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

TagContent
EnhancerAtlas ID
HS048-11357 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr14:54514900-54516330 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs116848211chr1454515235hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE40MA0464.2chr14:54515215-54515225ATCACGTGAC+6.02
TFAP4MA0691.1chr14:54515331-54515341AACAGCTGAT+6.02
TFEBMA0692.1chr14:54515215-54515225ATCACGTGAC+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr145451578054515873
Number: 1             
IDChromosomeStartEnd
GH14I054048chr145451495854516255
Enhancer Sequence
AGTTCTTTCC CAACGGCTCA GCCTTTATCA TTCTGACAGG GACTCCAAAG CCCAGAAGAG 60
CCCTTACCAA GGTCACACAG TGAGTGACTA GCTAGGAATA GTCCTAGTGG TTCCTGGACC 120
CAATTCCATG CCCTAAATAC CAGATGACAA AACCCGCTGC ATAAAAATAG TTCAATTAAA 180
ATCTAAAATA AAATCGTCAC TTACTCTCGA AAAGAAAGCT AGCACAGTAT TTCATGAAAA 240
TGTCATGAAC CTGAATGAAA CTGTAATTTG GGAAGTTGTA AAAATATGGT TGCACCATTC 300
TGAGGGCCAA CGCCTATCAC GTGACCCTGA ACCGCGGGCT CCGCCCTGCT GTTCCACCTT 360
GCCTGGCTTG TGCAAGGCTG TGTGCAGAAG GAAACGAGAG TGGGAAGTCA GCTACCCAGG 420
ATGGTCCATT TAACAGCTGA TCTGCTGGGA CCAGTGCCTA AGAAGTTAAT TTCTAGCTTT 480
GAGATGGTTT CTGGTAATTG TAGGTAATTT AAAATATAAT TGCAATTTAG TTAAAAAAAA 540
AAAAAAAAAA CTCTGTTTGC AGTGTTTATG CTCATCACTC TAATTTAAGG TCTAGAATGT 600
TGGATGAACT GCACTTGAGT ACACGCTCAT TTTGCGTCTT CCTGATTTTA CCACCAGTGA 660
TTATAAAAAC AGCCTCAGCA AACTCAGTCT GCATTGCAAG ACAGATGCTG CAAAGTTCAG 720
ATATAAAGTT TCACATTTCC GGAAGGTTAA CTATTGAGCA TGTTAATGAT TATTGAAGAG 780
ATGAAGAAAA CCACAAGGCT TCAAAATGCA AACACCTCTC AAAAATATCC AGCTTCCTCG 840
TGTTTATAAT AAAGCCACCT TTTTTTTTTT TTTTTTTTCA AAGAAAGACT ATGGTTGAGT 900
TCAGTGTGGT CTGCATATAG GCTTAATGGA GGAATAATTA CACGAGGCTG CTTGTGAGTA 960
GGCCAATGGA GCTTGCATCT GGGTTGTATG TTATAAACTG CTCTGTGCTA AGCCAGGGCA 1020
TCTACAGCTT TGCAAGGTTC ACAGAAATTT CTTACCACAG TGACAGCATA TGTTTTAAAT 1080
GCAGAGAAAT TCTAAGATCT ATTGTGTGTG GATTTATACA GAATTTTCAA AATAATCCAA 1140
AATATAGGTA GGACAGCTAC TTAATGGCAG GCATCTCAGC AATCAATTTA CATTCCAAAG 1200
CACCATCATG GGCCCAATCA GCCATCGTTG CGAACCTAGA CAAGTGGAGC TAAATGAGAA 1260
AACAGCTGAA ATGAGCACTC AATCTAATAA CCTCACATAC AGTCTCCCAT CTCCCAGCTT 1320
GCAAAACTTA ATAGAATGGA GCTTAGGGCT GAAGCAGTAC TGCATTGCAC AGCAATTACA 1380
CCATGTTAAC ACTGGCATTG GAAATCACTT TCTGAATTTG AAAACTCAGA 1430