EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS121-11018 
Organism
Homo sapiens 
Tissue/cell
LNCaP 
Coordinate
chr14:65204090-65205450 
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PLAG1MA0163.1chr14:65204999-65205013CACCCGAGGGCCCC-6.31
RREB1MA0073.1chr14:65205165-65205185TGGGGTGGGGTGGTGGGGGC-6.32
ZNF263MA0528.1chr14:65204812-65204833GGAGGAGGAGGAGCAGGAGGA+10.05
ZNF263MA0528.1chr14:65204665-65204686GGAGGAGGAAGAGGAAGAGGA+10.52
ZNF263MA0528.1chr14:65204704-65204725GGAGGAGGAGGAGGAGGAAGA+11.36
ZNF263MA0528.1chr14:65204695-65204716GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr14:65204698-65204719GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr14:65204701-65204722GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr14:65204674-65204695AGAGGAAGAGGAGGAGGTGGT+6.18
ZNF263MA0528.1chr14:65204677-65204698GGAAGAGGAGGAGGTGGTGGA+6.45
ZNF263MA0528.1chr14:65204809-65204830GGAGGAGGAGGAGGAGCAGGA+7.03
ZNF263MA0528.1chr14:65204671-65204692GGAAGAGGAAGAGGAGGAGGT+7.15
ZNF263MA0528.1chr14:65204686-65204707GGAGGTGGTGGAGGAGGAGGA+7.31
ZNF263MA0528.1chr14:65204689-65204710GGTGGTGGAGGAGGAGGAGGA+7.54
ZNF263MA0528.1chr14:65204680-65204701AGAGGAGGAGGTGGTGGAGGA+7.74
ZNF263MA0528.1chr14:65204806-65204827AGAGGAGGAGGAGGAGGAGCA+8.08
ZNF263MA0528.1chr14:65204683-65204704GGAGGAGGTGGTGGAGGAGGA+8.15
ZNF263MA0528.1chr14:65204707-65204728GGAGGAGGAGGAGGAAGAGCA+8.5
ZNF263MA0528.1chr14:65204815-65204836GGAGGAGGAGCAGGAGGAGAG+8.79
ZNF263MA0528.1chr14:65204668-65204689GGAGGAAGAGGAAGAGGAGGA+9.18
ZNF263MA0528.1chr14:65204692-65204713GGTGGAGGAGGAGGAGGAGGA+9.68
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_01667chr14:65202771-65205303Aorta
SE_03953chr14:65202725-65204661Brain_Anterior_Caudate
SE_04856chr14:65202485-65204956Brain_Cingulate_Gyrus
SE_05821chr14:65202540-65206717Brain_Hippocampus_Middle
SE_06781chr14:65202547-65204736Brain_Hippocampus_Middle_150
SE_23289chr14:65202217-65204661Colon_Crypt_1
SE_24426chr14:65202664-65204703Colon_Crypt_2
SE_26750chr14:65202614-65204661Esophagus
SE_27717chr14:65202030-65204504Fetal_Intestine
SE_28783chr14:65202126-65204423Fetal_Intestine_Large
SE_32308chr14:65204333-65204939Gastric
SE_47632chr14:65203606-65204366Pancreas
SE_65298chr14:65202574-65205228Pancreatic_islets
SE_68953chr14:65202683-65204783H9
Number: 2             
IDChromosomeStartEnd
GH14I064735chr146520201865204240
GH14I064737chr146520433465204939
Enhancer Sequence
AAGGTAAAGG CCAGTGGGAG GAGGGGACTG GCTGACAGAG GAGGGTGGGA CTGCCCAGGT 60
CAGCCCCCGG CCCCTTCAGC CCTCATTGTC TTCATTCATT CAACAAATGC CTACTAAGCA 120
CCCACTGTGT ACCAGGCTGT GTGGCTTAGG GCCACAGAGA TGAATAAGAC ATGGGCCTTG 180
CCCTGGGGGC CCTTCTGCAC CCTCTGCCTA GAACAGCACC CTGCTGGGGG CCTGCCCAGT 240
GTGGACCTAC TCAGATTTCC CTCTCCCTAG GGTAGACAAG TAGGCAGGCC TGTTTGGGTT 300
CTGAAGTTTT GACCAGGTCC CAGCCTTTCC ACCATGAGAA TGCCCACCCC TCCCTGGACC 360
CCAGTGGCAA CCTGAGTTGG GCATCTAGGT GTGGCTTTCT GTGTGAAGGC TCCCCCCCCG 420
CAGCTGCCTG CAGGAGGACG GGAGGTTGCC CAAGAGGCTG GTCACGAGGG GGTCTTGTGC 480
TCTGAACAGC ATGCAGGCAG TGCTGGAACC CTCCTGGACT TTGGGCAGCC CTCCCGTACT 540
CGGGGCCTGC AGCCAGAGGC TGAAGGGGCT ACCCAGGAGG AGGAAGAGGA AGAGGAGGAG 600
GTGGTGGAGG AGGAGGAGGA GGAGGAGGAG GAAGAGCAGG CCTTTCAGGT CTCTCTGGAG 660
GACCTGACAG GGCATGAAGG CAACGAGAAG GGGGCTGGGC CGGAGCCCCC AGGCTCAGAG 720
GAGGAGGAGG AGGAGCAGGA GGAGAGCCTG GCGGTGGCGG AGCAGGTAGC CGACTTTGCC 780
AGCTCCCTGC TGGCCGCCCT CCACTGCTGG CACTATCGGG CCAACGCTTT ACTTTTCTCC 840
CGGGGCGCTA TGGTGAGGTG TCTCTTCGAT CTCCCCTCCT CCTTGCATGC TCCCTGGGAT 900
GTGCATGCCC ACCCGAGGGC CCCCTCTGCT GCCCTCCTCA CCCCACCCTG CCCTGGTTTT 960
ACTCCTCCCC TCAGCACTTA ACACCATCGC TCGCTGTCAC ACCCTGGTGA GCCCCTGGCA 1020
TGCTCTGTTC CAGTACTGGG CACTAATCAA TATAACGCCC AACAAGCATG ACAAGTGGGG 1080
TGGGGTGGTG GGGGCAGGGA GAAGCTAGCA CACAGTGGGG CTGGAAAGGT CAAGTCCACT 1140
TTGGAGGGAC AGAAAGGTGG GCTGAGGTTT TTTGAAGCTG CATGCCTGAC AAGGCTTTCC 1200
GCAGCCCCAG GCCTGGCAGT TCAGGTTGGC TCTGGAATGG CTCAGGTCCA AGACTGGCTC 1260
TCAGCTCAGC CCAGCCCCTT GGGGCGTGGG AGGCACTGCC CGTGTTGGGA TGCAGAAGGG 1320
ATCAGCTTCC AGTTGTCTTG GAGTTGATGA CTGACCTCTA 1360