Variant report

Variant	nsv557497
Chromosome Location	chr12:11234850-11279407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:11237956-11238445	GM12878	blood:	n/a	n/a
2	ATF2	chr12:11238009-11238486	GM12878	blood:	n/a	n/a
3	BATF	chr12:11263799-11264109	GM12878	blood:	n/a	n/a
4	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
5	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
6	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
7	BATF	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
8	BATF	chr12:11263857-11264113	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:11263900-11264159	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
12	CEBPB	chr12:11260954-11260970	HepG2	liver:	n/a	n/a
13	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
14	CTCF	chr12:11270380-11270463	GM13977	blood:	n/a	n/a
15	CTCF	chr12:11257042-11257094	GM20000	blood:	n/a	n/a
16	CTCF	chr12:11248748-11248798	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr12:11247641-11247704	GM20000	blood:	n/a	n/a
18	CTCF	chr12:11265530-11265560	GM13976	blood:	n/a	n/a
19	CUX1	chr12:11238241-11238349	GM12878	blood:	n/a	n/a
20	E2F4	chr12:11278096-11278419	MCF10A-Er-Src	breast:	n/a	n/a
21	ELF1	chr12:11261505-11261735	K562	blood:	n/a	n/a
22	ELK1	chr12:11278900-11278906	GM12878	blood:	n/a	n/a
23	EP300	chr12:11238104-11238440	GM12878	blood:	n/a	n/a
24	EP300	chr12:11238133-11238438	GM12878	blood:	n/a	n/a
25	FOXM1	chr12:11238005-11238472	GM12878	blood:	n/a	n/a
26	GATA3	chr12:11270848-11270991	SH-SY5Y	brain:	n/a	n/a
27	HCFC1	chr12:11260107-11260159	K562	blood:	n/a	n/a
28	IKZF1	chr12:11238336-11238561	GM12878	blood:	n/a	n/a
29	IRF1	chr12:11274892-11274895	K562	blood:	n/a	n/a
30	IRF4	chr12:11247411-11247911	GM12878	blood:	n/a	n/a
31	IRF4	chr12:11247559-11247865	GM12878	blood:	n/a	n/a
32	IRF4	chr12:11263795-11264158	GM12878	blood:	n/a	n/a
33	KAP1	chr12:11279200-11279719	K562	blood:	n/a	n/a
34	KAP1	chr12:11258085-11258322	K562	blood:	n/a	n/a
35	MAFF	chr12:11234615-11234942	HepG2	liver:	n/a	n/a
36	MAFK	chr12:11234616-11234980	HepG2	liver:	n/a	chr12:11234789-11234806
37	MAFK	chr12:11262939-11263117	HepG2	liver:	n/a	n/a
38	MAFK	chr12:11263010-11263067	HepG2	liver:	n/a	n/a
39	MAFK	chr12:11234655-11234917	H1-hESC	embryonic stem cell:	n/a	chr12:11234789-11234806
40	MAFK	chr12:11234630-11234922	HepG2	liver:	n/a	chr12:11234789-11234806
41	MAFK	chr12:11262928-11263070	IMR90	lung:	n/a	n/a
42	MAFK	chr12:11234617-11234968	IMR90	lung:	n/a	chr12:11234789-11234806
43	MAFK	chr12:11254181-11254247	HepG2	liver:	n/a	n/a
44	MXI1	chr12:11238156-11238251	GM12878	blood:	n/a	n/a
45	NFATC1	chr12:11238014-11238349	GM12878	blood:	n/a	n/a
46	NFATC1	chr12:11237942-11238414	GM12878	blood:	n/a	n/a
47	NFIC	chr12:11247511-11247905	GM12878	blood:	n/a	n/a
48	NFIC	chr12:11237984-11238521	GM12878	blood:	n/a	n/a
