| Tag | Content |
|---|
EnhancerAtlas ID | HS048-35162 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr8:8820740-8821840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr8:8821040-8821061 | TCCAGCACCTTTGGCAGCTCC | + | 6.45 |
| | | 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 |
| GH08I008962 | chr8 | 8820301 | 8821581 |
| Enhancer Sequence | TTCCTTCACT GTCCAGTTTG CAGAGCCGTC TTGGAGCTGG CGCGGGTCCT CCCTCTGTCG 60
TCCTGGCTCT TGGAAAGGAA CCAGGCGGGC TGAGGAACTG GCGCGCCCTC GTCCGCCCAC 120
AAGTCCTTGG AAAGCGCAGG CCTCGTGCGC TCTCCAGCGC CCTTCCAGGG CGCAAGGGCA 180
GGACAGGTAC ATCCCGCGTG CTGCGGTGGC GATCAGCGCG GACACGGAGC CTGGCTCCAC 240
CCGTCCGCCC AGCCTTGGGG TTCTGCCAGA GCGCCGGGCG CAGAGCAAGC GGGTCTGAGC 300
TCCAGCACCT TTGGCAGCTC CCGGCCCCGG GGTGCGAACG GCGGCCGTGG CTCACCGCTT 360
CAGGAGCAGG CGACCAGGAC ACTAGGAAGA GAAGCCCGGA CCAGGGCTAG TTTGTTTCCC 420
CAACTCCTCT GGCCAGCTCA GGTTCTTAAA CCCGCCGTGC AACAGACGCA GGTACCGGCT 480
CAGAAAGCTC AGTCAGTGGT GCAGGAAGCC TGGGTCGCGG TGCATCGTGT TTAAAAATAA 540
ACACACACTT CCCTTGGGGC CAGTGGCATT TATTCTATTT AAATTACATA GATCGTTTCC 600
ATTCCTTGGT GTCTGAAGTA TTAAGGCTGA AGTCTGCTTT CCCAGCTATT TGCATGTATT 660
TGTTTAGGGA TGGAGTCGCC CTGCAACACG GGCTGCTCCT ATGGCAACTG CTACAAAACA 720
AGATCAGGCT TCACCAGGGT CGGGAGAAGA AACCTCCCAA GAAAGCCAGG CGCTAGAGTC 780
ATGGGTGTGG ATGTCCTTTT AGGGCCTAGG AAAGTAGGGT CTGATGAGGA GGCATTGAAG 840
AAAAGCCAGT ATGACGACGA TGCTTTCATG GTGAAGTTTT GTGCATCTTC TACTGAACAT 900
TTTTTAAAGT ATGCTCTTCT TTTTTGAGTT AGAAGGAAAT ATTGGCATTC AGAGTTAATG 960
CTTCTTAAAA ACAGTTACGT GGAAAGGAAA GCATTCCATC TTAGCTCATT TGCAAACAAT 1020
TGCATTATTC TTGATCTTTG TTTATATCTA TGTATGTGTC CAATGAATAT ACTGTAGGAT 1080
GTATATGTAA TTATATATCG 1100
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