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

TagContent
EnhancerAtlas ID
HS105-21156 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr12:125229300-125232640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11057793chr12125230287hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr12:125230278-125230296AGAATGAATGAAGGAAGG+6.56
EWSR1-FLI1MA0149.1chr12:125230290-125230308GGAAGGAAGGAATGACAG+6.96
EWSR1-FLI1MA0149.1chr12:125230282-125230300TGAATGAAGGAAGGAAGG+7.69
EWSR1-FLI1MA0149.1chr12:125230286-125230304TGAAGGAAGGAAGGAATG+8.2
GLI2MA0734.2chr12:125232542-125232557GGACCACACACTTCG+6.17
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_00859chr12:125228424-125232056Adrenal_Gland
SE_03938chr12:125228436-125232323Brain_Anterior_Caudate
SE_05231chr12:125226828-125232740Brain_Cingulate_Gyrus
SE_05839chr12:125221607-125233847Brain_Hippocampus_Middle
SE_07622chr12:125226704-125231650Brain_Hippocampus_Middle_150
SE_08157chr12:125228062-125232528Brain_Inferior_Temporal_Lobe
SE_09272chr12:125229706-125233190CD14
SE_26949chr12:125225146-125232662Esophagus
SE_29720chr12:125229758-125231460Fetal_Muscle
SE_32333chr12:125228235-125232144Gastric
SE_33494chr12:125228482-125231266H2171
SE_38622chr12:125229570-125231990HUVEC
SE_42285chr12:125229246-125232185Lung
SE_47311chr12:125218497-125233711Panc1
SE_47856chr12:125230228-125232093Pancreas
SE_47856chr12:125232192-125232641Pancreas
SE_48725chr12:125229544-125232344Right_Atrium
SE_49850chr12:125229177-125232684RPMI-8402
SE_53614chr12:125229548-125231831Spleen
SE_54773chr12:125224509-125232672Stomach_Smooth_Muscle
SE_65686chr12:125230166-125232109Pancreatic_islets
SE_65686chr12:125232245-125232927Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12125229309125231390
chr12125230587125231048
chr12125231951125232267
Number: 1             
IDChromosomeStartEnd
GH12I124737chr12125221960125232737
Enhancer Sequence
TATTCTCAGG CAGGCTCTCC CGTCCTAAGG TAAGAATCTC ACTGATACCC GACTACATCA 60
TGTGACCCTC CTTTGGACCA ATGACTGCTG TCAGAGGATG GGATGACCTG ATTGGCCAAG 120
CCTTGGTCAT GTGCTCCTCC AGGAGCCAGG GAGGCGGGGT CAGCCCCACC TGAACTACAG 180
ATGATGAGAG AAAAGAAGAA AGCTGTTTTC CTCAACGAGA TCCGGGGCGC CATTACCAGG 240
AGGAACAGAT GCTGAGTTGG TAAAAGCAAC AGCTGTCCCC AACAGAAGCA AACTCCTATT 300
TCCCAGGCCC CTTGGCTAAG TCTCACCACC ACCCATTTTA CAGCTGAGTA AACTGAGGTC 360
TTGGAGGTGA AGTCAGTCTC CTTCTTTGGT GATGCAGTCG GCACCCCAGT CCCAATCTAG 420
GTCTGATTCA TGCTCAGGCT GTTCACATTG ACCAGCGTGC ATCTCTAATC CTGCCCTCCA 480
AGAAGCCTGC ACACAGTTGG TGTGCAATAA ATGCACAGCA CATCAAATTG TTGTTAAGAG 540
TCTGCCCCTG CCCACTGGAC CATAAGATGC CTGAGGGCAG AGACCATGTC TGTCCTGTTC 600
ACTGTGGCAC CCCAACACCC AGAGCGTAGT AGGTGCCCCC CCCAACGCTT GGTAAATGAA 660
TGAATGACTC CCTGGCGTAT AGTACGCGCT CCACAAATAC TGGACAAACA TGTATCTCTG 720
TGGATGCTCC ACAAATACCT GCTAAGTGAA TGCAAGTCTG TCTAGGGCCT CACGCACAGT 780
AGGTACTCCA CAAACAGTGG TAAATGAACA GATTCTTAGT GCCTGCACAT AGTGGGTGCT 840
TAGTAAATAT TTAGTGAATC AATGAGTGGA TCTCGATGGG AACCAAGCTG CCTGGATGCT 900