49	PAX5	chr12:11238021-11238288	GM12878	blood:	n/a	n/a
50	POLR2A	chr12:11248225-11248247	ProgFib	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244939-11244989	HMEC	breast:	n/a
2	chr12:11244939-11244989	LNCaP	prostate:	n/a
3	chr12:11244939-11244989	H1-hESC	embryonic stem cell:	embryo
4	chr12:11244899-11244949	U87	brain:	n/a
5	chr12:11244939-11244989	PrEC	prostate:	n/a
6	chr12:11244939-11244989	GM19239	blood:	n/a
7	chr12:11244899-11244949	NHBE	bronchial:	n/a
8	chr12:11244899-11244949	NT2-D1	testis:	n/a
9	chr12:11244939-11244989	NHDF-neo	bronchial:	n/a
10	chr12:11244899-11244949	NHDF-neo	bronchial:	n/a
11	chr12:11244939-11244989	Hepatocyte	liver:	n/a
12	chr12:11244939-11244989	GM12878	blood:	n/a
13	chr12:11244899-11244949	HRPEpiC	eye:	n/a
14	chr12:11244939-11244989	AG04450	lung:	fetal
15	chr12:11244899-11244949	AG09309	skin:	n/a
16	chr12:11244899-11244949	GM19239	blood:	n/a
17	chr12:11244939-11244989	HCPEpiC	choroid plexus:	n/a
18	chr12:11244939-11244989	MCF-7	breast:	n/a
19	chr12:11244939-11244989	HUVEC	blood vessel:	n/a
20	chr12:11244939-11244989	NB4	blood:	n/a
21	chr12:11244899-11244949	A549	lung:	n/a
22	chr12:11244939-11244989	NT2-D1	testis:	n/a
23	chr12:11244899-11244949	GM12878	blood:	n/a
24	chr12:11244899-11244949	HEK293	kidney:	embryo
25	chr12:11244899-11244949	IMR90	lung:	fetal
26	chr12:11244899-11244949	SK-N-MC	brain:	n/a
27	chr12:11244899-11244949	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:11244899-11244949	HUVEC	blood vessel:	n/a
29	chr12:11244939-11244989	ovcar-3	ovarian:	n/a
30	chr12:11244939-11244989	GM12891	blood:	n/a
31	chr12:11244939-11244989	HAEpiC	amniotic membrane:	n/a
32	chr12:11244899-11244949	HRCEpiC	kidney:	n/a
33	chr12:11244939-11244989	U87	brain:	n/a
34	chr12:11244939-11244989	A549	lung:	n/a
35	chr12:11244939-11244989	HCF	heart:	n/a
36	chr12:11244899-11244949	PANC-1	pancreas:	n/a
37	chr12:11244939-11244989	AG04449	skin:	fetal
38	chr12:11244899-11244949	HCT-116	colon:	n/a
39	chr12:11244899-11244949	HMEC	breast:	n/a
40	chr12:11244899-11244949	AG10803	skin:	n/a
41	chr12:11244939-11244989	T-47D	breast:	n/a
42	chr12:11244899-11244949	GM12891	blood:	n/a
43	chr12:11244899-11244949	Hepatocyte	liver:	n/a
44	chr12:11244899-11244949	HIPEpiC	eye:	n/a
45	chr12:11244899-11244949	K562	blood:	n/a
46	chr12:11244899-11244949	PFSK-1	brain:	n/a
47	chr12:11244939-11244989	GM12892	blood:	n/a
48	chr12:11244939-11244989	AG09309	skin:	n/a
49	chr12:11244899-11244949	ProgFib	skin:	n/a
50	chr12:11244899-11244949	HCF	heart:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
2	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:
3	chr12:11271454..11274346-chr12:11279643..11282306,2	MCF-7	breast:
4	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
5	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11273609-11273779	NONHSAT026916
2	lnc-PRH1-1	chr12:11273435-11273779	NONHSAT026920

