Variant report

Variant	nsv899504
Chromosome Location	chr12:106095906-106135942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:395)
CpG islands
(count:183)
Chromatin interactive
region (count:21)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:106099507-106099870	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr12:106115130-106115535	GM12878	blood:	n/a	n/a
3	BATF	chr12:106114837-106115571	GM12878	blood:	n/a	n/a
4	BATF	chr12:106115773-106115932	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:106114891-106115636	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:106134161-106134377	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr12:106114906-106115239	GM12878	blood:	n/a	n/a
8	BRCA1	chr12:106117152-106117158	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:106126397-106126610	HepG2	liver:	n/a	chr12:106126529-106126540
10	CEBPB	chr12:106126376-106126686	A549	lung:	n/a	chr12:106126529-106126540
11	CEBPB	chr12:106116763-106116923	IMR90	lung:	n/a	chr12:106116825-106116838 chr12:106116825-106116836
12	CEBPB	chr12:106126369-106126647	H1-hESC	embryonic stem cell:	n/a	chr12:106126529-106126540
13	CEBPB	chr12:106126371-106126598	IMR90	lung:	n/a	chr12:106126529-106126540
14	CHD1	chr12:106115591-106115603	GM12878	blood:	n/a	n/a
15	CHD2	chr12:106114974-106115354	GM12878	blood:	n/a	n/a
16	CTCF	chr12:106099859-106099861	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr12:106099120-106099270	HMEC	breast:	n/a	n/a
18	CTCF	chr12:106099735-106099861	GM19238	blood:	n/a	n/a
19	CTCF	chr12:106099560-106099710	BJ	skin:	n/a	n/a
20	CTCF	chr12:106099540-106099690	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr12:106099788-106099790	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:106099500-106099650	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr12:106099920-106100070	GM12865	blood:	n/a	n/a
24	CTCF	chr12:106099500-106099650	HCT-116	colon:	n/a	n/a
25	CTCF	chr12:106099560-106099710	GM12868	blood:	n/a	n/a
26	CTCF	chr12:106099580-106099730	GM12864	blood:	n/a	n/a
27	CTCF	chr12:106099531-106099841	GM10248	blood:	n/a	n/a
28	CTCF	chr12:106099544-106099753	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr12:106099580-106099730	GM12875	blood:	n/a	n/a
30	CTCF	chr12:106099920-106100070	GM12868	blood:	n/a	n/a
31	CTCF	chr12:106100149-106100226	Fibrobl	skin:	n/a	n/a
32	CTCF	chr12:106099550-106099740	Lung_OC	lung:	n/a	n/a
33	CTCF	chr12:106099509-106099910	LNCaP	prostate:	n/a	n/a
34	CTCF	chr12:106099440-106099848	K562	blood:	n/a	n/a
35	CTCF	chr12:106099580-106099730	AG04450	lung:	n/a	n/a
36	CTCF	chr12:106099240-106099390	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr12:106099150-106099968	A549	lung:	n/a	n/a
38	CTCF	chr12:106097924-106098016	MCF-7	breast:	n/a	chr12:106097963-106097981
39	CTCF	chr12:106100060-106100210	HMEC	breast:	n/a	n/a
40	CTCF	chr12:106099640-106099790	GM12874	blood:	n/a	n/a
41	CTCF	chr12:106099560-106099710	GM12875	blood:	n/a	n/a
42	CTCF	chr12:106099560-106099710	K562	blood:	n/a	n/a
43	CTCF	chr12:106099600-106099750	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr12:106099560-106099710	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr12:106099503-106099793	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr12:106099778-106099863	GM19239	blood:	n/a	n/a
47	CTCF	chr12:106100000-106100150	GM12871	blood:	n/a	n/a
48	CTCF	chr12:106099540-106099690	GM12869	blood:	n/a	n/a
49	CTCF	chr12:106099620-106099770	WI-38	lung:	n/a	n/a
50	CTCF	chr12:106099560-106099710	GM06990	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:106100228-106100278	SK-N-SH_RA	brain:	n/a
2	chr12:106135284-106135334	AG09309	skin:	n/a
3	chr12:106100228-106100278	AG09309	skin:	n/a
4	chr12:106100228-106100278	HIPEpiC	eye:	n/a
5	chr12:106100228-106100278	AG09319	gingival:	n/a
6	chr12:106100228-106100278	HEEpiC	esophagus:	n/a
7	chr12:106133609-106133659	NH-A	brain:	n/a
8	chr12:106135284-106135334	K562	blood:	n/a
9	chr12:106133609-106133659	AG09309	skin:	n/a
10	chr12:106135284-106135334	AoSMC	blood vessel:	n/a
11	chr12:106135284-106135334	HCPEpiC	choroid plexus:	n/a
12	chr12:106135284-106135334	PANC-1	pancreas:	n/a
13	chr12:106100228-106100278	NB4	blood:	n/a
14	chr12:106100228-106100278	HCM	heart:	n/a
15	chr12:106133609-106133659	HRE	kidney:	n/a
