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

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EnhancerAtlas ID
HS182-15361 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr22:50179380-50180880 
Target genes
Number: 3             
NameEnsembl ID
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs763236chr2250179640hg19
rs138834chr2250180497hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GLIS1MA0735.1chr22:50180831-50180847AGGCCCCCCACGAAGG+6.93
GLIS2MA0736.1chr22:50180832-50180846GGCCCCCCACGAAG+6.48
GLIS3MA0737.1chr22:50180832-50180846GGCCCCCCACGAAG+7.01
ZBTB18MA0698.1chr22:50180391-50180404TATCCAGATGTGC+6.57
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr225017973650179934
Number: 2             
IDChromosomeStartEnd
GH22I049784chr225017843450179657
GH22I049786chr225017976150179910
Enhancer Sequence
GTAGAAAATT TCTACACATT CAGTTACGTG CAAAATTTTC ATACAAATCA AAATGAAATT 60
TACCAGAAAT TACTTTGGCA ACAAGACGCA TGACCTGCTT GCTGGCAAGG GTAGGAAGTG 120
AGCCTCCTTC TGCACAAAGA CCTTTGACAG TGCCTGGTCT CACTCCCCTC CCCGGACGCT 180
TCAGGCCAGA GACCAGCAGA AGGAACAGGG ACAAGATGTG AGGGAGTGGC CTGGGCAGGT 240
CTTGCCCACC ACAGCCTTCC ATCTGCACCC GGCCTGGTGA GGCTCCATGA CACAGGACTC 300
ACTTGCTGCC ACTCTGGGAA ATAAGCAACA CCCACCCAGC CCCACCCTCT CTCACTGCTC 360
AAGTGCACGA GGCACCACGG CACACCAGCA CAGCCAGGAG AAAATGCGCA TCTCCTTATC 420
TAGGTATAAC AGGCAGACAG GACAGACGGG AACCAAGCCT TGACTCGGGA CAAAAACCAA 480
AATGACAAAC ATGCTCCAGA CACGCTTCCA GAAAAGAGTC GCTGGCAACC TGAGCCGGCA 540
CCTCCAGAAG CGCAGCCAGT ACCGAAGAAG CAAACCGATG ACAGCTGCTC CTCTTTAAAG 600
GACAAACTCC TCAGCTTCCT CTGAGGGGCG GGGAGCAGAG GCTGCAGGAA CACAGCGGCC 660
TCCTCAAAGT GCTCCCAGCA CAGCACACAC ACGGCAACAC CCTCACCGAG GAATTCAACA 720
GAGTTCAGTT ACAAAAGCGC AGCAAGAGAT GAGAAGCGCT TTCCAGTGCT ATTTCAGCAG 780
GTCCTAATAC CTCATCACAT ATGTGGCTAA GAGGGCCACA TAAAACAATG AGTAAATGTT 840
GCTGAAATCA ACTGCAAAGT ACTGCATTTA CCACAGGGGC AGGTCCTCTC AGAGGTCCAG 900
GGAAGGGCCA GGCTCAACCC CAGGTCCTAG GTCTGTGGGG CTGCAAGGAG ACCTGACTGA 960
GGGTTGCAGA GTCGAGCTCC CACAAGTGCT GGGAGCGGCC AGTCACCAGC TTATCCAGAT 1020
GTGCACAGCA AAGTCAAGAT GACCAATTAA AACTACACCT GAATTCATTC TCAGTACTTT 1080
TTTAAAGATC AGAAGGGGCC AGGTGCAGCG GCTCACACAT CTAATCCCAA CACTTTGGGA 1140
GTCAGAGGCC AGGAGTTCAA GACCAGCCGG GACAACACAG CGAGACCCCC ATCTCTACCA 1200
AAAATTTTCA AATTAGCTGG GAGTGGTGGT GTGCACCTGT AGTCCCAGCT ACACAAGAGG 1260
CTGAGGCAGG AGGATCACCT GAGCCCAGGA GTTGGAGGCT GCAGTGAGCC ACTCACTCCA 1320
GCCTGGGTGA CAAAGCAAGA CTCTCTTAAA AAAAAATCAG AGAGGAAGTA TGTGGCAGAA 1380
GACAGGACCA AGGACCATCG ACCCCTGGCC CAGGGCAGCC CAGCAAGGTT GCACAATCTC 1440
TCGTGGCAAA CAGGCCCCCC ACGAAGGCGC CGGCCTCAGA CCCGCAACTC AAGGCTTTTC 1500