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

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EnhancerAtlas ID
HS180-01476 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:44037120-44038290 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3001723chr144037685hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Znf423MA0116.1chr1:44038128-44038143GGCACCTAAGGGGCC+6.41
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_00616chr1:44036802-44039405Adipose_Nuclei
SE_04240chr1:44038071-44039804Brain_Anterior_Caudate
SE_05040chr1:44033899-44037467Brain_Cingulate_Gyrus
SE_05040chr1:44037598-44040003Brain_Cingulate_Gyrus
SE_05962chr1:44033964-44040045Brain_Hippocampus_Middle
SE_08033chr1:44036769-44039793Brain_Inferior_Temporal_Lobe
SE_27645chr1:44037146-44038216Fetal_Intestine
SE_28595chr1:44037272-44038173Fetal_Intestine_Large
SE_41575chr1:44036638-44039606LNCaP
SE_52524chr1:44037150-44038079Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14403783044038114
Number: 1             
IDChromosomeStartEnd
GH01I043570chr14403663944041999
Enhancer Sequence
ATTCGACCTG CCTTCTGGTC ACCCTGACCA GTGGTGATCA GTGATGAGTG ATGACCTTCT 60
TTTCAGACAG CTGTACCCTC TTTCCATAAG TGGCACCCTC CAACCTGGAA CATGGGTCTC 120
AAGTTGGTTT GAGAGCTCTC AAATGTACCA CCCTCGTGGC TCTCAAATTG GCCCCCTTCT 180
CCCCTCCTGC TGCGTCAGTC CTATCCCAGG CACCAGACAC TGCTTTCCCT GCCTCCGGGC 240
CCTCCCGAGA ATCCATCATC CTGTAGGTCA GGTTTGCTGC TCATACCTTC CTGTGCCTCA 300
GTGGTGTCTC CTTGCCTACC TGGTCAAGTG ACGCTCCCAA GCAAGGCTTA GAGGGCCCTT 360
CTTGGTCTTC CCCTGCCCGT GTCTCATCGG GTCCTGGCTA CACCACTTAC CAGCTCTCTG 420
GCATTGGTTA ACTTTTTCGT GTGTCAGTTT TCTCATGTTT GAAAAGGAGT TACAGTAAGC 480
AGTGAGTGAG TCAATGGCAG TCAAACCTTG AGTTGATGGC CTGGCCTCTG GTAAGGGCTT 540
CATGGAGCTC TTTCTACTTT CTGTGCCCTT GACCCTCCTA ACACTGAGCT GTGCTGACCC 600
GTCCTTGGTC CTTGCCCACC TCCGGCCCTC TGCTCACCTT CCGGCTGCTC CACTTGAAAA 660
CCTCCACCCT GCTCAGCCTC TGGCTGCTGC CTCAGGCCTC ACCTTGCTTT ACATTGTCAC 720
CATCTGGCTC CAGTTCTGCT CAGCTAGGCC TTGCAGGGAG GGCCTGGGTC TGATCACACT 780
TGGTGAGGTC AGCTGTAGGA CAGGTCTTCT CTGAGCCCTT GTCAAGTGAA TGATTTCATG 840
AACTTGACCT TTGGCACTTG TCCCTGTAGG CTAATATCTG CTCTAATGTT CACTCCTCCT 900
TCTGCTTTCC AGGTCCAAGG AAGACTTCCT TATTTGTCTT CCTGCCACCT GGAAGTTGTG 960
ACCTCAGGGT CGTGGGCCCA GGGTCCAGCT CCTGGGATGG AGCCAGATGG CACCTAAGGG 1020
GCCTCAACCA TCCCACCTCT GCAGTAATAA CTGGGCTCTC TCCCCTCCCT GCCTGACCTG 1080
GCCTGGGACC GTTGGCCTCA GTTGTTGCTG GCCTTATCCC ATTACCATTT AGAAGGGTGC 1140
TAAGGCTATT CCGTGCACAT TTTTCAGGGA 1170