Tag | Content |
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EnhancerAtlas ID | HS048-31750 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:41429460-41431990 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF1 | MA0595.1 | chr6:41430998-41431008 | GTGGGGTGAT | - | 6.02 | ZIC1 | MA0696.1 | chr6:41431219-41431233 | CCCAGCAGGGGGCC | - | 6.34 | ZIC3 | MA0697.1 | chr6:41431218-41431233 | GCCCAGCAGGGGGCC | - | 6.19 | ZIC4 | MA0751.1 | chr6:41431218-41431233 | GCCCAGCAGGGGGCC | - | 6.57 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 41429797 | 41430066 | chr6 | 41429800 | 41430200 |
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Enhancer Sequence | AGTGGTTCCG TTTCGTTAGG AACTGTGATG CCTCGTTGGG GTATGTGGTG GGTGGAGGTC 60 TGTGTGAGGG ACAGGTAGGA GATGGCAAAG CAAAAAGAAT AGATAAGCAA GCAGGAGGGA 120 AATGGGCATG GGAGGGCAGA AAAGGAACTA GAGGGAAGCC ATGTGCCAGG GCGAGCCCAG 180 CACCCCTCTG AGATGCCACT CAAGTGCTTT CATTGCCTGA GCTGGGCTGT GAACTCTGTC 240 CTCTGGCTTT AGTTGATATG CCCCAAAGGC CCCTACTTCT GACCCAATTC CTCAAGCTTT 300 ATCCCCAACC TCCAAAGATA GGTTCTCTTT TCTAACCTCT GGTCTTCCAG CCCTGACACC 360 CTCTCCCAAA GACTCATAGA GGAGCTGGTT GGCTAGTCCT TCTGTGGTAG CATTACACGG 420 TGAACTGTGG ACCATGCTCT AACCCCTATA GCTAAGCTGC CAGAGCTCTG TGGGCAGATT 480 CCTGGGGCTG CTTCCATGTA TTTCCCAGGC CAGAGGTGAG CACGCAGTTC CTGGCTCATA 540 CCGGAGCAGG GTGGATACAG AAAGAAGCAG CAGCTTGCAC CGGCTGGAGA AGCTGACAGC 600 TGCCTCTCTG CCCCAGGGCT GCAGAAGCAG TGTGTTTTAG CTATGGCATG ACTTAATAGT 660 TAAAAAGCAG GCCCAGCACA TGCCAAGGAC ATAGCTGGTC ACACTGGGCA CTCAGGCATT 720 CAACCTCCAC TGGAGGCACT TGGAGAGGCT CTTTGCCTTC TCTGCTTCCC AGAGCTCAGG 780 TGCCTCAATG GAAAACAGCA AGAAAGGTGC AACCACATTT GCCAATGAGA TGGAGACAGA 840 GAGAGGGCTC AGCTGCAGAT AGCAGAGTTC AGTTTCTTGC CACTCTTTTA AAAGCAAACT 900 CCACCAACTG ATGTGCAGTG AGGCTGGCAT TTCCAGGCGC CTGACAGGCT GGAATTAAAC 960 ACCTGTCCGT TAAACTGACA GCCCCTGGAA GGAAAGTGAG GGAAAGAGAA GGTAGAGGGG 1020 GAGAGCTGGA AACCCAACAG CAGGCCGGCT CCTTCCTTGT AGGAGGCATT GTGTGTGCCC 1080 AAGAGAGAGT CCAGGATCAG AGTAAGCGGC ACCTCTGGGT CCCTGCCCTC TGGTTTCTGA 1140 GGGAGCGTGT AGGCAGGCCC ACAACAAACT AATACTCAGA CCTGGACATT AGGGATAGAG 1200 AAGGAGGCCG GGCCAAGGAG AAGCTGAGAG GCTTACCATC ATTTGCTCAA AGCTCCAGCT 1260 CAAAGGCTAG TTGCACCCTG ACAGCCTCCC TGCTCTCTCC TTCCTCACCC ACATACACAA 1320 CATCTTAACT GCTCTGAACC CTTCAGGCAC ATGCCAGGCA CTAGGCAACC CGTCCTGAAC 1380 TTCCCTGAGA CACCTCTTGG GCTGTTGTTT AACATTTGAA TGGGTCGGTC CTGGCTCCCC 1440 AACTCCCCAG CGTAAGCTCC TAGGGAGAAG GAAGCTTGTC TTTGACTTCA AAGATGCTCC 1500 CCTACAGTCT TCAGTGCATC CTAGTGGGTG GGGCCAGTGT GGGGTGATAG GTTTACAGAT 1560 GGATGGGAAT CATGGGTAAA TGAACAGATG GATGAGTGGA TGGATGCAAC ACTGATCACT 1620 AGGTGCTGTA TGTCACTGTG CCGAGGCTGG TTGTTAAAGT TAGTAAGTAG TCGTTGCCCC 1680 TAACCAGGGA AGGCCAACCT CCAACCATCT GGGACTTGCT GGACCTCATA CCATTCAGCA 1740 AGTAAACATT AGCACCCCGC CCAGCAGGGG GCCTCAGGCC CCTGCTCCAT TGCTATGACC 1800 AGCGTCCATT CTTATTGGTC AGTATACGGG ATTATTATTT TAACCAACAC TCCTGAGTGG 1860 GCAGATGAAC AGAGGCCAGG ACTGAATGTG AAATTAGATG ATTTTAGGGA AGGAAGAACT 1920 GGAAGGAAGT AGGTAGGAAC TTGTGACAAG CCAACTCGCT TGTCAGGTGA GTGGGTTTTT 1980 GTTTCTCACA CTCAACCATG ACCTTGGGCT ATTTAGTAGA ACTCTGAGCC TCAGTCTGCT 2040 CACCTCTCAA GTGAGAACAG TATCTGCCTT GCCCACTTTA GAGGGTGGTC GTGCCTGGTT 2100 GGAATCTGTC CCTCGCTCCT CTAGGCATTA TTCTTTGCTC TGCACGTGCC CGTTTCTCTA 2160 ATAGATAATG AGCTCTTTGC AAACAAGGAT GCAGTATAAA ACATCTTTAT ATCCCAGAGC 2220 GTGCTTGGTA AATGTTGGTT GAATGGATGA ATGCAGGAGT AATGAATGAG TGAATGAAAA 2280 AAAGAGCAGA CTCTGAAAAG TATAGCAGGA GAGAGTAGGG TGCACATGGG GGAAGTTGTT 2340 GTAAGATGGA TGGGAGGTGG AGAGGGGGAA GACCAGGGAG GGGCACTGCC CAGTATCAGA 2400 AGGGATCTTC TCGCACCCTT GATCAACTCC TCATGTGCCT CCTTCACTAC CCTGGTGATG 2460 CCCAAGTTTT GGGAGCATGA GGCCAGCATA TGTCCTCGTG GGAGAGTGGG CCCCTGAAGG 2520 CAGATCCTAG 2530
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