Variant report

Variant	nsv516262
Chromosome Location	chr12:11458806-11575570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:732)
Chromatin interactive
region (count:2)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:11501400-11501725	K562	blood:	n/a	n/a
2	BCL3	chr12:11501365-11501771	GM12878	blood:	n/a	n/a
3	BCL3	chr12:11501361-11501642	GM12878	blood:	n/a	n/a
4	CBX3	chr12:11569521-11569734	K562	blood:	n/a	n/a
5	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
6	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
9	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
10	CEBPB	chr12:11478711-11479007	HepG2	liver:	n/a	chr12:11478828-11478841 chr12:11478830-11478839 chr12:11478828-11478839 chr12:11478829-11478840
11	CREB1	chr12:11501439-11501709	A549	lung:	n/a	n/a
12	CREB1	chr12:11501156-11501972	K562	blood:	n/a	n/a
13	CREB1	chr12:11501322-11501785	K562	blood:	n/a	n/a
14	CREB1	chr12:11501341-11501827	HepG2	liver:	n/a	n/a
15	CREB1	chr12:11501275-11501755	HepG2	liver:	n/a	n/a
16	CTCF	chr12:11500860-11501010	GM12864	blood:	n/a	n/a
17	CTCF	chr12:11501520-11501609	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:11500840-11500990	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr12:11545806-11545841	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:11569479-11569545	MCF-7	breast:	n/a	n/a
21	CTCF	chr12:11500880-11501030	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr12:11505978-11506004	Lung_OC	lung:	n/a	n/a
23	CTCF	chr12:11500820-11500970	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr12:11500860-11501010	HCFaa	heart:	n/a	n/a
25	CTCF	chr12:11544846-11544963	GM13976	blood:	n/a	n/a
26	CTCF	chr12:11501578-11501581	A549	lung:	n/a	n/a
27	CTCF	chr12:11552280-11552316	GM13977	blood:	n/a	n/a
28	CTCF	chr12:11566785-11566861	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr12:11500780-11500930	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr12:11500860-11501010	GM06990	blood:	n/a	n/a
31	CTCF	chr12:11501300-11501450	SAEC	small airway:	n/a	n/a
32	CTCF	chr12:11500858-11500977	GM12878	blood:	n/a	n/a
33	CTCF	chr12:11500820-11500970	GM12801	blood:	n/a	n/a
34	CTCF	chr12:11500900-11501050	GM12878	blood:	n/a	n/a
35	CTCF	chr12:11490383-11490444	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr12:11500860-11501010	Caco-2	colon:	n/a	n/a
37	CTCF	chr12:11500800-11500950	GM12871	blood:	n/a	n/a
38	CTCF	chr12:11500867-11500968	HepG2	liver:	n/a	n/a
39	CTCF	chr12:11500860-11501010	GM12873	blood:	n/a	n/a
40	CTCF	chr12:11500539-11501299	A549	lung:	n/a	n/a
41	CTCF	chr12:11500900-11501050	GM12864	blood:	n/a	n/a
42	CTCF	chr12:11545746-11545856	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:11505990-11506144	K562	blood:	n/a	n/a
44	CTCF	chr12:11500840-11500990	GM12875	blood:	n/a	n/a
45	CTCF	chr12:11500880-11501030	GM12869	blood:	n/a	n/a
46	CTCF	chr12:11500860-11500982	LNCaP	prostate:	n/a	n/a
47	CTCF	chr12:11500891-11501001	LNCaP	prostate:	n/a	n/a
48	CTCF	chr12:11556054-11556104	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr12:11500840-11500990	HPF	lung:	n/a	n/a
50	CTCF	chr12:11528342-11528385	LNCaP	prostate:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11463937-11463987	AoSMC	blood vessel:	n/a
2	chr12:11463937-11463987	HAEpiC	amniotic membrane:	n/a
3	chr12:11463937-11463987	GM12891	blood:	n/a
4	chr12:11460710-11460760	HAEpiC	amniotic membrane:	n/a
5	chr12:11463379-11463429	HRE	kidney:	n/a
6	chr12:11549555-11549605	HPAEpiC	pulmonary alveolar:	n/a
7	chr12:11460710-11460760	PrEC	prostate:	n/a
8	chr12:11548867-11548917	BJ	skin:	n/a
9	chr12:11464607-11464657	BE2_C	brain:	n/a
10	chr12:11463844-11463894	AG10803	skin:	n/a
11	chr12:11460710-11460760	HEK293	kidney:	embryo
12	chr12:11508049-11508099	GM12878	blood:	n/a
13	chr12:11464607-11464657	HNPCEpiC	eye:	n/a
14	chr12:11463844-11463894	NB4	blood:	n/a
15	chr12:11461798-11461848	HIPEpiC	eye:	n/a
16	chr12:11509583-11509633	NH-A	brain:	n/a
17	chr12:11548867-11548917	ProgFib	skin:	n/a
18	chr12:11463844-11463894	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:11463844-11463894	A549	lung:	n/a
20	chr12:11461798-11461848	A549	lung:	n/a
21	chr12:11549192-11549242	SK-N-MC	brain:	n/a
22	chr12:11464607-11464657	H1-hESC	embryonic stem cell:	embryo
23	chr12:11549192-11549242	BJ	skin:	n/a
24	chr12:11548019-11548069	SAEC	small airway:	n/a
25	chr12:11463937-11463987	NB4	blood:	n/a
26	chr12:11461798-11461848	IMR90	lung:	fetal
27	chr12:11548867-11548917	CMK	blood:	n/a
28	chr12:11464607-11464657	MCF-7	breast:	n/a
29	chr12:11548867-11548917	Hepatocyte	liver:	n/a
30	chr12:11549192-11549242	AG04449	skin:	fetal
31	chr12:11509583-11509633	HRE	kidney:	n/a
32	chr12:11509583-11509633	MCF-7	breast:	n/a
33	chr12:11463844-11463894	K562	blood:	n/a
