Variant report

Variant	nsv898761
Chromosome Location	chr12:10496724-10564329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1555)
CpG islands
(count:550)
Chromatin interactive
region (count:27)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1555 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10536954-10536986	K562	blood:	n/a	n/a
2	ARID3A	chr12:10514385-10514386	K562	blood:	n/a	n/a
3	ARID3A	chr12:10515922-10516407	K562	blood:	n/a	n/a
4	ARID3A	chr12:10513720-10513857	K562	blood:	n/a	n/a
5	ARID3A	chr12:10519484-10519894	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:10517306-10518105	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
8	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:10548121-10548681	HepG2	liver:	n/a	n/a
10	ATF1	chr12:10518698-10519024	K562	blood:	n/a	n/a
11	ATF1	chr12:10515987-10516344	K562	blood:	n/a	n/a
12	ATF1	chr12:10518006-10518279	K562	blood:	n/a	n/a
13	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
14	ATF2	chr12:10516513-10517982	GM12878	blood:	n/a	n/a
15	ATF2	chr12:10516736-10518064	GM12878	blood:	n/a	n/a
16	ATF2	chr12:10517788-10518192	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr12:10544776-10545621	GM12878	blood:	n/a	n/a
18	ATF2	chr12:10515391-10516378	GM12878	blood:	n/a	n/a
19	ATF2	chr12:10515378-10516482	GM12878	blood:	n/a	n/a
20	ATF2	chr12:10517765-10518225	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr12:10547858-10548386	GM12878	blood:	n/a	n/a
22	ATF3	chr12:10515933-10516347	K562	blood:	n/a	n/a
23	BACH1	chr12:10517085-10517124	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr12:10516901-10517786	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:10517007-10517370	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:10544909-10545281	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:10547793-10548282	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:10544925-10545336	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:10547875-10548349	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:10516986-10517620	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:10515491-10515913	GM12878	blood:	n/a	n/a
32	BCL3	chr12:10515498-10515948	GM12878	blood:	n/a	n/a
33	BCLAF1	chr12:10544936-10545515	GM12878	blood:	n/a	chr12:10545490-10545499
34	BCLAF1	chr12:10516769-10517765	GM12878	blood:	n/a	n/a
35	BCLAF1	chr12:10544894-10545448	GM12878	blood:	n/a	n/a
36	BCLAF1	chr12:10516740-10517803	GM12878	blood:	n/a	n/a
37	BCLAF1	chr12:10547846-10548369	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:10516330-10516752	GM12878	blood:	n/a	n/a
39	BHLHE40	chr12:10559427-10559772	K562	blood:	n/a	n/a
40	BHLHE40	chr12:10515601-10515915	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:10516495-10517792	K562	blood:	n/a	n/a
42	BHLHE40	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:10547847-10548665	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:10516861-10517974	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:10562058-10562261	K562	blood:	n/a	n/a
46	BHLHE40	chr12:10515999-10516244	K562	blood:	n/a	n/a
47	BRCA1	chr12:10517548-10518007	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr12:10544899-10545539	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr12:10507323-10507343	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr12:10546999-10547736	Hela-S3	cervix:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10560602-10560652	SK-N-SH_RA	brain:	n/a
2	chr12:10560602-10560652	SK-N-SH_RA	brain:	n/a
3	chr12:10544636-10544686	Hepatocyte	liver:	n/a
4	chr12:10532046-10532096	MCF10A-Er-Src	breast:	n/a
5	chr12:10545083-10545133	HRE	kidney:	n/a
6	chr12:10545083-10545133	HCPEpiC	choroid plexus:	n/a
7	chr12:10544636-10544686	GM12878	blood:	n/a
8	chr12:10532046-10532096	IMR90	lung:	fetal
9	chr12:10525233-10525283	Hela-S3	cervix:	n/a
10	chr12:10516240-10516290	U87	brain:	n/a
11	chr12:10525233-10525283	HIPEpiC	eye:	n/a
12	chr12:10515091-10515141	PFSK-1	brain:	n/a
