Variant report

Variant	nsv899349
Chromosome Location	chr12:82931646-83114286
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1876)
CpG islands
(count:1221)
Chromatin interactive
region (count:75)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1876 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:83021707-83022007	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:83079498-83079859	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:83044464-83044541	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:83079569-83079766	K562	blood:	n/a	n/a
5	ATF1	chr12:83043553-83043580	K562	blood:	n/a	n/a
6	ATF2	chr12:83079423-83079832	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:83080135-83080691	GM12878	blood:	n/a	n/a
8	ATF2	chr12:83044271-83044754	GM12878	blood:	n/a	n/a
9	ATF2	chr12:83044248-83044789	GM12878	blood:	n/a	n/a
10	ATF3	chr12:83079429-83079917	A549	lung:	n/a	n/a
11	ATF3	chr12:83045164-83045791	HCT-116	colon:	n/a	n/a
12	BACH1	chr12:83080125-83080301	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr12:83080541-83081200	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr12:83016592-83016711	K562	blood:	n/a	n/a
15	BATF	chr12:83079501-83079775	GM12878	blood:	n/a	n/a
16	BATF	chr12:82948434-82948657	GM12878	blood:	n/a	n/a
17	BATF	chr12:82987634-82987976	GM12878	blood:	n/a	n/a
18	BATF	chr12:83044408-83044763	GM12878	blood:	n/a	chr12:83044538-83044549
19	BATF	chr12:82986851-82987326	GM12878	blood:	n/a	n/a
20	BATF	chr12:82987581-82987963	GM12878	blood:	n/a	n/a
21	BATF	chr12:82986910-82987255	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:82986805-82987286	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:82987643-82987969	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:82987585-82987949	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:82986936-82987223	GM12878	blood:	n/a	n/a
26	BCL3	chr12:83044415-83044639	GM12878	blood:	n/a	chr12:83044604-83044613 chr12:83044605-83044614
27	BCL3	chr12:83059273-83059591	GM12878	blood:	n/a	n/a
28	BCL3	chr12:83059236-83059628	GM12878	blood:	n/a	n/a
29	BCL3	chr12:83079406-83080044	A549	lung:	n/a	n/a
30	BCLAF1	chr12:83080074-83080737	GM12878	blood:	n/a	n/a
31	BCLAF1	chr12:83081358-83081835	GM12878	blood:	n/a	n/a
32	BCLAF1	chr12:83079455-83079908	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:82987541-82988424	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:83080069-83081162	GM12878	blood:	n/a	chr12:83080366-83080382 chr12:83080358-83080374
35	BHLHE40	chr12:83045133-83045147	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:83079477-83079836	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:83079639-83079844	K562	blood:	n/a	n/a
38	BHLHE40	chr12:83081426-83082338	GM12878	blood:	n/a	n/a
39	BRCA1	chr12:83044386-83044808	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr12:83080953-83081041	HepG2	liver:	n/a	n/a
41	BRCA1	chr12:83079484-83080605	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr12:83079544-83079928	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr12:83079499-83079784	HepG2	liver:	n/a	n/a
44	CBX3	chr12:83079572-83079786	K562	blood:	n/a	n/a
45	CBX3	chr12:83044148-83044993	HCT-116	colon:	n/a	chr12:83044817-83044828
46	CBX3	chr12:83044197-83044987	HCT-116	colon:	n/a	chr12:83044817-83044828
47	CBX3	chr12:83079485-83079786	K562	blood:	n/a	n/a
48	CBX3	chr12:83045217-83045776	HCT-116	colon:	n/a	n/a
49	CCNT2	chr12:83080794-83081014	K562	blood:	n/a	n/a
50	CEBPB	chr12:83045261-83045751	A549	lung:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:83080838-83080888	T-47D	breast:	n/a
2	chr12:83080838-83080888	T-47D	breast:	n/a
3	chr12:83081048-83081098	HAEpiC	amniotic membrane:	n/a
4	chr12:83079551-83079601	SK-N-SH	brain:	n/a
5	chr12:83079681-83079731	MCF-7	breast:	n/a
6	chr12:83080838-83080888	ECC-1	luminal epithelium:	n/a
7	chr12:83080830-83080880	SAEC	small airway:	n/a
8	chr12:83079969-83080019	HRE	kidney:	n/a
9	chr12:83053229-83053279	IMR90	lung:	fetal
10	chr12:83082074-83082124	AG09319	gingival:	n/a
11	chr12:83089601-83089651	HNPCEpiC	eye:	n/a
12	chr12:83102075-83102125	NHDF-neo	bronchial:	n/a
13	chr12:83079681-83079731	AG10803	skin:	n/a
14	chr12:83053229-83053279	MCF10A-Er-Src	breast:	n/a
15	chr12:83079551-83079601	AG04450	lung:	fetal
16	chr12:83089601-83089651	PANC-1	pancreas:	n/a
17	chr12:83080830-83080880	H1-hESC	embryonic stem cell:	embryo
18	chr12:83080830-83080880	BE2_C	brain:	n/a
19	chr12:83041928-83041978	MCF-7	breast:	n/a
20	chr12:83081389-83081439	HRE	kidney:	n/a
