Variant report

Variant	nsv899387
Chromosome Location	chr12:85427691-85629241
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	BRCA1	chr12:85430006-85430438	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr12:85486417-85486899	HCT-116	colon:	n/a	n/a
3	CCNT2	chr12:85446186-85446386	K562	blood:	n/a	n/a
4	CEBPB	chr12:85536096-85536348	A549	lung:	n/a	chr12:85536185-85536196
5	CEBPB	chr12:85451223-85451554	K562	blood:	n/a	n/a
6	CEBPB	chr12:85619290-85619582	IMR90	lung:	n/a	chr12:85619428-85619439
7	CEBPB	chr12:85619295-85619549	A549	lung:	n/a	chr12:85619428-85619439
8	CEBPB	chr12:85551145-85551452	A549	lung:	n/a	n/a
9	CEBPB	chr12:85451209-85451528	A549	lung:	n/a	n/a
10	CEBPB	chr12:85451207-85451539	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:85599606-85599840	A549	lung:	n/a	n/a
12	CEBPB	chr12:85451182-85451527	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:85536088-85536377	HepG2	liver:	n/a	chr12:85536185-85536196
14	CEBPB	chr12:85619275-85619599	HepG2	liver:	n/a	chr12:85619428-85619439
15	CEBPB	chr12:85451193-85451587	MCF-7	breast:	n/a	n/a
16	CEBPB	chr12:85451199-85451430	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr12:85451200-85451523	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr12:85429910-85430498	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr12:85429936-85430402	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr12:85430009-85430335	A549	lung:	n/a	n/a
21	CREB1	chr12:85430000-85430187	A549	lung:	n/a	n/a
22	CTCF	chr12:85451063-85451598	HCT-116	colon:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
23	CTCF	chr12:85549660-85549810	AG04450	lung:	n/a	n/a
24	CTCF	chr12:85451044-85451453	MCF-7	breast:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
25	CTCF	chr12:85451283-85451421	NHEK	skin:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
26	CTCF	chr12:85549644-85549848	A549	lung:	n/a	n/a
27	CTCF	chr12:85562317-85562433	GM10248	blood:	n/a	n/a
28	CTCF	chr12:85451240-85451390	GM12871	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
29	CTCF	chr12:85450640-85450790	BJ	skin:	n/a	n/a
30	CTCF	chr12:85451280-85451430	GM06990	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
31	CTCF	chr12:85470269-85471237	SK-N-SH	brain:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
32	CTCF	chr12:85549640-85549790	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:85537065-85537096	GM10266	blood:	n/a	n/a
34	CTCF	chr12:85470521-85470632	GM20000	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
35	CTCF	chr12:85470600-85470750	HVMF	connective:	n/a	n/a
36	CTCF	chr12:85470511-85470654	K562	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
37	CTCF	chr12:85451280-85451430	GM12868	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
38	CTCF	chr12:85470920-85471070	AG04450	lung:	n/a	n/a
39	CTCF	chr12:85470900-85471050	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr12:85470660-85470810	GM12870	blood:	n/a	n/a
41	CTCF	chr12:85550507-85550617	A549	lung:	n/a	chr12:85550533-85550554
42	CTCF	chr12:85549640-85549790	HMEC	breast:	n/a	n/a
43	CTCF	chr12:85451239-85451471	Lung_OC	lung:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
44	CTCF	chr12:85549540-85549690	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr12:85470440-85470590	HAc	cerebellar:	n/a	chr12:85470580-85470588
46	CTCF	chr12:85470403-85470706	A549	lung:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
47	CTCF	chr12:85549660-85549810	NB4	blood:	n/a	n/a
48	CTCF	chr12:85550499-85550627	MCF-7	breast:	n/a	chr12:85550533-85550554
49	CTCF	chr12:85451260-85451410	HPF	lung:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
50	CTCF	chr12:85470520-85470670	HRE	kidney:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85430029-85430079	AG09309	skin:	n/a
2	chr12:85430145-85430195	K562	blood:	n/a
3	chr12:85430174-85430224	HUVEC	blood vessel:	n/a
4	chr12:85473162-85473212	ProgFib	skin:	n/a
5	chr12:85430145-85430195	MCF10A-Er-Src	breast:	n/a
6	chr12:85430250-85430300	HRE	kidney:	n/a
7	chr12:85430336-85430386	AG09309	skin:	n/a
8	chr12:85430123-85430173	BJ	skin:	n/a
9	chr12:85430174-85430224	T-47D	breast:	n/a
10	chr12:85430123-85430173	K562	blood:	n/a
11	chr12:85430145-85430195	HL-60	blood:	n/a
12	chr12:85430250-85430300	AG04449	skin:	fetal
13	chr12:85430336-85430386	HMEC	breast:	n/a
14	chr12:85430123-85430173	HAEpiC	amniotic membrane:	n/a
15	chr12:85430192-85430242	HCT-116	colon:	n/a
16	chr12:85430123-85430173	IMR90	lung:	fetal
17	chr12:85430192-85430242	GM12891	blood:	n/a
18	chr12:85430336-85430386	CMK	blood:	n/a
19	chr12:85430123-85430173	HIPEpiC	eye:	n/a
20	chr12:85430029-85430079	AoSMC	blood vessel:	n/a
21	chr12:85430215-85430265	HRPEpiC	eye:	n/a
22	chr12:85430029-85430079	IMR90	lung:	fetal
23	chr12:85430085-85430135	NHBE	bronchial:	n/a
24	chr12:85430145-85430195	HCF	heart:	n/a
25	chr12:85430123-85430173	AG04450	lung:	fetal
26	chr12:85430085-85430135	Caco-2	colon:	n/a
27	chr12:85430174-85430224	NH-A	brain:	n/a
28	chr12:85430025-85430075	HRPEpiC	eye:	n/a
29	chr12:85430174-85430224	HIPEpiC	eye:	n/a
30	chr12:85430025-85430075	U87	brain:	n/a
31	chr12:85430145-85430195	U87	brain:	n/a
32	chr12:85430025-85430075	AG10803	skin:	n/a
33	chr12:85430336-85430386	HEK293	kidney:	embryo
34	chr12:85430215-85430265	BE2_C	brain:	n/a
