Variant report

Variant	nsv558257
Chromosome Location	chr12:33681398-33897481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1014)
CpG islands
(count:122)
Chromatin interactive
region (count:130)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:33740984-33742025	K562	blood:	n/a	n/a
2	ARID3A	chr12:33806348-33806595	K562	blood:	n/a	n/a
3	ARID3A	chr12:33831095-33831857	K562	blood:	n/a	n/a
4	ARID3A	chr12:33807257-33807627	K562	blood:	n/a	n/a
5	ATF1	chr12:33807257-33807582	K562	blood:	n/a	n/a
6	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
7	ATF1	chr12:33740996-33741606	K562	blood:	n/a	n/a
8	ATF1	chr12:33749134-33749614	K562	blood:	n/a	n/a
9	ATF2	chr12:33740950-33741433	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr12:33740922-33741468	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:33741735-33742256	GM12878	blood:	n/a	n/a
12	ATF3	chr12:33740980-33741602	K562	blood:	n/a	n/a
13	ATF3	chr12:33806344-33806588	K562	blood:	n/a	n/a
14	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr12:33812366-33812495	K562	blood:	n/a	n/a
16	BACH1	chr12:33847319-33847363	K562	blood:	n/a	n/a
17	BACH1	chr12:33740516-33741383	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:33807354-33807505	K562	blood:	n/a	n/a
19	BACH1	chr12:33751125-33751167	K562	blood:	n/a	n/a
20	BATF	chr12:33741913-33742237	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:33802958-33803315	H1-hESC	embryonic stem cell:	n/a	chr12:33803028-33803037
22	BCL11A	chr12:33741023-33741182	H1-hESC	embryonic stem cell:	n/a	n/a
23	BHLHE40	chr12:33759769-33760039	K562	blood:	n/a	n/a
24	BHLHE40	chr12:33867451-33867477	K562	blood:	n/a	n/a
25	BHLHE40	chr12:33806387-33806560	K562	blood:	n/a	n/a
26	BHLHE40	chr12:33734583-33735390	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:33741030-33741823	K562	blood:	n/a	n/a
28	BHLHE40	chr12:33697751-33697753	K562	blood:	n/a	n/a
29	BHLHE40	chr12:33759702-33760074	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:33741303-33741660	GM12878	blood:	n/a	n/a
31	BRCA1	chr12:33713910-33713913	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr12:33740352-33740651	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr12:33715396-33715617	K562	blood:	n/a	n/a
34	CBX3	chr12:33703185-33703489	K562	blood:	n/a	n/a
35	CBX3	chr12:33740710-33741670	K562	blood:	n/a	n/a
36	CBX3	chr12:33770775-33771015	K562	blood:	n/a	n/a
37	CBX3	chr12:33770729-33771117	K562	blood:	n/a	n/a
38	CBX3	chr12:33803718-33804191	K562	blood:	n/a	n/a
39	CBX3	chr12:33772340-33772799	K562	blood:	n/a	n/a
40	CBX3	chr12:33715352-33715613	K562	blood:	n/a	n/a
41	CBX3	chr12:33803725-33804117	K562	blood:	n/a	n/a
42	CBX3	chr12:33770149-33770498	K562	blood:	n/a	n/a
43	CBX3	chr12:33703953-33704297	K562	blood:	n/a	n/a
44	CCNT2	chr12:33741067-33741621	K562	blood:	n/a	n/a
45	CEBPB	chr12:33802974-33803262	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr12:33762321-33762756	MCF-7	breast:	n/a	n/a
47	CEBPB	chr12:33821454-33821714	HepG2	liver:	n/a	chr12:33821568-33821579
48	CEBPB	chr12:33712455-33712704	A549	lung:	n/a	chr12:33712545-33712556
49	CEBPB	chr12:33740841-33741369	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr12:33704584-33704792	HepG2	liver:	n/a	chr12:33704654-33704665

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33787337-33787387	NT2-D1	testis:	n/a
2	chr12:33750494-33750544	HNPCEpiC	eye:	n/a
3	chr12:33750494-33750544	HAEpiC	amniotic membrane:	n/a
4	chr12:33750494-33750544	MCF10A-Er-Src	breast:	n/a
5	chr12:33750494-33750544	HL-60	blood:	n/a
6	chr12:33787337-33787387	AG09319	gingival:	n/a
7	chr12:33750494-33750544	MCF-7	breast:	n/a
8	chr12:33750494-33750544	PrEC	prostate:	n/a
9	chr12:33787337-33787387	SKMC	muscle:	n/a
10	chr12:33787337-33787387	T-47D	breast:	n/a
11	chr12:33750494-33750544	SKMC	muscle:	n/a
12	chr12:33750494-33750544	HMEC	breast:	n/a
13	chr12:33750494-33750544	NT2-D1	testis:	n/a
14	chr12:33787337-33787387	HRE	kidney:	n/a
15	chr12:33787337-33787387	HL-60	blood:	n/a
16	chr12:33787337-33787387	U87	brain:	n/a
17	chr12:33750494-33750544	GM12891	blood:	n/a
18	chr12:33787337-33787387	AG04449	skin:	fetal
19	chr12:33750494-33750544	HEEpiC	esophagus:	n/a
20	chr12:33750494-33750544	HCT-116	colon:	n/a
21	chr12:33787337-33787387	BE2_C	brain:	n/a
22	chr12:33750494-33750544	IMR90	lung:	fetal
23	chr12:33750494-33750544	SK-N-SH_RA	brain:	n/a
24	chr12:33787337-33787387	NH-A	brain:	n/a
25	chr12:33787337-33787387	HCT-116	colon:	n/a
26	chr12:33750494-33750544	AG09309	skin:	n/a
27	chr12:33750494-33750544	RPTEC	kidney:	n/a
