Variant report

Variant	nsv832375
Chromosome Location	chr12:39599362-39784722
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1288)
CpG islands
(count:305)
Chromatin interactive
region (count:96)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:39782854-39783156	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:39708632-39708643	K562	blood:	n/a	n/a
3	ARID3A	chr12:39734843-39735216	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:39713017-39713303	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:39726981-39727045	K562	blood:	n/a	n/a
6	ATF1	chr12:39681654-39681982	K562	blood:	n/a	n/a
7	ATF2	chr12:39734914-39735478	GM12878	blood:	n/a	n/a
8	ATF2	chr12:39599817-39600262	GM12878	blood:	n/a	n/a
9	ATF3	chr12:39748780-39749070	K562	blood:	n/a	n/a
10	BACH1	chr12:39713137-39713293	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr12:39626959-39627154	GM12878	blood:	n/a	chr12:39627086-39627097
12	BATF	chr12:39599839-39600242	GM12878	blood:	n/a	n/a
13	BATF	chr12:39626610-39626815	GM12878	blood:	n/a	n/a
14	BATF	chr12:39766731-39767112	GM12878	blood:	n/a	chr12:39766904-39766915
15	BATF	chr12:39734939-39735488	GM12878	blood:	n/a	n/a
16	BATF	chr12:39599781-39600204	GM12878	blood:	n/a	n/a
17	BATF	chr12:39734956-39735511	GM12878	blood:	n/a	n/a
18	BATF	chr12:39671281-39671667	GM12878	blood:	n/a	n/a
19	BATF	chr12:39626976-39627170	GM12878	blood:	n/a	chr12:39627086-39627097
20	BATF	chr12:39671306-39671625	GM12878	blood:	n/a	n/a
21	BATF	chr12:39693284-39693435	GM12878	blood:	n/a	n/a
22	BATF	chr12:39693282-39693429	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:39734955-39735370	GM12878	blood:	n/a	n/a
24	BCL3	chr12:39630667-39631248	A549	lung:	n/a	n/a
25	BCL3	chr12:39630714-39631296	A549	lung:	n/a	n/a
26	BCLAF1	chr12:39766698-39767293	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:39667041-39667224	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:39671371-39671521	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:39599801-39600047	GM12878	blood:	n/a	n/a
30	BRCA1	chr12:39694055-39694061	GM12878	blood:	n/a	n/a
31	BRCA1	chr12:39618264-39618265	GM12878	blood:	n/a	n/a
32	CEBPB	chr12:39681603-39682092	MCF-7	breast:	n/a	chr12:39681826-39681837
33	CEBPB	chr12:39681640-39682014	H1-hESC	embryonic stem cell:	n/a	chr12:39681826-39681837
34	CEBPB	chr12:39681750-39681908	HepG2	liver:	n/a	chr12:39681826-39681837
35	CEBPB	chr12:39681563-39682066	ECC-1	luminal epithelium:	n/a	chr12:39681826-39681837
36	CEBPB	chr12:39735556-39735740	HepG2	liver:	n/a	chr12:39735638-39735649
37	CEBPB	chr12:39681567-39682036	ECC-1	luminal epithelium:	n/a	chr12:39681826-39681837
38	CEBPB	chr12:39612419-39612607	A549	lung:	n/a	n/a
39	CEBPB	chr12:39681629-39681971	K562	blood:	n/a	chr12:39681826-39681837
40	CEBPB	chr12:39707718-39707730	K562	blood:	n/a	n/a
41	CEBPB	chr12:39681650-39682021	IMR90	lung:	n/a	chr12:39681826-39681837
42	CEBPB	chr12:39712949-39713260	HepG2	liver:	n/a	chr12:39713116-39713127
43	CEBPB	chr12:39712964-39713245	MCF-7	breast:	n/a	chr12:39713116-39713127
44	CEBPB	chr12:39681542-39682062	K562	blood:	n/a	chr12:39681826-39681837
45	CEBPB	chr12:39630887-39631318	A549	lung:	n/a	n/a
46	CEBPB	chr12:39681517-39682075	A549	lung:	n/a	chr12:39681826-39681837
47	CEBPB	chr12:39681602-39681955	A549	lung:	n/a	chr12:39681826-39681837
48	CEBPB	chr12:39671094-39671647	Hela-S3	cervix:	n/a	chr12:39671434-39671447 chr12:39671239-39671252 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
49	CEBPB	chr12:39671251-39671626	K562	blood:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
50	CEBPB	chr12:39671277-39671610	HepG2	liver:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39763210-39763260	HNPCEpiC	eye:	n/a
2	chr12:39706834-39706884	SK-N-SH	brain:	n/a
3	chr12:39706834-39706884	NH-A	brain:	n/a
4	chr12:39706834-39706884	U87	brain:	n/a
5	chr12:39706834-39706884	H1-hESC	embryonic stem cell:	embryo
6	chr12:39763210-39763260	AoSMC	blood vessel:	n/a
7	chr12:39726715-39726765	HRPEpiC	eye:	n/a
8	chr12:39763210-39763260	HMEC	breast:	n/a
9	chr12:39726715-39726765	GM12878	blood:	n/a
10	chr12:39706834-39706884	AoSMC	blood vessel:	n/a
11	chr12:39706834-39706884	LNCaP	prostate:	n/a
12	chr12:39726715-39726765	U87	brain:	n/a
13	chr12:39687917-39687967	ProgFib	skin:	n/a
14	chr12:39727030-39727080	HCF	heart:	n/a
15	chr12:39763210-39763260	Caco-2	colon:	n/a
16	chr12:39763210-39763260	Jurkat	blood:	n/a
17	chr12:39706834-39706884	BJ	skin:	n/a
18	chr12:39727030-39727080	Hela-S3	cervix:	n/a
19	chr12:39763210-39763260	HCM	heart:	n/a
20	chr12:39727030-39727080	HCPEpiC	choroid plexus:	n/a
21	chr12:39726715-39726765	NHDF-neo	bronchial:	n/a
