Variant report

Variant	nsv559557
Chromosome Location	chr12:83334204-83453620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:702)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:83409707-83410354	K562	blood:	n/a	n/a
2	ARID3A	chr12:83398443-83398586	K562	blood:	n/a	n/a
3	ARID3A	chr12:83413340-83413383	K562	blood:	n/a	n/a
4	ARID3A	chr12:83446120-83447651	K562	blood:	n/a	n/a
5	ATF1	chr12:83409890-83410267	K562	blood:	n/a	n/a
6	ATF3	chr12:83410012-83410345	K562	blood:	n/a	n/a
7	BACH1	chr12:83409673-83410314	K562	blood:	n/a	n/a
8	BACH1	chr12:83358454-83358480	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:83390166-83390478	GM12878	blood:	n/a	n/a
10	BATF	chr12:83336816-83337031	GM12878	blood:	n/a	chr12:83336939-83336950
11	BATF	chr12:83353717-83353948	GM12878	blood:	n/a	n/a
12	BATF	chr12:83390229-83390442	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:83390132-83390497	GM12878	blood:	n/a	chr12:83390379-83390388 chr12:83390380-83390389
14	BCL3	chr12:83390244-83390523	GM12878	blood:	n/a	chr12:83390379-83390388 chr12:83390380-83390389
15	BHLHE40	chr12:83346748-83347174	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:83409167-83410333	K562	blood:	n/a	n/a
17	CBX3	chr12:83404224-83404502	K562	blood:	n/a	n/a
18	CBX3	chr12:83409364-83410378	K562	blood:	n/a	chr12:83409365-83409376
19	CBX3	chr12:83398517-83398829	K562	blood:	n/a	n/a
20	CBX3	chr12:83404126-83404531	HCT-116	colon:	n/a	n/a
21	CBX3	chr12:83404132-83404575	K562	blood:	n/a	n/a
22	CBX3	chr12:83404125-83404631	HCT-116	colon:	n/a	n/a
23	CCNT2	chr12:83446672-83447166	K562	blood:	n/a	chr12:83446846-83446866
24	CEBPB	chr12:83360156-83360339	H1-hESC	embryonic stem cell:	n/a	chr12:83360195-83360212 chr12:83360196-83360209
25	CEBPB	chr12:83374978-83375251	A549	lung:	n/a	chr12:83375100-83375111 chr12:83374988-83375001
26	CEBPB	chr12:83409690-83410375	K562	blood:	n/a	n/a
27	CEBPB	chr12:83421175-83421409	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:83450162-83450166	K562	blood:	n/a	n/a
29	CEBPB	chr12:83409835-83410602	HCT-116	colon:	n/a	n/a
30	CEBPB	chr12:83358952-83359152	K562	blood:	n/a	n/a
31	CEBPB	chr12:83408928-83409231	K562	blood:	n/a	n/a
32	CEBPB	chr12:83437540-83437749	HepG2	liver:	n/a	chr12:83437684-83437697 chr12:83437643-83437654 chr12:83437643-83437656
33	CEBPB	chr12:83421172-83421490	A549	lung:	n/a	n/a
34	CEBPB	chr12:83374950-83375260	HepG2	liver:	n/a	chr12:83375100-83375111 chr12:83374988-83375001
35	CEBPB	chr12:83390558-83390906	Hela-S3	cervix:	n/a	chr12:83390848-83390859
36	CEBPB	chr12:83409529-83410360	K562	blood:	n/a	n/a
37	CEBPB	chr12:83362448-83362714	K562	blood:	n/a	chr12:83362592-83362603
38	CEBPB	chr12:83425252-83425259	A549	lung:	n/a	n/a
39	CEBPB	chr12:83374924-83375261	IMR90	lung:	n/a	chr12:83375100-83375111 chr12:83374988-83375001
40	CEBPB	chr12:83409470-83410432	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:83442400-83442578	K562	blood:	n/a	n/a
42	CEBPB	chr12:83421206-83421358	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr12:83409818-83410473	HCT-116	colon:	n/a	n/a
44	CEBPB	chr12:83362563-83362638	A549	lung:	n/a	chr12:83362592-83362603
45	CEBPD	chr12:83446751-83447380	K562	blood:	n/a	n/a
46	CHD2	chr12:83346908-83346912	GM12878	blood:	n/a	n/a
47	CHD2	chr12:83390339-83390366	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr12:83446963-83447427	K562	blood:	n/a	chr12:83447282-83447292
49	CTCF	chr12:83398504-83398735	Fibrobl	skin:	n/a	n/a
50	CTCF	chr12:83398540-83398690	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:83436797-83436847	PANC-1	pancreas:	n/a
2	chr12:83436797-83436847	HMEC	breast:	n/a
3	chr12:83436797-83436847	NHBE	bronchial:	n/a
4	chr12:83436797-83436847	K562	blood:	n/a
5	chr12:83436797-83436847	AoSMC	blood vessel:	n/a
6	chr12:83436797-83436847	HRCEpiC	kidney:	n/a
7	chr12:83436797-83436847	AG09309	skin:	n/a
8	chr12:83436797-83436847	AG04450	lung:	fetal
9	chr12:83436797-83436847	NB4	blood:	n/a
10	chr12:83436797-83436847	SK-N-MC	brain:	n/a
11	chr12:83436797-83436847	NH-A	brain:	n/a
12	chr12:83436797-83436847	HNPCEpiC	eye:	n/a
13	chr12:83436797-83436847	GM06990	blood:	n/a
14	chr12:83436797-83436847	GM19239	blood:	n/a
15	chr12:83436797-83436847	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:83436797-83436847	A549	lung:	n/a
17	chr12:83436797-83436847	HCF	heart:	n/a
18	chr12:83436797-83436847	Caco-2	colon:	n/a
19	chr12:83436797-83436847	GM12892	blood:	n/a
20	chr12:83436797-83436847	SKMC	muscle:	n/a
