Variant report

Variant	nsv976579
Chromosome Location	chr12:12253001-12266723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:12263903-12264159	GM12878	blood:	n/a	n/a
2	BCL11A	chr12:12263900-12264228	GM12878	blood:	n/a	n/a
3	BCL11A	chr12:12263916-12264097	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:12257494-12257665	K562	blood:	n/a	chr12:12257591-12257602
5	CEBPB	chr12:12253546-12253578	K562	blood:	n/a	chr12:12253564-12253575
6	CEBPB	chr12:12257452-12257725	IMR90	lung:	n/a	chr12:12257591-12257602
7	CEBPB	chr12:12257452-12257771	A549	lung:	n/a	chr12:12257591-12257602
8	CEBPB	chr12:12257446-12257772	HepG2	liver:	n/a	chr12:12257591-12257602
9	CEBPB	chr12:12253520-12253669	HepG2	liver:	n/a	chr12:12253564-12253575
10	CEBPB	chr12:12257451-12257773	Hela-S3	cervix:	n/a	chr12:12257591-12257602
11	CEBPB	chr12:12253566-12253573	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr12:12264011-12264099	GM13976	blood:	n/a	n/a
13	CTCF	chr12:12264276-12264328	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr12:12264116-12264199	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr12:12264130-12264206	GM10266	blood:	n/a	n/a
16	CTCF	chr12:12258820-12258970	GM12868	blood:	n/a	n/a
17	EBF1	chr12:12264363-12264681	GM12878	blood:	n/a	n/a
18	EBF1	chr12:12264323-12264643	GM12878	blood:	n/a	n/a
19	EP300	chr12:12253407-12254948	SK-N-SH	brain:	n/a	n/a
20	EP300	chr12:12253834-12254159	SK-N-SH_RA	brain:	n/a	n/a
21	FOS	chr12:12261635-12261703	MCF10A-Er-Src	breast:	n/a	n/a
22	FOSL2	chr12:12263793-12264168	HepG2	liver:	n/a	n/a
23	GATA3	chr12:12253885-12254076	SH-SY5Y	brain:	n/a	n/a
24	GATA3	chr12:12253734-12254321	SK-N-SH	brain:	n/a	n/a
25	GATA3	chr12:12253758-12254235	SK-N-SH	brain:	n/a	n/a
26	HEY1	chr12:12263868-12264172	HepG2	liver:	n/a	n/a
27	HEY1	chr12:12264921-12265145	K562	blood:	n/a	n/a
28	HEY1	chr12:12263743-12264249	HepG2	liver:	n/a	n/a
29	HEY1	chr12:12263805-12264259	K562	blood:	n/a	n/a
30	HEY1	chr12:12264338-12264656	K562	blood:	n/a	n/a
31	HEY1	chr12:12263801-12264171	K562	blood:	n/a	n/a
32	JUND	chr12:12263896-12264090	HepG2	liver:	n/a	n/a
33	MAFF	chr12:12257979-12258169	HepG2	liver:	n/a	n/a
34	MAFF	chr12:12265007-12265113	HepG2	liver:	n/a	n/a
35	MAFK	chr12:12257979-12258164	HepG2	liver:	n/a	n/a
36	MAFK	chr12:12265082-12265151	HepG2	liver:	n/a	chr12:12265085-12265096 chr12:12265085-12265096
37	MAFK	chr12:12257949-12258213	HepG2	liver:	n/a	n/a
38	PAX5	chr12:12264416-12264613	GM12878	blood:	n/a	n/a
39	PAX5	chr12:12263901-12264123	GM12878	blood:	n/a	n/a
40	PBX3	chr12:12263925-12264103	GM12878	blood:	n/a	n/a
41	POLR2A	chr12:12263741-12264276	U87	brain:	n/a	n/a
42	POLR2A	chr12:12260384-12260557	MCF-7	breast:	n/a	n/a
43	POLR2A	chr12:12263869-12264021	Gliobla	brain:	n/a	n/a
44	POLR2A	chr12:12263827-12264026	A549	lung:	n/a	n/a
45	POLR2A	chr12:12263793-12265063	GM12878	blood:	n/a	n/a
