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

TagContent
EnhancerAtlas ID
HS121-23291 
Organism
Homo sapiens 
Tissue/cell
LNCaP 
Coordinate
chr2:242176180-242178060 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs113492892chr2242176395hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr2:242176212-242176223GACAGCTGCTG+6.14
Sox3MA0514.1chr2:242177318-242177328AAAACAAAGG-6.02
Tcf12MA0521.1chr2:242176212-242176223GACAGCTGCTG+6.02
ZNF740MA0753.2chr2:242176392-242176405GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr2:242176393-242176406GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr2:242176394-242176407GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr2:242176395-242176408GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr2:242176396-242176409GGGGGGGGGGGGG-6.03
ZNF740MA0753.2chr2:242176399-242176412GGGGGGGGGGCGG-6.64
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2242176533242176742
Enhancer Sequence
TGAACTAGAG AGAAAGGGGA AAAGGGACAG CTGACAGCTG CTGGAAGAGA CCCCACACCT 60
TGTTCAGAAT GCATATGTCT GTGAGGCACC TGCTGGGTGC TGGGTGGTAA AAGGGAGGGA 120
AAACCACTCC TGTCCTTCAG GAGGTCTTGG TCTGGTCAGG GAGAGCAGAT AGGACGTCCC 180
CACAGCAGCC TCAAAGAGGG CTCCCAGACC TTGGGGGGGG GGGGGGGGGC GGCAATGAAG 240
GCTTTGCCGG GAGGCCGTGA GCTCTGTGTC TCCCTTCTTC ACCTTGAAGA TGAAGCTAAC 300
AGCAACTAAC TACAGCAGAG GCTTCAGTGA GATCAGATGA GTTAGTTCAT GGGAGGAACA 360
CAGGGCAGAC CCACTGCACA AGTGAGGCTT GACTGTGAGG CAGGGCTCAT CAGGGAAGGC 420
GGCCAGCACG CAGCCCCACC CAGGAGAGGC AGTGGGAAGG GGGGTGAGAG GTCTAGGGGA 480
GACAGAAAGG GCAAGGCCAA GGTAAACCTG TGCCAGCTCC TTATGCCAGA AAGCGAGAGC 540
CCCAGAAGTG AAGAGGCGTG TGAACAGGAC ACAGAAGACA GCTGGAGGGG CTCCTACAGG 600
CCACACTGGG ACACCGCGTG TGTACCAAAA TAGACACCAC AACAATAAGT GTCACAAAAC 660
AGACACAACA ATAATTATCA CTAAGACAGA ACCCAGGAGG TGTGTGATGT AAATAAATGA 720
GCAGGAGACC AGACAGACGC CTGCCTGAAA TCAAGGGTGA TCCTAGGATG GGGAAGTAGG 780
TGTTTCTGAA GGAGAAAAAC TGGCAAATTT GAATACCGAC AACATATTAG ATACTACTGT 840
TATATAATGT TAAATCCGAT TCCGATAAAT GTGCTAGAAT TATGTAAGAG AATGTCCTTG 900
TTCTAAGAAA ATACCCACCA TGAATAAAGG GACATGTCTA AAAATGACAT TCAGAAAAAA 960
AACGTGTGTA AAAGGGGAGA AGTTGAGAAA AGAAACTGGT GCCACAGGAT GTGTCTTTAT 1020
ACTATTCTGT GAAATTCTAT CAAAATCAAA GTTTTAAATA ACCACTGAAG TGTAAAACAT 1080
AGACAGAGTG CAGTATGAGT TTATTAGTTT CCTACTCAAA ACACCCTGTA TTCTCAGGAA 1140
AACAAAGGGG CTTGAATGGC TGTGTGTGAC ATGCTTCCTG GATGCCCAGA GAGATGACAC 1200
TATGTGCACT CAGCAGGCTG CAGGGCCACC TGCCGCCCAA ACAGCTCAAC CAAGACTGAT 1260
AACACAGAGT GGAGGGCGGG CATCTGATAA CACAGAGTGG AGGGCATACC TTTTGTTTCA 1320
CAAATGCAGA GCAAGTGAGA GAGAGGCAAC CGACCCGCAT CCCACAGGTC GCCTCCCCAC 1380
CACCAGGTGC ATGAGCAGAG CTGGGGGCAA GCATGGTACG GGGAACTGAA TGCTCTCCTA 1440
GAACTGCCGG CCACTTGGAT GGTGCCCTCT GGCCAGCCAG AGGCTGCAGC TGCCTGCCTC 1500
ACAGGGGACA CCCCACAGTG ATGGGAGATG TGGAGGAGGA AGCTCTACGA CGGGGCTCAT 1560
GCGATCCAAA CGATGTCATG AGAATCACTG GGACTGAACT CGGGACACCC GAGGATGAGG 1620
CTGCACGCTC CTCATCGCCT TGGGACTGGC TACCTTGTGT GTCTCTAGGA CCTATGAAGG 1680
TCACCTGGTC ACTCTGTCAG TAACTGACGT GGTCCATCTT TTAAAGGCCA GGGAGTGACC 1740
CTGAACCTCT GGAAGCCCCC AGAATACATA GATGGTTTTC CAGCAGAGAC AGGAAAGAGC 1800
CTCACCAGTA TGTGCGACAG CCCCGCCTCT CACATGGGAG GCGCCACTAT TAACAAGCAG 1860
AGCAGGGCTA ATGGGGGACC 1880