EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-04671 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr11:1357010-1359120 
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
TGGATGAGTT TGTAAAAGGA AGGTCGATTC TGCATGATGA AGCTAAATTG GAGCCCAAAA 60
TTCTCTCTTC CGGCCCCCAG TAGAATATTA TGGGTGCACC CAAAGGAATG TAAAAAGACC 120
AGATGCCCAG GACACGGGGC GGTGCCTGAT GAAACAGCTG CATTAGAGAG TGACTTTGCA 180
ACTCTGGAGA GAAGCCACTG AAACCCAGCG CTCCTATAAA TAGCAGCTCT TGCAAAGCAT 240
CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT TCAGAGATTG AGAAATCCAG AGACGTTCAT 300
GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG GAGGTCGCAA GCAATGCCAT CTTCAGGAAC 360
AAAACTCCTG CATAACGAAG CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC CGGGCACCTT 420
CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG TCTCTCCTGG CTGTGGACGA ATGGACGCCT 480
GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT TGTGGGTGTC GGCTCCCATC CCGGGGTCCT 540
CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT CTCTCCCACC CTCCTCCCTC CTCCCACCTC 600
CCCTGCCCTC TCCCACCGGC GTGCACCCCC CCGCCCCGCT GCTCACCGCC CACCACTCCC 660
CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC CTGGGCCCCC AGTACCGCCC CGTGCCCCCC 720
TCACTTCTCC CCCGGAAGCG CATCCGTCAG GGAAACCGTC CTAAGACCGT CCGCACTCGC 780
TTCAGAGCCG CTGCAAACGG CCGTCAATCC GTCATTCAGA CGCGAAGACA AAGCGTCCCT 840
GGCTCAGCCC TGAGAAGCAG CGGGACGGCG GCGCGTTCCT GAGTTCCCGC CACGCGGGCG 900
CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG GGCGGGGGGG 960
CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG GGGGCGGGGG 1020
CGGGGCGTGG GGGCGGGGCG TGGAGGGCGG GGGGGCGGGG CGTGGAGGGC GGGGGGCGGG 1080
GGGATGGGGA CAAGGTAGGG GTCGTGGGGC GCTGGGCTCA CCCCAGGCCC TCAGGTGTCT 1140
CGAGATGGCC CGGGCTCCGA GCGCTCCCGG CGCTTACGCT AGAGCCTCCT CCTGTGCGAA 1200
ACGCGTCCGT GCCCAGGCGC GGGGACCCTG CAGGGCTGTG GGTTCGCGCT GCCGCTGATC 1260
CTGCGTCTTC CCCCCTCCCA GGCCCCGCGT CCAGCCCGCC CCGCCCGCGG TGGGAGACGC 1320
GCCCTCCAGG TGCGGATGAG ACGCGCGGAC AGCGGGATGG AGAAGGTGAG ACCTGTCCGG 1380
CCCCCGCCTC GCGCTCCCGC TTCTCCAGGA AGAGGTGTCG CCGCCGCCCG GGGGTCCCCG 1440
TCCCTCCCTA GCCCGATCCC CCGGAGCCGC GGCCCCACCA CCGCCTGGCA CTCCCGGGAG 1500
CGCGCGGCCT CGGAGCCCCC AGCCCCGCAC AGCCCCTTGT CCCCGGCTGG GAATGGCGCC 1560
TCGCACGGGG TCCCTCGGAG GCCGCGAGGC TCCGCTCGGC GTGTTCGGAA GCCACCCCCA 1620
GCTCCCCCGG CAGCTTGGAG CCTCAGAAAC GCGGGGCAGA GACGCGACAC GGAGCCGCCT 1680
GGCACTGAGA CTCCCCAGTG GCTGCGCCGC CTTCCCGGGG GCCCGAGGCG GGGGCGGGGG 1740
GCGCGCTCGC TTCTTCCCCT CGCGGGGGTC TTCCCAGCCC ACCGGCCACG GCCGCTCCGT 1800
TCCAAGCGCG CTTTTCATTC CGCGTCATCT TATCTGACAA ACGTTAAAAA GAGGGAGGGT 1860
GGGAGGCCCC GAAGTCCCAC CCGAGTCCCC GCGGGGCCGC TGCCCCCTGG AAGTCCCCGC 1920
GGCCATATGG CGGCTCCGTG GAGGGCGCGG TCCTGTCCCC GGAGCCACCG CGGGGAGGGA 1980
CCCCAGGGCC TGGGGGGCGC CTCCGGGGGA CAGAGGCGGC CACGGAGGGG CTCCCGGGAC 2040
ACTCGCGAAA TTCAGATTCA CGGGGCAACC GGCTTCAGAC CTCCTCACTC CCTTCTTCAC 2100
CAGAGCCGCC 2110