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

TagContent
EnhancerAtlas ID
HS018-15486 
Organism
Homo sapiens 
Tissue/cell
CD19+ 
Coordinate
chr3:4909210-4911040 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2053500chr34909440hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr3:4910267-4910278GCCCCGCCCCC+6.02
KLF5MA0599.1chr3:4910267-4910277GCCCCGCCCC+6.02
NRF1MA0506.1chr3:4910169-4910180GCGCCTGCGCG+6.14
SP4MA0685.1chr3:4910264-4910281ATCGCCCCGCCCCCTCC+6
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_18602chr3:4908063-4912293CD4p_CD25-_Il17-_PMAstim_Th
SE_19590chr3:4908204-4911214CD4p_CD25-_Il17p_PMAstim_Th17
SE_20241chr3:4907902-4911210CD56
SE_49889chr3:4905767-4910143RPMI-8402
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr349099174910799
chr349103934911000
Number: 1             
IDChromosomeStartEnd
GH03I004866chr349078454911822
Enhancer Sequence
TAATTGTAAG AGTAAATTTA GAAAAAATAA TCAATGAAAT GCTTCCTTTA TCTTTTCTAA 60
AACACTAAAC TAGAAAGATG TGCAAAGTAA GACTGAGCAG CTTTTTCTAC GGCAGGGATC 120
AATGGGAGTG TACGTAATAA ATGAATAATT GCATTCCTTC TCCCTGGCCA GCCGACAGAG 180
TGGAAATCGA CCTCTGTTCG GCGGGCATGC ACAACCGGCT GGCATGGTGT CTGCGTTCCC 240
CTCCTATGAA AGGATCAGCT CTAGTTACAT GCCCTGTGCG CGGCCTGAAG CCTGTAACCG 300
GGATTACGAG CCCACTATGA GCCAGGGACT AAAGGTGACA CAGATTTCAC CTCTTTTCAT 360
TACCTTTGAA GGAAGTTCTG TGCCCTGACG AGGAAACTGG GGCCAAGCTC GCATAGGCAG 420
TGCGGCCGAG TCAGCCCTGT GGCCCCCAAG CTGGGGCACG AACCCACCGC AGTGCTTGCA 480
CCAGGCACTG GCTCCGAGAG CAAAGGCATG ACTGGGCACC TAAATACCCA CTAGGCAGGC 540
AGTGACTGCG ACAGTAACTC TCTTCTTTTT GGCCACTCTC AGGCCGCAAG TCCTCCAGAA 600
AACGGAAAAC TGAGGCGCGA GCCAAGTCAC TTTCCAAAGG TCACAGCTGG TAGCAGGCCG 660
AGGAGGGCCT CCAGGCCTGG TGCTTGCGAC CCTCAACGAC CATCTGTAAT AATGCCCAGA 720
GCCTCTGCCA GGATTCCCCA GCCCTATGTT CCCGCGGCCT TTGAGGGGAA AGGGCCAGGG 780
CCTAGACGTT CCCCTCCCGC GTGGTTTTCC CGTCAGCAGC TTTCGTCTGC AAGGGAAAGC 840
GGCGGCCCCA CCCGCAGACA GCTGCGAGGC ACCGCGCCAA GCGTATGCGC CTGTTCCCAG 900
GCACTCCCTC CTCCGCCTTC ACCCTTTTGC CACCTCCGCC CTCCACCCAG CCCCGCCGTG 960
CGCCTGCGCG CCCCGGCCCG TGGGCCAGCG GGCAGTCTAC TCACGTGGGC CTCCGCATGG 1020
CCCAGCGCCG CCAAGGGCAA GGCGGAGCCT CGCGATCGCC CCGCCCCCTC CGTGCCCCGC 1080
CTCCTGTAGG GAGCGCGGGA CCCTCGGCTG GCGCGGGCAC TTCCCAGCCC AGCCCGGGGC 1140
GCCGGCTTCG CCGCGTGCGC GTGCGCATGG TGGGGTTTGG CTGGCTGCGG GATGCGGTCG 1200
AGGCCGCCGA GGCCGCAAAC TCCAGTGGGA AGGCGGCGTG CCGCGGCCGG CTTCGGTGGA 1260
GGAGGGGGCG TTTCCCCGGA AAAGGAAGGA AGTGGGTGTC ACGGGCCTCA ATACGGCCCC 1320
TTTGACGTCT TGAGTGGGAA ATCACAAGAT ACTGCTCCAG ATTTTCCCAT TTTATGGCTA 1380
AATCCAAATG ACTCGGACCC CCTGCCCCAT CACATCAGGA ACTTCAGCAG TTCCTTCCAC 1440
CAAAGCTCAA CTATTGCTGC AAGCGCTTTG GTAATCACGA GCATTATCTA TGAAGCTACT 1500
GCTGTGGTCA GGGCCCCAGT CGTCCTGCTG AGTAGCAGAC TTTGAAAGAC GGTGTCCAAG 1560
GCCACCCTGC TGGTCAGTGA CCTGCTCTAG AGGCTAAGCC AGGGCATGCT TAGAACTTTG 1620
ATATTTAGAC TTCTTACATT AACTTAACCC AGTTAACAGG TTTGTGGGGG CATTTTTTGT 1680
TTGTTTTTTT GAGACCGAGT CTCGCTGTGT CACCCAGGCT GGAGTGCAGT GGCACAATCT 1740
CTGCTCACTG CAGCTTCTGC CTCCCGGATT CAAGCAATTC TCTCACCTCA GCCTCCAGAG 1800
TAGCTGGGAT TAGACGTGTG CCACCACACC 1830