16	chr12:106100228-106100278	IMR90	lung:	fetal
17	chr12:106133609-106133659	MCF-7	breast:	n/a
18	chr12:106135284-106135334	Hela-S3	cervix:	n/a
19	chr12:106100228-106100278	NT2-D1	testis:	n/a
20	chr12:106100228-106100278	T-47D	breast:	n/a
21	chr12:106133609-106133659	HRPEpiC	eye:	n/a
22	chr12:106133609-106133659	HNPCEpiC	eye:	n/a
23	chr12:106135284-106135334	HCM	heart:	n/a
24	chr12:106100228-106100278	HAEpiC	amniotic membrane:	n/a
25	chr12:106133609-106133659	HCPEpiC	choroid plexus:	n/a
26	chr12:106133609-106133659	Jurkat	blood:	n/a
27	chr12:106100228-106100278	PANC-1	pancreas:	n/a
28	chr12:106135284-106135334	IMR90	lung:	fetal
29	chr12:106135284-106135334	Hepatocyte	liver:	n/a
30	chr12:106133609-106133659	HCT-116	colon:	n/a
31	chr12:106135284-106135334	RPTEC	kidney:	n/a
32	chr12:106100228-106100278	H1-hESC	embryonic stem cell:	embryo
33	chr12:106135284-106135334	SK-N-SH	brain:	n/a
34	chr12:106133609-106133659	H1-hESC	embryonic stem cell:	embryo
35	chr12:106135284-106135334	Jurkat	blood:	n/a
36	chr12:106100228-106100278	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:106135284-106135334	SKMC	muscle:	n/a
38	chr12:106135284-106135334	BJ	skin:	n/a
39	chr12:106135284-106135334	HEK293	kidney:	embryo
40	chr12:106133609-106133659	HCM	heart:	n/a
41	chr12:106100228-106100278	HRE	kidney:	n/a
42	chr12:106133609-106133659	AG04449	skin:	fetal
43	chr12:106100228-106100278	NH-A	brain:	n/a
44	chr12:106135284-106135334	ovcar-3	ovarian:	n/a
45	chr12:106100228-106100278	HepG2	liver:	n/a
46	chr12:106135284-106135334	PrEC	prostate:	n/a
47	chr12:106133609-106133659	GM12892	blood:	n/a
48	chr12:106100228-106100278	PrEC	prostate:	n/a
49	chr12:106100228-106100278	Caco-2	colon:	n/a
50	chr12:106100228-106100278	PFSK-1	brain:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:106114982..106116504-chr12:106117187..106119638,2	K562	blood:
2	chr12:106128999..106131037-chr12:106139408..106142036,2	MCF-7	breast:
3	chr12:106099637..106100474-chr12:106529654..106530671,3	MCF-7	breast:
4	chr12:106123113..106125890-chr12:106127769..106130574,2	MCF-7	breast:
5	chr12:106099656..106103215-chr12:106103450..106106049,3	MCF-7	breast:
6	chr12:106125356..106127672-chr12:106133504..106135544,2	MCF-7	breast:
7	chr12:106134598..106137615-chr12:106531407..106534871,3	MCF-7	breast:
8	chr12:106123113..106125890-chr12:106127769..106130574,2	MCF-7	breast:
9	chr12:106114982..106116504-chr12:106117187..106119638,2	K562	blood:
10	chr12:106125356..106127672-chr12:106133504..106135544,2	MCF-7	breast:
11	chr12:106105066..106107920-chr12:106531148..106533033,2	MCF-7	breast:
12	chr12:106126086..106128636-chr12:106139690..106141510,2	MCF-7	breast:
13	chr12:106133184..106135047-chr12:106140177..106142971,2	K562	blood:
14	chr12:106099358..106100248-chr12:106529662..106530556,3	K562	blood:
15	chr12:106135266..106136098-chr12:106254116..106254831,3	MCF-7	breast:
16	chr12:106127208..106129011-chr12:106532051..106534056,2	MCF-7	breast:
17	chr12:106126183..106128065-chr12:106252083..106254658,2	MCF-7	breast:
18	chr12:106122688..106125088-chr12:106125191..106126814,2	MCF-7	breast:
19	chr12:105814204..105815049-chr12:106099199..106100140,3	MCF-7	breast:
20	chr12:106122688..106125088-chr12:106125191..106126814,2	MCF-7	breast:
21	chr12:106133734..106136085-chr12:106136351..106138075,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf75-2	chr12:106135534-106136007	ENSG00000257859
2	lnc-C12orf75-2	chr12:106135534-106137841	NR_110110
3	lnc-C12orf75-2	chr12:106131034-106131175	NR_110108
4	lnc-C12orf75-2	chr12:106135534-106137840	ENSG00000257859
5	lnc-C12orf75-2	chr12:106097981-106098034	NR_110108
6	lnc-C12orf75-2	chr12:106135534-106137841	NR_110108
7	lnc-C12orf75-2	chr12:106100552-106100634	ENSG00000257859
8	lnc-C12orf75-2	chr12:106131034-106131175	NR_110110
9	lnc-C12orf75-2	chr12:106097981-106098034	ENSG00000257859
10	lnc-C12orf75-2	chr12:106097981-106098034	NR_110109
11	lnc-C12orf75-2	chr12:106100552-106100634	NR_110110
12	lnc-C12orf75-2	chr12:106100552-106100634	NR_110111
13	lnc-C12orf75-2	chr12:106135534-106137841	NR_110111
14	lnc-C12orf75-2	chr12:106108940-106108997	NR_110109
15	lnc-C12orf75-2	chr12:106116001-106116059	NR_110109
16	lnc-C12orf75-2	chr12:106135534-106137841	NR_110109
17	lnc-C12orf75-2	chr12:106131034-106131175	ENSG00000257859
