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

TagContent
EnhancerAtlas ID
HS184-23531 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr5:1127490-1132530 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12517665chr51128736hg19
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HSF1MA0486.2chr5:1130320-1130333GAATCTTCCAGAA-6.09
HSF1MA0486.2chr5:1128622-1128635GAAGGTTCTAGAA-7.12
KLF14MA0740.1chr5:1128251-1128265GAGTGGGCGTGGCT-6.51
KLF16MA0741.1chr5:1130559-1130570GCCCCGCCCCC+6.02
KLF5MA0599.1chr5:1130559-1130569GCCCCGCCCC+6.02
NR2C2MA0504.1chr5:1130056-1130071GAGGGTCAGGGGTCA+6.47
RARA(var.2)MA0730.1chr5:1132257-1132274TGACCTCTGGTTGTCCT-6.62
RREB1MA0073.1chr5:1130883-1130903GGTGGGCGGGTGGTGGGAGG-6.07
SP1MA0079.4chr5:1128252-1128267AGTGGGCGTGGCTGG-6.32
SP1MA0079.4chr5:1130556-1130571AAAGCCCCGCCCCCA+6.51
SP2MA0516.2chr5:1130555-1130572GAAAGCCCCGCCCCCAC+6.39
SP3MA0746.2chr5:1128252-1128265AGTGGGCGTGGCT-6.54
SP4MA0685.1chr5:1130556-1130573AAAGCCCCGCCCCCACC+6.71
SP4MA0685.1chr5:1128250-1128267GGAGTGGGCGTGGCTGG-6.73
SP8MA0747.1chr5:1128252-1128264AGTGGGCGTGGC-7.22
SPI1MA0080.4chr5:1130129-1130143TGAAAGAGGAAGTT+6.03
STAT1MA0137.3chr5:1132428-1132439TTTCCTGGAAA-6.62
Stat4MA0518.1chr5:1132425-1132439CCCTTTCCTGGAAA-7.64
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_23448chr5:1127976-1132214Colon_Crypt_1
SE_23989chr5:1128079-1132174Colon_Crypt_2
SE_24840chr5:1128000-1128624Colon_Crypt_3
SE_24840chr5:1128652-1132261Colon_Crypt_3
SE_28283chr5:1129844-1132139Fetal_Intestine
SE_29290chr5:1129882-1132174Fetal_Intestine_Large
SE_31577chr5:1127256-1132504Gastric
SE_40750chr5:1126628-1130046Left_Ventricle
SE_41639chr5:1127884-1132182LNCaP
SE_42534chr5:1127296-1132332Lung
SE_47514chr5:1128007-1131783Pancreas
SE_48976chr5:1127774-1129305Right_Atrium
SE_49487chr5:1128081-1129127Right_Ventricle
SE_50482chr5:1127887-1132021Sigmoid_Colon
SE_52622chr5:1127966-1132104Small_Intestine
SE_53895chr5:1127979-1128693Spleen
SE_57916chr5:1128138-1128944VACO_9m
SE_57916chr5:1130439-1131776VACO_9m
SE_61441chr5:1092795-1176993Toledo
