EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS110-03832 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr5:1128120-1132460 
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: 1             
IDChromosomeStartEnd
GH05I001127chr511279661132045
Enhancer Sequence
GGTGGTGACA GGCGCGTGAT CTCTGGTTAT TCCAGAAGCA GTGAATGTAG GATGTGTGTC 60
ATTTAGCTTC TCACGCCATG CACTGGGGCA AGTTCACTGA GGAAACAGAT CTCATCCTTA 120
AGGCAGGCTG GGAGTGGGCG TGGCTGGGAG GTGGGTGCCT GAGGAACACT CTCGCCCCTT 180
CCCCTGCACC TGTGGTCTCA ACCTGGCGGG AAGTCCGCTC CAGCTCCTGT GGGACCAGGG 240
TTGCTGGATC CAAGTTGCCA GGTAAACTCC CGCTGATCTG CAGCACAAGA GCCAAATCCC 300
AGGACGAGCT CTCACGGAGC AGTCAGGCCC AGTGGAAACT GGTGGCCTCG CTCCAGGAAA 360
TGAAGCCAGA CTCAGACAAA CAAAAGCCAC CAGCAATGCA TGGAGGCAGG ATGGGACATC 420
TCACGCGGAC CCAGTGACCC TGGAGCATGC CTGGGTACAG ATGGAGCCCC CAACAGGGGT 480
TTCCTTCCTC ATGTGGTTGA TGGAAGGTTC TAGAATTCAT CTTCTCATAG GGAGGAAAAG 540
TGCTGCCCAG CCCCCAACAC TCTGAGACCT CTGGGGCTCA GTAAATATTT GATAAACAAC 600
AGGCTCAGCA GGTGCGGTGG CTAGTGAGAC TGGTACAGAC CAGGTGGCCC ATGGGTATTG 660
GGTCTGCCCT GTGACCACCA GTCCTGACAG GCTGCAGCGG AGCATGTGTG CACGTGTGTG 720
CATGTATGTG TGCGTGTGTG TGTGCATGCG TGCACACCAA TGGGAGTGGC CCCAAGTGCC 780
TGCCTGGTCT CTACACGGCT TCCAGCCTTT TCCTAGAATG GATCACATGT TTGCATACAC 840
ACATATGTGC ACACACATGC AGAAACCAGA CCCACTCCCA CCATCCACCC ACACAAGCTG 900
GACCCTCAGT CACGCGGCTC CCTGCCACGT GCTCCATCCC CATGTGCGTC CAACACACCT 960
GCCAGCTCTG CTTTCAGCTT TCCCTGATGG CCAAGCATAC CCCGCTGCCC CTGCAAGGCT 1020
TGGGAGCACT CCTGGGATCC CCTGCAAGGC TTGGGAGCAC CCCTGGGATC CCAAGTCTGA 1080
TGGCCTCTAG AAGTCCCTCT CCTCAAACCT CGGTCACAGC TGCTGCCTAG GGCCTGCCAG 1140
GCCAGGGGGA CAGCCACGTC TCTCCTAGAC ACACGAGGAC ACCCCTCCAA GAGGCCTCCC 1200
TCAGCCAGCC GCCACTGCTG CCGGCCCCTC TGTGCATCCC CAAGGGCTGA GCTGTTGCAG 1260
GGTACAACGC CTCCTGGCTC CAAGTGAAAG TCGGAGGTGG GCAGGACGTT CAGGTAACAC 1320
CCCCACCTCC GAAGTCCAGT CTCACAGAGC CTTAGCAGCC ACCCAAGGCA AGGAGGTGGC 1380
CATGGGCCAC CAGGAGTGTC CCGAGCATCC CAGGCCCACA AGGGCCAGAG AAAGTTCCGG 1440
GCTTCCCCTA GCGTAAGGGA CAGAACCAGG CGCCCTCCCC TCCTGGCCCC CTCAGCTTTC 1500
CTGTGACGCC CAGGACCAGG ACCAGGACCA GGGAAACCAC AGCGTCCCAG GCGACAGGGT 1560
GGAGGGCGGC TCCAGGAGCC CAGCTGGGGC ATCGGCCAAC CCCCGAGAGA CACACTTGCT 1620
CAGGCATCCC TGGCAAGGTT TCCAAAGCCC TCACGCGGAT GAACACGGGA ACACCTGGGG 1680
CACCCACTGT TTCACGGAAA AAGTCACAGG GGTCACCCTG ATGGGATGTA ATTTCTGGAT 1740
ATGATTAAAC AGGAAGAAAA GATCCCGGCT GAGATTACCG TTCAGAAGCA CCTTGGAGCC 1800
GGGCTCTCGA CACTGCTGAC CCGAAACCTG GTGATTCAAG AGGAAAAGAA CGCCCTGCTG 1860
CCGTCAGAGC TGGAAACTGC ACAGCCCATT GTGTCCTGGG CGTGAAGCCA TCACCTGACT 1920
CCCAGGTGAG GAGCCAGAGG GTCAGGGGTC AGAGCTCAAG GGACGCCCTG GCCAGCTGGG 1980
GCAGTCAAAG CTACCTCTGC TTCTTCCCCT GAAAGAGGAA GTTTAGATAC CCAAGAAGTT 2040
