| Tag | Content |
|---|
EnhancerAtlas ID | HS034-20104 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr22:42721020-42722850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr22:42722477-42722498 | AGCAGCACCTTGGACAGACCC | + | 7.21 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23330 | chr22:42721152-42722047 | Colon_Crypt_1 | | SE_23842 | chr22:42720953-42721931 | Colon_Crypt_2 | | SE_25072 | chr22:42720853-42722021 | Colon_Crypt_3 | | SE_65474 | chr22:42720842-42721636 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I042325 | chr22 | 42721059 | 42721590 |
|
Enhancer Sequence | GGATGCTCCC TCTTTGTCTT CCCACCCTGC TGGGACTCAG GAAACCGCAT GGGCGGGTGG 60
GAGGATGCTG AGCTCTCTGC CGGCAGCCCC AACTACAGAT GCCTCTCCGT GCTCAGGCTT 120
CTGGGCCAGC GCCCCCCTAA CCAGAGCTCT GCTCCTCTGG GCCTCCTCCC GACTGGGCAC 180
TCGGATACTC TATGGTGCTG GAGCCACCAC CTCTGTGCTC CCCTGGATGT TCTGGGCGGG 240
GCCAGGCAAG GAAATGTTCC TCCCTGGGAA GCCCAGGGCA GCAGCAGCCA CTCCCAGGCT 300
GGCTCTGAGA GGCAAAACCT CCAGGAAAAG TGCCTCTGCC CGGTGGCCCC CACTCAGCCA 360
CTCCTCACCT CAACAGGTGG GGCCCTTGGG GCCAGGCCCA CGTGACTGTC ACAGCAAGAC 420
CACCCTTTCC TGCCCAGTAA ACCCTGATTT CCTCCCCCAA GAGGCAGGGC TGGCACCAGC 480
CCAAGCAGTA CTCATGCACA CGGTGGCAAG TCACACCAGC TCGGGGGGAG GGGAGGGCAT 540
GAGACTTCAT TCAATTCTGG CCACGTCTGT GTAGTGAGCC CTTCGGCCTG GGCATTGTGC 600
CAGGCATCCC AGGTAGGCAG GACAAAGGGA GGCCCTCAAG GAGCTCACAG TCCAAAACAG 660
GGTAGAAGCT GGGCCGCACC CAAGGACGGC ACCCTGAGGC TACGCAGGAC AGGGAACCAT 720
CACCTGCCAG AGCTGGGAAG TGGAGGCCGT GGGGAGCAAG GCACTGCATT TCCGAGCCCC 780
AATTCTGCAG CCGACTTGCC TGGAGCCAGC GCGCCTCTCT GAGGTTCAGC CTCTCATGTC 840
AAAAGTGGGG GTCAGGGCCC TAGCTTGCAG GATTAGCAGG GTTCAGAGGC ACAGGTACTG 900
CTATTATTGC CGTCCTCAGG TGAGTAAGAC ATGGTTTCTC CCAGGCACCA GCATCTGTCT 960
TGCTCTGGTT GTTGTCACAG GACATCTGGC CTGTGCACCA CCTAAGGCCC CCTTTCAAGA 1020
CCAAAATACA GGCTTCTCTG GCTGCCAGGG GTGCCAGCTG CTGAGGGTCC CTTTGGTGAA 1080
GGAGCCAACT CCCCCCAGGA GAGGAAGGAG CCATCCTCTC CTGGGGACAG CTAACCACTG 1140
ACCAGTCAAC GCAGGATGTA ATGGCTGAGC CCCTGCCTTG GTCTGGAACC AAGCGGGACC 1200
ACCCCTGCTC CCAAGTGCCC GTGAGATCAC CTGAGGCCTC TGTTTCTATT GCACTGCAGC 1260
CCAACCTCAC CCTCTGCCCC CCACAGGAGT TGTTATTAAG AGTGTTCCCC AGTAAACCTC 1320
TCCAGGGTCA CCCTGGATTC TGATTCTGGT GAAGCCGCCC TGTGACAATG CCCCTTCCCA 1380
TCTCGGCTGG GGCCCAAGAG CCGTGCACCA AATCCCTCAT AGAAATGAGA CATAGCACCG 1440
TCGCCTGCTA TGCTGCCAGC AGCACCTTGG ACAGACCCTG TGACATGCTT CCAACTCTCC 1500
GCTCTTCAAT CTAGGGCAGG CATTTGTGCC CAGCTGACAG ATGCCAGGTT CTGGGTAAGG 1560
ATGGGGGCCA CCAGCGAGAG CCCTGGACTC AAAGCCTCAG GGAGCCAGGT ACAGGCTCAG 1620
CCCTGCCGTT TAGCCAGGCC ACCCAAGGCC AGCACATCAC CCCTCTGGGC CTCAGTTTCC 1680
TCATCTGTAA AACCATAACT GTAGTCTGGA CAGAACCTTT ACATTGGCAA AGAGCTGCCA 1740
TGTCCCCTCT TAGGGGGCTC CACCAGAGCA GCATCAACCT TGCTAATCTT CAACTGAAGA 1800
GCCCAGAGAG GGCCACACTT GCCCGATGCC 1830
|
