EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS125-00231 
Organism
Homo sapiens 
Tissue/cell
Lung 
Coordinate
chr1:54802980-54805340 
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr1:54804129-54804140GCTTCCCGCCC-6.02
ELF1MA0473.2chr1:54803761-54803773AAACCGGAAGTG+6.27
ELF4MA0641.1chr1:54803761-54803773AAACCGGAAGTG+6.27
ELK1MA0028.2chr1:54803763-54803773ACCGGAAGTG+6.02
ELK4MA0076.2chr1:54803763-54803774ACCGGAAGTGC-6.02
ERGMA0474.2chr1:54803763-54803773ACCGGAAGTG+6.02
ETS1MA0098.3chr1:54803763-54803773ACCGGAAGTG+6.02
FEVMA0156.2chr1:54803763-54803773ACCGGAAGTG+6.02
FLI1MA0475.2chr1:54803763-54803773ACCGGAAGTG+6.02
Foxd3MA0041.1chr1:54803959-54803971GAATGTTTATTT+6.74
IRF1MA0050.2chr1:54804835-54804856AAAAAAAAAGAAAAAGAAAAA-6.09
MNX1MA0707.1chr1:54804544-54804554TTTAATTACC-6.02
MecomMA0029.1chr1:54804881-54804895TCTTATCTTATCCC-6.12
NFAT5MA0606.1chr1:54804196-54804206AATGGAAAAT-6.02
NFATC1MA0624.1chr1:54804196-54804206AATGGAAAAT-6.02
NFATC3MA0625.1chr1:54804196-54804206AATGGAAAAT-6.02
NFICMA0161.2chr1:54804995-54805006TTCTTGGCAGA+6.02
Nr2f6(var.2)MA0728.1chr1:54803387-54803402TGAACTCCTGACCTC-6.22
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_04901chr1:54799713-54803367Brain_Cingulate_Gyrus
SE_05919chr1:54788288-54803304Brain_Hippocampus_Middle
SE_07802chr1:54804140-54809587Brain_Inferior_Temporal_Lobe
SE_24449chr1:54803720-54804070Colon_Crypt_2
SE_29698chr1:54803479-54805037Fetal_Muscle
SE_31383chr1:54800045-54804738Gastric
SE_31383chr1:54805057-54809910Gastric
SE_33414chr1:54803684-54812351H2171
SE_39253chr1:54799970-54803315IMR90
SE_41605chr1:54803705-54803983LNCaP
SE_50141chr1:54800071-54803314Sigmoid_Colon
SE_63284chr1:54754699-54809827NCI-H82
SE_66951chr1:54803684-54812351H2171
SE_68686chr1:54801913-54803319H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr15480382854804057
Number: 2             
IDChromosomeStartEnd
GH01I054339chr15480501454807090
GH01I054329chr15479486154804767
Enhancer Sequence
GTGTTGCAGA AGCTGGTTTA ACCCTTGCTT TGCAATAACC CACCCTGGCC TGCCCTCTCA 60
AGGAAGAGGC GCAGGGATCT TAGGGCAGGC TTTGTGCTGC TGAGGCTGTT CTCGCTCCAG 120
TCTCTGACTT CAAGCAGCAA AAGGTTGGCT GAACCAAAGC ATTTTGTTTT CCTCAAGCTT 180
TTTTTTTTTT TTTTTTTTTT TTTTTTTTGA GATGGAGTCT CAGTCTGTTG CCCAGGCTGG 240
AGTGCAGTGG CACCATCTCC GCTCACTGCA ACCTCCCTCC GTCTCCCGGG TTCCAGCGAT 300
TCCCTTGCCT CATGAGTAGC TGGGACTACA GGCATCCACC ACCACACCCG ACTAATTTTT 360