13	chr12:10545083-10545133	HEEpiC	esophagus:	n/a
14	chr12:10532046-10532096	HCPEpiC	choroid plexus:	n/a
15	chr12:10545083-10545133	H1-hESC	embryonic stem cell:	embryo
16	chr12:10543073-10543123	MCF10A-Er-Src	breast:	n/a
17	chr12:10545083-10545133	SK-N-SH_RA	brain:	n/a
18	chr12:10543073-10543123	LNCaP	prostate:	n/a
19	chr12:10544636-10544686	HCPEpiC	choroid plexus:	n/a
20	chr12:10515574-10515624	HL-60	blood:	n/a
21	chr12:10560602-10560652	SKMC	muscle:	n/a
22	chr12:10516240-10516290	NHDF-neo	bronchial:	n/a
23	chr12:10515574-10515624	HMEC	breast:	n/a
24	chr12:10545083-10545133	HNPCEpiC	eye:	n/a
25	chr12:10544636-10544686	AoSMC	blood vessel:	n/a
26	chr12:10515574-10515624	PrEC	prostate:	n/a
27	chr12:10515574-10515624	Jurkat	blood:	n/a
28	chr12:10532046-10532096	HEK293	kidney:	embryo
29	chr12:10560602-10560652	NHBE	bronchial:	n/a
30	chr12:10515091-10515141	K562	blood:	n/a
31	chr12:10543073-10543123	AG10803	skin:	n/a
32	chr12:10543073-10543123	SAEC	small airway:	n/a
33	chr12:10545083-10545133	GM12892	blood:	n/a
34	chr12:10525233-10525283	PANC-1	pancreas:	n/a
35	chr12:10532046-10532096	HPAEpiC	pulmonary alveolar:	n/a
36	chr12:10544636-10544686	ECC-1	luminal epithelium:	n/a
37	chr12:10515091-10515141	HepG2	liver:	n/a
38	chr12:10543073-10543123	HCPEpiC	choroid plexus:	n/a
39	chr12:10515091-10515141	GM12878	blood:	n/a
40	chr12:10532046-10532096	HUVEC	blood vessel:	n/a
41	chr12:10515091-10515141	H1-hESC	embryonic stem cell:	embryo
42	chr12:10515574-10515624	MCF10A-Er-Src	breast:	n/a
43	chr12:10544636-10544686	NT2-D1	testis:	n/a
44	chr12:10544636-10544686	HRPEpiC	eye:	n/a
45	chr12:10543073-10543123	HEK293	kidney:	embryo
46	chr12:10544636-10544686	BE2_C	brain:	n/a
47	chr12:10515574-10515624	HRE	kidney:	n/a
48	chr12:10515574-10515624	AG10803	skin:	n/a
49	chr12:10543073-10543123	MCF-7	breast:	n/a
50	chr12:10560602-10560652	AoSMC	blood vessel:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10515701..10517485-chr12:10526352..10529351,3	K562	blood:
2	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
3	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
4	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
5	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
6	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
7	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
8	chr12:10536735..10538905-chr12:10543028..10545121,2	MCF-7	breast:
9	chr12:10534850..10537741-chr12:10540764..10542364,2	MCF-7	breast:
10	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
11	chr12:10516092..10519058-chr12:10537972..10540241,2	K562	blood:
12	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
13	chr12:10506746..10508549-chr12:10514255..10516412,2	K562	blood:
14	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
15	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
16	chr12:10509675..10512643-chr12:10514341..10517366,3	K562	blood:
17	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
18	chr12:10537029..10538774-chr12:10541549..10544546,2	K562	blood:
19	chr12:10518506..10519182-chr16:20688297..20688797,2	HCT-116	colon:
20	chr12:10548044..10548696-chr9:117267865..117268396,2	Hela-S3	cervix:
21	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
22	chr12:10515701..10519228-chr12:10526352..10529377,4	K562	blood:
23	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
24	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
25	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
26	chr12:10528733..10530247-chr12:10762165..10764402,2	K562	blood:
27	chr12:10519323..10520144-chr12:10902384..10903013,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRD1-1	chr12:10516368-10516632	ENSG00000245648
2	lnc-RP11-277P12.7.1-1	chr12:10511063-10511162	ENSG00000256155
3	lnc-RP11-277P12.7.1-1	chr12:10513183-10513644	ENSG00000256155
4	lnc-KLRD1-1	chr12:10526634-10526735	ENSG00000245648
5	lnc-KLRD1-1	chr12:10532301-10532435	ENSG00000245648
6	lnc-KLRD1-1	chr12:10548778-10551105	ENSG00000245648

