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

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EnhancerAtlas ID
HS077-06902 
Organism
Homo sapiens 
Tissue/cell
H128 
Coordinate
chr2:218661740-218662650 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr2:218661815-218661836AAAGAAAAAAAGAAAGAAAGA-6.34
Nr2f6(var.2)MA0728.1chr2:218662107-218662122TGACCTCCTGACCTC-7.19
TCF3MA0522.2chr2:218662507-218662517AGCAGGTGTT-6.02
ZNF263MA0528.1chr2:218661918-218661939GCCCCATCCACTTCCTCCTCC-6.99
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_00005chr2:218652544-218667684Adipose_Nuclei
SE_01533chr2:218661708-218662912Aorta
SE_26522chr2:218661742-218662752Esophagus
SE_36939chr2:218660099-218663160HSMMtube
SE_42142chr2:218661810-218662890Lung
SE_46622chr2:218661846-218662038Ovary
SE_48080chr2:218661820-218663137Psoas_Muscle
SE_48661chr2:218661829-218662804Right_Atrium
SE_51206chr2:218661726-218662831Skeletal_Muscle
SE_54481chr2:218660446-218667341Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr2218661949218662000
chr2218661903218662378
Number: 1             
IDChromosomeStartEnd
GH02I217797chr2218661924218662603
Enhancer Sequence
ACTGCACTCC AGCCTCCTGG GTGACGGAGT GAGATTCTGT CTCGAAAGAA AAAAAGAAAA 60
GAAAGAAAGA AAAGAAAAGA AAAAAAGAAA GAAAGAAAAT GCAAAGGTCC TTTGGGTATT 120
CTGTGTGATA ATGTGTGTCA GAAGAGCTGC CCTTCCTCAA CCAGAGCCCT CCACTGCTGC 180
CCCATCCACT TCCTCCTCCT TGAGGCACCA AGAGCACAGC CACCTCACTG CTGAGTCCCC 240
TGAAAGGCCA GCTGCATCAG CTCGGCTCAC AGGCCGTAGC TTGTCTCTCT CATCAGACAC 300
TCCTCCCCTG TACCAGGCCC ACCCCTGAGG TACCTACATC CCTCTGCAGC TGGCCAGTGT 360
CAGGGGATGA CCTCCTGACC TCCCCCATCA CACACCCAGG AGCCCTGGTC CACACCCTGG 420
GAAGCCAGCC TACAGTCTAG CCCGTGACCC CCTATCTGAC CAGTGACATC AGTTTGGCTT 480
CCCACTTGCC CATGGCTCAT CAGAGTCTGT CTCTCCCCTC AGAAGCCAGC CCTGAGAGCA 540
GAGAAAGAGG CAAGAGCTAG GAAGAGCCTG GCTGAGAAGT CAGCTCACCT GGGTTCGTAG 600
CCTGGCTGGG CCACTTACCC CAACTCTGTG ATTTTGAGTA AGTGTCTTCA CCTCTTTGAA 660
CTCCAGTTTC TTCAACTGTG AAATGAGGAC AAGGATAGCC CTTACCTCTC AGGTGCACGT 720
GCGTGAGAAA TGATACCCAA GTGCTTAGCA CAGGCTCTCT GGCACGTAGC AGGTGTTGGC 780
TGAGTGCCAG CCTTCACCGG TGGTGGTGAT GCTGAGTACA AGTTCTGCCA GCTAGAAACT 840
GTGTGACCTC TCAGAGCCTC GGTTTCCTTA CTTGTCCCTG TGTATAACAG CGCCTACCTC 900
ATGGGTTTGT 910