Variant report

Variant	nsv898742
Chromosome Location	chr12:9473157-9518222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:913)
CpG islands
(count:671)
Chromatin interactive
region (count:30)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9495326-9496012	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:9493327-9493396	K562	blood:	n/a	n/a
3	ATF1	chr12:9515879-9516104	K562	blood:	n/a	n/a
4	ATF1	chr12:9492605-9492785	K562	blood:	n/a	n/a
5	ATF1	chr12:9499390-9499755	K562	blood:	n/a	n/a
6	ATF1	chr12:9500046-9500362	K562	blood:	n/a	n/a
7	ATF1	chr12:9517037-9517719	K562	blood:	n/a	n/a
8	ATF1	chr12:9493010-9493521	K562	blood:	n/a	n/a
9	ATF2	chr12:9514231-9515229	GM12878	blood:	n/a	n/a
10	ATF2	chr12:9483870-9484266	GM12878	blood:	n/a	n/a
11	ATF2	chr12:9515316-9516084	GM12878	blood:	n/a	n/a
12	ATF2	chr12:9483724-9484288	GM12878	blood:	n/a	n/a
13	ATF2	chr12:9516298-9518464	GM12878	blood:	n/a	n/a
14	ATF2	chr12:9514144-9518351	GM12878	blood:	n/a	n/a
15	BACH1	chr12:9486740-9486998	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr12:9507019-9507395	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr12:9490118-9490128	K562	blood:	n/a	n/a
18	BACH1	chr12:9496419-9496420	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:9516711-9516911	K562	blood:	n/a	n/a
20	BATF	chr12:9516818-9517792	GM12878	blood:	n/a	n/a
21	BATF	chr12:9507017-9507310	GM12878	blood:	n/a	n/a
22	BATF	chr12:9515676-9516129	GM12878	blood:	n/a	chr12:9515939-9515950
23	BATF	chr12:9506976-9507254	GM12878	blood:	n/a	n/a
24	BATF	chr12:9516696-9517884	GM12878	blood:	n/a	n/a
25	BATF	chr12:9514492-9515074	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:9516825-9517859	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:9507015-9507175	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:9514518-9515013	GM12878	blood:	n/a	chr12:9514548-9514557
29	BCL11A	chr12:9514587-9514903	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:9506964-9507320	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:9516896-9517726	GM12878	blood:	n/a	n/a
32	BCL3	chr12:9514179-9515157	GM12878	blood:	n/a	chr12:9514548-9514557
33	BCL3	chr12:9514536-9515106	GM12878	blood:	n/a	chr12:9514548-9514557
34	BCL3	chr12:9516773-9518016	GM12878	blood:	n/a	n/a
35	BCL3	chr12:9516906-9517768	GM12878	blood:	n/a	n/a
36	BCLAF1	chr12:9514268-9515127	GM12878	blood:	n/a	chr12:9514548-9514557
37	BCLAF1	chr12:9516391-9518359	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:9516321-9518443	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:9514439-9515090	GM12878	blood:	n/a	chr12:9514548-9514557
40	BHLHE40	chr12:9514468-9515061	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:9516856-9517910	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:9507008-9507323	HepG2	liver:	n/a	n/a
43	BHLHE40	chr12:9507035-9507312	HepG2	liver:	n/a	n/a
44	BHLHE40	chr12:9493114-9493281	K562	blood:	n/a	n/a
45	BHLHE40	chr12:9499426-9499609	K562	blood:	n/a	n/a
46	BHLHE40	chr12:9483724-9484100	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:9495267-9495730	HepG2	liver:	n/a	n/a
48	BHLHE40	chr12:9515984-9516100	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:9483761-9484064	K562	blood:	n/a	n/a
50	BRCA1	chr12:9480340-9480381	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9493259-9493309	HEEpiC	esophagus:	n/a
2	chr12:9478612-9478662	AG09319	gingival:	n/a
3	chr12:9478612-9478662	T-47D	breast:	n/a
4	chr12:9478612-9478662	HCM	heart:	n/a
5	chr12:9479566-9479616	H1-hESC	embryonic stem cell:	embryo
6	chr12:9489057-9489107	Jurkat	blood:	n/a
7	chr12:9479566-9479616	PFSK-1	brain:	n/a
8	chr12:9479566-9479616	HUVEC	blood vessel:	n/a
9	chr12:9486542-9486592	HCF	heart:	n/a
10	chr12:9478906-9478956	GM19239	blood:	n/a
11	chr12:9489057-9489107	HCM	heart:	n/a
12	chr12:9501915-9501965	NT2-D1	testis:	n/a
13	chr12:9479566-9479616	Hela-S3	cervix:	n/a
14	chr12:9479566-9479616	AG04449	skin:	fetal
15	chr12:9501783-9501833	HL-60	blood:	n/a
16	chr12:9493259-9493309	Hepatocyte	liver:	n/a
17	chr12:9486542-9486592	GM12891	blood:	n/a
18	chr12:9478612-9478662	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:9489057-9489107	NH-A	brain:	n/a
