Variant report

Variant	nsv916679
Chromosome Location	chr12:38805678-38963660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:372)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:372 , 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	CEBPB	chr12:38950379-38950387	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:38871205-38871508	A549	lung:	n/a	chr12:38871344-38871353 chr12:38871342-38871353 chr12:38871343-38871354 chr12:38871342-38871355
3	CEBPB	chr12:38951466-38951741	HepG2	liver:	n/a	chr12:38951566-38951577
4	CEBPB	chr12:38871156-38871532	Hela-S3	cervix:	n/a	chr12:38871344-38871353 chr12:38871342-38871353 chr12:38871343-38871354 chr12:38871342-38871355
5	CEBPB	chr12:38950329-38950425	A549	lung:	n/a	n/a
6	CEBPB	chr12:38821030-38821227	HepG2	liver:	n/a	chr12:38821151-38821162 chr12:38821150-38821163
7	CEBPB	chr12:38871174-38871515	HepG2	liver:	n/a	chr12:38871344-38871353 chr12:38871342-38871353 chr12:38871343-38871354 chr12:38871342-38871355
8	CEBPB	chr12:38895683-38896190	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:38876099-38876195	HepG2	liver:	n/a	chr12:38876146-38876159 chr12:38876148-38876159 chr12:38876146-38876157
10	CEBPB	chr12:38871221-38871436	H1-hESC	embryonic stem cell:	n/a	chr12:38871344-38871353 chr12:38871342-38871353 chr12:38871343-38871354 chr12:38871342-38871355
11	CEBPB	chr12:38919074-38919216	A549	lung:	n/a	n/a
12	CEBPB	chr12:38871177-38871501	ECC-1	luminal epithelium:	n/a	chr12:38871344-38871353 chr12:38871342-38871353 chr12:38871343-38871354 chr12:38871342-38871355
13	CEBPB	chr12:38951490-38951690	A549	lung:	n/a	chr12:38951566-38951577
14	CEBPB	chr12:38880197-38880223	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:38933170-38933247	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:38871207-38871470	K562	blood:	n/a	chr12:38871344-38871353 chr12:38871342-38871353 chr12:38871343-38871354 chr12:38871342-38871355
17	CEBPB	chr12:38951464-38951704	IMR90	lung:	n/a	chr12:38951566-38951577
18	CEBPB	chr12:38821116-38821316	Hela-S3	cervix:	n/a	chr12:38821151-38821162 chr12:38821150-38821163
19	CEBPB	chr12:38949928-38950461	Hela-S3	cervix:	n/a	chr12:38950417-38950428
20	CEBPB	chr12:38851865-38851866	A549	lung:	n/a	n/a
21	CEBPB	chr12:38871178-38871522	IMR90	lung:	n/a	chr12:38871344-38871353 chr12:38871342-38871353 chr12:38871343-38871354 chr12:38871342-38871355
22	CEBPB	chr12:38856956-38857149	H1-hESC	embryonic stem cell:	n/a	chr12:38857015-38857028
23	CHD2	chr12:38910620-38910626	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr12:38831395-38831416	LNCaP	prostate:	n/a	n/a
25	CTCF	chr12:38927977-38928058	GM20000	blood:	n/a	n/a
26	CTCF	chr12:38938600-38938750	GM12878	blood:	n/a	n/a
27	CTCF	chr12:38847620-38847770	HEK293	kidney:	n/a	n/a
28	CTCF	chr12:38938600-38938750	HMF	breast:	n/a	n/a
29	CTCF	chr12:38949626-38949662	HepG2	liver:	n/a	n/a
30	CTCF	chr12:38874065-38874123	LNCaP	prostate:	n/a	n/a
31	CTCF	chr12:38938627-38938716	GM19239	blood:	n/a	n/a
32	CTCF	chr12:38938580-38938730	GM12874	blood:	n/a	n/a
33	CTCF	chr12:38938600-38938750	HepG2	liver:	n/a	n/a
34	CTCF	chr12:38938660-38938810	BE2_C	brain:	n/a	n/a
35	CTCF	chr12:38938580-38938730	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr12:38938630-38938705	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:38949520-38949670	BE2_C	brain:	n/a	n/a
38	CTCF	chr12:38938600-38938750	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr12:38938600-38938750	GM12873	blood:	n/a	n/a
40	CTCF	chr12:38938620-38938770	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr12:38938620-38938770	HCT-116	colon:	n/a	n/a
42	CTCF	chr12:38949536-38949876	HCT-116	colon:	n/a	n/a
43	CTCF	chr12:38938600-38938750	GM12865	blood:	n/a	n/a
44	CTCF	chr12:38938320-38938470	HCT-116	colon:	n/a	n/a
45	CTCF	chr12:38949535-38949717	LNCaP	prostate:	n/a	n/a
46	CTCF	chr12:38895057-38895083	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr12:38938580-38938730	GM12873	blood:	n/a	n/a
48	CTCF	chr12:38940541-38940568	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:38949500-38949650	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr12:38874012-38874126	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:38806793-38806843	GM12892	blood:	n/a
