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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-21568
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr17:79912170-79913270
Target genes
Number: 55
Name
Ensembl ID
C17orf56
ENSG00000167302
SLC38A10
ENSG00000157637
RP13
ENSG00000229848
ACTG1
ENSG00000184009
FSCN2
ENSG00000186765
C17orf70
ENSG00000185504
Y
ENSG00000207021
TSPAN10
ENSG00000182612
NPLOC4
ENSG00000182446
PDE6G
ENSG00000185527
CCDC137
ENSG00000185298
C17orf90
ENSG00000204237
HGS
ENSG00000185359
ARL16
ENSG00000214087
MRPL12
ENSG00000262814
SLC25A10
ENSG00000183048
GCGR
ENSG00000215644
AC174470.1
ENSG00000215621
FAM195B
ENSG00000225663
PPP1R27
ENSG00000182676
RP11
ENSG00000262831
P4HB
ENSG00000185624
ARHGDIA
ENSG00000141522
ANAPC11
ENSG00000141552
ALYREF
ENSG00000183684
NPB
ENSG00000183979
PCYT2
ENSG00000185813
SIRT7
ENSG00000187531
MAFG
ENSG00000197063
PYCR1
ENSG00000183010
AC137723.5
ENSG00000235296
MYADML2
ENSG00000185105
NOTUM
ENSG00000185269
ASPSCR1
ENSG00000169696
STRA13
ENSG00000169689
LRRC45
ENSG00000169683
RAC3
ENSG00000169750
DCXR
ENSG00000169738
RFNG
ENSG00000169733
GPS1
ENSG00000169727
DUS1L
ENSG00000169718
FASN
ENSG00000169710
CCDC57
ENSG00000176155
SLC16A3
ENSG00000141526
AC132872.1
ENSG00000184551
CSNK1D
ENSG00000141551
CD7
ENSG00000173762
SECTM1
ENSG00000141574
TEX19
ENSG00000182459
UTS2R
ENSG00000181408
HEXDC
ENSG00000169660
C17orf101
ENSG00000181396
C17orf62
ENSG00000178927
NARF
ENSG00000141562
FOXK2
ENSG00000141568
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
ZNF263
MA0528.1
chr17:79912818-79912839
CTCTCTCTCTCTCTCTCCTCT
-
6.22
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
79912644
79912694
Enhancer Sequence
AAGCTGGCCC TGTTGGAGAG GAGACAGTGG CTTGTGAGCT CCTTACCCCC TCAGCCCCTT 60
TTCCACCCCC ACTCCCCTAG AGCTGTCCCC CGCCTGGCCA TCACCCCTTC CTGTTGCTAT 120
GGCTGCCAGC TGTTCCTCTG GCCCGGGCCT CCCCCTAGTT GGCCAGCTCC CGGCTGACCC 180
TTATCGCTTT GTGCCTCAAA TCCCTGCTCA GAGTCCACCT CTTCCAGGCA GGCCCTCCCA 240
GGTGATGGCA AGAGGCTGCC CTAGACAGGC AAATATTCTG CTACTATCTA GAACTCTATT 300
TTCATTTTAT TTTGAGTCGG GGTCTGGCTC TATCGCCCCA GCTGGAGTGT AGTGGTACAA 360
TCGAAGCTTG CTTGCCTCCC ACAGGCAAGG TTAGCTCACT GTAACCTTGA ACTCCTGGGC 420
TCAAGGGATC CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGTGA TGCCACCATG 480
CCTGGATAAT TTCTGTATGT GCAGTAGAGA CACGGTTTCA CCATGTTGCC CTGGCTGGTC 540
TTAGACTCCT GGCCTCCAGC AATCCTGCTG CCTCGGCCTC CCAAAGGGGT GGGATTATAG 600
GCGTGAGCCA GTGTGCCAGG CCCAAGACCG ATCTCGATCT CTCTCTCTCT CTCTCTCTCT 660
CTCTCCTCTC TCTCTTTCTC TCTCTCTCTA TATATGTATT TTTTGAGACA GAGTCTTACT 720
CCGTCACCCA GGCTGGAGTG CAGTGGCACA ATCTCAGCTC ACTGCAACCT CCACCTCCCA 780
GTTCAAGTGA TTCTCCTGCC TCAGCCTCTT GAGTAGCTGG GATTACAGGC GCCTGCCACT 840
ACACCGGACT AATTTTTTGC ATATTTTGTG GAGATAGGGT TTTGCCATGT TGGCCAGGCT 900
GGTCTCGCAC TCCTGACCTC AGGTGATCCA CCTGCATGGG CCTCCCAAAG TGCTGGGATT 960
ATAGGTGTGA GTCACTGCGC CCGGCCTACA AGACCTCTAT TTTTTTTTGT TCTGGTTTTT 1020
CTTCTTTTGT TTTCTCAGGA CCTCTATTTT TAAATAAGGA GGGAGCTACC CGGCGTGGGG 1080
CTCCCGGGGC CCACACACTC 1100