Tag | Content |
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EnhancerAtlas ID | HS012-24628 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr8:103412530-103414430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr8:103413579-103413589 | ACCAACTGTC | + | 6.02 | PBX1 | MA0070.1 | chr8:103413176-103413188 | TCATCAATCAAT | + | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH08I102400 | chr8 | 103412741 | 103412850 | GH08I102402 | chr8 | 103414229 | 103417028 |
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Enhancer Sequence | AAAAACAATA CATGGCATAC CCACCTGATG CCACTCCCTG AGCTCGCTAA TCTATAACCT 60 CACTCTTCTC CAAGCTTTCT CCCTGAGCCA GAAAAAGTTC CAAACACGTC TCAACCCGAA 120 GTTTCAGGAC GGTTTGGTGT GGCAATTGAA ACACACCAGC TATCCCTGGC CTAGCACACT 180 TTTTGCACAT GAGAAGCACA CAAGCATTTA CTCAACAAGA AAAACTAATC TAACACTGTT 240 CTCAAACTCT GTGCAAGCAA TAGCATGGCA AATATTTACA CAGCCCAAAC TCTACCTCTT 300 GTAGCAGTCT TTCATAGTGC TACTATCTAT GGATGAGCCT CATTTCTCCC AACTAGACTG 360 TGACCTTACA AGCACCGAAA TGCATTTTAA AAAGCTATCC TTTCAGTATC TCACAGTTGT 420 GTAGAGGACC TAGAATTTAT GTAACTTAAT CTAAATTTTT CCAATTTCGT GGTTAAAAAA 480 AAAGAAGCGA ACAAAAATAA ACTACTCTAG CTTAGAGAGA GACACACAAA ATCAAGGAAC 540 AGGAAAATAC CCTATTCTCA AACAGACAGG TATAAAACCT GTAAGTCTAA GGGGAAAAGG 600 AAGGTTGGAG GCAGTGAAGA ACTGGCAAGT TTGGCCCTAT TTGCCATCAT CAATCAATGT 660 TAAGACAAAG AAAAGAGGGT AAAAGAGCCT TTTTACTCAG TGGTCTTCAA GTTTTGCTGC 720 TCCTGATGAC GGTCCATCCC ATGAGAAGCA CTGTTTTAAA TCAAGAGACC TCCTAACTGG 780 GAAAAGCCAC CACAATCCAT GATTTTACTA CAATTTGACT AGGTTATGTT ACTCATACAA 840 TAATTTCAAT TCAACTGTCC GAAAAACCTT CTACTTTAAA AAAGCTTAAC CATATCATGT 900 CCCCGATCCC CAAAAAATGC TATTACCTCT CAATAATGTC TTAAAATTGA CCAAAGGAAG 960 ACAAAGACTG AATCTACATG TCAATTGAAG AAGCTTTTAC ATTCCCAGAG CCCTCTGAAG 1020 AGCAGAGAGA CCCTAGAGAA AAGCAAAATA CCAACTGTCC TCGAGTCCCT GCCACTCTAG 1080 AGTTTCATGA AACCAGAAAC ATTCAGGGAT GGTATGGGGT GGCTGCTAAT TCCTGTACTG 1140 TACTACAGTA CTGACTCCTG TCTCTGCAGG CAAGTGTCGT ATGTACTCTT CAGTAGCTCT 1200 CAGCTCTCAA AAGTAGCAGA AAGATGAACA GATGCCAACA AAATCAGTCC ACATGTCATC 1260 TCTGACCTGC AAACCATGGC CTGCCAACCT ACACTACAGA AGTCACTCAT TTCTGTTTCT 1320 GCATCCCCTA GGCAGTGACA AAATCCTACC AGGAATCGTC TCAGGTAGCA GGAATTTGGG 1380 TTAATCTTCT ATTGGCGACT ATAGGAGGCA AAAAAAAAAA AGTACTTCCC CCAAAAAACA 1440 ACTACAGAAA CAAAAGGTCC CACTGCCCAT ACTCCCCCTA CTCAATTATT CTCTAATCTA 1500 CATGTAATAA TCAGAATACC TGATAAGCAG AAAAAACACA ATCACTTAAG GAAAACACCT 1560 AAGGATTTCC TGGAGATGAA GACAAGTTTA AACATCACTA GAAATATAAG CCTATTAAGA 1620 GAATGAATGT TTAGCCAGGC ATGGTGGCTC ATGCTTATAA TCCAAGCACT TTGGGGGCTG 1680 AGGCAGGAGA ATCACTTGAG TGTCAGAGTT TGAGACCAGC CTGGGCAACA TGCTGAAACC 1740 CCATCTCTAT GAAAAACACA AAAATTAGCC AGGTGTGGTG GCACGCACCT GTAGTCCCAG 1800 CTACTAGGGA AGCTGAGGTG GGAGAACTAC CTGGGCCTGG GAGATTGAGA TTGCAGTGAG 1860 CCAATATTGC ATCACTGCAC TCCAGCCTGA GTGACAGAGT 1900
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