28	chr12:33750494-33750544	SAEC	small airway:	n/a
29	chr12:33787337-33787387	RPTEC	kidney:	n/a
30	chr12:33750494-33750544	GM12892	blood:	n/a
31	chr12:33750494-33750544	Hela-S3	cervix:	n/a
32	chr12:33787337-33787387	HRPEpiC	eye:	n/a
33	chr12:33787337-33787387	K562	blood:	n/a
34	chr12:33787337-33787387	AG10803	skin:	n/a
35	chr12:33787337-33787387	SK-N-SH_RA	brain:	n/a
36	chr12:33750494-33750544	ProgFib	skin:	n/a
37	chr12:33787337-33787387	HUVEC	blood vessel:	n/a
38	chr12:33787337-33787387	SAEC	small airway:	n/a
39	chr12:33750494-33750544	U87	brain:	n/a
40	chr12:33750494-33750544	AG09319	gingival:	n/a
41	chr12:33787337-33787387	HRCEpiC	kidney:	n/a
42	chr12:33787337-33787387	LNCaP	prostate:	n/a
43	chr12:33750494-33750544	SK-N-MC	brain:	n/a
44	chr12:33750494-33750544	SK-N-SH	brain:	n/a
45	chr12:33787337-33787387	HepG2	liver:	n/a
46	chr12:33787337-33787387	SK-N-MC	brain:	n/a
47	chr12:33750494-33750544	HRE	kidney:	n/a
48	chr12:33787337-33787387	HCPEpiC	choroid plexus:	n/a
49	chr12:33787337-33787387	Hela-S3	cervix:	n/a
50	chr12:33787337-33787387	GM06990	blood:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:33785580..33788231-chr12:33795540..33797279,2	MCF-7	breast:
2	chr12:33700293..33703250-chr12:33739121..33741427,2	K562	blood:
3	chr12:33817225..33819690-chr12:33823230..33824769,2	MCF-7	breast:
4	chr12:33807598..33810256-chr12:33811118..33813511,2	K562	blood:
5	chr12:33073552..33076364-chr12:33762087..33763941,2	MCF-7	breast:
6	chr12:33737682..33739227-chr12:33743519..33746177,2	K562	blood:
7	chr12:33588584..33590612-chr12:33792019..33793766,2	K562	blood:
8	chr12:33688358..33691054-chr12:33691826..33694361,2	K562	blood:
9	chr12:33741049..33744622-chr12:33756451..33760061,5	MCF-7	breast:
10	chr12:33697913..33700088-chr12:33701563..33703139,2	K562	blood:
11	chr12:33589747..33593267-chr12:33745774..33749514,5	MCF-7	breast:
12	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
13	chr12:33041897..33044565-chr12:33740312..33741870,2	K562	blood:
14	chr12:33732468..33735660-chr12:33738194..33740414,4	MCF-7	breast:
15	chr12:33785580..33788231-chr12:33795540..33797279,2	MCF-7	breast:
16	chr12:33748144..33750127-chr12:33751970..33754633,2	K562	blood:
17	chr12:33757088..33759339-chr12:33761312..33763614,2	K562	blood:
18	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
19	chr12:33590753..33592625-chr12:33706633..33709299,2	K562	blood:
20	chr12:31834709..31836887-chr12:33736084..33739059,2	K562	blood:
21	chr12:33740590..33741231-chr12:33762284..33763123,2	MCF-7	breast:
22	chr12:33740590..33741231-chr12:33762284..33763123,2	MCF-7	breast:
23	chr12:33719195..33722497-chr12:33723252..33727386,3	MCF-7	breast:
24	chr12:33589726..33596989-chr12:33737254..33743557,12	MCF-7	breast:
25	chr12:33737682..33739227-chr12:33743519..33746177,2	K562	blood:
26	chr12:33795537..33797751-chr12:33801352..33803205,2	MCF-7	breast:
27	chr12:33726328..33728110-chr12:33734687..33736717,2	MCF-7	breast:
28	chr12:33752276..33753246-chr12:33762327..33763192,5	MCF-7	breast:
29	chr12:33667255..33668975-chr12:33733951..33735986,2	MCF-7	breast:
30	chr12:33799617..33801183-chr8:42749699..42752602,2	MCF-7	breast:
31	chr12:33720010..33722634-chr12:33727963..33730491,2	K562	blood:
32	chr12:33590801..33593904-chr12:33746085..33748903,3	MCF-7	breast:
33	chr12:33680785..33683680-chr12:33685838..33687484,3	MCF-7	breast:
34	chr12:33738598..33741307-chr8:42697129..42698949,2	MCF-7	breast:
35	chr12:33828756..33830899-chr12:33837528..33839909,2	MCF-7	breast:
36	chr12:33579807..33580648-chr12:33758471..33759360,2	MCF-7	breast:
37	chr12:33735767..33737470-chr12:33737741..33739409,2	K562	blood:
38	chr12:33711689..33714048-chr12:33717879..33720013,2	MCF-7	breast:
39	chr12:33762278..33765239-chr12:33769487..33771063,2	K562	blood:
40	chr12:33734204..33736505-chr12:33740513..33742206,2	K562	blood:
41	chr12:33757088..33759339-chr12:33761312..33763614,2	K562	blood:
42	chr12:33732468..33735660-chr12:33738194..33740414,4	MCF-7	breast:
43	chr12:33694299..33696215-chr12:33697909..33700735,2	MCF-7	breast:
44	chr12:32908939..32909783-chr12:33758798..33759372,2	MCF-7	breast:
45	chr12:33586288..33588588-chr12:33738098..33741571,3	MCF-7	breast:
46	chr12:33758791..33761325-chr12:33805781..33808679,2	K562	blood:
47	chr12:33730883..33732707-chr12:33745155..33746710,2	MCF-7	breast:
48	chr12:33748329..33751340-chr12:33752553..33756348,4	K562	blood:
49	chr12:33700293..33703250-chr12:33739121..33741427,2	K562	blood:
50	chr12:33831200..33833987-chr12:33837460..33839264,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-6	chr12:33870788-33871152	NONHSAT027645