35	chr12:85430123-85430173	HUVEC	blood vessel:	n/a
36	chr12:85430192-85430242	NB4	blood:	n/a
37	chr12:85430145-85430195	BJ	skin:	n/a
38	chr12:85430215-85430265	IMR90	lung:	fetal
39	chr12:85430336-85430386	PrEC	prostate:	n/a
40	chr12:85430336-85430386	H1-hESC	embryonic stem cell:	embryo
41	chr12:85430123-85430173	HL-60	blood:	n/a
42	chr12:85430025-85430075	GM12878	blood:	n/a
43	chr12:85430085-85430135	AG09309	skin:	n/a
44	chr12:85473162-85473212	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:85430025-85430075	GM12892	blood:	n/a
46	chr12:85430085-85430135	H1-hESC	embryonic stem cell:	embryo
47	chr12:85430215-85430265	H1-hESC	embryonic stem cell:	embryo
48	chr12:85430336-85430386	SK-N-SH	brain:	n/a
49	chr12:85430123-85430173	NHBE	bronchial:	n/a
50	chr12:85473162-85473212	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85454595..85457151-chr12:85457581..85459222,2	MCF-7	breast:
2	chr12:85496315..85499030-chr12:85506456..85509353,2	K562	blood:
3	chr12:85625880..85629090-chr12:85630770..85633051,3	K562	blood:
4	chr12:85268014..85268964-chr12:85450937..85451485,2	MCF-7	breast:
5	chr12:85549530..85550247-chr12:86266080..86266618,2	MCF-7	breast:
6	chr12:85269198..85269791-chr12:85451134..85451813,2	MCF-7	breast:
7	chr12:85550574..85552513-chr12:85557330..85559057,2	MCF-7	breast:
8	chr12:85549387..85549978-chr12:85835659..85836204,2	MCF-7	breast:
9	chr12:85469399..85472134-chr9:139733502..139735289,2	MCF-7	breast:
10	chr12:85500330..85501960-chr12:85504219..85505982,2	K562	blood:
11	chr12:85549075..85550214-chr12:85841829..85842800,6	MCF-7	breast:
12	chr12:85470147..85471061-chr12:85788737..85789303,2	MCF-7	breast:
13	chr12:85500330..85501960-chr12:85504219..85505982,2	K562	blood:
14	chr12:85496315..85499030-chr12:85506456..85509353,2	K562	blood:
15	chr12:85470175..85471007-chr12:86313905..86314467,2	MCF-7	breast:
16	chr12:85535998..85538330-chr12:85580098..85581911,2	K562	blood:
17	chr12:85454595..85457151-chr12:85457581..85459222,2	MCF-7	breast:
18	chr12:85470481..85471011-chr12:86260831..86261575,2	MCF-7	breast:
19	chr12:85268266..85268773-chr12:85451270..85451782,2	MCF-7	breast:
20	chr12:85550574..85552513-chr12:85557330..85559057,2	MCF-7	breast:
21	chr12:85470092..85470900-chr12:85818409..85819385,3	MCF-7	breast:
22	chr12:85535998..85538330-chr12:85580098..85581911,2	K562	blood:

Variant related genes	Relation type
LRRIQ1	TF binding region
TSPAN19	TF binding region
LRRIQ1	CpG island
TSPAN19	CpG island
ENSG00000072041	chromatin interactions

Extended variants
information (count: 2179 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2179 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10506910	chr12:85427691-85427692	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145965060	chr12:85427710-85427711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547098011	chr12:85427725-85427726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565399165	chr12:85427726-85427727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs117764997	chr12:85427797-85427798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547857462	chr12:85427818-85427819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569971158	chr12:85427826-85427827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536939336	chr12:85427855-85427856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558765686	chr12:85427881-85427882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138702676	chr12:85427888-85427889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191576764	chr12:85427906-85427907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116820581	chr12:85427907-85427908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554323944	chr12:85427938-85427939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572545734	chr12:85427953-85427954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543078362	chr12:85427969-85427970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79319505	chr12:85427985-85427986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576719439	chr12:85428011-85428012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562098841	chr12:85428032-85428033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184001796	chr12:85428039-85428040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565530809	chr12:85428049-85428050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141769365	chr12:85428122-85428123	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs547553973	chr12:85428126-85428127	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs559048161	chr12:85428152-85428153	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs150762274	chr12:85428162-85428163	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs542100483	chr12:85428204-85428205	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs548212339	chr12:85428256-85428257	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs569548494	chr12:85428274-85428275	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs529348363	chr12:85428279-85428280	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs369200199	chr12:85428280-85428281	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs13377881	chr12:85428374-85428375	