EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS107-03156 
Organism
Homo sapiens 
Tissue/cell
Jurkat 
Coordinate
chr11:1356990-1358450 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs199527622chr111357872hg19
TF binding sites/motifs
Number: 32             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr11:1357943-1357954GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1357965-1357976GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1357986-1357997GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358006-1358017GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358025-1358036GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358038-1358049GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358060-1358071GGGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357922-1357932GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357927-1357937GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357944-1357954GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357966-1357976GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357987-1357997GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358007-1358017GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358026-1358036GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358039-1358049GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358061-1358071GGGGCGGGGC-6.02
SP2MA0516.2chr11:1357984-1358001CGGGGGGCGGGGCGTGG-6.27
SP2MA0516.2chr11:1358036-1358053GTGGGGGCGGGGCGTGG-6.32
SP2MA0516.2chr11:1357941-1357958GGGGGGGCGGGGCGTGG-6.63
SP2MA0516.2chr11:1357963-1357980GGGGGGGCGGGGCGTGG-6.63
SP2MA0516.2chr11:1358058-1358075GGGGGGGCGGGGCGTGG-6.63
SP3MA0746.2chr11:1357942-1357955GGGGGGCGGGGCG-6.11
SP3MA0746.2chr11:1357964-1357977GGGGGGCGGGGCG-6.11
SP3MA0746.2chr11:1357985-1357998GGGGGGCGGGGCG-6.11
SP3MA0746.2chr11:1358059-1358072GGGGGGCGGGGCG-6.11
ZNF263MA0528.1chr11:1357320-1357341AAAGGAGTGGGGTGGGGAGGG+6.08
ZNF263MA0528.1chr11:1357590-1357611CTCCTCCCTCCTCCCACCTCC-6.19
ZNF263MA0528.1chr11:1357560-1357581CCTCCCCCCTCCCCCGCCCTC-6.3
ZNF263MA0528.1chr11:1357547-1357568CCTCCCCCGCCGTCCTCCCCC-6.45
ZNF263MA0528.1chr11:1357579-1357600TCTCTCCCACCCTCCTCCCTC-6.67
ZNF263MA0528.1chr11:1357583-1357604TCCCACCCTCCTCCCTCCTCC-7.51
ZNF263MA0528.1chr11:1357576-1357597CCCTCTCTCCCACCCTCCTCC-8.03
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1113578631358286
Number: 1             
IDChromosomeStartEnd
GH11I001335chr1113564721359269
Enhancer Sequence
ACAAACAGTG AGTGGATGGC TGGATGAGTT TGTAAAAGGA AGGTCGATTC TGCATGATGA 60
AGCTAAATTG GAGCCCAAAA TTCTCTCTTC CGGCCCCCAG TAGAATATTA TGGGTGCACC 120
CAAAGGAATG TAAAAAGACC AGATGCCCAG GACACGGGGC GGTGCCTGAT GAAACAGCTG 180
CATTAGAGAG TGACTTTGCA ACTCTGGAGA GAAGCCACTG AAACCCAGCG CTCCTATAAA 240
TAGCAGCTCT TGCAAAGCAT CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT TCAGAGATTG 300
AGAAATCCAG AGACGTTCAT GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG GAGGTCGCAA 360
GCAATGCCAT CTTCAGGAAC AAAACTCCTG CATAACGAAG CCCAGGTTTC TGTGTTTTCG 420
TGGGTGTTCC CGGGCACCTT CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG TCTCTCCTGG 480
CTGTGGACGA ATGGACGCCT GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT TGTGGGTGTC 540
GGCTCCCATC CCGGGGTCCT CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT CTCTCCCACC 600
CTCCTCCCTC CTCCCACCTC CCCTGCCCTC TCCCACCGGC GTGCACCCCC CCGCCCCGCT 660
GCTCACCGCC CACCACTCCC CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC CTGGGCCCCC 720
AGTACCGCCC CGTGCCCCCC TCACTTCTCC CCCGGAAGCG CATCCGTCAG GGAAACCGTC 780
CTAAGACCGT CCGCACTCGC TTCAGAGCCG CTGCAAACGG CCGTCAATCC GTCATTCAGA 840
CGCGAAGACA AAGCGTCCCT GGCTCAGCCC TGAGAAGCAG CGGGACGGCG GCGCGTTCCT 900
GAGTTCCCGC CACGCGGGCG CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG CGGGGGGGCG 960
GGGCGTGGAG GGCGGGGGGG CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG GAGGGCGGGG 1020
GCGGGGCGTG GGGGCGGGGG CGGGGCGTGG GGGCGGGGCG TGGAGGGCGG GGGGGCGGGG 1080
CGTGGAGGGC GGGGGGCGGG GGGATGGGGA CAAGGTAGGG GTCGTGGGGC GCTGGGCTCA 1140
CCCCAGGCCC TCAGGTGTCT CGAGATGGCC CGGGCTCCGA GCGCTCCCGG CGCTTACGCT 1200
AGAGCCTCCT CCTGTGCGAA ACGCGTCCGT GCCCAGGCGC GGGGACCCTG CAGGGCTGTG 1260
GGTTCGCGCT GCCGCTGATC CTGCGTCTTC CCCCCTCCCA GGCCCCGCGT CCAGCCCGCC 1320
CCGCCCGCGG TGGGAGACGC GCCCTCCAGG TGCGGATGAG ACGCGCGGAC AGCGGGATGG 1380
AGAAGGTGAG ACCTGTCCGG CCCCCGCCTC GCGCTCCCGC TTCTCCAGGA AGAGGTGTCG 1440
CCGCCGCCCG GGGGTCCCCG 1460