EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS095-04810 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr11:1357070-1358390 
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
TTCTCTCTTC CGGCCCCCAG TAGAATATTA TGGGTGCACC CAAAGGAATG TAAAAAGACC 60
AGATGCCCAG GACACGGGGC GGTGCCTGAT GAAACAGCTG CATTAGAGAG TGACTTTGCA 120
ACTCTGGAGA GAAGCCACTG AAACCCAGCG CTCCTATAAA TAGCAGCTCT TGCAAAGCAT 180
CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT TCAGAGATTG AGAAATCCAG AGACGTTCAT 240
GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG GAGGTCGCAA GCAATGCCAT CTTCAGGAAC 300
AAAACTCCTG CATAACGAAG CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC CGGGCACCTT 360
CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG TCTCTCCTGG CTGTGGACGA ATGGACGCCT 420
GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT TGTGGGTGTC GGCTCCCATC CCGGGGTCCT 480
CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT CTCTCCCACC CTCCTCCCTC CTCCCACCTC 540
CCCTGCCCTC TCCCACCGGC GTGCACCCCC CCGCCCCGCT GCTCACCGCC CACCACTCCC 600
CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC CTGGGCCCCC AGTACCGCCC CGTGCCCCCC 660
TCACTTCTCC CCCGGAAGCG CATCCGTCAG GGAAACCGTC CTAAGACCGT CCGCACTCGC 720
TTCAGAGCCG CTGCAAACGG CCGTCAATCC GTCATTCAGA CGCGAAGACA AAGCGTCCCT 780
GGCTCAGCCC TGAGAAGCAG CGGGACGGCG GCGCGTTCCT GAGTTCCCGC CACGCGGGCG 840
CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG GGCGGGGGGG 900
CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG GGGGCGGGGG 960
CGGGGCGTGG GGGCGGGGCG TGGAGGGCGG GGGGGCGGGG CGTGGAGGGC GGGGGGCGGG 1020
GGGATGGGGA CAAGGTAGGG GTCGTGGGGC GCTGGGCTCA CCCCAGGCCC TCAGGTGTCT 1080
CGAGATGGCC CGGGCTCCGA GCGCTCCCGG CGCTTACGCT AGAGCCTCCT CCTGTGCGAA 1140
ACGCGTCCGT GCCCAGGCGC GGGGACCCTG CAGGGCTGTG GGTTCGCGCT GCCGCTGATC 1200
CTGCGTCTTC CCCCCTCCCA GGCCCCGCGT CCAGCCCGCC CCGCCCGCGG TGGGAGACGC 1260
GCCCTCCAGG TGCGGATGAG ACGCGCGGAC AGCGGGATGG AGAAGGTGAG ACCTGTCCGG 1320