EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-17783 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:69212750-69214480 
TF binding sites/motifs
Number: 45             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:69213976-69213994TCTTCCTTCCTTCCTTCC-10.05
EWSR1-FLI1MA0149.1chr16:69214127-69214145CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr16:69214131-69214149CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr16:69214059-69214077TCTTCCCTCCCTCCCTCC-6.16
EWSR1-FLI1MA0149.1chr16:69214102-69214120TCTTCCCTCCCTCCCTCC-6.16
EWSR1-FLI1MA0149.1chr16:69214076-69214094CCTGCCTGCCTGCCTCCC-6.27
EWSR1-FLI1MA0149.1chr16:69214114-69214132CCCTCCTTCCCTCCCTTC-6.33
EWSR1-FLI1MA0149.1chr16:69214084-69214102CCTGCCTCCCTTCCTCTC-6.34
EWSR1-FLI1MA0149.1chr16:69213980-69213998CCTTCCTTCCTTCCTCTT-6.84
EWSR1-FLI1MA0149.1chr16:69214110-69214128CCCTCCCTCCTTCCCTCC-6.84
EWSR1-FLI1MA0149.1chr16:69214139-69214157CCTTCCTTCCTTCTTTTT-6.84
EWSR1-FLI1MA0149.1chr16:69214028-69214046CCTTCCCTCCCTCCTTTC-7.12
EWSR1-FLI1MA0149.1chr16:69214106-69214124CCCTCCCTCCCTCCTTCC-7.12
EWSR1-FLI1MA0149.1chr16:69214119-69214137CTTCCCTCCCTTCCTTCC-7.46
EWSR1-FLI1MA0149.1chr16:69213972-69213990TTTTTCTTCCTTCCTTCC-7.54
EWSR1-FLI1MA0149.1chr16:69214080-69214098CCTGCCTGCCTCCCTTCC-7.64
EWSR1-FLI1MA0149.1chr16:69214008-69214026CCTCCCTTCCTTCTTTCC-7.93
EWSR1-FLI1MA0149.1chr16:69214024-69214042CCTTCCTTCCCTCCCTCC-8.45
EWSR1-FLI1MA0149.1chr16:69214020-69214038CTTTCCTTCCTTCCCTCC-8.84
EWSR1-FLI1MA0149.1chr16:69214016-69214034CCTTCTTTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr16:69214135-69214153CCTTCCTTCCTTCCTTCT-9.09
EWSR1-FLI1MA0149.1chr16:69214012-69214030CCTTCCTTCTTTCCTTCC-9.17
EWSR1-FLI1MA0149.1chr16:69214123-69214141CCTCCCTTCCTTCCTTCC-9.42
MEF2AMA0052.3chr16:69213074-69213086TTTATTTTTAGA-6.07
MEF2CMA0497.1chr16:69213073-69213088TTTTATTTTTAGATA-6.26
ZNF263MA0528.1chr16:69214003-69214024TTTTCCCTCCCTTCCTTCTTT-6.04
ZNF263MA0528.1chr16:69214114-69214135CCCTCCTTCCCTCCCTTCCTT-6.04
ZNF263MA0528.1chr16:69213979-69214000TCCTTCCTTCCTTCCTCTTTC-6.05
ZNF263MA0528.1chr16:69214000-69214021TTCTTTTCCCTCCCTTCCTTC-6.28
ZNF263MA0528.1chr16:69214094-69214115TTCCTCTCTCTTCCCTCCCTC-6.34
ZNF263MA0528.1chr16:69214110-69214131CCCTCCCTCCTTCCCTCCCTT-6.46
ZNF263MA0528.1chr16:69214055-69214076CTTCTCTTCCCTCCCTCCCTC-6.52
ZNF263MA0528.1chr16:69213976-69213997TCTTCCTTCCTTCCTTCCTCT-6.66
ZNF263MA0528.1chr16:69214051-69214072CTCTCTTCTCTTCCCTCCCTC-6.6
ZNF263MA0528.1chr16:69214119-69214140CTTCCCTCCCTTCCTTCCTTC-6.71
ZNF263MA0528.1chr16:69214123-69214144CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr16:69214020-69214041CTTTCCTTCCTTCCCTCCCTC-6.79
ZNF263MA0528.1chr16:69214106-69214127CCCTCCCTCCCTCCTTCCCTC-6.82
