Variant report

Variant	nsv541458
Chromosome Location	chr12:33010643-33079667
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1153)
CpG islands
(count:854)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1153 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:33048500-33048992	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:33054568-33055429	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:33072127-33072538	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:33049969-33050169	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:33018464-33018796	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:33046390-33046742	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:33054647-33054650	K562	blood:	n/a	n/a
8	ARID3A	chr12:33044860-33045278	HepG2	liver:	n/a	n/a
9	ATF1	chr12:33036761-33036922	K562	blood:	n/a	n/a
10	ATF1	chr12:33014709-33014760	K562	blood:	n/a	n/a
11	ATF2	chr12:33059615-33059979	GM12878	blood:	n/a	n/a
12	ATF2	chr12:33059586-33060007	GM12878	blood:	n/a	n/a
13	BACH1	chr12:33049894-33050256	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr12:33030623-33030822	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr12:33032847-33033059	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr12:33059630-33060046	GM12878	blood:	n/a	n/a
17	BATF	chr12:33059634-33059995	GM12878	blood:	n/a	n/a
18	BATF	chr12:33028971-33029262	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:33059600-33060059	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:33059729-33059987	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:33059577-33060084	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:33059721-33059989	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:33049632-33050306	HepG2	liver:	n/a	chr12:33049870-33049886
24	BHLHE40	chr12:33059661-33060049	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:33049923-33050303	K562	blood:	n/a	n/a
26	BHLHE40	chr12:33041372-33041391	K562	blood:	n/a	n/a
27	BRCA1	chr12:33050089-33050272	HepG2	liver:	n/a	n/a
28	BRCA1	chr12:33019723-33019749	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr12:33049921-33050446	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr12:33044615-33045258	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:33059278-33059755	Hela-S3	cervix:	n/a	n/a
32	CCNT2	chr12:33049670-33050245	K562	blood:	n/a	n/a
33	CEBPB	chr12:33014741-33014848	K562	blood:	n/a	n/a
34	CEBPB	chr12:33046386-33046732	MCF-7	breast:	n/a	n/a
35	CEBPB	chr12:33073361-33073863	A549	lung:	n/a	n/a
36	CEBPB	chr12:33070175-33070494	HepG2	liver:	n/a	chr12:33070338-33070351 chr12:33070339-33070350
37	CEBPB	chr12:33044836-33045355	ECC-1	luminal epithelium:	n/a	chr12:33045100-33045111
38	CEBPB	chr12:33045913-33046786	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr12:33072087-33072788	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr12:33029081-33029169	K562	blood:	n/a	n/a
41	CEBPB	chr12:33046383-33046786	MCF-7	breast:	n/a	n/a
42	CEBPB	chr12:33048686-33048922	K562	blood:	n/a	n/a
43	CEBPB	chr12:33018459-33018655	HepG2	liver:	n/a	chr12:33018570-33018581
44	CEBPB	chr12:33070217-33070429	K562	blood:	n/a	chr12:33070338-33070351 chr12:33070339-33070350
45	CEBPB	chr12:33070126-33070498	A549	lung:	n/a	chr12:33070338-33070351 chr12:33070339-33070350
46	CEBPB	chr12:33072386-33072677	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:33069974-33070624	Hela-S3	cervix:	n/a	chr12:33070338-33070351 chr12:33070339-33070350
48	CEBPB	chr12:33046416-33046785	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:33070128-33070536	MCF-7	breast:	n/a	chr12:33070338-33070351 chr12:33070339-33070350
50	CEBPB	chr12:33044543-33045712	Hela-S3	cervix:	n/a	chr12:33045100-33045111

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33050217-33050267	BE2_C	brain:	n/a
2	chr12:33049650-33049700	SK-N-SH	brain:	n/a
3	chr12:33048913-33048963	ProgFib	skin:	n/a
4	chr12:33031216-33031266	HAEpiC	amniotic membrane:	n/a
5	chr12:33031065-33031115	A549	lung:	n/a
6	chr12:33050217-33050267	AG04449	skin:	fetal
7	chr12:33047018-33047068	LNCaP	prostate:	n/a
8	chr12:33036765-33036815	GM12891	blood:	n/a
9	chr12:33036765-33036815	U87	brain:	n/a
10	chr12:33047018-33047068	U87	brain:	n/a
11	chr12:33050050-33050100	AG09309	skin:	n/a
12	chr12:33036765-33036815	HCPEpiC	choroid plexus:	n/a
13	chr12:33048259-33048309	SK-N-SH_RA	brain:	n/a
14	chr12:33049671-33049721	ECC-1	luminal epithelium:	n/a
15	chr12:33049671-33049721	HRE	kidney:	n/a
16	chr12:33050173-33050223	HAEpiC	amniotic membrane:	n/a
