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

TagContent
EnhancerAtlas ID
HS044-02636 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr11:86229890-86231040 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
LMX1BMA0703.2chr11:86230575-86230586TTAATTAAAAC-6.14
MEF2AMA0052.3chr11:86230739-86230751GCTATTTTTAGA-6.52
MEF2BMA0660.1chr11:86230739-86230751GCTATTTTTAGA-6.22
MEF2CMA0497.1chr11:86230738-86230753TGCTATTTTTAGAGC-6.29
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_37591chr11:86229369-86231214HSMMtube
SE_38572chr11:86225520-86232167HUVEC
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr118622989286231005
Number: 1             
IDChromosomeStartEnd
GH11I086513chr118622441186231883
Enhancer Sequence
GCAGGAAGAA ATAGCCAAGG GATGATAGAA ACAGAGATTG GACTGATGCA TCCAGAGGCA 60
AGGAATGCCA AGGATTGCCA GCAAATAACA GAAGCTAGAA GGGGCGGCAA GGAGTGTCCC 120
CCACAGGTGT CAGAGGGAGC ACGACCTGCT GACACCTGAT TTTGGACTTC TTGCTGTTAG 180
AACTATGAGA AAATAAATTT CTGTTGTTTT AAGCCATCCA ATTTGTAGTA TTTTGTTACA 240
TACAGTAGCC CTAGGAAGCA AATATGCCAA CCATCCAATT TTTGTGTAGT AGCTATGAGT 300
AGTGGTGATA TCACAATTCC TTCCCTGTAC ATTTCTTAAA GCTCAAAGTC TGTTGGAATT 360
TCATCAAGGC AAGTGTAAGT GAAGTTTCCT CCATCTGACA AAGGCATGCA AATTACATCA 420
CTATCTTCAG TTTCCATCAG GAGCCAGAAA AATCCTCTTG AATGTTTGAA TTCAGTTACA 480
CGAGAGAGAA AGAAAAACAA AGATAATGTT CACTTAGGAG AATGTTATTT CTTGAGAAAA 540
AGACTCTTAA CCCTTATCTC GGCCTGTAGA AGAGTGATTC TTGCAAATTT CCTAAAATAG 600
AATTGAAAAA AGAACCCTGA ACAACACCCA CTCAAGTAGA CATGTTCATT TAGGCTTCTT 660
GGCACCAAGT CCAGCAATAA AGGGCTTAAT TAAAACAGAG TCAGTGACAT TAGGCAAACC 720
CCTGCAGCTG GGCTCAGGAG GAGGGATATG CACTTTCAAC TCTAACAAAG GCTCGCTGTT 780
GCCAATGGAA CCACCATTCC ACATATTTTT TGGCAGGAAG GGAACCTGTC CTCTGAGAAC 840
CTGCAAGATG CTATTTTTAG AGCTCAGTAG CAGTCTCCCA GAGGCAACAG TACAGCAAGA 900
AAACATAGCT AGGTCTAAGA AGCCCAGGAA GCAGATCTAA GAAATCCTCG AAGGCTGTGT 960
AGGCCTGGAG GGCAGAACTG GAGAGACTCA AGTGAGGTAA CTGTCCATGC CTTGGAAGAG 1020
CTTTAAAATC ACACTTTCCA CTGCTTTCTG TGGAACGTCC TCAGGGACGT GTGACTGAAG 1080
TGCGGGATGG GGTGGCCACA GACAACTGAA CATGTTAGTG GTGGTTCACT CATAATCCTT 1140
CTTTGGTGTT 1150