20	chr12:9493259-9493309	K562	blood:	n/a
21	chr12:9478612-9478662	HRE	kidney:	n/a
22	chr12:9489057-9489107	GM12892	blood:	n/a
23	chr12:9501783-9501833	ovcar-3	ovarian:	n/a
24	chr12:9517562-9517612	Jurkat	blood:	n/a
25	chr12:9478906-9478956	HUVEC	blood vessel:	n/a
26	chr12:9478612-9478662	HIPEpiC	eye:	n/a
27	chr12:9493259-9493309	HNPCEpiC	eye:	n/a
28	chr12:9486542-9486592	Jurkat	blood:	n/a
29	chr12:9478906-9478956	HIPEpiC	eye:	n/a
30	chr12:9501783-9501833	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:9478906-9478956	AG10803	skin:	n/a
32	chr12:9489057-9489107	Hela-S3	cervix:	n/a
33	chr12:9501845-9501895	SAEC	small airway:	n/a
34	chr12:9517562-9517612	PANC-1	pancreas:	n/a
35	chr12:9478612-9478662	HNPCEpiC	eye:	n/a
36	chr12:9517562-9517612	BJ	skin:	n/a
37	chr12:9479566-9479616	HCF	heart:	n/a
38	chr12:9501845-9501895	NHDF-neo	bronchial:	n/a
39	chr12:9478906-9478956	K562	blood:	n/a
40	chr12:9493259-9493309	HRE	kidney:	n/a
41	chr12:9517562-9517612	Caco-2	colon:	n/a
42	chr12:9479566-9479616	HAEpiC	amniotic membrane:	n/a
43	chr12:9478627-9478677	Jurkat	blood:	n/a
44	chr12:9489057-9489107	HUVEC	blood vessel:	n/a
45	chr12:9478627-9478677	SAEC	small airway:	n/a
46	chr12:9478612-9478662	LNCaP	prostate:	n/a
47	chr12:9501845-9501895	Caco-2	colon:	n/a
48	chr12:9517562-9517612	HCF	heart:	n/a
49	chr12:9479566-9479616	BJ	skin:	n/a
50	chr12:9501845-9501895	Hepatocyte	liver:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9216104..9218306-chr12:9470179..9473467,3	MCF-7	breast:
2	chr11:62379397..62380044-chr12:9496046..9496903,2	HCT-116	colon:
3	chr12:9492767..9495377-chr12:9497278..9499065,2	K562	blood:
4	chr12:9499156..9500827-chr12:9501599..9503470,2	MCF-7	breast:
5	chr12:9514676..9517481-chr12:9908794..9910668,2	K562	blood:
6	chr12:9514472..9517285-chr12:9517571..9520331,3	K562	blood:
7	chr12:9485621..9488613-chr17:57864279..57867030,2	MCF-7	breast:
8	chr12:9215856..9217597-chr12:9482273..9484056,2	MCF-7	breast:
9	chr12:9216106..9218386-chr12:9489612..9493915,4	MCF-7	breast:
10	chr12:9225166..9226787-chr12:9475945..9478723,2	MCF-7	breast:
11	chr12:9475880..9477662-chr12:9479960..9482900,2	K562	blood:
12	chr12:9475880..9477662-chr12:9479960..9482900,2	K562	blood:
13	chr12:9483454..9485642-chr12:9487208..9489749,3	K562	blood:
14	chr12:9431917..9434887-chr12:9485752..9487325,2	MCF-7	breast:
15	chr12:9492332..9494947-chr12:9501072..9502931,2	MCF-7	breast:
16	chr12:9494429..9497191-chr12:9497385..9498990,2	MCF-7	breast:
17	chr12:9483454..9485642-chr12:9487208..9489749,3	K562	blood:
18	chr12:9512017..9514493-chr12:9517939..9520276,2	MCF-7	breast:
19	chr12:9215714..9219195-chr12:9470456..9473261,3	MCF-7	breast:
20	chr12:9492767..9495377-chr12:9497278..9499065,2	K562	blood:
21	chr12:9483967..9484695-chr12:9530892..9531873,3	MCF-7	breast:
22	chr12:9494429..9497191-chr12:9497385..9498990,2	MCF-7	breast:
23	chr12:9492332..9494947-chr12:9501072..9502931,2	MCF-7	breast:
24	chr12:9516871..9518767-chr12:9528942..9530878,2	MCF-7	breast:
25	chr12:9499156..9500827-chr12:9501599..9503470,2	MCF-7	breast:
26	chr12:9471764..9473665-chr12:9564371..9566160,2	MCF-7	breast:
27	chr12:9493453..9495524-chr12:9502233..9505001,2	K562	blood:
28	chr12:9483413..9484009-chr12:9524583..9525215,2	MCF-7	breast:
29	chr12:9483381..9483965-chr12:9531043..9531743,2	MCF-7	breast:
30	chr12:9493453..9495524-chr12:9502233..9505001,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-5	chr12:9504271-9504480	XLOC_009651
2	lnc-CLEC2D-7	chr12:9492506-9492537	XLOC_009649
3	lnc-PZP-10	chr12:9502714-9503413	NONHSAT026583
4	lnc-PZP-10	chr12:9495983-9496596	NONHSAT026583
5	lnc-CLEC2D-6	chr12:9499308-9499722	NONHSAT026706
6	lnc-CLEC2D-7	chr12:9493053-9493304	XLOC_009649
7	lnc-CLEC2D-5	chr12:9504271-9504944	NONHSAT026731
8	lnc-CLEC2D-5	chr12:9502564-9502713	NONHSAT026731
9	lnc-CLEC2D-5	chr12:9502422-9502713	XLOC_009651
10	lnc-CLEC2D-6	chr12:9500555-9500599	XLOC_009650
11	lnc-PZP-10	chr12:9499320-9499524	NONHSAT026583
12	lnc-CLEC2D-6	chr12:9499309-9499722	XLOC_009650
13	lnc-PZP-10	chr12:9489902-9490170	NONHSAT026583
14	lnc-PZP-10	chr12:9500060-9500507	NONHSAT026583
15	lnc-PZP-10	chr12:9486480-9486891	NONHSAT026583
