Variant report

Variant	nsv898778
Chromosome Location	chr12:11108281-11165394
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:672)
Chromatin interactive
region (count:8)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:11134866-11135249	GM12878	blood:	n/a	n/a
2	BATF	chr12:11134883-11135228	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:11134926-11135203	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:11121545-11121715	A549	lung:	n/a	chr12:11121638-11121649
5	CEBPB	chr12:11148042-11148079	K562	blood:	n/a	n/a
6	CEBPB	chr12:11121449-11121832	IMR90	lung:	n/a	chr12:11121638-11121649
7	CEBPB	chr12:11121480-11121758	HepG2	liver:	n/a	chr12:11121638-11121649
8	CEBPB	chr12:11122383-11122390	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:11121480-11121817	ECC-1	luminal epithelium:	n/a	chr12:11121638-11121649
10	CEBPB	chr12:11135657-11135714	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:11121485-11121799	Hela-S3	cervix:	n/a	chr12:11121638-11121649
12	CTCF	chr12:11112500-11112650	HepG2	liver:	n/a	n/a
13	CTCF	chr12:11112500-11112650	Caco-2	colon:	n/a	n/a
14	CTCF	chr12:11112482-11112636	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr12:11112460-11112610	AG09319	gingival:	n/a	n/a
16	CTCF	chr12:11112440-11112590	HMF	breast:	n/a	n/a
17	CTCF	chr12:11112538-11112598	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr12:11112556-11112633	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr12:11113870-11114070	GM12878	blood:	n/a	n/a
20	CTCF	chr12:11131072-11131138	LNCaP	prostate:	n/a	n/a
21	CTCF	chr12:11112500-11112650	NHLF	lung:	n/a	n/a
22	CTCF	chr12:11112420-11112570	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr12:11143647-11143668	GM13977	blood:	n/a	n/a
24	CTCF	chr12:11112447-11112778	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:11112540-11112690	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr12:11112500-11112650	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr12:11112480-11112630	HAc	cerebellar:	n/a	n/a
28	CTCF	chr12:11112504-11112638	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr12:11112564-11112604	K562	blood:	n/a	n/a
30	CTCF	chr12:11112520-11112670	HCM	heart:	n/a	n/a
31	CTCF	chr12:11112480-11112630	BE2_C	brain:	n/a	n/a
32	CTCF	chr12:11112501-11112667	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:11112420-11112570	BE2_C	brain:	n/a	n/a
34	CTCF	chr12:11112520-11112670	HPF	lung:	n/a	n/a
35	CTCF	chr12:11112544-11112636	NHEK	skin:	n/a	n/a
36	CTCF	chr12:11112470-11112662	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:11112500-11112650	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr12:11112509-11112629	HepG2	liver:	n/a	n/a
39	CTCF	chr12:11112500-11112650	HMEC	breast:	n/a	n/a
40	CTCF	chr12:11112420-11112570	HMF	breast:	n/a	n/a
41	CTCF	chr12:11112480-11112630	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr12:11112480-11112630	GM12875	blood:	n/a	n/a
43	CTCF	chr12:11112561-11112637	GM19239	blood:	n/a	n/a
44	CTCF	chr12:11147020-11147170	GM12869	blood:	n/a	n/a
45	CTCF	chr12:11112460-11112610	HPF	lung:	n/a	n/a
46	CTCF	chr12:11119020-11119170	A549	lung:	n/a	n/a
47	CTCF	chr12:11112478-11112661	HepG2	liver:	n/a	n/a
48	CTCF	chr12:11112387-11112746	GM12878	blood:	n/a	n/a
49	CTCF	chr12:11112480-11112630	GM12873	blood:	n/a	n/a