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs377730591	chr12:85428380-85428381	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs552197978	chr12:85428393-85428394	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs139204755	chr12:85428394-85428395	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs527705666	chr12:85428440-85428441	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs534834124	chr12:85428482-85428483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1144678	chr12:85428628-85428629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541370110	chr12:85428888-85428889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564433064	chr12:85428893-85428894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560095090	chr12:85428936-85428937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553183298	chr12:85428973-85428974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572613028	chr12:85428999-85429000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149945044	chr12:85429002-85429003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200849758	chr12:85429025-85429026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572468790	chr12:85429047-85429048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554999268	chr12:85429094-85429095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533458010	chr12:85429109-85429110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76165724	chr12:85429124-85429125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543762430	chr12:85429175-85429176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570428553	chr12:85429181-85429182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577096969	chr12:85429199-85429200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85424400-85429600	Weak transcription	Hela-S3	cervix
2	chr12:85425400-85429600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:85427400-85429600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:85429400-85430600	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr12:85429600-85429800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:85429600-85429800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:85429600-85429800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr12:85429600-85429800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:85429600-85429800	Flanking Active TSS	Fetal Brain Male	brain
10	chr12:85429600-85429800	Enhancers	Rectal Smooth Muscle	rectum
11	chr12:85429600-85430000	Active TSS	Right Atrium	heart
12	chr12:85429600-85430000	Enhancers	Stomach Mucosa	stomach
13	chr12:85429600-85430600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr12:85429600-85430600	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr12:85429600-85430600	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr12:85429600-85430600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr12:85429600-85430600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:85429600-85430600	Active TSS	Brain Anterior Caudate	brain
19	chr12:85429600-85430600	Active TSS	Fetal Brain Female	brain
20	chr12:85429600-85430600	Active TSS	Fetal Kidney	kidney
21	chr12:85429600-85430600	Active TSS	Hela-S3	cervix
22	chr12:85429600-85430600	Active TSS	NH-A	brain
23	chr12:85429600-85430600	Active TSS	NHDF-Ad	bronchial
24	chr12:85429600-85430800	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr12:85429600-85430800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:85429600-85430800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:85429600-85430800	Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr12:85429600-85430800	Active TSS	Brain Angular Gyrus	brain
29	chr12:85429600-85430800	Active TSS	Brain Cingulate Gyrus	brain
30	chr12:85429600-85430800	Active TSS	Brain Hippocampus Middle	brain
31	chr12:85429600-85430800	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr12:85429600-85430800	Active TSS	Brain Substantia Nigra	brain
33	chr12:85429600-85430800	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr12:85429600-85430800	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr12:85429600-85430800	Active TSS	Stomach Smooth Muscle	stomach
36	chr12:85429600-85430800	Active TSS	A549	lung
37	chr12:85429600-85430800	Active TSS	HMEC	breast
38	chr12:85429600-85431000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:85429600-85431000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr12:85429600-85431000	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr12:85429800-85430000	Enhancers	Primary B cells from peripheral blood	blood
42	chr12:85429800-85430000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr12:85429800-85430000	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
44	chr12:85429800-85430000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
45	chr12:85429800-85430000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:85429800-85430000	Active TSS	Fetal Muscle Trunk	muscle
47	chr12:85429800-85430000	Enhancers	Placenta	Placenta
48	chr12:85429800-85430000	Active TSS	Fetal Stomach	stomach
49	chr12:85429800-85430000	Active TSS	Rectal Mucosa Donor 31	rectum
50	chr12:85429800-85430000	Active TSS	Skeletal Muscle Female	skeletal muscle

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