Variant report

Variant	nsv558598
Chromosome Location	chr12:40742363-40828264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:278 , 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	CEBPB	chr12:40765667-40765959	HepG2	liver:	n/a	chr12:40765812-40765823
2	CEBPB	chr12:40818440-40818807	HepG2	liver:	n/a	chr12:40818529-40818540 chr12:40818717-40818728
3	CEBPB	chr12:40767587-40767770	HepG2	liver:	n/a	chr12:40767650-40767661
4	CEBPB	chr12:40765714-40765997	A549	lung:	n/a	chr12:40765812-40765823
5	CEBPB	chr12:40755590-40755779	HepG2	liver:	n/a	n/a
6	CEBPB	chr12:40791302-40791514	A549	lung:	n/a	n/a
7	CEBPB	chr12:40748360-40748390	A549	lung:	n/a	n/a
8	CEBPB	chr12:40791310-40791585	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:40818598-40818846	IMR90	lung:	n/a	chr12:40818717-40818728
10	CEBPB	chr12:40826439-40826590	A549	lung:	n/a	n/a
11	CEBPB	chr12:40818440-40818848	A549	lung:	n/a	chr12:40818529-40818540 chr12:40818717-40818728
12	CTCF	chr12:40768992-40769169	HepG2	liver:	n/a	n/a
13	CTCF	chr12:40769053-40769154	GM19239	blood:	n/a	n/a
14	CTCF	chr12:40769040-40769190	BJ	skin:	n/a	n/a
15	CTCF	chr12:40769020-40769170	HMF	breast:	n/a	n/a
16	CTCF	chr12:40768980-40769130	GM06990	blood:	n/a	n/a
17	CTCF	chr12:40768984-40769180	HepG2	liver:	n/a	n/a
18	CTCF	chr12:40769000-40769150	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr12:40768894-40769274	GM12878	blood:	n/a	n/a
20	CTCF	chr12:40769060-40769210	GM12865	blood:	n/a	n/a
21	CTCF	chr12:40805024-40805091	LNCaP	prostate:	n/a	n/a
22	CTCF	chr12:40769020-40769170	HEK293	kidney:	n/a	n/a
23	CTCF	chr12:40769086-40769118	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:40823200-40823350	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr12:40768965-40769182	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr12:40769000-40769150	HepG2	liver:	n/a	n/a
27	CTCF	chr12:40768958-40769209	Gliobla	brain:	n/a	n/a
28	CTCF	chr12:40768997-40769190	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:40768975-40769173	K562	blood:	n/a	n/a
30	CTCF	chr12:40769140-40769290	WI-38	lung:	n/a	n/a
31	CTCF	chr12:40768960-40769110	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr12:40769021-40769161	GM10266	blood:	n/a	n/a
33	CTCF	chr12:40768963-40769213	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:40769000-40769150	HMEC	breast:	n/a	n/a
35	CTCF	chr12:40768960-40769110	HMF	breast:	n/a	n/a
36	CTCF	chr12:40768840-40768990	RPTEC	kidney:	n/a	n/a
37	CTCF	chr12:40769020-40769170	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr12:40768980-40769130	HL-60	blood:	n/a	n/a
39	CTCF	chr12:40768960-40769110	Caco-2	colon:	n/a	n/a
40	CTCF	chr12:40769020-40769170	GM12875	blood:	n/a	n/a
41	CTCF	chr12:40769000-40769150	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr12:40768980-40769130	GM12873	blood:	n/a	n/a
43	CTCF	chr12:40769000-40769150	AG09319	gingival:	n/a	n/a
44	CTCF	chr12:40769060-40769210	GM12873	blood:	n/a	n/a
45	CTCF	chr12:40769040-40769190	HVMF	connective:	n/a	n/a
46	CTCF	chr12:40768961-40769208	GM12878	blood:	n/a	n/a
47	CTCF	chr12:40769000-40769150	HPF	lung:	n/a	n/a
48	CTCF	chr12:40769000-40769150	BE2_C	brain:	n/a	n/a
49	CTCF	chr12:40768980-40769130	Caco-2	colon:	n/a	n/a
50	CTCF	chr12:40769040-40769190	GM12865	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40747204-40747254	T-47D	breast:	n/a
2	chr12:40747204-40747254	AG09309	skin:	n/a
3	chr12:40747204-40747254	H1-hESC	embryonic stem cell:	embryo
4	chr12:40747204-40747254	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:40747204-40747254	HNPCEpiC	eye:	n/a
6	chr12:40747204-40747254	AG04449	skin:	fetal
7	chr12:40747204-40747254	ovcar-3	ovarian:	n/a
8	chr12:40747204-40747254	HL-60	blood:	n/a
9	chr12:40747204-40747254	SK-N-SH_RA	brain:	n/a
10	chr12:40747204-40747254	BJ	skin:	n/a
11	chr12:40747204-40747254	Hela-S3	cervix:	n/a
12	chr12:40747204-40747254	NHDF-neo	bronchial:	n/a
13	chr12:40747204-40747254	K562	blood:	n/a
14	chr12:40747204-40747254	HCM	heart:	n/a
15	chr12:40747204-40747254	HCF	heart:	n/a
16	chr12:40747204-40747254	U87	brain:	n/a
17	chr12:40747204-40747254	NH-A	brain:	n/a
18	chr12:40747204-40747254	NHBE	bronchial:	n/a
