Tag | Content |
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EnhancerAtlas ID | HS141-01378 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:172467060-172468500 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ONECUT1 | MA0679.1 | chr1:172467857-172467871 | GTTATTGATTTTTT | - | 7.1 | ONECUT2 | MA0756.1 | chr1:172467857-172467871 | GTTATTGATTTTTT | - | 7.28 | ONECUT3 | MA0757.1 | chr1:172467857-172467871 | GTTATTGATTTTTT | - | 7.95 | Zfx | MA0146.2 | chr1:172468440-172468454 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29101 | chr1:172467425-172471329 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I172496 | chr1 | 172465702 | 172470802 |
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Enhancer Sequence | ATAGTAAATA CATTGGAACT ATGCCTAGTG CATAGTAAGC AGTCAAAAAA TATCAATATG 60 TGTTTTTGTG AGGAATCTGG AGCACAGAGA GGTTAAATAA TTTGGCCAGG ATCACACAGC 120 TTGTAAAATA AGGCCAAGAT TCAAACCCCG GTAGTTTGGC CCCAGAGCCT GCTCTCCTAA 180 TGGCAGCGTT ATTTGCTGTG CTGCTCTGCT GCACAAAACA ATTAAAGAGT AACAAGAAAC 240 CAGTGACTTT GGGTGGCTAG AGAGAAGCTG GGGAACCCCT TGAGTTTGTG TAAATGAGTG 300 GTTCTCAAAA TGTGCCCCCC TGGCAGCATC CTCCCCATTT CCTTAGGAAC TTGTTATAAA 360 TGCAACTTCT CAGGCTACAT CCCAGATCTA CTGAATCTCC AACTCTGGGG TGAGACCCAG 420 GATACTATGT TTTAAAGCGT TCTCCAGGGG ATTTAGAGGC ACACTGATAT CCCAGAAGCA 480 CTGGAGTCGA CTTTTAACTG TTATATCTAC TACGCACCCA GCCTCCATAG CAGAACATGG 540 CTCTCAAGTT GCTTCCACTG CTTTATGATA TTCTTCAACC CATCCCTCAC CCAAGCTGGT 600 GATAGAGGTT TTGAAAGGGC TTGGTACAGG GCAATCTTGC AGCAGAGGGC TGCAAATGTG 660 AATTATTAGA AATGTGGGCA GTCTGGAAAT GTGAATTAAC TTTTGGCCTC ATGGCCACAT 720 CATATGGAGG CCTCCGTTTT CTGAGATGCT AAGTCACAGA TGGAGAAAAC AGATTTGGTA 780 CCTGGGTTTT TGGGGTGGTT ATTGATTTTT TTCACCAAAT TCCCTGGAAA TATAATTTAA 840 GGGCCAGAGA AGCTAAAAGG AAAGCGACCA AATGAATCCT GCCTCCTGGG GAGTGTTGTC 900 TGTGTGTTGT GGGGGTGGGC AGCAGTATGG CCAAGGCAAC TGTAGCTTTA TAAACTGGGT 960 GAGGTGAGGT GAGATAGCTA CAATGTCAGA GAACAATTCT GAGTTTTATA AAGACACAAA 1020 AGTACTAAAA TTTTCTCAAG ATCAAGGAAG GGGAAGGGTT GGCCCATGAA AGTTGCTAAA 1080 CAACTTTCTT TAGCAACTTG ATATTCCACG CTGCTTCCGC CAGGCTCAGC CTGCAGCTGC 1140 AACCTTCAGA GAGCTGCAAG GAGTATCATT GTTATTACCT AATACTGCCA TTTATTGAGT 1200 ACAGCCCCTG TGCCAGGCAC TATTCATTGT GCATGTGCTC ATTGTTTTAA TTCTCTTAGA 1260 ACTTGGAGTA GGTATCATTA TTTTCATCCT TCTATTACAG ATGGATTTAA GGAAATTAAA 1320 GCACATAAAA CTTAAGTAGG CCAGGCACGG TGGCTCATGC CTGTAATCCC AGCACATTGG 1380 GAGGCCGAGG CGGGCAGATC ACCTGAGGTC AGGAGTTCGA GACCAGCCTA GCCAACATGG 1440
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