16	lnc-PZP-10	chr12:9495275-9495398	NONHSAT026583
17	lnc-PZP-10	chr12:9494143-9494640	NONHSAT026583
18	lnc-CLEC2D-6	chr12:9500409-9501023	NONHSAT026706
19	lnc-PZP-10	chr12:9489581-9489812	NONHSAT026583
20	lnc-CLEC2D-6	chr12:9498751-9498941	NONHSAT026706
21	lnc-PZP-4	chr12:9516719-9517139	XLOC_010009

No data

Variant related genes	Relation type
ENSG00000255753	TF binding region
ENSG00000260423	TF binding region
ENSG00000255753	CpG island
ENSG00000260423	CpG island
ENSG00000245105	chromatin interactions
ENSG00000260423	chromatin interactions
ENSG00000149499	chromatin interactions
ENSG00000149489	chromatin interactions
ENSG00000214851	chromatin interactions

Extended variants
information (count: 1308 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7294479	chr12:9473157-9473158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113562602	chr12:9473203-9473204	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182743582	chr12:9473204-9473205	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs140847093	chr12:9473207-9473208	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs187712763	chr12:9473309-9473310	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374085119	chr12:9473496-9473497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193243251	chr12:9473527-9473528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184860613	chr12:9473544-9473545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367895944	chr12:9473586-9473587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189329692	chr12:9473597-9473598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142979821	chr12:9473604-9473605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191906724	chr12:9473631-9473632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184381530	chr12:9473636-9473637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6487821	chr12:9473720-9473721	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs7311758	chr12:9473725-9473726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs377205311	chr12:9473784-9473785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188446452	chr12:9473837-9473838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145123331	chr12:9473866-9473867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181396718	chr12:9473880-9473881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6487824	chr12:9473882-9473883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs547312095	chr12:9473897-9473898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544769421	chr12:9473961-9473962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372985177	chr12:9474010-9474011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567037481	chr12:9474011-9474012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371520932	chr12:9474078-9474079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186031099	chr12:9474104-9474105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138382084	chr12:9474175-9474176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7954383	chr12:9474204-9474205	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs149234955	chr12:9474264-9474265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10771531	chr12:9474305-9474306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs569431488	chr12:9474321-9474322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112643590	chr12:9474335-9474336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10771532	chr12:9474404-9474405	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs201893220	chr12:9474505-9474506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10743665	chr12:9474509-9474510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4883236	chr12:9474538-9474539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397842535	chr12:9474541-9474542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200040621	chr12:9474542-9474543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7299213	chr12:9474543-9474544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71045249	chr12:9474544-9474545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535852642	