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

TagContent
EnhancerAtlas ID
HS094-25672 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr22:31645980-31647130 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4820043chr2231647094hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat6MA0520.1chr22:31646353-31646368ACTTCTCAGGAAGAG-7.07
ZNF263MA0528.1chr22:31646982-31647003GAGGGAGCAAGGGAATGAAGA+6.17
ZNF263MA0528.1chr22:31646975-31646996GGAGGAAGAGGGAGCAAGGGA+6.3
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_26106chr22:31645649-31647755Duodenum_Smooth_Muscle
SE_27205chr22:31643647-31647694Esophagus
SE_27790chr22:31643391-31650686Fetal_Intestine
SE_28888chr22:31643343-31650784Fetal_Intestine_Large
SE_31902chr22:31643646-31647232Gastric
SE_37292chr22:31642944-31647660HSMMtube
SE_42312chr22:31643665-31647360Lung
SE_52405chr22:31644955-31648226Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223164647531646616
Enhancer Sequence
AGCTTTTTCT GTCTTCCTGA CTTTCTCTCA TCCTTCAGGG GGCTGCAGGT TTGTTTTCTT 60
CTCCTAGTGG AGAGGAAATT CTCAGGTTTG TTTTCCTCTC CTAGCAGAGA GTAAAAAAAG 120
GGATAGTTTG CCTGACTTGT TGAAGGTGTG GCTGAGATTG TTTTCTAAAG AGCCAATGGA 180
AATTGATCTT GAGTTTAGGA GAAAGCTTTT ACATGTGGAA TTAAGATGCC AAGTGTTGAA 240
GTAGCCACAT TTCAGGTCCT CATTAATTTC TCTTAATCCT GGGAAGGCAG CTTAGGAGAA 300
GGGTTGTTCC TTTAGGAGCC AGGAACTATA CCCCTTTTAC CCTTGGAGAG GCAGGGAAGC 360
CAGGGAGGAC ACAACTTCTC AGGAAGAGGA GAAGCTAGAG CAGATAGTGA ACTCTCAACC 420
TGAACCTTTA AGGGCCAGAC CACTAATGCC ACCCAAGTCC ACCTGCCGTT TGTCTTGTTC 480
TGTCCCAGGC TTTCTGGAGA ACCTGATCTT CTTGCCCCTA CCCCCAAGCT CCGTTTGCCC 540
AGCTAGAGTC TGGGGGGTAC TGACTGACTT TCGTAGACAT TCTTCCCTTC CCCAAATAAG 600
AGGCCACATT CCTGAAGTCA CTTCTGAAGA GATAGCTGCC ACACAGGGCT CTTTCCCCCC 660
AGGGAGGGAC CACCCAGACC CTCTGCTCTC CCAGGTATCC GTTACCACAT CACTACCTGG 720
TCAGAAAGCT GTTTCTGCCA TTAGCCCCTC CCTCTTTTAT TATAGGATAT CCTCAAGGGC 780
TCCTCTTTGG GCCTCAGTTT CATCCTTGGC AGAAAGTAGA AGCTAGACTT CTTGGGCTCC 840
TGAACAGGGT CCTTGCTGGA TTCTGTGAAA CAAATTAAGT TCTTGACCCT AGGCCTCTGG 900
GGGAGTACAA AGTCTATGGG AGTTCTGGGG CTGTGGTTGC AAGGAAAGTG ACGCAACCAG 960
ATTCCATGGG GACATGATCA GGCGTGACAT GTGAGGGAGG AAGAGGGAGC AAGGGAATGA 1020
AGAATACAAC TTCTGTGTCC CATACACCCC TGCCTGACAG GCCATACATA CTCAGCAGAG 1080
AATGCACTGT CTTTCCTACC ACACTAGCGT GAGAAGTGAG CTGCAATTAC CACTGTGCTT 1140
CCAAGTAAGA 1150