Variant report

Variant	nsv1052245
Chromosome Location	chr12:33606238-33766502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:910)
CpG islands
(count:61)
Chromatin interactive
region (count:115)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:910 , 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	chr12:33740984-33742025	K562	blood:	n/a	n/a
2	ATF1	chr12:33740996-33741606	K562	blood:	n/a	n/a
3	ATF1	chr12:33749134-33749614	K562	blood:	n/a	n/a
4	ATF2	chr12:33740950-33741433	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:33740922-33741468	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:33741735-33742256	GM12878	blood:	n/a	n/a
7	ATF3	chr12:33740980-33741602	K562	blood:	n/a	n/a
8	BACH1	chr12:33613710-33613715	K562	blood:	n/a	n/a
9	BACH1	chr12:33625286-33625549	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr12:33751125-33751167	K562	blood:	n/a	n/a
11	BACH1	chr12:33740516-33741383	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr12:33741913-33742237	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:33741023-33741182	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr12:33734583-33735390	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:33741030-33741823	K562	blood:	n/a	n/a
16	BHLHE40	chr12:33741303-33741660	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:33759769-33760039	K562	blood:	n/a	n/a
18	BHLHE40	chr12:33759702-33760074	GM12878	blood:	n/a	n/a
19	BHLHE40	chr12:33697751-33697753	K562	blood:	n/a	n/a
20	BRCA1	chr12:33740352-33740651	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr12:33713910-33713913	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr12:33715352-33715613	K562	blood:	n/a	n/a
23	CBX3	chr12:33673832-33674319	K562	blood:	n/a	n/a
24	CBX3	chr12:33740710-33741670	K562	blood:	n/a	n/a
25	CBX3	chr12:33715396-33715617	K562	blood:	n/a	n/a
26	CBX3	chr12:33703953-33704297	K562	blood:	n/a	n/a
27	CBX3	chr12:33703185-33703489	K562	blood:	n/a	n/a
28	CCNT2	chr12:33741067-33741621	K562	blood:	n/a	n/a
29	CEBPB	chr12:33740992-33741470	MCF-7	breast:	n/a	n/a
30	CEBPB	chr12:33762321-33762756	MCF-7	breast:	n/a	n/a
31	CEBPB	chr12:33740841-33741369	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr12:33740890-33741531	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:33740839-33741631	K562	blood:	n/a	n/a
34	CEBPB	chr12:33740927-33741311	K562	blood:	n/a	n/a
35	CEBPB	chr12:33672207-33672491	HepG2	liver:	n/a	chr12:33672352-33672365 chr12:33672352-33672363 chr12:33672354-33672365
36	CEBPB	chr12:33741120-33741314	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:33708093-33708429	K562	blood:	n/a	chr12:33708261-33708272 chr12:33708344-33708357
38	CEBPB	chr12:33704517-33704702	Hela-S3	cervix:	n/a	chr12:33704654-33704665
39	CEBPB	chr12:33608367-33608484	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:33758688-33759108	MCF-7	breast:	n/a	n/a
41	CEBPB	chr12:33712455-33712704	A549	lung:	n/a	chr12:33712545-33712556
42	CEBPB	chr12:33673343-33673349	K562	blood:	n/a	n/a
43	CEBPB	chr12:33741024-33741433	MCF-7	breast:	n/a	n/a
44	CEBPB	chr12:33640896-33641346	MCF-7	breast:	n/a	n/a
45	CEBPB	chr12:33708082-33708506	IMR90	lung:	n/a	chr12:33708261-33708272 chr12:33708344-33708357
46	CEBPB	chr12:33648317-33648399	A549	lung:	n/a	n/a
47	CEBPB	chr12:33758802-33759002	K562	blood:	n/a	n/a
48	CEBPB	chr12:33712422-33712635	H1-hESC	embryonic stem cell:	n/a	chr12:33712545-33712556
49	CEBPB	chr12:33740994-33741335	IMR90	lung:	n/a	n/a
50	CEBPB	chr12:33753026-33753436	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33750494-33750544	LNCaP	prostate:	n/a
2	chr12:33750494-33750544	HNPCEpiC	eye:	n/a
3	chr12:33750494-33750544	SK-N-SH_RA	brain:	n/a
4	chr12:33750494-33750544	HAEpiC	amniotic membrane:	n/a
5	chr12:33750494-33750544	U87	brain:	n/a
6	chr12:33750494-33750544	AG10803	skin:	n/a
7	chr12:33750494-33750544	HRCEpiC	kidney:	n/a
8	chr12:33750494-33750544	HEEpiC	esophagus:	n/a
9	chr12:33750494-33750544	MCF10A-Er-Src	breast:	n/a
10	chr12:33750494-33750544	NHDF-neo	bronchial:	n/a
11	chr12:33750494-33750544	SAEC	small airway:	n/a
12	chr12:33750494-33750544	T-47D	breast:	n/a
13	chr12:33750494-33750544	HUVEC	blood vessel:	n/a
14	chr12:33750494-33750544	IMR90	lung:	fetal
15	chr12:33750494-33750544	HIPEpiC	eye:	n/a
16	chr12:33750494-33750544	BE2_C	brain:	n/a
17	chr12:33750494-33750544	BJ	skin:	n/a
18	chr12:33750494-33750544	Hepatocyte	liver:	n/a
19	chr12:33750494-33750544	HepG2	liver:	n/a