No data

Variant related genes	Relation type
ENSG00000256400	TF binding region
TAS2R43	TF binding region
TAS2R64P	TF binding region
ENSG00000256400	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island

Extended variants
information (count: 2152 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2152 , 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	rs34521533	chr12:11234850-11234851	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117916118	chr12:11234857-11234858	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116781272	chr12:11234886-11234887	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs191959666	chr12:11234944-11234945	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs142043792	chr12:11234957-11234958	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs574500541	chr12:11234968-11234969	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs11524287	chr12:11234981-11234982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549996695	chr12:11235007-11235008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199573581	chr12:11235034-11235035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151138649	chr12:11235067-11235068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367808653	chr12:11235098-11235099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139483870	chr12:11235105-11235106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200667857	chr12:11235131-11235132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145127678	chr12:11235172-11235173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114874254	chr12:11235269-11235270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534750353	chr12:11235310-11235311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147599271	chr12:11235371-11235372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574673643	chr12:11235372-11235373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142493216	chr12:11235385-11235386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112859169	chr12:11235435-11235436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112712158	chr12:11235473-11235474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146767705	chr12:11235502-11235503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113189717	chr12:11235537-11235538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577062977	chr12:11235545-11235546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11533165	chr12:11235565-11235566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112982783	chr12:11235569-11235570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559528268	chr12:11235581-11235582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528872953	chr12:11235593-11235594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528183544	chr12:11235600-11235601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200315110	chr12:11235616-11235617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548922416	chr12:11235623-11235624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111686571	chr12:11235634-11235635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78780197	chr12:11235681-11235682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145850362	chr12:11235686-11235687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530342775	chr12:11235687-11235688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78327516	chr12:11235717-11235718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11534426	chr12:11235731-11235732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184329776	chr12:11235769-11235770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571851512	chr12:11235779-11235780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77179636	chr12:11235793-11235794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79562448	chr12:11235801-11235802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143834982	chr12:11235815-11235816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80260552	chr12:11235838-11235839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188636496	chr12:11235847-11235848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74971268	chr12:11235864-11235865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113015984	chr12:11235865-11235866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532529314	chr12:11235883-11235884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79038950	chr12:11235890-11235891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75160883	chr12:11235906-11235907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77737160	chr12:11235910-11235911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11203600-11240000	Weak transcription	Ovary	ovary
2	chr12:11203800-11261200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:11204800-11247600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr12:11205800-11269200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:11208600-11259600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr12:11218200-11256800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:11221200-11259600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:11225200-11236200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:11225200-11261000	Weak transcription	Fetal Stomach	stomach
10	chr12:11233800-11243400	Weak transcription	Fetal Heart	heart
11	chr12:11233800-11252200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:11234400-11236600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr12:11234400-11236600	Weak transcription	Fetal Lung	lung
14	chr12:11234400-11261200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:11234400-11261400	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr12:11236000-11236800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr12:11236200-11236400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:11236200-11237200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:11236600-11237000	ZNF genes & repeats	Fetal Muscle Trunk	muscle
20	chr12:11236600-11237200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
21	chr12:11236600-11237200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
22	chr12:11236600-11237200	ZNF genes & repeats	Fetal Lung	lung
23	chr12:11236800-11237200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:11237000-11237200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:11237000-11237200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:11237000-11243600	Weak transcription	Fetal Muscle Trunk	muscle
27	chr12:11237200-11239400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:11237200-11241400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:11237200-11256400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr12:11237200-11262200	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr12:11237800-11246400	Weak transcription	Fetal Muscle Leg	muscle
32	chr12:11238000-11238800	Enhancers	Primary B cells from peripheral blood	blood
33	chr12:11238800-11241200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:11238800-11243800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr12:11239000-11241400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr12:11239200-11283600	Weak transcription	Fetal Thymus	thymus
37	chr12:11239400-11240200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:11239600-11261600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr12:11239800-11243800	Weak transcription	Fetal Intestine Small	intestine
40	chr12:11239800-11261400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:11240200-11244600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:11240200-11253800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:11241200-11242000	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr12:11241400-11242000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:11241400-11242000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:11241800-11259400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr12:11242000-11243800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr12:11242000-11244200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:11242000-11257200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:11243800-11244800	Strong transcription	Primary B cells from peripheral blood	blood

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