No data

Variant related genes	Relation type
ENSG00000270807	TF binding region
RNU6-400P	TF binding region
ENSG00000270807	CpG island
RNU6-400P	CpG island
ENSG00000171148	chromatin interactions
ENSG00000266044	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000212475	chromatin interactions
ENSG00000250151	chromatin interactions
ENSG00000241553	chromatin interactions
ENSG00000110975	chromatin interactions
ENSG00000120925	chromatin interactions
ENSG00000131931	chromatin interactions

Extended variants
information (count: 3955 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3955 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561580601	chr12:33681606-33681607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185586432	chr12:33681611-33681612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539018783	chr12:33681650-33681651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10128813	chr12:33681653-33681654	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570417441	chr12:33681714-33681715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539305168	chr12:33681729-33681730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546291352	chr12:33681740-33681741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139247365	chr12:33681868-33681869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566616838	chr12:33681894-33681895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144016164	chr12:33681924-33681925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191427515	chr12:33681959-33681960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369275930	chr12:33681963-33681964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115688191	chr12:33681975-33681976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575953044	chr12:33682028-33682029	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs181492804	chr12:33682040-33682041	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs538440699	chr12:33682061-33682062	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs534010897	chr12:33682126-33682127	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555577599	chr12:33682185-33682186	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs558337232	chr12:33682202-33682203	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs145816925	chr12:33682211-33682212	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186939363	chr12:33682262-33682263	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs191784833	chr12:33682281-33682282	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs183173333	chr12:33682310-33682311	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs118041165	chr12:33682347-33682348	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs542793857	chr12:33682357-33682358	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs538330425	chr12:33682377-33682378	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs66760012	chr12:33682385-33682386	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs1994135	chr12:33682405-33682406	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545033343	chr12:33682452-33682453	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs148971385	chr12:33682460-33682461	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs371516182	chr12:33682492-33682493	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs563903409	chr12:33682523-33682524	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs377196317	chr12:33682582-33682583	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs554462578	chr12:33682682-33682683	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs572630606	chr12:33682694-33682695	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs533097182	chr12:33682726-33682727	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs546850511	chr12:33682743-33682744	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs77268575	chr12:33682821-33682822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535423055	chr12:33682872-33682873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374179703	chr12:33682970-33682971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142988070	chr12:33682994-33682995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537902696	chr12:33683017-33683018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs151124646	chr12:33683053-33683054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145166573	chr12:33683075-33683076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs578197951	chr12:33683121-33683122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111689248	chr12:33683140-33683141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534254186	chr12:33683142-33683143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554435912	chr12:33683145-33683146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573994702	chr12:33683287-33683288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543008140	chr12:33683293-33683294	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	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