20	chr12:33750494-33750544	HRE	kidney:	n/a
21	chr12:33750494-33750544	HRPEpiC	eye:	n/a
22	chr12:33750494-33750544	HL-60	blood:	n/a
23	chr12:33750494-33750544	PANC-1	pancreas:	n/a
24	chr12:33750494-33750544	GM19239	blood:	n/a
25	chr12:33750494-33750544	H1-hESC	embryonic stem cell:	embryo
26	chr12:33750494-33750544	ProgFib	skin:	n/a
27	chr12:33750494-33750544	AG04449	skin:	fetal
28	chr12:33750494-33750544	Jurkat	blood:	n/a
29	chr12:33750494-33750544	GM12878	blood:	n/a
30	chr12:33750494-33750544	AG09309	skin:	n/a
31	chr12:33750494-33750544	HEK293	kidney:	embryo
32	chr12:33750494-33750544	ECC-1	luminal epithelium:	n/a
33	chr12:33750494-33750544	NT2-D1	testis:	n/a
34	chr12:33750494-33750544	HCT-116	colon:	n/a
35	chr12:33750494-33750544	CMK	blood:	n/a
36	chr12:33750494-33750544	SK-N-MC	brain:	n/a
37	chr12:33750494-33750544	PrEC	prostate:	n/a
38	chr12:33750494-33750544	Caco-2	colon:	n/a
39	chr12:33750494-33750544	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:33750494-33750544	NHBE	bronchial:	n/a
41	chr12:33750494-33750544	HCM	heart:	n/a
42	chr12:33750494-33750544	GM06990	blood:	n/a
43	chr12:33750494-33750544	AoSMC	blood vessel:	n/a
44	chr12:33750494-33750544	GM12892	blood:	n/a
45	chr12:33750494-33750544	A549	lung:	n/a
46	chr12:33750494-33750544	K562	blood:	n/a
47	chr12:33750494-33750544	HMEC	breast:	n/a
48	chr12:33750494-33750544	SK-N-SH	brain:	n/a
49	chr12:33750494-33750544	HCF	heart:	n/a
50	chr12:33750494-33750544	NH-A	brain:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:33688358..33691054-chr12:33691826..33694361,2	K562	blood:
2	chr12:33667255..33668975-chr12:33733951..33735986,2	MCF-7	breast:
3	chr12:33730883..33732707-chr12:33745155..33746710,2	MCF-7	breast:
4	chr12:33749840..33752814-chr12:33754848..33757190,2	K562	blood:
5	chr12:33738598..33741307-chr8:42697129..42698949,2	MCF-7	breast:
6	chr12:33740467..33741676-chr12:33762290..33763074,5	MCF-7	breast:
7	chr12:33757088..33759339-chr12:33761312..33763614,2	K562	blood:
8	chr12:33673191..33674096-chr7:136092701..136093461,2	MCF-7	breast:
9	chr10:58407921..58410026-chr12:33604212..33606934,2	MCF-7	breast:
10	chr12:33590684..33593436-chr12:33756476..33760229,4	MCF-7	breast:
11	chr12:33601474..33603509-chr12:33613032..33615014,2	K562	blood:
12	chr12:33753748..33755380-chr12:33758835..33761146,2	K562	blood:
13	chr12:33632921..33635641-chr12:33638680..33640584,2	K562	blood:
14	chr12:33749943..33752525-chr12:33753325..33754973,2	MCF-7	breast:
15	chr12:33680785..33683680-chr12:33685838..33687484,3	MCF-7	breast:
16	chr12:33757088..33759339-chr12:33761312..33763614,2	K562	blood:
17	chr12:33590681..33593666-chr12:33611371..33613830,2	K562	blood:
18	chr12:33636131..33639117-chr12:33639347..33641138,2	MCF-7	breast:
19	chr12:33762278..33765239-chr12:33769487..33771063,2	K562	blood:
20	chr12:33697913..33700088-chr12:33701563..33703139,2	K562	blood:
21	chr12:33593109..33594784-chr12:33753664..33755603,2	MCF-7	breast:
22	chr12:33592469..33594296-chr12:33715860..33717717,2	MCF-7	breast:
23	chr12:33667255..33668975-chr12:33733951..33735986,2	MCF-7	breast:
24	chr12:33652466..33655399-chr12:33657814..33659678,2	K562	blood:
25	chr12:33737757..33739747-chr12:33741389..33743027,2	MCF-7	breast:
26	chr12:33762584..33764416-chr12:33765590..33768500,2	MCF-7	breast:
27	chr12:33663952..33667378-chr12:33671771..33674594,3	MCF-7	breast:
28	chr12:33726328..33728110-chr12:33734687..33736717,2	MCF-7	breast:
29	chr12:33590785..33592619-chr12:33667736..33669567,2	MCF-7	breast:
30	chr12:33748144..33750127-chr12:33751970..33754633,2	K562	blood:
31	chr12:33704309..33707491-chr12:33710515..33713446,4	K562	blood:
32	chr12:33590760..33594067-chr12:33739942..33743332,4	K562	blood:
33	chr12:33589747..33593267-chr12:33745774..33749514,5	MCF-7	breast:
34	chr12:33673352..33675554-chr12:33738881..33741351,2	MCF-7	breast:
35	chr12:33749299..33751532-chr12:33760036..33763741,3	MCF-7	breast:
36	chr12:33732468..33735660-chr12:33738194..33740414,4	MCF-7	breast:
37	chr12:33615181..33617280-chr12:33622628..33625177,2	MCF-7	breast:
38	chr12:33762272..33764150-chr8:42748547..42750407,2	MCF-7	breast:
39	chr12:33586288..33588588-chr12:33738098..33741571,3	MCF-7	breast:
40	chr12:33726328..33728110-chr12:33734687..33736717,2	MCF-7	breast:
41	chr12:33101880..33104767-chr12:33761445..33763993,2	MCF-7	breast:
42	chr12:33758071..33760342-chr12:33762792..33765785,2	MCF-7	breast:
43	chr12:33758071..33760342-chr12:33762792..33765785,2	MCF-7	breast:
44	chr12:32906746..32910896-chr12:33738987..33744699,5	MCF-7	breast:
45	chr12:33694299..33696215-chr12:33697909..33700735,2	MCF-7	breast:
46	chr12:33748329..33751340-chr12:33752553..33756348,4	K562	blood:
47	chr12:33737682..33739227-chr12:33743519..33746177,2	K562	blood:
48	chr12:33590801..33593904-chr12:33746085..33748903,3	MCF-7	breast:
49	chr12:33752192..33755696-chr12:33757650..33764170,6	MCF-7	breast:
50	chr12:33741049..33744622-chr12:33756451..33760061,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000256070	TF binding region
RNU6-400P	TF binding region
ENSG00000256070	CpG island
RNU6-400P	CpG island
ENSG00000110975	chromatin interactions
ENSG00000131931	chromatin interactions
ENSG00000212475	chromatin interactions
ENSG00000139131	chromatin interactions

Extended variants
information (count: 3252 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3252 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111847099	chr12:33606257-33606258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74072812	chr12:33606267-33606268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs572970081	chr12:33606287-33606288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115891280	chr12:33606294-33606295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565919876	chr12:33606308-33606309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539536664	chr12:33606424-33606425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561974010	chr12:33606435-33606436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186289311	chr12:33606455-33606456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191480030	chr12:33606485-33606486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61927698	chr12:33606507-33606508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564037630	chr12:33606510-33606511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527413949	chr12:33606576-33606577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181482139	chr12:33606591-33606592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150629384	chr12:33606601-33606602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548667174	chr12:33606610-33606611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546655700	chr12:33606658-33606659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567002483	chr12:33606814-33606815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536040960	chr12:33606822-33606823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376725325	chr12:33606832-33606833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549267853	chr12:33606868-33606869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78641972	chr12:33606879-33606880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569209727	chr12:33606888-33606889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538117872	chr12:33606967-33606968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369766461	chr12:33607014-33607015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577599420	chr12:33607021-33607022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566966207	chr12:33607023-33607024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114397119	chr12:33607106-33607107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373362628	chr12:33607221-33607222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572993803	chr12:33607246-33607247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537454985	chr12:33607275-33607276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11052715	chr12:33607285-33607286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs374179747	chr12:33607309-33607310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115365058	chr12:33607342-33607343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575624816	chr12:33607347-33607348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544503524	chr12:33607374-33607375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146400050	chr12:33607385-33607386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138493600	chr12:33607391-33607392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539996149	chr12:33607407-33607408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61746207	chr12:33607418-33607419	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs528933386	chr12:33607436-33607437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201175982	