19	chr12:40747204-40747254	IMR90	lung:	fetal
20	chr12:40747204-40747254	GM19239	blood:	n/a
21	chr12:40747204-40747254	SK-N-MC	brain:	n/a
22	chr12:40747204-40747254	HRCEpiC	kidney:	n/a
23	chr12:40747204-40747254	Caco-2	colon:	n/a
24	chr12:40747204-40747254	AG09319	gingival:	n/a
25	chr12:40747204-40747254	LNCaP	prostate:	n/a
26	chr12:40747204-40747254	SKMC	muscle:	n/a
27	chr12:40747204-40747254	HCPEpiC	choroid plexus:	n/a
28	chr12:40747204-40747254	NT2-D1	testis:	n/a
29	chr12:40747204-40747254	PFSK-1	brain:	n/a
30	chr12:40747204-40747254	A549	lung:	n/a
31	chr12:40747204-40747254	GM06990	blood:	n/a
32	chr12:40747204-40747254	MCF-7	breast:	n/a
33	chr12:40747204-40747254	HEK293	kidney:	embryo
34	chr12:40747204-40747254	AG04450	lung:	fetal
35	chr12:40747204-40747254	Jurkat	blood:	n/a
36	chr12:40747204-40747254	RPTEC	kidney:	n/a
37	chr12:40747204-40747254	HepG2	liver:	n/a
38	chr12:40747204-40747254	HCT-116	colon:	n/a
39	chr12:40747204-40747254	Hepatocyte	liver:	n/a
40	chr12:40747204-40747254	ProgFib	skin:	n/a
41	chr12:40747204-40747254	PANC-1	pancreas:	n/a
42	chr12:40747204-40747254	PrEC	prostate:	n/a
43	chr12:40747204-40747254	SAEC	small airway:	n/a
44	chr12:40747204-40747254	AG10803	skin:	n/a
45	chr12:40747204-40747254	NB4	blood:	n/a
46	chr12:40747204-40747254	BE2_C	brain:	n/a
47	chr12:40747204-40747254	AoSMC	blood vessel:	n/a
48	chr12:40747204-40747254	SK-N-SH	brain:	n/a
49	chr12:40747204-40747254	HUVEC	blood vessel:	n/a
50	chr12:40747204-40747254	HRE	kidney:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:40730810..40731494-chr12:40768592..40769125,2	MCF-7	breast:
2	chr12:40802843..40805068-chr12:40806902..40808859,2	K562	blood:
3	12:40793507-40812339..12:40836437-40839614	H1-hESC	embryonic stem cell:	embryo
4	chr12:40803393..40806032-chr12:40844478..40846629,2	K562	blood:
5	12:40703633-40711447..12:40765226-40767074	GM12878	blood:
6	chr12:40768243..40769926-chr12:40782774..40784277,2	K562	blood:
7	chr12:40718929..40719819-chr12:40768166..40769419,3	MCF-7	breast:
8	chr12:40802735..40804254-chr12:40811941..40814562,2	K562	blood:
9	chr12:40768243..40769926-chr12:40782774..40784277,2	K562	blood:
10	chr12:40802843..40805068-chr12:40806902..40808859,2	K562	blood:
11	chr12:40730058..40730795-chr12:40768301..40769589,4	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC19-1	chr12:40827566-40827715	NONHSAT027728
2	lnc-SLC2A13-3	chr12:40814022-40814113	ENSG00000258167.1
3	lnc-MUC19-1	chr12:40820209-40820419	NONHSAT027728
4	lnc-MUC19-1	chr12:40791681-40791713	NONHSAT027728
5	lnc-MUC19-1	chr12:40805835-40805984	NONHSAT027728
6	lnc-MUC19-1	chr12:40815015-40815125	NONHSAT027728
7	lnc-SLC2A13-3	chr12:40810105-40810240	XLOC_010054
8	lnc-MUC19-1	chr12:40826429-40826566	NONHSAT027728
9	lnc-SLC2A13-3	chr12:40792362-40792466	ENSG00000258167.1
10	lnc-SLC2A13-3	chr12:40814022-40814118	XLOC_010054
11	lnc-MUC19-1	chr12:40787197-40787301	NONHSAT027728
12	lnc-MUC19-1	chr12:40812976-40813035	NONHSAT027728
13	lnc-MUC19-1	chr12:40826180-40826264	NONHSAT027728
14	lnc-SLC2A13-3	chr12:40814022-40814113	XLOC_010054
15	lnc-MUC19-1	chr12:40823344-40823479	NONHSAT027728
16	lnc-SLC2A13-3	chr12:40810103-40810240	XLOC_010054
17	lnc-MUC19-1	chr12:40811932-40811982	NONHSAT027728
18	lnc-SLC2A13-3	chr12:40807837-40807921	XLOC_010054
19	lnc-SLC2A13-3	chr12:40814022-40814118	XLOC_010054
20	lnc-MUC19-1	chr12:40805409-40805429	NONHSAT027728
21	lnc-SLC2A13-3	chr12:40789712-40789790	XLOC_010054
22	lnc-MUC19-1	chr12:40815906-40816003	NONHSAT027728
23	lnc-MUC19-1	chr12:40821772-40821895	NONHSAT027728
24	lnc-SLC2A13-3	chr12:40789655-40789788	ENSG00000258167.1
25	lnc-MUC19-1	chr12:40815642-40815702	NONHSAT027728
26	lnc-MUC19-1	chr12:40825428-40825520	NONHSAT027728
27	lnc-SLC2A13-3	chr12:40810105-40810240	XLOC_010054
28	lnc-MUC19-1	chr12:40814009-40814237	NONHSAT027728
29	lnc-MUC19-1	chr12:40821176-40821298	NONHSAT027728

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRK2	hsa-miR-205-5p	chr12:40761683-40761690
2	LRRK2	hsa-miR-205-5p	chr12:40761670-40761690

Variant related genes	Relation type
MUC19	TF binding region
MUC19	CpG island
ENSG00000188906	chromatin interactions
