| Tag | Content |
|---|
EnhancerAtlas ID | HS101-16125 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr16:88000-90340 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr16:88793-88804 | ACAGATAAGGA | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 88678 | 89600 | | chr16 | 88144 | 88281 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I000037 | chr16 | 87233 | 89811 |
| Enhancer Sequence | GAACTCCTGA CCTCATGATC CGCCCGCCTC AGTCTCCCAC AGTGCTGGGA TTACAGGCAT 60
GAGCCACCAT GCCTGGCCCA GCATGCATGC TCTTAAGGAA CTCACACACT CTCAACAGGC 120
AGTAGGCACT ACTCTAACCC CACTCCTGCA GCCTACCCAG GTACCCACAG GACAGTCCCC 180
TGTTAAGACT GATGATCGGG AAGACTCACC CTTCCCTAGA ATGGAGCGTG CAGTCTGGCA 240
CCACCGGCCA CAACATGAAA CACCGTGGCA AGTTCTCTGC AGCAACGTCT GTCCCTTCTT 300
GCAGCAGCTA CTGGAAAGGT GGGAATGGGG AAGACAGTCA GCCTGCTCTT GGGATATCTG 360
AGGGCGGGGT TGGAGTGACC ACCAGGACCT GGGGAAGCAC AGGCACAACA GCCACAGCTG 420
AGAGCTGACC CAGGCCCCAG GATGGCCGAC CGCTGCCCCA GCAGTGGAGA AACACCCACG 480
TCGGTGTAGA ATCAGGCCAG GCCAGCCACA GGCTAACCCA GGAGCAGACG GCTTGAGAGC 540
AGGGAGTGGG GCGGCTCCAA GCTCAGCAGT CCTCATTTCT AGAAAGGGAG AGGGGATGGT 600
AGGGCAAGAC CCACATGTGA CACCTGAGAG CTACAAAGGA GGAGCCCAGG ACACTCCCTA 660
GGGGAGCATT AGAGTGTTGG GTATAGCGAC AAGGGGGTAT GGCCATCTGA GGGGAAGGTC 720
TCTGCTTTTC CTCTGCACTG AAAACTCACA GCTGCACCTG GTAAGCTGAG CAGGGCAGGG 780
TTACCACCCT CCTACAGATA AGGAGACTGA GGCTCAGAGA CCTAGGACCT GCCCAATACC 840
TGGCTCCTGA CACCTCTGTT CTTGGCACAT TCCCATCAGC TTCTACACAA GCCTGTGAAC 900
TTCCCGAGGG CAGTGCCTGC GAGGCACCAC TCAGCACATG CCCCAGCAGA AGGCACCACA 960
GTGCTTTACA AATAGGGTGG AGCTACAGGC AGATCTACCT TCCCCCATCC TTGACCACAG 1020
GACCAGGAAG TCAGGGCAGG TGCACACACC CCCACCCACA TGCTCCGTGC TCCTCTGTGT 1080
CACCAGGGAG GCCTCACCAC AGCTCAGACA CCAGGTCACA GGACAGTTGT GAGAGCAAGA 1140
GGGGAAGCCA GTGTCTGCCA CCTGGGAAAG AGCTGCCCCG ACACCCCCAG TCCTGCTAGG 1200
GAGCCTGGCT GACATCACTG CCCAGGACAC CCTCTCCTGC ACTGGGTCTG TGGACATAGC 1260
CTCCAGCCCA TGGTCACTCT GGGCCCTTCT TAGAGCCTCA CCTGTTCCAT GGCCTCAGCA 1320
TCAAGGCCTG GCCCAGATGA CCACTGGGCC TCACGGCCTG CCTGCCCTGG TTCCCTGGGC 1380
CACTGTGAAG CTGTGCGCTG CCCTGCAGCT AGACCCCTCC CTCAGACCAC AGGCTCTGCC 1440
ACACCCACGG GAGGGTCTTC AGGCAAGCTC AGCCATTCAC CCTCCCTTAG CTGGGCAGGG 1500
TGGCCCACGC CTATAGTCCC AGCTCCTTGG GAGGCTGAGG TGGGAGGATC TCCTGAGCCC 1560
GGCAATTTCA GGTTGTGGTG AGTCGTTATT GCGCCACTTT ACTCCAACCT AGGTGACAGT 1620
GAAACCCTGT CTCAAAAAAA AAAAAAAACA ACTGCAGCAA GAATATTCCC AAAGATGAGA 1680
CACTAATGCA GCAAAAAAGG AAGTGTAAAT ATGTGTTAAA ACTGGCGGCG GTAAAAGCAT 1740
GTGTGGGGCA GGAAAAAGCT TAGGTGGACA AATGTACGAA GCTTATGAAA ACATAAAGTG 1800
CTTAAAGTGT ATGGTTTTCA CTCCATCATC ATTATTATTA TTATTATTAT TATCATTATT 1860
ATTATTGAGA CGGAGTCTCA CTCTGTCACC CAGGCTGGAG TGCAATGACA CGATCTCAGC 1920
TCACTGCAAC CTCTGCCTTC CAGGTTCCAG TGATTCTCCT ACCTCAGCCT CCAGAATAGC 1980
TGGGATTACA AGCTGTGCCA CCATGCCCAG CATGAGCCAC TGCACCCAGA TTAATTTTTG 2040
TATTTTTAGT AAAGATGAGG TTTCGCCGTG TTCGCCAGGC TGGTCTCGAA CCCCTGACCT 2100
GAGGTGATCC GCCAACCTCA GCCTCAAAGT GCTAGGATTA CAGGCGTGAG CCACTGTGCC 2160
TGACTTCACT GCATTATTCA ACAGCAAGAA CTCTGTGGGA AATATCTGAA TCCATTATCA 2220
GTGGTGAATC TATTGACTCT ATCAGTGGTG TCAATGGTAT ACTTCATTTG CTCTCCTGGA 2280
TGTAACCAGC ATTCACAGAT GCACATTTGC AATTGATTTC AATGACAGGG AACACTAACT 2340
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