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

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EnhancerAtlas ID
HS133-29116 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr7:99052840-99054050 
Target genes
Number: 37             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13243267chr799053314hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr7:99053097-99053112CAGGTCACAAGGTCA+6.49
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr79905377299053856
Enhancer Sequence
TGTCACCCCA TTAATGTCAG AGACACTTCA TGTAAGTCCT GGATTCCCCA GAGTCAGCTG 60
TGGGGTCCGA CAGACATGCC AGATGCCGTG AGCAGGGTGT GTGGTCCCTC CCCCAGCCAT 120
CATGTTAGCC CTACAGCCCA TCGGCAGCCT CTCCATACAG AGTCACACCT GCAGATCAGA 180
CAAAGTTGAA AACACAGGGA CAGCTGGGTG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT 240
TGGGAGGCCG AGGGGAGCAG GTCACAAGGT CAGGAGTTCG AGACCATCCT GGCCAACATA 300
GAAGAAAGAA AACAGGAATT GCAGAGCCAG GGAATAGAGC TGGCAAGAGT GTTGGGTGCC 360
AACTGGGCAG AGCCCCTCAG GGCAGCAGGG ACTCAGGGGT GGGTGTCAGT ACAGAGTCAG 420
TGCCCCCAGC TGCCTCCTGA CCCTTTTGTT CAGTGCTTGA GGCTGCCGTT TTAGGAGTCA 480
TAGAGTAAAG AGAAGCTATG GAAGGGCCTG GATAATCAGG ACTGGGATGA GGCAGGGTCA 540
GGGCTGGATT TGTCATGTGG CTCTGCAGGC TCCCCTTACC CAAGTCTAAG CATCGTCCCA 600
TCTCTCTGAT CCTGTAATCA AAACCTGTCC CCAAGGTAGC TTAGGTGTGT CACAGCCACG 660
AGGGAAAACG TTGGGTACAG CCCACCCTCT GTCCCCAGCA GTGGCTCCCC AAGGGAGGGG 720
AGGCTGGGAC ACTTCTGATG CTGTTCCCTC CCATCTCCTG CCAGGGAACC CCAGACCTTG 780
GCTCAGAGGT AAGTGACTGG CCTGTGGTGC AGAAGGGCTT GGTCCCCAGA CGGGGTGGCG 840
GAGCTCAGGT GCCACGGGCT TCTCTTTGTC CTGCTACCCA CTTGGGAGTC CCTCCCTGGG 900
CAGGCCATGT GTCCAGGTGG GAGAGTTGTG GGCCTGAAAG AGCAGGTCGC TAGCAGGTCG 960
CCTTCTGGCG GCCTTGTTCT CCCTTGCATC TGCGGAGTTG CTGGCTAGTT TCTGCACCAC 1020
TGCACTTTCC ATCCTGAGCT CCCTCACCCT CTAATTTGAA AGAAACTCTG TACCACTGAG 1080
AATTTCAGAG TCATGTCCCG ACTGGGGACT TGGTGGATGA TTTGGGATTT GGTGGGCACT 1140
CCCTTAGTTG AAAACTGCAT TTGAACAGTG TTGTTGTCTG TCTCTCCTCT TCCCCCACTT 1200
CCTGCTGTTC 1210