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

TagContent
EnhancerAtlas ID
HS182-13931 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr20:43243420-43246170 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr20:43245418-43245432GGCCACGCCCACTC+7.19
Klf12MA0742.1chr20:43245418-43245433GGCCACGCCCACTCC+6.25
RELAMA0107.1chr20:43244206-43244216GGGAATTTCC+6.02
SP1MA0079.4chr20:43245416-43245431CGGGCCACGCCCACT+6.02
SP3MA0746.2chr20:43245418-43245431GGCCACGCCCACT+6.92
SP4MA0685.1chr20:43245416-43245433CGGGCCACGCCCACTCC+6.28
SP8MA0747.1chr20:43245419-43245431GCCACGCCCACT+7.22
TFAP2CMA0524.2chr20:43243829-43243841TGCCCTGGGGCA+6.44
TFAP2CMA0524.2chr20:43243829-43243841TGCCCTGGGGCA-7.22
ZNF263MA0528.1chr20:43244769-43244790TGCTTCTCCCCTCCCTCCCCT-6.2
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_00279chr20:43242343-43246269Adipose_Nuclei
SE_01271chr20:43244070-43245098Adrenal_Gland
SE_01849chr20:43241967-43245916Aorta
SE_03744chr20:43242191-43246486Brain_Angular_Gyrus
SE_04325chr20:43241985-43249405Brain_Anterior_Caudate
SE_05260chr20:43240623-43249747Brain_Cingulate_Gyrus
SE_05994chr20:43240850-43251946Brain_Hippocampus_Middle
SE_07387chr20:43240502-43249639Brain_Hippocampus_Middle_150
SE_08237chr20:43241683-43249633Brain_Inferior_Temporal_Lobe
SE_10988chr20:43236447-43252402CD20
SE_25405chr20:43241977-43245373DND41
SE_40873chr20:43242209-43246478Left_Ventricle
SE_42448chr20:43242079-43246286Lung
SE_48409chr20:43242859-43246238Psoas_Muscle
SE_48778chr20:43242182-43246514Right_Atrium
SE_51576chr20:43243305-43246070Skeletal_Muscle
SE_54142chr20:43243411-43245157Spleen
SE_54929chr20:43242304-43245486Stomach_Smooth_Muscle
SE_58424chr20:43199983-43247676Ly1
SE_60908chr20:43204757-43248014DHL6
SE_61654chr20:43199842-43247312Toledo
SE_62478chr20:43204535-43247707Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr204324458843245603
chr204324495643245554
Number: 1             
IDChromosomeStartEnd
GH20I044613chr204324233843245708
Enhancer Sequence
TCCTAGACTG CCCATACTTT CTTAGAGAAG AAACCACATT TAAGTCAGGC CTGCCCCATG 60
GTCAGTGGCA GAGTCCAGCA ATCTCTAGGT TGGAAGATGT TTGAGTCTCA GGCCCCAAGG 120
ACTCCTCTGG ACAGGCATCC GGGACTCTTC CTGTCCCCCT GCCCCCTAGC CCAGGTCCCT 180
CCACTTCTCG CTATCCCCAC AGCTATACCT GGCTCTGGCC ACTCACAGCT CTCACCTGGC 240
TGACTTTAGC GGCCGGCTTC CCTGGGCTCC CTACACCCAT CTCCGCCCTT CCTGTTCAGC 300
TCTATGCAGC AGCCAGCAGA CCCCATTTAA ACCATTCTGT CCATCATGCT TCTGCCAAAA 360
AAAAAAAATC CCCCAGTGGC TTCACTGAGT GAAGCTAAGC TTGTCACATT GCCCTGGGGC 420
AGTCCTGCTG TAGGCCGGGC CCTGCCCAAG TCTCACCCGG TGCCACTCCT CTCCCTGACA 480
CCCTCCAGCT ACATCTACCT TTGGTCTGTT TCTCAGTCAA GCCTCTCCAA GGGGCCTTCT 540
