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

TagContent
EnhancerAtlas ID
HS060-16914 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr19:7607970-7609140 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr19:7608028-7608043TGACCTCTGATCCCT-6.23
NR2C2MA0504.1chr19:7607977-7607992TGACCCCTGACCTGT-6.54
ZNF263MA0528.1chr19:7608539-7608560GGAGGAGGAGGAGGAAGAAGA+10.29
ZNF263MA0528.1chr19:7608536-7608557GTAGGAGGAGGAGGAGGAAGA+6.77
ZNF263MA0528.1chr19:7608548-7608569GGAGGAAGAAGAAGAGGAAAG+7.82
ZNF263MA0528.1chr19:7608542-7608563GGAGGAGGAGGAAGAAGAAGA+9.59
ZNF263MA0528.1chr19:7608545-7608566GGAGGAGGAAGAAGAAGAGGA+9.79
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_54401chr19:7607678-7608883Spleen
SE_54401chr19:7608971-7611185Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1976085517608716
Number: 1             
IDChromosomeStartEnd
GH19I007543chr1976080317611193
Enhancer Sequence
GTGAGGCTGA CCCCTGACCT GTAACCATGC CACCTGAGAT CATTCCCTAT GACTTCTGTG 60
ACCTCTGATC CCTGCCCTTT GACTGTAAGA CCAGCACCTT CTCCCATAGA AGCAGACCTC 120
TCTCATCCTA TCATTTCCAA CCTCTAACCC TTGGGTCCTG TGACCCCCAC CCCCTAACCC 180
CACCCTATGT CCTCTGGACC TGTCAACCCT TCACCTGTGA CCCCTGAACC TTTTGCCCTA 240
GGACTCCAAC TCCTAGATCT CTCCTGCCTG CCCTGGCTCT TCCTGTAATT CTGTTTTCTG 300
AACTTCTGAT CCTGCAGTAT TCACTAACAT GTCTGCTTCT CATGCTGACC GCTGCCAGGA 360
TAGGGGCTCA ATAAATGGCT ACAAATCGCC ATCTGGCCTC GGAAGGCCAT GAACCAGCCC 420
TGGGTCGGGG TTTCAGGGCC TTGTGGCGGC ACCCAGGATG TGTAGGAAAA TGTATCCTAC 480
CATTCTGTCC ACTGTCCATA TGGGGAAACT GAGGCCCATC AAGGGTTAGT GACCCGACTA 540
CCAGCTGAAA GTCAGGAAGC CTCAGGGTAG GAGGAGGAGG AGGAAGAAGA AGAGGAAAGT 600
TGAAACCCAC ACTCTGTCCC CAGAGTGTGG CAGATGATCT AGAAAGTTCT CTGCTTCCTC 660
ATCAGTGGAA TGAGGTAATA AAGAAGAGAT GCCTAGTTCG CAGAACCCCA GTAAGACTTC 720
TTTTTTTTCT TTTTTTTTTT TTTTGAGACG GAGTCTCGCT CTGTCACCCA GGCTGGAGTG 780
CTGCAGTGGC GTGACGGTGG CTCACTGCAA GCTCCGCCTC CCGGGTTCAC GCCATTCTCC 840
TGCCTCAGCC TCCCGAGTAG CTGGGACTAC AGGCGCCTGC CACCATGCCC GGCTAATTTT 900
TTGTATTTTT ACTAGAGAGG GGGTTTCACT GTGTTAGCCA GGGTGGTCTC GATCTCCTGA 960
CCTCGTGATC CGCCCGCCTA GGCCTTCCAA AGTGCTGGGA TTACAGGCGT GAGCCACTGC 1020
GCCCGGCCTT TTTTTTTTTG TTTTGAGACA GAGTCTTGCT GTTGTCACCC AGGCTGGAGT 1080
GCAGTGGCAC AATCTCAGCT CACTGCAACC TCCGCCTCCT GGGTTCAAGC AATTCTCCTG 1140
CCTCAGCCTC CCGAGTAGCT GGGATTACAG 1170