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

TagContent
EnhancerAtlas ID
HS133-17090 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr2:70791890-70793000 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxa2MA0047.2chr2:70792416-70792428TGTTTACTTTGG+6.74
HNF4GMA0484.1chr2:70792718-70792733TGACCTTTGACCTTT-6.97
NR2C2MA0504.1chr2:70792718-70792733TGACCTTTGACCTTT-7.68
NR2F1MA0017.2chr2:70792721-70792734CCTTTGACCTTTG-7.22
Nr2f6MA0677.1chr2:70792718-70792732TGACCTTTGACCTT-8.12
RxraMA0512.2chr2:70792718-70792732TGACCTTTGACCTT-7.82
Stat6MA0520.1chr2:70792669-70792684ATTTCCCAAGAAATG-6.12
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_07395chr2:70790185-70795547Brain_Hippocampus_Middle_150
SE_35718chr2:70790838-70794537HepG2
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr27079224170792561
chr27079260570792998
Number: 1             
IDChromosomeStartEnd
GH02I070565chr27079268170792830
Enhancer Sequence
TTACAATATA TTCCTAAAAA TGTACAGTAT GATCCAATTT TTGTCCCTCC CCATAAATAT 60
ATTATATACA TGCATAGAGA AACAGAAAGC TGCAGATATA GCAAAATGTT TCAATACTGT 120
GGGTGGTAAA ATTGAGTGAT TCTTTGTCTA TTCTCTGTTT CTTTATTTAA ATTTTCCACA 180
ATAAATCTAT TTCGCTTTTG TAATAAGAAA CAGATTAATT TCTTTCAGAA GGAAAAGCAG 240
TGAGAATGGT TTGGTTGGTT ACAGAGCTAC AGGAATGAGA GGTGGGAGAG TTTCTCTTCC 300
TTTGTGGGTA GAGATGATTA GGGGGTCGTG GAGAGTGAAG TTTGAACATC AACTGTTTGC 360
ACTGGTGCAC CAGGGCAGGC AGGAATCAGA GGCTGTCTGG GCCAATCTCA CTGCCTGGAC 420
ACAGGCGCCT CAGTGTGAAC CGGGGCCTGT GATGGGCCGA TACTGCTCGT TCCTGGAACA 480
AGGGCCCTGT GTCTTCCACT GTCCAACACA AAGGACAGAG TTCCCCTGTT TACTTTGGAT 540
TAGAAATGTT CAAATGAAGG ACAGCAACAA CATTTGAGTT TTTCCTCTTT TCAGTTTCTT 600
ACAAAAAAAC AAATTGTAGT AAGTCAGAGA TTTTTTTGGC ATCTTCGGTG AATAAAATCA 660
ATCAGACTAG ATCGCTGAAG GAGTCTTAAA GAGCTTCCCT TGTTTACTAT GTTTTTTAGA 720
TTTATGGCTT AAAGCTTAAG AAGTAGCAGT GACTGACTAG GCCTCTGAAT TGTCCATTCA 780
TTTCCCAAGA AATGAGGCAT TCCCAATTCC TTGGTCAGTT GGGCGAAGTG ACCTTTGACC 840
TTTGGCAATA AGCTCATTCT AGGCTGGAAG TAATCACATA ATTATGGAAA CACTCCTTCC 900
TTTTGTCCAA CCTCCCACAC ACTTCGAAAT ACTCCTTTCC TTTCAGATGC TCATTCAAAA 960
CCCCCCTCAA TTAGACCTGC TAAGACATAG AGTTTGTATC AGACATAGAA GTCTTTAAAT 1020
CATCAAAGTC TAAGTGGTCC CATGTTGAAA GACTGTGCCT AACACTATAG GGAATAAGAC 1080
CTTGAATACC ATGGTGGTAA GGTGGAAACT 1110