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

TagContent
EnhancerAtlas ID
HS180-14172 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr14:20895270-20896490 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1713450chr1420896245hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NKX2-5MA0063.2chr14:20896137-20896147ACCACTTGAG+6.02
SPICMA0687.1chr14:20895990-20896004AGAAAGAGGAAGCA+6.04
ZNF263MA0528.1chr14:20895933-20895954GGAGAAAGAAGAGAAAGAAAA+6.03
ZNF263MA0528.1chr14:20895930-20895951GAGGGAGAAAGAAGAGAAAGA+6.42
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_28028chr14:20895260-20896705Fetal_Intestine
SE_29051chr14:20895241-20896718Fetal_Intestine_Large
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr142089538320896384
chr142089593120896136
Number: 1             
IDChromosomeStartEnd
GH14I020426chr142089492120897612
Enhancer Sequence
AGCATGGCAC ATGTATACAT ATGTAACTAA CCTGCACATT GGGCACATGT ACCCTAAAAC 60
TTAAAGTATA ATAATAATAA AATAAAATAA ATTAAAAAAA AAAAAAGAAA AAGAAAATTG 120
ACCTAAACAC ACACAAAAAA ACTGACCCTT TTTTGCTCTC AGCTGTCCAG TAGGCAGAAA 180
TGGAAAGAGC AGACAGGAAG GATAGAGGTG AGTCATAGAG GGCGGGAATA CACAATCATT 240
AAGTGAAAGC CATTATCCTC AGGAAGGCTC CAGAGAAGAG AGTAGGTGGC AAGAGCAGCA 300
GAATTATCTG AAAAGCCTCT GGAATACCCA CTTCCTCTTT GCTATGGAGA AACAGGGCAT 360
GGCATGCCCC ACTTCTTTCT GTTTCAAATG CATTCCCCCT TCTCTAATGG GTGAGACTCT 420
AGGCAGCCTT TAAGATCCAG TTCAAAATAC ACCCATCGGA TGACACCTTT CCTAACAGAA 480
GCCTTCCTGA GCAGAGTTCA CTGCTCTATC CTCTGGGCTC TCGCAAGACT CGTCCATACA 540
TGTAAGTCCA CTCAAAATTT GTATTTGTTT ATGTCTATCT GCTGGTCAGG AGCTCTCTGA 600
CCTCTGTATC TTGGTGCCTC CTACAGTGCC TGCCACACAG TAGGTAATTA ATAACTGTGT 660
GAGGGAGAAA GAAGAGAAAG AAAAAAGAGA GGCAGTGGGG AGAGCAGGAT GGGGGAAGAG 720
AGAAAGAGGA AGCACCTGAC TACCTTCCCT GGCCAAGATA AAGGGAAATG GATTTAAAAA 780
TAACTCTGGG GGAAAGGAAC TGAAAGGGGG AAATGACTTT TCTGAGTCTT GTCTGCTTCT 840
CACTCTTCTC TCCCCCCACA TCCTCTCACC ACTTGAGACC TCAGGCAACA ACGGTCTCAT 900
TTTCACTCCT GATTCCTCAG TTTGCCCAAA AGAAAGAAGG CACACAGGCT TCTGACTTCT 960
TCCACCCCAT CTCCTTAAAC CTCAGATCAT CTGTTTTTCC ACTGTGGGCC TCTCCCTCCT 1020
TGGCCTCTGC CCCCATCATC TTTCCCACAC AACACTCCTG CCACATGGCC CTGGGGGGCC 1080
CGTCAGGCCT CTCAGGCCCC TGTGCCGTGC ATGTCCATGT GGGAGCTTCT GCCTCAGAAG 1140
GAAACCAAGA GGTTCTCAGG GGCAGCCTGT GGTGTCTCGC TGGGAAACGC TAGACCAGGC 1200
CTACAAAGTT ACCCGGGAGA 1220