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

TagContent
EnhancerAtlas ID
HS195-01489 
Organism
Homo sapiens 
Tissue/cell
VCaP 
Coordinate
chr12:31901820-31902760 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr12:31902606-31902627TCATTGTTTCTTTTTCTTTTT+6.02
JUN(var.2)MA0489.1chr12:31902261-31902275CTGAGTCATTTCCT-6.73
NFE2L1MA0089.2chr12:31902257-31902272TGTGCTGAGTCATTT-6.91
Nfe2l2MA0150.2chr12:31902259-31902274TGCTGAGTCATTTCC-6.41
RREB1MA0073.1chr12:31902205-31902225TGTTGTGGATTGGTTGGGGG-6.33
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_09906chr12:31898377-31905721CD14
SE_15277chr12:31901388-31902876CD4_Memory_Primary_7pool
SE_35168chr12:31898555-31904362HeLa
SE_38691chr12:31898993-31904489HUVEC
SE_40045chr12:31900620-31902995K562
SE_54023chr12:31901634-31902971Spleen
SE_61892chr12:31867411-31932528Toledo
SE_62563chr12:31867177-31913478Tonsil
SE_63403chr12:31879241-31906059NCI-H69
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr123190213631902566
Number: 1             
IDChromosomeStartEnd
GH12I031745chr123189879731905733
Enhancer Sequence
TTCAAGTACA TGTATCTTCA AAATACAAAT ATACTTCAAA GCTACTGTAC TTTGAAATAT 60
GTTATCTTCA AAAATGACAT TATCACTAAG AATATAGGAA GCCTTAAGAA TTGAATATGG 120
TGGTTCAAAA TTAGTATTTT TCCTCTTTGT AGGGGAAATC ACCCAAAAGT AACAATCAGA 180
ACTGTTACCA CCTGACTGGT TCTTGCCCAC TGCACAGATA AAACCAAAAC ACTGAGCCAG 240
CAGGAGTTGC AGCAGAGAAA GAGTTTGATT ATTGCAAGGC AATAGAGTGA GGAGGACGGG 300
ATACATTTCC CAGATCCACC TCACCAAGAA TTCAGAGGCT AAGGTTTTTA AGGATGATTT 360
GGCAGGTAGG GCATTAGGAA ACAGATGTTG TGGATTGGTT GGGGGATGAA ATCATAGGAG 420
TGTTGAAACT GTCTTCATGT GCTGAGTCAT TTCCTGCAGG GGAGTGGTCA GAGGACCGGT 480
TGAGTCAGTT CCTTTGTTGC AGTCACGGTC ACTGTTCAAG CTGGTGTCAG TTGATTCACC 540
TGAAGGCAAA GTCTGAAAAA TATCTCAGAG ATCAGTCTCA GGTTTCACAA TAGCGCTTGT 600
GACTGCCTGT TACATAACTC CTGAGCAATA AGCAATTATA GAAAAGCAAA CAAGAGAACA 660
ATGATGGGCT ATCATTCAAC TACGCCTACA GCTTAAGAGG TGAGCTCCCT GGTGATTGAA 720
ACTGCTTGCA CTCCTCAGTT GATCCAACTT CTGGAAAATA CAAAGGCAGT CTGCATGACT 780
TAAAGATCAT TGTTTCTTTT TCTTTTTTTT TTTTTTTTTG AGACAGAGTC TTGGTCTGTC 840
GCCGAGGCTG GAGTGCAGTG GCACAACCTG GGCTCACTGC AACCTCCGCC TCCTGGGTTC 900
AAGCGATTCT CCTGCTTCAG CCTCCCGAGT AGCTGGGATC 940