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

TagContent
EnhancerAtlas ID
HS073-02046 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr10:121060610-121061560 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr10:121060991-121061002ACAGGGTGTGG-6.14
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_00490chr10:121060377-121062038Adipose_Nuclei
SE_01929chr10:121060533-121063667Aorta
SE_10590chr10:121060459-121061857CD19_Primary
SE_11224chr10:121059325-121070010CD20
SE_18649chr10:121059241-121063302CD4p_CD25-_Il17-_PMAstim_Th
SE_27473chr10:121060607-121062391Esophagus
SE_31412chr10:121060338-121063812Gastric
SE_42191chr10:121060469-121062237Lung
SE_48573chr10:121060605-121061537Right_Atrium
SE_50131chr10:121060491-121062817Sigmoid_Colon
SE_52365chr10:121060481-121063136Small_Intestine
SE_54449chr10:121060459-121062073Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10121060989121061309
Number: 1             
IDChromosomeStartEnd
GH10I119300chr10121059772121067576
Enhancer Sequence
GTCCCAAAAG AAAAAAAAAA AAGTGCAGAA CCCATAGACA TACTGCTGGA TGGTTTTTCA 60
TAAAGTGATG AAGTGCATAC CCTGTGGAAC CCTAGTCAAG AAGCACGTCA TCTACACCCC 120
AGGACCCTCC GGGAGCCCCT TCCAGGCCCC ATCTACCTTG TGGTGGTTCT AACGCCATGG 180
GTTAGTCTTG CCTGCCTCTG AACTCTGGGT GAAAGGAGCC ACGCAGCCTT GGCCCTTTTG 240
AGGCTGGCTC CTTTCACTCA CCATTGTCTT TGAGATTTGG GCCTGTGGCT GTGTGCAGTT 300
GTGTTTGGTT CATTCTCGCT GCTGAGTCCT ATTCCCCTGT CTCCACACAT AGTGGGTGTT 360
CACAGCAGCC CCACGAAGTA CACAGGGTGT GGACTGTTCC TCCTGTTTTA TAAGAAAGGA 420
AGCCCAGGCT TGGTGTTACC CACAGCACAG AGGTGGCTCT AGAGCACGCC CCATCCGATG 480
GCTGCTGAGG AAGTGACTTG ATCTTTCTAG GAGCGTCTTG TCCTCTGCCC AAGAAGTTGC 540
CAGCAGCTTT CTCTTTAGTC TTCCAGAAGC CCCTGGCTCT CCTTTTGAGT CACTTTGACC 600
ACGCCTCCTT ACCAGTCAAA CCGTGGGTTT TCTGAATTCC TGGAAGTGCT CTTTTAGCTG 660
CTTTTCTGAT CCCTGAACAG CAAACACTTA TCGTGGGTAG CATTTTCCTC TGCCAGGCCA 720
ATGGCAGACA TTACTAACTA ATTGTGGGAC TCCTGTTCAT TGAGCCTGGA CCCTGTCTTG 780
AGTTCCAGGA TTCCCGGCAG CCACTGCCAT CTTTTTGGAG CTCATTCACT TAATGAAATC 840
TTTCTGCTTT TGTAGTGCCA GGTGGTACAA GCAGAGTTGC ACTTTCTGCT GAGGAGACTT 900
GATTTCTTAT GAAAATACCA AGCAATGAAG GAACGCTGCA TTTCTAAAGC 950