chr12:33607451-33607452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185904170	chr12:33607452-33607453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113347823	chr12:33607464-33607465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569071661	chr12:33607471-33607472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531916038	chr12:33607542-33607543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73313980	chr12:33607576-33607577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs571353459	chr12:33607642-33607643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150625325	chr12:33607662-33607663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190663635	chr12:33607680-33607681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567770963	chr12:33607782-33607783	Weak transcription	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
Schizophrenia	20967226	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33595400-33615800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:33609200-33609600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr12:33609400-33610000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr12:33609800-33610000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr12:33615600-33616000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr12:33615600-33616200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr12:33615800-33616000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:33629400-33629600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:33629400-33629800	Enhancers	HSMM	muscle
10	chr12:33629400-33630000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr12:33635400-33635600	Enhancers	K562	blood
12	chr12:33635600-33636400	Weak transcription	K562	blood
13	chr12:33635600-33637600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:33636400-33637800	Enhancers	Fetal Heart	heart
15	chr12:33636400-33638000	Enhancers	K562	blood
16	chr12:33637200-33637400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:33637400-33639200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:33637600-33637800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:33637800-33638200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:33638200-33640800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:33639000-33640600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr12:33639200-33639600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:33639600-33646200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:33640800-33641400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:33641000-33641200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:33641000-33642000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:33641000-33642200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr12:33641200-33645200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:33641600-33642200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:33641600-33642600	Enhancers	Placenta Amnion	Placenta Amnion
31	chr12:33641800-33642200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr12:33641800-33642200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr12:33642200-33645200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr12:33645200-33645400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
35	chr12:33645200-33645600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:33645200-33645800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr12:33645200-33645800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:33659600-33659800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:33659800-33661200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:33661000-33661400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:33661200-33661600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:33668400-33669400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:33669400-33669600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:33672600-33672800	Enhancers	K562	blood
45	chr12:33672800-33673000	Flanking Active TSS	K562	blood
46	chr12:33673000-33673200	Active TSS	K562	blood
47	chr12:33673200-33673400	Flanking Active TSS	K562	blood
48	chr12:33673200-33673800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr12:33673400-33673600	Enhancers	HepG2	liver
50	chr12:33673400-33674200	Active TSS	ES-I3 Cell Line	embryonic stem cell

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