18	lnc-C12orf75-2	chr12:106131034-106131175	NR_110109

No data

Variant related genes	Relation type
CASC18	TF binding region
CASC18	CpG island
ENSG00000257859	chromatin interactions
ENSG00000074590	chromatin interactions
STK40	miRNA target sites
MAP4	miRNA target sites
MAP3K7	miRNA target sites
ZNF275	miRNA target sites
YY1	miRNA target sites

Extended variants
information (count: 1597 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1597 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11112681	chr12:106095906-106095907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181947686	chr12:106095933-106095934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116798422	chr12:106095958-106095959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536985369	chr12:106095963-106095964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559248836	chr12:106095965-106095966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528351051	chr12:106095991-106095992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544943985	chr12:106095994-106095995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200041477	chr12:106096013-106096014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs398076935	chr12:106096016-106096017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573359127	chr12:106096059-106096060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547948902	chr12:106096066-106096067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568239552	chr12:106096096-106096097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550260361	chr12:106096120-106096121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570155785	chr12:106096126-106096127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534056759	chr12:106096150-106096151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547472405	chr12:106096154-106096155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7133279	chr12:106096157-106096158	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs535349605	chr12:106096171-106096172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185725631	chr12:106096184-106096185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571819782	chr12:106096240-106096241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537237730	chr12:106096265-106096266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7133311	chr12:106096284-106096285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs190434298	chr12:106096294-106096295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542246756	chr12:106096297-106096298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368767357	chr12:106096316-106096317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79528348	chr12:106096357-106096358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572480896	chr12:106096418-106096419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576953848	chr12:106096429-106096430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545293350	chr12:106096432-106096433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564994785	chr12:106096482-106096483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78280798	chr12:106096487-106096488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544075201	chr12:106096499-106096500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375668631	chr12:106096500-106096501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529391229	chr12:106096514-106096515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375722661	chr12:106096548-106096549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549470158	chr12:106096556-106096557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61529194	chr12:106096611-106096612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182980076	chr12:106096649-106096650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78456279	chr12:106096680-106096681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534685441	chr12:106096695-106096696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111510990	chr12:106096703-106096704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537677644	chr12:106096740-106096741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145517300	