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

TagContent
EnhancerAtlas ID
HS087-00493 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr1:27321100-27323080 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs148609498chr127321794hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Six3MA0631.1chr1:27321807-27321824CCAGGTGATACCCTTTA-6.36
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_26796chr1:27320100-27322233Esophagus
SE_26796chr1:27322265-27329040Esophagus
SE_31795chr1:27319283-27327051Gastric
SE_34461chr1:27319108-27326655HCT-116
SE_36077chr1:27320120-27329970HMEC
SE_47963chr1:27320102-27321641Pancreas
SE_49333chr1:27319936-27322236Right_Atrium
SE_49333chr1:27322274-27323394Right_Atrium
SE_65116chr1:27320938-27323497NHEK
SE_68709chr1:27322416-27327853H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12732145227321840
Enhancer Sequence
GAGGTGCGGT CTTAGCGGCT GGTGCGTTCG AGGGTCGGTC ATGGCGTGTG GGGGGCTGGT 60
CCAGGGCCCG GGAACTCCCT TCCCTGGAGC TTCTGGCGTC TGCTGGGTCC CTAGTAAAGC 120
TGCCACTTTC TGTTGCCGCC TCTCCCGACC ATCTGGAGAG TGAGAGGTGG TAGCATCAAG 180
TCTCCATTAT AAGAGTTGGA CTCTTGAGGG GGCTCAGATC CCAGGAACGG GTTGGCGGCA 240
AACTTTTACC ACTTGGAACC TGCCGCACGG ATGCAGCACC CCCCATCCTC ACCCCCACTT 300
GCGTGGCCTT TCCCGGGCCC CTCGGAGCTG TGAGCAGTCT TGCCCTTGAG GATGCTGCTT 360
CCTGGCGCCG CCCAGCTCCG TGCCTTCGGG AGGACAGAAT AATGAGGCCC CAGGATGGGG 420
TGGAGGCTGG CACAGGGCTG TACCACTGAA TTCCCCCTCT AGGCCTGTTT CACCTTTGGG 480
GAGACGGAAT CCCAGAGAGG TTTAGGATTT GTTCTCTTCA TACTTAGGCC CTTCTTCTTC 540
TAGGAGACAG CTTTTCTTAT GCCGTCATGC AGGTTCGCAA AAATTACAGC CTGACTCACA 600
TAACCAGGAC AGGATGTCTG GCACCTGCTC ACCCAGGGAT CCTTACATAG CAGAACCTAG 660
AGGCTTAACT CCCAACCTGT TACTAAGATG GCTCGGCCAG GTTGGAACCA GGTGATACCC 720
TTTAACAGGC CCCAAGGGGG CAGGTGTGGT ATCAGCTTCC AGAAAGGGGG GCCTTAAAGA 780
GCCAGATCTG AGGTGAGATC TGCTTCTCTT CCTGTCCAGA TGCCCTTCAG TCTCCCATTC 840
CTCTGTCCCC ACTGTGAATG ACCTGGCTAC CACATTGCTG CTCACCAGCT GAGTTAATTT 900
CACTCTCACT TATCAGTCTG CGAAGTGGAT CTCTTAACCT CCCAGAGGGG CTGTGGTGAC 960
GTTAACCCAG GGCAGAGGTC CTTCTTCTTC CTCACTAAAT CATGGAAAGA TAATTTTTTT 1020
GTTGTTGTTG TTTGTTTTGA GACAGTGTTT CGCTCTTGTT GCCCAGGCTG AAGTGCAATG 1080
GTGCGATCTT GGCTCACTGC AACCTCCACC TCCCGGATTC AAGCGATTCT CCTGCCTCAG 1140
CCTCCCAAGT AGCTGGGATT ACAGGCATGT GCCACTATGC CCATCTCATT TTGTATTTTT 1200
GGTAGAGACC GGGTTTCTCC ATGTTGGTCA GGCTGTTCTT GAACTCCCGA CCTCCGGTGA 1260
TCTGTCCGCT TCGGCCTCCC AAAGTGTTGG GATTACAGGT GTGAGCCACT GCACCTGGCT 1320
GATAATGTAT TATTTTAACT CACACCTGGA AACAGGCACT GCTTTTGCTG ATAGAGCCAT 1380
GAGCTAATTT AAAGTCCTAC TTTTGCAGGG TGGAGAGGGG ATTTCTCAAG GTCACATGCC 1440
AGTGAGGGAA GAATCAAGGT CCCTGGCCTG TGTGTGCACC TCCCACAGTA CCCTGGGCAG 1500
GGGCTAGGGA GAGTTGTCCT CTGGATCCTG TCTGCTCTGT GACTTAGAAC AACTCTGCCC 1560
CCTCTCTGGG CCTCTTTCCT CAGTCCCTCC TTGAGTCAGG GCTTGGGAAT GGGGTGAAGT 1620
GGGGAGGATG CTTCCTTCCA CAGGAATCTG GGAGGGTCAG GTGCACTGCT CTGATAGGCT 1680
GAGGCTTGGG GCCCTTATGG GATCCTCCCT CATCAGCCCT TCTCCCTGGA TACCAAACTT 1740
TTTGGCTGGT TTCTCGGCTA ACAGCAAGGC TTTCCTGAAC CCTTTCTTAG CTGGGGAAGG 1800
GAGGTTCAGG AGGGAGTCTC AGAGCCTCTG ACAAAGTTAG GGAACCCCAG GGAAGTAATG 1860
AAGGGGGCAA TGCCATCCTC TGGTCTTTCC AAACAGGGAA CACCTTCCAA AGCCACTTGG 1920
GTCATTTGGG GTCTAGAGGC TTAGAGAGGA CAGGACATCT TGGAAAGAGC TGAGCTCAGG 1980