CAAATATTTC CAGATCATTA ACAAGATAGA GAGAGGAGAG AGATTAGGGG GCTGGTGGGG 960
GAGGAATGAA TGAGTGAAAG AATGAATGAA GGAAGGAAGG AATGACAGAA ACCTTTGCTG 1020
GACTTTAGTG CTCAGACAAG GATCCACAGT CCTTGCGGCT CCACAGCGAG AATCAAGGCT 1080
GCCTGGAAGG AAGACCCAGT TTTGGAAAGG GCGCTGGGTC TTTGTGAGCT AGGAGAGGGG 1140
GCGGCGGGGC TGGCAGCAGA GTCAGGAGGA AGGGAGGTCA GCCAGGGCGG GCGAGCAACG 1200
GGGCCGTGCC AGGGACACCG CGCCCCGGGC AGGGCCTGCT CCCCCTGCCC CGACCTTGCC 1260
TCCCGTTCCA CAATAGAGCA TCCATTGTAA GTGGGTAATT GGGTTCCGGC ACATCCCCTC 1320
CCCCGGCTGG GGGTGGAAGC AAAGGGAAAC ACAATCTGTT TTCTATTTGT CACGGCTGCC 1380
AAGACGCCAC TCCCTCCCCC AGCCTCCGCT CTGGCTGGCC CGCTGAGCCA CAGCCGCTGC 1440
GACATTCCTT GGCCTGGGCT GAGCCTGCAT TCAGAGCTGC CCACCCCCGC TGGCTGACCC 1500
AAGAGAAACC ACGTGACAGA GACCCAGAAT CAGCCTCAGG GGCCTCCTGG CCTCGTTCCC 1560
CAGCCTCCCC CATGGGAAGC CAAAACCACA GCCCTCGCTG GAGGCTTTCC ACCCCAAGGA 1620
GGACTCACAT CCTGGCTCCC TCTCTTTTTA GCTGTGTGAC CTTGAGCCAG TCACTCAGCC 1680
TCTCTGTGCC TGTTTCCTTC TCTAAAATGG GGAGGATAGT AATGATAGAG AGGCCCTCTT 1740
GCGTGTTAAA CATACTCCTC CAGGCAGAGT GCAGAGCACA TAGAAAGGGT TTGGTCGCTG 1800
TTAGCTGTCA TTTGATTTAT TCTTTTAGGG AGTGAGTGGG ACCTTCCTGG TTTCAGTGTA 1860
ATTCGCAGAG TTGGGTGTCT CTGTTCCCGA ACAATTTGAA GTGGGGGAGA CAAGGGTAAA 1920
TGCTCAGGGG GCCCCATGCC TGAGCCGCAG GCTGCCTCAC TGCACTGCCC ACTCACACGC 1980
AAAGGGCCTG TTGGATGCCT CATGTGCGCC CAGCTCACAC TGACCTGACA GGAGAGGATC 2040
AGAGAGGTGA GAGGAGGAAC ATACAGAAAA GTCAAAGGTC TGAGCTCTGC CTATGAGGGG 2100
CTGGCGACCC GTAGTGTTGG GTTAGAAAGC AAACAGGCTC TGCTGACATG TCCCTAAGCC 2160
CCTGAGTTCT GTGGGAGTTG GGGAACTGCA GCAGGCTTGG AGGACTTCCT GGAGGAGGGG 2220
AGCCAGGTTT GAATCCTGCC TCTGCTGTGG GTCTTGGGCA ATGTCTTCAC CGCTCTGGAC 2280
TTTGTGATTT CATCTTTTGG GGACTTCTTC AAGAAAAAGA ACAGCACAAG TCAGCCAGGC 2340
CTTTAACAGG TAAGGTTAGG GCAATTTCAG AAGAAACCAA GACACCTTGA ACTTGGCTTT 2400
CGTTGTTGGA TGAAATCCCG GGGTGGCCTT GACTTGGATG TTCAGAGTAA TCCTGCTTCA 2460
GCCCCGCAAA GGGCCTGTGT GGACAGATGT GCACCTGGGG CTCCAACCCC AAGCCCCTCC 2520
ACACCTTGGG CAATCACTGA ACCTCCCAGA CTCAGTCTCC ACATCTGTAA AAGGGGACTT 2580
CAGAGGCACC AGCGTGAGAG CTTAAGCTAA CAGACTTGGC ACACAGCAAC TGTTCAATAG 2640
ATCTTAGCAA CTACCCCTAA TTCCCAGAGG CAGAGGCGTC TGAGAAAAGC GGAGGCAACA 2700
GACAGCAGAG GCCACAGCTT ATTTGTGGAC AGCAGCGGGG CCCTCACTCC CCTCTTGATG 2760
AATAAACCTG CACATGGTAG TAATGGTCCA CATGAGTTCT TTCATGACCT CAGGTGCATA 2820
AAATCGGATT AATCATTGTC TTGTGACTCA CTCCCATGGT TGGTGAAGCC TGACCTGTTT 2880
TGTTTTATGG GTTTATTTCT TCATTTCTTT TTGTGGTTTT GAATTTGTTT CACAATATAA 2940
TGGACACTCA TGAAGCTACC CCCAATGCAA GAACAGAACA TAGGCAGGGA CACATCTGCC 3000
CCCAGACTCT CCCCAGAAGT AAGCCCCACT CCTCGATTTA AATAAACACG TATTTTGTCC 3060
TCACTGTGGG CTTTGGGCAT GAGCATGTTT GTGCCTAAAC CGGTGCTTCT CACACGACAG 3120
TGTGCTCAGT CACTTGGGAG ACTGTGGCCC AGCCCAGAGC ATCCAACTCA ACAAGTCTGG 3180
AGGAGAGCCC GAGAATGTGC ATTGCCAACA CGTTTCCAGG AGCTTTTGCT GCTGCAGCTC 3240
TGGGACCACA CACTTCGAGA AGCTCACCCT AAAGAATGTA TTATCAGGCC GGGCGAGGTG 3300
GCTCACACCT GTAATCCCAA CTCTGTGGGA GGCCAAGGCG 3340