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

TagContent
EnhancerAtlas ID
HS191-38612 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr9:38018560-38021330 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4878737chr938020544hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:38020089-38020107GGAAGGAGGGAAGGACTT+6.33
MEF2CMA0497.1chr9:38020234-38020249GGCTATTTTTGGTAC-6.28
MyogMA0500.1chr9:38019484-38019495CTGCAGCTGTT-6.02
Tcf12MA0521.1chr9:38019484-38019495CTGCAGCTGTT-6.62
ZfxMA0146.2chr9:38021094-38021108GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00446chr9:38016624-38019194Adipose_Nuclei
SE_01843chr9:38018555-38019965Aorta
SE_02310chr9:38015828-38020539Astrocytes
SE_03893chr9:38015988-38020718Brain_Anterior_Caudate
SE_04803chr9:38015709-38020845Brain_Cingulate_Gyrus
SE_05785chr9:38015646-38020684Brain_Hippocampus_Middle
SE_06784chr9:38015807-38020377Brain_Hippocampus_Middle_150
SE_07767chr9:38015675-38020809Brain_Inferior_Temporal_Lobe
SE_26555chr9:38018516-38019701Esophagus
SE_26555chr9:38020251-38021183Esophagus
SE_27864chr9:38018395-38020013Fetal_Intestine
SE_28791chr9:38018036-38021048Fetal_Intestine_Large
SE_31580chr9:38018069-38019901Gastric
SE_33929chr9:38016211-38021311HCC1954
SE_34811chr9:38019880-38021080HeLa
SE_38030chr9:38016459-38020860HUVEC
SE_38998chr9:38015698-38021143IMR90
SE_40993chr9:38018585-38019719Left_Ventricle
SE_41666chr9:38018522-38019979LNCaP
SE_41666chr9:38020029-38021146LNCaP
SE_42283chr9:38018623-38020033Lung
SE_44329chr9:38018392-38019871NHDF-Ad
SE_44779chr9:38018343-38019940NHLF
SE_45758chr9:38015670-38020868Osteoblasts
SE_47196chr9:38016020-38021300Panc1
SE_47459chr9:38018602-38019666Pancreas
SE_48861chr9:38018605-38019837Right_Atrium
SE_51847chr9:38018333-38020537Skeletal_Muscle_Myoblast
SE_55662chr9:38015908-38020711u87
SE_57367chr9:38018604-38019070VACO_503
SE_57367chr9:38019217-38019687VACO_503
SE_63571chr9:38018333-38020316HSMM
SE_65279chr9:38018566-38019885Pancreatic_islets
SE_67542chr9:38015908-38020711u87
SE_69063chr9:38018583-38019783H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr93801856238021000
chr93802112438021174
chr93802080238021011
Number: 1             
IDChromosomeStartEnd
GH09I038014chr93801466738021190
Enhancer Sequence
AAAATGTATA TTTAATCAAT TTGCTTTTGA ACTTCAAAGT GAGGTTGGTG GAGGGAAAGA 60
AATTTGAGGT TTGAGCAACC TGAAACTTTG CAAACACTAC ACTGAACTGT CTGATCTTTT 120
GCAAAATGAT GTCCTAGTTT TGGGAATAAA AATTCAACCA GGTGTTAGGA GAGTTGAGCA 180
GGCAGTCAAC CAGAGTGCCC TGTGAAGTAC CATGGGCCCC AGCCATCAGG ACTGGGCAGT 240
GTGACCACTG TCCAAGCTGC CTGGGGCTCA CCGCCAGTCC AGATGGCCAT GCAGAAGGTT 300
TGTGTGAAGC GTGCTGCTTT TTTGAGCTAA AAGAAAGAGA ATGAGTTTTC TCCAGATGTG 360
AGATTGGATT TCTGACGGGA TTGCTTTTGC TTTGCTTTAA AACTTCCCAG TTAGTGGACA 420
