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

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EnhancerAtlas ID
HS044-07950 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr20:4225160-4226440 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12481514chr204225920hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE41MA0636.1chr20:4225749-4225759GTCACGTGAC+6.02
BHLHE41MA0636.1chr20:4225749-4225759GTCACGTGAC-6.02
HNF4GMA0484.1chr20:4225701-4225716AAGGAGCAAAGGTCA+6.18
Stat4MA0518.1chr20:4225730-4225744TGACTTCCTGGAAG-6
ZNF263MA0528.1chr20:4226094-4226115GAGGAAGGGACAGGAGGAGGG+6.11
ZNF263MA0528.1chr20:4226078-4226099GAGGCAGGGAGAGAAAGAGGA+6.68
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2042253344226099
Number: 1             
IDChromosomeStartEnd
GH20I004244chr2042251394226813
Enhancer Sequence
TTTGATCCCT GCATCCAAGT TTCCAATGTT CTCTATCCCC TACCACACAC CTGGTACCTC 60
CACACCAACA TATACCAGCC CCTGGGGGTC CACATTCCCC CCAAAAGTTG CTGCTCAGTG 120
TTCCCTGTTC CTTCAAAGGT ATCTCCCTCC TCCCAGGCCT GGGCCTCATG CTGGGGGTGT 180
CAGGACCTCC TGGCCCCCTC TCCTTCCTGC ACAGCCTCCA GACCCCTCCT GCTCCAAATG 240
GGCTCTGCCC TCCCTCTCTG CTGCTTCTGC CCTCCAAGCC ATACTGGGGC AGATCGGAAT 300
ATTTTGTTTC CTTGTTTGGC CTCTGTCCTG TTTGCTCATC ATTGCCAGAT TCAACTCAAT 360
TCAGCTCCAC CAGTGTCCCT GGGCTCTGCT CTGAGGCACT CGGAAAGGTG CCCTGAGAAG 420
CCTGGTGCAG CACAGACCAT TAGGAAGGAG GATTTAGGGC CTCCTCCACC CCCCAATTCC 480
CTACACCACA TGTGAGGCGC AGCAGAAATG TAAGGATTGA GAAAGAGCTG TGCGTGCCAG 540
CAAGGAGCAA AGGTCATGGA AATTAAGGGA TGACTTCCTG GAAGAGGGAG TCACGTGACG 600
TGGACCTCAA AGAAAGCAGT GGCCTTTTGC AGTGTTGATT GGAACAAGGA AGAGTTAGAA 660
AAACCTAACA TTCAGCAGGA TCAACGCACT GTGGAATACT CTCAAATGTA CTGCTGTGAA 720
AATGGCCCAG CATGGATAAA TCTCAGCCAC ATAATGTTGG GTGAAATGGC AAATTGAAGA 780
ACGGTGATAC GCATGGCAAG GTGCCATTCA TATAAATCTC AAAGACAAAC AAAACAGTAT 840
ATTATTATGG ATACAGATGT TTGTAGTAAG AGTATGAACA TCTGTATAAG AGTGATATAC 900
TCCAGATTTA TCTCTGGCGA GGCAGGGAGA GAAAGAGGAA GGGACAGGAG GAGGGGATCT 960
AGTTATGGCT TGTTCTATTT ATTTGAAAAG AGAGAGGAAG GGGTCTGAGG CAAATATGGC 1020
AAAATGTTAA CATCTGTTCA GTATAGGTGA TTACAGGCAT GTGGGTGCTT GTTTTATTGT 1080
TTTCTCCTTA TTTGTGCATT AAGCTAAAAT TTTAAAGGAA GTTAAAAGGA AAAAAAAACA 1140
GGGAGCTGGC ATTCTACACA GGTTGGGCGT TCCCTACAGG GGCCCAGTGT GAACCGAGGG 1200
GCAGGGGTTG AATGAGGGCA CCCAGGAGCC CAGCACAGCT GGGCAAGGCT GGAGCAGGGG 1260
CTGGGGCGAT GGGCCTGGGG 1280