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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS139-22233
Organism
Homo sapiens
Tissue/cell
Myotube
Coordinate
chr17:7616770-7617570
Target genes
Number: 35
Name
Ensembl ID
EIF5A
ENSG00000132507
GPS2
ENSG00000132522
PLSCR3
ENSG00000187838
C17orf61
ENSG00000205544
NLGN2
ENSG00000169992
FGF11
ENSG00000161958
RP11
ENSG00000263301
CHRNB1
ENSG00000170175
ZBTB4
ENSG00000174282
POLR2A
ENSG00000181222
TNFSF12
ENSG00000239697
TNFSF13
ENSG00000161955
SENP3
ENSG00000161956
EIF4A1
ENSG00000161960
SNORA48
ENSG00000209582
SNORD10
ENSG00000238917
SNORA67
ENSG00000207152
CD68
ENSG00000129226
MPDU1
ENSG00000129255
AC113189.5
ENSG00000233223
FXR2
ENSG00000129245
SAT2
ENSG00000141504
WRAP53
ENSG00000141499
TP53
ENSG00000141510
EFNB3
ENSG00000108947
CYB5D1
ENSG00000182224
CHD3
ENSG00000170004
LSMD1
ENSG00000183011
SCARNA21
ENSG00000252835
AC025335.1
ENSG00000179859
CNTROB
ENSG00000170037
TRAPPC1
ENSG00000170043
VAMP2
ENSG00000220205
SNORD118
ENSG00000200463
C17orf59
ENSG00000196544
TF binding sites/motifs
Number: 2
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
RREB1
MA0073.1
chr17:7617471-7617491
TGTGTGTGTGTGTTGGGGGT
-
6.17
RREB1
MA0073.1
chr17:7617469-7617489
TGTGTGTGTGTGTGTTGGGG
-
7.29
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr17
7616944
7617000
chr17
7616842
7617443
Enhancer Sequence
CCTTGGCCTC CCAAAGTGCT GGGATGACAG GCATGAGCCA CCGCACCCGG CCTGGAGCTG 60
CTTTAGATGA GGAGGTCAGG AAGGTCCCTT TGAAAGAGAT GCCCTTGATC AGGACCTTAA 120
GTCATGAGAC AGGAGTAAGC CATGCACACT GGGGACGGGC ATGCTAGACA GAGGAACAGC 180
AAGTGCACGG GCACAGAGGT GAGATTGTGG TGTGTTTGGG AACAGTAAGA AGGACATCAC 240
CACCACATGC ATGTTTCGGA TGTGTCCTGT TCTTCCCTAG CCTCGGCCTG GAGGGGAGTA 300
AGTCACTTAG GGTCTTGGAT CCACATTAAG GAAGTTGATC TCACTCAGTC TCCCATCCCC 360
TTGCCTTTTG TTTCTTGTGT GTCTGTGACT TGTGTTTTCC TCGTCTAAAT TTTAAGCTCT 420
GGGAGGGCAA GGATGATGCT CTGAGCTTTT TTGGGGGCTG TGGCACAGCT GCTGGCAGAG 480
TCCAGAGCAG GAAGGCAGAG CGGAAGTAAA GGAACCGAGA GGGCTGGGAC CACAGAAGCT 540
AGAGCTGTCG CCCTGCCATC CCCAAACCGC ATAGGATTGA GGCTGTCTTG GGGCTGAGCT 600
GTAGAGTGAA GCTCAGGCTT TGCCCTCCTT CCAAATAACG GCAGCTGAGG GATACTATTC 660
AGCCCGAGGT GCGTGTGTGT GTGCGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTTGGGGG 720
TTTTTAGGGA AAGGGGAATG GGGCAAGGAG TGGCAGTGGG AATTTCTTTT CTTTTTCTTT 780
TCTTTTTTTT TTTTTTTGAG 800