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

TagContent
EnhancerAtlas ID
HS148-13244 
Organism
Homo sapiens 
Tissue/cell
NHLF 
Coordinate
chr4:3389460-3390290 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6828057chr43389811hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr4:3389921-3389942AGAGGAGGAGACGGGAGGGAG+6.06
ZNF263MA0528.1chr4:3389938-3389959GGAGGAGGAGACGGGAGGGAG+6.83
ZNF263MA0528.1chr4:3389955-3389976GGAGGAGGAGACGGGAGGGAG+6.83
ZNF263MA0528.1chr4:3389972-3389993GGAGGAGGAGACGGGAGGGAG+6.83
ZNF263MA0528.1chr4:3389935-3389956GAGGGAGGAGGAGACGGGAGG+6.92
ZNF263MA0528.1chr4:3389952-3389973GAGGGAGGAGGAGACGGGAGG+6.92
ZNF263MA0528.1chr4:3389969-3389990GAGGGAGGAGGAGACGGGAGG+6.92
ZNF263MA0528.1chr4:3389834-3389855TCCACCCCCTGCTCCTCCTTC-7.24
ZNF263MA0528.1chr4:3389831-3389852CTTTCCACCCCCTGCTCCTCC-7.43
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_09504chr4:3385958-3393092CD14
SE_27206chr4:3385813-3392719Esophagus
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr433896423390154
Number: 1             
IDChromosomeStartEnd
GH04I003384chr433861283392596
Enhancer Sequence
TGTTCATGCT TTCTCTTTCT GCCGTGTTCT CACTTCTCCT TTCTGGCAGA AGACATTCAT 60
TTCTTGCAGG CAATTTATAC ATGAAAGATT TGCCTAATAT GTTTAGTTTC ACCATATATA 120
ATAAGTTTTA TTTGCCTCCA AAAGATTGCT TCTGTCAGCA ATAGATGCAG GAACCCAGAG 180
TTGTGTTATG TGTCCATTTT ACAGTTGTTT AAAAACCTGC ACCTCCCAAG GGTGGGAAGT 240
CTCTAGCTCC TCGCCGTGCT GGCTCTGTGT GTCCCTCTGA GGAAGTGTGT CCTGGCTCCT 300
CGCCACGCTG GCTCTGTGTG TCCCTCTGAG GAAGTGTATC CTGGCCACGC AGAGATCCCC 360
TGGTGCTAGG GCTTTCCACC CCCTGCTCCT CCTTCTTTTC CCAGTGTCAG ACCCTGGGGC 420
CACTGGGACA GGCCCGTCCC TCCATGGAGA GCCCCAGTCA CAGAGGAGGA GACGGGAGGG 480
AGGAGGAGAC GGGAGGGAGG AGGAGACGGG AGGGAGGAGG AGACGGGAGG GAGGAGACAG 540
TCATCAGCAC ACCCTGAATT TCAGGAACCG CAGTGGGCGG GCTGGATGTT TATTTAGTTC 600
CTTTTTGTGT TTTTGTTATT TTTCCATCTT CAGTTTCTTT GCTTATAAGA GTAAAAAGAG 660
CCAGTTATCT TGTTTAATGT GCACATGAGC TCTAGATCGG TGTCACATTC TGCCGTTGTT 720
AGATGTAGGG CACCGAGGCA GAGTGGGGAG ATCCAGCAGC TCACAGTAGT CTGCAGGTGA 780
GATGGCCAGA CTCAGGCCTG CAGGGGAAAG CCCTGGCTGA GAGGCCCCTC 830