Variant report

Variant	rs11831581
Chromosome Location	chr12:85306637-85306638
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:85306502-85307327	Hela-S3	cervix:	n/a	n/a
2	MAX	chr12:85305083-85307492	H1-hESC	embryonic stem cell:	n/a	chr12:85307310-85307318 chr12:85305659-85305670 chr12:85306627-85306640 chr12:85306629-85306638 chr12:85305660-85305669 chr12:85305660-85305669 chr12:85305175-85305184 chr12:85305660-85305670 chr12:85305661-85305668 chr12:85306630-85306637 chr12:85306627-85306642 chr12:85306628-85306638 chr12:85307311-85307321 chr12:85306627-85306636 chr12:85305659-85305669 chr12:85306628-85306639
3	CTCF	chr12:85306600-85306750	GM12864	blood:	n/a	n/a
4	CTCF	chr12:85306612-85306721	Pancreas_OC	pancreas:	n/a	n/a
5	REST	chr12:85306271-85306718	SK-N-SH	brain:	n/a	chr12:85306688-85306701
6	MAZ	chr12:85306348-85306819	Hela-S3	cervix:	n/a	chr12:85306627-85306640 chr12:85306629-85306638 chr12:85306630-85306637 chr12:85306627-85306642 chr12:85306628-85306638 chr12:85306627-85306636 chr12:85306628-85306639
7	MAX	chr12:85305054-85307032	A549	lung:	n/a	chr12:85305659-85305670 chr12:85306627-85306640 chr12:85306629-85306638 chr12:85305660-85305669 chr12:85305660-85305669 chr12:85305175-85305184 chr12:85305660-85305670 chr12:85305661-85305668 chr12:85306630-85306637 chr12:85306627-85306642 chr12:85306628-85306638 chr12:85306627-85306636 chr12:85305659-85305669 chr12:85306628-85306639
8	POLR2A	chr12:85306200-85306947	Hela-S3	cervix:	n/a	n/a
9	BACH1	chr12:85306376-85307360	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr12:85305891-85306852	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr12:85306580-85306730	HCPEpiC	choroid plexus:	n/a	n/a
12	HA-E2F1	chr12:85306351-85306859	Hela-S3	cervix:	n/a	chr12:85306697-85306706 chr12:85306695-85306705
13	TAF1	chr12:85306280-85306866	PFSK-1	brain:	n/a	n/a
14	ELK1	chr12:85306593-85307011	Hela-S3	cervix:	n/a	n/a
15	NRF1	chr12:85306124-85306910	SK-N-SH	brain:	n/a	n/a
16	SIN3AK20	chr12:85306348-85306867	SK-N-SH	brain:	n/a	n/a
17	FOXP2	chr12:85306192-85306892	PFSK-1	brain:	n/a	n/a
18	SIN3A	chr12:85304934-85307509	H1-hESC	embryonic stem cell:	n/a	chr12:85306407-85306415 chr12:85306813-85306826 chr12:85307311-85307320 chr12:85306473-85306484 chr12:85305737-85305746 chr12:85306698-85306709
19	CTCF	chr12:85306600-85306750	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr12:85306520-85306670	HEK293	kidney:	n/a	n/a
21	CTCF	chr12:85306540-85306690	HFF-Myc	foreskin:	n/a	n/a
22	RFX5	chr12:85306464-85306795	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr12:85306600-85306750	AG04449	skin:	n/a	n/a
24	CTCF	chr12:85306560-85306710	HCM	heart:	n/a	n/a
25	CTCF	chr12:85306500-85306650	HMEC	breast:	n/a	n/a
26	RAD21	chr12:85306440-85306833	SK-N-SH_RA	brain:	n/a	n/a
27	TAF1	chr12:85304946-85307521	H1-hESC	embryonic stem cell:	n/a	n/a
28	SIN3AK20	chr12:85306151-85306849	PFSK-1	brain:	n/a	n/a
29	E2F6	chr12:85306347-85306866	A549	lung:	n/a	chr12:85306697-85306706 chr12:85306695-85306705
30	CTCF	chr12:85306560-85306710	AG04449	skin:	n/a	n/a
31	CTCF	chr12:85306510-85306790	NHEK	skin:	n/a	n/a
32	POLR2A	chr12:85304226-85307325	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr12:85304075-85307349	MCF10A-Er-Src	breast:	n/a	n/a
34	TAF1	chr12:85306430-85306799	SK-N-SH	brain:	n/a	n/a
35	CTCF	chr12:85306600-85306750	A549	lung:	n/a	n/a
36	RCOR1	chr12:85306508-85307138	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr12:85306580-85306730	HVMF	connective:	n/a	n/a
38	MYC	chr12:85306433-85306787	HUVEC	blood vessel:	n/a	chr12:85306627-85306640 chr12:85306629-85306638 chr12:85306630-85306637 chr12:85306627-85306642 chr12:85306628-85306638 chr12:85306627-85306636 chr12:85306628-85306639
39	CREB1	chr12:85306288-85306860	A549	lung:	n/a	n/a
40	MAX	chr12:85305123-85307338	Hela-S3	cervix:	n/a	chr12:85307310-85307318 chr12:85305659-85305670 chr12:85306627-85306640 chr12:85306629-85306638 chr12:85305660-85305669 chr12:85305660-85305669 chr12:85305175-85305184 chr12:85305660-85305670 chr12:85305661-85305668 chr12:85306630-85306637 chr12:85306627-85306642 chr12:85306628-85306638 chr12:85307311-85307321 chr12:85306627-85306636 chr12:85305659-85305669 chr12:85306628-85306639
41	CTCF	chr12:85306600-85306750	GM12865	blood:	n/a	n/a
42	TAF1	chr12:85306350-85306838	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr12:85306302-85306891	SK-N-MC	brain:	n/a	n/a
44	CTCF	chr12:85306600-85306750	HRE	kidney:	n/a	n/a
45	SIN3AK20	chr12:85306379-85306830	PFSK-1	brain:	n/a	n/a
46	CTCF	chr12:85306580-85306730	HFF	foreskin:	n/a	n/a
