Variant report

Variant	nsv1046514
Chromosome Location	chr12:554091-633417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1052)
CpG islands
(count:1405)
Chromatin interactive
region (count:77)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1052 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:597161-597361	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:597107-597347	K562	blood:	n/a	n/a
3	ATF1	chr12:596988-597372	K562	blood:	n/a	n/a
4	ATF3	chr12:562458-562788	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr12:562477-562737	GM12878	blood:	n/a	n/a
6	BACH1	chr12:562530-562764	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:569939-570255	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:562151-562738	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:562203-562719	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:562080-562805	GM12878	blood:	n/a	n/a
11	BCL3	chr12:596925-597490	A549	lung:	n/a	n/a
12	BCL3	chr12:596868-597484	A549	lung:	n/a	n/a
13	BHLHE40	chr12:593358-593595	K562	blood:	n/a	chr12:593518-593527 chr12:593518-593527
14	BHLHE40	chr12:568683-568808	K562	blood:	n/a	n/a
15	BHLHE40	chr12:562200-562747	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:588389-588670	K562	blood:	n/a	n/a
17	BHLHE40	chr12:570572-570903	HepG2	liver:	n/a	n/a
18	BHLHE40	chr12:559708-559969	K562	blood:	n/a	n/a
19	BHLHE40	chr12:632323-632391	HepG2	liver:	n/a	n/a
20	BHLHE40	chr12:597146-597299	K562	blood:	n/a	n/a
21	BHLHE40	chr12:593499-593640	GM12878	blood:	n/a	chr12:593518-593527 chr12:593518-593527
22	BRCA1	chr12:597261-597370	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr12:562047-562747	K562	blood:	n/a	n/a
24	CBX3	chr12:561932-562822	K562	blood:	n/a	n/a
25	CEBPB	chr12:568309-568542	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:568214-568497	A549	lung:	n/a	n/a
27	CEBPB	chr12:596933-597254	K562	blood:	n/a	n/a
28	CEBPB	chr12:596925-597353	A549	lung:	n/a	n/a
29	CEBPB	chr12:559882-559914	K562	blood:	n/a	n/a
30	CEBPB	chr12:596867-597386	A549	lung:	n/a	n/a
31	CEBPB	chr12:596959-597290	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:568205-568608	MCF-7	breast:	n/a	n/a
33	CEBPB	chr12:631994-632121	HepG2	liver:	n/a	chr12:632053-632064
34	CEBPB	chr12:562227-562742	K562	blood:	n/a	n/a
35	CEBPB	chr12:590620-590912	HepG2	liver:	n/a	n/a
36	CEBPB	chr12:617359-617732	MCF-7	breast:	n/a	chr12:617501-617512
37	CEBPB	chr12:576926-577203	HepG2	liver:	n/a	chr12:577070-577081
38	CEBPB	chr12:576949-577149	A549	lung:	n/a	chr12:577070-577081
39	CEBPB	chr12:596902-597398	IMR90	lung:	n/a	n/a
40	CEBPB	chr12:617299-618599	ECC-1	luminal epithelium:	n/a	chr12:617501-617512
41	CEBPB	chr12:617379-617657	IMR90	lung:	n/a	chr12:617501-617512
42	CEBPB	chr12:596960-597311	MCF-7	breast:	n/a	n/a
43	CEBPB	chr12:562026-562699	GM12878	blood:	n/a	n/a
44	CEBPB	chr12:617459-617658	H1-hESC	embryonic stem cell:	n/a	chr12:617501-617512
45	CEBPB	chr12:558416-558642	A549	lung:	n/a	n/a
46	CEBPB	chr12:577001-577239	K562	blood:	n/a	chr12:577070-577081
47	CEBPB	chr12:619249-619306	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:617352-617672	HepG2	liver:	n/a	chr12:617501-617512
49	CEBPB	chr12:568253-568483	HepG2	liver:	n/a	n/a
50	CEBPB	chr12:617319-617691	A549	lung:	n/a	chr12:617501-617512

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:562065-562115	GM12892	blood:	n/a
2	chr12:568931-568981	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:562065-562115	GM12892	blood:	n/a
4	chr12:568931-568981	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:569733-569783	ECC-1	luminal epithelium:	n/a
6	chr12:569111-569161	HRE	kidney:	n/a
7	chr12:569733-569783	GM12891	blood:	n/a
8	chr12:630773-630823	HRPEpiC	eye:	n/a
9	chr12:569679-569729	BE2_C	brain:	n/a
10	chr12:562065-562115	HRE	kidney:	n/a
11	chr12:630892-630942	AG10803	skin:	n/a
12	chr12:573270-573320	LNCaP	prostate:	n/a
13	chr12:568931-568981	HRE	kidney:	n/a
14	chr12:566229-566279	HIPEpiC	eye:	n/a
15	chr12:562272-562322	IMR90	lung:	fetal
16	chr12:630773-630823	T-47D	breast:	n/a
17	chr12:562065-562115	AG09309	skin:	n/a
18	chr12:568826-568876	HCF	heart:	n/a
19	chr12:630807-630857	GM12878	blood:	n/a
20	chr12:569221-569271	HAEpiC	amniotic membrane:	n/a
