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

TagContent
EnhancerAtlas ID
HS127-31221 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr8:144300700-144302570 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56960668chr8144300760hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr8:144301184-144301199GAGGTCAGAAGTTCA+6.38
Nr5a2MA0505.1chr8:144300732-144300747GAGCTCAAGGTCACA+6.38
RARAMA0729.1chr8:144301184-144301202GAGGTCAGAAGTTCACGT+7.2
RFX2MA0600.2chr8:144302497-144302513CGTTGCCTTGGAAACG-6.19
RFX2MA0600.2chr8:144302497-144302513CGTTGCCTTGGAAACG+6.3
RFX5MA0510.2chr8:144302497-144302513CGTTGCCTTGGAAACG-6.41
RFX5MA0510.2chr8:144302497-144302513CGTTGCCTTGGAAACG+6.65
ZNF263MA0528.1chr8:144302420-144302441CCATCCCTTTCCTCCTCCTTA-6.29
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8144301806144302247
Number: 1             
IDChromosomeStartEnd
GH08I143217chr8144299859144303931
Enhancer Sequence
GTACGAAAGC CTGCAGCTGC GACATGAGGC TCGAGCTCAA GGTCACACAG CTGGGCGGTG 60
CAGATCCAGG ATCCAGTCCC CGGGCTTCCT GCCAACCGCA CCCAGCTTCC CAGAGGTGTC 120
CCAGGCTCCA GGACGCCTCA GCTGGGGAGG AGCTGGATGT CAGCCAAGAG CCAGCCAGAT 180
TCCCAGGCCA AGTCGAGTCT GAGCCAGGCA AGTCAGCGGT GCCAACGGGC GGATGGTCAC 240
AGCCAAGACA CCCTGGGCCC CGTCTCAGAG CCCAACGCAT GCTGTCAGTC TCAAGAGTGA 300
ACATAGAGGG ACCTCCCTTT CTCATCCAGC CCAGCAGCAG GGAGACTGGG GGCTGGGGGG 360
CTGGGCAGGG AGGGGGCAGG GCCCTGGCCC AAGAACCCAT GTCCCTCTGT ACCAGTTTCC 420
CAGGGCTGCC ATAACAAATC ACCACGAACC TAGTGACTTA ACACAAGTTC ATGCTGTGGC 480
TCTGGAGGTC AGAAGTTCAC GTCAGGGCTC TGGCTGGGCT GCGTTTTCTT GGGAGAGAAT 540
CCACCCCCGC CCTCTCAGCT TCAAGAGGCC ACCTGCTCTC CTTGGCTCAT GGCCCTTCCT 600
CCACCTTCGA AGCCGCTCCA ACCACTGCTC CCTCACCAGC TTCCCGAGTC AGCTCTCCCT 660
CGGCCTCCTT CTTACAGGGA TCCTGTGACC ACAGTTAGGA CTCGCCTGGA GAATCCGGAG 720
CCATCTCCCA TCTCAGATCC TCCGCTTCCT CATGGCTGCA AAGTCCCTTT TGCCATAGAA 780
GGCACATTCA CAGGCTTGAG GATTTGAACC TGGGTATGTC AAAGACCTTT CCTGAGCCCA 840
CATCAGCCCT TCCCTGGACA CCTGCTCCGA GACTAGCTGT GCTCTGGAAG CCACGGTCCT 900
GGGGAGGATA AAGCCCAGCT CCCTGGCTCA AGGGGGCCAC AGTCCCAGGA AGGAGGCCTT 960
GCCGGGCCCC TGGTGGCCAC AGTCCAGAAG TCAGTCCCAC AGTGGTCTCT TCCTGCCCCA 1020
GAAGAATTCA GGCCCCTTCG CCTGTGCTCA TCACGAGAAG CCGGGCAGAG GCTTGTTCTC 1080
ACTCTGTCTC TCCCGCACCC CTTGGGTCTG CCCACACCCA GGTCTCCCCG CCATCAAAAC 1140
TGACCAAGAC CAGGGTGCAG TGCCTGACTC ACTCATGGGA CAAACCCTAA CCACGCCTCC 1200
CTCCTGACTC AACTCATGGG ACAGACCCTA ACCACGCCTC CCTCCTGACT CAACTCATCG 1260
GACAAACCTT AACCACGCCT CCCTCCTGAC TCAACTCATG GGACAGACCC TAACCACACC 1320
TCCCTCCTGA CTCAACTCAT CGGACAAACC CTAACCACGC CTCCCTCCTG ACTCAACTCA 1380
TGGGACAAAC CCTAACCACG CCTCCCTCCT GACTCAACTC ATGGGACAGA CCCTAACCAC 1440
ACCTCCCTCC TGGCTCAACT CATCGGACAA ACCTTAACCA CGCCTCCCTC CACCATGAGC 1500
TCTGGCCACT CCCACATAAG GACACACGAG GACACAAGGG GCGTCTGACA CCCCCGGGAC 1560
TGGGCCCCCA ACCTCTGCCC GCCAGCCATT CGGGGACAGG TGGACTCAGA TACGTGGGTG 1620
GGGGAGACCT GGGTGTGGCA GAGCCGAGGG AGTGCAGGAG AGACCGTGAG AGCAGGACTC 1680
TGCCTAGCAC CCTGGAGATC CTCCCCAGAA CCCACCAGAT CCATCCCTTT CCTCCTCCTT 1740
AGGGACTGGG GCCGGCAGGC ACTGCTCCGG CACCCACTCT CTGGAGGATG GAGCCAACGT 1800
TGCCTTGGAA ACGGGCATCC AGGAGTGGAG TTCATTCCTA ACACGTTCGG CTTTTTGTCT 1860
CTTAATTCAT 1870