21	chr12:83079551-83079601	AG10803	skin:	n/a
22	chr12:83059257-83059307	ECC-1	luminal epithelium:	n/a
23	chr12:83079969-83080019	HCT-116	colon:	n/a
24	chr12:83053229-83053279	PANC-1	pancreas:	n/a
25	chr12:83080834-83080884	BJ	skin:	n/a
26	chr12:83080681-83080731	SKMC	muscle:	n/a
27	chr12:83053192-83053242	SK-N-MC	brain:	n/a
28	chr12:83102075-83102125	Jurkat	blood:	n/a
29	chr12:83078195-83078245	HL-60	blood:	n/a
30	chr12:83080208-83080258	U87	brain:	n/a
31	chr12:83082074-83082124	BJ	skin:	n/a
32	chr12:83080830-83080880	GM06990	blood:	n/a
33	chr12:83080208-83080258	AG04449	skin:	fetal
34	chr12:83080838-83080888	HPAEpiC	pulmonary alveolar:	n/a
35	chr12:83059257-83059307	HUVEC	blood vessel:	n/a
36	chr12:83079681-83079731	GM06990	blood:	n/a
37	chr12:83080681-83080731	Caco-2	colon:	n/a
38	chr12:83079551-83079601	NH-A	brain:	n/a
39	chr12:83079681-83079731	NH-A	brain:	n/a
40	chr12:83080681-83080731	AG04450	lung:	fetal
41	chr12:83059257-83059307	HRPEpiC	eye:	n/a
42	chr12:83079551-83079601	HEK293	kidney:	embryo
43	chr12:83102075-83102125	HEK293	kidney:	embryo
44	chr12:83053315-83053365	NH-A	brain:	n/a
45	chr12:83082074-83082124	HMEC	breast:	n/a
46	chr12:83053229-83053279	GM06990	blood:	n/a
47	chr12:83102075-83102125	AG10803	skin:	n/a
48	chr12:83082074-83082124	AG10803	skin:	n/a
49	chr12:83081046-83081096	ovcar-3	ovarian:	n/a
50	chr12:83059257-83059307	Hepatocyte	liver:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:83069857..83072718-chr12:83073334..83076243,4	MCF-7	breast:
2	chr12:83078982..83081661-chr3:63848631..63850534,2	MCF-7	breast:
3	chr12:83045168..83046859-chr12:83077129..83078918,2	MCF-7	breast:
4	chr12:83042183..83044298-chr12:83079732..83081351,2	MCF-7	breast:
5	chr12:83030541..83031126-chr2:73772566..73773410,2	MCF-7	breast:
6	chr12:83052210..83053962-chr12:83070728..83072436,2	MCF-7	breast:
7	chr12:83079302..83080209-chr12:83828151..83829089,2	MCF-7	breast:
8	chr12:83104932..83106856-chr12:83113427..83114996,2	K562	blood:
9	chr12:83079543..83083074-chr12:83085664..83088459,4	MCF-7	breast:
10	chr12:83080249..83082936-chr12:83085734..83087836,2	K562	blood:
11	chr12:83082650..83084238-chr12:83109960..83112390,2	MCF-7	breast:
12	chr12:83079877..83081535-chr12:120728404..120731286,2	MCF-7	breast:
13	chr12:83078910..83080496-chr12:83405630..83407973,2	MCF-7	breast:
14	chr12:83088398..83090839-chr12:83090924..83092850,2	MCF-7	breast:
15	chr12:83079157..83079752-chr12:84896786..84897429,2	MCF-7	breast:
16	chr12:83038079..83039947-chr12:83043283..83045373,2	MCF-7	breast:
17	chr12:82920672..82921613-chr12:83021112..83021885,4	MCF-7	breast:
18	chr12:82753521..82754075-chr12:83021392..83022207,3	MCF-7	breast:
19	chr12:83027721..83031479-chr12:83077251..83081760,5	MCF-7	breast:
20	chr12:82971566..82972433-chr13:51277425..51278166,2	MCF-7	breast:
21	chr12:83079259..83080112-chr12:83782817..83783839,5	MCF-7	breast:
22	chr12:83079605..83080356-chr12:83398378..83399038,2	MCF-7	breast:
23	chr12:83097820..83099718-chr12:83101247..83102887,2	MCF-7	breast:
24	chr12:83103199..83104985-chr12:83114072..83116122,2	MCF-7	breast:
25	chr12:83075987..83078783-chr12:83079698..83081470,2	K562	blood:
26	chr12:83041018..83042538-chr12:83044192..83045758,2	MCF-7	breast:
27	chr12:82920686..82921567-chr12:83021333..83022314,4	MCF-7	breast:
28	chr12:83072653..83078667-chr12:83078860..83082223,14	MCF-7	breast:
29	chr12:83042670..83045643-chr12:83080310..83082308,2	MCF-7	breast:
30	chr12:82920677..82921535-chr12:83019931..83020685,2	MCF-7	breast:
31	chr12:83078627..83080390-chr12:83781749..83784378,2	MCF-7	breast:
32	chr12:83053691..83056419-chr12:83078760..83082343,3	MCF-7	breast:
33	chr12:83054169..83057951-chr12:83058253..83061323,3	MCF-7	breast:
34	chr12:82752165..82753058-chr12:83021424..83022313,3	MCF-7	breast:
35	chr12:83078166..83081005-chr12:83099084..83103387,3	MCF-7	breast:
36	chr12:83080196..83081829-chr12:83092014..83094612,2	MCF-7	breast:
37	chr12:83103199..83104985-chr12:83114072..83116122,2	MCF-7	breast:
38	chr12:82936658..82939200-chr2:183214684..183217154,2	MCF-7	breast:
39	chr12:83080246..83081011-chr12:112123306..112123880,2	NB4	blood:
40	chr12:83079314..83080074-chr12:83165496..83166214,2	MCF-7	breast:
41	chr12:83067087..83068686-chr12:83071892..83073446,2	MCF-7	breast:
42	chr12:83052210..83053962-chr12:83070728..83072436,2	MCF-7	breast:
43	chr12:83079558..83081676-chr12:83103138..83105199,2	MCF-7	breast:
44	chr12:83088398..83090839-chr12:83090924..83092850,2	MCF-7	breast:
45	chr12:83079676..83081707-chr12:83150851..83153057,2	MCF-7	breast:
46	chr12:83038079..83039947-chr12:83043283..83045373,2	MCF-7	breast:
47	chr12:83077655..83080172-chr12:83389847..83391869,2	MCF-7	breast:
48	chr12:83079205..83080097-chr12:84217208..84218130,4	MCF-7	breast:
49	chr12:83097820..83099718-chr12:83101247..83102887,2	MCF-7	breast:
50	chr12:83079271..83080216-chr12:84217192..84217878,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC59-4	chr12:82950644-82950876	XLOC_010141
2	lnc-CCDC59-4	chr12:82954894-82954933	XLOC_010141

No data

Variant related genes	Relation type
TMTC2	TF binding region
TMTC2	CpG island
ENSG00000089234	chromatin interactions
ENSG00000163634	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000133773	chromatin interactions
ENSG00000127720	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000111271	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000179104	chromatin interactions
N4BP1	miRNA target sites
NAA15	miRNA target sites

Extended variants
information (count: 4804 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4804 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56175170	chr12:82938409-82938410	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs137896599	chr12:82938413-82938414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114595733	chr12:82938467-82938468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149467118	chr12:82938473-82938474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113676482	chr12:82938474-82938475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113183362	chr12:82938485-82938486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555541220	chr12:82938486-82938487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571595623	chr12:82938568-82938569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187730547	chr12:82938576-82938577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368926430	chr12:82938585-82938586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35486299	chr12:82938595-82938596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117303314	chr12:82938615-82938616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562804880	chr12:82938659-82938660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111882144	chr12:82938664-82938665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545336601	chr12:82938696-82938697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12425234	chr12:82938719-82938720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs192704175	chr12:82938721-82938722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193068556	chr12:82943816-82943817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537107373	chr12:82943818-82943819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368324245	chr12:82943829-82943830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138656871	chr12:82943884-82943885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552112046	chr12:82943905-82943906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185694924	chr12:82943914-82943915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530013159	chr12:82943918-82943919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142719844	chr12:82943967-82943968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12832018	chr12:82944040-82944041	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574126526	chr12:82944057-82944058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535113462	chr12:82944067-82944068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535249536	chr12:82944075-82944076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568888032	chr12:82944082-82944083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539504237	chr12:82944092-82944093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557535589	chr12:82944106-82944107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372531677	chr12:82944127-82944128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373926966	chr12:82944149-82944150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4641549	chr12:82944171-82944172	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141692861	chr12:82944174-82944175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530825408	chr12:82944181-82944182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555651785	chr12:82944186-82944187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573987422	