34	chr12:11548867-11548917	RPTEC	kidney:	n/a
35	chr12:11461798-11461848	HEEpiC	esophagus:	n/a
36	chr12:11508049-11508099	HCF	heart:	n/a
37	chr12:11463379-11463429	BE2_C	brain:	n/a
38	chr12:11464607-11464657	SKMC	muscle:	n/a
39	chr12:11548019-11548069	T-47D	breast:	n/a
40	chr12:11463379-11463429	HL-60	blood:	n/a
41	chr12:11548867-11548917	HCF	heart:	n/a
42	chr12:11463844-11463894	GM12891	blood:	n/a
43	chr12:11548867-11548917	MCF10A-Er-Src	breast:	n/a
44	chr12:11508049-11508099	HRE	kidney:	n/a
45	chr12:11461798-11461848	HEK293	kidney:	embryo
46	chr12:11461798-11461848	HCPEpiC	choroid plexus:	n/a
47	chr12:11549192-11549242	LNCaP	prostate:	n/a
48	chr12:11463937-11463987	HEK293	kidney:	embryo
49	chr12:11463379-11463429	SAEC	small airway:	n/a
50	chr12:11508049-11508099	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:
2	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRB4-1	chr12:11462305-11462339	NONHSAT026935
2	lnc-PRB4-1	chr12:11461584-11461816	NONHSAT026935
3	lnc-PRB1-1	chr12:11552784-11552937	ENSG00000255790.1
4	lnc-PRB1-1	chr12:11552315-11552411	ENSG00000255790.1
5	lnc-PRB1-1	chr12:11559632-11559826	ENSG00000255790.1
6	lnc-PRB4-1	chr12:11461162-11461375	NONHSAT026935
7	lnc-PRB4-1	chr12:11463270-11463369	NONHSAT026935
8	lnc-PRB1-1	chr12:11554419-11554457	ENSG00000255790.1

No data

Variant related genes	Relation type
PRB4	TF binding region
PRB2	TF binding region
PRB1	TF binding region
PRB4	CpG island
PRB2	CpG island
PRB1	CpG island

Extended variants
information (count: 4644 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4644 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1427751	chr12:11460231-11460232	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1863843	chr12:11460257-11460258	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs548772551	chr12:11460326-11460327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548089769	chr12:11460328-11460329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571019605	chr12:11460366-11460367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537566782	chr12:11460389-11460390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149101469	chr12:11460396-11460397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571181141	chr12:11460470-11460471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72477466	chr12:11460471-11460472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2900128	chr12:11460475-11460476	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs115993427	chr12:11460478-11460479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186260950	chr12:11460549-11460550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556016658	chr12:11460577-11460578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575872410	chr12:11460672-11460673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544408212	chr12:11460679-11460680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556189009	chr12:11460687-11460688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558231044	chr12:11460705-11460706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577990203	chr12:11460711-11460712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540633819	chr12:11460712-11460713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576020336	chr12:11460713-11460714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377666404	chr12:11460738-11460739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542481755	chr12:11460743-11460744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112885101	chr12:11460792-11460793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189063606	chr12:11460795-11460796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200327304	chr12:11461178-11461179	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs374451714	chr12:11461188-11461189	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs75004563	chr12:11461190-11461191	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs146162362	chr12:11461217-11461218	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs576626342	chr12:11461218-11461219	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs77514395	chr12:11461223-11461224	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs371842116	chr12:11461228-11461229	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs375278204	chr12:11461241-11461242	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs574597591	chr12:11461259-11461260	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs141102420	chr12:11461272-11461273	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs368003440	chr12:11461282-11461283	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs372237042	chr12:11461285-11461286	