EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-05103 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr10:104427920-104431150 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr10:104428879-104428890GGGCGGGAAAG+6.32
GATA2MA0036.3chr10:104431128-104431139GAAGATAAGAA-6.02
RREB1MA0073.1chr10:104428479-104428499GCTGTGGGCGTGGGTTGGGG-6.73
STAT3MA0144.2chr10:104429029-104429040CTTCCCAGAAG-6.14
ZNF263MA0528.1chr10:104430672-104430693TCTCCTCCCTGCCCCTGCTCC-6.56
ZNF263MA0528.1chr10:104430666-104430687TCTTTCTCTCCTCCCTGCCCC-6.68
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_03928chr10:104427506-104431130Brain_Anterior_Caudate
SE_04957chr10:104427296-104431189Brain_Cingulate_Gyrus
SE_05850chr10:104427212-104431574Brain_Hippocampus_Middle
SE_06794chr10:104428204-104430033Brain_Hippocampus_Middle_150
SE_07900chr10:104427056-104431396Brain_Inferior_Temporal_Lobe
SE_19414chr10:104427492-104429411CD4p_CD25-_Il17p_PMAstim_Th17
SE_23338chr10:104429017-104429873Colon_Crypt_1
SE_23909chr10:104429052-104429868Colon_Crypt_2
SE_26660chr10:104428913-104429898Esophagus
SE_29601chr10:104427183-104430217Fetal_Muscle
SE_31421chr10:104428022-104430107Gastric
SE_36963chr10:104426876-104431090HSMMtube
SE_40696chr10:104427420-104431290Left_Ventricle
SE_42120chr10:104427400-104431252Lung
SE_47510chr10:104428121-104430088Pancreas
SE_48604chr10:104428497-104431201Right_Atrium
SE_52411chr10:104428768-104430079Small_Intestine
SE_53301chr10:104427988-104431128Spleen
SE_55138chr10:104427981-104428923Thymus
SE_55138chr10:104429059-104429442Thymus
SE_62334chr10:104369841-104439105Tonsil
SE_65286chr10:104428376-104430360Pancreatic_islets
SE_65286chr10:104430443-104431278Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr10104429200104430400
chr10104429194104430031
chr10104428227104429146
Number: 3             
IDChromosomeStartEnd
GH10I102667chr10104427367104430502
GH10I102670chr10104430561104430710
GH10I102671chr10104430761104431010
Enhancer Sequence
CTGATAAGTC CATTAAAAAG GTTTGGGGTC AGATCAGCAG GGCCTTGAAT AACAGGATAA 60
ATGGTTTGGC TGGAGGGACC CACAGCAGCA GGGCCTCTGA AGGCATCTTA GCAGGGTACT 120
GCATTTTAAT AATGGCGCTA ACCCCTCAAA GGAGGATCAG GCAGGGGAGT CCAGCCCAAG 180
CTGGGAGGCA GTGGGAGGGC CAAGGGAGAG ACAGGTGGGG TTCAGGGTGC ACCCTCAACC 240
CAGTCTAAGG AGTGGGAAGG CAGGTGGCTG GGTGTCCAGG TCCTGCTGCT CAGCCAAGGG 300
ATGGAAGCCT GGATCAAGCT TTCCCCTTCC CTGCCAGCTA GCCATGGGCC CCAGAGTCAG 360
CAGAAAATCC CGGCTCCAGG GAGGAGGCGG CGTGGAGCCA GAAGCTGCTG AGGGAGCACT 420
GGCAGCAAGA TGCCATTGTA CATCCGCAAT CAAGATGCTT CAGAGGAAAT CAAAAGCACC 480
AACCAGGGAA ATGATGTGTG CACTCTCTTT CTCTCAAACA CACATACAAA CTTCTGCCTC 540
CAAAATGGGT CAAGTGAAGG CTGTGGGCGT GGGTTGGGGA GGGAGGGCTG GGAGAAGTGG 600
GGGCCTGGGA GCCCGGGAGC AGGCTGGGCC CTGGTGCCCA CTCACCCTCC TGGCATAGGG 660
GATGGCAGCA GCTGCAGGGT GGGGCGGGAT GTGAGGATAA ATATACACCT CCCATGCATA 720
TGGATCATGC TCACAGCTGC CCTGCTTGCT TAGTGTTCAT TAGGACCAAC TGTTTCAGGA 780
