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

TagContent
EnhancerAtlas ID
HS091-23114 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:8092720-8094950 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs882951chr198093265hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr19:8094916-8094926GGCACGTGCC+6.02
HES2MA0616.2chr19:8094916-8094926GGCACGTGCC-6.02
HNF4GMA0484.1chr19:8094112-8094127AAAGGCCAAAGGTCA+7.01
Nr2f6(var.2)MA0728.1chr19:8093008-8093023TGAACTCCTGACCTC-6.22
Nr2f6MA0677.1chr19:8094113-8094127AAGGCCAAAGGTCA+6.73
RREB1MA0073.1chr19:8093678-8093698TGGGGTTGGGGGGTGTGGGG-6.22
RxraMA0512.2chr19:8094113-8094127AAGGCCAAAGGTCA+6.09
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1980931298093432
chr1980934728094571
Number: 1             
IDChromosomeStartEnd
GH19I008028chr1980929708095351
Enhancer Sequence
CACTGGCCTT CCTCGTCCTC CTCTTTATAC CATTGCACCC AGGTTTGTTT GTCTGTTTTT 60
AGTGACAGAG GCTTGCTGTG TCACCCAGGA TGGAGTGCAG TGGCACATTC TCAGCTCACT 120
GCAACCTCTG CCTCCCAGAT TCAAGCAATT CTCCTGCCTC AGTCTCCTGA GTAGCTGGGA 180
TTATAGGCAT GTGCCACCGC ATCCGGCTAA TTTTTGATTT TTTTTTTTTT TTTTTTTTTT 240
TTTTTTTTTA GTGGAGACGG GGATTCATTA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC 300
CTCCAGTGAT CCACCTGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGACA TGAGCCACTG 360
CACCCAGCCC CTGGGGTTTT ATTTACCCAG ATCCCCACTG CCTTTCCTTC CTGTGGCTGA 420
CATCTCCCTA CACTGTCCCC CAGAAACACA GCTGTTTTGC CCTCAACCAC AGCTCCTGCA 480
TCCAGTGCAG GGCCTGGCTC TTGACTGAGA CATCAGCAAA TGTGAGCCCT GCTCTCCTGG 540
GTCAATGCAG GCTCCTTCAG GAAGGAGGCG GGGATCTGTC CCCCTTGGCA TCCCCAGTGC 600
CCAGCATGGG GGGCCTGGCA CCCATGAGGC AGCCAAGGCT TTCAGACCAA ATGAACAAGC 660
AGTGAGCCCT GCCTTCGAGG GCCCGTCTTG AGGACACCAG GTGGGTTTAT GACATCCCAG 720
TGGACATGAG GCCCCCAGGG ACCAGTTCCT CTCCGGCATT GGCACCAGGG CCCCTGCCCC 780
ACTGGATCAG ACCTCCCAAG CTTGGGGTCC CTTTTCCAGT AGGCAAGAGA GGCACCCGAC 840
TCCTGCTTCA GCCCAAGGAG AACCTGCCGA CTCCAAGGGG TGGCCATTGA GGGGATCAGT 900
GACGTAAGTC CTTCAGAGGC AGCAGGGACA AGGAGCTGTA GGGAAAACAG GGCAGGCCTG 960
GGGTTGGGGG GTGTGGGGTG CTGACAAGGT GCAGACCCAC CACCCCAACC AAGCCCCTCC 1020
TCCGCAGATC CATCACCTCT GCCCCGTGCC CCATGAATGA ACCAGCTCAT TCCCCGGCCC 1080
AGTGACCAGC ACAGGCTCCA GACGTTTCCC TCGGACATTG TCTGCCTGAC CACCTCTTCC 1140
AGCACAGTGA GGGGCCTGGG ATCTGGAGGC CAGAGTGGGC CAGGCCTAGG GGTGGGGGGA 1200
AAAACGTCAC TATTCTTAGA TCCCTCGTCC TCCAGGGCCC AGGCCAGGCG GAGCAGTCAC 1260
ATTCCAGAGG TAGAAACCAT CAGCCCACAC AAATGCTTGT GTTCCCTGAG GAGGCCAAGG 1320
GTCACCAGGA ACTAAAATCA GCTTTTCCCA AGAAAGGCGG GAGACAGGGT GGGGGGCGGG 1380
GGGCAGGGTT AGAAAGGCCA AAGGTCACCC AATAAACCCT TCCAGCTGCC CCTGGTGGAA 1440
AGCCCCTCTG AGTCCGGAGG GATGAGGACA GAGGGATTCT CGCCCTCTAA GCTACTCTGC 1500
GGGCTGGCTG ATTCTTCCTG GTAGGGGGCG GTCCTGTGCA GTCTAGATTA TTTAGCAGCT 1560
CTCTGGCAGC CCACCGCCCC CCCAGCCTCC CAGTGGTGAC AGCCAAATCT CTCTCCAGGC 1620
ACGGGCCAGG TGTCCCCTGG GGAAAAATCG ACCCCAGATG AGAACTGTAC TTTCCCAAAC 1680
AGAGCTTCCA GGTGGCGTCT GGGGTAGATA TTTAGGATCC TGCTGTTCTA TGGACTCTGT 1740
TCTCTCAGCC TGGAATCCTC TTCCCGCATA GCACAATCCC CCACCAGCCC TGCAATCTTC 1800
CAGAACTAAA CCCACACATC ACCTCCCTCA GGAAGTGTCC TGTGGGCCCC CCATCTTATG 1860
ATTTTGGCCC CCACGGATGC TGTGGTAGGT AAAATAAAGC CCCTTTGGCC AGATATGGTG 1920
GCTTACACCT GTAATCCCAA CATTTTGGGA CGCCGAGGAG GGAGGATCAC TTGAGCCTAG 1980
GAGTTAGAGA CCAGCCTGGA CAACATAGCA AGACACAGTC TCTACAAAAA AAAATAAAAA 2040
AATTAGCTGG GGCTGGGCGC GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCAA 2100
GGCGAGCGGA TCACAAGGTC AAGAGATCGA GACCATCCTG GCCAAGATGG TGAAACCCTG 2160
TCTCTACTAA AAATACAAAA ATTAGCTGGG CGTGTTGGCA CGTGCCTGTA ATCTCAGCTA 2220
CTCTGGAGGC 2230