| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00782 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:24893950-24895550 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:24894986-24895007 | AGAGGTGGAGGAGGGGAGAGA | + | 6.4 | | ZNF263 | MA0528.1 | chr1:24894246-24894267 | GGAGGAGGGAAGAAGTGGAGG | + | 6.68 | | ZNF263 | MA0528.1 | chr1:24894989-24895010 | GGTGGAGGAGGGGAGAGAAAG | + | 7.05 | | ZNF263 | MA0528.1 | chr1:24894992-24895013 | GGAGGAGGGGAGAGAAAGGAA | + | 7.19 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28444 | chr1:24892273-24895724 | Fetal_Intestine | | SE_29333 | chr1:24892170-24895939 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I024565 | chr1 | 24892389 | 24895732 |
|
Enhancer Sequence | CAGGCATTCT GCTAGGGGGT TAACGTGCAC TGCTAAGTGA CTTATGCACA CAAAACCCTT 60
ACACAGGCCT GGTCTATACA GTAAGGCTAA GTGATTGACA CTTAATATTA ACAATTATCA 120
TCTCCTTTGA GTGTAACAAG AAGGAACTAG AGAGGAGTCG CAAAGCCTCC TTTACAGTTG 180
AGGAAACAGG CATGGAGGCT AAGTTGTGAG CCCAAGGGGA CATAACTAAG CCGGAGTTCA 240
ATCCCCAATT TAATTCTAAA GTCCTGATCT CTGTCTCCAC CCTCTTTCTA GTTCATGGAG 300
GAGGGAAGAA GTGGAGGACA TTCCCAAAGA GGGGACAAAC CTTGGGAAAA CTCAATAGTC 360
TCAAGGAGCC AGGGTGTGGA GTATGTGGGT GCCCAGGTGG GATGGGAGAG GAGGCAGGAG 420
AGAGGTGGCG GGGGCTGAAG TGTAAAGGGC ATTGAACACC AGGTGGGGTA GGAGAGTGGG 480
CTTGATTCTA CCCATAGAGA GAATCGACCG AGGGTTCCGC GACGCCCTGG CCGTATTGGA 540
ATCTCTCCTT CCAGGTCACA CTCCCGTGAC CGCTCGTCAC CTAATTAGGC ACCCGCCTGT 600
GACCCGTTCA CATCCTTCCA GGCAGGGCTG GGCCTGGAAC ACGGGGCAAC TCACAGTCCA 660
GAGCTTCCTC CTTGTCACGG CCTCCCTCTC AGGCTGTGGT ATTTGCTCAG AACCTGAGCC 720
CGGGGGCAGA GAGCACAGAA ATATTTATTT ATGTCACTGC CAACCCTGCC TCCTGGAGGC 780
CCGCACGGGG CACCTCACAG AGAAGCTCAG TTATATAACT CAGAGTTGAC ACAGCAGGAA 840
GGAGAGGGAA ACAAGTTCTA GTTATTCCTT TTTCTCAGTC TTAGACACAT TTGGAAACTG 900
GATGGCTTGA CATTGCCCTG TCTTCTTCCT CCCTCACCTT ACTGACCTGG GGTCCCCAGG 960
GACCTCGGTG ATGCTAGATC CATTGCTGAT TTTAACCTCG ATTCTCATGT GGCTGGGGGT 1020
TTGGGGAGAT CTTCCTAGAG GTGGAGGAGG GGAGAGAAAG GAAATATATT AAAGGGCTGC 1080
TTTGTGCCAA ACACTGCCAG AGACTTTATA TTTATTATTA TTAGTAGTAG TATTAAACAG 1140
CAATCCCATG AAGAGGGTCC TGTTATTACC TCCACTTTAC AGAAAAGGAG ATGAAGGCAC 1200
AGAGAGGTTA AGTAACTTTC TAAAGGCCAC CCAGCCGAGC CAGGTCAGTC TGGCTCTGAC 1260
CACTACTGGT TCATTTTCAA GCATCTCAAA CTGAATCCAT AATAAACTGA ATCCCATAAT 1320
AGGGATCCTT TTTGTTGTTG TTATTAGAGA CAGGGGTCTC GATATATTGC CCAGGCTGGA 1380
CTCAAACTCC TGGGCTCAAG AGATCCTCCC ACCTCAGCCT TCCAAGTAGC TAGGACTAGA 1440
GGCATGCGTC ACCATACCCG GCTCATAATG TAGGGGTTCT TGAGAGCCCA GAGCATGCTA 1500
GTTTCTTATT GTGGAGGAAG TTCTTCCACA GCTTTAATTC CTAATATATT TGTTTTGTTT 1560
TGTTTTGTTT TTTTTTGGAG ACTTGCTCTG TCGCCCAATG 1600
|