SE_65274chr5:1127036-1132318Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr511308001131471
chr511296001130521
Number: 2             
IDChromosomeStartEnd
GH05I001128chr511273441127787
GH05I001127chr511279661132045
Enhancer Sequence
GAGATGGAGG CAGAGGCTGA GGCGATGGGG CCACAGACCC AGGGATGCCT GGAGCCGCAG 60
AAGTTGGAAG GGGCAGGAAG GAGCCTCTTT TAGAGCCTCC GGAGGGCGTG CAGCCCTGCC 120
CACACCTGGA CTTCAGATTT CCTTTCTCCA CCACTGAGAA GGCAGATCTG TGAAGCCACA 180
GTGTGTGGTG ATCACAGCAG TCCGAGGAAA CTGATGGATA TACAAATACC ACAGATAACT 240
CTGTGATAAC GATCTTGTAA ATGGAGATAA AATAGACACA TTCTCCAAAA TCCATACAAA 300
AAGAAACAGA AGCTCTGAAT AGTACTATGT CTCATGAAGA AATTAAATCC TTGATTTAAC 360
TTTGCCCCCC TCCTGCACAT AAAACCTTCA GGGCCACACA GACTCACTGG TAAACTTTTC 420
CAAACACTGA AGGAAGAAAT AATACCAGTT ACATTGAAGT CTTTCAGAGA ATTTTAAAAA 480
AGAAGTAATT TTGCACATCT CCTGTTATCA AATTAGCACT TGTCATCAAG GAAGGGAAGA 540
TAAAGCACGA GGAGATGCCC ACACCCCAGG AAAGTGTCCC AAGAGTGGCT CAGATTCTCC 600
AGGGCTGCGA CGTCCTGGTT TTCATCTGGG GGTGGTGACA GGCGCGTGAT CTCTGGTTAT 660
TCCAGAAGCA GTGAATGTAG GATGTGTGTC ATTTAGCTTC TCACGCCATG CACTGGGGCA 720
AGTTCACTGA GGAAACAGAT CTCATCCTTA AGGCAGGCTG GGAGTGGGCG TGGCTGGGAG 780
GTGGGTGCCT GAGGAACACT CTCGCCCCTT CCCCTGCACC TGTGGTCTCA ACCTGGCGGG 840
AAGTCCGCTC CAGCTCCTGT GGGACCAGGG TTGCTGGATC CAAGTTGCCA GGTAAACTCC 900
CGCTGATCTG CAGCACAAGA GCCAAATCCC AGGACGAGCT CTCACGGAGC AGTCAGGCCC 960
AGTGGAAACT GGTGGCCTCG CTCCAGGAAA TGAAGCCAGA CTCAGACAAA CAAAAGCCAC 1020
CAGCAATGCA TGGAGGCAGG ATGGGACATC TCACGCGGAC CCAGTGACCC TGGAGCATGC 1080
CTGGGTACAG ATGGAGCCCC CAACAGGGGT TTCCTTCCTC ATGTGGTTGA TGGAAGGTTC 1140
TAGAATTCAT CTTCTCATAG GGAGGAAAAG TGCTGCCCAG CCCCCAACAC TCTGAGACCT 1200
CTGGGGCTCA GTAAATATTT GATAAACAAC AGGCTCAGCA GGTGCGGTGG CTAGTGAGAC 1260
TGGTACAGAC CAGGTGGCCC ATGGGTATTG GGTCTGCCCT GTGACCACCA GTCCTGACAG 1320
GCTGCAGCGG AGCATGTGTG CACGTGTGTG CATGTATGTG TGCGTGTGTG TGTGCATGCG 1380
TGCACACCAA TGGGAGTGGC CCCAAGTGCC TGCCTGGTCT CTACACGGCT TCCAGCCTTT 1440
TCCTAGAATG GATCACATGT TTGCATACAC ACATATGTGC ACACACATGC AGAAACCAGA 1500
CCCACTCCCA CCATCCACCC ACACAAGCTG GACCCTCAGT CACGCGGCTC CCTGCCACGT 1560
