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

TagContent
EnhancerAtlas ID
HS108-18951 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr19:510380-511790 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:510762-510781CACTGCCCCCTGCAGGTCA-6.99
ZNF263MA0528.1chr19:511236-511257CCTTCCTCTTCCTCCTCCTCC-10.3
ZNF263MA0528.1chr19:511233-511254CTGCCTTCCTCTTCCTCCTCC-6.87
ZNF263MA0528.1chr19:511239-511260TCCTCTTCCTCCTCCTCCCTC-8.84
ZfxMA0146.2chr19:511619-511633CAGGCCTGGGCCAG-6.14
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_17708chr19:505979-515548CD4p_CD25-_CD45RAp_Naive
SE_23026chr19:505960-513081CD8_primiary
SE_54247chr19:510330-511994Spleen
SE_68663chr19:506207-533817TC71
SE_68664chr19:506207-533817TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr19511222511648
Number: 1             
IDChromosomeStartEnd
GH19I000510chr19510241513382
Enhancer Sequence
AAAAAGAGAA GCTCAGAGCC TGGCAGATTT GTCCCCACTC AGTCCAGTGT GTTGACCCCC 60
AAAGGCTGAG GGGCTGACTG GGGCTGCTCC TGAGAGCATC ACCGTGGTAG GCTGGGGGAG 120
AAGTCACCCC AGATCCTCCC TGGCACCTTC TTTTGAGAAA TGGCAAGCTC CGGCCGCCAG 180
GGCTGGTGAT GGCAGCCACA GTGTCCCCCT CCTGCCACCT TCCTGGTCGT CTCCAAGGCC 240
CCCTGGAGCA CACACACAGA CGTTACATGA CTTGCTGAAG GCCACACGGC CACCGAGGGC 300
AGAGCTGGGG TCAGAGAGCC CCAGAGTGCA GCCCCGGAGG CCTCCTCAGC CACCACGTTG 360
CTCATCCTGG CAGCAAGGGC TGCACTGCCC CCTGCAGGTC ACTGCCAGGA AAACGTGCAC 420
GAAAACGAAG CCCCAGCTGA TCTGGGCCAG GGTTCCCCCG ACTCGTCCTC TGGGGGCCGT 480
CCTGGGTACT GCAGGGCCCT GAGCAGCGTC CCTGGCCTCC ACCCACTCCT TGCCAGGAGC 540
TCCCCGAGTC GTGACAACCA CAGATGTCCC AGACACCGCC CGGCGTCTGC TGGGGGCAGG 600
AGTGGGAAGC AGAAGTCTAA GGTGTAGGGT GGCTCCTGTC TCTTTCTGGA GACGTTCCAT 660
AAATAGAATC TTTCCTGTAT TAACAAATGC TCACACGCCT TACAAACCGC TCTGTGTAGG 720
AGCCGACACA GACGGAGCCC TGGCTGGGCT CCCGCTTTCC ATTTTGCAAT CAGGGAAACC 780
AAGGCCCAGA GGCCACCGTC ACAGGCAGAG CTGACGTTCC AGCCCCGGCC TCCTCCTCCG 840
AGCCCAGAGC TTGCTGCCTT CCTCTTCCTC CTCCTCCCTC ACCCGATGAT TCTGCTGGGA 900
GCCGCCCGGG AGCCCAGGAG GGGCGGGTAT GCGGCCGCCT TGAAGTGGGC TGTCACCTTC 960
CTGTCTCCTG CCGTCATCAT GGCTGTGATC TCACCAGGCT GTAATTACCT CTTTGTGTGT 1020
CTTCCTGCCC CTCAAGGCAG CTGTGGCTGA GCTGCAGCCC TAATTACAGC CCAAAATAAG 1080
CAGGTGGGGC CTCCCACACG TATGCCAGCT GCTGTCCTGA GCACCTGGCT CCAGCCCCGT 1140
TCTCCCGTCC TCACAAGAAC CCCCACTCCG TAGATGCACA AGGCCAGGTG CAGAAAAGGA 1200
GAGTGCACAC AGCTGGGAGG GGCAGACGAA CACCCGAGGC AGGCCTGGGC CAGGCACAGA 1260
GCCCTGCACA CCGAGGGGCC GCGTGGATGC TTGCGGAGCT GGACCAGGGC TGCCGCCCCC 1320
AGAGAGGAGA GCATTTATGC AGAAGTGGTG GTGGATGGCG CTGGGTAATC CCGGCCCACA 1380
GACCTGTCAG TCAGAAGCTG CGAGCACGAC 1410