Tag | Content |
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EnhancerAtlas ID | HS141-00559 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:44478610-44479720 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr1:44478725-44478741 | GGTTGTTTACTTAGGG | - | 7.34 | Foxa2 | MA0047.2 | chr1:44478728-44478740 | TGTTTACTTAGG | + | 7.22 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_04236 | chr1:44476144-44484011 | Brain_Anterior_Caudate | SE_05099 | chr1:44474958-44484186 | Brain_Cingulate_Gyrus | SE_06661 | chr1:44475060-44484159 | Brain_Hippocampus_Middle | SE_07053 | chr1:44475106-44484097 | Brain_Hippocampus_Middle_150 | SE_23374 | chr1:44476677-44482159 | Colon_Crypt_1 | SE_24099 | chr1:44478286-44478727 | Colon_Crypt_2 | SE_24099 | chr1:44478732-44479259 | Colon_Crypt_2 | SE_24099 | chr1:44479608-44480705 | Colon_Crypt_2 | SE_24883 | chr1:44478765-44483361 | Colon_Crypt_3 | SE_27482 | chr1:44479315-44480785 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I044010 | chr1 | 44476163 | 44482159 |
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Enhancer Sequence | CATTTTTTGG AGGGTGTGAG GCCTGCTGGG GGTGGTCTAT CTGGTCCCAA ACAAATGCCA 60 GCCAAATAGG GCTCCTATAT GTTGACCCTA CAATACCAGT TTTATTCTGT CCCAGGGTTG 120 TTTACTTAGG GGCACAATGC CTGATTGTGC CAGCAGCACA GTACACGGAT GGGGTCACAG 180 AGCAGCAGTT ACAGCTGTAA AAGGGACAAC TGATGGTCCA GGATGGACCC ATGGGCAGGG 240 TAAGGGCAAG GCCCTTTGCA GAGATCCAGG TTCCCAAGGC TTGAAGATCA AGGCCTGTCT 300 CCTGTTCCCA GCAGGATGAG GGACAGATGC CCCATACCCC CTGACCAAGT GGGACCACAT 360 TTGGATCCCT GAAGTCTGCT CCTTCCCTGG CAGGGGGAGG TACGGGGAAG GTGGTGATGC 420 TTCCAGCCAC GTGCCACAGA CAGCCGCCTG CCTGAGCCCT CAAGAGCCAG CCACTGCTCC 480 GTTAATGAGC CGTGTGCTAA CCAGCTTAGC CGTGCGGGCT GTAACCCAGG GAGGCCACAG 540 CCCCCGCGAC AGGGCTGAAC CGGGGTTGGC GACGGGGCTC TGGCAGGAAG TTTCTGACAA 600 CACTAAAGGT CTGCTGTATG CAGAGGATCC TTGCAGAAGC AGCACCCACT TCTGCTTGGG 660 CCTGGGTCCC AGCACTGTGG CGCTCGACCA CGGGAATCTG GCCCAGGCTT GGCCTCTGTC 720 TTCAACTCCA GGGCTGTCTA CGCTCAGGTG GCTTGGCTGG GGAGGGCTGA GCTCTCAGCG 780 GACGACAGAG CAGGCCTACC TTTCTCCAAG CAAACTGGAG GAAAGACTCT CCAAAAAAAA 840 ATCCAGGCAC TTTCTGGGTG TTCTAGTTCC CTTCCTTGTC CAGATCTCCT CTGGGGACCA 900 CCCTCTGACT TCCCTCCTGA GCAGCTAAAT CTTTTTCAAT ACTGTATGGC TTTTTTTCTC 960 CCTCCTTGCA TAATCTTTCC TATTCTAAGC CTCTAGTTTT TCTTGATCTG CTGGGTGGAC 1020 GGCTGTGTCA CTGATATGAA CTGTCCCTGC AGTGGTCATC AGCTGAGGTA CCCACGGAAA 1080 AATCCCTTTG TGCTCACGAT TTGACTCAGA 1110
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