50	CTCF	chr12:11112580-11112730	RPTEC	kidney:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11151622-11151672	ProgFib	skin:	n/a
2	chr12:11151622-11151672	ProgFib	skin:	n/a
3	chr12:11151522-11151572	ECC-1	luminal epithelium:	n/a
4	chr12:11151224-11151274	HepG2	liver:	n/a
5	chr12:11139304-11139354	SK-N-SH_RA	brain:	n/a
6	chr12:11151478-11151528	PrEC	prostate:	n/a
7	chr12:11149362-11149412	BE2_C	brain:	n/a
8	chr12:11151224-11151274	HL-60	blood:	n/a
9	chr12:11149362-11149412	NHDF-neo	bronchial:	n/a
10	chr12:11139962-11140012	AG09319	gingival:	n/a
11	chr12:11140560-11140610	SKMC	muscle:	n/a
12	chr12:11151224-11151274	GM19239	blood:	n/a
13	chr12:11149362-11149412	ProgFib	skin:	n/a
14	chr12:11149362-11149412	AG04450	lung:	fetal
15	chr12:11139304-11139354	T-47D	breast:	n/a
16	chr12:11151478-11151528	HRPEpiC	eye:	n/a
17	chr12:11151622-11151672	HNPCEpiC	eye:	n/a
18	chr12:11151430-11151480	NT2-D1	testis:	n/a
19	chr12:11151478-11151528	SK-N-SH_RA	brain:	n/a
20	chr12:11151224-11151274	HRCEpiC	kidney:	n/a
21	chr12:11140560-11140610	AoSMC	blood vessel:	n/a
22	chr12:11140560-11140610	NH-A	brain:	n/a
23	chr12:11127185-11127235	GM12878	blood:	n/a
24	chr12:11139962-11140012	HEEpiC	esophagus:	n/a
25	chr12:11140560-11140610	SAEC	small airway:	n/a
26	chr12:11151522-11151572	RPTEC	kidney:	n/a
27	chr12:11151622-11151672	NHDF-neo	bronchial:	n/a
28	chr12:11151478-11151528	SK-N-SH	brain:	n/a
29	chr12:11151522-11151572	A549	lung:	n/a
30	chr12:11139304-11139354	AG10803	skin:	n/a
31	chr12:11151522-11151572	AG09319	gingival:	n/a
32	chr12:11127185-11127235	BE2_C	brain:	n/a
33	chr12:11151430-11151480	PFSK-1	brain:	n/a
34	chr12:11127185-11127235	PrEC	prostate:	n/a
35	chr12:11151478-11151528	IMR90	lung:	fetal
36	chr12:11139710-11139760	HRCEpiC	kidney:	n/a
37	chr12:11151622-11151672	RPTEC	kidney:	n/a
38	chr12:11149362-11149412	MCF10A-Er-Src	breast:	n/a
39	chr12:11139710-11139760	HL-60	blood:	n/a
40	chr12:11151430-11151480	NB4	blood:	n/a
41	chr12:11139962-11140012	GM12891	blood:	n/a
42	chr12:11151622-11151672	T-47D	breast:	n/a
43	chr12:11139304-11139354	SK-N-MC	brain:	n/a
44	chr12:11139962-11140012	HUVEC	blood vessel:	n/a
45	chr12:11151522-11151572	HMEC	breast:	n/a
46	chr12:11139962-11140012	NHDF-neo	bronchial:	n/a
47	chr12:11127185-11127235	PANC-1	pancreas:	n/a
48	chr12:11127185-11127235	HRE	kidney:	n/a
49	chr12:11140560-11140610	PANC-1	pancreas:	n/a
50	chr12:11139962-11140012	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
2	chr12:11111049..11113421-chr12:11322867..11324787,2	MCF-7	breast:
3	chr12:11153714..11156559-chr12:11162296..11164278,2	MCF-7	breast:
4	chr12:11154648..11156385-chr12:11157901..11159498,2	K562	blood:
5	chr12:11157746..11159406-chr12:11165545..11167423,2	K562	blood:
6	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
7	chr12:11153714..11156559-chr12:11162296..11164278,2	MCF-7	breast:
8	chr12:11154648..11156385-chr12:11157901..11159498,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11126254-11126320	NR_037918
2	lnc-PRH1-1	chr12:11126254-11126305	NONHSAT026910
3	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026912
4	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026908
5	lnc-TAS2R50-1	chr12:11117024-11117951	NONHSAT026913
6	lnc-PRH1-1	chr12:11158533-11158868	NONHSAT026915
7	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026907
8	lnc-PRH1-1	chr12:11125883-11126320	NONHSAT026914

