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

TagContent
EnhancerAtlas ID
HS101-17685 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr16:89734450-89735620 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2377058chr1689734831hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HSF1MA0486.2chr16:89735275-89735288TTCTAGAACATTC+7.52
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr168973485889735409
Number: 1             
IDChromosomeStartEnd
GH16I089668chr168973500989735208
Enhancer Sequence
GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC AGGTAGATCA CCTGAGGTCG 60
GGAGTTCAAG ACCAGCCTGG CCAACATGGA GAAACCCTGT CTCTACTAAT AATACAAAAA 120
TTCCCCAGGT GTGGTGGCAG GAGCCTGTAG TCCCAGTTGC TCAGGAGGCT GAGGCAGGAG 180
AATCACTTGA ACTCAGGAGG TGGAGGTTGC AGTGAGCCGA GATCACACCA CTGCACTCCA 240
GCCTGGGTGA CAGAGCGAGA CTCCGTCTCA AAAACTAAGA AGAAGATTAA TAATAAACCA 300
GCACTGCCAT TGCCAGCAGT CCATCCTACC TCGCATCCAG GTTCGTGAGC TACCAAGTGT 360
CCCCACAAAG CTGTAAAACA ACATGACCAC TGTAGTTACG TTTCTGTAAA AAGGTGACTG 420
AGTCTTCTAA CCCTGACCAC ACATATGTGT GCAGAGAGAG CCAGCTCCAT CCTGCTCTCC 480
CAGAAGCCTG AACAGCTGTG CCCTAGCTCG TAGCAGTGGC ACTCCAGGAA GGGGGCGGGC 540
GGCTGTGCCC GAGCTCGTAG CAGTGGCACT CCAGGAAGGG GGCGGGCGGC TGTGTCTGAG 600
CTCGTAGCAG TGGCACTCCA CGAAGGGGGT GGGCGGCTGT GCCCGAGCTT GTAGCAGTGG 660
CACTCCAGGA AGGGGCGGCC GGCCAGCCAG GAGAGCAGCC GGTGAAGGAG CACTTTTGCT 720
TTGTACGTGG CAACGCTCGG CAGGCTCAGC AGTTTCACAG GTCTCAGGCG TTCCTTGTAA 780
CCTTAACAGG TTTAAGAAAA TGTGAGCAAC ATCAGACATG TCCATTTCTA GAACATTCTA 840
ATGGATGAAG TTCTGTACAG AGGGCTTTAG CAGAATTAGA GACCTTTGGA GTGGAAATGA 900
TGTCTCTGAA CCTTGAGCTC TGAGGCGGTT CCTGCCTGGA CGTGTGCCCT CCCTCCTTCC 960
TTTGCTGGTC GCCCTGACAC CATCCTGCCA CGGATAGTGG AAGTGTTTCT CCTGTTTTCT 1020
TCCCTGAAAA AGGGTGTCCA GCATCAGCAA CCTTCATGGC TGAGTTGCAC ATCCCTTAAG 1080
CCCTGTAATG TTCATGGACA GTTTTGATCA CTTTTGGACT CACCCATTTT TTCTGCTAAC 1140
CATACATCTT AATTCCTTTA CTCTGACCAA 1170