	chr12:85535998..85538330-chr12:85580098..85581911,2	K562	blood:
10	chr12:85470092..85470900-chr12:85818409..85819385,3	MCF-7	breast:
11	chr12:85469399..85472134-chr9:139733502..139735289,2	MCF-7	breast:
12	chr12:85470147..85471061-chr12:85788737..85789303,2	MCF-7	breast:
13	chr12:85550574..85552513-chr12:85557330..85559057,2	MCF-7	breast:
14	chr12:85549530..85550247-chr12:86266080..86266618,2	MCF-7	breast:

Variant related genes	Relation type
LRRIQ1	TF binding region
LRRIQ1	CpG island

Extended variants
information (count: 550 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186862785	chr12:85469049-85469050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190910505	chr12:85469058-85469059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76162638	chr12:85469109-85469110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142512891	chr12:85469159-85469160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146704407	chr12:85469165-85469166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139365274	chr12:85469175-85469176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574504114	chr12:85469198-85469199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570718250	chr12:85469199-85469200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542824385	chr12:85469219-85469220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531727721	chr12:85469232-85469233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183371407	chr12:85469261-85469262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188206422	chr12:85469358-85469359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531844516	chr12:85469462-85469463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113983810	chr12:85469473-85469474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565280583	chr12:85469498-85469499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532359959	chr12:85469506-85469507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377244141	chr12:85469538-85469539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184847947	chr12:85470616-85470617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148192426	chr12:85470624-85470625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552430402	chr12:85470630-85470631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11116696	chr12:85470641-85470642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189980583	chr12:85470655-85470656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377345988	chr12:85470671-85470672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553060573	chr12:85470715-85470716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552653513	chr12:85470731-85470732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73379770	chr12:85470790-85470791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370917740	chr12:85470832-85470833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182097560	chr12:85470852-85470853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs137921983	chr12:85470859-85470860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142577745	chr12:85470889-85470890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144566010	chr12:85470896-85470897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373367261	chr12:85470897-85470898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543585528	chr12:85470898-85470899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145988781	chr12:85470906-85470907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577426620	chr12:85471001-85471002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541716614	chr12:85471012-85471013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs3847769	chr12:85471016-85471017	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs186302792	chr12:85471027-85471028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191296775	chr12:85471052-85471053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78958616	chr12:85471062-85471063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563751876	chr12:85471085-85471086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181355649	chr12:85471086-85471087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs359984	chr12:85471087-85471088	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs74488102	chr12:85471096-85471097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570667978	chr12:85471134-85471135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528327815	chr12:85471136-85471137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546869243	chr12:85471138-85471139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535183818	chr12:85478801-85478802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552776155	chr12:85478818-85478819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374677408	chr12:85478822-85478823	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
abnormal development	18461090	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
Cancer	20164920	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85469000-85469600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:85470600-85471000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:85470600-85471000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr12:85470600-85471000	Enhancers	Duodenum Smooth Muscle	Duodenum
5	chr12:85470600-85471200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr12:85470600-85471200	Enhancers	NHEK	skin
7	chr12:85470800-85471000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr12:85470800-85471200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:85470800-85471200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:85470800-85471200	Enhancers	Hela-S3	cervix
11	chr12:85478800-85479400	Enhancers	Fetal Lung	lung
12	chr12:85483600-85484000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr12:85483600-85484000	Enhancers	H9 Cell Line	embryonic stem cell
14	chr12:85483600-85484000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr12:85483600-85484000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr12:85483600-85484000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:85483800-85484200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr12:85483800-85484200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr12:85486000-85487400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:85486200-85487800	Enhancers	HMEC	breast
21	chr12:85486400-85487400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:85486600-85486800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:85486600-85487200	Enhancers	NHEK	skin
24	chr12:85487000-85487600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:85490600-85491200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:85511800-85512200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:85527800-85528200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr12:85527800-85528400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:85527800-85528400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr12:85528000-85528600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:85531400-85531800	Active TSS	Fetal Kidney	kidney
32	chr12:85547800-85550000	Active TSS	Fetal Kidney	kidney
33	chr12:85549200-85549400	Enhancers	Hela-S3	cervix
34	chr12:85549400-85549800	Flanking Active TSS	Hela-S3	cervix
35	chr12:85549800-85550400	Enhancers	Hela-S3	cervix
36	chr12:85550000-85551400	Active TSS	A549	lung
37	chr12:85550400-85550600	Weak transcription	Hela-S3	cervix
38	chr12:85550600-85551200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:85550600-85551200	Enhancers	HUVEC	blood vessel
40	chr12:85550600-85551600	Active TSS	Hela-S3	cervix
41	chr12:85550800-85551800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:85551600-85557200	Weak transcription	Hela-S3	cervix

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