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

TagContent
EnhancerAtlas ID
HS059-07801 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr11:44580510-44582140 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs77796218chr1144580581hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr11:44581100-44581121AAATGGAAACAGAAAGTGTGG-6.36
RFX1MA0509.2chr11:44580788-44580804AGTTGCTATGGCAACA+6.78
RFX1MA0509.2chr11:44580788-44580804AGTTGCTATGGCAACA-6.78
RFX2MA0600.2chr11:44580788-44580804AGTTGCTATGGCAACA-7.13
RFX2MA0600.2chr11:44580788-44580804AGTTGCTATGGCAACA+7.15
RFX5MA0510.2chr11:44580788-44580804AGTTGCTATGGCAACA+7.38
RFX5MA0510.2chr11:44580788-44580804AGTTGCTATGGCAACA-7.42
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_10955chr11:44576513-44583494CD20
SE_18725chr11:44580645-44581856CD4p_CD25-_Il17-_PMAstim_Th
SE_25709chr11:44580490-44581799DND41
SE_62566chr11:44577989-44637584Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr114458075844581672
chr114458121544581415
chr114458058344582000
Number: 1             
IDChromosomeStartEnd
GH11I044559chr114458072844582208
Enhancer Sequence
CAAATGACAT ATATTGGGAT GTATATAACC CTACCATGGG TTTAAGCTGA TGCCTAAAAA 60
GAAAAATAAA CGGGTAGAAC AGGGAATTTG GGGAGGGGGG GACATGATTT AATAGTTTCA 120
AAGACTTACC CAAGTGCCAC AGTTGTAAGA TAAATATAAA TAAGCTTTAG AATATGTAAA 180
GTGCTACGCA AATGCTAGTT ATCAAATTAG TTAAATATAT TTAAATTAGT TATTTTACAG 240
CTTACTTTTA AAACGGTGGC TGCCATTATT AGTGTCGTAG TTGCTATGGC AACATGGCAA 300
TGTACAGGGG CTAAAAGCCC CCTGAAGAGT AACCCCTGGA CCTTCAGATG TAGTAGGCGG 360
CAGGGCAGGA TTTGAGCAGG GGCCTCACTG ATCTTTCTGA AATGACTGAG ACAGGAACAA 420
ATCAATGGCT CAGTGTCTTC TGTGGGAACT CAGCCCCTGT CCTCAGCTAC AACCCAGCTA 480
TAATGGGCTT AGAGTTCCAA TCCCCTTTAA GTGCTTTGGA GAAAAAAATA AAGGTCGGTG 540
GTCCTGCTGA GCCCATTCAA ATGCAGGAAT GACTGTGTTC AGGAATAGAG AAATGGAAAC 600
AGAAAGTGTG GGAAAGTGCT ATTAACCACT TCCTGGCCTG AGACTCGGCA AGAGGACAGA 660
GGATAGGGCG GGGTTATGCC AAGCAAGTGC TGGAGCCCAG CTTTCTGGGG CCAGCCTTCT 720
TTCTGTAAGC AGGAAGCAGG GTCCCTTCAA GGCCCTGGGG AACCTCCTTG ATCCAGTGCG 780
AGCTTTTGCG ATTCAGTGTT GGGCGCTCAC TGGGTCCCAA CTTGGGCCTT TCCCCTAGGG 840
CTCAATTTCA GGAACTGAAA ATTGGGTTAG CTATATATAA GCTGCAACTT CACTTTCCTC 900
CATCACTTGT TAGTTGTATG ACTTTAGCAT CTGAGTGCTC CATTTCCACA TCTTGGGAAT 960
GGGCCTCATA ATAGTATGTG CCTCACTGGG TTGTTGCTAT CAGGATTAAA TGAGTGCAAT 1020
TTTTAAGTTT GTAACTTTAA GGAAACAGTG CAGGTTTAGG GAGGGAAGTG CTAACTCTAT 1080
TCTGAGGACT CTTGAAGAAA GATCTTAAGA CATCCACTTA CTAGGCCAGG CGCGGTGGCT 1140
CACGCCTGTA ATCCCAGGAT TATGGGAGGC CGAGGTGGGT GGATCACGAG GTCAGGAGAT 1200
CGAGGTCATC CTGGCTAACA TGGTGAAACC CAGTCTTTAC TAAAAACACA AAAAAATTAG 1260
CTGGGCGTGG TGGCACACAC CTGTAGTTCC AGCTACTCAC AAGGCTGAGG CAGGAGAATC 1320
ACTTGAACCT GGGAGGCAGA GGTTGCAGTG AGCCGAGGTC GCACGACCAC ACTCCAGCCT 1380
GAGCAACAGA GTGAGACTCC ATCTAAAAAA AAAACAAAAA AAAGACATCC AGCTACTCAA 1440
GACCAGTTGT CCACTGCTGA ACTTCTTATT CATTTGTGCA CAAATGCTTG TGTGATACAT 1500
ACTGTATACC ATTTTTTAAA ACAATCAATT GAGTTTGAAC TCTCAGCTCC CATCAGAGAA 1560
ACCCTCCTCC AGTCATTCTG AGGACTCGCT TGGGGCAGAT TGTATTTTTC ACAGATGGCT 1620
GCAACAATAT 1630