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

TagContent
EnhancerAtlas ID
HS098-14338 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr12:105776340-105777520 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr12:105777300-105777319TACTTCCCCCTGGTGGACT-6.3
FOSMA0476.1chr12:105776556-105776567TCTGACTCATT+6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12105776400105777369
Number: 1             
IDChromosomeStartEnd
GH12I105382chr12105776296105777580
Enhancer Sequence
CTATAAGAGA GACAGGAAAT ACTGGCTTTC TGTTTGTGAT GAAATGCAAA TTCCTTATGT 60
ATTTTTCCAA AATGTTTAAA ATGAGGCTTT TGTAATCAGA AGTATATAAG CCCCCTTCCC 120
CCAAAGAAAA TGATTATTCT ACTGCCCGTC TTGACTGTAT TCTTACTTGG GGGCAGGGTG 180
GGTGGCGTGA ACAGGGAGAG CTAATCTCTC CTTCTTTCTG ACTCATTCCA CAGTCAATCC 240
TTTTTCTTAT TATTTTCCAA AGGCATGAGG ACCTTCCATG TTCCGAAACC ATTGTCCAGA 300
GTATTTCTTC TGGACTATTT TCCACTTCCT TCCATCTGAC CGGCCAGCTG TTCTGCATTT 360
GTAAAAGCTG GTTTCTGATG TCATCTCTAG GCAGGACCGC TCCCTCCCTC TCCTGCACTC 420
CTATACTTCG TGGCATATCC GCCCCAAGAT AACACTTGTC ACTCTGTTTT CCAAATTCAG 480
TTTCATTCAT TTGCTTCACA TGTGCACTGA GCCCACTGAC TTCTTTCCCT GTCTGTTGCC 540
AGCACTGGAG ACCAAGCCTG CACGCTTTGG CCCAGACCAT CTCATTCACC TTTTAACACA 600
GAATCAGGGT GAGTGGAGAG TGGGGGAGTG GTGTGGTGGG TCTTTGCCTC TCGCTGTTCA 660
GTGAACTTCA TGCCTGTCCT CCTGATCCCC AGCGCTAACA CAGGGTCAGG CTCGCGGGAG 720
TGAACAACCA CCATTTATCT CCGGCTTGTT GGGGGAAGCC CTTTCATTTA CTTGACAGTT 780
TACCTGTCAA TTTTACGTGC GTGGTCATTT TTAATCCTCT GCACTTTCAG GTAATAGGAA 840
AATAATTTGA ATCAAGTTCT TCCTTCACCA TTGGCGTAAA ATCGGTGATT AAACTTTTAA 900
TATTTAACGT CTTAAAAAAA ATTCCCCGGG CTAGCGTCAT GCCTAAGTAA TGCATGCATC 960
TACTTCCCCC TGGTGGACTC ATCTTCTAAT AGCAGCTTTG TTTTCCCCCC TTTATTATTG 1020
GCAGGAGTAA TCCATCTCTC ACTTTCCTTA ACACAGATAT TCATGGATTG CAGGATTCAG 1080
CAGTGTCTTC ATAATAGCAG GAAGTTTATG TTCTGGCTTT GCCACTTACT AGCTGTGTAA 1140
CTTGGGCAAT TTACTTAACT TCTCTGCGTC TCGGTTTCTT 1180