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

TagContent
EnhancerAtlas ID
HS110-03278 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr22:37899220-37900190 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr22:37899769-37899788TTGCCACCAGAGGGTGCGC+6.04
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_00910chr22:37896561-37901467Adrenal_Gland
SE_24000chr22:37897867-37901007Colon_Crypt_2
SE_26741chr22:37898489-37900917Esophagus
SE_28072chr22:37896512-37901348Fetal_Intestine
SE_29196chr22:37896513-37901262Fetal_Intestine_Large
SE_31997chr22:37894291-37901218Gastric
SE_34331chr22:37896665-37900927HCT-116
SE_42998chr22:37894978-37901425Lung
SE_47921chr22:37897095-37899990Pancreas
SE_47921chr22:37899994-37900723Pancreas
SE_54082chr22:37895467-37901259Spleen
SE_56940chr22:37897777-37899488VACO_400
SE_65664chr22:37894011-37902867Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223789932637899639
chr223789970637900164
Number: 1             
IDChromosomeStartEnd
GH22I037498chr223789448137901287
Enhancer Sequence
CTGGGCAGAG AGAGGGCAGG GAGGGGGCAG GAGGTGAGGC ACAGTGGGCA CTCTGCCCCG 60
CTCCCTCCTC CTGCCCCCAC ACCAGATAAA TGTCTCACAG CCCCCAAGCA AATGCAGGCT 120
AGACTCAAGG CAGGGTCCCA GGTACAGGGC ACCCATGCCA CCTGGCTCCC CTAAACTCCC 180
AGGGTAAGAA GTTAATGTCC TGGCCTCTGT CCAATGTTGT TCCACCTACA ATGCCCTGGC 240
ATGCCCTTCA AAGCCAGCTC TTTCAATGCC ACCTCCTCCT GGAAGCCACC CCTGATCTCT 300
CACCCCTCAC CTCACCCTCA CTTGCCACCT TTGTGGTTTG TGACTCCCAG GTACGCCTCC 360
TAAATTAAAC CATGACCTCC TCATCAGACA CCTCCTTGGG ACAGATTTAC GCAGATCAAG 420
GCCATACTGA CCACAGCCTC CCAGGGCCCA GCCTCTCACC AGTAAAGGAA TAAATCAAGG 480
GCTGCTTACA GGGGAAAAGC AGTGACAAGG ATCGCGCCCC AGGAGGCAGG CTATCTCCCG 540
CCCTTGGTCT TGCCACCAGA GGGTGCGCCT TGGTTTTTCT GGTCCCTATT TGCTGCTGAT 600
GCCCAAACCT GGGGCCTGGC TTTCTTGCCG GAGGTCCCTG ATACCTTGAA ACATTCTCCA 660
CGCCCCCTAG TCCTGAACCA TCAAGCTTCT CCTTGGGTAT AGGATCTTCA AGGCTTGACC 720
CCCAGTGACC CTCCTGCCAG GATGCTTGGC TAGGACTGAG TTCGCTCTGC CCATCGGCCT 780
TATCTTAAGC CTGACCTTGG TCGCCCCTGT GACTCACAGG ACCTGGGTTT CCAGAGCTCC 840
AGCCATCTGA GGGCAATAAA GGGAAGTGAC TGCCTGGACC TGACTTTGGC ATTGCAGATT 900
CTGGGAGGTG GCTGTTCGGG AAACGGCAGC CCCACCTCCC TGGGTGTCTA CTGCTATCCC 960
CAGCCATCTC 970