Tag | Content |
---|
EnhancerAtlas ID | HS050-13176 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:77625010-77626890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr11:77625030-77625042 | TAAATCACTGCA | + | 6.92 | TP63 | MA0525.2 | chr11:77626093-77626111 | GACATATTTCAACTTGTT | - | 6.08 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I077912 | chr11 | 77623796 | 77626758 |
|
Enhancer Sequence | TGTGATACAG GAATCCCCTG TAAATCACTG CACATCACAG AATATGGATT TTAGAGTTGA 60 CAAAGCTGAA CTCAAATCCT GCTTCTGCCT CTTCTTAGCA AATTACTTCA TGTCTGCAAT 120 GATGGTTGTA AAACATCGCA GGTGCCCTCA GTGCTATGGT CCATCTGCTT CCCTTTCCAG 180 ATTTTTCACC ATCCTGCCTA TGCTCCTGAA TACACACTCA AGCTAGAAAC ACAGAGCCCC 240 AAACTTAGGA CAGTGATCTG GCCGGCCACT GCCTAGCAAG ACTATCATCT CAGGAAACCC 300 AGACCATGAA GGCGAGTACC TTCTAAGAGC CAGCACTGCA GCTGATCACC AAATTGGCTA 360 GCTTTTGTGC CTTTTGCACT TGCTTTAGTG CCAACAGGAT AAAACTGTCA AGGACAAAAT 420 CTAAATGTTT ATTTAGGTGG GGATGAGTCA GGAAGTAGAC TGTATTTTAC TGGGCTCAGG 480 GCCAACAACC TCATTCAGTG GCCTCCAAAA CTAAACACTT TGTTGAGGGA GAAGAGAAAT 540 CGCTTCACAA GAGGTATAGA AAGGACTGGA ATCTCCGCTT ACAGAGCTGT GGACTGCCCA 600 GAGCTTACAG CAGGGTCAGC AAATTTTTTC TGTAAAAGGT CAAATAGTAA ATATGTTAGC 660 TTTTACAGGC CGTATGGTCT CTGTGGCAAC TACTCAACTC TGTGATTGTA GCATGAAAGC 720 AACTATAGAC AATACCTAAA CAAATGAGCG TGGGTGTGCT TCAATCAGAT CTTACATACA 780 AAAGCAGGCA ACAGGCCAGC TTTGGTCCAC AGGCTGTAGT CTGGGGACTC CTAGTTTAGA 840 GTACTGTTAC TGGCACATCA CAGGCACACA ATAAATATCA AGTATATGAT TCAATGTACA 900 GTGGCAAGAG AACAAACTGC CATGCTAAAA TCATTTCAAC CTAAAAAATA ATTCAGTTTT 960 CCCTATCTTT TATTGTTACT GATTACAGTG ATGGTATTCA GGTGAACACT CTGCCATTTG 1020 GAATATCATT TAGGCTTAGC CTGTGCAGCT AATGCAGCTT CTTCACACCA CACAGCCATC 1080 TTTGACATAT TTCAACTTGT TAACGATTCA TGTTCTGCAG CCCTTTTGGC TGATGCTATC 1140 ACTGCAAAGC AGTGATATGT GTGAGTCCAT TCATTACGGT AACAAGCTTT CACTCAAGCT 1200 TTGTTTCTTG CAGTATCTAT CATTTCTAGT GTGATCTCCT CCACTGATTT TTAAAAATCC 1260 AGTCAACAGT AGGATTTTCT TGTTGAACTG TGAAGGCCTG TGCTAGGTAG GGACTTTGTG 1320 AATCATCCCT GCTTGGGTCC CAGAGCTACT GGGGGGCCCA TCACTGGAGT GGCTGGTGAG 1380 ACCCTCCAGG GCATGAGAGT TGCTATGGGC CTCTGTGTGG CTTCTAGAGG CTTCCCAGGG 1440 GCACAAAGAC TAAGTGACCC AGGTGGAAGC TCAGGAGGCT CACGCTGGAC ACATGCTGCA 1500 CACTCTGGCT CTCCTGTGGC TGCAGCTGCA CCCACCTACC CAGCATTCTC CCCACGACCT 1560 GTCCAGCCCA AGCCCACGGC ACTCCCAGGG GAGCCCAGGA CACCCTCAAC TTTTTATTGG 1620 ATTACTAGAG TATCAGACCA CCCATTTATC TCTCAGTTCC TCACTCCCAC CCCTGCACCC 1680 AGCAAGTCAC CAAGTCCCCC AGGTGAGTAA ACTGGAGCTA ACAGCAGTTG GTACTTATGG 1740 CATATACTGG ATTTGGCTCA CTCACTCGTG GTATTCCTAT CTTCATCTAC TGTATCTTCC 1800 TAGACTACAT AAGCTGCAAA GTTAAAAACT GCATTTCTCA GATTCCCTTG AGCTAGGTTC 1860 CAGACATGAT TTATTATCAG 1880
|