Variant report

Variant	nsv1040033
Chromosome Location	chr12:20914439-21078855
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	chr12:20961418-20961995	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:20983563-20983814	HepG2	liver:	n/a	n/a
3	ATF1	chr12:20937716-20937850	K562	blood:	n/a	n/a
4	BATF	chr12:21021928-21022137	GM12878	blood:	n/a	chr12:21022019-21022030
5	BCL3	chr12:20983287-20983862	A549	lung:	n/a	n/a
6	BHLHE40	chr12:21017099-21017177	GM12878	blood:	n/a	n/a
7	BRCA1	chr12:20975364-20975513	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr12:20946993-20947034	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:21036286-21036659	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
10	CEBPB	chr12:20983497-20983867	A549	lung:	n/a	chr12:20983711-20983722
11	CEBPB	chr12:21036155-21036832	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
12	CEBPB	chr12:20961462-20961896	HepG2	liver:	n/a	chr12:20961744-20961757
13	CEBPB	chr12:21038089-21038427	A549	lung:	n/a	n/a
14	CEBPB	chr12:20983561-20984147	A549	lung:	n/a	chr12:20983711-20983722
15	CEBPB	chr12:20982312-20982493	IMR90	lung:	n/a	chr12:20982413-20982424
16	CEBPB	chr12:20961440-20961862	HepG2	liver:	n/a	chr12:20961744-20961757
17	CEBPB	chr12:20983601-20983801	Hela-S3	cervix:	n/a	chr12:20983711-20983722
18	CEBPB	chr12:20961578-20961819	HepG2	liver:	n/a	chr12:20961744-20961757
19	CEBPB	chr12:21056070-21056238	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:21036268-21036667	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
21	CEBPB	chr12:20932046-20932199	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:20982284-20982555	A549	lung:	n/a	chr12:20982413-20982424
23	CEBPB	chr12:21036282-21036646	Hela-S3	cervix:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
24	CEBPB	chr12:21036323-21036549	HepG2	liver:	n/a	chr12:21036463-21036474
25	CEBPB	chr12:20915410-20915535	A549	lung:	n/a	n/a
26	CEBPB	chr12:21065012-21065124	HepG2	liver:	n/a	chr12:21065034-21065045
27	CEBPB	chr12:20991943-20992076	A549	lung:	n/a	chr12:20992038-20992049
28	CEBPB	chr12:20975351-20976142	A549	lung:	n/a	n/a
29	CEBPB	chr12:21037942-21038507	A549	lung:	n/a	n/a
30	CEBPB	chr12:20982280-20982503	HepG2	liver:	n/a	chr12:20982413-20982424
31	CEBPB	chr12:21015510-21015751	A549	lung:	n/a	n/a
32	CEBPB	chr12:20991877-20992081	HepG2	liver:	n/a	chr12:20992038-20992049
33	CEBPB	chr12:21038060-21038439	A549	lung:	n/a	n/a
34	CEBPB	chr12:20983420-20984015	A549	lung:	n/a	chr12:20983711-20983722
35	CEBPB	chr12:20983564-20983877	HepG2	liver:	n/a	chr12:20983711-20983722
36	CEBPB	chr12:21071557-21071721	A549	lung:	n/a	n/a
37	CEBPB	chr12:20975368-20976107	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr12:20975360-20975559	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr12:20922240-20922355	Fibrobl	skin:	n/a	n/a
40	CTCF	chr12:20951560-20951710	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr12:20951560-20951710	HEK293	kidney:	n/a	n/a
42	CTCF	chr12:20951640-20951790	WERI-Rb-1	eye:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
43	CTCF	chr12:20951640-20951790	MCF-7	breast:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
44	CTCF	chr12:20951640-20951790	GM06990	blood:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
45	CTCF	chr12:20951488-20951864	H1-hESC	embryonic stem cell:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
46	CTCF	chr12:20951680-20951830	NHDF-neo	bronchial:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
47	CTCF	chr12:20951640-20951775	Kidney_OC	kidney:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
48	CTCF	chr12:20951580-20951730	HepG2	liver:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
49	CTCF	chr12:21065523-21065625	Lung_OC	lung:	n/a	n/a
50	CTCF	chr12:21009590-21009613	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21015340-21015390	CMK	blood:	n/a
2	chr12:20966524-20966574	GM06990	blood:	n/a
3	chr12:20935799-20935849	SAEC	small airway:	n/a
4	chr12:21014317-21014367	HAEpiC	amniotic membrane:	n/a
5	chr12:20935799-20935849	SK-N-SH_RA	brain:	n/a
6	chr12:20966439-20966489	NB4	blood:	n/a
7	chr12:20960409-20960459	SK-N-SH	brain:	n/a
8	chr12:20966524-20966574	CMK	blood:	n/a
9	chr12:20966524-20966574	HEK293	kidney:	embryo
10	chr12:20962423-20962473	HEEpiC	esophagus:	n/a
11	chr12:20935754-20935804	HCPEpiC	choroid plexus:	n/a
12	chr12:20960446-20960496	ECC-1	luminal epithelium:	n/a
13	chr12:20983111-20983161	NH-A	brain:	n/a
14	chr12:21015340-21015390	SKMC	muscle:	n/a
15	chr12:20966524-20966574	HepG2	liver:	n/a
16	chr12:20983111-20983161	H1-hESC	embryonic stem cell:	embryo
17	chr12:20935811-20935861	HEEpiC	esophagus:	n/a
18	chr12:20960409-20960459	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:20935811-20935861	MCF-7	breast:	n/a
20	chr12:20960409-20960459	HCT-116	colon:	n/a
21	chr12:20960446-20960496	HMEC	breast:	n/a
22	chr12:20983111-20983161	LNCaP	prostate:	n/a
23	chr12:20983111-20983161	GM12892	blood:	n/a
