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

TagContent
EnhancerAtlas ID
HS182-01254 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr1:112190720-112192290 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs494453chr1112192122hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr1:112191044-112191063CTTCCAGCAGGTGGTGGTA+6.04
ESRRBMA0141.3chr1:112191084-112191095TTTGACCTTGA-6.14
HNF4GMA0484.1chr1:112190849-112190864TGACCTTTGAACTTT-7.07
NR2C2MA0504.1chr1:112190849-112190864TGACCTTTGAACTTT-6.06
Nr2f6MA0677.1chr1:112190849-112190863TGACCTTTGAACTT-7.12
RORAMA0071.1chr1:112191086-112191096TGACCTTGAT-6.02
RxraMA0512.2chr1:112190849-112190863TGACCTTTGAACTT-7.12
SPI1MA0080.4chr1:112191538-112191552TACTTCCCCTTTAT-6.15
SPICMA0687.1chr1:112191538-112191552TACTTCCCCTTTAT-6.64
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_11566chr1:112185460-112190935CD20
SE_18422chr1:112189725-112190974CD4p_CD25-_Il17-_PMAstim_Th
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1112190885112191239
Number: 1             
IDChromosomeStartEnd
GH01I111647chr1112189900112191645
Enhancer Sequence
CTTGCTCTGT TGCCCAGGCT GGAGTGCAGT GGCACAATCT TGGCTCACTG GAGCCTCTGC 60
CTCCCAGGTT CAAACAGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTATTT TTTTTTTTTT 120
GACTTCCAGT GACCTTTGAA CTTTTTATTG GCTTCCTGCT CCCCAAAGGG TACCCTGCTT 180
CTGCTGGCTT AATTCTCAGA ACTTTGGTGT CATTGGTCTC AGATACCACT TTGCCATCCA 240
CTATCTGGTG GATGGTCGTC TTTTGGATGG TTCGCATGGA GTTGCTGCTG TCCAGGGCAT 300
CACCAAGATT GAAGTCCTTG CCATCTTCCA GCAGGTGGTG GTAGGTGGCG ATCTCAGCCT 360
CTAGTTTGAC CTTGATATTC AGCAGGGCCT CGTACTCACT CCTGGGCCTG GCGTTGCCCC 420
TCTGCCCGGG TCTGTGCCAG CTCTGACTGC AGTTGCAGCA GGATCCCGTT TAGCTGCTCC 480
ATCTGCAGGA AGTAGAGGGC CTCCACCTCC CTCAGTCTGT TCTACAAACT GGCCTTCACA 540
TTTCTCACTG AGTCCAGGTC AATCTTTAAG GACTGGACTG TATGTCTCAG CTCTGTGAGC 600
GTCATCTTAG CCTCTCCAGC CTCAGCAGAC TGCGTGGTGA CCACTGTGGT GCCCTCCTCA 660
ATCTGCTGAG ACCAGTACTT GTCTAGCTCC TGTCGATTCT TTCAAGCCAG CTCATTGTAT 720
TGGGCCGAGA TGTCTGCCAT GATCTTGCTG TCCTGAGATT TGGGGGCATC TGCCTCCATG 780
GTCAACCCAG AGCTGGCAAT CTGGGCTTGT AGGCCTTTTA CTTCCCCTTT ATGGTTCTTC 840
TTCATGAAGA ACAGCTCTTC GTTGAGAGCC TCGATCTCTG GCTTCAGCTG CAGCCAAGTG 900
ACATTGATGT CATCATTGAC CTTGTGGAGT CCGTGGATGT CACTCTCCAC AGACTGGCAC 960
ATGGCCAGCT CTGTCTCATA CTTGACTCTA AAGTCATCAG TAGCAAGATG GGCATTGTCA 1020
ATCTGCAGAA CGATGTGGGC ATTGTCCACA GTATTTAAGA AGATCTGAGC TCTCACGTCC 1080
TCGATGGTCT TGAAGTAATG GCCCCAGTCC CTGAGCTGGG GTCCCTTCTT CTCCAGGTGC 1140
TCCTGGATTT TGCTCTCCAG CTTCCGGTTC TCGGTTTCCA GGCTCTCACT CTGTCCAGGT 1200
AGGAGGCCAG GCATTGAGGC GTTGCATGGT CTCCTCATTC TGGATGCCTC CCATTCCTGC 1260
CAGCCCCTCG GCCATCCCTG CAGCCAGACC CCAAGCTGTC CCAGAAGCTG GTGGAGTGGG 1320
ACACGGAGAT CTGGGAACCA GAGCCCCCAG CACCTGGATA GACGCTGGCC AGGCGCCATA 1380
GCTGGCTGCC TTGACAGAGC TTAGGGACTG GTAGTTGGTG GATAAGGTGA AGCGAGTGGT 1440
AAAGCTCATG CTCTCTGGGG AGGAGAGTGA GAGGATAGGA CTCAGGCTTT GCCGACGACC 1500
AGAATATTAG ATATTATCAT TGCCTAATAT CCCTTTCTTC TTTTGCTGTT GATAATCAAA 1560
ACTTTATTAC 1570