Variant report

Variant	nsv869
Chromosome Location	chr12:105363425-105394904
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:744)
CpG islands
(count:549)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:105379908-105380194	HepG2	liver:	n/a	n/a
2	ATF1	chr12:105390338-105390481	K562	blood:	n/a	n/a
3	ATF1	chr12:105379134-105379580	K562	blood:	n/a	n/a
4	ATF2	chr12:105368276-105368956	GM12878	blood:	n/a	n/a
5	ATF2	chr12:105368342-105368854	GM12878	blood:	n/a	n/a
6	ATF3	chr12:105379699-105380335	A549	lung:	n/a	chr12:105380067-105380076
7	BACH1	chr12:105380109-105380242	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:105368453-105368784	GM12878	blood:	n/a	n/a
9	BATF	chr12:105368373-105368802	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:105368354-105368777	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:105368445-105368735	GM12878	blood:	n/a	n/a
12	BCL3	chr12:105379658-105380446	A549	lung:	n/a	chr12:105380396-105380409 chr12:105380430-105380443 chr12:105380296-105380309 chr12:105380433-105380446 chr12:105380368-105380381
13	BCL3	chr12:105368433-105368763	GM12878	blood:	n/a	n/a
14	BCL3	chr12:105368529-105368781	GM12878	blood:	n/a	n/a
15	BCLAF1	chr12:105368296-105368960	GM12878	blood:	n/a	n/a
16	BCLAF1	chr12:105368367-105368796	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:105379836-105380637	GM12878	blood:	n/a	chr12:105380424-105380440 chr12:105380363-105380379
18	BHLHE40	chr12:105379952-105380424	HepG2	liver:	n/a	chr12:105380363-105380379
19	BHLHE40	chr12:105368464-105368900	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:105380099-105380343	A549	lung:	n/a	n/a
21	BHLHE40	chr12:105379976-105380650	K562	blood:	n/a	chr12:105380424-105380440 chr12:105380363-105380379
22	BRCA1	chr12:105379811-105380307	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr12:105379812-105380343	K562	blood:	n/a	n/a
24	CCNT2	chr12:105379907-105380629	K562	blood:	n/a	chr12:105380067-105380076 chr12:105380405-105380414
25	CEBPB	chr12:105368479-105368690	GM12878	blood:	n/a	n/a
26	CEBPB	chr12:105368390-105368693	K562	blood:	n/a	n/a
27	CEBPB	chr12:105369368-105369855	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr12:105368388-105369022	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr12:105368378-105368696	IMR90	lung:	n/a	n/a
30	CEBPB	chr12:105379848-105380203	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:105369456-105369811	IMR90	lung:	n/a	n/a
32	CEBPB	chr12:105368454-105368676	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:105368364-105368737	MCF-7	breast:	n/a	n/a
34	CEBPB	chr12:105377991-105378053	K562	blood:	n/a	n/a
35	CEBPB	chr12:105368386-105368728	A549	lung:	n/a	n/a
36	CEBPB	chr12:105368380-105368712	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:105368300-105368908	GM12878	blood:	n/a	n/a
38	CEBPB	chr12:105381460-105381714	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:105368378-105368687	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPD	chr12:105379884-105380285	HepG2	liver:	n/a	n/a
41	CHD1	chr12:105380079-105380313	GM12878	blood:	n/a	n/a
42	CHD2	chr12:105379922-105380278	HepG2	liver:	n/a	chr12:105380065-105380075
43	CHD2	chr12:105380042-105380225	K562	blood:	n/a	chr12:105380065-105380075
44	CHD2	chr12:105368436-105368903	GM12878	blood:	n/a	n/a
45	CHD2	chr12:105379845-105380659	Hela-S3	cervix:	n/a	chr12:105380065-105380075
46	CHD2	chr12:105379785-105380299	GM12878	blood:	n/a	chr12:105380065-105380075
47	CHD2	chr12:105380083-105380261	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr12:105368421-105368912	GM12878	blood:	n/a	n/a
49	CREB1	chr12:105379885-105380466	A549	lung:	n/a	n/a
50	CREB1	chr12:105368256-105368910	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:105379910-105379960	HCF	heart:	n/a
2	chr12:105379979-105380029	HCT-116	colon:	n/a
3	chr12:105379977-105380027	T-47D	breast:	n/a
4	chr12:105379977-105380027	HEK293	kidney:	embryo
5	chr12:105379977-105380027	IMR90	lung:	fetal
6	chr12:105380444-105380494	GM12891	blood:	n/a
7	chr12:105383497-105383547	BJ	skin:	n/a
8	chr12:105379893-105379943	HCPEpiC	choroid plexus:	n/a
9	chr12:105379893-105379943	MCF-7	breast:	n/a
10	chr12:105380772-105380822	A549	lung:	n/a
11	chr12:105377807-105377857	NH-A	brain:	n/a
12	chr12:105377807-105377857	SK-N-SH	brain:	n/a
13	chr12:105383497-105383547	SKMC	muscle:	n/a
14	chr12:105380444-105380494	IMR90	lung:	fetal
15	chr12:105379977-105380027	NHDF-neo	bronchial:	n/a
16	chr12:105379977-105380027	HUVEC	blood vessel:	n/a
