| Tag | Content |
|---|
EnhancerAtlas ID | HS101-24769 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:122617330-122618590 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:122618345-122618366 | CCTCCCCTCCTGTTCTCCTCC | - | 6.5 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I121859 | chr2 | 122617430 | 122618730 |
|
Enhancer Sequence | TACAGGGAGG GGAGAGGGGC TGAAGGTCAA GTTGATCGCC AATGGCCAAT GATTTTGTCA 60
ATCATGCCTA TGTAATGAAG CCTCCAACAA ATCCAAAAGG ATAGACTTAG GAGAGCTTCC 120
AGGTAGTTGA ATGCCTGGAG GTTCCTGGAG GGATGTGTAC CCGGAGGGCA TGGAAGCTCC 180
ACGCCCCTTC CCACATAATT TGCCCTGTGC GTTTCTTTAT CTGTGTCCTT TGTAATATCC 240
TTTATAATAA ACCAGTAAAT GCAAATAAGT GTTTTCCTAA ATTCTGTGAG CTGCTCTAGC 300
AAACAAATTG AATCTGAGGA GGGGGTTGTG GGAACTTTGA TTTAGGCTGG TTGGTCAGAA 360
GCACAGGTAA GACAACCTGC GGCTCGTGAC TGGTGTCTGA AGAGGGGCCA GTCTTCTGGG 420
ACTGAGCTTT CAACTTATGG GATCTGATGC AATCTCCAGA TAAACAGTGT CAGAATGGAA 480
TTGAATTGGA GGATTCTCAG CTGGTGTCCA CTGTAGAACT GCTTGCTTAC TTATTGGTGG 540
GGAGGAACCT CAACACATTT GCTCACAGAA GTCTGCTTTG ATTGTTGTGG TATGAAGGCA 600
GAGGAAAAAC AGTTTGTTTT TTTTCACAGT TTGTGTTTTC CCACTCATTT CCACAACAGG 660
CTGCCTCAAG GAAACCCACA GGCTCCTTCT CATGGAAGTG GCTTCTTTTA GGAACATTGG 720
CTCTGGCCAT TCAGTGAAGG ACTAAGACAA CCACGCTGCC TTCCTTAAGG CCACCTCGAC 780
ATTCCTGCTG CACTTGTCAG TAGGAATCAT GCAACAAGGC TAGGCTTTGC TGATCTCATA 840
AAGACTGACT GTGTCATGAG TTGTGCTGAC TCAAGGTAGT AGGACTTCTG GGGCATGCAG 900
CAGGAAGTCA AACAGATGTT AGCCAGGCGA TCTTAGTAGG AAGGTGATGA ATGAGGACGG 960
GAGGCAGCAG CAAGCTTTGA TGGAGACACA TAATGGAACT AATACAAGCC CCTCTCCTCC 1020
CCTCCTGTTC TCCTCCCTGT CAAGAGGTGA ACAGCTCATA GAGGACTAGA GTCCAGGCTG 1080
CAACACAGAC CCCAGCGTCC ATGAAAAGGA TCTGCATCTG TGATGGGAAG GAGAAGTTCA 1140
ATTAAAAGAT ATCAAAGGGC AAAATGTTTC CAGGCTAGTG TTCTTAAATT CCCTTACATT 1200
TATCTTGCTC AAATTGCCTC CTCTCTGTGC AGGGTTCAGC CTGCCCGGAA ATGACCTCTC 1260
|