GCTCCATCCC CATGTGCGTC CAACACACCT GCCAGCTCTG CTTTCAGCTT TCCCTGATGG 1620
CCAAGCATAC CCCGCTGCCC CTGCAAGGCT TGGGAGCACT CCTGGGATCC CCTGCAAGGC 1680
TTGGGAGCAC CCCTGGGATC CCAAGTCTGA TGGCCTCTAG AAGTCCCTCT CCTCAAACCT 1740
CGGTCACAGC TGCTGCCTAG GGCCTGCCAG GCCAGGGGGA CAGCCACGTC TCTCCTAGAC 1800
ACACGAGGAC ACCCCTCCAA GAGGCCTCCC TCAGCCAGCC GCCACTGCTG CCGGCCCCTC 1860
TGTGCATCCC CAAGGGCTGA GCTGTTGCAG GGTACAACGC CTCCTGGCTC CAAGTGAAAG 1920
TCGGAGGTGG GCAGGACGTT CAGGTAACAC CCCCACCTCC GAAGTCCAGT CTCACAGAGC 1980
CTTAGCAGCC ACCCAAGGCA AGGAGGTGGC CATGGGCCAC CAGGAGTGTC CCGAGCATCC 2040
CAGGCCCACA AGGGCCAGAG AAAGTTCCGG GCTTCCCCTA GCGTAAGGGA CAGAACCAGG 2100
CGCCCTCCCC TCCTGGCCCC CTCAGCTTTC CTGTGACGCC CAGGACCAGG ACCAGGACCA 2160
GGGAAACCAC AGCGTCCCAG GCGACAGGGT GGAGGGCGGC TCCAGGAGCC CAGCTGGGGC 2220
ATCGGCCAAC CCCCGAGAGA CACACTTGCT CAGGCATCCC TGGCAAGGTT TCCAAAGCCC 2280
TCACGCGGAT GAACACGGGA ACACCTGGGG CACCCACTGT TTCACGGAAA AAGTCACAGG 2340
GGTCACCCTG ATGGGATGTA ATTTCTGGAT ATGATTAAAC AGGAAGAAAA GATCCCGGCT 2400
GAGATTACCG TTCAGAAGCA CCTTGGAGCC GGGCTCTCGA CACTGCTGAC CCGAAACCTG 2460
GTGATTCAAG AGGAAAAGAA CGCCCTGCTG CCGTCAGAGC TGGAAACTGC ACAGCCCATT 2520
GTGTCCTGGG CGTGAAGCCA TCACCTGACT CCCAGGTGAG GAGCCAGAGG GTCAGGGGTC 2580
AGAGCTCAAG GGACGCCCTG GCCAGCTGGG GCAGTCAAAG CTACCTCTGC TTCTTCCCCT 2640
GAAAGAGGAA GTTTAGATAC CCAAGAAGTT TTGATATCTC CTCCACGACT TTACTTCTGG 2700
ATGTGGTTCA GAAAAATCTG CGGAAAATCA CCCAGAATTG CACCCGTTTG GTTTACAGGA 2760
GTATTAGCTG TGGGGGCCCC TTTTCCACCA CCCCCATCAA GCAGCCTCCC GGGCAGCCCA 2820
GGACCCTCCA GAATCTTCCA GAAGCCGCAC CACTCGCTTC AGTCGTAACC TGCAGGACCC 2880
CACCGGGCGA GGCTGGCTGG GAGGAGGCAC TCTCAGGACA AGGGACCTGG GCAGGCACCT 2940
CCTGTCTCCG CTCAACACCC AGCGAGGACA GGAGGACCCA GGGTGCACCT GCATCTGCGT 3000
CTGGGCAGAG GAGCAAAGAC CTGGCCTTCC CAGAGCTTGA GCTGTGGGAG GAAGAGAGGC 3060
TGAATGAAAG CCCCGCCCCC ACCCCACCCC AGGAGAGGCC ACCTGGGGCC TCCCACAGCC 3120
CTGCCCACGG CTGCACACGC GTGTCCCCTC ACCTCCTTAG CCAGGGCGGC TGCCCGCGCA 3180
GGTCCCCTCA CCTCCTTAGC CAGGGCGGCT GCCCGCGCAG GTCCCCTCAC CTCCTTAGCC 3240
AGGGTGGGGG CAGCAGGGAG GGAGGGCGTG CTGCATTCTT CCCTGGGCCT GCAGGTGCAC 3300