21	chr12:573270-573320	GM12878	blood:	n/a
22	chr12:569733-569783	CMK	blood:	n/a
23	chr12:618772-618822	AG09319	gingival:	n/a
24	chr12:569221-569271	ovcar-3	ovarian:	n/a
25	chr12:562272-562322	AG09319	gingival:	n/a
26	chr12:630892-630942	MCF-7	breast:	n/a
27	chr12:566229-566279	HepG2	liver:	n/a
28	chr12:562065-562115	A549	lung:	n/a
29	chr12:630892-630942	NHBE	bronchial:	n/a
30	chr12:568798-568848	HRCEpiC	kidney:	n/a
31	chr12:630773-630823	AG10803	skin:	n/a
32	chr12:569679-569729	ProgFib	skin:	n/a
33	chr12:562848-562898	PrEC	prostate:	n/a
34	chr12:562848-562898	LNCaP	prostate:	n/a
35	chr12:573270-573320	AG04449	skin:	fetal
36	chr12:630892-630942	HRPEpiC	eye:	n/a
37	chr12:568543-568593	SAEC	small airway:	n/a
38	chr12:570249-570299	LNCaP	prostate:	n/a
39	chr12:570155-570205	GM12891	blood:	n/a
40	chr12:590469-590519	NH-A	brain:	n/a
41	chr12:568826-568876	HRE	kidney:	n/a
42	chr12:630807-630857	SAEC	small airway:	n/a
43	chr12:570249-570299	K562	blood:	n/a
44	chr12:564731-564781	PANC-1	pancreas:	n/a
45	chr12:569111-569161	HRCEpiC	kidney:	n/a
46	chr12:569679-569729	PFSK-1	brain:	n/a
47	chr12:618772-618822	PFSK-1	brain:	n/a
48	chr12:569679-569729	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:618772-618822	SK-N-SH	brain:	n/a
50	chr12:563019-563069	NB4	blood:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:622355..623083-chr12:633209..633927,4	MCF-7	breast:
2	chr12:622362..623146-chr12:632963..633907,2	MCF-7	breast:
3	chr12:558395..561077-chr12:566153..568160,2	K562	blood:
4	chr12:552972..554536-chr12:556070..557992,2	MCF-7	breast:
5	chr12:579325..581351-chr12:586759..589716,2	MCF-7	breast:
6	chr12:618073..620518-chr12:625351..628084,2	MCF-7	breast:
7	chr12:563912..565642-chr12:570833..573151,2	K562	blood:
8	chr12:627385..629195-chr12:632325..634029,2	K562	blood:
9	chr12:565368..565882-chr12:633415..633928,2	MCF-7	breast:
10	chr12:561777..563247-chr12:653593..656972,77	MCF-7	breast:
11	chr12:568218..570488-chr12:587646..590152,3	K562	blood:
12	chr12:562235..562796-chr12:678736..679457,3	MCF-7	breast:
13	chr12:562076..562781-chr12:1058723..1059610,2	K562	blood:
14	chr12:592627..596074-chr12:611199..615537,4	K562	blood:
15	chr12:610332..613763-chr12:616552..619652,4	MCF-7	breast:
16	chr12:563912..565642-chr12:570833..573151,2	K562	blood:
17	chr12:553314..555353-chr12:563794..566581,2	MCF-7	breast:
18	chr12:553314..555353-chr12:563794..566581,2	MCF-7	breast:
19	chr12:595976..598882-chr12:613425..615039,3	MCF-7	breast:
20	chr12:622277..623146-chr12:632963..633980,6	MCF-7	breast:
21	chr12:561825..562818-chr12:694443..695023,2	MCF-7	breast:
22	chr12:611154..613945-chr12:632166..635023,2	MCF-7	breast:
23	chr12:562103..563075-chr12:634406..635587,3	MCF-7	breast:
24	chr12:633000..634118-chr12:680824..681736,4	MCF-7	breast:
25	chr12:563329..565508-chr12:567009..569483,2	MCF-7	breast:
26	chr12:626830..629195-chr12:631126..633825,2	K562	blood:
27	chr12:589171..589964-chr12:633097..633983,2	MCF-7	breast:
28	chr12:626830..629195-chr12:631126..633825,2	K562	blood:
29	chr12:610332..613763-chr12:616552..619652,4	MCF-7	breast:
30	chr12:611154..613945-chr12:632166..635023,2	MCF-7	breast:
31	chr12:592281..595019-chr12:599966..602441,2	MCF-7	breast:
32	chr12:562096..563077-chr12:923022..923690,2	MCF-7	breast:
33	chr12:609770..612442-chr12:616470..618259,2	MCF-7	breast:
34	chr12:558395..561077-chr12:566153..568160,2	K562	blood:
35	chr12:618074..619807-chr12:641547..643283,2	MCF-7	breast:
36	chr12:627385..629195-chr12:632325..634029,2	K562	blood:
37	chr12:562216..562824-chr12:680454..681003,2	MCF-7	breast:
38	chr12:559544..561291-chr12:645812..647419,2	K562	blood:
39	chr12:622362..623146-chr12:632963..633907,2	MCF-7	breast:
40	chr12:567792..568717-chr12:633148..633750,3	MCF-7	breast:
41	chr12:595976..598882-chr12:613425..615039,3	MCF-7	breast:
42	chr12:579325..581351-chr12:586759..589716,2	MCF-7	breast:
43	chr12:562112..562967-chr12:655719..656711,9	K562	blood:
44	chr12:589171..589964-chr12:633097..633983,2	MCF-7	breast:
45	chr12:633000..634015-chr12:680744..681736,4	MCF-7	breast:
46	chr12:562294..562804-chr12:608079..608940,2	MCF-7	breast:
47	chr12:562205..562756-chr12:650853..651426,2	MCF-7	breast:
48	chr12:563544..564514-chr12:655825..656615,2	MCF-7	breast:
49	chr12:602358..605293-chr12:611922..614455,2	MCF-7	breast:
50	chr12:631879..633874-chr12:643555..645936,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC77-2	chr12:623386-625305	ucscGeneNc_uc009zdl_1
2	lnc-CCDC77-2	chr12:622408-623144	ucscGeneNc_uc009zdl_1

No data

Variant related genes	Relation type
B4GALNT3	TF binding region
B4GALNT3	CpG island
ENSG00000139044	chromatin interactions
ENSG00000002016	chromatin interactions

Extended variants
information (count: 3522 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3522 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10774192	chr12:554091-554092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139966109	chr12:554121-554122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559423340	chr12:554125-554126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149834896	chr12:554126-554127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187154186	chr12:554133-554134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563150278	chr12:554174-554175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527436662	chr12:554213-554214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111900780	chr12:554245-554246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs59021353	chr12:554258-554259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552235557	chr12:554300-554301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12833509	chr12:554331-554332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs571679078	chr12:554416-554417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538688939	chr12:554468-554469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147928426	chr12:554471-554472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9669448	chr12:554479-554480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11063005	chr12:554492-554493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs192643777	chr12:554502-554503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184767753	chr12:554503-554504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117137043	chr12:554522-554523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61916595	chr12:554548-554549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375561307	chr12:554550-554551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558702052	chr12:554551-554552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60911799	chr12:554564-554565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536947854	chr12:554618-554619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147669346	chr12:554647-554648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540716220	chr12:554657-554658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552924332	chr12:554676-554677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573172871	chr12:554682-554683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149128857	chr12:554689-554690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534059777	chr12:554731-554732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541724118	chr12:554751-554752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530413779	chr12:554763-554764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs60087360	chr12:554811-554812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs77668223	chr12:554884-554885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201685982	chr12:554912-554913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200418475	chr12:554913-554914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187642630	chr12:554914-554915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117557671	chr12:554930-554931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368164843	chr12:554934-554935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369335955	chr12:554984-554985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549885097	chr12:554999-555000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143195863	chr12:555035-555036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139072271	