Tag | Content |
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EnhancerAtlas ID | HS040-18096 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:15812260-15814910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:15813515-15813534 | AAGCGCCACCTCCTGGCTG | - | 6 | Klf1 | MA0493.1 | chr19:15813151-15813162 | TGGGTGTGGCT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 15812394 | 15812794 | chr19 | 15812811 | 15814040 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I015701 | chr19 | 15812346 | 15814365 |
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Enhancer Sequence | ATTTATTTTT TTCCTGAGAT GGTGGATTGG AGGGATTGTT AGCATGCTTC TCCCACTTGG 60 AAGACAACAT AGTGTGTAAA GATTCACACT GTGAAGTTTT TTCCAAGAAG TGACACAGGA 120 ACTTAACAGG AAAACTGAAA GAAACCACCC TTTGAAAGAA GCATCAGGCT GCAGCCTACA 180 CCACGAGCCA GGTGGACAAC TGTAAGTCCC CAGAGTGTGA GAGAGGGTAA AGTGCCTCCA 240 GGATATACAG TCCCACCGGG GAACCTGGTA ATCCAGGCCA CAGGGAAGGT CTTAATCCTT 300 CCTTGTGGCA GGCCAACTGG GTGGCTGGGT CTTAATCCTT CTGAGTACTG GAGCTGACTT 360 AGTAAGTGGT GGGAGTATAT GAGAAGTGGC ATCAGGGCAG GCATTCCCAG TCTCTGGCAT 420 TCCCAGTCTC CAGCAGGACA AAGGGAAGCC ATTCCTGATC CTACCTCACA GGGGACCTCA 480 TGGACGTCTG CCAGCTAACA CAGGTGGTGG TCACAGGTTG AGAGAAACTC CCAACTGAGA 540 TTCACAATAT AATCTCAAGT AGGGATAACT CCCCCGTGGT CAGACCAAGA GGCAAGTGGG 600 AAGTGAGCTG CAGCAACCAG CACAGGAGCT TGGTGTTCCT GCTTAATGGG CAAACCTGGA 660 GAGGTGTGGC CTGAAAGCTG CAGATACTGG CTCAGCATTG GACTTTTGTG TCCCTGCTTA 720 ATGGGCAAAC CTGGAGAGGT GTGGCCTGAA AGCTGCAGAT ACTGGCTCCT CAGGGAAGGC 780 GTATGGCCTG GGGCACATTT GAATTCTGAG CACAGACTGC CTGGAACCTA GCTAGCTGCT 840 GCTAGTGGAA CACTGTGGGT GCAAGACCTG TCTTGCCAAG AGTGTAGGAG CTGGGTGTGG 900 CTTATTGCCA CCTGCTACTC CCCATTCCCC ATACAGACTC TTCTGTGAAG CAGAGGCAGC 960 TGTGCTCCTC CCTGGACATT ATTCCTGCAA CCAGAGAACC ACTCTCTGAT CCCCAGTGGG 1020 GCTACTGCTT TTGTCCAGAG GTGGAGAGCC AGAGTGCGGA CTTGCCTGAT TGAGCTCTCA 1080 CTTGGCTTTG CCCCTCCACC TGCCCTGATA TATTAATACG TAGGGCAGAA ATTTTTGGGA 1140 GCCCTATGGC CCCCCCGCCC GGCCCGCCAC TGCCTGAGAC GCGAGAGTAC CTCCTCTGGG 1200 TAACATAAGA CAGACACAAA TTCCACTGCT ACCACCACAG CTGGTGTTAT TTTGCAAGCG 1260 CCACCTCCTG GCTGTGGGCC AATTGACAGA GTCCATTATA GTATCTGCTT GCAAGCACAA 1320 TAACAGCCAG CAGGAAGGAG AAAACTTGTG CATGACCTCA GCTATCACTA TTGCCTGCAT 1380 CCATCTGGTT AATCAGGAAG TTCTGAGTCT GTCCACATGA CCAGTTTGTT AGTACCACAG 1440 CTGGCATTTG AGAAAGCCAA CACACTAAGG CTACTTATAA CTGAGCAATC TCACAGAATC 1500 TACATCACTC CCCTTCTTCC CCCATCAGAG CTGGGGCTGG TACCACTGCT GGGGGTTTTG 1560 AGGATCCGTT ACTTGATTGG CCCCTTGCAG ATATTCTCCA GCACCAGCAT AAATTGTGGC 1620 AGCCCCACTG GGTGGCTAGA CCAAGAGGAG CCGCAGCCTT CATAGTAGTC TGGCTCTCTG 1680 AGACTCCTAC TTCTAGGGGG AAGGGGAGTG CACCGTATCA ATGGAGCACA CCATGGGACA 1740 AAAGATTCCA GATGGTAGAC CTTGAGTCCC ACTTTCCGCA TATGAGAAGT TGCTTTTCTT 1800 TTTCTTTTTT TTTTTTTTTG AGACAGACTT TCGCTCTGTC CCCCAGGCTG GAGTGCAGTG 1860 GCGCAATCTC GGCTCACTGC ACCTGGGTTC AGGCAATTCT CCTGCCTCAG CTTGCTGAGT 1920 AGCTGGGGTT ACAGGCGCCT GCCACCGTGC CCAGCTAACT TCTTGTATTT TTAGTAGAGA 1980 TGAGGATTTG CCATCTTGGC CGGCTAGTTT TCAACTCGTG ATCCACTCGC CTCAGCCTCC 2040 CAAAGTGTTG GGATTACAGG CTTGAGCCGC TGTGCCTGGC AAGAAGTTTC TTTCAGCAGA 2100 GGCATAGGTG CAGTGCTGGG TTCAGTGGCG GAAATGTCTG CAGATCTACT TCAACAGTCA 2160 GGCACTTCTG GGGATCAATG AAGGGTCTTA GAGAAGGGGA CTTTTTCTTC CCCTTGTCCA 2220 CTACTGCAGA CACAGCTGCA GCTTCTCCCA TGACAGCTTG GCATGGCTAC ACATGTAGAC 2280 ATTCATTCTC TCTGGAATAG TTCAGAGTGA CTGCATTCTA TAGGAGGAGC ACTCTCCAGG 2340 TTCAGGCTTG CATGAGTGGC AGAGCCCCAG TCCCTCTCTA CAGGGAATAT CAGCATTCCT 2400 GCAAATGAAA AGAGGTGCCT ATCTGATCTG ACTAGTCAGA TCACTGGGTC AGGAGTGTAT 2460 CTGGGAGGTG GGTAGGTTTC CTGCTGTCCT GGCAGGGGAG CTGAGGAGGC TCCCTCCCTT 2520 CCCCTTGAAA AGACCTCCAT GTGTTTCCCT GAGAGCTCCC CCAACCACAT CTGTCAAGGA 2580 TGGCACCTTT GCCCCCCACT GGGAACTGCA TTGACCAAAC TGCTTTAACC ACAGCTGGTT 2640 TTTATTCATG 2650
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