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KLRK1	hsa-miR-9-5p	chr12:10525600-10525624

Variant related genes	Relation type
KLRK1	TF binding region
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000256155	TF binding region
ENSG00000245648	TF binding region
KLRK1	CpG island
KLRC4	CpG island
KLRC4-KLRK1	CpG island
ENSG00000256155	CpG island
ENSG00000245648	CpG island
ENSG00000270103	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000167900	chromatin interactions
ENSG00000213809	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000256888	chromatin interactions
ESR1	miRNA target sites
SMAD4	miRNA target sites
KIAA1967	miRNA target sites

Extended variants
information (count: 2735 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2735 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7137853	chr12:10496724-10496725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115940442	chr12:10496741-10496742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188473285	chr12:10496749-10496750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572337486	chr12:10496757-10496758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548902438	chr12:10496766-10496767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6488282	chr12:10496774-10496775	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs35514947	chr12:10496781-10496782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6488283	chr12:10496783-10496784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs79119364	chr12:10496803-10496804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550160672	chr12:10496860-10496861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6416265	chr12:10496867-10496868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs557647088	chr12:10496871-10496872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532678399	chr12:10496872-10496873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7304620	chr12:10496891-10496892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533318732	chr12:10496966-10496967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115541456	chr12:10496985-10496986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147764617	chr12:10497001-10497002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11053752	chr12:10497003-10497004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557000250	chr12:10497008-10497009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530012199	chr12:10497026-10497027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138790369	chr12:10497031-10497032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9738661	chr12:10497033-10497034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11502910	chr12:10497036-10497037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9738662	chr12:10497039-10497040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192746537	chr12:10497047-10497048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61648448	chr12:10497052-10497053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576531650	chr12:10497055-10497056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568351296	chr12:10497066-10497067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200796033	chr12:10497094-10497095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536913324	chr12:10497115-10497116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183127757	chr12:10497117-10497118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141130096	chr12:10497129-10497130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539029854	chr12:10497130-10497131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552692073	chr12:10497164-10497165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147435872	chr12:10497174-10497175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139738190	chr12:10497188-10497189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566946722	chr12:10497195-10497196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561284109	chr12:10497204-10497205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138952468	chr12:10497217-10497218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575095651	chr12:10497261-10497262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544103111	chr12:10497283-10497284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7959173	chr12:10497287-10497288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369953731	chr12:10497304-10497305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563951899	chr12:10497309-10497310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532586697	chr12:10497321-10497322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373400411	chr12:10497328-10497329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375968873	chr12:10497334-10497335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367992892	chr12:10497376-10497377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60521315	chr12:10497390-10497391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559887352	chr12:10497405-10497406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1782 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10492800-10507000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:10494600-10507000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:10504000-10504200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:10504200-10507000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr12:10505000-10505600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:10505600-10505800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr12:10505600-10507000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:10505800-10506800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:10506600-10506800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr12:10506800-10507200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr12:10506800-10507200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr12:10506800-10507200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr12:10506800-10507200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr12:10506800-10507200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr12:10506800-10507200	Enhancers	GM12878-XiMat	blood
16	chr12:10506800-10507400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr12:10506800-10507400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
18	chr12:10506800-10507400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr12:10506800-10508000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr12:10506800-10508000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:10506800-10508200	Enhancers	Hela-S3	cervix
22	chr12:10507000-10507200	Enhancers	Gastric	stomach
23	chr12:10507000-10507200	Enhancers	Pancreas	Pancrea
24	chr12:10507000-10507400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr12:10507000-10507400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr12:10507000-10507400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:10507000-10507400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:10507000-10507400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:10507000-10507400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr12:10507000-10507400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr12:10507000-10507400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr12:10507000-10507400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr12:10507000-10507400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:10507000-10507400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:10507000-10507400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr12:10507000-10507400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr12:10507000-10507400	Enhancers	Placenta Amnion	Placenta Amnion
38	chr12:10507000-10507400	Enhancers	HSMM	muscle
39	chr12:10507000-10507600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr12:10507200-10507400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr12:10507200-10507400	Enhancers	HMEC	breast
42	chr12:10507200-10513000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr12:10507400-10510200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr12:10507400-10512800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr12:10507400-10512800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr12:10507400-10513400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:10507400-10513400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:10507400-10513400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:10507400-10515800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr12:10507600-10513400	Weak transcription	HMEC	breast

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