Variant report

Variant	esv17347
Chromosome Location	chr12:20892854-21029179
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	BRCA1	chr12:20907821-20907893	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:20915410-20915535	A549	lung:	n/a	n/a
11	CEBPB	chr12:20961578-20961819	HepG2	liver:	n/a	chr12:20961744-20961757
12	CEBPB	chr12:20961462-20961896	HepG2	liver:	n/a	chr12:20961744-20961757
13	CEBPB	chr12:20982312-20982493	IMR90	lung:	n/a	chr12:20982413-20982424
14	CEBPB	chr12:20897500-20897722	HepG2	liver:	n/a	chr12:20897639-20897650
15	CEBPB	chr12:20982280-20982503	HepG2	liver:	n/a	chr12:20982413-20982424
16	CEBPB	chr12:20983561-20984147	A549	lung:	n/a	chr12:20983711-20983722
17	CEBPB	chr12:20961440-20961862	HepG2	liver:	n/a	chr12:20961744-20961757
18	CEBPB	chr12:20991877-20992081	HepG2	liver:	n/a	chr12:20992038-20992049
19	CEBPB	chr12:20975368-20976107	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:20983497-20983867	A549	lung:	n/a	chr12:20983711-20983722
21	CEBPB	chr12:20983601-20983801	Hela-S3	cervix:	n/a	chr12:20983711-20983722
22	CEBPB	chr12:21015510-21015751	A549	lung:	n/a	n/a
23	CEBPB	chr12:20983420-20984015	A549	lung:	n/a	chr12:20983711-20983722
24	CEBPB	chr12:20932046-20932199	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:20983564-20983877	HepG2	liver:	n/a	chr12:20983711-20983722
26	CEBPB	chr12:20982284-20982555	A549	lung:	n/a	chr12:20982413-20982424
27	CEBPB	chr12:20975351-20976142	A549	lung:	n/a	n/a
28	CEBPB	chr12:20991943-20992076	A549	lung:	n/a	chr12:20992038-20992049
29	CHD2	chr12:20975360-20975559	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr12:20951446-20951829	A549	lung:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
31	CTCF	chr12:20951560-20951793	K562	blood:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
32	CTCF	chr12:21022085-21022282	A549	lung:	n/a	n/a
33	CTCF	chr12:20951660-20951810	HEEpiC	esophagus:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
34	CTCF	chr12:20951640-20951790	NB4	blood:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
35	CTCF	chr12:21016100-21016250	Caco-2	colon:	n/a	n/a
36	CTCF	chr12:20951500-20951650	A549	lung:	n/a	n/a
37	CTCF	chr12:20932865-20932879	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr12:20951640-20951790	GM06990	blood:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
39	CTCF	chr12:20951680-20951830	HAc	cerebellar:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
40	CTCF	chr12:20951640-20951790	AG09309	skin:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
41	CTCF	chr12:21022178-21022245	GM19238	blood:	n/a	n/a
42	CTCF	chr12:20921692-20921773	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr12:21009487-21009574	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:20951640-20951790	MCF-7	breast:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
45	CTCF	chr12:21022142-21022253	GM12892	blood:	n/a	n/a
46	CTCF	chr12:20989086-20989127	GM10248	blood:	n/a	n/a
47	CTCF	chr12:21009478-21009610	LNCaP	prostate:	n/a	n/a
48	CTCF	chr12:20951660-20951810	WERI-Rb-1	eye:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
49	CTCF	chr12:20951620-20951770	HPAF	blood vessel:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
50	CTCF	chr12:20951560-20951710	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21014317-21014367	BJ	skin:	n/a
2	chr12:20962423-20962473	CMK	blood:	n/a
3	chr12:20966439-20966489	NB4	blood:	n/a
4	chr12:20960409-20960459	Caco-2	colon:	n/a
5	chr12:20935811-20935861	U87	brain:	n/a
6	chr12:20935799-20935849	MCF-7	breast:	n/a
7	chr12:20983111-20983161	RPTEC	kidney:	n/a
8	chr12:20935754-20935804	AG10803	skin:	n/a
9	chr12:20966524-20966574	SK-N-MC	brain:	n/a
10	chr12:20966439-20966489	AG09309	skin:	n/a
11	chr12:20935799-20935849	PFSK-1	brain:	n/a
12	chr12:21014317-21014367	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:20966439-20966489	HL-60	blood:	n/a
14	chr12:20935754-20935804	HNPCEpiC	eye:	n/a
15	chr12:20966439-20966489	HCPEpiC	choroid plexus:	n/a
16	chr12:20960409-20960459	HIPEpiC	eye:	n/a
17	chr12:20906250-20906300	ProgFib	skin:	n/a
18	chr12:20960409-20960459	HRCEpiC	kidney:	n/a
19	chr12:20962423-20962473	HNPCEpiC	eye:	n/a
20	chr12:20935754-20935804	HEK293	kidney:	embryo
21	chr12:20906250-20906300	SAEC	small airway:	n/a
22	chr12:20935799-20935849	NHDF-neo	bronchial:	n/a
23	chr12:21014317-21014367	HUVEC	blood vessel:	n/a
24	chr12:20966524-20966574	Hepatocyte	liver:	n/a
25	chr12:20960409-20960459	ProgFib	skin:	n/a
26	chr12:20966439-20966489	SK-N-SH	brain:	n/a
27	chr12:20966439-20966489	IMR90	lung:	fetal
28	chr12:20962423-20962473	SAEC	small airway:	n/a
29	chr12:20906250-20906300	GM06990	blood:	n/a
30	chr12:21015340-21015390	AG04450	lung:	fetal
31	chr12:21014317-21014367	AoSMC	blood vessel:	n/a
32	chr12:20966524-20966574	GM12891	blood:	n/a
33	chr12:20966524-20966574	SK-N-SH	brain:	n/a
34	chr12:20983111-20983161	HEK293	kidney:	embryo
35	chr12:20960409-20960459	HEK293	kidney:	embryo
36	chr12:20906250-20906300	U87	brain:	n/a
37	chr12:20983111-20983161	PANC-1	pancreas:	n/a
38	chr12:20935811-20935861	SKMC	muscle:	n/a
39	chr12:20960409-20960459	CMK	blood:	n/a
40	chr12:20960409-20960459	GM19239	blood:	n/a
41	chr12:21014317-21014367	CMK	blood:	n/a
42	chr12:20935799-20935849	HCF	heart:	n/a
43	chr12:20935811-20935861	PFSK-1	brain:	n/a
44	chr12:20935811-20935861	HRE	kidney:	n/a
45	chr12:20966524-20966574	ECC-1	luminal epithelium:	n/a
46	chr12:20935799-20935849	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:20960446-20960496	CMK	blood:	n/a
48	chr12:20935754-20935804	CMK	blood:	n/a
49	chr12:20960409-20960459	LNCaP	prostate:	n/a
50	chr12:20935799-20935849	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:20639028..20639571-chr12:20951385..20952022,2	MCF-7	breast:
2	chr12:20798864..20799798-chr12:20951213..20952118,4	MCF-7	breast:
3	chr12:20886731..20889299-chr12:20891417..20893433,2	K562	blood:
4	chr12:20798899..20799416-chr12:20951641..20952181,2	MCF-7	breast:

