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

TagContent
EnhancerAtlas ID
HS133-26070 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr6:683140-684400 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4960188chr6684034hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NHLH1MA0048.2chr6:683931-683941CGCAGCTGCG+6.02
NHLH1MA0048.2chr6:683931-683941CGCAGCTGCG-6.02
ZNF263MA0528.1chr6:684166-684187GAAGGATGAGGTTAGGGAGGG+6.17
ZNF263MA0528.1chr6:684208-684229GGGGGAGGGGAGACAGGAGAG+6.8
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr6683515683626
Number: 1             
IDChromosomeStartEnd
GH06I000679chr6679921685725
Enhancer Sequence
CTGACCTTGC GGGAAGATGT GAGTGGCCTA GACTTTCTAA TCCTTGACAA ACATCAACAC 60
CACCAACTCC ATTCCAGCAA GACTGCCAGG AAGACATGAA AATAAAGAAG CTAAACAATG 120
CAAAATCCCA AGTGATATCA AGAGTCTACA TATGTTTATT CAAATAACAA AATACTTGAC 180
CATCTCAACA ATAATGTTCA GGAATGAGAG AGGAACAAAA TCAAGAAAAT ATTACTAAGC 240
TATTCATAAT GAAAGGATTG GATAAAAAGA TATTCTCCTA AATTTATACT ACTACATAAA 300
AACAAAGTTT CATTTGTCTC GACTTGTCAA ATCTTTAGGA TGAAATAAAC CAATATCACC 360
GCTGACAAAT ATAATAACTA TGGTAAACAG GCATGCCAAA ATCAATGCAG AGTTTCAGAA 420
AAGGTCAAGA AACCAACCGT CAGCTTAAAT TGGTTAATTT CATTAAAACT GTTAAACATG 480
ACAGGATGTC GCTAACTCCC AGGTTCTTTT ATATGAGCAA AGTTGGATTA ATTTGACCCA 540
AATTTTGTAT AATAGCTTTT CCAATTTCCA AAAATACATC AACTTTGTCA CTGATCTTAC 600
AAATTCTGCT TTCCTTCTCT AGCTCTATCT CAAAAGAAGC TTCTCGAAGG CCATAAATCT 660
TGACATAGTG AAAGCAAAAT AATCACAGCA CTCAACAGTG CCGTTAACAT TTCTGAGCCG 720
TGAGGGATTA AGCAGGCAGA TGCTATGGAA AGTGCCTGTC AGGAAAGGAC AGCCCAGAGT 780
TCAGAACGCA CCGCAGCTGC GAAGGATTGA AGCTGCTAGC TATGGAATCA AGCTCAGGAG 840
AAACTCTGGG CACAATTCCG GCATCCGAAA TAAATTAAAG TAAACAGTGT TGCTCTCTCT 900
CTCATCCACC CTGTTAGCAG CCTCTCGGCT GAGCGGGAGA CCACACACTC GGACCACACA 960
GCGCCAGCTG AACTCCCTCG CACGCAACAT CTACAAGCTG TCACTCTGCA GCAGCCCAGA 1020
GAGGGAGAAG GATGAGGTTA GGGAGGGGGA GACAGGACCG CAGGAAGAGG GGGAGGGGAG 1080
ACAGGAGAGT CTTCCCTATG TGCAGCTGGA GAGAGTGATG TGTGGTTTAG AGAAGGGGGA 1140
GGGGTGGAAT CCATAAACCT CCCTGAGAAA ACAAGCTGGT CATGGCCTTG TGTAGTCTTG 1200
ACCTGTACTC CCCCATACCA ATTTAGTAGC TGATGAAGGA TTAACAAAGC ATCCATTTAA 1260