EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-13290 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr14:93509440-93511970 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35584079chr1493511641hg19
TF binding sites/motifs
Number: 14             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr14:93511661-93511676AGGTCAGAGTGGCCT+6.66
FOSL2MA0478.1chr14:93510658-93510669CTGAGTCACCC-6.02
GATA2MA0036.3chr14:93509989-93510000TTCTTATCTGT+6.14
Gata1MA0035.3chr14:93509989-93510000TTCTTATCTGT+6.62
HES2MA0616.2chr14:93511862-93511872GGCACGTGCC+6.02
HES2MA0616.2chr14:93511862-93511872GGCACGTGCC-6.02
JUNBMA0490.1chr14:93510658-93510669CTGAGTCACCC-6.02
Klf12MA0742.1chr14:93511071-93511086AAGAAGGGTGTGGCC-6.25
Klf1MA0493.1chr14:93511075-93511086AGGGTGTGGCC-6.32
MYCNMA0104.4chr14:93509512-93509524GGCCACGTGGGC+6.27
MYCNMA0104.4chr14:93509512-93509524GGCCACGTGGGC-6.27
RUNX1MA0002.2chr14:93511647-93511658AAACCACAGAG-6.14
ZNF263MA0528.1chr14:93511134-93511155AAAGGAGGAAGAGGAAGAAGC+6.88
ZNF263MA0528.1chr14:93511890-93511911GGAGGAGGAGGTGAGAGGAGG+7.65
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_03181chr14:93510068-93510583Brain_Angular_Gyrus
SE_03888chr14:93504983-93513044Brain_Anterior_Caudate
SE_04808chr14:93494251-93514329Brain_Cingulate_Gyrus
SE_05777chr14:93493302-93514911Brain_Hippocampus_Middle
SE_06743chr14:93509612-93512256Brain_Hippocampus_Middle_150
SE_07721chr14:93492779-93514769Brain_Inferior_Temporal_Lobe
SE_09265chr14:93510048-93513026CD14
SE_23185chr14:93505279-93514419Colon_Crypt_1
SE_23918chr14:93509314-93512076Colon_Crypt_2
SE_26366chr14:93505659-93512899Duodenum_Smooth_Muscle
SE_26889chr14:93505113-93512411Esophagus
SE_27639chr14:93505251-93519390Fetal_Intestine
SE_28556chr14:93505100-93524844Fetal_Intestine_Large
SE_34796chr14:93505024-93514368HeLa
SE_40660chr14:93505046-93514961Left_Ventricle
SE_41563chr14:93509310-93512004LNCaP
SE_42451chr14:93505095-93514218Lung
SE_48575chr14:93505057-93512067Right_Atrium
SE_49689chr14:93509996-93512067Right_Ventricle
SE_50538chr14:93509223-93514489Sigmoid_Colon
SE_52403chr14:93505242-93519331Small_Intestine
SE_57475chr14:93510071-93511486VACO_503
SE_65267chr14:93507414-93512032Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr149350944693510834
Number: 1             
IDChromosomeStartEnd
GH14I093038chr149350488193524683
Enhancer Sequence
CCGAGGCCCA CACTTTGGGG AAAACCCTTA GAAACTTCTT GTCATTGGTT AAAAAAATAT 60
TGACCCAGGA TTGGCCACGT GGGCCACAGG TGGTTTCACA GCACACACAG AACCAGAAGC 120
TGGGGCTCAG AGAAGCAAAA TAACTTGCCC AAGATCACAC AGCTAAGGAG ATCGGATTGA 180
AATCCACCCC AGTTTATGTG CACAGACAGA AGGGGAGAAA AGAGATGTGG GGCAGGTGGA 240
TTTCTGAGGG CAGGAAATAC CAGTGGGAAA GCCGAAGACA GCACAGTAGA GACTGCAAAA 300