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
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Cancer	21272361	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33681600-33686600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr12:33682000-33682200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr12:33682200-33682400	Active TSS	Monocytes-CD14+_RO01746	blood
4	chr12:33682400-33682800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr12:33682600-33683200	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr12:33682800-33684200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr12:33685800-33686000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr12:33699000-33699200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:33699200-33704000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:33704000-33704800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr12:33704800-33714600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr12:33709800-33710000	Enhancers	H9 Cell Line	embryonic stem cell
13	chr12:33710000-33710600	Enhancers	Placenta Amnion	Placenta Amnion
14	chr12:33710000-33713600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr12:33711200-33711600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr12:33711600-33713200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr12:33712200-33712400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr12:33712400-33712600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr12:33712400-33712600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr12:33712400-33713600	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr12:33712600-33713400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr12:33712800-33713800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr12:33713200-33713600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr12:33713400-33713600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr12:33713400-33714400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr12:33713600-33713800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr12:33713600-33713800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr12:33713600-33714000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr12:33713600-33714000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr12:33713600-33714000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr12:33713600-33714400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr12:33713600-33714400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:33713600-33714600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr12:33713800-33714000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr12:33713800-33714400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr12:33713800-33714400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr12:33714000-33714200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr12:33714000-33714600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr12:33714000-33714800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr12:33714200-33714600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr12:33714600-33714800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:33714600-33714800	ZNF genes & repeats	Pancreas	Pancrea
43	chr12:33714600-33715000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:33715600-33716200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr12:33733200-33741400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:33733800-33735600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr12:33733800-33736000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:33734400-33734800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr12:33734600-33735200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr12:33734600-33735400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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