ZNF263MA0528.1chr16:69214115-69214136CCTCCTTCCCTCCCTTCCTTC-6.86
ZNF263MA0528.1chr16:69214012-69214033CCTTCCTTCTTTCCTTCCTTC-6.93
ZNF263MA0528.1chr16:69214127-69214148CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr16:69214131-69214152CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr16:69214098-69214119TCTCTCTTCCCTCCCTCCCTC-7.08
ZNF263MA0528.1chr16:69214024-69214045CCTTCCTTCCCTCCCTCCTTT-7.85
ZNF263MA0528.1chr16:69214102-69214123TCTTCCCTCCCTCCCTCCTTC-8.66
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr166921305269214130
Number: 1             
IDChromosomeStartEnd
GH16I069178chr166921273669214468
Enhancer Sequence
AGTAGACTTT TAATTTAATT TTTATTTTTT TATTTTTTTT GAGACAGTCT CGCTTTGTCA 60
CCCAGGCTTG AGTGCAGTGG CACGATCATG GCCCACTGCA ACCTCCGCCT CCCGGGTTCA 120
AGCGATTCTC CTGCCTCAGC TTCCCAAGTA GCTGGGATTA CAGGTGCCTG CCACCATGGC 180
TGGCTAATTT TTGTATTTTT AGTGGAGACA GGGTTTCACC ACGTTGACCA GGCTGGTCTC 240
GAACCCCTGA CCTCAAATGA TCCACCCACC TCGGCCTCCC AAAGTGCTAG GATTACAGGC 300
GTGAGCCACC GTGCTGGGCT GACTTTTATT TTTAGATATT ATTTGAATTT CATGACAAAT 360
TATGTAATTT CCATGATTGT CAATAAAAAA AAGAAAAAAG AAAACACTGG TGATTTTCCG 420
TAACTAAGTG GATTCAATGA AACTAAACTT CTATTTAGTG TGTCCTTGCT AATATTTTCC 480
TTTAAAAAGT CACAGTGCTA CAAAACTGTC ACCAGCTGCT GCTTATTAGG AATGTGGTTA 540
GCAGATGTGG GTTTTCATAG TCATGCTGTA TGAGATCGTT AGTCCATTTT TGCGGGTTTC 600
AGATGGTTAG TGATTTATCT TGGTGGGATG AATTAAAAAT GTGCTTGCAT CAGCTAAAGG 660
ACATATGCAC CTTTCTCTCT TTCGTGACAT GTTTGTGCTG GAGTGAAAAT ATATTGCAGG 720
ATATTTCTAC TGGAAGGTAA AGTAGTACTA TTCATTGAAA AGGATAACTG ATCCTGCTGC 780
CTTCTTAGTG GGGAAGAGTT ATGCATAGAT AATTTTTCAA AGCTGGATGT TGGATCAGTT 840
ATTTTATAAG CTTATTTCTC CCTTTGGCTT CTTCCTTAGT AGTAATTGAG TGGCTCCTGC 900
TTTTGTTCCT CTGGCATCAG GCCACCTTTG TGGCAGTGAC CTTCAGGCTT GCTAAGGGCT 960
GCAATTTTGC TTGAGGCCCT CCTTCCTTAT GAAATTACAC AACACTCAAA CGTTGGAACC 1020
AGCCCCAGAT CCACTAATTC TTTTCCTTTG ACGGACTCTT GGCAATCTAT ACTGTCTTTC 1080
AGCCAAAGTG TAGCTTTATA CAAGATCTGT TTGTCACCGA AATTAATTTG GCCATTTGCC 1140
CTTTAAGCAT GGCATCAAAT GGTGTTATGG CATACTCATT CCTAGATAAA GTATAGACTA 1200
GCAGCTGGAG AGTTTCTTTT TTTTTTTCTT CCTTCCTTCC TTCCTCTTTC TTCTTTTCCC 1260
TCCCTTCCTT CTTTCCTTCC TTCCCTCCCT CCTTTCTTGC TCTCTCTTCT CTTCCCTCCC 1320
TCCCTCCCTG CCTGCCTGCC TCCCTTCCTC TCTCTTCCCT CCCTCCCTCC TTCCCTCCCT 1380
TCCTTCCTTC CTTCCTTCCT TCTTTTTGAG ACAGGGTCTC ACTGTGTCAC CCAGGCTGGA 1440
GTGCAGTGGT CTGATCACAG CCCACTACAG CCTTGAACTC CTGGGCTCAA GTGATCCTCC 1500
CACCTTAGGC TACCTAGTAG CTAGGACTAC AGGTGCCCAC CACCACACCC AGTTAGTTTT 1560
TGTATTTTTT ATAGAGATGG GGTTTTGCCA CATTGCCCAG TCTGGGCTCA AGTGATCCTC 1620
CTGCCTCGGC CTCCCAAAAT GCTAGGATTA TAGGCTTGAG CCACTGTGCC CAGCCAAGAG 1680
TTTCTATCAA AGGTTTTATT GTTGGTGCTG CTGAAAGTCA ACTGGTAATA 1730