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

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EnhancerAtlas ID
HS048-10216 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr13:30982170-30983170 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TCF7L2MA0523.1chr13:30982916-30982930CAAGATCAAAGGAC+6.15
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_00375chr13:30975726-30985706Adipose_Nuclei
SE_27321chr13:30981976-30984779Esophagus
SE_30915chr13:30982126-30984107Fetal_Thymus
SE_39413chr13:30982745-30984312Jurkat
SE_49940chr13:30982654-30983769RPMI-8402
SE_53158chr13:30982099-30984380Small_Intestine
SE_54302chr13:30982107-30983659Spleen
SE_55176chr13:30982233-30982599Thymus
SE_55176chr13:30982659-30983496Thymus
SE_58519chr13:30968372-31042217Ly1
SE_59984chr13:30968520-31022227Ly4
SE_60928chr13:30968309-30997757DHL6
SE_61447chr13:30927785-31042444Toledo
SE_62285chr13:30943739-31052350Tonsil
SE_66282chr13:30982745-30984312Jurkat
SE_68356chr13:30968406-30997248TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr133098280030983087
Number: 1             
IDChromosomeStartEnd
GH13I030407chr133098213430984790
Enhancer Sequence
GGGAGTCCGA GGCGGGTGGA TCACGAGGTG GATCACGGGT GGCCAGAGAA CAAGCTGGCC 60
AGCCTAAGGG AACATAAAAG AAATCGAATG AGGCTTTGCT CTCTCTATTT TAGTGACCGC 120
TGACTGCGGA GCAACGCTCT TGTGTTCTGC GGGCCCAGCA GCTCCGGGAA CGGTCAGCGT 180
CGGGGGCCAG CCTGGCGGGA CATTTGGGGT CCCCCATACG TGGACCTATG CCTGTTGTAA 240
GATGTTTGGA AGAGCGTCGA AAGATGAGAT CATGTTGTGT CCTTGGAAGC TGAATGAAGA 300
ACCGGCTTGC AAAGGAGAAG CGCGTGCAGT CCCGGCGCGG CCCGCTCTGC TCAGTTCTCC 360
AGGGCGGGCC TTGGCCTGGA CTGCGTGTCG GGAGGACTCG CGGGCCCCGC ATTGCCGCAT 420
GCCACCGGCA GGTGTCTCTT TCCTGGCTTG GGAACCTATT GTGAGTTCAC CAAATGGAGG 480
CGCGAGGAGG AGGGGGCGGG CAGGGGAGGG GCGCCGAGAG CCGGAGCGGG CACCGCCCCC 540
TGCCTGCCCG CTCCCCGAGC GCACCGCGGC CCAGCCACGA GGCTGCCGGT CCTCACCTTT 600
GAAACGCCGG CAGCTGCGCG CGCTGCGGCA GGCGCGGAGA GGAGCCACCT CGTCACGTGG 660
GGAGGAAATG CCTTGCCGGC CTCCAAACCT ACTGGCTCTT GTTTCTGGGG TTTTATGGCC 720
AGGAGAGTGG GCTCAGCTCT CAAACCCAAG ATCAAAGGAC AGTGCAGGAC CCATCACCCT 780
GGGAAGTTTT CTCCCTTTCC CGTCTTTCTC CTTCTCACCT TCTCAGAAAG CGTAGCGAAA 840
GGGGCCTGCC ACCCTACTGG CTTTTCCTTT TAGGGAAATT CCATTTCCTA ACGTGTCCTG 900
TTTTGAAAGA GGCCAATTTA TTGGGTAATG ACGGCAGCCT GCTAGGCAGA AGTCAGGCCA 960
GGAGCAGTCG CTTTTATTAT TTTATTCAAC GAATGCCTAC 1000