ACTCCTGTAT ATCTAATTGA ACAATTCAAC CAAAAGGGAG CCAGCCGGGA CTCCTCTGCA 480
GGCCAGGCCA CCTGGGTCCA CAAGAAGCTT TCCTTTTAGT CTCAGATTGG CAGAGACCTG 540
GCAGCCACAG AGGCAGAGCT GAGCAGTAGC AGAAAAAAAG GCTGTAGAGT GCGGCTGCTT 600
AGTCAGTGAG CCACGTCATC TTTTGTTTGC TCGGCCTCTT GGGATGAGTG CTAAACCCCA 660
GGCAAGCACC TTTCTTGCTT TCAGACAAAA CTACAGACCC CAGGTCAGCC CAAAGCCCCT 720
ACAGGGCTTC CACAGGTTTG TCCTCCTGGA GACCTGCTCT GACCTCCCCT TGTTTTCCAC 780
AGGGCCCACT GCAGGGCGTT GTCAGTCACC TAGCAAACCA GCAGTGGCCT GGGGATGGCC 840
TCTCCATGCC TCCTCTCTGG AACGCACACT GCTGGGGCCC CTGTGTTTTT ATCTTAGAAA 900
CTTCACTTTG TGATAGGAAG TAGTCTGCAG CTGTTCATCC CAAAGGAAAG GACTAGAGGA 960
AGGTGGGTGT TGCCCCTTGG CCACACTTCC CTATGGACTG GTCAGAGTTT TAGTTGCTTT 1020
TGTGGGACAG CTGCACTTGT GAGCAGAATT GGGTCCTCTC CACATGCTTT CAGTGGAAAT 1080
GCACTTGGGT GGAGACACTT ACAAGGGTAA CTTTGGGCAG AATCCATTAA AATCCCCAAA 1140
TGCGCCAAGT TTGACCCAGC AATTTTACTT CTCAGTATTT ATTCCCAAAT GTGCATAAGG 1200
GTCCATGGGA AGGATGCTGC CTGAAGTAAT CATGAGAAAC CACCCGAAAC TACTGCATCC 1260
ATCAATAGAG GAATCGCTAA ATAAACTGTG CTAGTTCCAT ACGATGTAAC ATTATGCAGC 1320
AGGCTGAAAA AAAAAATTTA AAAAAAGCAG TTGCTCTGTG TGAGCTGGCA CAGCACTCCA 1380
TGACATAGCT CTGAATGGAA AGCAAGCAAG CTGTAGAATG ATAACTACAA CATCATACCT 1440
ACTTAATGAA AAACAAAACA GAAACCTGTA TCTCTATTAA GTTAAAGAAA GGGTCTGGGA 1500
GATGCACACT CCAAACTGAC CCCTCTTTGG GAAGGAGGGA AGGACTTGGA ATGGGGTGCT 1560
TAGGGGAAGT CAAAAGAGAC CTTCTCTGCA ATGTTAAAAC ATTTTCAAAC AAGGAGAACC 1620
TATTCATGTA CTATGTGCAA AACTAAACTT GCTTAAAAGC ACTCCTCTTC CACAGGCTAT 1680
TTTTGGTACA GTAGACAGAA TGTTTCCCAA ACTTGCCTGA AGACAGGAAT GGCTTGGAAC 1740
GCTTGTTAAG GAAACAGATT CCTAGCCCCA ATAATCTGTA TTTTAACAAG CAAGCCAGGT 1800
GATCCTTATC AGGAAAGCTT GGGAAACAAT AAGCTAGAGC CAGCACCCTT CCCCACCAGT 1860
CTAGAGACAA GCCTCCAGAT ATTACTCTGG AATTGTACTT TTCCCAGGTA TTGCTCAGCC 1920
CTGTTCGTTG AAGTGAAGCA AGAAGTTTGT GCTAACATGC AGCTCTTTTG TTTTCTTCCC 1980
TGGTGGTCAA CTGGAGAAAA AGAGGACCCG ACGTGCCATC TCCAGGATCT AAGACATGGA 2040
GGAAATGGTA ACCCCTCTGC AATCATGTGG GCTGGCTCCA GATTGAGCAA TTCGGCCTGT 2100
GCAGGGGGAG AGGGCTACCA AAATCTCACA AATCACCACT AAAGAACTTA GTCATGTAAC 2160
CAAACACCAC CTGTTCTCCA ATAACCTATG AAAATAAAAA TTTAAATAAA TTTAAAAAAA 2220
GACTTCTGCC CTGTCACCAC CCTGAAAGTG ACGGGGTGGG GGGGTGGCCC AACAGGGATC 2280
CTAGCCCCGA GGATCTTGCA AGGCAAGGCT TTCTGTTTGA AACCCACAGC AGCTTTCAGG 2340
CCAAGGCCAA TTTACTCTCA GCAAACTCGT TCTAGGAAGA TCACCCGGCT ACAGGAAGGG 2400
CTGGTGGCAC TTCAGAAGAG GAGCCACTGC AGAAATGCAA AGGGAATCTC TGCTGAAATT 2460
GCTCAAACCT GCTAAAAAGA ATGATGAGGC ATGTCCGGGC TTAGTGGCTC ACATCTGTAA 2520
TCCCAGCATT TTGGGAGGCC GAGGCGGGCG GATTACCTGA GGTCAGCAGT TCGAGACCAG 2580
CCCGACCAAC GTGGAGAAAC CCAGTCTCTC CTAAAAACAC AAAAAAATTA GCTGGGCCTG 2640
GTGGTGCATG CCTGTAATCC CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CACTTGAACC 2700
CGGGAGGTGG AGGTTGTGGT GAGCCGAGAT CGCGCCATTG CACTCCAGCC TGGGCAGTAA 2760
GAGCGAAACT 2770