EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-12503 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr11:1356400-1358810 
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: 3             
ChromosomeStartEnd
chr1113581051358800
chr1113566001357964
chr1113578631358286
Number: 1             
IDChromosomeStartEnd
GH11I001335chr1113564721359269
Enhancer Sequence
TTTGGGTCAT ATCTAAGTAA ACCAAGCTCA AAAAGATTCA CCCCATGTCT TCTCAGTGAT 60
TTATAGTTTG AATTTCTACA TCTAGGTCTT TAACCCACTT TAAACTAATT GTTCTATGTG 120
GTATGAGGCA CCTGTCTCTT CCTAGAGACC ACTGCACTCC ACCTGTCCCT GAGAATGACT 180
CCTGACTCCA CTGCATACGA GTCCCTCTCC CCCACCTTCT ACCTGGAAAA CTCCTATTCA 240
TCCCATCAAG ACCCAGCCCT GGGTTGCTCC TGGGTGGCTT TTTTCACTCT CCTTGGCAGC 300
TTTAACTGCT GCCTGGGATG TGGGCTCAGG GCCAGTGCCC TGGAGGGCCC CTGTCATAGC 360
CCTTCTCACC AGCACTGAGA TTGGTCACCT CCGAGTCTGG TGGGCCCGGG GCCCCCATGC 420
AGGTGCACAC AAGTGCTGCT GAGTGACTGG TGATCATACA GCCAACATTC GCGGTGACAT 480
TCATGCACCG GGGACTTCAC AATTCCCCGG ACTCGTCATA AGGGCTGCTC GGCCCCATCT 540
TACAAATGGG GAAACTGAGC CTGGGGGGTT CAGTAACTTG CTGAGTTCAC ACAAACAGTG 600
AGTGGATGGC TGGATGAGTT TGTAAAAGGA AGGTCGATTC TGCATGATGA AGCTAAATTG 660
GAGCCCAAAA TTCTCTCTTC CGGCCCCCAG TAGAATATTA TGGGTGCACC CAAAGGAATG 720
TAAAAAGACC AGATGCCCAG GACACGGGGC GGTGCCTGAT GAAACAGCTG CATTAGAGAG 780
TGACTTTGCA ACTCTGGAGA GAAGCCACTG AAACCCAGCG CTCCTATAAA TAGCAGCTCT 840
TGCAAAGCAT CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT TCAGAGATTG AGAAATCCAG 900
AGACGTTCAT GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG GAGGTCGCAA GCAATGCCAT 960
CTTCAGGAAC AAAACTCCTG CATAACGAAG CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC 1020
CGGGCACCTT CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG TCTCTCCTGG CTGTGGACGA 1080
ATGGACGCCT GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT TGTGGGTGTC GGCTCCCATC 1140
CCGGGGTCCT CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT CTCTCCCACC CTCCTCCCTC 1200
CTCCCACCTC CCCTGCCCTC TCCCACCGGC GTGCACCCCC CCGCCCCGCT GCTCACCGCC 1260
CACCACTCCC CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC CTGGGCCCCC AGTACCGCCC 1320
CGTGCCCCCC TCACTTCTCC CCCGGAAGCG CATCCGTCAG GGAAACCGTC CTAAGACCGT 1380
CCGCACTCGC TTCAGAGCCG CTGCAAACGG CCGTCAATCC GTCATTCAGA CGCGAAGACA 1440
AAGCGTCCCT GGCTCAGCCC TGAGAAGCAG CGGGACGGCG GCGCGTTCCT GAGTTCCCGC 1500
CACGCGGGCG CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG 1560
GGCGGGGGGG CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG 1620
GGGGCGGGGG CGGGGCGTGG GGGCGGGGCG TGGAGGGCGG GGGGGCGGGG CGTGGAGGGC 1680
GGGGGGCGGG GGGATGGGGA CAAGGTAGGG GTCGTGGGGC GCTGGGCTCA CCCCAGGCCC 1740
TCAGGTGTCT CGAGATGGCC CGGGCTCCGA GCGCTCCCGG CGCTTACGCT AGAGCCTCCT 1800
CCTGTGCGAA ACGCGTCCGT GCCCAGGCGC GGGGACCCTG CAGGGCTGTG GGTTCGCGCT 1860
GCCGCTGATC CTGCGTCTTC CCCCCTCCCA GGCCCCGCGT CCAGCCCGCC CCGCCCGCGG 1920
TGGGAGACGC GCCCTCCAGG TGCGGATGAG ACGCGCGGAC AGCGGGATGG AGAAGGTGAG 1980
ACCTGTCCGG CCCCCGCCTC GCGCTCCCGC TTCTCCAGGA AGAGGTGTCG CCGCCGCCCG 2040
GGGGTCCCCG TCCCTCCCTA GCCCGATCCC CCGGAGCCGC GGCCCCACCA CCGCCTGGCA 2100
CTCCCGGGAG CGCGCGGCCT CGGAGCCCCC AGCCCCGCAC AGCCCCTTGT CCCCGGCTGG 2160
GAATGGCGCC TCGCACGGGG TCCCTCGGAG GCCGCGAGGC TCCGCTCGGC GTGTTCGGAA 2220
GCCACCCCCA GCTCCCCCGG CAGCTTGGAG CCTCAGAAAC GCGGGGCAGA GACGCGACAC 2280
GGAGCCGCCT GGCACTGAGA CTCCCCAGTG GCTGCGCCGC CTTCCCGGGG GCCCGAGGCG 2340
GGGGCGGGGG GCGCGCTCGC TTCTTCCCCT CGCGGGGGTC TTCCCAGCCC ACCGGCCACG 2400
GCCGCTCCGT 2410