17	chr12:105379979-105380029	PANC-1	pancreas:	n/a
18	chr12:105377807-105377857	NB4	blood:	n/a
19	chr12:105380444-105380494	NHDF-neo	bronchial:	n/a
20	chr12:105379910-105379960	SK-N-SH	brain:	n/a
21	chr12:105379977-105380027	GM12878	blood:	n/a
22	chr12:105380772-105380822	Hela-S3	cervix:	n/a
23	chr12:105379893-105379943	HAEpiC	amniotic membrane:	n/a
24	chr12:105380171-105380221	HRCEpiC	kidney:	n/a
25	chr12:105380171-105380221	AG09319	gingival:	n/a
26	chr12:105377807-105377857	BJ	skin:	n/a
27	chr12:105380171-105380221	ProgFib	skin:	n/a
28	chr12:105377807-105377857	HNPCEpiC	eye:	n/a
29	chr12:105383497-105383547	HMEC	breast:	n/a
30	chr12:105379910-105379960	HNPCEpiC	eye:	n/a
31	chr12:105379910-105379960	AG09309	skin:	n/a
32	chr12:105380444-105380494	AG10803	skin:	n/a
33	chr12:105379910-105379960	Caco-2	colon:	n/a
34	chr12:105379893-105379943	Jurkat	blood:	n/a
35	chr12:105380772-105380822	HEK293	kidney:	embryo
36	chr12:105383497-105383547	GM12878	blood:	n/a
37	chr12:105379979-105380029	SK-N-SH_RA	brain:	n/a
38	chr12:105383497-105383547	HNPCEpiC	eye:	n/a
39	chr12:105379977-105380027	SAEC	small airway:	n/a
40	chr12:105379910-105379960	BJ	skin:	n/a
41	chr12:105379979-105380029	HRCEpiC	kidney:	n/a
42	chr12:105377807-105377857	MCF10A-Er-Src	breast:	n/a
43	chr12:105379893-105379943	AG04450	lung:	fetal
44	chr12:105380171-105380221	K562	blood:	n/a
45	chr12:105380444-105380494	SK-N-SH	brain:	n/a
46	chr12:105383497-105383547	AG09319	gingival:	n/a
47	chr12:105380444-105380494	AG04450	lung:	fetal
48	chr12:105379977-105380027	NHBE	bronchial:	n/a
49	chr12:105379977-105380027	U87	brain:	n/a
50	chr12:105377807-105377857	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:105376961..105378683-chr12:105383835..105385377,2	K562	blood:
2	chr12:105378619..105382506-chr12:105382781..105387261,4	MCF-7	breast:
3	chr12:105351138..105353772-chr12:105378582..105380234,3	MCF-7	breast:
4	chr12:105380127..105381694-chr12:105412344..105413961,2	MCF-7	breast:
5	chr12:105378452..105381595-chr12:105388431..105392391,5	MCF-7	breast:
6	chr12:105349646..105353787-chr12:105376379..105382982,10	MCF-7	breast:
7	chr12:105379691..105382014-chr12:105391921..105394682,4	MCF-7	breast:
8	chr12:105372994..105375958-chr12:105380772..105382455,2	K562	blood:
9	chr12:105379932..105381513-chr12:105500073..105501775,2	MCF-7	breast:
10	chr12:105384826..105387201-chr12:105391835..105393587,2	K562	blood:
11	chr12:105391022..105393004-chr12:105396428..105398011,2	MCF-7	breast:
12	chr12:105368507..105370397-chr12:105372355..105374469,3	MCF-7	breast:
13	chr12:105363885..105366874-chr12:105377038..105378762,2	MCF-7	breast:
14	chr12:105367392..105369569-chr12:105378392..105380770,2	MCF-7	breast:
15	chr12:105368507..105370397-chr12:105372355..105374469,3	MCF-7	breast:
16	chr10:120938058..120938919-chr12:105379858..105380461,2	NB4	blood:
17	chr12:105379925..105380593-chr5:79950231..79951164,2	HCT-116	colon:
18	chr12:105376931..105378676-chr12:105378687..105380549,2	MCF-7	breast:
19	chr12:105379990..105383317-chr12:105392457..105395172,3	MCF-7	breast:
20	chr12:105379993..105381811-chr12:105382055..105386132,5	K562	blood:
21	chr12:105373554..105375601-chr12:105378341..105380639,2	K562	blood:
22	chr12:105379411..105381004-chr12:105501090..105502694,2	MCF-7	breast:
23	chr12:105349138..105353350-chr12:105380237..105383582,4	MCF-7	breast:
24	chr12:105365761..105368091-chr12:105378210..105380629,2	MCF-7	breast:
25	chr12:7052689..7053433-chr12:105379811..105380628,2	HCT-116	colon:
26	chr12:105372994..105375958-chr12:105380772..105382455,2	K562	blood:
27	chr12:105350976..105355078-chr12:105366279..105369986,4	MCF-7	breast:
28	chr12:105352802..105355166-chr12:105362542..105365310,2	MCF-7	breast:
29	chr12:105376961..105378683-chr12:105383835..105385377,2	K562	blood:
30	chr12:105384826..105387201-chr12:105391835..105393587,2	K562	blood:
31	chr12:105394211..105395980-chr12:105415862..105418537,2	K562	blood:
32	chr12:105379882..105380391-chr2:26256742..26257507,2	MCF-7	breast:
33	chr12:105363885..105366874-chr12:105377038..105378762,2	MCF-7	breast:
34	chr12:105371850..105375601-chr12:105378341..105381533,4	K562	blood:
35	chr12:105391750..105393633-chr12:105396940..105398737,2	K562	blood:
36	chr12:105374222..105376739-chr12:105379905..105381631,3	MCF-7	breast:
37	chr12:105368926..105370513-chr12:105372160..105373896,2	MCF-7	breast:
38	chr12:105368926..105370513-chr12:105372160..105373896,2	MCF-7	breast:
