EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS145-03884 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr11:1356890-1359370 
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
GGGACTTCAC AATTCCCCGG ACTCGTCATA AGGGCTGCTC GGCCCCATCT TACAAATGGG 60
GAAACTGAGC CTGGGGGGTT CAGTAACTTG CTGAGTTCAC ACAAACAGTG AGTGGATGGC 120
TGGATGAGTT TGTAAAAGGA AGGTCGATTC TGCATGATGA AGCTAAATTG GAGCCCAAAA 180
TTCTCTCTTC CGGCCCCCAG TAGAATATTA TGGGTGCACC CAAAGGAATG TAAAAAGACC 240
AGATGCCCAG GACACGGGGC GGTGCCTGAT GAAACAGCTG CATTAGAGAG TGACTTTGCA 300
ACTCTGGAGA GAAGCCACTG AAACCCAGCG CTCCTATAAA TAGCAGCTCT TGCAAAGCAT 360
CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT TCAGAGATTG AGAAATCCAG AGACGTTCAT 420
GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG GAGGTCGCAA GCAATGCCAT CTTCAGGAAC 480
AAAACTCCTG CATAACGAAG CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC CGGGCACCTT 540
CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG TCTCTCCTGG CTGTGGACGA ATGGACGCCT 600
GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT TGTGGGTGTC GGCTCCCATC CCGGGGTCCT 660
CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT CTCTCCCACC CTCCTCCCTC CTCCCACCTC 720
CCCTGCCCTC TCCCACCGGC GTGCACCCCC CCGCCCCGCT GCTCACCGCC CACCACTCCC 780
CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC CTGGGCCCCC AGTACCGCCC CGTGCCCCCC 840
TCACTTCTCC CCCGGAAGCG CATCCGTCAG GGAAACCGTC CTAAGACCGT CCGCACTCGC 900
TTCAGAGCCG CTGCAAACGG CCGTCAATCC GTCATTCAGA CGCGAAGACA AAGCGTCCCT 960
GGCTCAGCCC TGAGAAGCAG CGGGACGGCG GCGCGTTCCT GAGTTCCCGC CACGCGGGCG 1020
CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG GGCGGGGGGG 1080
CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG GGGGCGGGGG 1140
CGGGGCGTGG GGGCGGGGCG TGGAGGGCGG GGGGGCGGGG CGTGGAGGGC GGGGGGCGGG 1200
GGGATGGGGA CAAGGTAGGG GTCGTGGGGC GCTGGGCTCA CCCCAGGCCC TCAGGTGTCT 1260
CGAGATGGCC CGGGCTCCGA GCGCTCCCGG CGCTTACGCT AGAGCCTCCT CCTGTGCGAA 1320
ACGCGTCCGT GCCCAGGCGC GGGGACCCTG CAGGGCTGTG GGTTCGCGCT GCCGCTGATC 1380
CTGCGTCTTC CCCCCTCCCA GGCCCCGCGT CCAGCCCGCC CCGCCCGCGG TGGGAGACGC 1440
GCCCTCCAGG TGCGGATGAG ACGCGCGGAC AGCGGGATGG AGAAGGTGAG ACCTGTCCGG 1500
CCCCCGCCTC GCGCTCCCGC TTCTCCAGGA AGAGGTGTCG CCGCCGCCCG GGGGTCCCCG 1560
TCCCTCCCTA GCCCGATCCC CCGGAGCCGC GGCCCCACCA CCGCCTGGCA CTCCCGGGAG 1620
CGCGCGGCCT CGGAGCCCCC AGCCCCGCAC AGCCCCTTGT CCCCGGCTGG GAATGGCGCC 1680
TCGCACGGGG TCCCTCGGAG GCCGCGAGGC TCCGCTCGGC GTGTTCGGAA GCCACCCCCA 1740
GCTCCCCCGG CAGCTTGGAG CCTCAGAAAC GCGGGGCAGA GACGCGACAC GGAGCCGCCT 1800
GGCACTGAGA CTCCCCAGTG GCTGCGCCGC CTTCCCGGGG GCCCGAGGCG GGGGCGGGGG 1860
GCGCGCTCGC TTCTTCCCCT CGCGGGGGTC TTCCCAGCCC ACCGGCCACG GCCGCTCCGT 1920
TCCAAGCGCG CTTTTCATTC CGCGTCATCT TATCTGACAA ACGTTAAAAA GAGGGAGGGT 1980
GGGAGGCCCC GAAGTCCCAC CCGAGTCCCC GCGGGGCCGC TGCCCCCTGG AAGTCCCCGC 2040
GGCCATATGG CGGCTCCGTG GAGGGCGCGG TCCTGTCCCC GGAGCCACCG CGGGGAGGGA 2100
CCCCAGGGCC TGGGGGGCGC CTCCGGGGGA CAGAGGCGGC CACGGAGGGG CTCCCGGGAC 2160
ACTCGCGAAA TTCAGATTCA CGGGGCAACC GGCTTCAGAC CTCCTCACTC CCTTCTTCAC 2220
CAGAGCCGCC CCTCCCAGGT TCACCTGCCA GCCCCTGAGT CTCCTCTGCC AATCTCTCTT 2280
CTCCTCCTGG TCTCTCTCTG TCTCTTCTTT GTCTCTCCGT CTCTATCTCT TTATCTTTTG 2340
TCTCTCTCTA TTTCTGTCTC TCTGTGTCTC TCTCATCTCT GCCTCTATCT CTCATTACTC 2400
TTGTTTCTCT CTATCTCTTT CTGTCTCTCT CTGTTCTCTG TCTCTCTCTG TTCTCTGTCT 2460
CTCTCTGTTT TCTGTCTCTG 2480