ENSG00000205592	chromatin interactions
ENSG00000258167	chromatin interactions
STXBP3	miRNA target sites
MORF4L1	miRNA target sites
BLOC1S3	miRNA target sites
SLC25A37	miRNA target sites
SEC23IP	miRNA target sites

Extended variants
information (count: 2924 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2924 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11176143	chr12:40742363-40742364	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534638081	chr12:40742424-40742425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549303363	chr12:40742514-40742515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567467823	chr12:40742604-40742605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534855780	chr12:40742605-40742606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187998728	chr12:40742661-40742662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571800172	chr12:40742670-40742671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7294958	chr12:40742689-40742690	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs61915610	chr12:40742701-40742702	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs180819448	chr12:40742728-40742729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535232124	chr12:40742732-40742733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556641218	chr12:40742797-40742798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7294952	chr12:40742876-40742877	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs78560388	chr12:40742908-40742909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367587469	chr12:40743039-40743040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558748255	chr12:40743108-40743109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529938813	chr12:40743130-40743131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116004538	chr12:40743235-40743236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544786129	chr12:40743295-40743296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145677990	chr12:40743312-40743313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113510284	chr12:40743314-40743315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146989832	chr12:40743361-40743362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59096461	chr12:40743363-40743364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111722387	chr12:40743368-40743369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs398055493	chr12:40743371-40743372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563250147	chr12:40743424-40743425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17491611	chr12:40743428-40743429	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs115625901	chr12:40743473-40743474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34169929	chr12:40743485-40743486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs59980086	chr12:40743492-40743493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs397964698	chr12:40743499-40743500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561201723	chr12:40743519-40743520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12306725	chr12:40743610-40743611	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs143887108	chr12:40743664-40743665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571369701	chr12:40743665-40743666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532600403	chr12:40743737-40743738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185224699	chr12:40743755-40743756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201760414	chr12:40743757-40743758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75043706	chr12:40743787-40743788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4768233	chr12:40743788-40743789	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs4768234	chr12:40743830-40743831	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs566795041	chr12:40743831-40743832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534237159	chr12:40743870-40743871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148633876	