EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-04157 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr11:65068660-65070290 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs655433chr1165069275hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr11:65069728-65069743GTGCTGAGTCAGCAG-7.55
MAFFMA0495.3chr11:65069728-65069743GTGCTGAGTCAGCAG+7.61
MAFGMA0659.1chr11:65069725-65069746TTCGTGCTGAGTCAGCAGGCC+6.31
MAFGMA0659.1chr11:65069725-65069746TTCGTGCTGAGTCAGCAGGCC-6.39
MAFKMA0496.2chr11:65069726-65069745TCGTGCTGAGTCAGCAGGC-6.04
MAFKMA0496.2chr11:65069726-65069745TCGTGCTGAGTCAGCAGGC+6.36
Myod1MA0499.1chr11:65069555-65069568AGGGACAGCTGCT-7.52
MyogMA0500.1chr11:65069558-65069569GACAGCTGCTG+6.14
RESTMA0138.2chr11:65069095-65069116ATCCGCACCATGGAGAGGACT+6.59
Tcf12MA0521.1chr11:65069558-65069569GACAGCTGCTG+6.02
ZNF263MA0528.1chr11:65069176-65069197GGGGCAGGGGAGGGAAGAGGG+7.06
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_00332chr11:65063191-65070540Adipose_Nuclei
SE_03505chr11:65068922-65069370Brain_Angular_Gyrus
SE_03505chr11:65069377-65070108Brain_Angular_Gyrus
SE_04140chr11:65068501-65070288Brain_Anterior_Caudate
SE_06057chr11:65068011-65070679Brain_Hippocampus_Middle
SE_07047chr11:65068386-65070521Brain_Hippocampus_Middle_150
SE_27474chr11:65069029-65070158Esophagus
SE_28272chr11:65068900-65070402Fetal_Intestine
SE_29490chr11:65068821-65070419Fetal_Intestine_Large
SE_29716chr11:65067995-65070685Fetal_Muscle
SE_34967chr11:65069370-65070426HeLa
SE_36992chr11:65057722-65070777HSMMtube
SE_42714chr11:65068484-65070270Lung
SE_44186chr11:65068329-65070376NHDF-Ad
SE_44803chr11:65069503-65070138NHLF
SE_46915chr11:65069009-65069441Ovary
SE_46915chr11:65069455-65070073Ovary
SE_50465chr11:65068319-65070347Sigmoid_Colon
SE_51908chr11:65068413-65070520Skeletal_Muscle_Myoblast
SE_53043chr11:65068791-65070200Small_Intestine
SE_53693chr11:65068747-65070343Spleen
SE_54859chr11:65068703-65070413Stomach_Smooth_Muscle
SE_63700chr11:65068312-65070534HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116506900365069988
chr116506892465069931
Number: 1             
IDChromosomeStartEnd
GH11I065288chr116505600765070529
Enhancer Sequence
GTAAAAGAAA AGAGGGAAAG GGAAGGGAGG CAGTGATGGG CCCGGAATGG TGCTTCAGAG 60
CCAGATTGTG AAGTCTTGCT AAGGCATTTG GACCTGATTC TTTCTGCCCC AGAGAATCTT 120
GGAAGGGTTT GCCTCCCACC CCCTGTGCCT CACCCTGACC ACCCAACAAG GACCAACTTA 180
AGAGGAGTCC CAGGTGCAGC CTCAGTACCT GGTAGCATGT AGCAAAGGGG TGGTTTGAGG 240
GGAGAGGGGC TCAGGGGAGG GGCCTGGGTC TGTTGGGGCA GGTCGGGAGG AAGAGGGGCA 300
CCAAGTGGGC CATTGGAATA CTGGAAGCAG CACTCCAGTG AGACATGGGC GTTGGAGGGG 360
TAGATGTGGG AGTCACTGCA GTCAAAAGCC ACAGAACTGG GTGCTGGGAG GGTGGCCGAG 420
AGATGGATGG GCAACATCCG CACCATGGAG AGGACTCTGG CCAGCACTTG CACTTAGCAT 480
CACTGATCAA CAAGGCAAAA GGGTGGGACT GGCCTGGGGG CAGGGGAGGG AAGAGGGATG 540
GCAACAGAGA GGTGCTGGGA TTTCTGGCTA AAGAGACCAG AAGACACCCA TGGTTGTTCA 600
TGGCAAGACT CCCAGCTGCA TTCAGGCATT TGGGACCTTC TGTCACCGTC ATTGGTCATT 660
CTGGGTCTTC AGTCCCCAAG CGACCATGCC TACTGCTGCT TTCGTGGGTC AGCCCTGGAA 720
ATGCCCAGGG GCCTAGGGGC TGGCCTGCCC TCAGACCCAG CTGGACTGCC GCTGGCTCTG 780
AATTCCTCCA TCCTGCCCCG CCTCTTCCCG GGGCTCTAGG CTCCTCCCCA CCCAGAGCCT 840
GCCTGACAGC TGAGGCCCTG CAGCTGCCCA GGCAAAGGGG CCCCTGGGAG GTCTCAGGGA 900
CAGCTGCTGC CCATAACCTT GCTGACCCTG GCCCCTGCAC ACTGCTCCCT GAGATCCCAG 960
GCTTCTGCCC AGCAGCCAGC AGGACCCTAC CAAGCCCCAT CTTCTCTGCT CACTCCCATC 1020
GCTCCCAGAT CTTCCCAGGG GCTGAAGCAT TTTGGGCTGA GCATTTTCGT GCTGAGTCAG 1080
CAGGCCCCAC CCAAAGAGTG AGAAAAGCTG CTGGGTAGAG GCACCCCTAG CCCCGCTCCT 1140
GCTTCAGAGG AAGTGCCTTT CAGGGGTGGA TGAGGGGTAC ACCTGCCTCC GTCAGGCAGG 1200
CTTGGCCCTG TTCAACAGGG TGGGGACCCT GCCCTCCCAC CACCTGCCTC CTACCACAGA 1260
ACAGGGCACA AGGGTGGCAC AAGGGGAAAA AGGAGAAGGC ACCATCACTC CTGATTCCCA 1320
GCGAATAGGG GGAAAAGGCA TACTCACTCC TGATTCCTGG CAGCTTCTTC CCTTGAAGGT 1380
CCACTTTCCT CCTGAGGACT CGAGGCCCCT TCAAATTGCC CCTTAGAATG TTTCTAGTAA 1440
TAGTAGTTGC CTCTGGGGAC GGGTGTCCAA GGGCTAGGGG TCAGGAGTAG GAGGGCTCAG 1500
AGAACGATTT GTCATGTCCA CACTCAACCT GTTTGAATTT TTTTTTTTAT TTTTTTGGAG 1560
ACAGAGTCTC ACTCTGTCGC CCAGTCTAAG TGCTGTGGTG CCATCACAGC TCGCTGCAGC 1620
CTCAACCTCC 1630