EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-22065 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr3:129297280-129299690 
TF binding sites/motifs
Number: 20             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr3:129298037-129298055TGAAGGATGGAAGGGAGG+6.53
EWSR1-FLI1MA0149.1chr3:129298033-129298051GGGATGAAGGATGGAAGG+6.56
EWSR1-FLI1MA0149.1chr3:129297987-129298005GGAACGAAAGAAGGAGGG+6.65
EWSR1-FLI1MA0149.1chr3:129298041-129298059GGATGGAAGGGAGGGAGG+6.72
EWSR1-FLI1MA0149.1chr3:129298002-129298020GGGAGGAGGGAGGGAAGG+6.94
EWSR1-FLI1MA0149.1chr3:129298006-129298024GGAGGGAGGGAAGGAAAG+7.62
EWSR1-FLI1MA0149.1chr3:129298010-129298028GGAGGGAAGGAAAGAAGG+7.85
EWSR1-FLI1MA0149.1chr3:129298018-129298036GGAAAGAAGGAAGGAGGG+8.34
EWSR1-FLI1MA0149.1chr3:129298014-129298032GGAAGGAAAGAAGGAAGG+9.17
Klf1MA0493.1chr3:129298478-129298489AGCCACACCCA+6.14
RREB1MA0073.1chr3:129299371-129299391GGGTAGGTGTTGATGTGGGG-6.66
ZNF263MA0528.1chr3:129298042-129298063GATGGAAGGGAGGGAGGGGAG+6.08
ZNF263MA0528.1chr3:129298011-129298032GAGGGAAGGAAAGAAGGAAGG+6.23
ZNF263MA0528.1chr3:129298015-129298036GAAGGAAAGAAGGAAGGAGGG+6.2
ZNF263MA0528.1chr3:129298023-129298044GAAGGAAGGAGGGATGAAGGA+6.38
ZNF263MA0528.1chr3:129298007-129298028GAGGGAGGGAAGGAAAGAAGG+6.76
ZNF263MA0528.1chr3:129298038-129298059GAAGGATGGAAGGGAGGGAGG+7.19
ZNF263MA0528.1chr3:129298000-129298021GAGGGAGGAGGGAGGGAAGGA+7.74
ZNF263MA0528.1chr3:129297996-129298017GAAGGAGGGAGGAGGGAGGGA+7.94
ZNF263MA0528.1chr3:129298003-129298024GGAGGAGGGAGGGAAGGAAAG+8.89
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_00112chr3:129296408-129298337Adipose_Nuclei
SE_05951chr3:129296904-129298206Brain_Hippocampus_Middle
SE_09767chr3:129294545-129298343CD14
SE_25754chr3:129296269-129297924DND41
SE_25754chr3:129298095-129298948DND41
SE_31151chr3:129293199-129298320Fetal_Thymus
SE_31569chr3:129294892-129298060Gastric
SE_33524chr3:129292858-129302344H2171
SE_40701chr3:129295308-129297722Left_Ventricle
SE_42115chr3:129295052-129298666Lung
SE_51354chr3:129295342-129298113Skeletal_Muscle
SE_53375chr3:129294696-129297954Spleen
SE_62855chr3:129293187-129347490Tonsil
SE_65523chr3:129293511-129298361Pancreatic_islets
SE_67059chr3:129292858-129302344H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr3129297291129297400
chr3129297400129297482
Number: 1             
IDChromosomeStartEnd
GH03I129575chr3129294244129298501
Enhancer Sequence
AGAGGAAACA GAAGGAGAGG GTGACACAGG GGCATTTCAG AGAAGAGGCA GGAGGACTCA 60
CTGCACCCCA GCCTGCCTGG TTCAGTCCTG CCTTCCTGAG GAGAAAACAC TAGTCATTCA 120
GTCCTAACGG CCACCAGCCC CACCCCGTGC CTCCCACTCG CCACCACCCT CCATCCTATG 180