CTGTGCCTGC CCAGAGGGAG CAGCGGGAGC TTCCAGCAGA CACACCTGGA CAGGTGCACA 3360
GAGCTCCTGC CAGGGAAACC CAGCACAGAC GCAGGTGGGC GGGTGGTGGG AGGGTGGCAG 3420
AAGCGGAAAG AGGAGGAGGC TGAGCTCAGC ACAGCCCATG CAGTCTCCTT CCGGCCAAGG 3480
GGAGCGGCTG GGCCAGTCTG AGCCGGGAGG CAGCTCAGGG AGTAAGCCCT GGGGACAACA 3540
TTGGAGTAGC ACAGGGTTCC CTGACAGAAC CTCACGTCGG AGGGTGGTCT GAGGGCTGCT 3600
GGGGGCCCAC CTAGGAGATG GGGTCCCAGG ACACAGAACA GGGAGGGGGT GGTGTTTCCA 3660
GGGTGAGGCC TGGGGGAGGG TAGCAAGGCC TGGACTAGGA GATGGAGGCC TAATCAAAGC 3720
AAAACAGAGA CTCAGAGCTC AGCGCCTGTA TTCGCAGGGA CACACAGGGA CTCACAGGGA 3780
CGTCCCGGAT CGCTAGGGGA CTCACGGGGA CACGTGGGGA CACGCTCGGA CTCACGGGGA 3840
CTTGCAGGGG CCCATGGGGA TGTGCAGGGA CACCGTCCCT CCCGGCCGTC CTGCTCCTTG 3900
CCAAGAGTCA CCCAGAGGCT GGGGCCTGGC ACCACTTGCA GACAGGGGCA TTCCTGGGCC 3960
CCTCCTTTTG GCACCTCAGC CTCAGCAGCT GCTGAAGGGT GTGGGGGAGG GAGCCGGTAT 4020
TGGTGCAACA GGCAGATGGT TCCAGAAACT CAGGATTCTA CACAATCCTA GCACCTGAGG 4080
CACAGTCCTG CACGGCCGCC ACGCTGTCGG AAGCAGGCAC CGGCCCTGGT GGTCAACACA 4140
AGCCCTGAGG ACCTCCCAGA GGGCATGCTC CGGGCAACCT GCCAGGACCA CCTCTCCTGC 4200
CTGGTGTTGG GGGCCTCACC TGACCTCTCC GGGTCCCTAA CCAGGCGCTA GGGCTGCCTC 4260
CCTTGGGGCC CCCAGAATCC ACCCTGGAAC GGCTGCTGGG ACTGAGACCC TGAGTCAGGC 4320
CAATCCCCAG AGCCTTGCCT AGCCATGGCT TGTCTGGGGT GGGTTCCCAG ATCCTCGTCC 4380
AGGACACGGG AAAGGGGCTC CTTTTGTGGC CTGTGCTGTG GAAGGGCTCA GTAAGCAAGG 4440
TGATCCTCCT GGGAGGTAGG GCAATGCCTG CCAGGAGCAG CTTCCCAGGT GGGGCCCAGC 4500
GCCCTGGCTG TGTACACGGC AAAGCTCACT GCCCCTGGTT CTGTCAGGGG CGTTTGAACC 4560
AGAGTGACTC CATCTTGAAC AGGGGCTGGG TCTGATGAGG CTGAGGCCTG CTGCGCTGCA 4620
TTCCCAGGAG CTTAGGGATT CTCAGTCACA AGGTGAGACG GGACGACCGC GCAAGAGGCA 4680
GGTCGTTAAA ACCTTATTAA TAAAACAAGT TGTGGTCAGG AAGCCATCCA ATACCCAGTA 4740
CCCACCAAAA CCAAGGCGGC ATGAAAGTGA CCTCTGGTTG TCCTCACTGC TCATTACACG 4800
CTAATTCGAA TGCATTAGCA TCTAAGAGAC ACTCCTACCA GCACGGTGGC AGTTTACAGA 4860
GGCCACGGCA ACGTCGGGAA GCTACCCTCT ATGGCCTAAA AAGGGGAGGA GCCCACAGTT 4920
CTGGGAATTT TGCACCCCTT TCCTGGAAAA TTCATGAAAA ATCCACCCCT TGTTCAGCGC 4980
ATAATGAAGA AGTAACAGTA AGTGTCCTTG GTCGGGGAGC CATTCTTCAT CCCTTCACTT 5040