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

TagContent
EnhancerAtlas ID
HS073-05064 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr16:11707200-11708160 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr16:11707745-11707757GAATGTTTATTT+6.74
Gata1MA0035.3chr16:11707756-11707767TCCTTATCTCT+6.02
IRF1MA0050.2chr16:11708133-11708154CTCTTCTTTCTTTTTCTTTTC+6.32
KLF4MA0039.3chr16:11707570-11707581GGAGGGTGTGG-6.32
ZNF263MA0528.1chr16:11708102-11708123GCCTTCTCCTTCTCCTTCTCC-6.5
ZNF263MA0528.1chr16:11708108-11708129TCCTTCTCCTTCTCCTTCTTC-7.15
ZNF263MA0528.1chr16:11708105-11708126TTCTCCTTCTCCTTCTCCTTC-7.89
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_10082chr16:11705586-11708566CD14
SE_23656chr16:11705744-11708148Colon_Crypt_1
SE_27070chr16:11705764-11708228Esophagus
SE_31920chr16:11705719-11708162Gastric
SE_42648chr16:11705745-11708264Lung
SE_50207chr16:11705709-11708328Sigmoid_Colon
SE_52871chr16:11705643-11708238Small_Intestine
SE_53430chr16:11705562-11708227Spleen
SE_61608chr16:11668804-11735966Toledo
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr161170727711708060
Number: 1             
IDChromosomeStartEnd
GH16I011611chr161170565811710497
Enhancer Sequence
CAGAGAGACC AGACCTCCTG GGTCACCTGG GGGAATAAGC AATGCAGCCA GCTGCCAGGT 60
CCCAGGGCTG CCTTCTCCTG ACCATCTGGG CAATTCAGAC ACAGCTGGGT CTGAGGTGCC 120
AGAGTGTGTT GTTCCGCCTG TTTAGACCTG CCCCACCTCG AAGACATCGG TGATTCACAA 180
TCTTCCCTAG AACGGACAAC TCCTGGAGGG TGGGGCCCCT GCTGATTCAA ACTGGGCTCC 240
TATGAAAGCT CCCAGAGGGT GAGGGCAGTC AGGGAAGGCT TCCAGGAGGA AGTGGCTCTT 300
GTTGAAGGCT AAGCCAGAGT TAGGTGGGAG AGGAGCAGGA AAGGTGTCCT TACAGGGAGC 360
ACAGCCGGAC GGAGGGTGTG GCGTGTGCCG GCTAGGCAGT TCACACTGGT GGAACCGAGG 420
GCACAGAGGT GGCTGGGGCA AAGCCCAGAC AGAAAGGACA TCTCAGAAAT GAGGATCTGT 480
ACTCCGAGAG CCGGCCTCAC CCTGCCACAT GTTGTCAGAT GACCGGGCGG GCCACTTCTC 540
TCGCTGAATG TTTATTTCCT TATCTCTAAA ACGGAACTGA CAGTTGAGAT CAACGCCTGT 600
GTTCTGTGGG GTCCCTCTGC TTCCTGGCAG GTCCTGAGAT TTGGACACTT GCACATGACT 660
CATTCATTCC CAGCAACACC AGTCAACAGT GGAGCCGTTG TGCCCATTGT ACAGACGGGG 720
CAGCTGAGGC TTGTGCAGGC TCAGAAGGAT GTCCTAGTCT CTCTCACTCT CCTTTCTCCC 780
TCCTACGGAT GCTGTGACAA ATGACCACAA ACTAGGTGGC TTAAAACAAC AGAAACTGAT 840
TGTCACAGTT CTGGAGGCTA GAAGTCTGAA ATCAAGATGT CAGCGGGCTG GTCCTTCTGG 900
AGGCCTTCTC CTTCTCCTTC TCCTTCTTCT TTCCTCTTCT TTCTTTTTCT TTTCTTTTTT 960