2	chr12:38806793-38806843	Jurkat	blood:	n/a
3	chr12:38938054-38938104	AG04449	skin:	fetal
4	chr12:38806793-38806843	H1-hESC	embryonic stem cell:	embryo
5	chr12:38806793-38806843	HPAEpiC	pulmonary alveolar:	n/a
6	chr12:38938054-38938104	GM06990	blood:	n/a
7	chr12:38806793-38806843	GM12891	blood:	n/a
8	chr12:38806793-38806843	ovcar-3	ovarian:	n/a
9	chr12:38806793-38806843	HEEpiC	esophagus:	n/a
10	chr12:38938054-38938104	ProgFib	skin:	n/a
11	chr12:38806793-38806843	RPTEC	kidney:	n/a
12	chr12:38938054-38938104	SK-N-SH	brain:	n/a
13	chr12:38938054-38938104	NHBE	bronchial:	n/a
14	chr12:38806793-38806843	SAEC	small airway:	n/a
15	chr12:38938054-38938104	AG04450	lung:	fetal
16	chr12:38938054-38938104	SK-N-SH_RA	brain:	n/a
17	chr12:38806793-38806843	NHDF-neo	bronchial:	n/a
18	chr12:38938054-38938104	PANC-1	pancreas:	n/a
19	chr12:38938054-38938104	NH-A	brain:	n/a
20	chr12:38806793-38806843	HIPEpiC	eye:	n/a
21	chr12:38938054-38938104	HCM	heart:	n/a
22	chr12:38806793-38806843	AG04450	lung:	fetal
23	chr12:38938054-38938104	HCF	heart:	n/a
24	chr12:38806793-38806843	AG09309	skin:	n/a
25	chr12:38806793-38806843	HEK293	kidney:	embryo
26	chr12:38806793-38806843	HCPEpiC	choroid plexus:	n/a
27	chr12:38938054-38938104	NT2-D1	testis:	n/a
28	chr12:38938054-38938104	GM12891	blood:	n/a
29	chr12:38938054-38938104	Caco-2	colon:	n/a
30	chr12:38806793-38806843	AG04449	skin:	fetal
31	chr12:38806793-38806843	CMK	blood:	n/a
32	chr12:38806793-38806843	AG09319	gingival:	n/a
33	chr12:38806793-38806843	GM06990	blood:	n/a
34	chr12:38806793-38806843	GM12878	blood:	n/a
35	chr12:38938054-38938104	LNCaP	prostate:	n/a
36	chr12:38938054-38938104	HepG2	liver:	n/a
37	chr12:38806793-38806843	SK-N-SH_RA	brain:	n/a
38	chr12:38938054-38938104	IMR90	lung:	fetal
39	chr12:38938054-38938104	U87	brain:	n/a
40	chr12:38938054-38938104	HEK293	kidney:	embryo
41	chr12:38938054-38938104	T-47D	breast:	n/a
42	chr12:38938054-38938104	MCF10A-Er-Src	breast:	n/a
43	chr12:38806793-38806843	ProgFib	skin:	n/a
44	chr12:38806793-38806843	GM19239	blood:	n/a
45	chr12:38938054-38938104	NHDF-neo	bronchial:	n/a
46	chr12:38806793-38806843	K562	blood:	n/a
47	chr12:38806793-38806843	MCF10A-Er-Src	breast:	n/a
48	chr12:38806793-38806843	LNCaP	prostate:	n/a
49	chr12:38938054-38938104	CMK	blood:	n/a
50	chr12:38938054-38938104	HAEpiC	amniotic membrane:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38845594..38847956-chr12:38851662..38853438,2	K562	blood:
2	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
3	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:
4	chr12:38917479..38920369-chr12:38920412..38922084,2	K562	blood:
5	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
6	chr12:38876753..38877648-chr6:116268599..116269448,2	MCF-7	breast:
7	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
8	chr12:38917479..38920369-chr12:38920412..38922084,2	K562	blood:
9	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:
10	chr1:186105531..186106141-chr12:38883322..38883955,2	MCF-7	breast:
11	chr12:38954957..38957532-chr12:38958850..38960983,2	K562	blood:
12	chr12:38845594..38847956-chr12:38851662..38853438,2	K562	blood:
13	chr12:38954957..38957532-chr12:38958850..38960983,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPNE8-1	chr12:38937980-38938333	XLOC_010050
2	lnc-CPNE8-5	chr12:38837923-38838124	l_629_chr12:38821325-38838592_lung
3	lnc-CPNE8-1	chr12:38940187-38940310	ENSG00000258119
4	lnc-CPNE8-1	chr12:38940187-38940279	ENSG00000258119
5	lnc-CPNE8-5	chr12:38832098-38832212	l_629_chr12:38821325-38838592_lung
6	lnc-CPNE8-5	chr12:38824250-38824373	l_629_chr12:38821325-38838592_lung
7	lnc-CPNE8-5	chr12:38821326-38822703	l_629_chr12:38821325-38838592_lung
8	lnc-CPNE8-5	chr12:38838505-38838592	l_629_chr12:38821325-38838592_lung
9	lnc-CPNE8-1	chr12:38940187-38940310	XLOC_010050
10	lnc-CPNE8-1	chr12:38938130-38938378	ENSG00000258119
11	lnc-ALG10B-3	chr12:38836308-38836412	NONHSAT027682
12	lnc-ALG10B-3	chr12:38846321-38846419	NONHSAT027683
13	lnc-ALG10B-3	chr12:38847317-38847681	NONHSAT027682
14	lnc-CPNE8-1	chr12:38937979-38938333	ENSG00000258119
15	lnc-ALG10B-3	chr12:38847317-38847776	NONHSAT027683

