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

TagContent
EnhancerAtlas ID
HS098-30461 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr2:70172540-70174380 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6756513chr270172587hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArntlMA0603.1chr2:70173453-70173463GGTCACGTGC+6.02
ESR1MA0112.3chr2:70173986-70174003AAGGTCAAAACGACCCT+6.27
FOSL2MA0478.1chr2:70173903-70173914GGGTGACTCAG+6.02
INSM1MA0155.1chr2:70173007-70173019TGCCTGGGGGCA+6.04
JUNBMA0490.1chr2:70173903-70173914GGGTGACTCAG+6.02
SP8MA0747.1chr2:70173227-70173239AGTGGGCGTGGG-6.14
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_09668chr2:70170084-70175672CD14
SE_65154chr2:70171871-70174956NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr27017354070174234
chr27017256770172868
chr27017262770172794
Number: 1             
IDChromosomeStartEnd
GH02I069945chr27017193470176194
Enhancer Sequence
AGCCCAAACT GGGTGGCGAG GCAGCTCCCT GCCCACTCTG TTCCATGCAG AATTCTGGAG 60
TCATTGCCTC TGCGAGTGTC CTTGTGGAGA CTAGATGAGG TAGATGTGGC TGCTGGCTGC 120
TGGCTGGGTT GAACATGTTG CCCAGAGGAA AGGGAAGCTT TGTGTTGGGA CAGAGTGACT 180
AACCCACTTT CAGGCAGACG GCAGGGCAGG CTCTAACTGG CTGAAGCTTC CGGGAGCCTC 240
CCCGGCTGTG GGTGAAGGCA GCGTGTCTGG TGAAGGCAGG CTAGGGATGT AATGGGACAG 300
GCGAACCATC TTATCCAAAG GGATGACCAC AGGAAGAGCC AGGACGGAGG CCAAGGGCAT 360
GCACCTGAGG CCAGGTCTGA GCGGGTGGAC TGGGGGTATT GGAGCTAGAG AGGCCCACTC 420
AGGCCCTGGA GAAAAGGGCA GGGGCTTTTC TAGGATGCTC TTGGCCTTGC CTGGGGGCAG 480
AGGTGAGGAA GACAGTCAAC GCAGGGAGCT CTGTGTCAGA AATACGTCTG CCTTCAAAGA 540
AAGCAGCCAT CCTGGAGGAG AAGGCACCTG GGAGGGCCTT AGGGATAGGG GAAAGAGAGA 600
AAGGCACTGG CCAACCAACA CCATTGGCCA GCCAGACAGC CGGGCTGGGT GACACCTGGA 660
GATAGCCCCC AGCCATGCAC AGGGACCAGT GGGCGTGGGA GAACCAGTAT CTGTTTAGTT 720
ACAAGCAGAA CATCCAACAC ACTCGCCTTG CCACGCTGAT ACTGTCATCC CCCAGAAGGC 780
GGAAAAAACC ATTGCTGTGA AGCATTCGAG CCAGTAATGA CCAACAGAGA CCAATAGGCT 840
GGCCAAGTGG AAATAGAAAC TCAGGGGGAG TGCCCATGTC CCCTAGGTAC CCCGGAAGGT 900
GGTCCTGGGT GATGGTCACG TGCACAGACT CTGGTCAAAT GGAGCTAAGG GTCGATGCCA 960
ACTCCACCCT TAACACCCTC GGTGACCCCA GGCAAGTATC TGGGACTCTG CTGACCCGGT 1020
CTGTAGAGTG AGGATAATAA CAGCATGTAC TTCCCAGGGC TGCTAGGGGG ATTAAGTAAG 1080
GTAAAGTATG CAAACAGCTT TTCCCCATGC CTGACATGCA GAAAGCATTC AGTACATATG 1140
AGCAATTATA ATCATTTTCC CAGCCAAGGA GAGAACGTTC GAACACTGTC TGGCATGTGA 1200
CTTGGATTTT CAGAATACAA AATTCCAACA CTCAGAGAAG AAATAAGCTT GGAAGGGAAA 1260
ATTACATTAG AGGGTGGGGA AGTGTTCAAA TATGTCATTC TGACTGTGCT GTTTAGACAA 1320
CAAACAGTAG GCAGGAAGTG GTTAAACCGA AAGGGGGAGC AGAGGGTGAC TCAGGGACAG 1380
AATGTGGGCA TTGACAGTGG AGGGGTGGCT ATTTTCCAGG TAGTATCTCA CCTATGTGCT 1440
GTTCGGAAGG TCAAAACGAC CCTAAGACCC CGCCAGCCCT ACAGGGCAGT TCCTCTCATA 1500
GAGAGACCAG ATCATACAGA GGTGGCTCAG AGAGAGAGAC AGAGGGAAGC CCTTGCTAAA 1560
ATGCCCATAT GTTGCAAGTA TCTCATCAGA AGAGGCCAAA TGACTTCAGT TCCCGCATTC 1620
ACACGTACCT TTGCACTGCA AATTCAGAAC AACCGTAGGT AGAGCTCTAC CCAGACGGGG 1680
ACAACTCCAC ACTTCAAGTA TGACCTCTGA GCAACTGCAG AGGTTGTGAT GATTCTTGGC 1740
TACTTTGCAG TTAATAACTT TGGTCAAAGA AGCTACCAGT CAATGCAGAC TAGCACAGGG 1800
CATGGAACAG TGTGTGGCCC AGAAGAGGTA TCAGTGGAAG 1840