EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS091-19796 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:40971630-40972790 
Target genes
Number: 46             
NameEnsembl ID
STAT5BENSG00000173757
STAT3ENSG00000168610
PTRFENSG00000177469
ATP6V0A1ENSG00000033627
AC067852.1ENSG00000256929
NAGLUENSG00000108784
HSD17B1ENSG00000108786
COASYENSG00000068120
MLXENSG00000108788
PSMC3IPENSG00000131470
TUBG1ENSG00000131462
FAM134CENSG00000141699
TUBG2ENSG00000037042
PLEKHH3ENSG00000068137
CCR10ENSG00000184451
CNTNAP1ENSG00000108797
CTDENSG00000239671
EZH1ENSG00000108799
HMGN2P42ENSG00000214578
RAMP2ENSG00000131477
AC100793.1ENSG00000197291
VPS25ENSG00000131475
WNK4ENSG00000126562
CCDC56ENSG00000183978
CNTD1ENSG00000176563
BECN1ENSG00000126581
PSME3ENSG00000131467
AOC2ENSG00000131480
AOC3ENSG00000131471
RP11ENSG00000260105
AC100793.2ENSG00000213373
G6PCENSG00000131482
SNORA40ENSG00000212149
AARSD1ENSG00000108825
RUNDC1ENSG00000198863
RPL27ENSG00000131469
IFI35ENSG00000068079
VAT1ENSG00000108828
RND2ENSG00000108830
NBR2ENSG00000198496
BRCA1ENSG00000012048
NBR1ENSG00000188554
TMEM106AENSG00000184988
ARL4DENSG00000175906
AC087650.1ENSG00000237888
ETV4ENSG00000175832
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr17:40972137-40972156CTGCCTGCAGGGGGCGCTG+6.99
RUNX1MA0002.2chr17:40971738-40971749AAACCACAGAG-6.14
ZNF263MA0528.1chr17:40972758-40972779TGAGGAGGATAGGGGAGAGGG+6.89
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174097203740972433
Number: 1             
IDChromosomeStartEnd
GH17I042820chr174097208140972250
Enhancer Sequence
GGAAAGAAAT AAGAGGGCAT TACAACTCTG GCAGCTTAGA GGTAGAGTTC ATCTCCCAAA 60
CAGCCTCAGA ACTATATGGC TTTAGTCTTG ATAACCACAA GACTTGATAA ACCACAGAGA 120
CTTAAAAAAT GGGTATTATC GAAGCAATCC TTGTGTATGT GGACTAAGAA AGGACCCACG 180
ATACAGACAA ACCTTAAGTC CCATTTGATT TTTTTTTTGT GGGGAACAGC ATTTCCTAAC 240
TATGTTACAC TCTATGTATG GTTAAATTTG CATTTCTCAA CACTTAGCAG TCAGGGGCAG 300
AGGACAGAAT GCCCTAAATC ATAGTACAAG GAAAAAGCCA GATCAGACTG CAATGAAGTC 360
TGCCACAGTA CAAAGTAGAA AATTTATATG TTTTCAGTAT TTTGAGATTA CTCATATGTG 420
ACCAAAATCT CACAGCATCT ATTGACTTCA AATGCCAGAC CCCTTTGCCT CCTTGCTTAA 480
AGGCTTCTCT GGCTCCTGGA CTCTTCACTG CCTGCAGGGG GCGCTGGCCA GAATTAATGA 540
CCTCCACTAA ACCTGACATC AGCACTCCCC CAGTGACTGG CAGCTGTGGG TAAATAAATA 600
CTCCAGCTCC CTTGCTACTT GAGAAGAAAT CTCAGGTGTG TATTCAATAG TATCTCACAG 660
GATGTTGCTC CACAGGATCC CTGATATTAT CACAGCTTAA AATGACATGT TCTCTAACAC 720
TGACAATTCT TTCTGTCCAG GGCAATCATA CAATTCACTG TCCTAACCAG GATGCTTTTG 780
AGAATGGAAA GGAGTGGATA TTAACAACTA GCTAGAACAA CAGATGCAAA TCAATGCTCT 840
AGAACGACCT GGACACACAG GTCATCCCAT CTCCAACCTA CAATAATTTA TAATTCTGCT 900
TCAAATAAAG AGCCCTTTCC AACATTTTAA AATGACTAAT TCAGTAACCC TGTGACCTCA 960
GGTGCAGATC TGTACCTCCA ATGGTGCATA GCAGCCTGAT CATGTAGAAT GTCTCATTAC 1020
CCAGAGATCC CAAAAGTCCG GGAGCTCTAG AAGCGCCAAG TAGCCTGCAG AAACCAAGCC 1080
TGCATTCCTG TTTTCATATC ATATCTCTCA TTTGGAATGT TTACTACATG AGGAGGATAG 1140
GGGAGAGGGC ACTTCTATTA 1160