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

TagContent
EnhancerAtlas ID
HS145-11477 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr19:6800820-6802030 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs332426chr196801966hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
POU2F2MA0507.1chr19:6801934-6801947CTGATTTGCATAT+6.5
POU4F2MA0683.1chr19:6801069-6801085ATCATCAATTATTCAC-6.42
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_17561chr19:6798623-6803806CD4p_CD25-_CD45RAp_Naive
SE_18804chr19:6799714-6804369CD4p_CD25-_Il17-_PMAstim_Th
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1968011166801467
Number: 1             
IDChromosomeStartEnd
GH19I006799chr1967995996804367
Enhancer Sequence
GCAGTCGGGG TTTCACCATG TTGCCCAGGC TGGTCTTGAA CCCCTGACCT CAAGTGATCC 60
GCCCGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCA CCCAGCCGCT 120
CACCATCTCT TTGTCGCCTG CATGGCACCA TTCTCTCCTG TACCACCCCA AAGCCTTACC 180
AGGTGCCTCC TGCATTTAAC CAGGTCCCAT AGCTCTCTGT GCTTCCCGGC ACACCCTCTC 240
ACCACCCTCA TCATCAATTA TTCACCTTGC TGACTGCTTA GTGTTTGTCT CCTGGCTGGA 300
TTACATAAGC CCTGTAAGGG CAGAGCTCTG TTTGTCTTGA TCACCATTAG GTTCTGGTGC 360
TTGGCATACA GTAGGCATTC CACACATGCT TGCTGAATTA ATGCATGACC GGGTCTGGGG 420
TGCTGGGTTT CACACCAGGC TCTACCGCAA ACATTGGGTC AAGTATTTTC ATTCCCGACG 480
TACAGATGAG TCAATTGAAT CAACGGAAAG CAAAATGATC CCATCCAAGC TCCCTCAACT 540
TGCCGGGCTG GTCTGGGAGT CGAACCAGAT CTGCCTGACC CTCCCACCGG TGCTGAAAAG 600
TGGAGTGTGT GCTGGGGTGG TAGGGGATGG GGCAGAAGAG AGACGGGCTT CCTCACAGAA 660
GGGTTTGAGG GCTAGGATGA GGCGTGCACA CTCTGCACCC CTGCTTCGGA GCTTTGAAAG 720
GGTGCACAGC ACACCCGCCC TCTCTGGGAA CCCTCGGGAG CTTGAGGTTG CCTGATGAAG 780
GGGCTGATGG GTTGAACGCA AAGGGCCCCT CCACCCACCC TTTTTTCTAT CTCCCCAACC 840
AAGCCCTGGT AACAGGCATT TCCGGTTTCC GGCCGGCTCC CTGGTGCTGG GGTGGGGGTG 900
GGGAGTTGAT TGCTGCCGTC GTGCTTGGCT CTGGGTCCCC TTCTCCCAGA CCCCAGAGGC 960
CTCTGTCCCT GCACACTGCT TCCCCGAAGG AGCGTGGAAA GCCAGCCGAC CTTTCTGGCT 1020
CTTTCTTCAT CTTGGGCAGG GGTTTTGTTG ATGGGAGGCT GGCTGGCAAA TGGGGAAGAA 1080
TGAACCTCAG GGTTCACCGC AGTGCGCCTG GGTGCTGATT TGCATATGGG CACGATGCCA 1140
GCACAGTGGG TGCCCGCCTC TTCCTGGAGG AAGGAAGAGG GGCACTGAGG GGGGTTGCCC 1200
CCAGCAGGGA 1210