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

Extended variants
information (count: 6190 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6190 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10770714	chr12:20892859-20892860	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34596286	chr12:20892870-20892871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140048658	chr12:20892885-20892886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10770715	chr12:20892897-20892898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs562748009	chr12:20892917-20892918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369712864	chr12:20892960-20892961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537631464	chr12:20893006-20893007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76663762	chr12:20893009-20893010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189627094	chr12:20893010-20893011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112455944	chr12:20893023-20893024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567261307	chr12:20893034-20893035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536123768	chr12:20893036-20893037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2037154	chr12:20893052-20893053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs373531958	chr12:20893084-20893085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2271656	chr12:20893108-20893109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs12304500	chr12:20893109-20893110	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs558577357	chr12:20893145-20893146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149798560	chr12:20893163-20893164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145739313	chr12:20893176-20893177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376458164	chr12:20893205-20893206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537883974	chr12:20893219-20893220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369753500	chr12:20893226-20893227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79135860	chr12:20893248-20893249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147735206	chr12:20893259-20893260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373688341	chr12:20893351-20893352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139978368	chr12:20893353-20893354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12368368	chr12:20893354-20893355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs577327680	chr12:20893370-20893371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545984506	chr12:20893462-20893463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201331067	chr12:20893482-20893483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563043965	chr12:20893493-20893494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531682443	chr12:20893546-20893547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181143347	chr12:20893556-20893557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2138332	chr12:20893572-20893573	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs529957810	chr12:20893580-20893581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575630483	chr12:20893589-20893590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77817238	chr12:20893631-20893632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12816049	chr12:20893714-20893715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199577812	chr12:20893715-20893716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546385088	chr12:20893717-20893718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs68150818	chr12:20893720-20893721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10770716	chr12:20893721-20893722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61289547	chr12:20893736-20893737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71039980	chr12:20893741-20893742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71935790	chr12:20893742-20893743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56659656	chr12:20893752-20893753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs2176141	chr12:20893753-20893754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185391382	chr12:20893798-20893799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60960983	chr12:20893888-20893889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552079298	chr12:20893912-20893913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:206 , 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	chr12:20902200-20905600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr12:20903200-20903800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr12:20903600-20903800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:20903600-20904200	Enhancers	Brain Germinal Matrix	brain
6	chr12:20903800-20904800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr12:20904400-20904600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:20904800-20905000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:20909800-20910200	Enhancers	HepG2	liver
10	chr12:20913200-20917000	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr12:20913600-20915800	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr12:20914400-20915800	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr12:20916600-20917400	Active TSS	H9 Cell Line	embryonic stem cell
14	chr12:20917000-20922200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr12:20917400-20921800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr12:20919000-20919200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr12:20919200-20922200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr12:20920600-20921000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:20921000-20921400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:20921000-20921600	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr12:20921400-20922400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:20921600-20922400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr12:20921800-20922200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:20921800-20922200	Weak transcription	Adipose Nuclei	Adipose
25	chr12:20921800-20922400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
26	chr12:20922000-20922400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
27	chr12:20922200-20922400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
28	chr12:20922200-20922400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
29	chr12:20922200-20922400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr12:20922200-20922400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:20922200-20922400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:20922200-20922400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr12:20922200-20922400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr12:20922200-20922400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr12:20922200-20922400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
36	chr12:20922200-20922400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
37	chr12:20922200-20922400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
38	chr12:20922200-20922400	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr12:20922200-20922400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:20922200-20922400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:20922200-20922400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
42	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
43	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
44	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
45	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
46	chr12:20922200-20922400	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
47	chr12:20922200-20922400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
48	chr12:20922200-20922400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
49	chr12:20922200-20922400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr12:20922200-20922400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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