| Tag | Content |
|---|
EnhancerAtlas ID | HS012-17808 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr22:38180470-38181640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr22:38181245-38181257 | ATGTAAACAGAG | + | 6.32 | | FOXP2 | MA0593.1 | chr22:38181245-38181256 | ATGTAAACAGA | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23557 | chr22:38178148-38181893 | Colon_Crypt_1 | | SE_26673 | chr22:38177304-38182313 | Esophagus | | SE_34613 | chr22:38176901-38182015 | HCT-116 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I037781 | chr22 | 38177376 | 38181967 |
|
Enhancer Sequence | TTAAACCTCT CCAGAAGGAT TTGCACACAT ACATTTGTGC ACACACACCC CCAGGGTGAG 60
GGAACCCAGT GTGAAGGGGC CCTGGACACA CAAGACCCTG GGAATAGTGG TTGCCTCCTC 120
GGGGAGGGAG CCAGAAGGCC AGGGGACAGG GGTGGTGGGA CACATTTCAG TGTTAAATGC 180
TTTCATATGT TCTGCACTAT TTCCCATGTG CATGTGATAT TTATTCCAAA ATAAAGTTTT 240
AAAAAATACT AAAATAGTCC TGAACGGAGC ATGGTAGGGG AGTGGCAGGG CTGGCACCAA 300
ACTCAGGGCT CACTGGCTGG CTCTGCCACA CACCTGCTTC AATCAATGAT CTTCCCTGGA 360
AATTCACTTC CTCACCTGAG ATGAGATGAA GAAATGGGAT TAAGTGAGGC CCTGAGCGTG 420
GCCAGGCCCA CTGAGTCTGA GTAGCAGCTG TTATTCCTGT TAATATCCTG GTCAAGCCTG 480
TTCCAGGCAC CTGAGTGACA CAGACATGAA GGGACACGCC CTGTCCCTGC GCTCACCCTG 540
CAAGGGCAAG GGGAGAGACA GCAACACCAG GGAGAGCTGA TGCAACTGAC CCGGTGCAAC 600
TAACTCGGCC AGAGGAGCCA GGGAAGGCTG CACAGGACAG GTGACGCCTG CACCGAGGCT 660
TCAAAGATAA ATAGGTGTAA TCGGGGGACC AAAGGAGAGA GGGTGCTCCA GGCTGGGGAA 720
GCAGAGCCTG CCAAGACTGT AAAAAACTCA TGCTGGGCAC ACCCACGTCC ACAGCATGTA 780
AACAGAGCCA TATATGCACT CATGAACACC TGTGCTCACA GCTGCCCCAT TCTATACACT 840
CCTGCTCACA TACACAGCCC ATGTGCATGC CTGTATATGC CCCCCATGTG CACAGCAGAC 900
CGCCTGCCAG TTACCTGTGT GACCCACTTA TGTCTCTCAA CCTCTCTGGG CCTCAGTTCG 960
CTCACCTCTT ACATGTGGAA AATGACAGGG ACATGGTGAG TGTTATATGA GACAGTACCT 1020
GTGGAGCACT AAGGGCAATG TCCAGTAAAT GTTCGCTGTA TGATCCTTTT GTCGTTCATA 1080
AGCATGACGA TTGGGCTTTC ATGCTCATGC ATGAGATGGG CCTCCCTTCA GTCTTGTTAC 1140
AGGCCGGCTC TGTGGCTCAT GCCTGTAATC 1170
|