No data

Variant related genes	Relation type
TAS2R15	TF binding region
TAS2R20	TF binding region
TAS2R50	TF binding region
PRR4	TF binding region
TAS2R15	CpG island
TAS2R20	CpG island
TAS2R50	CpG island
PRR4	CpG island
ENSG00000256537	chromatin interactions
ENSG00000111215	chromatin interactions
ENSG00000212127	chromatin interactions
ENSG00000256712	chromatin interactions

Extended variants
information (count: 2174 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2174 , 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	rs11054083	chr12:11108281-11108282	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534373363	chr12:11108284-11108285	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs79877303	chr12:11108326-11108327	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs7139132	chr12:11108336-11108337	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs536389749	chr12:11108516-11108517	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs555950118	chr12:11108537-11108538	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs116374925	chr12:11108577-11108578	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs576316084	chr12:11108581-11108582	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs115771040	chr12:11108595-11108596	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs558404171	chr12:11108609-11108610	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs188289934	chr12:11108643-11108644	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs191969845	chr12:11108678-11108679	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs11611502	chr12:11108686-11108687	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs150154693	chr12:11108759-11108760	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs370251016	chr12:11108760-11108761	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs538956371	chr12:11108791-11108792	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs182578567	chr12:11108795-11108796	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs78296485	chr12:11108834-11108835	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs117901142	chr12:11108861-11108862	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs552227900	chr12:11108913-11108914	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs117338647	chr12:11108927-11108928	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs528034846	chr12:11109014-11109015	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs547968957	chr12:11109035-11109036	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs142761174	chr12:11109068-11109069	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs562358420	chr12:11109088-11109089	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs536863962	chr12:11109093-11109094	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs527986205	chr12:11109119-11109120	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs115044966	chr12:11109180-11109181	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs538627431	chr12:11109184-11109185	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs186855786	chr12:11109237-11109238	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs147502593	chr12:11109240-11109241	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs572006498	chr12:11109242-11109243	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs557187012	chr12:11109272-11109273	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs79706381	chr12:11109294-11109295	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs367708846	chr12:11109319-11109320	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs554856983	chr12:11109341-11109342	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs574510805	chr12:11109360-11109361	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs138480097	chr12:11109413-11109414	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs201466212	chr12:11109421-11109422	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs117413621	chr12:11109458-11109459	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs191286565	chr12:11109467-11109468	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs141978322	chr12:11109477-11109478	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs116204767	chr12:11109483-11109484	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs150690447	chr12:11109513-11109514	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs184327216	chr12:11109525-11109526	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs561643608	chr12:11109533-11109534	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs117011299	chr12:11109562-11109563	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs190787989	chr12:11109576-11109577	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs369967967	chr12:11109610-11109611	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs538795068	chr12:11109612-11109613	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Incontinentia Pigmenti	22033527	CNVD
Recurrent pregnancy loss	19789632	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11095200-11148800	Weak transcription	HepG2	liver
2	chr12:11095600-11114000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:11095600-11121600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:11096000-11113600	Weak transcription	Hela-S3	cervix
5	chr12:11099800-11112000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:11100000-11112600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr12:11100800-11134200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr12:11101800-11110400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:11102000-11111200	Weak transcription	HMEC	breast
10	chr12:11102000-11114000	Weak transcription	Ovary	ovary
11	chr12:11102000-11114200	Weak transcription	Pancreas	Pancrea
12	chr12:11102000-11121200	Weak transcription	Gastric	stomach
13	chr12:11102000-11122600	Weak transcription	Spleen	Spleen
14	chr12:11102000-11127600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:11102000-11135600	Weak transcription	Aorta	Aorta
16	chr12:11102200-11111200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:11105600-11112600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr12:11105600-11121200	Weak transcription	Left Ventricle	heart
19	chr12:11105600-11121200	Weak transcription	Psoas Muscle	Psoas
20	chr12:11106000-11121400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr12:11106400-11121200	Weak transcription	Placenta	Placenta
22	chr12:11107800-11110400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:11108600-11108800	ZNF genes & repeats	Primary B cells from cord blood	blood
24	chr12:11108800-11126000	Weak transcription	Primary B cells from cord blood	blood
25	chr12:11109400-11110200	ZNF genes & repeats	Fetal Brain Male	brain
26	chr12:11109400-11112400	Weak transcription	Primary T cells from cord blood	blood
27	chr12:11109600-11110000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
28	chr12:11110000-11128600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr12:11110200-11120000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:11110400-11111000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:11110400-11111400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:11110400-11113800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr12:11110600-11127200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr12:11111000-11111200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr12:11111000-11114000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:11111200-11111400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:11111200-11111400	Enhancers	Brain Hippocampus Middle	brain
38	chr12:11111200-11111800	Enhancers	HMEC	breast
39	chr12:11111200-11112000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr12:11111200-11112600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr12:11111400-11111600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:11111400-11116000	Weak transcription	Brain Hippocampus Middle	brain
43	chr12:11111400-11123600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:11111600-11121200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:11111800-11142800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:11112000-11114000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr12:11112000-11114000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr12:11112000-11115200	Weak transcription	Fetal Kidney	kidney
49	chr12:11112400-11114000	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr12:11112400-11114200	Enhancers	Primary T cells from cord blood	blood

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