| Tag | Content |
|---|
EnhancerAtlas ID | HS101-18012 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:16362560-16364200 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr17:16362768-16362779 | AGAGGGTGTGG | - | 6.02 | | ZNF263 | MA0528.1 | chr17:16363120-16363141 | CCTCCCACCCCTGCCTCATCC | - | 6.12 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23256 | chr17:16362602-16364481 | Colon_Crypt_1 | | SE_24469 | chr17:16363328-16364011 | Colon_Crypt_2 | | SE_24469 | chr17:16364026-16364451 | Colon_Crypt_2 | | SE_28155 | chr17:16362053-16364329 | Fetal_Intestine | | SE_28963 | chr17:16362293-16364398 | Fetal_Intestine_Large | | SE_52412 | chr17:16362116-16364450 | Small_Intestine | | SE_54064 | chr17:16362062-16364244 | Spleen | | SE_69090 | chr17:16362559-16364715 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I016459 | chr17 | 16362514 | 16364250 |
|
Enhancer Sequence | AAGGTAATTT CAGAGACCAG TAAGTAAAAC AGAGAAACGA ATGGAAAAAT AAATGGGGCT 60
CGAGACAGGC TGATCAGGAG CCTACACTAG GCAGGCTTGT CAACGAAGGC CTCTCAGAGG 120
CCGTAGGCTC AGTCTGAACT CAGGAGAAGG CAACTCAGAC AGAAGAGGCT GGAGCAGTCA 180
AAGGGAGCAG CGACGTCCCT AAGATAGGAG AGGGTGTGGA GGTGTCAGGA ACAGAGGAGG 240
GAGGCCCACG TGCTAGAGCA GAGCTCGCAG GGTGGCAAGT GGGAGAGGGG AGCTCAAGAG 300
ACTCAGGCAA AGCCAGATGA GGAGTTTGGG TTTTGTTTAA ACTACAGCAC AGCCCCTCAC 360
TAAAGGATGT TCAGTGAGGT CCGTGTAGTA TCCAATTTAC CTTTGGAACG AGCTCTCCGG 420
TCTTGACACC TCTGCCTATA ATCTCTAGAC CCATAACGTG GGCTGACATG AACTTCTCAG 480
ATGCAAATTG CTCTGACCAG GATGTCCTGG TCAGCCCTCT GGGGTGGATG GAGGGGCTGC 540
TCCTACCACC AGCCTGGGGA CCTCCCACCC CTGCCTCATC CAGAGAGCCT CGCTTGCCAC 600
ATGGGCACGA AAGGGGCCTT CCAGGTCTCT GGGCTTTAGC AGGGCTCACC CACTCTGGCT 660
GGCTCTGATT TTGTTTTGAG GAAAACAAAG TCCAGGTGTT GAAGTGGTCT GAGGAAGGTT 720
ACACCATGCA ATGGACTGAA TGTTGGTATC TCCCCAGAAT TCACGTGTTG AAACCTAATC 780
CCCAGGGTGA TGGTATTTAG AGGTGGGGCC TTTGGGAGGT GATTAGGCCA GGGGGGTGGA 840
GCTCTCACAA TGGGATTCCT GCTCCTTTGC CCATTTCCTG CCATGTGAGG ACACAGGAAG 900
GTGACTGTCT GTAACCCAGA AAAAGGTCCT TGCCAGTCAC CAACCAGGCT GGCACCCAGA 960
TCTCAGACTT CCAGCCTTCA GAAGTGTGAG AGATAAATTT CTACTGTTTG TAAGCCACCC 1020
AGTCTACGAT AATTTGTTAC AGCCACCTGA ATGGACCACA ACAACCCAGG TATGCACCCC 1080
CTGGCCCCGC CTCTACCCAG ATGGAAAGGG AAGATCAGAA GGCAGGAGTT CCCGCCCCTC 1140
CTCCTGGCCT TGCCTGGTCC TGTCTCACAG GGTCTCACAG TGGCCCTTAC CCACTCCCTG 1200
GCCTGCCTCT CTCTCTGAGA GGGTGGGTCC TTCTCCCCAC ACAGGCTGTC CATGAGGCAA 1260
CCTGTGAGGG GCAGGTTGGG GAGGGAGGGG AGCTCGGCTG CTCCCACCAG GCCCCTCCTC 1320
CTGCCCCCAT GGGCACTGAC CACCCAGGGA CCACCGGCCT GTGTCCCGCC CGGCTCTGGG 1380
TCACTGCATA GGCCCAAATC ACACCTGTGG TTCTCCTCGG AGGTGTAACC TTGCTCAGAT 1440
CACTTGATTA CCTGAATTTT GTTTTCCTTA ACTCAAAGAT GGGCATATAC ATAGCCCTCC 1500
TATTTCTTTT TTGCTTTTTT GAGAGCCCCA TCGCCTTTCA CCCTCTCATC TGTGAGCAAC 1560
TCCATTGCTG CTCTAGGAAA GGCAGAGTCT GGCACCTGGC AAGGCCTCCT CACAGGCCTG 1620
ACTCCCGTCC CTTCCCACCT 1640
|