chr12:106096766-106096767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575411929	chr12:106096778-106096779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567483751	chr12:106096808-106096809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148303167	chr12:106096809-106096810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552606110	chr12:106096827-106096828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79971769	chr12:106096853-106096854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538249401	chr12:106096884-106096885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141401001	chr12:106096909-106096910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106095200-106099600	Weak transcription	Aorta	Aorta
2	chr12:106095800-106099600	Weak transcription	Right Atrium	heart
3	chr12:106096400-106096600	Enhancers	Psoas Muscle	Psoas
4	chr12:106096600-106099600	Weak transcription	Fetal Brain Male	brain
5	chr12:106097000-106097200	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr12:106097000-106099000	Weak transcription	Psoas Muscle	Psoas
7	chr12:106097200-106097400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr12:106097200-106098600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr12:106097200-106099000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:106097400-106098200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr12:106097400-106099800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr12:106097400-106101000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:106098000-106098200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:106098000-106098200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr12:106098000-106098400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr12:106098000-106098400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr12:106098000-106098800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr12:106098000-106099200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr12:106098000-106100600	Enhancers	Fetal Muscle Trunk	muscle
20	chr12:106098000-106101200	Enhancers	Fetal Heart	heart
21	chr12:106098000-106101400	Enhancers	Fetal Muscle Leg	muscle
22	chr12:106098200-106098400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:106098200-106098600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:106098200-106099600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:106098200-106099800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr12:106098400-106098800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:106098400-106099600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr12:106098400-106099800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr12:106098400-106100200	Enhancers	Fetal Lung	lung
30	chr12:106098400-106101400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:106098600-106098800	Enhancers	Left Ventricle	heart
32	chr12:106098600-106098800	Enhancers	Right Ventricle	heart
33	chr12:106098600-106099800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:106098600-106099800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr12:106098600-106100000	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr12:106098600-106100200	Enhancers	Lung	lung
37	chr12:106098600-106101600	Enhancers	HSMMtube	muscle
38	chr12:106098800-106099200	Enhancers	Brain Angular Gyrus	brain
39	chr12:106098800-106099800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr12:106098800-106099800	Weak transcription	Left Ventricle	heart
41	chr12:106098800-106099800	Weak transcription	Right Ventricle	heart
42	chr12:106098800-106101400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:106098800-106101400	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr12:106099000-106099600	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr12:106099000-106100000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:106099000-106100200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:106099000-106100200	Enhancers	Brain Cingulate Gyrus	brain
48	chr12:106099000-106101000	Enhancers	Psoas Muscle	Psoas
49	chr12:106099000-106101200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:106099200-106099600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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