Variant report

Variant	rs2469568
Chromosome Location	chr15:76478268-76478269
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr15:76478120-76478270	RPTEC	kidney:	n/a	n/a
2	CTCF	chr15:76478160-76478310	HFF-Myc	foreskin:	n/a	n/a
3	RAD21	chr15:76477821-76478542	HCT-116	colon:	n/a	n/a
4	CTCF	chr15:76478140-76478290	HRE	kidney:	n/a	n/a
5	RAD21	chr15:76478001-76478301	SK-N-SH_RA	brain:	n/a	n/a
6	CTCF	chr15:76478120-76478270	GM12866	blood:	n/a	n/a
7	CTCF	chr15:76478200-76478350	HAc	cerebellar:	n/a	n/a
8	CTCF	chr15:76478063-76478314	GM19240	blood:	n/a	n/a
9	RAD21	chr15:76477913-76478548	A549	lung:	n/a	n/a
10	TEAD4	chr15:76477911-76478399	ECC-1	luminal epithelium:	n/a	n/a
11	CTCF	chr15:76478049-76478313	GM19238	blood:	n/a	n/a
12	SMC3	chr15:76478017-76478441	K562	blood:	n/a	n/a
13	CTCF	chr15:76478099-76478270	GM10248	blood:	n/a	n/a
14	CTCF	chr15:76478046-76478333	Gliobla	brain:	n/a	n/a
15	CTCF	chr15:76478120-76478270	HPF	lung:	n/a	n/a
16	CTCF	chr15:76477937-76478471	MCF-7	breast:	n/a	n/a
17	CTCF	chr15:76478052-76478292	MCF-7	breast:	n/a	n/a
18	JUND	chr15:76478021-76478346	K562	blood:	n/a	n/a
19	RCOR1	chr15:76478123-76478393	K562	blood:	n/a	n/a
20	CTCF	chr15:76477939-76478410	A549	lung:	n/a	n/a
21	RAD21	chr15:76477955-76478541	ECC-1	luminal epithelium:	n/a	n/a
22	CTCF	chr15:76478120-76478270	MCF-7	breast:	n/a	n/a
23	RAD21	chr15:76478011-76478287	K562	blood:	n/a	n/a
24	CTCF	chr15:76478076-76478276	Medullo	brain:	n/a	n/a
25	CBX3	chr15:76477995-76478351	K562	blood:	n/a	n/a
26	CTCF	chr15:76478120-76478270	HCT-116	colon:	n/a	n/a
27	RAD21	chr15:76478045-76478291	HepG2	liver:	n/a	n/a
28	RAD21	chr15:76477990-76478451	HepG2	liver:	n/a	n/a
29	CTCF	chr15:76478240-76478390	WI-38	lung:	n/a	n/a
30	TEAD4	chr15:76477995-76478388	K562	blood:	n/a	n/a
31	GTF2F1	chr15:76478093-76478286	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr15:76478055-76478310	NHEK	skin:	n/a	n/a
33	CTCF	chr15:76478140-76478290	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:76478067-76478293	MCF-7	breast:	n/a	n/a
35	CTCF	chr15:76477999-76478354	ECC-1	luminal epithelium:	n/a	n/a
36	CTCF	chr15:76478016-76478335	T-47D	breast:	n/a	n/a
37	CTCF	chr15:76477987-76478513	K562	blood:	n/a	n/a
38	CTCF	chr15:76478073-76478294	ProgFib	skin:	n/a	n/a
39	ZNF143	chr15:76478003-76478321	GM12878	blood:	n/a	n/a
40	CTCF	chr15:76478120-76478270	BE2_C	brain:	n/a	n/a
41	CTCF	chr15:76478096-76478268	Fibrobl	skin:	n/a	n/a
42	CTCF	chr15:76478120-76478270	HMF	breast:	n/a	n/a
43	POLR2A	chr15:76478032-76478985	Hela-S3	cervix:	n/a	n/a
44	ZNF143	chr15:76478048-76478344	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr15:76478140-76478290	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr15:76477977-76478391	K562	blood:	n/a	n/a
47	RAD21	chr15:76478040-76478367	A549	lung:	n/a	n/a
48	CTCF	chr15:76477894-76478483	MCF-7	breast:	n/a	n/a
49	ZNF143	chr15:76478059-76478349	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr15:76478120-76478270	Caco-2	colon:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76478115..76478633-chr15:76622409..76623267,2	MCF-7	breast:
2	chr15:76478027..76479862-chr15:76483019..76485634,3	MCF-7	breast:
3	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
4	chr15:76478149..76479732-chr15:76481760..76484387,3	K562	blood:
5	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
6	chr15:76477747..76478594-chr15:76625784..76626375,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259422	TF binding region
ENSG00000169758	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs17456573	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1801591	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs1914816	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2291449	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs2456027	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2456040	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2456042	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2456047	1.00[CHB][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2456054	0.90[CEU][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2456066	1.00[CHB][hapmap];0.95[YRI][hapmap];0.89[AMR][1000 genomes]
rs2456067	0.94[AMR][1000 genomes]
rs2456070	1.00[CHB][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2456072	1.00[CHB][hapmap];0.84[YRI][hapmap];0.81[ASN][1000 genomes]
rs2456074	0.94[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2456075	0.81[ASN][1000 genomes]
rs2456078	0.81[ASN][1000 genomes]
rs2460146	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2460151	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.81[ASN][1000 genomes]
rs2460153	1.00[CHB][hapmap];0.80[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2460155	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.96[ASN][1000 genomes]
rs2460158	1.00[CHB][hapmap]
rs2469211	1.00[CHB][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes]
rs2469214	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs2469215	1.00[CHB][hapmap];0.95[YRI][hapmap];0.89[AMR][1000 genomes]
rs2469216	0.84[AMR][1000 genomes]
rs2469538	0.94[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2469539	1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2469552	0.89[AMR][1000 genomes]
rs2469559	0.90[CEU][hapmap];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2469564	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2469573	1.00[CHB][hapmap];0.84[YRI][hapmap]
rs2938691	0.81[ASN][1000 genomes]
rs2956875	1.00[CHB][hapmap];0.95[YRI][hapmap];0.89[AMR][1000 genomes]
