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

TagContent
EnhancerAtlas ID
HS047-07237 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr12:726240-727330 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TFAP4MA0691.1chr12:726629-726639AACAGCTGAT+6.02
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_00367chr12:726365-727464Adipose_Nuclei
SE_05306chr12:726363-729970Brain_Cingulate_Gyrus
SE_06214chr12:723128-729920Brain_Hippocampus_Middle
SE_09786chr12:724884-728477CD14
SE_30303chr12:726299-727391Fetal_Muscle
SE_40967chr12:726136-727429Left_Ventricle
SE_42232chr12:726198-729719Lung
SE_48311chr12:723105-729807Psoas_Muscle
SE_48881chr12:726269-727408Right_Atrium
SE_53753chr12:723125-729061Spleen
SE_62689chr12:719155-796233Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12726826727017
chr12726277726327
Number: 1             
IDChromosomeStartEnd
GH12I000615chr12724465727490
Enhancer Sequence
GCACACCTGT AATCCCTGCT ACTCGGGAGG CTGAGGCAGG AGAATCGCTG GAACCTGGGA 60
GGCGGAGGTT GCAGTGAGCT GATCACTCCA TTGCACTCCA GCCTGGGCGA CAAAGCAAGA 120
CTCCATCTCA AAAACAAAAA AGTGTGTTCA CCCCCTGTTC TTGCCCTAGG TCCCTAATCT 180
AAGCGAAGTT GTTGTAGTAA AGCCTGGGAT GCGCTAAGAG GACAACAGAG GAAAGACACT 240
GGGGGAAGAG CCCACAGCAG TCAGAGCACG TCCTCCCCTC ACGAAGCCTT CCCTAAAGCC 300
CTGGCCGCGT GCTGAGAATC CTTCCTTCTA ATCCTGCCCC TGCATATCCG TGGCCCAAGC 360
ATTCCTTCTG CCTCCAGACC TGCCTCCACA ACAGCTGATG AGGCAAGTGT CCTGGCTGAA 420
GCGCAGCAGT TCACATCCCC TTTCTTTCTG GCCTTGACAT TAGAGGATGC CTGTGCAGCT 480
CTGAAGCTCC TGGGGATAAA AGGCTCAGGC TGCTGTGCTT CTTCTCACAG GTCCCTGAGC 540
TCCCCCAGGG CTTTCCTACA CAGAAGGCCG GCTGGCTGAG CACTCCCAGC TGCAGCCCCG 600
CTGGCGTCGC CGTGTTTTCT GTGCTCTGCG CTCACTCCCC AGGACGTTCT GGTTTCCTCA 660
TCTCAGCTCT CTTTGTTTAG CCACAGAGAT TGGGCAACTT CTGTTGGGCA GCGAGGTCAG 720
GGCCCTGCCT CCTAAGAAGG GGCCTCTCCC TCACAGGTCA GTCTGAAGTC ACTTGTTCTC 780
CAAGCCCTTG CTCACCCCAG GGCCCTGACA CTCAAGTCCA TCCAACACCA GGTGCCTCTT 840
TCTCTGGGCA CTTGGTGCCC AGGTAAAATT TTCAGATATT ATTGCTGTTT TTAACATTAT 900
TCAGTGAATA ACGTACTCTG GTGGTCTGAA AGGGATAAGG GGGGATTCTG ATTTACGGAT 960
TTAATGTCAG ACTGCATAAA AGCCTCCTCT CTCTCCTTCG GAAGTTTTCT AGGGTGCTAG 1020
GTGGCAGCAA CCCTGTTCTG TCAATAGGAC CATCTGAACC CGTAGGAGCT CCTTGCTGGA 1080
CAATGCCAAA 1090