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

TagContent
EnhancerAtlas ID
HS147-10297 
Organism
Homo sapiens 
Tissue/cell
NHEK 
Coordinate
chr11:129722970-129724500 
Target genes
Number: 6             
NameEnsembl ID
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFE2L1MA0089.2chr11:129724313-129724328AGGTGACTCAGCACA+6.38
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_27353chr11:129722906-129725277Esophagus
SE_27846chr11:129723063-129724609Fetal_Intestine
SE_35121chr11:129721033-129725996HeLa
SE_36539chr11:129723345-129724382HMEC
SE_64293chr11:129722901-129725891NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr11129723044129723175
chr11129723853129724184
chr11129723312129724437
Number: 1             
IDChromosomeStartEnd
GH11I129852chr11129722635129725772
Enhancer Sequence
CCCACTGGCT TATCTTCATC CTCAAGTCTC AAGCGCTTAT AGAGAGTTTA TGTAGATTCG 60
TAAATTAGCC AGTGGGAGAG AAAAAGCAGC AGAGGGCTGT TGAAGAGGAA TTTTCCTTCA 120
CTCTGCCCCA TTCCAACAAG ATCCACCCAC TCCCACTGTT TCCTTCGCAT CCACTCCGCT 180
CCACTGCGGC CCTCCAGGAA CAAGCAGTGA TGACAGTAAC AAGTGTTCTT CCTCAGGACC 240
AGCCCCACCT GGGGGGAATG AGGGGTCTTA ATCTGCAACT GACAATTACC ACTTGTCATC 300
AGTGGCCTAT GGCTTCTTGG AGAGAGTGAA GCAACATCGC TTCTCTTGGA GGAAGCAAAG 360
CTTCACAGGG CTTTGTTGGT CTCATCCTGC TGAATGTCCC CACTCACCAT TCAGGCATCA 420
GAGAGGCCTC CCGTGAGAAG TGACAGGGAC CTGTGGCTTA AAGGATCAGG ACAGCATCAA 480
CCTTGCCTAA ATAAAGCTAG GACAATTACA ATATTTGGCC CCTTGACTGG GTGAAAATGG 540
TACTCATTCA ACAGCTCTCT GGCACTCCTA CCACAAGCCA GGAAGTCACT GTTCCAGGCA 600
TAGGAGATAC ACTGGGGAAC CACACAGCCG CTGCTGTCAC AGGGCTTCCA TTCTAGTGTC 660
ACTGGGACTT TTCCTGGGTC ATTTCCACAA CTTCCTGACT CTGTGTGTGG GAATTCAAAA 720
AGGGTCTGGC TTGAGAAACA AGTATCTGGG AAACGGAGTC CAAAATGTCA TCATGGAGGA 780
TTTCTTCTAG GCTTCCCCAA GAACACTTTG GGTACCAGGC ATAAAGACAA ATCTTTTGCC 840
TTCCAAATTA GCTGATAAAA GTAGAAGGGA TAAGAACTAA GAGCTATCCT GTGTCGCAGT 900
TTCGTCATTT TCTGGCCCAC ATCCTGGGGC CTCTGCCTTG TTTACCCGGT GTTTTAAAAC 960
ACACAGCTGG GAGGGGCGCA GGGCTTGCAG AGCTGGCTCT GTGCCCAGGA AGGACACGCA 1020
CTCAAAATCA GCCCTGCAGA CACGCACCTG GGAGCCGCTT CCCTCCCTTG GCACGTACAG 1080
GTATCTTCAT TACCAGTGTG TCTCTGCTCA GATTCTGCTT TCAGCCTAAT TGTTTCTGTC 1140
TGGGATTTCT TTCACTGCTC ACTTGGCAGG GAAGCCCAGA GATTATTCTA TCAGCCACAC 1200
TCCGACTTAA GTGATGATGT CTTGCTCATC TCTGCTCCTG GACAAACCTC CTGGGGATCT 1260
ATGTGTGTGT GGTTGTGTTC ATTGATTCTT CTACCCTCAA CCCCAAACCC CTAAAAGGAA 1320
CAACAATGGC AAGATGTCTA CACAGGTGAC TCAGCACACA CCCTACTTTA TACTGAAGCA 1380
GCTGCACCTG AGGCAGCAAA GTAGCTCTGC TGACCCGCGG GCCACCCTCA CCTCACCCCA 1440
TCTCCGCTTC GCTCATGCCT TTGGGTTATT CCTTGCTCCT ATTTGTCTTA GAGCTACTCT 1500
TCCCTCTAAA ACATCCATCC TCATTTCCCT 1530