22	chr12:39727030-39727080	HEEpiC	esophagus:	n/a
23	chr12:39727030-39727080	GM19239	blood:	n/a
24	chr12:39763210-39763260	NT2-D1	testis:	n/a
25	chr12:39726715-39726765	CMK	blood:	n/a
26	chr12:39687917-39687967	HCPEpiC	choroid plexus:	n/a
27	chr12:39706834-39706884	Hepatocyte	liver:	n/a
28	chr12:39763210-39763260	HepG2	liver:	n/a
29	chr12:39763210-39763260	NHDF-neo	bronchial:	n/a
30	chr12:39687917-39687967	GM19239	blood:	n/a
31	chr12:39726715-39726765	Jurkat	blood:	n/a
32	chr12:39706834-39706884	HNPCEpiC	eye:	n/a
33	chr12:39687917-39687967	HEK293	kidney:	embryo
34	chr12:39763210-39763260	BE2_C	brain:	n/a
35	chr12:39706834-39706884	AG10803	skin:	n/a
36	chr12:39687917-39687967	PFSK-1	brain:	n/a
37	chr12:39687917-39687967	AG04449	skin:	fetal
38	chr12:39727030-39727080	PFSK-1	brain:	n/a
39	chr12:39763210-39763260	HRPEpiC	eye:	n/a
40	chr12:39763210-39763260	BJ	skin:	n/a
41	chr12:39763210-39763260	NH-A	brain:	n/a
42	chr12:39727030-39727080	HL-60	blood:	n/a
43	chr12:39727030-39727080	AG09309	skin:	n/a
44	chr12:39706834-39706884	NHBE	bronchial:	n/a
45	chr12:39687917-39687967	NT2-D1	testis:	n/a
46	chr12:39763210-39763260	A549	lung:	n/a
47	chr12:39687917-39687967	HAEpiC	amniotic membrane:	n/a
48	chr12:39726715-39726765	GM06990	blood:	n/a
49	chr12:39726715-39726765	AG04449	skin:	fetal
50	chr12:39726715-39726765	HEK293	kidney:	embryo

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:39707021..39709923-chr12:39830984..39833005,2	K562	blood:
2	chr12:39708405..39711742-chr12:39713944..39715751,3	K562	blood:
3	chr12:39775530..39777936-chr12:39825264..39827786,2	K562	blood:
4	chr12:39770581..39773028-chr12:39775151..39777027,2	K562	blood:
5	chr12:39300107..39301045-chr12:39666439..39667709,7	MCF-7	breast:
6	chr12:39708198..39710149-chr12:39835781..39837977,2	MCF-7	breast:
7	chr12:39706735..39709135-chr12:39713252..39715316,2	K562	blood:
8	chr12:39701709..39705031-chr12:39707216..39710861,3	K562	blood:
9	chr12:39707343..39709850-chr12:39833796..39835957,2	K562	blood:
10	chr12:39769582..39772161-chr12:39835841..39837638,2	K562	blood:
11	chr12:39724474..39727162-chr12:39736483..39738898,2	K562	blood:
12	chr12:39771043..39772683-chr12:39784560..39786078,2	MCF-7	breast:
13	chr12:39685600..39687183-chr12:39700503..39702703,2	K562	blood:
14	chr12:39748533..39750921-chr12:39755964..39757616,2	K562	blood:
15	chr12:39757176..39762110-chr12:39835391..39838507,4	MCF-7	breast:
16	chr12:39779513..39783139-chr12:39785165..39787752,3	K562	blood:
17	chr12:39751967..39753839-chr12:39754682..39757326,2	K562	blood:
18	chr12:39711735..39712649-chr12:40077357..40078312,2	K562	blood:
19	chr12:39755090..39757754-chr12:39764621..39766612,2	MCF-7	breast:
20	chr12:39729399..39730971-chr12:39733599..39736235,2	MCF-7	breast:
21	chr12:39762097..39763744-chr12:39766808..39769516,2	MCF-7	breast:
22	chr12:39747712..39750921-chr12:39754829..39757616,3	K562	blood:
23	chr12:39708222..39708926-chr12:39836719..39837524,2	MCF-7	breast:
24	chr12:39768164..39770883-chr12:39771123..39773923,3	K562	blood:
25	chr12:39742374..39745219-chr12:39747056..39748871,3	K562	blood:
26	chr12:39679471..39682455-chr12:39683067..39685661,2	MCF-7	breast:
27	chr12:39706735..39709135-chr12:39713252..39715316,2	K562	blood:
28	chr12:39784633..39788139-chr12:39834968..39838023,4	MCF-7	breast:
29	chr12:39770581..39773028-chr12:39775151..39777027,2	K562	blood:
30	chr12:39734809..39736531-chr12:39748406..39750857,2	K562	blood:
31	chr12:39705679..39708570-chr12:39709976..39712207,2	MCF-7	breast:
32	chr12:39759047..39762172-chr12:39834495..39838400,6	MCF-7	breast:
33	chr12:39701709..39705031-chr12:39707216..39710861,3	K562	blood:
34	chr12:39713760..39716372-chr12:39835448..39837014,2	MCF-7	breast:
35	chr12:39727146..39729804-chr12:39835867..39838331,2	K562	blood:
36	chr12:39738067..39741527-chr12:39743955..39747329,3	MCF-7	breast:
37	chr12:39768164..39770883-chr12:39771123..39773923,3	K562	blood:
38	chr12:39607982..39610891-chr12:39612624..39615291,2	K562	blood:
39	chr12:39725322..39729241-chr12:39730380..39734731,5	K562	blood:
40	chr12:39764517..39769063-chr12:39834166..39838574,6	K562	blood:
41	chr12:39752339..39754010-chr12:39754627..39757326,2	K562	blood:
42	chr12:39736502..39739070-chr12:39744339..39745945,2	K562	blood:
43	chr12:39742374..39745219-chr12:39747056..39748871,3	K562	blood:
44	chr12:39690972..39693239-chr12:39694761..39697625,2	MCF-7	breast:
45	chr12:39756404..39758819-chr12:39835044..39837136,2	MCF-7	breast:
46	chr12:39766807..39768997-chr12:39769052..39771333,2	MCF-7	breast:
47	chr12:39736502..39739070-chr12:39744339..39745945,2	K562	blood:
48	chr12:39743944..39745971-chr12:39833401..39836053,2	K562	blood:
49	chr12:38722084..38722866-chr12:39667246..39667987,2	MCF-7	breast:
50	chr12:39741674..39745219-chr12:39746773..39748556,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf40-4	chr12:39667587-39667691	NONHSAT027698
2	lnc-ABCD2-5	chr12:39750402-39750697	NONHSAT027704
3	lnc-C12orf40-3	chr12:39720338-39720424	NONHSAT027701
4	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027700
5	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027701
6	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027701
7	lnc-C12orf40-3	chr12:39720075-39720147	NONHSAT027700
8	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027702
9	lnc-ABCD2-5	chr12:39751050-39751089	NONHSAT027704
10	lnc-C12orf40-3	chr12:39721452-39721634	NONHSAT027702
11	lnc-C12orf40-4	chr12:39667024-39667150	NONHSAT027698
12	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027700

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KIF21A	hsa-miR-186-5p	chr12:39688170-39688191
2	KIF21A	hsa-miR-186-5p	chr12:39687380-39687401

Variant related genes	Relation type
KIF21A	TF binding region
KIF21A	CpG island
ENSG00000139116	chromatin interactions
ENSG00000252974	chromatin interactions
ENSG00000257718	chromatin interactions

Extended variants
information (count: 4666 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4666 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575260053	chr12:39611450-39611451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542634799	chr12:39611451-39611452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368490318	chr12:39611472-39611473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191133704	chr12:39611500-39611501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528167046	chr12:39611521-39611522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564833632	chr12:39611522-39611523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539975565	chr12:39611582-39611583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77726594	chr12:39611605-39611606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531400134	chr12:39611646-39611647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116316021	chr12:39611702-39611703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549706096	chr12:39611746-39611747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568806739	chr12:39611784-39611785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117776232	chr12:39611794-39611795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77807322	chr12:39620807-39620808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145714825	chr12:39620828-39620829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140462177	chr12:39620914-39620915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533345670	chr12:39620969-39620970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559604507	chr12:39620970-39620971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533473733	chr12:39620974-39620975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370409234	chr12:39621054-39621055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551729149	chr12:39621091-39621092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117915737	chr12:39621133-39621134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189686559	chr12:39621169-39621170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73266458	chr12:39621277-39621278	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549852816	chr12:39621278-39621279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4403835	chr12:39621324-39621325	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs7350605	chr12:39621331-39621332	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs78162718	chr12:39621335-39621336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572346355	chr12:39621358-39621359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145584968	chr12:39621441-39621442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558147827	chr12:39621488-39621489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146507287	chr12:39621519-39621520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77470244	chr12:39621521-39621522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75821956	chr12:39621538-39621539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181226968	chr12:39621544-39621545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375070526	chr12:39621549-39621550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141045680	chr12:39621557-39621558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559543438	chr12:39621558-39621559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533413174	