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

TagContent
EnhancerAtlas ID
HS061-08773 
Organism
Homo sapiens 
Tissue/cell
GM12892 
Coordinate
chr16:11707150-11708190 
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
TCCACTTCTG GATCCCCATG GGATGGAGAG AGACGGGACA CTCGCATTGA CAGAGAGACC 60
AGACCTCCTG GGTCACCTGG GGGAATAAGC AATGCAGCCA GCTGCCAGGT CCCAGGGCTG 120
CCTTCTCCTG ACCATCTGGG CAATTCAGAC ACAGCTGGGT CTGAGGTGCC AGAGTGTGTT 180
GTTCCGCCTG TTTAGACCTG CCCCACCTCG AAGACATCGG TGATTCACAA TCTTCCCTAG 240
AACGGACAAC TCCTGGAGGG TGGGGCCCCT GCTGATTCAA ACTGGGCTCC TATGAAAGCT 300
CCCAGAGGGT GAGGGCAGTC AGGGAAGGCT TCCAGGAGGA AGTGGCTCTT GTTGAAGGCT 360
AAGCCAGAGT TAGGTGGGAG AGGAGCAGGA AAGGTGTCCT TACAGGGAGC ACAGCCGGAC 420
GGAGGGTGTG GCGTGTGCCG GCTAGGCAGT TCACACTGGT GGAACCGAGG GCACAGAGGT 480
GGCTGGGGCA AAGCCCAGAC AGAAAGGACA TCTCAGAAAT GAGGATCTGT ACTCCGAGAG 540
CCGGCCTCAC CCTGCCACAT GTTGTCAGAT GACCGGGCGG GCCACTTCTC TCGCTGAATG 600
TTTATTTCCT TATCTCTAAA ACGGAACTGA CAGTTGAGAT CAACGCCTGT GTTCTGTGGG 660
GTCCCTCTGC TTCCTGGCAG GTCCTGAGAT TTGGACACTT GCACATGACT CATTCATTCC 720
CAGCAACACC AGTCAACAGT GGAGCCGTTG TGCCCATTGT ACAGACGGGG CAGCTGAGGC 780
TTGTGCAGGC TCAGAAGGAT GTCCTAGTCT CTCTCACTCT CCTTTCTCCC TCCTACGGAT 840
GCTGTGACAA ATGACCACAA ACTAGGTGGC TTAAAACAAC AGAAACTGAT TGTCACAGTT 900
CTGGAGGCTA GAAGTCTGAA ATCAAGATGT CAGCGGGCTG GTCCTTCTGG AGGCCTTCTC 960
CTTCTCCTTC TCCTTCTTCT TTCCTCTTCT TTCTTTTTCT TTTCTTTTTT TTTTTTTTTT 1020
CTTGAGACAG AGTCTCACTC 1040