chr12:82944243-82944244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12826548	chr12:82944265-82944266	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189113897	chr12:82944270-82944271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545813801	chr12:82944271-82944272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192423363	chr12:82944288-82944289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139572141	chr12:82944292-82944293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564111299	chr12:82944298-82944299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560541493	chr12:82944348-82944349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528296853	chr12:82944354-82944355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540388049	chr12:82944355-82944356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562002904	chr12:82944356-82944357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529184086	chr12:82944362-82944363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1382 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:82938400-82938800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:82938400-82938800	Enhancers	HMEC	breast
3	chr12:82943800-82944800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:82944800-82945000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:82944800-82945000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:82945000-82958400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:82946400-82946800	ZNF genes & repeats	Pancreas	Pancrea
8	chr12:82946800-82947000	ZNF genes & repeats	Gastric	stomach
9	chr12:82946800-82947400	Weak transcription	Pancreas	Pancrea
10	chr12:82947400-82947800	Enhancers	Pancreas	Pancrea
11	chr12:82947600-82950800	Enhancers	Hela-S3	cervix
12	chr12:82948200-82949800	Enhancers	HUVEC	blood vessel
13	chr12:82948400-82948800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr12:82948400-82949000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr12:82948400-82949000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:82948600-82949000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:82949000-82950000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr12:82950000-82951000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr12:82958000-82958200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr12:82958200-82958600	ZNF genes & repeats	Colon Smooth Muscle	Colon
21	chr12:82958400-82958600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
22	chr12:82958400-82958600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
23	chr12:82958400-82958600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr12:82958400-82958600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
25	chr12:82958400-82958600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
26	chr12:82958400-82958600	ZNF genes & repeats	Colonic Mucosa	Colon
27	chr12:82958400-82958600	ZNF genes & repeats	Esophagus	oesophagus
28	chr12:82958400-82958600	Bivalent/Poised TSS	Psoas Muscle	Psoas
29	chr12:82958400-82958800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr12:82958400-82958800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:82958400-82958800	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:82958400-82958800	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr12:82958400-82958800	ZNF genes & repeats	Gastric	stomach
34	chr12:82958400-82958800	ZNF genes & repeats	Spleen	Spleen
35	chr12:82958600-82958800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr12:82958600-82958800	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
37	chr12:82958800-82959200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr12:82959400-82960800	Enhancers	Stomach Mucosa	stomach
39	chr12:82959600-82961200	Enhancers	HUVEC	blood vessel
40	chr12:82959800-82960400	Enhancers	Liver	Liver
41	chr12:82959800-82960600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:82960400-82961600	Flanking Active TSS	Liver	Liver
43	chr12:82961600-82964000	Enhancers	Liver	Liver
44	chr12:82968000-82968600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:82972400-82973200	Enhancers	Hela-S3	cervix
46	chr12:82977200-82977800	Enhancers	HUVEC	blood vessel
47	chr12:82986800-82987200	Enhancers	GM12878-XiMat	blood
48	chr12:82986800-82988000	Enhancers	Fetal Heart	heart
49	chr12:82987000-82989200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr12:82987200-82987800	Weak transcription	GM12878-XiMat	blood

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