GCCCAGTGCT CTGTGGAGTC ACTGCAGAAA GCACCGAACA CATCCAAGGC TCAACCCATC 360
AGGCACTCTT TCCTTTGGGG CTACTTCCAA CAGGAAATTC CAAGTGTCCC TGTCAAGCAG 420
GGGAAATGCC ATCCTGGGTC CAAGGCAGCA GGGCAGCCTC CCTGCCCCGC CCAGCCCCAC 480
CTACATGAAG AACAAAGTGC ACCAGGCAGG AATGTGCACT CAGGCCGTAG CCAGCCTCAG 540
CCTGGCTCAT TCTTATCTGT GGCTTGATTA AAACAAGCTT GGATTACACC ACAATCTTTA 600
AGCCCCAAGG CTGGGGGTGG TGTCACCAGG AATCTGTTCC AAGCGCACGT CATGCCCAGG 660
CCACCGTTCT CCTTCCCCTC ATTGGTGGCA GGCTGGCATC CTGCAGGAGG CCCTTCCCAG 720
ACCACAGCCC CACCCTTCCT CTCCTGCCGC CCACCTGAAG GCCCCAATAC ACATCTTCCT 780
ACAGTTCTGG CTTCAACTCT GTTCCTGAGA CCTTTACTGC CCCAAGTCCA CTACCCTGAG 840
TTCTGGGCAA ATGAAAAATC TTTTCCCCTT CACCAGATTT CTCAAATCCA ACCATTCTGG 900
AACCCGGCTT GTGGATGGCT AGGCTCTAGC CTCCCTCCTC TTCTGTCCCA TCACCCTGGG 960
AAGACAGAGC CAGAGGGTAC TGAGGAATTC AGGTGGGAGG GGTTGGGGGG GAGGTGAGGA 1020
GGGGGTCCTA GGAGCAAATG GAGGGTCACA AACTGAAGCG CCCATGGGGC AAATGTAAAC 1080
CATGAGGCTG GTGGTGTGGG ACAACAGAGA ATGGTGGGGC CTAAGGGGCA ACCAGCTTAA 1140
ACACTGGCAA CAAATTCAAA GGAAAGAATG TAAAATTCCT GTGTGGGCCA AACAGATTGC 1200
ATGCAGGCCC AGGTATATCT GAGTCACCCA CGTGTAATCT GGTCCAACCC CCTCCGCAGA 1260
GATAGGAAAG CTGAAATCCA GACACAAGGA AGGGACCATG AATAAGTTTG TGCTGGCGAT 1320
TACTGAGAAA GTCTAGCATA AAAATTAAAC CGAAGCCTAG GCCGAACACT GGCATCCCTC 1380
TGCTTGGCTG TGAAGCTGGT GAGGATGCTG CACTCGGCCT GGCAGCAGAT GGAAACTCTG 1440
GAACTCGAGG GCCACGGATG AGCCACAGGG CCCCCCAGGT AAAGGACTGA CAGCCAGCCA 1500
TGCAAGCCCC TGGGACTGAC CCAGATGCAG AACTGACCAA TGTGGCGACA ACCATCACCC 1560
AACCCTGTGG GGCTGTAGAT CTCAGAGGAG GTGGGACAGT GGCCCAGCGG ACAGCAACAC 1620
GGCAGAGAGG GAAGAAGGGT GTGGCCTCTG TCTATGGCCT GGCCAGAAGG GCCACCGCAA 1680
GCACCAAGGC TAGCAAAGGA GGAAGAGGAA GAAGCAAGAA AAACCCGACA CCGTGACGGA 1740
CTAGCGTGGG CCGCAAGTCA GGGTTGTGGT TCTTTAGGAT ATATCTTAAC AGGGTAAGGG 1800
CCTTAAATGC CCTTTCCCCA CCAACCTGAC AGGGTTTAGC ACCAGGACTC CTGGCCAGGG 1860
CAGGCCCCAG GGCTCTAGGA TCTGTCAGAT CAGGAAGAAA GGGGCATTTA AGGTCTCCCT 1920
CCTGTAAGAT CTACCTTAAA GAACCAGATC CCTGACTTTG CAGCCCAGTG CCATGCTGCT 1980
TTTGAGCCTG AAATGGAAGT CTGTGCCTTA GTTCCAAGTC ACCAGGCACT GGTTCCTTGC 2040
CCTTGCAGGC ACAGGGCATC AAGATCAAAC CAAACCTCCA AGCCTCACCT CTCACAAATA 2100
AGCAGAGGCC AGTTACCCCT CTGGGCAAGA CCTCAGGCCC CTGTCCCTGC CAGTCAGCAG 2160
CTCTGCCTCC CGCAGCGCTT GAGGGCTGGT CCATGCAGCC GGCCAGGAAA CCACAGAGGC 2220
CAGGTCAGAG TGGCCTTTTA ATTCAACTCC CCTGGTGACC CTGAAGAGCA CTGCCGCAGA 2280
CTGAGAGGCT GGAAGTAGGC TATGCTGCCC CTGCCCCATA ACAAAGACTC TACAGCAAAT 2340
CACCAGGATG GGGGAAGATT AGCGCAAAGT GGGTGGAGAG TCTCCCTGAA ACGTACTGAC 2400
AGCACTTAAA AACCAATTAG ATGGCACGTG CCTGTAGTCC CAGCTACTCA GGAGGAGGAG 2460
GTGAGAGGAG GATCACTGGA GCCCAGGAGT TCAAGGCTGA AGTGCGCTAT GATTGCATCT 2520
GTGAAATAGC 2530