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

TagContent
EnhancerAtlas ID
HS182-19526 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr7:2529320-2530500 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs10282122chr72529623hg19
rs2969072chr72530431hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6MA0677.1chr7:2530086-2530100AAGGTCACAGGTCA+6.47
RREB1MA0073.1chr7:2529755-2529775CCCCCACCCACCCGCTATCC+6.61
RxraMA0512.2chr7:2530086-2530100AAGGTCACAGGTCA+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr725296412530385
chr725304092530497
Number: 1             
IDChromosomeStartEnd
GH07I002489chr725291342530412
Enhancer Sequence
AACCCTGGAG GGAGAGGCTG CAGTGAGCCG AGATTGTGCC ACCGCACTCC AGGCTGGGTG 60
ACAGAGTGAG ACTATCTCAA AAAGAAAAAG GAAAGAAAGA AAGGTGGGCT TGTGCGCCAG 120
GCTGGGAGCC AGGCAGAGGG TTCTGGGCGC TGACTGCCCA AGGAAAATGG TGTGAGAGGT 180
GCTGGCACAA GGCCTGGGAG GGGATGCTTG GATTTAGCAA CGAGAGGTCC TCAGAGGGCA 240
TGGAGTGAGT GGGCAGTGAG GAAACGGGGA CCCTTCCTCC CCCTTTCACC CCCCTTTCCT 300
GTCTCCCTCG GTCTCCACCC TCTCCACCCA CCATCCCAGG ACCCTGCGCT CTGGGGGCAG 360
AGCAGACACA AAGAGGGGCT CAGGGGCTGG AGTCTGGCTG CCACTCACCC TGGCCCCCAG 420
GGCCACCAGG GGCCACCCCC ACCCACCCGC TATCCCCGCT CCAACTGCTG CTCCCACTTC 480
CCTCGGCCGG GACGGGACAC AAGAGTCTTT CAAAAACATT TCCTTTGCAA AATAATCCTT 540
CCAAAAATGT TTTTGGAAAC GGACTCCTGA TCTGAACAGG AAGACGTTAA TTATGGTCCC 600
TCCCCAGAGG GGCAGGGGGA GGAAGCCTGG TGGTCGAAAC AGGAGCGGGG GCCAGGACAG 660
CCCCAGCCCA CACCCAGCCT CAGCCTCCTG CCCCCCAGGC CCCTGGGCCC AGCCCCTCCA 720
CCCACAATGG GGAGACAGAG ACTTAGGGAG GGCCAGCGAC ATGGCCAAGG TCACAGGTCA 780
GAAGCTGAGC AGGGTGGAGT CTTCTACTTC TGCTGCCACG TGGCATCCGT GCGAGAGCGT 840
GGCGAGGCGT TGTGCATTCG TGTGTCTCTG TGCCTTTGTG TGCAGGAGTG AAGGTGGGGC 900
GGGGGCAGGC AAGGAAGCTC CCAGGGTCCA CAGCCTCCCC AGGCCTGACT TCCTCCCCCA 960
GCAGGCCACT TTCCCCTGGT GCCCAGGTGT TGGCCGGACT CCGACTACAG CAAGGAGGAA 1020
GGAGACAGGG CTGAGGACCT CCCTTTCTGC TGCTGCTCTT AAGCGCCAAC CACCCTCCAA 1080
ACAAGTGCCA TCTGGGATCC CCCTGGGCCT AGATGAGGTC CCACCATAGA CGTTTTCTGA 1140
ATGTACCTAT GTCCATCTCA GTCAGCCCTG ATGCTTATGT 1180