CTGAGTGCTA GATCAGCCTT CCCCAATCAC ATGACCCTCA TCACTCTCTG ACAAGGTCTC 600
AGGGGTCTAA ATGTGAGCGC CGGGAGGGCA GAGGCCTTGC ATTCTGTTTG GCACACAGCA 660
GGTGCTTGGT AACCACAGAC CGAATGACAA AAGGAAACAG CATCCACCCA CCCAAGTCCT 720
GGCTGGAACA CCCCCACCCC CTCCATTCCC CCAGAGAACC CCTTGGCTCA AGTCCACAGT 780
CAGCCTGGGA ATTTCCTTGG GAAGCTTCCC TGACCCCTGC ACGGCTGAGG CCTTTCCCTC 840
CTGCTCTCAC AGCGCCACAG AGGCCGTGTG TGCTTCTCAC AGCACAGCCA TCAGGCTGCA 900
ACTGTCTCCC CGTGGGCTGT CCGGAGGGCC ACAGCCCTGC CCCTCCCTGG GTAGCCCTAG 960
TCTTCTTGCC CCTCACTGGC CAGAAGTGAA TCAAAAGTAC AGAACAGAGA AGACTTTGCC 1020
GGGGCTTGGA CCCAGCCCTC TCATGTTACA GATGGACAAA CTGAGGCCCA GAGAAGTTGG 1080
AGGACTTGCT CTGGGCCACC CAGGGAGTTA ACATAGAATC TGGCCGGCTT GAGAGAGAGC 1140
CCCCAGCACC CTGTCGACGG AACCCCACCC CAAAAGCCTT CCCTGTCCCA TAATCTATTC 1200
ATTCTCCTCT GTCACGTGGC CCAGGCAGAA CCTCCACAGG CTCACCCTGC TCGCCTCTCC 1260
AGCATCAACT CTCATCCTCT CGCCAGCCAT AGTCAAGTAC TTTGATCGCT CAGAAGCCCC 1320
TGTGGGCCTT CACACGCTGC ACCTCTGTTT GCTTCTCCCC TCCCTCCCCT TGCCTGGCTG 1380
GGTTCTCTTC ATTCTTAGAG ACCCAGGCAT CTGCTCAGCT GAGAAGCCTT CCCTGACCGC 1440
AGTACCCCTC CCAGACCGGG GAGGCACCTC TTCTCCCTGC TGCCTCCATG AGCCCACTGA 1500
GCATAATGGC CCTGCTCTAG ACTGAGCTTC TCCAGCACAG GCTCTGTGTC TTGTGCCCTC 1560
GGTGCCTGGT GGTGTTTGGC ACATGATGGA GGTACCGAGT CAATGGCTGT TCATTGACCG 1620
ACTGAATGAC CAGCATGTCC AGCTGCCACA CTGGGCACGC TGCCCTGGGC TCTCTCTCAA 1680
GGCTTCTGTG TCCTCACCCT CAGCTCTGGT GAGCTCTGTT CTGTCTCTCT CTCCCTCAGC 1740
AGTTGTAGCT GCTGGCCCAT GTGCCCAGGC TCTCCTAACA CCTGTTTTCC CTGACTCAGA 1800
TTCCCTAAAG TATGGGTCCT CTGGCTACAT GACATTCACC TGCCAGGGTG ACTGACATTT 1860
AAAAAGGGGG CCTGAGGAAA GAACAGTGCT CACTGAAGGA AAGGAAACAC TCACGGTGGC 1920
GTCCAGGCAA GAGTGACTGG CCAAGGAGCC TTCCAGGAAG CCCGCAGGGA GCAGTTCCGT 1980
TTCACAGGCG GGGCTGCGGG CCACGCCCAC TCCAGCGACT CCCCAAGGCA GGGGGAGTAC 2040
AGAGTTCCAG GCGCCACCCC GCTGGGAATA AAAGCAGGCT TTCCAGGCAG CGGGCTCGGA 2100
ATAGGGTCCC GAGCTACCAC CCACTTCCTA GCTTGCCGCA GGGGCACAGT GAGGCAGTGC 2160
TGATGTCAGG CCTCTATAAA CCTTCAGGAA TGCTGCTTAT TGGAGGAGGT TAAATTTGGT 2220
AGAAGGGGTA CTAGCCTTGG TGGCAGGCAG GGCTCTCCAC CCTTGATCCA GGCAAATCAG 2280
CTCACCTCGC TGGGCCTCGG TTTTCTCATG CATATCATGA CCCTAGTTAC ACCTCCATGT 2340
TACTGTGTGC ATTGCACGAG AAAGTGCCCA TCCATCTGCA GACCCTGGAG CTTGCTATAG 2400
GGTGGTGATT CTCCTGGTTC TGTGAAGGGC TTAGCCTGAA GGATAAAAAG GTGTGGTCTG 2460
GTTGGGCTGG ATTTGAACTC AGGCCCTCAG TGAGCTTGTA GGGCACCTAG TAACATTGCA 2520
CAGTGTCACT GGGGTTTAAG AATGTACCAC CTATTGAGCT CTGCCCACAT GCCAGGCCCC 2580
ACGTGGTGCA CCTTATGAAA AGACACCTGT TTATCATGCA GCCTGAGGAG GAAAGCATGG 2640
AGACTGGGGC CTGGGTGTGA GTTTGGCACT CCCCTCAACC TGCACTGCTG GTCCAGTGGG 2700
TGGCAGGAGC TGCCTGTCCC ACCTTGCACA GGGGGGCTCA AGGGAAGCTG 2750