24	chr12:20962423-20962473	AG04450	lung:	fetal
25	chr12:20960446-20960496	HRE	kidney:	n/a
26	chr12:20966439-20966489	NHBE	bronchial:	n/a
27	chr12:21014317-21014367	NHBE	bronchial:	n/a
28	chr12:20935799-20935849	HL-60	blood:	n/a
29	chr12:20935754-20935804	Hepatocyte	liver:	n/a
30	chr12:20935811-20935861	PFSK-1	brain:	n/a
31	chr12:20962423-20962473	U87	brain:	n/a
32	chr12:20966524-20966574	HCF	heart:	n/a
33	chr12:20935799-20935849	MCF10A-Er-Src	breast:	n/a
34	chr12:21014317-21014367	MCF10A-Er-Src	breast:	n/a
35	chr12:20960446-20960496	HL-60	blood:	n/a
36	chr12:20966524-20966574	PrEC	prostate:	n/a
37	chr12:20935799-20935849	GM12892	blood:	n/a
38	chr12:20966439-20966489	T-47D	breast:	n/a
39	chr12:20983111-20983161	BE2_C	brain:	n/a
40	chr12:21014317-21014367	NH-A	brain:	n/a
41	chr12:20960446-20960496	HIPEpiC	eye:	n/a
42	chr12:21015340-21015390	AG09319	gingival:	n/a
43	chr12:21014317-21014367	H1-hESC	embryonic stem cell:	embryo
44	chr12:20960446-20960496	AG09309	skin:	n/a
45	chr12:20983111-20983161	HIPEpiC	eye:	n/a
46	chr12:21015340-21015390	HL-60	blood:	n/a
47	chr12:20960409-20960459	HIPEpiC	eye:	n/a
48	chr12:20935799-20935849	GM19239	blood:	n/a
49	chr12:21014317-21014367	NHDF-neo	bronchial:	n/a
50	chr12:21014317-21014367	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:20639028..20639571-chr12:20951385..20952022,2	MCF-7	breast:
2	chr12:20798899..20799416-chr12:20951641..20952181,2	MCF-7	breast:
3	chr12:20798864..20799798-chr12:20951213..20952118,4	MCF-7	breast:

Variant related genes	Relation type
SLCO1B3	TF binding region
ENSG00000256157	TF binding region
ENSG00000257046	TF binding region
SLCO1B7	TF binding region
SLCO1B3	CpG island
ENSG00000256157	CpG island
ENSG00000257046	CpG island
SLCO1B7	CpG island

Extended variants
information (count: 7325 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:7325 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142774544	chr12:20914482-20914483	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533042210	chr12:20914504-20914505	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11045448	chr12:20914516-20914517	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs147404678	chr12:20914517-20914518	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528802126	chr12:20914588-20914589	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139160854	chr12:20914595-20914596	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535266280	chr12:20914596-20914597	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555082018	chr12:20914603-20914604	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs80263416	chr12:20914648-20914649	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534634408	chr12:20914675-20914676	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2090276	chr12:20914741-20914742	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs578204440	chr12:20914743-20914744	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77940834	chr12:20914744-20914745	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573289380	chr12:20914766-20914767	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557685523	chr12:20914802-20914803	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370885668	chr12:20914833-20914834	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2090275	chr12:20914883-20914884	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs112347390	chr12:20914905-20914906	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112460611	chr12:20914927-20914928	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559917845	chr12:20914947-20914948	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11045449	chr12:20914970-20914971	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545398710	chr12:20914982-20914983	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565089939	chr12:20914999-20915000	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11045450	chr12:20915000-20915001	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs10841618	chr12:20915065-20915066	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188251108	chr12:20915087-20915088	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192960023	chr12:20915095-20915096	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2090274	chr12:20915109-20915110	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs35040053	chr12:20915114-20915115	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565784161	chr12:20915137-20915138	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145104415	chr12:20915222-20915223	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148500072	chr12:20915240-20915241	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571203029	chr12:20915244-20915245	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372767463	chr12:20915267-20915268	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs955774	chr12:20915295-20915296	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs957164	