39	chr12:105392063..105394759-chr12:105462525..105464694,2	K562	blood:
40	chr12:105364467..105366636-chr12:105380045..105382271,2	MCF-7	breast:
41	chr12:53718302..53719271-chr12:105379712..105380362,2	NB4	blood:

No data

Variant related genes	Relation type
KRT18P20	TF binding region
C12orf45	TF binding region
KRT18P20	CpG island
C12orf45	CpG island
ENSG00000136052	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000228716	chromatin interactions
ENSG00000113318	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000151131	chromatin interactions
ENSG00000084733	chromatin interactions
ENSG00000165672	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000094914	chromatin interactions

Extended variants
information (count: 1140 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1140 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568614825	chr12:105363456-105363457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551612126	chr12:105363492-105363493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73193611	chr12:105363504-105363505	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548057667	chr12:105363510-105363511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35621730	chr12:105363515-105363516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151333516	chr12:105363559-105363560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539052271	chr12:105363596-105363597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555701337	chr12:105363618-105363619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575749391	chr12:105363657-105363658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140589468	chr12:105363671-105363672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555302462	chr12:105363685-105363686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541048212	chr12:105363730-105363731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78801548	chr12:105363790-105363791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541007566	chr12:105363885-105363886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564408397	chr12:105363918-105363919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150301620	chr12:105363926-105363927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546233598	chr12:105363951-105363952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562841845	chr12:105364003-105364004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117371798	chr12:105364016-105364017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542291977	chr12:105364042-105364043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs118119635	chr12:105364069-105364070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144872192	chr12:105364071-105364072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12297855	chr12:105364142-105364143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111339026	chr12:105364149-105364150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs80146717	chr12:105364216-105364217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35272765	chr12:105364217-105364218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79901499	chr12:105364224-105364225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184282222	chr12:105364315-105364316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569289211	chr12:105364357-105364358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189048231	chr12:105364381-105364382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374335311	chr12:105364431-105364432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79340904	chr12:105364455-105364456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571765532	chr12:105364523-105364524	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565591815	chr12:105364558-105364559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539698492	chr12:105364600-105364601	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534824529	chr12:105364643-105364644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181101011	chr12:105364644-105364645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs578014827	chr12:105364645-105364646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142070037	chr12:105364722-105364723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556628021	chr12:105364770-105364771	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373984881	chr12:105364777-105364778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545631701	