GGCAGGTCGC ATTGGCCCTG TTTAAAGATG AGGAAGGTGG GCACAGGCAG ATGGCATAAC 240
CCGCCCAGTG GTGGGGCCAA TTTCCTCCAT GAGTGCTCCC TGGCCTCAGA CGAGGCTGGG 300
AGGCTGAACT CCAGGCCCAG CTCCTCCCTG TCTCTGGGCC TCACCTTTCC CAATAGTAGA 360
ACAGGGGGGC TGCACCCACT CCCTGAGATG CCCCCAGGGC TGAAACTCCA GCTTCCTGAC 420
TGACCCGTGT TAAGCGATTC AGAAAAGAGA AACCTTGGGC TTCCAAACAG CCCATAGGAA 480
AGGCACAGGG AGGGCTCTGA ATACCAGGAG GACATTTCAG AGGGCCAGAT ACCACCGGTC 540
TCCAGGGGAC ACCCCTCCCC ACAGCCCGGG TATAAGTCAC AGCCTCTAGG TGAAGGTGCC 600
AGCCCCAGAT ACTCCCAGGA AGGGCCCCGG GCTCATGGGG GGACAGCACA TGGTTGGCTC 660
TTGTTTGGTG GTGGAGTCAC TGAGGCCTGG CAGAGCAGCT GCTTCATGGA ACGAAAGAAG 720
GAGGGAGGAG GGAGGGAAGG AAAGAAGGAA GGAGGGATGA AGGATGGAAG GGAGGGAGGG 780
GAGATTGAGC CTCCAAGAGC AGTGAGCTGC CTGAGGGCGG AGGACAGGGC TGGCCCCTGA 840
AGCCCCAGGT GTCTTGACTC TGGGGTCCTC CGAGCTGGGG CGCGTGTTAA GATGCAGAGG 900
TCTAGCCCCG CTGCAGGGAT TCAAGGCCTG GTTGGGAACT GCTGTCTCCA GGCTCCTGGG 960
ATCCATGCTC CACTGTACAG AATAAGAAAC TGAGGCCTGG GGGAGGGGCA GAGACCAGAG 1020
GCAGGGCTGT TCCCGCCATG TCCACCTTAG TGATCGCTCT GAGCTGGGAG GTATGGACCC 1080
CCCAACCTGC CCTGTGTTCT CCAGCTTTGG TGGCCCCAGT GAGCCATTCC TGCCTCCTCC 1140
TGCTCCCGAA TCTGACCTGC TGGGACCATG AGCAGGGCAG GACTGGGGAC CTTGGAGCAG 1200
CCACACCCAT GCCAAGGGGA CTACAACCAC CCTTCAGCTC AGGGACTTCC TACTCTGCCC 1260
TCCTTCCCAA GGCTGGTTGC AGAAGGATCT GGGTTAGAAT CAGGCCAGAA AGCAAAAGCG 1320
TCCATGGGCC ACGTGTGTCC ACGTGAGGTC ACCCAGCCAG GCCAAAGGCC TTGGGACAAA 1380
ATATGAGACG CTTCTTTATT CTACACCAGA TGAGAGCAGG ACAGGGACTG ATTCCCCTCA 1440
GGGACCCCAG CCCAAAACCG GACCTCGAGG GGATGCCAAT GCCAACAACA AGAACTGATG 1500
ACGATAATGC TAATAACAGT GGCAGTCACC AGCTCATCTA GCCCTCCCTC TGCTGGGACC 1560
GTTCTGAGCA CTTTGCACTC TTTTAATTTA CCAAATTCTA CTCCCAACAA CCCTAGGAGG 1620
TAGATACTAT CATTACACCC ACTTTACAGA ATAGGAAACT GAGGCACACA GAAGCAAAGC 1680
AGTTTGCCTA CAGTGGAATG AGCAACACAG GAAGGCTCCA GTTGTCCAGA CCATTTGCTG 1740
ACCACGAGAC CAGAGTGGTG AGTTCCCCTA GGGACAGGGT CTGGTGCAGA CCTCAGGGGC 1800
TTGGCAAGAG AAGCAGCATA GCCAGGCCCG GGTGCTGCTG GCTCCCTGTG CCAGAATACA 1860
CGAGCCACTG ACCCTCTCCG GGCCTCCGTG TTCCTACCAA GGAGGGGCCC AGACGGAGTC 1920
AGCGGCGGGC CCCCTGCAGA CCGCAGGCTG CCATCCTGTG CTGTGTGTAA ACCCCACGGA 1980
ATCCGAGGGC ATGGAATCCA TGTTTCCACT CAGGCCTCGA AGCCACTGCC AGGTCTGCTT 2040
TGCGGCTGGC TGGGGCCCAG CCTCTGTCCT CCTGGCCCCA GCCCACCCGG TGGGTAGGTG 2100
TTGATGTGGG GCTGAGGTGT GAGAGTCAGG GCAGGAGGCG CTCTCACAAG AGGGCCCCCA 2160
CAGTGAATGA TGTGTGACCA TCCCCGAGGG CCACCCCACT CCCCTTAGCC ACTTGTAACC 2220
TGTGGCCAGG TGGATGCTCA CCCCCATTCT AGAGAACCGA GGCTGGAGGA GTCCTCGTGG 2280
CTCTCACAGG GCCTCTCCTA AACTCCAGGG GAAGAACTGG TGTCCCAAAC CATCAAGGCA 2340
CTCAACAACC CAGGGACCCT GAATCCACCT GGTCCCTCCC TACGTCTCTG TACCCCCAGG 2400
GACCCCCACA 2410