chr12:20915299-20915300	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs35710865	chr12:20915421-20915422	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183125619	chr12:20915434-20915435	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536862266	chr12:20915435-20915436	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553567318	chr12:20915438-20915439	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113005343	chr12:20915451-20915452	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144204150	chr12:20915452-20915453	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs3938136	chr12:20915501-20915502	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545123101	chr12:20915514-20915515	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565374921	chr12:20915524-20915525	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372068424	chr12:20915537-20915538	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544184622	chr12:20915539-20915540	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538238669	chr12:20915543-20915544	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563271556	chr12:20915602-20915603	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7488626	chr12:20915617-20915618	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20892800-20922200	Weak transcription	Aorta	Aorta
2	chr12:20913200-20917000	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr12:20913600-20915800	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr12:20914400-20915800	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr12:20916600-20917400	Active TSS	H9 Cell Line	embryonic stem cell
6	chr12:20917000-20922200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr12:20917400-20921800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:20919000-20919200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr12:20919200-20922200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr12:20920600-20921000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:20921000-20921400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:20921000-20921600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr12:20921400-20922400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:20921600-20922400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr12:20921800-20922200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:20921800-20922200	Weak transcription	Adipose Nuclei	Adipose
17	chr12:20921800-20922400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr12:20922000-20922400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr12:20922200-20922400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
20	chr12:20922200-20922400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr12:20922200-20922400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:20922200-20922400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:20922200-20922400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:20922200-20922400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:20922200-20922400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr12:20922200-20922400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:20922200-20922400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
28	chr12:20922200-20922400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
29	chr12:20922200-20922400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
30	chr12:20922200-20922400	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:20922200-20922400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:20922200-20922400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr12:20922200-20922400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
34	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
35	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
36	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
37	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
38	chr12:20922200-20922400	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
39	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
40	chr12:20922200-20922400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
41	chr12:20922200-20922400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr12:20922200-20922400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr12:20922200-20922400	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
44	chr12:20922200-20922400	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr12:20922200-20922400	Enhancers	Aorta	Aorta
46	chr12:20922200-20922400	ZNF genes & repeats	Liver	Liver
47	chr12:20922200-20922400	ZNF genes & repeats	Brain Hippocampus Middle	brain
48	chr12:20922200-20922400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
49	chr12:20922200-20922400	ZNF genes & repeats	Colonic Mucosa	Colon
50	chr12:20922200-20922400	ZNF genes & repeats	Colon Smooth Muscle	Colon

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