17	chr12:33049620-33049670	GM19239	blood:	n/a
18	chr12:33050173-33050223	Hepatocyte	liver:	n/a
19	chr12:33031216-33031266	HL-60	blood:	n/a
20	chr12:33048913-33048963	SK-N-MC	brain:	n/a
21	chr12:33036765-33036815	GM12892	blood:	n/a
22	chr12:33050050-33050100	HRCEpiC	kidney:	n/a
23	chr12:33052596-33052646	HRE	kidney:	n/a
24	chr12:33031216-33031266	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:33049620-33049670	GM06990	blood:	n/a
26	chr12:33050050-33050100	NH-A	brain:	n/a
27	chr12:33048259-33048309	AG09319	gingival:	n/a
28	chr12:33049620-33049670	SKMC	muscle:	n/a
29	chr12:33052596-33052646	K562	blood:	n/a
30	chr12:33050173-33050223	U87	brain:	n/a
31	chr12:33031216-33031266	HCM	heart:	n/a
32	chr12:33031065-33031115	NHDF-neo	bronchial:	n/a
33	chr12:33049620-33049670	Jurkat	blood:	n/a
34	chr12:33030976-33031026	SK-N-MC	brain:	n/a
35	chr12:33050173-33050223	HUVEC	blood vessel:	n/a
36	chr12:33030976-33031026	AG09319	gingival:	n/a
37	chr12:33050217-33050267	U87	brain:	n/a
38	chr12:33030976-33031026	HIPEpiC	eye:	n/a
39	chr12:33030976-33031026	K562	blood:	n/a
40	chr12:33048913-33048963	GM12892	blood:	n/a
41	chr12:33049650-33049700	HL-60	blood:	n/a
42	chr12:33036765-33036815	Caco-2	colon:	n/a
43	chr12:33052596-33052646	HepG2	liver:	n/a
44	chr12:33049650-33049700	HRCEpiC	kidney:	n/a
45	chr12:33048913-33048963	NT2-D1	testis:	n/a
46	chr12:33052596-33052646	MCF10A-Er-Src	breast:	n/a
47	chr12:33048913-33048963	NH-A	brain:	n/a
48	chr12:33030976-33031026	HL-60	blood:	n/a
49	chr12:33048913-33048963	AoSMC	blood vessel:	n/a
50	chr12:33050217-33050267	AG09309	skin:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:33030910..33032926-chr12:33048801..33051266,2	MCF-7	breast:
2	chr12:33049986..33050843-chr19:40926643..40927147,2	Hela-S3	cervix:
3	chr10:60027892..60028588-chr12:33049924..33050500,2	Hela-S3	cervix:
4	chr12:33041543..33043753-chr12:33047901..33049581,2	MCF-7	breast:
5	chr12:33049077..33050069-chr16:2317510..2318347,2	Hela-S3	cervix:
6	chr12:32908063..32910245-chr12:33078669..33080621,2	MCF-7	breast:
7	chr12:33044433..33046332-chr12:33070929..33073660,2	MCF-7	breast:
8	chr12:33050014..33052233-chr12:33059225..33060757,2	MCF-7	breast:
9	chr12:33050014..33052233-chr12:33059225..33060757,2	MCF-7	breast:
10	chr12:32908961..32909825-chr12:33071724..33072321,3	MCF-7	breast:
11	chr12:33050887..33052544-chr4:134775575..134778473,2	MCF-7	breast:
12	chr12:33053524..33056632-chr12:33057306..33059409,3	MCF-7	breast:
13	chr12:32907857..32910579-chr12:33071009..33073541,2	MCF-7	breast:
14	chr12:33073552..33076364-chr12:33762087..33763941,2	MCF-7	breast:
15	chr12:32909198..32910124-chr12:33071777..33072639,3	MCF-7	breast:
16	chr12:33049269..33050202-chr17:42422178..42423144,2	Hela-S3	cervix:
17	chr12:33023484..33026312-chr12:33027563..33029941,2	K562	blood:
18	chr12:33034905..33037585-chr12:33047253..33049853,2	MCF-7	breast:
19	chr12:33046955..33049792-chr12:33071161..33073135,2	MCF-7	breast:
20	chr12:32906850..32908904-chr12:33070408..33072635,2	MCF-7	breast:
21	chr12:33053524..33056632-chr12:33057306..33059409,3	MCF-7	breast:
22	chr12:33047763..33049269-chr12:33060696..33063050,2	MCF-7	breast:
23	chr12:33049643..33050326-chr7:2393292..2394114,2	Hela-S3	cervix:
24	chr12:33049999..33050545-chr15:74832724..74833489,2	Hela-S3	cervix:
25	chr12:33044433..33046332-chr12:33070929..33073660,2	MCF-7	breast:
26	chr12:32907053..32910667-chr12:33044491..33046664,3	MCF-7	breast:
27	chr12:32908157..32910268-chr12:33048253..33050625,4	MCF-7	breast:
28	chr12:33041897..33044565-chr12:33740312..33741870,2	K562	blood:
29	chr12:33023484..33026312-chr12:33027563..33029941,2	K562	blood:
30	chr12:33050228..33050853-chr16:89882955..89883908,2	Hela-S3	cervix:
31	chr12:33049635..33052479-chr12:33052970..33055449,5	MCF-7	breast:
32	chr12:32909522..32911268-chr12:33072253..33074480,2	MCF-7	breast:
33	chr12:32907371..32910549-chr12:33046094..33048353,3	MCF-7	breast:
34	chr12:33049705..33050388-chr22:43011186..43011805,2	Hela-S3	cervix:
35	chr12:33049597..33050305-chr19:6424445..6424971,2	HCT-116	colon:
36	chr12:33049309..33052167-chr12:33052926..33054707,2	MCF-7	breast:
37	chr12:33050687..33051334-chr2:220117668..220118170,2	Hela-S3	cervix:
38	chr12:33047763..33049269-chr12:33060696..33063050,2	MCF-7	breast:
39	chr12:33022176..33023756-chr12:33047523..33049556,2	MCF-7	breast:
40	chr12:33044053..33044876-chr12:33059435..33060276,2	MCF-7	breast:
41	chr12:33044053..33044876-chr12:33059435..33060276,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNM1L-5	chr12:33016052-33016367	NONHSAT027633

No data

Variant related genes	Relation type
ENSG00000244743	TF binding region
PKP2	TF binding region
ENSG00000244743	CpG island
PKP2	CpG island
ENSG00000057294	chromatin interactions
ENSG00000106263	chromatin interactions
ENSG00000127824	chromatin interactions
ENSG00000243910	chromatin interactions
ENSG00000106266	chromatin interactions
ENSG00000088247	chromatin interactions
ENSG00000270022	chromatin interactions
ENSG00000187741	chromatin interactions
ENSG00000207715	chromatin interactions
ENSG00000030582	chromatin interactions
ENSG00000205937	chromatin interactions
ENSG00000260778	chromatin interactions
ENSG00000139131	chromatin interactions

Extended variants
information (count: 2629 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2629 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528652482	chr12:33010706-33010707	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551472772	chr12:33010719-33010720	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547526305	chr12:33010732-33010733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571712810	chr12:33010738-33010739	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527868525	chr12:33010766-33010767	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548058780	chr12:33010770-33010771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567952957	chr12:33010836-33010837	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76774152	chr12:33010856-33010857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12099507	chr12:33010899-33010900	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs554293978	chr12:33010908-33010909	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535846689	chr12:33010957-33010958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569614837	chr12:33010988-33010989	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113272738	chr12:33011014-33011015	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147960743	chr12:33011020-33011021	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200053982	chr12:33011022-33011023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370633467	chr12:33011024-33011025	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374336953	chr12:33011026-33011027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367913885	chr12:33011028-33011029	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1020666	chr12:33011045-33011046	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34727670	chr12:33011049-33011050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1020667	chr12:33011051-33011052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34480218	chr12:33011052-33011053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1020668	chr12:33011059-33011060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1020669	chr12:33011061-33011062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61139163	chr12:33011069-33011070	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3044534	chr12:33011073-33011074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561021901	chr12:33011084-33011085	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370398045	chr12:33011087-33011088	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189181479	chr12:33011107-33011108	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554942980	chr12:33011167-33011168	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192093147	chr12:33011202-33011203	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572477349	chr12:33011216-33011217	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540033672	chr12:33011254-33011255	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184315176	chr12:33011342-33011343	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573558897	chr12:33011345-33011346	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2389114	chr12:33011399-33011400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144080652	chr12:33011408-33011409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79688317	chr12:33011409-33011410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370452560	chr12:33011420-33011421	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146524189	chr12:33011424-33011425	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188659215	chr12:33011427-33011428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527436921	chr12:33011452-33011453	