Tag | Content |
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EnhancerAtlas ID | HS048-14138 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr16:27636000-27638110 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr16:27637166-27637187 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 27637462 | 27638002 | chr16 | 27636098 | 27636999 |
| | Number: 1 | ID | Chromosome | Start | End |
GH16I027625 | chr16 | 27635792 | 27638208 |
| Enhancer Sequence | TGTGGTGGCA CGCACCTGTA GTCCCTGCTA CTCGAGAGGC TGAGGTGGGA GGATTGCTTG 60 AGCCCAGGAG ATCAAGGCTG CAGTGAGCTG TGATCACACC ACTACACTCC AGCCTGGGCA 120 CCAGAGCAAG ACCCGGGAAA AAAAGAAAAG AAAGAAATAG CCATTGAGAG CTTTCCTCAT 180 TCAGCAGGCA CCATGGCCCA TAGGACAGAG GCTCAGAGTC CAGTGCGGGG GAAGAAGAAT 240 AAACAAATAC ACAGATACAT CCATAATATA ACATTAGCCA GTGATAGTGT GCCATTGGAA 300 AAAGTTGAAC CGGCAAGCCA GTAGAGGGTG GCAGGGCAGC AGGAGGGAAG AGTTCGATTT 360 TAGATAGGGC AGGAGAGGAA TCTGATTTAT CTGAGTCCCC TCTGCCCAGG ACAGCTTTTT 420 ATGCAAAGTA GGCTATCAAT TTTTAAAAAA CACTTTTCTT TGATGCCACC TGGATATTAC 480 TGATGCACTC CATTGCAGTA GGGGAGTTCC TTTAGCAATT CCTTTCCAGT CTGAATAATT 540 ATCTCCTAAT TTATCAGTTT CATAAATCTA CATTTTCATA AATCATTCTG CCTAAGGAGG 600 GGCACCCGTG GACTGCCAGT CTCAGATCCT GGATAGCTGG ATGCCGTGAC TGTTAACGTG 660 GCATCAGAAG GCAGGGAGAG AAGTTGAGGC AGGCTGTCTG CCTGGGTGAT CAGATTCCCC 720 ACTCTGCCCC GCCACAGGCC TCCCAGGACC TAGGCTCCTG CTCCCTCCCT GGAGACTGAC 780 GGTGCCTACA TTGTCCCTTG ATTGTTTGCT CTTGCAAGCG TAGCTATTGC TGTGTTTGGA 840 AATTGTCTCT TAGTTACTTG TGTTTTTCTT CCGTTTTATG TTGTTGCCCA ACAATCAGGC 900 ATCTCCCAGG CTTCCAAGGC TGGCAAGAGA TAAGCAGCCT GTAATAAATG TTCCTGCCAC 960 AATTGGTGAA AAGATGAATG TATCAGCTGC TAAAGAAACA TTTAAAAAAT AAACAAAGAA 1020 ATCACCCACA ATGCCACCAC CTTCCCTCAA CAACTCATTT CATGTTACAT TTATCACCTT 1080 CCACACTGGG TCCACAAACA CACAGTTTTC CAACATTACC TTTACTACAT ATGCCTTTTT 1140 CTTTTCATTT CATTTCTTTT CTTTTTTCTT TCTTTCTTTT TTTTTTTGGA GACAAGGTCT 1200 CTGTCTGTCA CCCGGGCTGG AGTGCAGTGG CATGATCATG TCTCACTACA GCCTCAACCT 1260 CCCCAGTTCA AGCCATCCTC CTGCCCCAGC CTCCCAAGTA GCTAGAACCA CAGGTGCACG 1320 CTACCACGCC CAGTTAATTT TTATATTTTT TATAGAGACG GGGTTTCACC ATGTTGCCCA 1380 GGCTAATCTC AGAACGCCTG GGCTCAAGCA GTCCAGTCTG CCTGCCCCAG CCTCCCAAAG 1440 TGCTGGGATT ACAGGCATGA GCCACTGTGC TCTGGCCTCT GTATCATTTT TATTCTGCCT 1500 TTTTCATCAC CACTCCCCCG CCCCCCACTG AACAGATCAC AGTCCCCCAT GTTTCTATAG 1560 AGTCTTCATA ATGATAACAT CTGTGTAATA GCAGCTTCCA CTTCTCTGGT GTTGGACATT 1620 TGGGTTGCTT CCAGAGTTTT GTTATTACTG AACACTGACT ATCTTCTTGC CCAGAGTTCA 1680 TATGCTTAGG AACAATTTGC CGGAATGTGC TTACTGGGCA AAGACCAAAC ATATGGCATT 1740 TTCTATATTT TCATACTACT TCTGAGAAGG TTCTATGAAT TACCAGCGAT GTCTAAGTTT 1800 GCCAGTTTCA ACATCATCTT GCTAGCTTTA CAAGTTGTCT TCGTTTTGGT GTAGACTCTG 1860 GAGCCAAATT GCCTAAGTTT GCATTCTACC CCTGCCACAT ACTATAATAG CTATGTGACC 1920 TTGGGCAAGT TCTTTAACCT TTCTATGCCT TATACTCCTT ATCTACTAAA TGGAGATAAT 1980 AAAAGTGATT ATGGCCAGGC ACAGTGGCTC ACGCCTGTAA TCCCAACACT CTGGGAGGCC 2040 GAAGTGGGCA GATGGTCAGG AGTTTAAGAC CAGCCTGGCC AACATGGTGA AACCCTGTCT 2100 CTACTAAAAA 2110
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