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

TagContent
EnhancerAtlas ID
HS184-15651 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr19:47234190-47235620 
Target genes
Number: 6             
NameEnsembl ID
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFE2L1MA0089.2chr19:47234457-47234472CACTGACTCAGCAGT+6.16
ZNF263MA0528.1chr19:47235013-47235034GCTTCCTCCTCCTGTTCCTCC-6.66
ZNF263MA0528.1chr19:47235004-47235025TCTTTCTCAGCTTCCTCCTCC-6.86
ZNF263MA0528.1chr19:47235016-47235037TCCTCCTCCTGTTCCTCCCTC-7.77
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194723478347235117
Number: 1             
IDChromosomeStartEnd
GH19I046727chr194723117347238057
Enhancer Sequence
GAAGGTGCCC TCCCAGGCTT GGTGGCCAGA GCCCAGACCC AGCTAACCCC CTAACCCCTG 60
AGCAGCCTTG ACTCTGGTCA CACACAGAGC CCCAACCCCA GCCTCTGCCC AACAAATGCT 120
CATTCCAACT GGAAGCCTCA CTCAGACCGC AAACGGGGCC CAGCTCCTCA ATGACCGCCG 180
ACCTGAGTTT CAGAGGGCCA GCCCCCAACC CTGGTCACAA ATCTCCATCC TGTGCTGAGT 240
CAGAAGGAAA GCTGGATGAG AAAGTGCCAC TGACTCAGCA GTCCCCATTC CCACAGCCCA 300
GTCAGACCAC AAGGGCAGGT CAGGCAGGAG GCAAACACGC CCTGCAGGAA AGAGGAACCG 360
GCCATTCTAC AAATGCTCTG GGAGGCGCCG AAAGCCAGCC AGCCTCGCGC AAGCAGGGGC 420
GCCGGCGATC CCTGCTACCC AGGAGCCTGC ACTATCCCCA GCAACAGATG GCACTCCTCC 480
TTCCACCTCC TGGCTTCCAA CTTCATGACA AGTTATAGCA GAGGAGGTAC TGACCCAGCC 540
TGACTGCGGG AGAAGGCAGG GTGCAATTCC AAGTGCAGAT CGACGAAAAC GTCCCCCCTT 600
TCTGCCATCA GGTTGATGCC CTGGAGGTCT TGTCAACTGC CAGTTACCAA CGGGTGCAGA 660
GGTCACTGCA GATGTACCCT CTCGCCTCAC GGCTGCCATC ACCAGAGCTC CACTCCATCC 720
TCAGAACACT CGCTGCACTT GCAGCGGGAC ACAGGACTCC ATTCTCACCG GCCTTCCTCC 780
CACAACGACA CTGACACGCC GCACAGGCTC AGCCTCTTTC TCAGCTTCCT CCTCCTGTTC 840
CTCCCTCCAG CCTCTAAGTG GGAGAGCACC CGGGCAGTCC CCAGATCTCT TCTCTGCGTC 900
ATCTACACTC ACTCCTGCAG GCACTGCAGA CGGCCATGGC TTTCCAAAGA ATGCCCATGT 960
GCTTGTTCAA CTAGACCTAT GTTTAGGGGC CAAATGCCCC GCAGCTCCAG ACGAGCTCTG 1020
CTTCTCCACA TGGGGGTAAA CAGGCCCCTC ACACTTCACA CAACCTCGGC GGCCCCCAGA 1080
ACTTCCACTC CCAGGCTTCC CCGTCTCAGG GGATGCTGCT CCAATGGCTC ACACCAAACC 1140
CTGGAGTCGC TCGTTTCTTT TCCTCTCCCC TTAGCTGCAG TCCTTCAGTG TCGACTGCCT 1200
GAAAGCCTCT GGGGAAGCTG ACACCTCTCG CCTCACCACC GCTAAAGTCC ATCAGCTCTG 1260
TCCCAGACAT CGAGCCATCT CCTAACTGGT CCGCCTGCCT CCTCTGTGAC CCTCCCACAC 1320
CTCTCCTTCT CAGAGTGGAT CAGGTACGTC AGATTATGTC ACCCCGCTGC TCGAAAGCAC 1380
TGGCTTCCCA CAACCCTGAG TCAAACTCAG ACTCTATCCC AGCCCAAGGC 1430