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

TagContent
EnhancerAtlas ID
HS060-14277 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr17:18078960-18080390 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs860568chr1718079075hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2F1MA0017.2chr17:18079156-18079169CCCATGACCTTTG-6.48
ZNF263MA0528.1chr17:18079171-18079192GCCTCCTCTCCCACCTCCCCC-6.64
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr171808027618080356
Enhancer Sequence
CTGTCTGATA CTGAGGCTTT CAAAACCATG TCTACCATCA CAGCATCCAT ACTTCTACCT 60
CCTGCCCAGA CTACCTGAGC TCCAGGCTCC CTCAGCATCC CCCTTGGAGA CCAACAGTCC 120
TCTCCAGCTT TCCTCCCGAT CCTCCCAGGC ACTCAGGCCC CAAATCTGGG AGTCCTTCCC 180
ATCCCTGTCC CTTCCTCCCA TGACCTTTGT GGCCTCCTCT CCCACCTCCC CCATCTCTGC 240
TCATTCCTCC AGCCACCCTG GCTCCCTTGT GCTGAGCTTG TTCTCCCTGC CCTGGGCCCT 300
CTGCCCTCAC TGTCCTCTCC ACCTGGAATG CTCTTCCTTG ATCCATCACA GGGCCCATTC 360
TCTCCCTTTA TTTGGGTTTC AGCACAAATA TCACCTTTTT CTAGAAGCTT TCCCTAACCT 420
TCCTCCCTAA GAACTCACGA TCCCTGCCCC CATAGCCCTA CTTATGGCTT GGAAATCATT 480
TAGTTATTTG TTTATGTATT GTCTCCTTAT ATTAGTCTGT TTTACGTTGC TATAAAGGAA 540
TATCCGAGGC TGCATAATTT ACAAAGAAAA GAGGTTTATC TGGCTCACGG TTCTGCAGGC 600
TGTGCAAGAA GCGTGGCACC AGCATCTGCT TGGCTTCTGT GGAGGCCTCA CGAAGCTTTT 660
ACTCAAGGCA GGAGGCAAAG GGGAAGCAGG CACATCACGT GGCAAGAGAG GGAACAAGAG 720
AGAGAGGGCC CAAACAGCCG TCTCTCGTGT GAACTATTAG AGTGAGGACT CACTCATTAC 780
CTTGGGTAAC CAAGCCATTC ATGAGGGATT TGCCTCCATG ACCCAACACC TCCCACCAGG 840
CCCTGTCTCC AACATTGGGG ATCACATTTC TTCTCTTTTC TTTTTTTTAC TTTTCTTTTT 900
TTTTTTTTTT TTTTTTTTAC TACAGTGTCT TGCTCTGTTG CCTAGGCTGG AGTAATCTCG 960
GCTCACTACA ACCTCTGCTT CCCCAGTTCA AGTGATTCTT CTGCCTCAGC CTCCCAAATA 1020
CCGGGATTAC AGGCATGTGC CACCATGCCC GGCTATTTTT TTGTATTTTA GTAGAGACGG 1080
GGTTTCACCA TGTTGGCCAG GCTGGTCTCA AACTCCTGGC CTCAAGTGAT CCACCCGCCT 1140
TGGCCTCCCA AAGTGCCGGA ATTACAGGCA TGAGCCACCA TGCCTGGCTG GGCATCACAT 1200
TTCAACACAA GATTTAGAAG GGACAAATAT CCAAACTGTA TCATTCCCCC ATCAGAATGT 1260
CAGCTCCAAG AGAGCAGGAC CGTATCCATC TTGTTCATGC TGTGTCCATA ACTCAGCGCC 1320
TGGCACATAG TAGATGCTCC ATACATATTT GTTGGTTGCA TGGGTGGGTG GGTGGATAGA 1380
TGGATGGATG AAGGCCTCTT TGCTTTTCCC ACTTCCTTGC AGCACCACCT 1430