46	POLR2A	chr12:12263634-12264320	SK-N-MC	brain:	n/a	n/a
47	POLR2A	chr12:12263765-12264284	GM12891	blood:	n/a	n/a
48	POLR2A	chr12:12265858-12265883	HepG2	liver:	n/a	n/a
49	POLR2A	chr12:12263803-12264183	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr12:12263759-12264180	PFSK-1	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12264390-12264440	HMEC	breast:	n/a
2	chr12:12264176-12264226	ECC-1	luminal epithelium:	n/a
3	chr12:12264176-12264226	HEEpiC	esophagus:	n/a
4	chr12:12264390-12264440	HRE	kidney:	n/a
5	chr12:12264075-12264125	ovcar-3	ovarian:	n/a
6	chr12:12264390-12264440	HCPEpiC	choroid plexus:	n/a
7	chr12:12264176-12264226	LNCaP	prostate:	n/a
8	chr12:12264176-12264226	IMR90	lung:	fetal
9	chr12:12264075-12264125	K562	blood:	n/a
10	chr12:12264075-12264125	PrEC	prostate:	n/a
11	chr12:12264176-12264226	GM06990	blood:	n/a
12	chr12:12264075-12264125	CMK	blood:	n/a
13	chr12:12264075-12264125	NHDF-neo	bronchial:	n/a
14	chr12:12264390-12264440	NHBE	bronchial:	n/a
15	chr12:12264075-12264125	BJ	skin:	n/a
16	chr12:12264390-12264440	HAEpiC	amniotic membrane:	n/a
17	chr12:12264176-12264226	HAEpiC	amniotic membrane:	n/a
18	chr12:12264075-12264125	GM12878	blood:	n/a
19	chr12:12264390-12264440	HL-60	blood:	n/a
20	chr12:12264390-12264440	HEEpiC	esophagus:	n/a
21	chr12:12264390-12264440	AG04449	skin:	fetal
22	chr12:12264390-12264440	HUVEC	blood vessel:	n/a
23	chr12:12264075-12264125	PFSK-1	brain:	n/a
24	chr12:12264075-12264125	SK-N-MC	brain:	n/a
25	chr12:12264390-12264440	U87	brain:	n/a
26	chr12:12264176-12264226	NB4	blood:	n/a
27	chr12:12264176-12264226	SK-N-SH_RA	brain:	n/a
28	chr12:12264390-12264440	NT2-D1	testis:	n/a
29	chr12:12264075-12264125	GM12891	blood:	n/a
30	chr12:12264176-12264226	PFSK-1	brain:	n/a
31	chr12:12264075-12264125	BE2_C	brain:	n/a
32	chr12:12264176-12264226	SAEC	small airway:	n/a
33	chr12:12264176-12264226	HIPEpiC	eye:	n/a
34	chr12:12264176-12264226	AG04450	lung:	fetal
35	chr12:12264390-12264440	ECC-1	luminal epithelium:	n/a
36	chr12:12264390-12264440	SAEC	small airway:	n/a
37	chr12:12264390-12264440	AG10803	skin:	n/a
38	chr12:12264390-12264440	HRPEpiC	eye:	n/a
39	chr12:12264075-12264125	HAEpiC	amniotic membrane:	n/a
40	chr12:12264390-12264440	NH-A	brain:	n/a
41	chr12:12264075-12264125	HepG2	liver:	n/a
42	chr12:12264075-12264125	HEK293	kidney:	embryo
43	chr12:12264176-12264226	HEK293	kidney:	embryo
44	chr12:12264075-12264125	SKMC	muscle:	n/a
45	chr12:12264176-12264226	U87	brain:	n/a
46	chr12:12264176-12264226	SK-N-MC	brain:	n/a
47	chr12:12264075-12264125	AG04450	lung:	fetal
48	chr12:12264390-12264440	LNCaP	prostate:	n/a
49	chr12:12264075-12264125	NB4	blood:	n/a
50	chr12:12264390-12264440	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:12261824..12262324-chr15:80352071..80352800,2	Hela-S3	cervix:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1244	chr12:12264940-12264965	MIMAT0005896_1

