EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-21594 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:79975280-79976270 
Target genes
Number: 58             
NameEnsembl ID
AC027601.1ENSG00000260005
C17orf56ENSG00000167302
LINC00482ENSG00000185168
RP11ENSG00000262877
BAHCC1ENSG00000171282
RP13ENSG00000229848
ACTG1ENSG00000184009
FSCN2ENSG00000186765
C17orf70ENSG00000185504
YENSG00000207021
TSPAN10ENSG00000182612
NPLOC4ENSG00000182446
PDE6GENSG00000185527
CCDC137ENSG00000185298
C17orf90ENSG00000204237
HGSENSG00000185359
ARL16ENSG00000214087
MRPL12ENSG00000262814
SLC25A10ENSG00000183048
GCGRENSG00000215644
AC174470.1ENSG00000215621
FAM195BENSG00000225663
PPP1R27ENSG00000182676
P4HBENSG00000185624
ARHGDIAENSG00000141522
ANAPC11ENSG00000141552
ALYREFENSG00000183684
NPBENSG00000183979
PCYT2ENSG00000185813
SIRT7ENSG00000187531
MAFGENSG00000197063
PYCR1ENSG00000183010
AC137723.5ENSG00000235296
MYADML2ENSG00000185105
NOTUMENSG00000185269
ASPSCR1ENSG00000169696
STRA13ENSG00000169689
LRRC45ENSG00000169683
RAC3ENSG00000169750
DCXRENSG00000169738
RFNGENSG00000169733
GPS1ENSG00000169727
DUS1LENSG00000169718
FASNENSG00000169710
CCDC57ENSG00000176155
SLC16A3ENSG00000141526
AC132872.1ENSG00000184551
CSNK1DENSG00000141551
CD7ENSG00000173762
SECTM1ENSG00000141574
TEX19ENSG00000182459
UTS2RENSG00000181408
HEXDCENSG00000169660
C17orf101ENSG00000181396
C17orf62ENSG00000178927
NARFENSG00000141562
FOXK2ENSG00000141568
WDR45LENSG00000141580
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr17:79976173-79976187CAGGGGGCGTGGCC-6.69
KLF16MA0741.1chr17:79976175-79976186GGGGGCGTGGC-6.62
SP1MA0079.4chr17:79976174-79976189AGGGGGCGTGGCCCG-6.01
SP3MA0746.2chr17:79976174-79976187AGGGGGCGTGGCC-6.82
SP8MA0747.1chr17:79976174-79976186AGGGGGCGTGGC-6.92
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177997593079975991
Enhancer Sequence
AACGCCTTCC TGTCATGCTT CCTCCAGAAA AGGGCCCCCG TCGTCTGCCC TGGCTCAGCT 60
GGACCGCAGT GTCCAGGCCT GAGAGCCTGG TGGACCATGG TGTGGGCCCC TGAGGAGCCT 120
GGTGGACCGT GGTGTGCATC CTGAACCCGC GTGGGTCTCC TCTTCGTTTT TAACCTAACA 180
GTTATTTACA CTTCCTCCAA GGAGAACAGA AGTGCTTGAG GAAAGTCTTT TGGGGGAAAT 240
CACCTGCAAC CCAGGAGCCA AGCCCTGGGC CAGGAGCTGG GGGAGGAGCT AGTAGGTCAC 300
CCCACATCCG TAGGGCAGGG CCTGGCCTCA GGCCTCCTGC TGCCCCCGAG CGGGCTATAG 360
TGCTGGGTTC TGGCCCTGGT CCACCCTGCA GCCAGCCTCC CCAGCAAGTC TGATGACTTC 420
TACAGGCTCC CAGGGCTTTC AAACTGACCT ACTGAGGTGG GCAGGGCGGG GAAGGGGTGG 480
ATCCCAGCAG CCCTGCCTGC CCGGGGCCAC TGGGGCTACA TCGAGGATGA AGAGGCTCGC 540
CTCAAAGTTG TCTTCGGGCA CCAGGGCAGG AGAGAGGCTG GGTCGCCTCC GATGGTTCCC 600
AGGGGCAGCT TTTGTGCTTC CCACCCTGGG GCCTGACTCC CTACCCTTTC CCCTCCCTGC 660
ACGGGGCTCC AGGATGGCGC TCAGCTGAGA GCCCCTGGGG TGCTTCCAGT CCTGGGCTCT 720
GACAAGAGAG AGAACGTGAG GTGGGCTGGA GGGGAAGTGG TCCAAGGCCC TGCCCGCTTC 780
CCAAGCGTTG GCACAAGTGG GGCTTATGCC AGAGGCCCCT GAGAGTCAGA GGGCAGCCAG 840
ACCTGGGTGG GGCATCCAGA CAGGTCCCAC AGCCCTGCGT CTCCAAGGGT GGGCAGGGGG 900
CGTGGCCCGA GGGGGCTGAC CTGCACCTCT CTGGCACTGC TTGGGAAAAG AGGAGGCCTT 960
CATTTCAGCA GGGCCTTGGG CCAGGGTCCC 990