47	KAP1	chr12:85304230-85306653	HEK293	kidney:	n/a	n/a
48	CTCF	chr12:85306540-85306690	HPF	lung:	n/a	n/a
49	MAX	chr12:85305012-85306965	SK-N-SH	brain:	n/a	chr12:85305659-85305670 chr12:85306627-85306640 chr12:85306629-85306638 chr12:85305660-85305669 chr12:85305660-85305669 chr12:85305175-85305184 chr12:85305660-85305670 chr12:85305661-85305668 chr12:85306630-85306637 chr12:85306627-85306642 chr12:85306628-85306638 chr12:85306627-85306636 chr12:85305659-85305669 chr12:85306628-85306639
50	CTCF	chr12:85306580-85306730	AG10803	skin:	n/a	n/a

Variant related genes	Relation type
SLC6A15	TF binding region

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11829477	0.83[AMR][1000 genomes]
rs11829799	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11829908	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11830709	1.00[EUR][1000 genomes]
rs11831467	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11833690	1.00[EUR][1000 genomes]
rs11833788	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11833789	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11833800	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11833807	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11834156	1.00[EUR][1000 genomes]
rs11834494	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11835173	1.00[EUR][1000 genomes]
rs11835174	1.00[EUR][1000 genomes]
rs11835496	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11835832	1.00[EUR][1000 genomes]
rs11837002	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1525544	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1525545	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1525546	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1554708	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35352631	0.83[AMR][1000 genomes]
rs35772840	0.83[AMR][1000 genomes]
rs3919777	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59509849	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs60246437	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61020514	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61268326	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61374184	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6539873	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6539874	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6539875	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7131949	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7132320	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs72542493	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7298505	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7304260	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7960028	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7960244	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7960525	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7966593	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7969872	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7973203	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7974606	0.83[AMR][1000 genomes]
rs7978190	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9668049	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035863	chr12:84710250-85331290	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1035236	chr12:84790507-85350433	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv899376	chr12:85157346-85339254	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv899377	chr12:85157346-85629241	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv1040452	chr12:85179586-85747907	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv899378	chr12:85219400-85315865	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv455666	chr12:85224141-85330496	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
8	nsv559645	chr12:85224141-85330496	Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
9	nsv470309	chr12:85224141-85339254	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
10	nsv899380	chr12:85232076-85330496	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
11	nsv899381	chr12:85232076-85339254	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
12	nsv899382	chr12:85232076-85345154	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
13	nsv559646	chr12:85233731-85330496	Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
14	nsv559647	chr12:85233731-85339254	Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
15	nsv899383	chr12:85233731-85339254	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
