EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS175-03897 
Organism
Homo sapiens 
Tissue/cell
SK-N-MC 
Coordinate
chr11:1356550-1358290 
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
chr1113566001357964
chr1113578631358286
Number: 1             
IDChromosomeStartEnd
GH11I001335chr1113564721359269
Enhancer Sequence
ACTGCACTCC ACCTGTCCCT GAGAATGACT CCTGACTCCA CTGCATACGA GTCCCTCTCC 60
CCCACCTTCT ACCTGGAAAA CTCCTATTCA TCCCATCAAG ACCCAGCCCT GGGTTGCTCC 120
TGGGTGGCTT TTTTCACTCT CCTTGGCAGC TTTAACTGCT GCCTGGGATG TGGGCTCAGG 180
GCCAGTGCCC TGGAGGGCCC CTGTCATAGC CCTTCTCACC AGCACTGAGA TTGGTCACCT 240
CCGAGTCTGG TGGGCCCGGG GCCCCCATGC AGGTGCACAC AAGTGCTGCT GAGTGACTGG 300
TGATCATACA GCCAACATTC GCGGTGACAT TCATGCACCG GGGACTTCAC AATTCCCCGG 360
ACTCGTCATA AGGGCTGCTC GGCCCCATCT TACAAATGGG GAAACTGAGC CTGGGGGGTT 420
CAGTAACTTG CTGAGTTCAC ACAAACAGTG AGTGGATGGC TGGATGAGTT TGTAAAAGGA 480
AGGTCGATTC TGCATGATGA AGCTAAATTG GAGCCCAAAA TTCTCTCTTC CGGCCCCCAG 540
TAGAATATTA TGGGTGCACC CAAAGGAATG TAAAAAGACC AGATGCCCAG GACACGGGGC 600
GGTGCCTGAT GAAACAGCTG CATTAGAGAG TGACTTTGCA ACTCTGGAGA GAAGCCACTG 660
AAACCCAGCG CTCCTATAAA TAGCAGCTCT TGCAAAGCAT CGGGTGTGAA TTTTCGTGGT 720
GTTGGCAAAT TCAGAGATTG AGAAATCCAG AGACGTTCAT GTTCCCGGAG AAAGGAGTGG 780
GGTGGGGAGG GAGGTCGCAA GCAATGCCAT CTTCAGGAAC AAAACTCCTG CATAACGAAG 840
CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC CGGGCACCTT CGGGCAGGTG GCCCCAGGCG 900
ATGTTGTGTG TCTCTCCTGG CTGTGGACGA ATGGACGCCT GGGGTGAGGC TGGGCCAGGG 960
ACCTGGGGCT TGTGGGTGTC GGCTCCCATC CCGGGGTCCT CCCCCGCCGT CCTCCCCCCT 1020
CCCCCGCCCT CTCTCCCACC CTCCTCCCTC CTCCCACCTC CCCTGCCCTC TCCCACCGGC 1080
GTGCACCCCC CCGCCCCGCT GCTCACCGCC CACCACTCCC CAGAGGCCGC TTGCTTCCCC 1140
GTCTTTGGCC CTGGGCCCCC AGTACCGCCC CGTGCCCCCC TCACTTCTCC CCCGGAAGCG 1200
CATCCGTCAG GGAAACCGTC CTAAGACCGT CCGCACTCGC TTCAGAGCCG CTGCAAACGG 1260
CCGTCAATCC GTCATTCAGA CGCGAAGACA AAGCGTCCCT GGCTCAGCCC TGAGAAGCAG 1320
CGGGACGGCG GCGCGTTCCT GAGTTCCCGC CACGCGGGCG CCCGGCGAGG GCGGGGCGGG 1380
GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG GGCGGGGGGG CGGGGCGTGG AGGGCGGGGG 1440
GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG GGGGCGGGGG CGGGGCGTGG GGGCGGGGCG 1500
TGGAGGGCGG GGGGGCGGGG CGTGGAGGGC GGGGGGCGGG GGGATGGGGA CAAGGTAGGG 1560
GTCGTGGGGC GCTGGGCTCA CCCCAGGCCC TCAGGTGTCT CGAGATGGCC CGGGCTCCGA 1620
GCGCTCCCGG CGCTTACGCT AGAGCCTCCT CCTGTGCGAA ACGCGTCCGT GCCCAGGCGC 1680
GGGGACCCTG CAGGGCTGTG GGTTCGCGCT GCCGCTGATC CTGCGTCTTC CCCCCTCCCA 1740