Tag | Content |
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EnhancerAtlas ID | HS101-01148 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:36102500-36104710 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr1:36102878-36102889 | AAGTAAACAAA | + | 6.62 | IRF1 | MA0050.2 | chr1:36103127-36103148 | TCTCACTTTCACTTTCACTTT | + | 10.73 | IRF1 | MA0050.2 | chr1:36103133-36103154 | TTTCACTTTCACTTTTCATTT | + | 8.57 | IRF2 | MA0051.1 | chr1:36103132-36103150 | CTTTCACTTTCACTTTTC | - | 6.41 | PRDM1 | MA0508.2 | chr1:36103129-36103139 | TCACTTTCAC | + | 6.02 | PRDM1 | MA0508.2 | chr1:36103135-36103145 | TCACTTTCAC | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I035636 | chr1 | 36102336 | 36104698 |
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Enhancer Sequence | TTAGAAGATT TTAATAGGTA ATGGTATCAA TTTTTCTCTT TCACTCTTCA TGTTAAACCA 60 TCAGCATATT GTGTAATGCC AATTTCGGTT GGAGAATATA CATGAAAGCT ACCAATTGAA 120 AATACAATTT AAAGCATTTA AAGGCATTTG AAATGCAAGG AACAGAACGA CAGAAGAAAC 180 TGAAGGAATC CAGCCAATGG CGATTATCTT TAGGCTCATG ATAACAAAGC CCTAAAATGT 240 TTCCACAACT ACAAATGTTA GTTATTATAT TTATACACAT ACAAAAGCAT ATATGAAAAG 300 GACTGGTGCT ATAATTAAAA TTAAGGAACC ATTTCAAGAA AGAATAGAAA ATCAACTGAG 360 AATATTAATC ACTTTAAAAA GTAAACAAAT TCCACTTCCA AAGAAAAAGA GAAAATTAAA 420 ATGATTGCCA AAGCAAAAAT TCTAGTGAAT ATTTTGACAG TAAGCTATTT AAAATACCTC 480 ACAAAAATCC TAATACTCTA ATCTTATCTA GCTGAACCAG AGTCATTCAG ATTAGACAGA 540 TAAATAAATA TTCAGGTTAC AGTTATTGCC TAAGGAAGAA AACTCCACAT TCAGTCTGCA 600 GCTTCAGAAA AGGCCTAAAT CTTCCTATCT CACTTTCACT TTCACTTTTC ATTTTTCAAA 660 TAGTGCTGAA TAATCCTCCC TGGGAGACAC GTTTCCTGTT TGAAAGCTTC TGAAATGCCA 720 AAATCCTTTA ATAGGATTTA AAGAACAAAA TGCTACTGTC AAATACTTTA CAAGTGTTTC 780 AGAGTTGTAG ATACCAGTAA TATGGCTTCT TAGACTTGGA GGGAAAAAAC ACACAAAATG 840 CACCTGTAGA TAATATCAAA TTGCCTCAAA ACTCCTAAAC AAACACACTT TTATTTGTTA 900 TGCAGGCTAG ATTTAAAGAT TGTTAGTTTG CAAACTTGTT AATAAACGAA AAACATTCAC 960 TTATATTATC TATGCAAAGA AAAAGGAGCA GAAGGGTATA TTCTAAGTGC TTGCCAGTGG 1020 TAAGAGTATG GGCAGTTTTC GTTTCCTTCT TTTGCTTGTT GGTTTTTCCT AAAACTTCTA 1080 TACTTAACAT GCCTCACTTT TATAAGAAAG CATTATTCAA TAAGTTCGCA TTATTTTTAT 1140 AATAAGAAAA AAGATATTTT TATTTGAAGG GGGAGCTTGT TTACAAAGAA CTTATGTCAC 1200 ACTTAGAAGA AAGGCTAAAA TCCTAGGCAG TAACCTGTTC AACTTTAAAA TTAGCTTAAT 1260 ACAAGGCCAA AAATGTTTTT TAAACACTGA ATATGTCCAA TGAGTAGCAG AGGGCAACAT 1320 ATTTAATAAA AACACAAGAG ATAGATACTT AGAGACCCCT GAGTTGTACA GGAAACTGCC 1380 TGTGTAGCTC TGGGGAATTT CTGATTCTTG ACGAGGAACT TACGAGATCC ACATACATGA 1440 AACAAATGGC CAACAAAATG AACAACATTA GCATGTCATA CTGTGGAAAA CCAACTGAAC 1500 TAGAATCCAA GAGACCTTGG TTATGATGTG GACTTGGCAC TCTGAACTTC GGCAAATTAC 1560 TTGTCCTCTC TAAGCCCCAG TTTCCAGATG TGTGAAATGT TATTTCCAAA TGTGTGAAAT 1620 GTTAATAATA TGACTTACCC CTGTCTAACT CACAAGTGAG AAAAACTAAT GAATTCTATA 1680 CATGTCCAAT ATTATGATAC TCAGTGTTAG ATAATGTAGT TCGGATTATA CATGCTATAG 1740 GAATTCAGAA AAGAGAGAAT TCTGTGTGGG CTGGAGTACT CCGAGTAACT TAAAAGCAAT 1800 TCTACATAGG CCAAGAGAAA AGAGACATGA AATGCGGCAT ATAAGCAAAC CAAAAGTTAT 1860 ACCACTTAAT AAGGTGGCAA TCCTCAGCAA ATGTCTACTC TATAGTATCA AAATGTTTTT 1920 ACAAAGTGAC ATACTGGACA ATTGATTGGA AGTTGTATTA TCATTTTATA CTTGGAGAAA 1980 GGAGTCCCAG AAGGTTACTA TTTTTTCAGC ATTCTTGCCT ACTCTAAACA AGCTCCATCG 2040 TGAAATGAAT GATTAGAAAA AAGTCATCAG ACGGCTGGGC ACGGTGGCTC ACGCCTGTAA 2100 TCCCAGCACT TTGGGAGGCG GAGGCAGGTG GATCACCTGA GGTCAGGAGT TTGAGACCAG 2160 CCTGGCCAAA CTGGTGAAAC CCCGTTTCTA CTAAAAATAC AAAAATTAGC 2210
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