GCAGTGGCAG GCGGGCGGGA GAGGGTGATG TACCCATTCA CAGACTGGGG GTAGGGGGGC 840
TGCCTGCAGC TGTGCAGATG CCTCCCCCAC TGCCTGGATC AGCATCTCAG CCCCTGAATG 900
CCCCTTCCTC CTGCTTTTTC TTCTTCCGAC CTGCTGCTAT GCCAGATCTG GAGGTCTCAG 960
GGCGGGAAAG GGGCCTGGGG CATGAGTAAG GATGAAATCC AGGCTGCATC CCCATAGGAG 1020
CTGGGGAGAG TGAGGGAAGA GTTGGGCTGG ATTGGATCCC TTGGTCCAGG ATGGGCTGTT 1080
GTTTACAAAC CAAAGCTTCT TATCCCCATC TTCCCAGAAG CCATCTGTAG CATTCCAGCA 1140
GGAAAACTGC TTTGGCACTG TCCCCTGGAG ACTCGAGGGA AGCCCCATTC CTATGTGACA 1200
ACCCTAGACC AGGCTTGCTC TGTGCCTCCA AAGGGAATCC AAGGGGGCTG AGGTTGGTGG 1260
ACCAGCATCA TTCTGCAGGA TTCTGACGTC CTGGCAGCAA GGAGGGCTAG GGAAGGAGAA 1320
TGCTGGGCTC CAGCCCGGGA CCAGGTGCTC TAGGTGGGCC TGGGCCTGGG CTGGGGAACA 1380
GTGCTGAAAT GTAGGCCCAG GGAAGGGTCT GGCTGGTGTC ACAGGCAGGG CCAAGTGTAG 1440
CTGTACAGCT TGTGCCCTAC CCAAGGGAAC TGGCTGAGGG GCCTGCAGCT GGTGCCACGC 1500
CTTGTACTCT GGTGTGGGGC ATAATCTCCC ACATGAGTCA GTGGTGGCCT GGGTGACAGG 1560
CCTCTCTAGT GTTAGGAATG TGGCCAAGAG GGCCTGCCTG TGGACGGAGC CCGTGTGTCT 1620
CCTATGGTGA GCTCTTTCTC CTCCTGCTCC AGCGGTCTTG GGGGGCTCCT AGGGCTGTGC 1680
CTCCAGGGGG CTGGCACAGG GGCTTCTGAG TCCTGGGTGG AAGTGGAGGC AGCTGATCCC 1740
AGGCCAAAGC CCCAACTACA ACAGCCTCCC CAGGCCCTTT CCTTGGTTGT AAGGGTGGGG 1800
CTGGGCACCT CCTGCCCCCT CTACTGGTGG CATCCAGAGC AGCAGCTGAC TCTGGGACCC 1860
CAGGGCAGGG TCTTCTGGAT CCTGAAAACA GGGTGAGTGG CAAAAAGCGA GGGCCGCCTC 1920
TCACCTACCT CCCTGGGGTG GCATCATGGA ATAAAATGGG CTTTCAGCAA GTGGGCTGGC 1980
GGGAATCACA GTCAAGCCAT TTCCTAGCTG TGTGACTCTG GGCAAGTGAC TTAACCTTTG 2040
TGAGCCTTGG TTTCATCATC TGGGAACTAG GGACAGTAAA CGGCTATCTT GTAGGGCTAA 2100
TCAAAGGATG AGACCCACTA ATGACTCAAA GGAGAAGCAG TTGGCTTAGC TAAATGGGAT 2160
TCTGACCCCA ACCCTGTACC TCTCAGCTTC AGGTATCCAA GCAAATTCTC CCTGCCCCCT 2220
CCTGGACACA GCTTGCTTTC TGCAGTTCTG TCATTAATAT TTCATTTCTT TAGCAAAGGC 2280
TTTTTGTCCC TGGGACACTG CTATTCGCTC TGGAGAAGAA ACTGTTCCGT GTTCCTTCGT 2340
GCAGAAGGAT TCCTTAGCTC CTTTTCTGAG AGCAGAGCAT TAGGAGCCAA AAGCAAACAG 2400
GTATTGTGGT ATAAATTTGG GACCCAGCAG TGAAATAGGC CTGAGTTCAA ATCCTGACTG 2460
TGCCCAGTTC TTCCTGTGCG ATCATGGGCG AGTGATTCAA ATTCTATGAG CCCCATCCTC 2520
ATACTGTGAA TGACAATACC TACAGTTAAC AGTGTCTTTG CGAGGATTAA ATAAGGTAAC 2580
TGTGAAGTAC CTGGTGCAAG TGGCTACCTC CTTAACTCTT TCCCCCGGTT CTGACACTGT 2640
GGGGGACTGG TTGTTGGCTG CACTTCCACG CCTGTGTGTG GTTGGTTCTG GACACACACA 2700
CACACCAGTG CTGGACCAGC AGAATGACTG CAGGGAGCCA GGGCTCTCTT TCTCTCCTCC 2760
CTGCCCCTGC TCCTGGTGGC TGCAGCTTCT CTGTGTTCTG CAGTGTTGGA AAAGGAAATT 2820
ACAGAACAGA TTGCAATTAA GGGGGATGAG GGGGAGACAG GGACAGAGGC CGTGAGATGC 2880
AGCTTGACTG AGCACTAAAC TGTGTTTGCG CCTGGAGCCA ATCAGGAGCC TCTGATAAGA 2940
GCCTTTCCCA CTTACAAAGC TAAGCAGGAG GTGTGGTTGG GGTGGCCCTG GGAGTCCCGA 3000
AGGGAGGGGG CTGCTGGCCT TGAAAGTCAC AGAGCCACAT GGGAGGGAAG GTGGGAGGTA 3060
GAGGTCTTAG GGGCCTTGGA AAGCCTGGAC TCCAGACTTT CTGCCAGCTG TTATATTTGC 3120
TACCATTGAT TTAGCACCTA CTACTCACTG TACGGACATC TCATCTCATC CTCTTGACAA 3180
CTGTGCAGCA TGATTATTGC CCAATTTTGA AGATAAGAAA CTGAGGGCCA 3230