GTATTTTTAG TAGAGACAGA GTTTCACCAT GTTGGCCAGG CTGGTCTTGA ACTCCTGACC 420
TCAGGTGATC ACCTGCCTTG GCCTCCCAAA GGGCTGGGAT GATAGGCGTG GGCCACCATG 480
CCCGGCCTCC TCAAACTTTT TGAAGACAGT GAGTTTTTTG GGCATAAAAA ATAAAATCTG 540
GCTGAGCATG GTGGCTCACG TCTGTAACCC CAAAACTCTG GGAGGCCAAG GCAGGGGGAT 600
CACTTGAGCC CAGTAGTTCA AGACCAACCT GGACAACATA ATGAGACCCC CATCTCTATC 660
TTTTAATTTA TTTTTGAAAA ATAATGAGAA TAAAGTCCCA GGCCGACTGA GAAATAAAAT 720
GAGATATAAT GATTGTAACC ATCCATGACA TCATGTGTGT ATATTACACT CAACAGCAAC 780
TAAACCGGAA GTGCTTCTCC AGTTTGTGAA GCCAGCTTCT GCACTCACTG CCTGCTCCAG 840
GAAGTTGCCT GTGACTGCCC CTGTGGTCCA GGTGTCCCTC TCCTGTGTTC ACAGCCTCGG 900
TGCCCCTACT GCAATGGGGC TGCATAGCCG GCACCTACGG CAGGGCGGGC TGATATGCTT 960
GCCTTGCATA TGCTAAAGCG AATGTTTATT TTTCCATTTC CCCAACTAGA CTGTAAAATC 1020
CTTGAGGGAC AATACCTTAT TCTACTTTAC TTTGCAAATA CCTGGGAAAA GATCTAGCAT 1080
GTATCTCACA CTGAAAAACC ATCTGTTGAA TAAATAACCA AAGTGATGAG CACATGGCTG 1140
CCCGCCTATG CTTCCCGCCC TCTCACTCCC GACCCCTAAC CCCACTTTCT CCACCCGCTA 1200
GAAGCATTCT GAAGAGAATG GAAAATCTCA GCCAACTATT CAGGGTAACT GTCCGGTCAC 1260
TCTGCGTCCA TTTGCCTTTA CGGCAATATA TATACTAAAG GGTATGAGCT CAAGTTTCCA 1320
TACATACCCA GGCAGCCAAG GGAGTTCTCT CTTCCCAGCC GAGGCTAAAC AGGGACCCAA 1380
CCACAAGCAT CCAGTAATTC TGAATATGAC GTGAACAACG TAAAAATAGC TCCTGTATCT 1440
CTTTGCCCCC ACCCTTCTCC CCAACAACAC AAAGGGCAGA AGAGAGTGAC ACCCCTAACA 1500
AACAGCCCCA GCCTCCTACA TCTGGACCAG CTGCTGTGAG CCAACAGGGT ATTCTAAATT 1560
ATACTTTAAT TACCATAATT TTTCACAGGT ACCTGAAACC AGATCATGAC GACGGTGCAA 1620
GAAATCCCCA AATAGGATGC ACGAGGTCCA AGTTAAAGCT AGTCTTCTAA ACACACACCT 1680
TTTCTCACAT GCCTTTTATT TCATGTAGCA CTTTACAGTC TGCAGAGTGC TTTCATGGGC 1740
CTTCTCTCTC CCACAGGCTC TGGATTAAGA CAACATGGTT CAATTCCAGC CTCCAAAGTA 1800
TCCTGCCCTC TCCAGAGACC CTTCACCTAT CACCATTTGG TGCAATCTGT AACAGAAAAA 1860
AAAAGAAAAA GAAAAAGAAT AGGAAATGGG GGAGAAGGGG GTCTTATCTT ATCCCATGGG 1920
TTACTAGGAA TGTTAAGGAT TAAATGGAAA GCATAGTTAA GATTTTTAAA GAGAAAGCAC 1980
TTATTGAGGA TAATTGATGC TGGACAGATA GCAGATTCTT GGCAGACACA CATTCTCAGT 2040
GTGGATGTGT CTATACAGCT AATGGTTAGA AGCGTGAGCT CTGAAATTAA TCTGCTTAGA 2100
TTTGAATCCT GTCTGCAACA TTTTAGCTAT GGGGCCTTGG GCCTCAGTTT CATCAACCAG 2160
AAAACAGGAA TGATAGCAGT AATTACTTCA CAGGCTCTTG CGGAGTTCAT GAAATAAATG 2220
CGAGTAAAAT ACTAGCCTAG CCCTAGCACA TAGTAACCAC TAAAAAAAAA AACATCATTG 2280
CAGGAGAGGG GAATCTCTAG TGCCTTAAGA AAGGGGAAAG ATCAGCCGGG CATGGTGGCT 2340
CACACCTATA ATCCTAGCAC 2360