chr12:555056-555057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56062329	chr12:555070-555071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs398018194	chr12:555071-555072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566076536	chr12:555076-555077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530070713	chr12:555090-555091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544014119	chr12:555123-555124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71045061	chr12:555221-555222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs398018195	chr12:555237-555238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Autism	22495309	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1625 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:512200-557800	Weak transcription	Fetal Heart	heart
2	chr12:524400-556800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:526200-557800	Weak transcription	Stomach Mucosa	stomach
4	chr12:528600-560200	Weak transcription	Colonic Mucosa	Colon
5	chr12:528600-562800	Weak transcription	Right Ventricle	heart
6	chr12:532000-554400	Weak transcription	Small Intestine	intestine
7	chr12:532600-555400	Weak transcription	K562	blood
8	chr12:534800-554200	Weak transcription	Esophagus	oesophagus
9	chr12:535000-558000	Weak transcription	Gastric	stomach
10	chr12:542200-559400	Weak transcription	Pancreas	Pancrea
11	chr12:542800-556200	Weak transcription	HSMMtube	muscle
12	chr12:542800-556400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:542800-560200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:544000-562200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr12:545000-562800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr12:545200-555200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr12:545400-560800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr12:546200-559400	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr12:546600-554200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:547600-555000	Weak transcription	Fetal Intestine Large	intestine
21	chr12:547800-556400	Weak transcription	Brain Substantia Nigra	brain
22	chr12:548000-560400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:548000-563000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:548400-561600	Weak transcription	A549	lung
25	chr12:549400-560000	Weak transcription	Fetal Intestine Small	intestine
26	chr12:550200-555000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr12:550200-555000	Weak transcription	Fetal Stomach	stomach
28	chr12:550400-560200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:550600-554200	Weak transcription	Brain Hippocampus Middle	brain
30	chr12:550600-555400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:550800-554400	Weak transcription	NH-A	brain
32	chr12:550800-559400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr12:550800-559400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr12:551200-554600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:551200-554800	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr12:551400-554600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:551400-554600	Weak transcription	Fetal Muscle Leg	muscle
38	chr12:551400-554800	Weak transcription	Primary B cells from cord blood	blood
39	chr12:551400-555000	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr12:551400-563800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr12:551600-554200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr12:551600-554600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr12:551600-559400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr12:551600-559400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr12:551600-561400	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr12:551600-561600	Weak transcription	Primary B cells from peripheral blood	blood
47	chr12:551800-559600	Weak transcription	Brain Germinal Matrix	brain
48	chr12:552000-554200	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr12:552000-554200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr12:552000-560000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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