EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS059-09296 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr11:120057040-120058450 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs508205chr11120057343hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr11:120057750-120057765GTGCCGAGTCAGCAT-6.37
MAFFMA0495.3chr11:120057750-120057765GTGCCGAGTCAGCAT+6.53
ZNF263MA0528.1chr11:120057212-120057233CCTTCATCTGCCTGCTCCTCC-6.18
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_05542chr11:120056921-120058407Brain_Cingulate_Gyrus
SE_06298chr11:120054796-120058689Brain_Hippocampus_Middle
SE_08308chr11:120056426-120059455Brain_Inferior_Temporal_Lobe
SE_23315chr11:120055000-120060848Colon_Crypt_1
SE_24076chr11:120055045-120058642Colon_Crypt_2
SE_27662chr11:120052269-120061818Fetal_Intestine
SE_28582chr11:120052177-120062136Fetal_Intestine_Large
SE_30245chr11:120054297-120060125Fetal_Muscle
SE_35389chr11:120053289-120058488HepG2
SE_50205chr11:120052336-120061675Sigmoid_Colon
SE_52530chr11:120052757-120060880Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11120057341120057971
Number: 1             
IDChromosomeStartEnd
GH11I120181chr11120052529120061573
Enhancer Sequence
GCAAAGCAAG GGGGTCTGAG GTGGCCCAGC TCTGTCCCTG CTCCCCACAG ACACCTGCTA 60
CCCTGGGCAT CCTACAGCTG CACTCAATCT GCCCCTCCTT CCTTCCTAGG CCTTAGGAAA 120
TATCTGTTCA TTTTGTTTCT TTCCACTTTC TCTCTCCCCT TCTTCCTGTC TCCCTTCATC 180
TGCCTGCTCC TCCCCAATCT GTCCTGAAGA GTACATTTCT TTCCCCATCA GGGAGCCTTG 240
TGGGAATCTG GGGGGCCTGG GGCTGAGGAA GAAGAGACTT CAGATCCAAG AGCAGCCCTG 300
AAGGATTGAG GGAGGCAGAA GGGGTGTCAG CCACTGGGCA GAGGAGTTCC TGGCAGCAGG 360
GAGGGCCATG AGATAATTAG CCCTAGAGCT TTCTAGGCCT CTGGAAAGAT GTGGGGTACA 420
GGAACAGAAG GGAAGGAAGA GGCAGGTCAG GACTGGGGGA ACTCAGGTTC CCTGGCCTGC 480
CTGACAGAGA CAGCACATGG TAGAGTTGAG AGGGGAGCCA GGGTCAGGGA CAGGGCAGGC 540
AATGGGAAAG AACAGGGACA TTCCCAGGCT CAGGAGTCCC CAGGTCTCCC AGGGGAGGGT 600
AGTCCTCGCC TGAGGTTAGG TGGCGGGCCC CGACTGGCTG GGAGTGGGTT TCTGTACGTG 660
GCTGGAGGTG AATCACACCT TCTGTGTGGG TTGCATGTTT ATATGTGGGT GTGCCGAGTC 720
AGCATGCGTT GTCCTGCGTG TCTGCTGGTG TATGTAGGTG TTACTGGTGG GTGACAGGTC 780
AAGGGTGTGC CCTGGTGAAG CGGGAGGGTG CCTGTGTGTG TCTGTGGGCC TCTAGACCTG 840
AGGAACCATG CTTGAGTTTG TTCTCAGAAT GTGCTGGCAT ATCTGTGTGC CACGTGTCCC 900
TTTCTCTGTC TCTGTGTGTC CTACTGAAAT CGGCTGTGTG CAGGAGTGTG TCTGCGTATG 960
TGGGTGTGTT TGTGCAGGGG CCAGGGAAGG GTTATTCATA GAAGCAAGAA CTGACTCTGG 1020
TGGGACACTC GTGCAGAGAT GGGGAGGCAC GTTGGGTGGG TAGGTGGGGG GCAGGCACTG 1080
TGTACACCAA CGTGCTCCGA ATTCCAGCAA ACTCCAGTGC CTGAGTTTCC AGCTGTCCCA 1140
GCTCAACTGT GCACAGATGT GTGCCGCTTT GCTACAGCCA TAAACAGACC TCCCAGGATT 1200
TTTCCAGAGG AAACGCAGAA ATATTTTGGT GTCTGCTCTT GGTAGTAGGA AAGAGAGTGG 1260
GGATGAGGCT TGAGGCTAGG GCTTCGAAAC AGAGGGACCA CAGTCAGAGG GGAGCTGAAG 1320
AGGCAACAGC ATCCCCCACA GGCCAGCAGG GTGGGGGAAG AGCTGTGATG GCTTCCAGTT 1380
GTGGGGTCCT CTCTAAGGCC CCAGCTAGCA 1410