TTGATATCTC CTCCACGACT TTACTTCTGG ATGTGGTTCA GAAAAATCTG CGGAAAATCA 2100
CCCAGAATTG CACCCGTTTG GTTTACAGGA GTATTAGCTG TGGGGGCCCC TTTTCCACCA 2160
CCCCCATCAA GCAGCCTCCC GGGCAGCCCA GGACCCTCCA GAATCTTCCA GAAGCCGCAC 2220
CACTCGCTTC AGTCGTAACC TGCAGGACCC CACCGGGCGA GGCTGGCTGG GAGGAGGCAC 2280
TCTCAGGACA AGGGACCTGG GCAGGCACCT CCTGTCTCCG CTCAACACCC AGCGAGGACA 2340
GGAGGACCCA GGGTGCACCT GCATCTGCGT CTGGGCAGAG GAGCAAAGAC CTGGCCTTCC 2400
CAGAGCTTGA GCTGTGGGAG GAAGAGAGGC TGAATGAAAG CCCCGCCCCC ACCCCACCCC 2460
AGGAGAGGCC ACCTGGGGCC TCCCACAGCC CTGCCCACGG CTGCACACGC GTGTCCCCTC 2520
ACCTCCTTAG CCAGGGCGGC TGCCCGCGCA GGTCCCCTCA CCTCCTTAGC CAGGGCGGCT 2580
GCCCGCGCAG GTCCCCTCAC CTCCTTAGCC AGGGTGGGGG CAGCAGGGAG GGAGGGCGTG 2640
CTGCATTCTT CCCTGGGCCT GCAGGTGCAC CTGTGCCTGC CCAGAGGGAG CAGCGGGAGC 2700
TTCCAGCAGA CACACCTGGA CAGGTGCACA GAGCTCCTGC CAGGGAAACC CAGCACAGAC 2760
GCAGGTGGGC GGGTGGTGGG AGGGTGGCAG AAGCGGAAAG AGGAGGAGGC TGAGCTCAGC 2820
ACAGCCCATG CAGTCTCCTT CCGGCCAAGG GGAGCGGCTG GGCCAGTCTG AGCCGGGAGG 2880
CAGCTCAGGG AGTAAGCCCT GGGGACAACA TTGGAGTAGC ACAGGGTTCC CTGACAGAAC 2940
CTCACGTCGG AGGGTGGTCT GAGGGCTGCT GGGGGCCCAC CTAGGAGATG GGGTCCCAGG 3000
ACACAGAACA GGGAGGGGGT GGTGTTTCCA GGGTGAGGCC TGGGGGAGGG TAGCAAGGCC 3060
TGGACTAGGA GATGGAGGCC TAATCAAAGC AAAACAGAGA CTCAGAGCTC AGCGCCTGTA 3120
TTCGCAGGGA CACACAGGGA CTCACAGGGA CGTCCCGGAT CGCTAGGGGA CTCACGGGGA 3180
CACGTGGGGA CACGCTCGGA CTCACGGGGA CTTGCAGGGG CCCATGGGGA TGTGCAGGGA 3240
CACCGTCCCT CCCGGCCGTC CTGCTCCTTG CCAAGAGTCA CCCAGAGGCT GGGGCCTGGC 3300
ACCACTTGCA GACAGGGGCA TTCCTGGGCC CCTCCTTTTG GCACCTCAGC CTCAGCAGCT 3360
GCTGAAGGGT GTGGGGGAGG GAGCCGGTAT TGGTGCAACA GGCAGATGGT TCCAGAAACT 3420
CAGGATTCTA CACAATCCTA GCACCTGAGG CACAGTCCTG CACGGCCGCC ACGCTGTCGG 3480
AAGCAGGCAC CGGCCCTGGT GGTCAACACA AGCCCTGAGG ACCTCCCAGA GGGCATGCTC 3540
CGGGCAACCT GCCAGGACCA CCTCTCCTGC CTGGTGTTGG GGGCCTCACC TGACCTCTCC 3600
GGGTCCCTAA CCAGGCGCTA GGGCTGCCTC CCTTGGGGCC CCCAGAATCC ACCCTGGAAC 3660
GGCTGCTGGG ACTGAGACCC TGAGTCAGGC CAATCCCCAG AGCCTTGCCT AGCCATGGCT 3720
TGTCTGGGGT GGGTTCCCAG ATCCTCGTCC AGGACACGGG AAAGGGGCTC CTTTTGTGGC 3780
CTGTGCTGTG GAAGGGCTCA GTAAGCAAGG TGATCCTCCT GGGAGGTAGG GCAATGCCTG 3840
CCAGGAGCAG CTTCCCAGGT GGGGCCCAGC GCCCTGGCTG TGTACACGGC AAAGCTCACT 3900
GCCCCTGGTT CTGTCAGGGG CGTTTGAACC AGAGTGACTC CATCTTGAAC AGGGGCTGGG 3960
TCTGATGAGG CTGAGGCCTG CTGCGCTGCA TTCCCAGGAG CTTAGGGATT CTCAGTCACA 4020
AGGTGAGACG GGACGACCGC GCAAGAGGCA GGTCGTTAAA ACCTTATTAA TAAAACAAGT 4080
TGTGGTCAGG AAGCCATCCA ATACCCAGTA CCCACCAAAA CCAAGGCGGC ATGAAAGTGA 4140
CCTCTGGTTG TCCTCACTGC TCATTACACG CTAATTCGAA TGCATTAGCA TCTAAGAGAC 4200
ACTCCTACCA GCACGGTGGC AGTTTACAGA GGCCACGGCA ACGTCGGGAA GCTACCCTCT 4260
ATGGCCTAAA AAGGGGAGGA GCCCACAGTT CTGGGAATTT TGCACCCCTT TCCTGGAAAA 4320
TTCATGAAAA ATCCACCCCT 4340