No data

Variant related genes	Relation type
ENSG00000198134	TF binding region
ENSG00000198134	CpG island
ENSG00000086666	chromatin interactions

Extended variants
information (count: 584 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35591290	chr12:12253013-12253014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145464009	chr12:12253044-12253045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183614684	chr12:12253091-12253092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543134224	chr12:12253119-12253120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561423080	chr12:12253132-12253133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144414143	chr12:12253153-12253154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568715304	chr12:12253165-12253166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572953583	chr12:12253186-12253187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552562255	chr12:12253195-12253196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547562269	chr12:12253196-12253197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146502555	chr12:12253233-12253234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533260083	chr12:12253249-12253250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569245166	chr12:12253306-12253307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551349297	chr12:12253310-12253311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570084247	chr12:12253321-12253322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533958021	chr12:12253332-12253333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565441657	chr12:12253333-12253334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545123017	chr12:12253336-12253337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386760450	chr12:12253338-12253339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542935827	chr12:12253345-12253346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530900390	chr12:12253359-12253360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4763270	chr12:12253360-12253361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567750668	chr12:12253361-12253362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532935517	chr12:12253370-12253371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143009395	chr12:12253372-12253373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553531699	chr12:12253375-12253376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112385468	chr12:12253377-12253378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188277557	chr12:12253390-12253391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539334801	chr12:12253400-12253401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557341982	chr12:12253409-12253410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575660138	chr12:12253411-12253412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554690875	chr12:12253415-12253416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574582903	chr12:12253420-12253421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536069100	chr12:12253421-12253422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573398799	chr12:12253435-12253436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552769242	chr12:12253448-12253449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148202795	chr12:12253449-12253450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11054688	chr12:12253453-12253454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141190838	chr12:12253459-12253460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146969414	chr12:12253461-12253462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530966366	chr12:12253464-12253465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549393898	chr12:12253465-12253466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567614746	chr12:12253484-12253485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528593464	chr12:12253532-12253533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546743305	chr12:12253535-12253536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138468855	chr12:12253562-12253563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538834538	chr12:12253573-12253574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4763780	chr12:12253591-12253592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
49	rs569200084	chr12:12253593-12253594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377686051	chr12:12253646-12253647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	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 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
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12225000-12255000	Weak transcription	Small Intestine	intestine
2	chr12:12232800-12257000	Weak transcription	HSMMtube	muscle
3	chr12:12234800-12259600	Weak transcription	Aorta	Aorta
4	chr12:12235400-12260200	Weak transcription	Gastric	stomach
5	chr12:12235400-12260800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr12:12235400-12278800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr12:12237400-12259800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:12240400-12254200	Weak transcription	Stomach Mucosa	stomach
9	chr12:12240600-12256800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr12:12241000-12260600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:12241000-12273400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:12241200-12256800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr12:12241200-12261000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr12:12241400-12272600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr12:12241800-12260400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:12242000-12257000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:12245600-12253600	Weak transcription	Colonic Mucosa	Colon
18	chr12:12245600-12257000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr12:12245600-12260400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr12:12245600-12260400	Weak transcription	Fetal Brain Female	brain
21	chr12:12245600-12260600	Weak transcription	Psoas Muscle	Psoas
22	chr12:12245800-12255600	Weak transcription	Brain Substantia Nigra	brain
23	chr12:12245800-12256600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:12245800-12256600	Weak transcription	Lung	lung
25	chr12:12245800-12260400	Weak transcription	Brain Germinal Matrix	brain
26	chr12:12245800-12260400	Weak transcription	Fetal Muscle Trunk	muscle
27	chr12:12245800-12260600	Weak transcription	Brain Hippocampus Middle	brain
28	chr12:12245800-12263800	Weak transcription	Pancreas	Pancrea
29	chr12:12245800-12266200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:12246000-12254400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr12:12246000-12256600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr12:12246200-12253600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr12:12246200-12253600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr12:12246200-12256000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr12:12246200-12260400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr12:12246200-12260400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:12246400-12257000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:12246400-12272000	Weak transcription	Osteobl	bone
39	chr12:12247600-12261400	Weak transcription	Colon Smooth Muscle	Colon
40	chr12:12248200-12271800	Weak transcription	Fetal Kidney	kidney
41	chr12:12248400-12260800	Weak transcription	Hela-S3	cervix
42	chr12:12248400-12261000	Weak transcription	NH-A	brain
43	chr12:12248800-12256600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr12:12248800-12256600	Weak transcription	Fetal Stomach	stomach
45	chr12:12249200-12256000	Weak transcription	Fetal Intestine Small	intestine
46	chr12:12249400-12256600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr12:12250000-12261400	Weak transcription	Primary T cells from cord blood	blood
48	chr12:12250200-12254400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:12250800-12260600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr12:12251000-12254800	Strong transcription	Liver	Liver

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