chr12:105364793-105364794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375938445	chr12:105364825-105364826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145907542	chr12:105364830-105364831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563243017	chr12:105364863-105364864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527746561	chr12:105364970-105364971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs186627923	chr12:105365058-105365059	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564313802	chr12:105365105-105365106	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533473950	chr12:105365120-105365121	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189020923	chr12:105365144-105365145	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
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
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
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105360400-105368000	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr12:105362000-105363600	Enhancers	GM12878-XiMat	blood
3	chr12:105363600-105368000	Weak transcription	GM12878-XiMat	blood
4	chr12:105365000-105365200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr12:105365000-105365400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr12:105365000-105365600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:105365000-105365800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr12:105365000-105365800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:105365000-105365800	Enhancers	HUVEC	blood vessel
10	chr12:105365200-105365600	Enhancers	NHEK	skin
11	chr12:105365200-105365800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:105365200-105368600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr12:105365400-105365800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:105365400-105368200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr12:105365600-105365800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:105365600-105365800	Enhancers	NHLF	lung
17	chr12:105365600-105365800	Enhancers	Osteobl	bone
18	chr12:105365600-105367000	Weak transcription	NHEK	skin
19	chr12:105365600-105368400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:105365800-105367000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:105365800-105368200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:105365800-105368400	Weak transcription	Osteobl	bone
23	chr12:105365800-105368600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:105365800-105368600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr12:105367000-105368000	Enhancers	NHEK	skin
26	chr12:105367000-105368200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:105367000-105368600	Enhancers	Placenta	Placenta
28	chr12:105367800-105368400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:105368000-105368200	Enhancers	GM12878-XiMat	blood
30	chr12:105368000-105368200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr12:105368000-105368800	Flanking Active TSS	NHEK	skin
32	chr12:105368000-105369000	Enhancers	Stomach Mucosa	stomach
33	chr12:105368000-105370800	Enhancers	HMEC	breast
34	chr12:105368000-105371800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:105368000-105371800	Enhancers	Primary B cells from peripheral blood	blood
36	chr12:105368200-105368400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:105368200-105368800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:105368200-105369000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:105368200-105369000	Enhancers	Adipose Nuclei	Adipose
40	chr12:105368200-105369000	Flanking Active TSS	GM12878-XiMat	blood
41	chr12:105368200-105369000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr12:105368200-105370000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr12:105368200-105370200	Enhancers	Hela-S3	cervix
44	chr12:105368200-105372000	Enhancers	Primary B cells from cord blood	blood
45	chr12:105368400-105368600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr12:105368400-105369800	Enhancers	Osteobl	bone
47	chr12:105368400-105370200	Enhancers	NHDF-Ad	bronchial
48	chr12:105368400-105370400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:105368400-105370800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr12:105368600-105368800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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