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs1052808	chr12:11461292-11461293	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs562435920	chr12:11461301-11461302	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs146939904	chr12:11461302-11461303	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs139306953	chr12:11461308-11461309	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs145416694	chr12:11461337-11461338	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs377238841	chr12:11461341-11461342	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs564883667	chr12:11461346-11461347	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs201691090	chr12:11461347-11461348	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs547141690	chr12:11461357-11461358	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs567304413	chr12:11461358-11461359	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs529711200	chr12:11461360-11461361	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs546117164	chr12:11461363-11461364	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs147670728	chr12:11461367-11461368	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs374921001	chr12:11461396-11461397	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11460200-11460800	Enhancers	HUVEC	blood vessel
2	chr12:11461200-11462200	Enhancers	Spleen	Spleen
3	chr12:11467000-11467200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:11473600-11475800	Enhancers	Fetal Heart	heart
5	chr12:11474600-11475000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:11475400-11478200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr12:11478200-11479200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr12:11478800-11479400	Enhancers	HMEC	breast
9	chr12:11479000-11479200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:11479200-11480200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr12:11479200-11493000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:11486800-11487000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:11493000-11493200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:11493000-11493400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:11493000-11494200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:11494200-11496400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:11496600-11496800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:11496800-11499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:11497200-11497800	Enhancers	HepG2	liver
20	chr12:11497800-11498600	Enhancers	Fetal Intestine Small	intestine
21	chr12:11498200-11498600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr12:11504000-11505000	Enhancers	HUVEC	blood vessel
23	chr12:11505000-11510400	Weak transcription	HUVEC	blood vessel
24	chr12:11506600-11507000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr12:11510000-11511000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr12:11510000-11511200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr12:11510400-11511000	Enhancers	HUVEC	blood vessel
28	chr12:11511000-11512400	Weak transcription	HUVEC	blood vessel
29	chr12:11511200-11519600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr12:11512400-11514000	Enhancers	HUVEC	blood vessel
31	chr12:11513000-11513800	Enhancers	HMEC	breast
32	chr12:11513000-11514000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:11513000-11514000	Enhancers	NHEK	skin
34	chr12:11513400-11513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:11513600-11514200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr12:11513600-11521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:11516600-11517000	Enhancers	HepG2	liver
38	chr12:11519600-11520200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr12:11520000-11520600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:11520200-11521200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:11521200-11521800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr12:11521400-11521600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:11529600-11529800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr12:11530200-11531200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:11539200-11539400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:11539400-11539800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr12:11544000-11544800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr12:11544000-11544800	Enhancers	HUVEC	blood vessel
49	chr12:11544800-11550000	Weak transcription	HUVEC	blood vessel
50	chr12:11544800-11550200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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