21	chr12:83436797-83436847	AG09319	gingival:	n/a
22	chr12:83436797-83436847	ovcar-3	ovarian:	n/a
23	chr12:83436797-83436847	HCPEpiC	choroid plexus:	n/a
24	chr12:83436797-83436847	T-47D	breast:	n/a
25	chr12:83436797-83436847	PFSK-1	brain:	n/a
26	chr12:83436797-83436847	HEEpiC	esophagus:	n/a
27	chr12:83436797-83436847	RPTEC	kidney:	n/a
28	chr12:83436797-83436847	NHDF-neo	bronchial:	n/a
29	chr12:83436797-83436847	HIPEpiC	eye:	n/a
30	chr12:83436797-83436847	PrEC	prostate:	n/a
31	chr12:83436797-83436847	CMK	blood:	n/a
32	chr12:83436797-83436847	HRPEpiC	eye:	n/a
33	chr12:83436797-83436847	Jurkat	blood:	n/a
34	chr12:83436797-83436847	ECC-1	luminal epithelium:	n/a
35	chr12:83436797-83436847	GM12878	blood:	n/a
36	chr12:83436797-83436847	SK-N-SH	brain:	n/a
37	chr12:83436797-83436847	HL-60	blood:	n/a
38	chr12:83436797-83436847	SAEC	small airway:	n/a
39	chr12:83436797-83436847	Hela-S3	cervix:	n/a
40	chr12:83436797-83436847	GM12891	blood:	n/a
41	chr12:83436797-83436847	BE2_C	brain:	n/a
42	chr12:83436797-83436847	H1-hESC	embryonic stem cell:	embryo
43	chr12:83436797-83436847	SK-N-SH_RA	brain:	n/a
44	chr12:83436797-83436847	MCF-7	breast:	n/a
45	chr12:83436797-83436847	HCT-116	colon:	n/a
46	chr12:83436797-83436847	HUVEC	blood vessel:	n/a
47	chr12:83436797-83436847	AG04449	skin:	fetal
48	chr12:83436797-83436847	AG10803	skin:	n/a
49	chr12:83436797-83436847	NT2-D1	testis:	n/a
50	chr12:83436797-83436847	IMR90	lung:	fetal

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:83079612..83081545-chr12:83368950..83370563,2	MCF-7	breast:
2	chr12:83443025..83445340-chr12:83453373..83455462,2	K562	blood:
3	chr12:83079421..83081926-chr12:83392730..83394368,2	MCF-7	breast:
4	chr12:83449205..83451472-chr12:83544040..83546509,2	K562	blood:
5	chr12:83449205..83452014-chr12:83544235..83546509,2	K562	blood:
6	chr12:83369189..83370820-chr12:83374868..83377615,2	MCF-7	breast:
7	chr12:83077655..83080172-chr12:83389847..83391869,2	MCF-7	breast:
8	chr12:83409479..83411224-chr12:83411247..83412794,2	K562	blood:
9	chr12:83435873..83438111-chr12:83445616..83447681,2	K562	blood:
10	chr12:83422630..83425371-chr12:83427227..83429667,2	K562	blood:
11	chr12:83404495..83407121-chr12:83413024..83415262,2	K562	blood:
12	chr12:83409329..83411312-chr12:83542800..83545681,4	K562	blood:
13	chr12:83376935..83379411-chr12:83411296..83413142,2	MCF-7	breast:
14	chr12:83376935..83379411-chr12:83411296..83413142,2	MCF-7	breast:
15	chr12:83422630..83425371-chr12:83427227..83429667,2	K562	blood:
16	chr12:83342058..83344006-chr12:83365931..83367769,2	MCF-7	breast:
17	chr12:83366836..83369224-chr12:84561366..84563438,2	MCF-7	breast:
18	chr12:83369189..83370820-chr12:83374868..83377615,2	MCF-7	breast:
19	chr12:83432652..83435598-chr12:83445768..83447475,2	K562	blood:
20	chr12:83410459..83412121-chr12:83415029..83417883,2	K562	blood:
21	chr12:83415930..83418702-chr12:83439696..83442546,2	K562	blood:
22	chr12:83341035..83343546-chr12:83347635..83350159,2	MCF-7	breast:
23	chr12:83443059..83446999-chr12:83447575..83450330,4	K562	blood:
24	chr12:83409479..83411224-chr12:83411247..83412794,2	K562	blood:
25	chr12:83078910..83080496-chr12:83405630..83407973,2	MCF-7	breast:
26	chr12:83396959..83399926-chr12:83808616..83810997,2	K562	blood:
27	chr12:83364622..83366289-chr12:83368200..83369793,2	K562	blood:
28	chr12:83079062..83081890-chr12:83395657..83398475,2	MCF-7	breast:
29	chr12:83423270..83425882-chr12:83433860..83436720,2	K562	blood:
30	chr12:83432652..83435598-chr12:83445768..83447475,2	K562	blood:
31	chr12:83079605..83080356-chr12:83398378..83399038,2	MCF-7	breast:
32	chr12:83404495..83407121-chr12:83413024..83415262,2	K562	blood:
33	chr12:83342058..83344006-chr12:83365931..83367769,2	MCF-7	breast:
34	chr12:83453334..83457247-chr12:83458920..83461547,4	K562	blood:
35	chr12:83436175..83438871-chr14:91881648..91884275,2	MCF-7	breast:
36	chr12:83364622..83366289-chr12:83368200..83369793,2	K562	blood:
37	chr12:83415930..83418702-chr12:83439696..83442546,2	K562	blood:
38	chr12:83398128..83399066-chr12:83782720..83783715,3	K562	blood:
39	chr12:83423270..83425882-chr12:83433860..83436720,2	K562	blood:
40	chr12:83079278..83081926-chr12:83348191..83350037,2	MCF-7	breast:
41	chr12:83443025..83445340-chr12:83453373..83455462,2	K562	blood:
42	chr12:83443059..83446999-chr12:83447575..83450330,4	K562	blood:
43	chr12:83341035..83343546-chr12:83347635..83350159,2	MCF-7	breast:
44	chr12:83448097..83450387-chr12:83473090..83475396,2	K562	blood:
45	chr12:83331086..83333520-chr12:83336090..83338497,2	MCF-7	breast:
46	chr12:83435873..83438111-chr12:83445616..83447681,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-977P	TF binding region
RNU6-977P	CpG island
ENSG00000252220	chromatin interactions
ENSG00000015133	chromatin interactions
ENSG00000179104	chromatin interactions
ENSG00000213270	chromatin interactions

Extended variants
information (count: 4807 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4807 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1796156	chr12:83334204-83334205	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560969896	chr12:83334229-83334230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12833489	chr12:83334230-83334231	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs76659463	chr12:83334250-83334251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73157650	chr12:83334271-83334272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs373370644	chr12:83334297-83334298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555970762	chr12:83334320-83334321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574140772	chr12:83334354-83334355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539668624	chr12:83334376-83334377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11115495	chr12:83334461-83334462	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs566947669	chr12:83334517-83334518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11380001	chr12:83334537-83334538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs398116680	chr12:83334545-83334546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566598780	chr12:83334575-83334576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35573775	chr12:83334582-83334583	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs555365348	chr12:83334691-83334692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190915448	chr12:83334719-83334720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182720981	chr12:83334732-83334733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149173258	chr12:83334746-83334747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185632283	chr12:83334805-83334806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545617990	chr12:83334811-83334812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560360736	chr12:83334830-83334831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11115496	chr12:83334862-83334863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371399609	chr12:83334889-83334890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75902659	chr12:83334909-83334910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531601758	chr12:83334926-83334927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550460847	chr12:83334927-83334928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562844311	chr12:83334944-83334945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532970720	chr12:83334966-83334967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs117636517	chr12:83334974-83334975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142357604	chr12:83334978-83334979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151292860	chr12:83334987-83334988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549101097	chr12:83334997-83334998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567265661	chr12:83335007-83335008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537880187	chr12:83335026-83335027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140552557	chr12:83335050-83335051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546825381	chr12:83335062-83335063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147103338	chr12:83335132-83335133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375268893	chr12:83335179-83335180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373447929	chr12:83335189-83335190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543142596	chr12:83335209-83335210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535265446	chr12:83335212-83335213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116175725	chr12:83335229-83335230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542666308	chr12:83335253-83335254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561094271	chr12:83335254-83335255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114648912	chr12:83335265-83335266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561952857	chr12:83335277-83335278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543448270	chr12:83335285-83335286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562621724	chr12:83335300-83335301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533229544	chr12:83335309-83335310	Weak transcription	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