No data

Variant related genes	Relation type
ENSG00000257645	TF binding region
ENSG00000258119	TF binding region
ENSG00000256878	TF binding region
ENSG00000257645	CpG island
ENSG00000258119	CpG island
ENSG00000256878	CpG island
SLC39A10	miRNA target sites
ZFP1	miRNA target sites
GREB1	miRNA target sites
NSF	miRNA target sites
HECTD3	miRNA target sites

Extended variants
information (count: 2130 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2130 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145611961	chr12:38805717-38805718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570412696	chr12:38805719-38805720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539238126	chr12:38805733-38805734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552468091	chr12:38805738-38805739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369499759	chr12:38805748-38805749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559222847	chr12:38805815-38805816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138083772	chr12:38805829-38805830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534975876	chr12:38805833-38805834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554588954	chr12:38805895-38805896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560583309	chr12:38805896-38805897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191191772	chr12:38805902-38805903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557440310	chr12:38805913-38805914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12301967	chr12:38805923-38805924	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs73093090	chr12:38805945-38805946	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs559265041	chr12:38805968-38805969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10881015	chr12:38805989-38805990	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553698992	chr12:38806005-38806006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11831125	chr12:38806006-38806007	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs530533327	chr12:38806027-38806028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543827756	chr12:38806029-38806030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182401222	chr12:38806053-38806054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532866256	chr12:38806104-38806105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542215222	chr12:38806179-38806180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76192994	chr12:38806193-38806194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377733495	chr12:38806210-38806211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11832065	chr12:38806239-38806240	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548482214	chr12:38806248-38806249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568377146	chr12:38806268-38806269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117409000	chr12:38806295-38806296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186579097	chr12:38806306-38806307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570956687	chr12:38806322-38806323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539543002	chr12:38806323-38806324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553253017	chr12:38806339-38806340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190003812	chr12:38806344-38806345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542007533	chr12:38806376-38806377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73265212	chr12:38806393-38806394	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs150131696	chr12:38806446-38806447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373124956	chr12:38806465-38806466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544224163	chr12:38806484-38806485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563911597	chr12:38806502-38806503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533094463	chr12:38806529-38806530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539953944	chr12:38806556-38806557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138043899	chr12:38806572-38806573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs61613123	chr12:38806579-38806580	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs532174933	chr12:38806656-38806657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547145225	chr12:38806667-38806668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528676467	chr12:38806706-38806707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74327990	chr12:38806793-38806794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138489721	chr12:38806794-38806795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531093982	chr12:38806813-38806814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38800200-38806600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:38804200-38805800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:38804600-38806200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:38805000-38807600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr12:38805000-38807600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr12:38805000-38807800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:38805200-38805800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:38805200-38807800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr12:38805400-38806200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr12:38805400-38806200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr12:38805600-38806000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:38806200-38806600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:38806200-38807200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr12:38806600-38806800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:38806600-38807400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr12:38807200-38807400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr12:38807200-38807400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr12:38818000-38818800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:38818800-38826200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:38819600-38821600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr12:38819800-38822200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:38820200-38821200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:38820200-38821400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr12:38820200-38821800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:38820200-38822400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:38820400-38821400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr12:38820400-38822200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:38820600-38821000	Enhancers	Primary hematopoietic stem cells	blood
29	chr12:38821200-38821600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr12:38821200-38822000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr12:38822400-38823800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:38823800-38824200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:38826200-38826600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr12:38830600-38831200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:38848800-38849200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:38848800-38851800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr12:38849200-38849800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:38849800-38850200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:38850000-38851000	Enhancers	Hela-S3	cervix
40	chr12:38850200-38851400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:38850600-38851600	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr12:38857000-38857600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr12:38858800-38859400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr12:38859400-38863200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr12:38861400-38861800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:38862600-38864200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:38863200-38863400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:38863200-38863400	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr12:38863200-38863400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:38863200-38863600	Enhancers	Adipose Nuclei	Adipose

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