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141068688	chr12:33011455-33011456	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79777031	chr12:33011583-33011584	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74556521	chr12:33011585-33011586	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547971989	chr12:33011656-33011657	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560244209	chr12:33011677-33011678	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565461778	chr12:33011680-33011681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567865464	chr12:33011687-33011688	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530393713	chr12:33011739-33011740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
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	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21272361	CNVD

Chromatin state (count:1438 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32941800-33033400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr12:32943800-33026800	Weak transcription	Fetal Kidney	kidney
3	chr12:32972000-33029000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:32974200-33030400	Weak transcription	Right Ventricle	heart
5	chr12:32975800-33020000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:32993000-33030400	Weak transcription	Colonic Mucosa	Colon
7	chr12:32993400-33013600	Weak transcription	Pancreas	Pancrea
8	chr12:32993800-33018000	Weak transcription	Fetal Stomach	stomach
9	chr12:32997800-33044400	Weak transcription	Hela-S3	cervix
10	chr12:32997800-33046000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr12:33000200-33012400	Weak transcription	Right Atrium	heart
12	chr12:33000400-33020000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr12:33003200-33019400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr12:33003200-33022800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr12:33003800-33012600	Weak transcription	HMEC	breast
16	chr12:33003800-33030400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr12:33004000-33011400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr12:33004000-33012400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr12:33004000-33012400	Weak transcription	NHEK	skin
20	chr12:33004000-33015000	Weak transcription	Fetal Intestine Small	intestine
21	chr12:33004000-33017400	Weak transcription	Placenta	Placenta
22	chr12:33004000-33020000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr12:33004000-33020000	Weak transcription	HepG2	liver
24	chr12:33004000-33020200	Weak transcription	Fetal Intestine Large	intestine
25	chr12:33004000-33030400	Weak transcription	Gastric	stomach
26	chr12:33004200-33011200	Weak transcription	Liver	Liver
27	chr12:33004200-33011600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr12:33004200-33015600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr12:33004200-33028800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr12:33004400-33019600	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr12:33006800-33012400	Weak transcription	Left Ventricle	heart
32	chr12:33007800-33016200	Weak transcription	Stomach Mucosa	stomach
33	chr12:33008000-33011600	Enhancers	Fetal Heart	heart
34	chr12:33008200-33019600	Weak transcription	Duodenum Mucosa	Duodenum
35	chr12:33008200-33019800	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr12:33008600-33012400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:33010200-33011800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:33010200-33011800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr12:33010400-33012400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:33010400-33013200	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr12:33010400-33019200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr12:33011200-33012600	Enhancers	Liver	Liver
43	chr12:33011400-33012000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr12:33011600-33011800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:33011600-33012600	Weak transcription	Fetal Heart	heart
46	chr12:33011800-33012000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr12:33011800-33012000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr12:33011800-33012400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:33011800-33012600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:33011800-33021800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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