16	nsv899384	chr12:85233731-85345154	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
17	nsv455667	chr12:85249218-85339254	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
18	nsv559648	chr12:85249218-85339254	Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
19	nsv899385	chr12:85249218-85339254	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
20	nsv899386	chr12:85249218-85345154	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
21	nsv559649	chr12:85257445-85330496	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
22	nsv455668	chr12:85257445-85339254	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
23	nsv559650	chr12:85257445-85339254	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
24	nsv559651	chr12:85281528-85325952	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
25	esv1842303	chr12:85284828-85356954	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
26	nsv559652	chr12:85285222-85339254	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85302600-85307000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr12:85303600-85307200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:85303800-85307000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:85304200-85306800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr12:85304200-85306800	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr12:85304200-85306800	Active TSS	Muscle Satellite Cultured Cells	--
7	chr12:85304200-85307200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr12:85304200-85307200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
9	chr12:85304200-85307200	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr12:85304200-85307200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:85304200-85307200	Bivalent/Poised TSS	Fetal Kidney	kidney
12	chr12:85304200-85307200	Active TSS	Hela-S3	cervix
13	chr12:85304200-85307200	Active TSS	NHDF-Ad	bronchial
14	chr12:85304200-85307400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:85304200-85307400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:85304200-85307400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:85304200-85307400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:85304200-85307400	Active TSS	Brain Angular Gyrus	brain
19	chr12:85304200-85307400	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr12:85304200-85307600	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr12:85304200-85307600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr12:85304400-85307000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:85304400-85307000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
24	chr12:85304400-85307000	Enhancers	Spleen	Spleen
25	chr12:85304400-85307200	Active TSS	H1 Cell Line	embryonic stem cell
26	chr12:85304400-85307200	Active TSS	H9 Cell Line	embryonic stem cell
27	chr12:85304400-85307200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
28	chr12:85304400-85307200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
29	chr12:85304400-85307800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr12:85304600-85307000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
31	chr12:85304800-85307200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:85304800-85307200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:85304800-85307400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr12:85304800-85307400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr12:85304800-85307400	Active TSS	Fetal Brain Male	brain
36	chr12:85305000-85306800	Active TSS	HMEC	breast
37	chr12:85305000-85307000	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
38	chr12:85305000-85307000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
39	chr12:85305000-85307000	Active TSS	Rectal Smooth Muscle	rectum
40	chr12:85305000-85307200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:85305200-85307000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
42	chr12:85305200-85307200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
43	chr12:85305400-85306800	Bivalent Enhancer	Fetal Thymus	thymus
44	chr12:85305400-85306800	Bivalent Enhancer	Left Ventricle	heart
45	chr12:85305400-85307200	Flanking Active TSS	NH-A	brain
46	chr12:85305400-85307400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:85305600-85307000	Flanking Active TSS	Lung	lung
48	chr12:85305600-85307000	Active TSS	NHEK	skin
49	chr12:85305600-85307200	Active TSS	Brain Anterior Caudate	brain
50	chr12:85305600-85307200	Active TSS	Brain Substantia Nigra	brain

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