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

TagContent
EnhancerAtlas ID
HS048-00402 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:16515160-16516130 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6656611chr116515805hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr1:16515443-16515454CCACACCCTGC+6.62
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_23091chr1:16515057-16516232Colon_Crypt_1
SE_23751chr1:16515130-16516087Colon_Crypt_2
SE_24743chr1:16515648-16516115Colon_Crypt_3
SE_26540chr1:16513910-16517815Esophagus
SE_28102chr1:16515172-16516184Fetal_Intestine
SE_29455chr1:16515096-16516063Fetal_Intestine_Large
SE_31527chr1:16515204-16516074Gastric
SE_34268chr1:16514127-16516193HCT-116
SE_34628chr1:16513819-16517068HeLa
SE_36144chr1:16514154-16516161HMEC
SE_50427chr1:16514084-16516281Sigmoid_Colon
SE_52536chr1:16514970-16516287Small_Intestine
SE_64726chr1:16514111-16515805NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11651535416516020
Number: 1             
IDChromosomeStartEnd
GH01I016187chr11651384116516098
Enhancer Sequence
GACCTAACAC CTGGCACTTG GGTTGGAGAG AATAACATGG CTGTCGTTAT ATACTAATCC 60
TTGGCCAGTC TGTCCTGGGA GATCAACTCC CCTTTGCATA GGGCTTTTTC GAAGTCCTTT 120
TCCAAGGCAT CACCTTCTTG TAGCTGCATT ATCATGCCCG TTTACCAGAT GAGGAAACTG 180
AGGCTCAGAG AGGGGAAGCA GCTTGCCTAG AGCATCGTGG CTTATAAGTT AAAGCAAGAC 240
TCAAGCCAGG TCCACCTGCC TCCAAACCCG GTGCTGGACT TTCCCACACC CTGCTTTGGA 300
AACTCTAAGG AACCTTCCAA TCCCCCAAAT CCTATTGCCT CATTTAAGTA AAGCAGGCCT 360
GGTTTCTGCC TCCTTCAGTG CCCCTCTTCT CCTCCCACAC CCTTCCAGCA GCCGAAACGC 420
TAGACCCAAT AGCTTACCCC TTCCTCCTTC CTGACCAGCT CCCAACCCTC AGGGCAGCTC 480
ATGAGCCAAG AGCTTGAGAG TGGCTTCCAA AGGTCATCCT CTCCACCCCG CTGTGCCCCA 540
CCCAAGCAGA TGACTGTTCA TCCTGTTCTT CACGCTGCTC AGGGGAAGAA ATTCCCCAGC 600
TTCACTCCCT CCACTCGCCC AGGTGTCTGA GACAGTTCCC ACAGTTGGCA AACTCTGCCT 660
TAAGTCCCAC CAGAGTCCCT CCTGCTACAA CGTCAGCCCA TTTATTTTAG TTCTTTCTCC 720
CAGTAGCATC AGAAATACAA TCTGGGGGGA GACAAACGCC GGGAGAGTGG GATCCTGGGA 780
AGGGGAAGGC ACACTTGGGG ACAGGAAGTG AGAGCAAACC CAGGTTCAAA TCCCGGTCAG 840
GGTGACAAGA GTGGCCAAGC GAGGCCAGGC GCAGTGGTTC ACACCTGTAA TCTTAGCACT 900
CTGGGAGGCT GAGGGGGGCA GATCACTTGA GGTCAGAAGT TCGAGACCAG CCTGACCAAC 960
ATGGTGAAAC 970