chr12:9474566-9474567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62819360	chr12:9474574-9474575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71441728	chr12:9474579-9474580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28754628	chr12:9474583-9474584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12303026	chr12:9474610-9474611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs182391626	chr12:9474709-9474710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186292779	chr12:9474751-9474752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7299515	chr12:9474794-9474795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs61914411	chr12:9474865-9474866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61914412	chr12:9474868-9474869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9437200-9485200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:9457400-9485800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr12:9463000-9479000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:9464400-9477600	Weak transcription	Lung	lung
5	chr12:9464600-9487600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:9464800-9490000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr12:9465000-9486400	Weak transcription	A549	lung
8	chr12:9465400-9485200	Weak transcription	Fetal Intestine Small	intestine
9	chr12:9465600-9477800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:9465600-9484000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr12:9465600-9488000	Weak transcription	Dnd41	blood
12	chr12:9466000-9484000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:9466200-9484000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:9466400-9477400	Weak transcription	Fetal Lung	lung
15	chr12:9466400-9485200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr12:9466400-9487200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:9466400-9487600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:9471600-9473400	Enhancers	Primary B cells from peripheral blood	blood
19	chr12:9472000-9473200	Enhancers	Stomach Mucosa	stomach
20	chr12:9472000-9473200	Enhancers	NHEK	skin
21	chr12:9472200-9473200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr12:9472200-9476000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr12:9472400-9479400	Weak transcription	Brain Germinal Matrix	brain
24	chr12:9472600-9474000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr12:9472600-9475800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:9472800-9479000	Weak transcription	Primary T cells from cord blood	blood
27	chr12:9472800-9487600	Weak transcription	Thymus	Thymus
28	chr12:9473000-9473200	Enhancers	Esophagus	oesophagus
29	chr12:9473000-9479400	Weak transcription	Fetal Thymus	thymus
30	chr12:9473000-9484000	Weak transcription	GM12878-XiMat	blood
31	chr12:9475800-9476400	Enhancers	K562	blood
32	chr12:9475800-9478200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:9476000-9476200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr12:9477400-9477600	Enhancers	Fetal Lung	lung
35	chr12:9477400-9477600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr12:9477600-9478000	Enhancers	Lung	lung
37	chr12:9477600-9479200	Enhancers	Fetal Muscle Leg	muscle
38	chr12:9477600-9479600	Flanking Active TSS	Fetal Lung	lung
39	chr12:9477600-9480200	Enhancers	Fetal Muscle Trunk	muscle
40	chr12:9477800-9478000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:9478000-9479400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:9478200-9478600	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:9478200-9479000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:9479000-9480000	Enhancers	HepG2	liver
45	chr12:9479000-9480400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr12:9479000-9480600	Enhancers	Primary T cells from cord blood	blood
47	chr12:9479000-9486800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:9479200-9480400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr12:9479200-9481000	Enhancers	Primary T cells fromperipheralblood	blood
50	chr12:9479200-9486600	Weak transcription	Fetal Muscle Leg	muscle

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