chr12:40743883-40743884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577367336	chr12:40743899-40743900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563071832	chr12:40743906-40743907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190316343	chr12:40743909-40743910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182495924	chr12:40743973-40743974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551828056	chr12:40743988-40743989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575161235	chr12:40743991-40743992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40640600-40768200	Weak transcription	Pancreas	Pancrea
2	chr12:40656800-40746400	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr12:40674400-40760400	Weak transcription	Lung	lung
4	chr12:40681200-40763000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:40687200-40765000	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr12:40712000-40743400	Weak transcription	Aorta	Aorta
7	chr12:40714200-40759200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr12:40716800-40761600	Weak transcription	Fetal Kidney	kidney
9	chr12:40722800-40755800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr12:40724600-40745400	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr12:40724800-40751000	Weak transcription	Brain Anterior Caudate	brain
12	chr12:40725200-40761200	Weak transcription	Psoas Muscle	Psoas
13	chr12:40726200-40766600	Weak transcription	A549	lung
14	chr12:40726200-40767800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:40729800-40756000	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr12:40730000-40745800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr12:40730000-40747000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr12:40730000-40760000	Weak transcription	Spleen	Spleen
19	chr12:40730400-40745400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr12:40732000-40745800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr12:40732000-40757200	Weak transcription	Right Ventricle	heart
22	chr12:40732200-40743000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr12:40732800-40764000	Weak transcription	Colon Smooth Muscle	Colon
24	chr12:40733200-40757000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr12:40733400-40745600	Weak transcription	Adipose Nuclei	Adipose
26	chr12:40733600-40761400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:40734600-40754200	Weak transcription	Esophagus	oesophagus
28	chr12:40735400-40745400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:40735600-40747000	Weak transcription	Brain Angular Gyrus	brain
30	chr12:40737000-40742800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:40737000-40743600	Weak transcription	Ovary	ovary
32	chr12:40737000-40751600	Weak transcription	Left Ventricle	heart
33	chr12:40737200-40754000	Weak transcription	Stomach Smooth Muscle	stomach
34	chr12:40740400-40744000	Strong transcription	Liver	Liver
35	chr12:40740400-40745600	Strong transcription	Primary B cells from cord blood	blood
36	chr12:40741000-40743400	Weak transcription	Primary B cells from peripheral blood	blood
37	chr12:40742800-40746800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:40743000-40744000	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr12:40743400-40744400	Strong transcription	Aorta	Aorta
40	chr12:40743400-40745600	Strong transcription	Primary B cells from peripheral blood	blood
41	chr12:40743600-40745200	Strong transcription	Ovary	ovary
42	chr12:40744000-40745400	Weak transcription	Liver	Liver
43	chr12:40744000-40745600	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr12:40744400-40754200	Weak transcription	Aorta	Aorta
45	chr12:40745200-40745600	Weak transcription	Ovary	ovary
46	chr12:40745400-40746000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr12:40745400-40746000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
48	chr12:40745400-40746200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr12:40745400-40746200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr12:40745400-40746200	Strong transcription	Liver	Liver

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