Tag | Content |
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EnhancerAtlas ID | HS048-31432 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:30118530-30119720 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK4 | MA0076.2 | chr6:30119551-30119562 | CCACTTCCGGC | + | 6.62 | Gabpa | MA0062.2 | chr6:30119550-30119561 | CCCACTTCCGG | - | 6.02 | MEOX2 | MA0706.1 | chr6:30118737-30118747 | AGTAATTAAC | + | 6.02 | ZBTB7A | MA0750.2 | chr6:30119550-30119563 | CCCACTTCCGGCC | - | 6.87 |
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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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Enhancer Sequence | CTAGGAGTAG GAGGAGACTG ACAGCCCCCA GGGTCTCTCC TCAGGAGAGA ATTCAGTTAT 60 ACTGAAGATG CCTTCCAGGC CCCCCTTGGT CCCTTCTGAC GTCACCACAG ATGATCAGGC 120 CAGGGGTGGG AGTCTGAACA GCAGATAATT GGCCAAACAA GTCTATGAGG TCACCTGTCA 180 AGGAAGACCT TATCAAAGAG GGACAATAGT AATTAACTGA AACCATCAGG TCCTCTCGGA 240 GATTCAGAAG GGATCCATGA TGAATGTGTC ATTAGTTGGC AAGAAGAGCA GACACAGAGA 300 GAATCAGAGA TGCATGTGCA GCCACGATGT ATTGGAACAG GTGTCCATGA CCCATGCTGC 360 TGAGAGGCCG CAGGAATATC CAGTCTTCAC GCTTCTTTGG ACTTCGAGCC CACTTCTTAC 420 CGGTAGGTCC TGGGCATACA ACATACCACT GCATAATGGT CATGAGCACA GACTCGGGAG 480 CCAAACCACA AGACTTCAAA TGCTGGCTCT GCGACTTACT ATCAGCTGAT TTGAGACCAG 540 CTGCTCGGCC TCCACATGTC TCAGTTCTCT TATGTACAAG ATGGGCACCT ACCTCCTGAG 600 GTTGTTGTGA GGATTAAATG AGTTAATATA TACAAATATT TATTATGGTG TTTGGCCAAA 660 ATAAGTTCTA TGTGTGTGAT TGTTATCAGC ATTTTTGGAA TCTCTAGTTC TTCCTACAGG 720 AACGAGTGGT GACCCCACCA ACTCGCTCAC GCCTGACATA GCTTCTCACG GGGCCTGGCT 780 CATGGTGGAA AATCGCATTT TCCTTATTTC TGCTTTTATA ATAAACTTAC CTATCATTTG 840 AACTAACTTG AGTGGGTCTC AGTTCTTTGC AATAGAAAGG GTTGCTACCA TGTAAGCTTT 900 GAAAAATGAG GTGTAAACTG TGGATGTTAC AAATGTGCAA CAGTCCTTCA GAGTCGGAAA 960 GGGTAGCTGG GACTCTGGGG CCTCTAGACT TGAGCACTTC CTGGGGAGGG AACCCAGAGT 1020 CCCACTTCCG GCCAGCAGAG CAAGGAGGTT CATTAAGCTG CCTTATCTTG AAGTTACCAG 1080 GTTTTAGGAT CTATCCACTT CCCCTGTGCT GACTCCATAC TCCGAAAGCA AGTAAACTTC 1140 AAGTAAAATT ACCCTAGGGG AGAAGCAGGT ACTGACAGAC CAACATGAGT 1190
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