Tag | Content |
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EnhancerAtlas ID | HS048-36996 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr9:35598560-35600280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr9:35599055-35599065 | GCCCCGCCCC | + | 6.02 | TEAD1 | MA0090.2 | chr9:35598822-35598832 | CACATTCCAT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 35598848 | 35599453 | chr9 | 35598618 | 35599419 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I035598 | chr9 | 35598601 | 35600532 |
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Enhancer Sequence | GAATCACTGG GGAAAAAAAG TAGCTGATAC CAGCTCTGGT CTAGATATGC ACAAAATGAG 60 TCCAGAACAT TTTATCATAT TGGATAGCAA GAAAACTGGA AATTTATGTC AGAAGGACTC 120 AGGAACTAAC TTGAATAAGT TCCCACTGGC CAAAATAGGA CAGTTTTGGC CAGTGGGAAC 180 AAAATAGTGA TGGCAGCAGC AGGCTGTCTG CAGTGGCTGC TGCCATCATG CCAGCTGCAG 240 CAGGGAGGCA TGGCCAGGGC TGCACATTCC ATGGAGCCAA CAGGAGCTGG GGACAAGCGG 300 GATCCTTGTC CCTTCCAAGT TGGGGTGGGA GCTCCCTGGG TGCTGCTGCA GCCGCCCAAG 360 CCACGGCTGT GGACCCAGGC ATCCCTGTGC TTTCAGGACC GGGAGCAGAC AGGAGCCCTA 420 CCTTTCCAGG CGCAGCTGCA GCCACCCAAA CCACAGCTGC AGACTCAGGC CTCCTGCTCA 480 GCAGAGCAGG CAGGAGCCCC GCCCCTGCCA GGTGTAGGTG CAGCCACTCA AAGAGTGGCT 540 GCAGACTCAG GAATCCCTGC CCTCTTGGGG CCCCAGAAGG CCTCACAGGC TCAGAAATTC 600 CTGCTCCAAC TGCCTGGCTT CTTCCTGCTG TTGGTGCCCA CTCCAATCTC AGAACAAAGT 660 CCGAGCAGAG CCTGGGCACT GTCACAGCCT GGCCGAGTGT GCACATACTC GGAGCAGTGC 720 TGACACACCA GTCCCCTGCT GCTTTGGTCC CCTACAGATT TTGGGTGCCA ATGAGCATAG 780 GAGGGAAGCC AAGTGGGGTC TGAAGGCAGC TCAGCACTGG CCTGCAGGCG CCTCTTGGCA 840 CCTACAGCCT GGGCACCATG AATGGCAGCA GGAGGCAGAC AGGCTTCTGA GCGGATGGGG 900 CAGGTCCCTG GTAAGGCCCC ACTTTCAGGC CAGGGAGGGC CTGAAGGCTG GGGACCGGGC 960 TGCCCATCAC ACTATGGGAG TGGGAACTTG TGGTGACACT TCCAGGCCCA CCCATGGCTG 1020 CCCAGGACCA ACTGGCATGC ACTTCCTCCC CTCTAAGGCC CATAAAAGCC CAGGCTCTGA 1080 GCAGACGTCA GGACAATCAG CTGCAGAGAG GAGCTACCCA CACCAAGGCC TCCTCTCTGT 1140 GAGAGCCGCA GATGTTGGGA CAACCAGCTG CAGAGAGGAG CAACCAACTT TGGGGCCTCC 1200 TCTCTGCTGA GAGCTGCAGA GACTACAGGA TGACATACCT GCAGAGAGAA GCCACCCACT 1260 CTAGGGCCTC CCCTCTGCTG AGAGCTGCAC AGATGACAGG ACAACCAGCT GCAGAGAGAC 1320 GCTACCCTCC CTGCTGATAG CTGAACACTT GTCAGGACGA CTTGCCTAGC AGAGAGGAGC 1380 TACCCTCTCT GCTAGGAGCT GAACATGCCT CAGGACACCC CTGCTAGGGA AAGGAGCTGC 1440 CCCCTGCAGG TTTCTTTTGA GCTGTTCTAT TGCTCAATAA AGCTACTCTT TGTCTTGCTC 1500 ACTCTTCACT TGTCTGCGTA CCTCATTCTT CCTGTCGCAG GACAAGAACT CAGGACCCAC 1560 CAAATGGTGA GGCTAAAAGA GCTGTAACAA ACGGGGGTGA GACATGACCC TTGCTTGCCA 1620 CGTTGTGGGT GAAGGCAAGG AAAGAAGAAC TGCAGCCCTT CGGGGAGCCT AGCCCTGGGA 1680 GCTCCCCAAG CCAGGGCTGT GACTTCCTCT TTGAGGACCT 1720
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