chr12:39621569-39621570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143119845	chr12:39621570-39621571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563881486	chr12:39621589-39621590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549853790	chr12:39621718-39621719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539599962	chr12:39621719-39621720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76650065	chr12:39621729-39621730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531336531	chr12:39621730-39621731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372966760	chr12:39621745-39621746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4768669	chr12:39621747-39621748	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186208522	chr12:39621766-39621767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148232174	chr12:39621791-39621792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572863438	chr12:39621796-39621797	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Breast cancer	21509527	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39611400-39611800	Enhancers	Esophagus	oesophagus
2	chr12:39620800-39622000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:39621000-39621400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:39621000-39621600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:39621200-39621400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr12:39622000-39624000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:39624000-39624600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:39624600-39629600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:39629400-39630200	Enhancers	Colon Smooth Muscle	Colon
10	chr12:39629600-39631400	Enhancers	NH-A	brain
11	chr12:39629600-39635000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr12:39629800-39630000	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr12:39629800-39630400	Enhancers	A549	lung
14	chr12:39629800-39631200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr12:39630000-39634000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr12:39630200-39631200	Enhancers	Hela-S3	cervix
17	chr12:39630200-39631400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr12:39630200-39631400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr12:39630400-39631200	Flanking Active TSS	A549	lung
20	chr12:39630600-39631000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:39630600-39631000	Enhancers	HSMMtube	muscle
22	chr12:39630800-39631200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:39630800-39631600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:39631200-39631400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr12:39631200-39631400	Enhancers	A549	lung
26	chr12:39631200-39632600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:39631200-39632600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr12:39631400-39632600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr12:39631400-39633200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:39631600-39632200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:39632200-39632800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr12:39632200-39632800	Bivalent Enhancer	A549	lung
33	chr12:39632400-39632800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr12:39632600-39632800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:39632600-39633400	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr12:39632600-39633800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr12:39632600-39634200	Enhancers	Fetal Intestine Large	intestine
38	chr12:39632600-39634400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr12:39632600-39634800	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr12:39632600-39635000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr12:39632800-39633200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:39632800-39633400	Enhancers	Brain Substantia Nigra	brain
43	chr12:39632800-39634200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr12:39633200-39634000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr12:39633200-39634200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:39633400-39633800	Enhancers	HepG2	liver
47	chr12:39633400-39634000	Active TSS	Rectal Mucosa Donor 29	rectum
48	chr12:39633400-39634400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr12:39633400-39634600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr12:39633400-39634800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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