rs2957037	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2959846	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8042255	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs874224	0.95[YRI][hapmap];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv569998	chr15:76232605-76550938	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1048760	chr15:76334544-76496977	Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv833057	chr15:76367848-76585868	ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv1039595	chr15:76431374-76483342	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
5	nsv1045860	chr15:76431374-76485536	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
6	nsv1053643	chr15:76431374-76485966	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
7	nsv1052496	chr15:76432823-76484981	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
8	nsv1036319	chr15:76432823-76489955	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
9	nsv1035806	chr15:76435640-76483342	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
10	nsv1047539	chr15:76435640-76485966	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
11	nsv1042750	chr15:76435640-76490547	ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
12	nsv1054289	chr15:76437970-76485966	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
13	nsv1035389	chr15:76444695-76483342	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
14	nsv1041435	chr15:76444695-76484981	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
15	nsv1046448	chr15:76444695-76485966	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
16	nsv1046099	chr15:76444695-76490547	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
17	nsv1054300	chr15:76445689-76483342	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
18	nsv1044603	chr15:76445689-76484981	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
19	nsv1043026	chr15:76445689-76485966	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
20	nsv1040683	chr15:76454194-76483342	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
21	nsv1041619	chr15:76454194-76484981	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
22	nsv1046485	chr15:76454194-76485536	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
23	nsv1053572	chr15:76454194-76485966	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
24	nsv1049916	chr15:76454194-76490547	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
25	nsv1046563	chr15:76460462-76483342	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
26	nsv1053775	chr15:76460462-76485966	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
27	nsv1054713	chr15:76460462-76505906	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2469568	ISL2	cis	Whole Blood	GTEx

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76443200-76483000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:76470600-76482800	Weak transcription	A549	lung
3	chr15:76471400-76482400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:76474200-76479800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr15:76475400-76478400	Weak transcription	HSMMtube	muscle
6	chr15:76476200-76482600	Weak transcription	Spleen	Spleen
7	chr15:76476400-76482800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr15:76477000-76479600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr15:76477200-76480000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr15:76477200-76480000	Weak transcription	Fetal Brain Female	brain
11	chr15:76477400-76479600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:76477600-76478800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr15:76477600-76479000	Enhancers	NHDF-Ad	bronchial
14	chr15:76477800-76478800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr15:76477800-76478800	Enhancers	HepG2	liver
16	chr15:76477800-76479000	Enhancers	NHLF	lung
17	chr15:76477800-76479200	Enhancers	Stomach Mucosa	stomach
18	chr15:76477800-76479800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr15:76478000-76478400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr15:76478000-76478400	Flanking Active TSS	Osteobl	bone
21	chr15:76478000-76478600	Enhancers	Pancreas	Pancrea
22	chr15:76478000-76478800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:76478000-76478800	Enhancers	HMEC	breast
24	chr15:76478000-76478800	Enhancers	NH-A	brain
25	chr15:76478000-76479000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr15:76478000-76479200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr15:76478000-76479800	Enhancers	Psoas Muscle	Psoas
28	chr15:76478200-76478400	Enhancers	Esophagus	oesophagus
29	chr15:76478200-76478600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr15:76478200-76478600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:76478200-76478600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr15:76478200-76478600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:76478200-76478600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:76478200-76478600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:76478200-76478600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr15:76478200-76478600	Enhancers	Placenta	Placenta
37	chr15:76478200-76478600	Enhancers	Placenta Amnion	Placenta Amnion
38	chr15:76478200-76478800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr15:76478200-76478800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr15:76478200-76478800	Enhancers	Hela-S3	cervix
41	chr15:76478200-76478800	Enhancers	HUVEC	blood vessel
42	chr15:76478200-76478800	Enhancers	NHEK	skin
43	chr15:76478200-76479000	Enhancers	HSMM	muscle
44	chr15:76478200-76480000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
45	chr15:76478200-76480200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:76478200-76488400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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