EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-08952 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr11:1356920-1358800 
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: 2             
ChromosomeStartEnd
chr1113581051358800
chr1113578631358286
Number: 1             
IDChromosomeStartEnd
GH11I001335chr1113564721359269
Enhancer Sequence
AGGGCTGCTC GGCCCCATCT TACAAATGGG GAAACTGAGC CTGGGGGGTT CAGTAACTTG 60
CTGAGTTCAC ACAAACAGTG AGTGGATGGC TGGATGAGTT TGTAAAAGGA AGGTCGATTC 120
TGCATGATGA AGCTAAATTG GAGCCCAAAA TTCTCTCTTC CGGCCCCCAG TAGAATATTA 180
TGGGTGCACC CAAAGGAATG TAAAAAGACC AGATGCCCAG GACACGGGGC GGTGCCTGAT 240
GAAACAGCTG CATTAGAGAG TGACTTTGCA ACTCTGGAGA GAAGCCACTG AAACCCAGCG 300
CTCCTATAAA TAGCAGCTCT TGCAAAGCAT CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT 360
TCAGAGATTG AGAAATCCAG AGACGTTCAT GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG 420
GAGGTCGCAA GCAATGCCAT CTTCAGGAAC AAAACTCCTG CATAACGAAG CCCAGGTTTC 480
TGTGTTTTCG TGGGTGTTCC CGGGCACCTT CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG 540
TCTCTCCTGG CTGTGGACGA ATGGACGCCT GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT 600
TGTGGGTGTC GGCTCCCATC CCGGGGTCCT CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT 660
CTCTCCCACC CTCCTCCCTC CTCCCACCTC CCCTGCCCTC TCCCACCGGC GTGCACCCCC 720
CCGCCCCGCT GCTCACCGCC CACCACTCCC CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC 780
CTGGGCCCCC AGTACCGCCC CGTGCCCCCC TCACTTCTCC CCCGGAAGCG CATCCGTCAG 840
GGAAACCGTC CTAAGACCGT CCGCACTCGC TTCAGAGCCG CTGCAAACGG CCGTCAATCC 900
GTCATTCAGA CGCGAAGACA AAGCGTCCCT GGCTCAGCCC TGAGAAGCAG CGGGACGGCG 960
GCGCGTTCCT GAGTTCCCGC CACGCGGGCG CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG 1020
CGGGGGGGCG GGGCGTGGAG GGCGGGGGGG CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG 1080
GAGGGCGGGG GCGGGGCGTG GGGGCGGGGG CGGGGCGTGG GGGCGGGGCG TGGAGGGCGG 1140
GGGGGCGGGG CGTGGAGGGC GGGGGGCGGG GGGATGGGGA CAAGGTAGGG GTCGTGGGGC 1200
GCTGGGCTCA CCCCAGGCCC TCAGGTGTCT CGAGATGGCC CGGGCTCCGA GCGCTCCCGG 1260
CGCTTACGCT AGAGCCTCCT CCTGTGCGAA ACGCGTCCGT GCCCAGGCGC GGGGACCCTG 1320
CAGGGCTGTG GGTTCGCGCT GCCGCTGATC CTGCGTCTTC CCCCCTCCCA GGCCCCGCGT 1380
CCAGCCCGCC CCGCCCGCGG TGGGAGACGC GCCCTCCAGG TGCGGATGAG ACGCGCGGAC 1440
AGCGGGATGG AGAAGGTGAG ACCTGTCCGG CCCCCGCCTC GCGCTCCCGC TTCTCCAGGA 1500
AGAGGTGTCG CCGCCGCCCG GGGGTCCCCG TCCCTCCCTA GCCCGATCCC CCGGAGCCGC 1560
GGCCCCACCA CCGCCTGGCA CTCCCGGGAG CGCGCGGCCT CGGAGCCCCC AGCCCCGCAC 1620
AGCCCCTTGT CCCCGGCTGG GAATGGCGCC TCGCACGGGG TCCCTCGGAG GCCGCGAGGC 1680
TCCGCTCGGC GTGTTCGGAA GCCACCCCCA GCTCCCCCGG CAGCTTGGAG CCTCAGAAAC 1740
GCGGGGCAGA GACGCGACAC GGAGCCGCCT GGCACTGAGA CTCCCCAGTG GCTGCGCCGC 1800
CTTCCCGGGG GCCCGAGGCG GGGGCGGGGG GCGCGCTCGC TTCTTCCCCT CGCGGGGGTC 1860
TTCCCAGCCC ACCGGCCACG 1880