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

TagContent
EnhancerAtlas ID
HS038-14298 
Organism
Homo sapiens 
Tissue/cell
ESC_neuron 
Coordinate
chr3:45208430-45209610 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr3:45208517-45208538TCCCTTCTCTCCCTCTCCTTC-6.43
ZNF263MA0528.1chr3:45208524-45208545TCTCCCTCTCCTTCCTTCTCT-7.02
ZNF263MA0528.1chr3:45208521-45208542TTCTCTCCCTCTCCTTCCTTC-7.09
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_26951chr3:45208004-45209572Esophagus
SE_34949chr3:45206745-45210367HeLa
SE_35922chr3:45207494-45210439HMEC
SE_46103chr3:45207847-45210517Osteoblasts
SE_55649chr3:45205730-45213596u87
SE_64277chr3:45207948-45210095NHEK
SE_67446chr3:45205730-45213596u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr34520854945209472
chr34520864845208845
chr34520910145209416
Number: 1             
IDChromosomeStartEnd
GH03I045165chr34520708245212390
Enhancer Sequence
TCCTCAAGAT TGTCATGGTT GTTCAAAAGA TGGCCAAAGT TTCTTTCTTT TTCTCACTCT 60
GTTCCCTCTC TAGCTGCACC CCTTGTCTCC CTTCTCTCCC TCTCCTTCCT TCTCTCTCCT 120
AATTGCATTT CTCAGTGTGC CTGCATCTGA CTGCCTGTCT GCCATTGGAA TGGGCACAGG 180
TGTTGGGGGA GGATGTCTCC ACCACAGGTC AGCCTGGGTA CCAAGGAAGT GTTTGGGGAA 240
CTGGCTTCAC TCCTTCCACC CAAGCCTATG TCACTTTTCA ACCGACCAAT GCAGTGAACA 300
GAACTCTGAG TCACGCAGGA AATACAGTAA TTTTCTGAGG AACAATAAGC ATCCATTCTG 360
CAGTTGCCAG TGGTGACTAT ATAGCCCTTC ACTGCCATTG AGCTCTTTAT TTTGGGGGGA 420
CCGGGGGTGG TATGTGCATA TCTGGCTCTC TATTTTATTT TTATACAAAC GATAGCATAT 480
ACTGTTTGTC TTGCCCTCAG GTTTGGTTTC TGTTGCCGCT GTTGTTTTCT TTTCCAACAT 540
CATAAGCCTC TTCCTTATCT TTCCATGTCT GCACACAGGA AGCGGCATCA CTTGTTTTTC 600
ATGTCCTGCG CATCGAGGCA CACTTTCTGC TCCTCTTTGT GCCGCCAGCC GGCCCAGGCC 660
CACAGATGGT AGGACTTGTG CCCCAGGCTG CTGTGTGAGT CAGAGTCAGG CAGGAAGCAA 720
ATGGCAACTT CACCGCGGTG ACTGAGGAAT GCTTAACGAA GGCGCCGCCC TTGACAACGG 780
TGTGGGTTGG TAAAAGGAAA CAGCCGGGAG CCCTGCAGCG CCGGTGCCGC CACCGTTTAG 840
TCTGACTGTG CATTTGACTA AGTCACAAGA GGCCAGGCCT GTGACTTGTC CGAGGGAAAA 900
ACCACCAGAA AACCAGGTGT CTGGGCTCCC AATCAGTAAT CTTCATTGGG TTTGCTTTGA 960
TTGTAAACGA ACAAAAAAAA AGCTTAGTTA TTTAAATTCC ATTCATGAAT CTAGGAAGGA 1020
GCTTAGAAAT TAGCCTTTTC CACAATCAAG ACCAATTAGT CAACTCTTCT ATTGTAAGTT 1080
TTCATCATTT TTCTGTTTAC CCAACTTACA AACTGCTTTT TAAGTCAGAA CTTGAAGATT 1140
TATTCCTGGC AAATGTTTTT AAGAGCAAAA ATTTGGAATC 1180