Tag | Content |
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EnhancerAtlas ID | HS048-29822 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:102553180-102554850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP3 | MA0746.2 | chr5:102554512-102554525 | GGTGGGCGTGGTG | - | 6.48 | SP8 | MA0747.1 | chr5:102554512-102554524 | GGTGGGCGTGGT | - | 6.32 |
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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: 1 | ID | Chromosome | Start | End |
GH05I103217 | chr5 | 102552965 | 102554845 |
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Enhancer Sequence | TATGACATTG AACTAGTATG AATGAGAAGA CAGCTTCATT GACCCATTGT TCTACTTGTA 60 TTACTAATAA GCTAATTGCC AAAACTGCAC AGAATATATT CCTAGTTTTG TTTCTGTTTT 120 CAGTTGGAAG AGACTAATTT GTAACAAAAT CTGTTTGGAT TGAAACATGC CAAACTTTTG 180 ATTCCTGATT TATTATTATT TTTTAAAGAC TTGATAAGTT CTAGTGACCT GATTCATTCT 240 TATCACACTA AAAATGAGCC ACTAAATATT TTGTGTGTAC ATCTCACCTT CCATGACAAC 300 TTTATGAGAA ACAAAAGTAG AAGCAAAATC ATAGATGAGG GTAGTCATTA GAAGATCAGG 360 AAGGAACATA AAGTTATGTA ATTACATTTT CAGAACTTTA TACATTTTAC CAGAAATAAA 420 ACACACAATT TAAAAAATGC TGGCCAGGCA CAGTAGCTCA CCCCTGTAAT CCCAGCACTT 480 TGGGATGCTG AGATGGGAGG ATCACTTGAT GTCAGGAGTT CAAGACCAGC CTGGCCAACA 540 TGGTGAAATC CTGTCTGTAG TAAAAATACA AAACTTAGCT GGGAGTGGTG GCAGGCACCT 600 GTAATCCCAG CCACTTGGGA GGCTGAGACA GGAGAATTGC TTGAACCTGG GAGGCAGAGG 660 TTGCAGTGAG CCGAGATCAT GCCCTGCACT CCAGCCTTGG TGACAGAGTG AGACTCTGTC 720 TCTAAAATAA ATAAATTAAC GTTAAAGCAG TCAAGCAAAT CAACTGCTGG CCCTTTATTT 780 GTATGGAGAC ATTCTTTTTA GCTGCATCAT AAATTGTTTT GCTGAGTTCT ACAAAAAGCC 840 CTGGGAAGTT AGCAAAGTAT GTATTATTGT TCTTACTTGA CAGATAAGAC AGTCGACACC 900 CAGAGAGGAA ACACGTAAGT CACTGACAAA ACTAGAAAAA GAATTCAAGT TGCCCAACCT 960 TTGTACATTT CTCTCTCAGG TTTATTTATG TTTAACTTTC AAACCTTGCT ACGTGGCTAT 1020 AGTTCTTAGG GATTTTTGTA GTTCATGATA CAAATAACTG AAGACGTATT TTCCAAATTA 1080 AAAGCAGTAT TTAGTTAGTA TACAAAAATT CAAGTAACTT GACTGGATAC CAATAGTCTT 1140 CATTCAAGAA ATATAGTTCA TTTTTGTTTT TTATTTATTC AGCTTACATC TTAACTCTTT 1200 CTTTTCTTTC TTTTTTTTAA TTATACTTAA GTTCCTGGGA GGCCGAGGCA GGCATATCAC 1260 AAGATCAGGA GATCAAGACC ATCCTGGCTA ACACAGTGAA ATCCCATCTC TACTAAAAAA 1320 TACAAAAAAC TAGGTGGGCG TGGTGGCAGG TGCCTATAGT CCCAGCTACT GGGGAGGCTG 1380 AGGCAGGAGA ATGGCATGAA CCCGGGGGGC GGAGCTTGCA GTGAGCCGAG ATCGAGATCG 1440 CATCACTGCA CTCCCGCCTG GGCGACAGAA CAAGACTCTG TCCCAAAAAT AATAATAATA 1500 ATAATTAAGT TCTAGGATAC ATGTGCAGAA CATGCAGGTT TGTTACATAG GTATACATGT 1560 GCCATGGTGG TTTGCTGCAC CCATCAACCC ATCACCTACA TTAGGTATTT CTCCTAATGC 1620 TATCCCTAGC CCCCAACCTC CCAACAGTAC CTGGTGTGTG GTGTTCCCCT 1670
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