Neurodevelopmental disorder	22521361	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
Breast cancer	21785460	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
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD

Chromatin state (count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83279000-83336400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr12:83305800-83336800	Weak transcription	Fetal Stomach	stomach
3	chr12:83307800-83336800	Weak transcription	Fetal Lung	lung
4	chr12:83323600-83334400	Weak transcription	Fetal Heart	heart
5	chr12:83324800-83336800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:83325000-83346400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:83325600-83348000	Weak transcription	Colon Smooth Muscle	Colon
8	chr12:83325800-83336800	Weak transcription	Brain Substantia Nigra	brain
9	chr12:83326000-83340200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr12:83328000-83334400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr12:83329000-83336400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:83331200-83336400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:83331400-83336800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr12:83331400-83348000	Weak transcription	Brain Hippocampus Middle	brain
15	chr12:83332400-83336400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr12:83334000-83335200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr12:83334400-83334800	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr12:83334400-83335200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr12:83334400-83335200	Enhancers	Fetal Heart	heart
20	chr12:83335200-83336800	Weak transcription	Fetal Heart	heart
21	chr12:83335200-83340200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr12:83336200-83337200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:83336400-83337000	Enhancers	Placenta Amnion	Placenta Amnion
24	chr12:83336400-83337200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:83336400-83337200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:83336400-83337200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr12:83336400-83338600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:83336600-83337000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr12:83336600-83337200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr12:83336800-83337200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:83336800-83337200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr12:83336800-83337200	Enhancers	Brain Anterior Caudate	brain
33	chr12:83336800-83337200	Enhancers	Brain Substantia Nigra	brain
34	chr12:83336800-83337200	Enhancers	Fetal Lung	lung
35	chr12:83336800-83337200	Enhancers	Fetal Stomach	stomach
36	chr12:83336800-83337400	Enhancers	Rectal Smooth Muscle	rectum
37	chr12:83336800-83337800	Enhancers	Fetal Heart	heart
38	chr12:83338600-83340000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:83340000-83340400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr12:83340200-83340400	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr12:83340200-83340800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
42	chr12:83340400-83348200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:83340800-83348400	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr12:83341800-83342000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:83342000-83352600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:83342800-83343200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr12:83343200-83343600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr12:83343600-83343800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr12:83343800-83346400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr12:83343800-83347600	Weak transcription	Brain Substantia Nigra	brain

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