Tag | Content |
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EnhancerAtlas ID | HS048-31925 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:46815950-46817140 |
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) |
IRF9 | MA0653.1 | chr6:46815990-46816005 | GCTTTCAGTTTTGTT | - | 6.01 |
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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 |
GH06I046848 | chr6 | 46816088 | 46817361 |
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Enhancer Sequence | AGCAACCTAT CTGGAATGGG TGAACCAGAT CATTTCTGGG GCTTTCAGTT TTGTTGTTAG 60 TGCCATAAAT GAGATTCAGT CAGTGAGGGG GGACAGAGAA AGGAAGGAGC TATCCCAGCG 120 AGTATGCCTC AGAAATGTAT GCCTGCCTGT GGATGTGCAA TGCACACTTG TAAACCGAAC 180 AGTCTCTGAG ACAGGTCTCA ATCAACTTAG AAGTTTATTT TGCCAAGGTT AAGAACACGA 240 CTGGAAGAAA GGAACACAGA ATCACAGAGA CAGTCTGTGG TCCGTTTTTC TGCAAAGATA 300 TTTTGAGGGC TTCAGTATTT AAAGGGGAAA AGTGGAGGCG AAGAGGGAGG GTATGGTCAC 360 AATGCATAAT CCATGCATTG CAGGAGAAAA GGAGCAGGTA GGGGAATAGT CAGTGATGTA 420 TTCATCTCAG TAAATCGGCA CTTTACATAA AAGGTGAACC TAGCGTAGCT ATCTGTGGAG 480 ATATCTGGCC TTTCATCTGT TAGCTATTCG CTTAGCAACA GAAGGAAAAG GCTGTTTCTT 540 GCATGACTTA GCTTCCATCT TAATTTTTTC CTTTTTGCAT AGTGAATTGG GGGCCTGAAA 600 TTTCCTTTGC CTTTCACACA CTGAAACTAC ATGACTGGGA TTTCCCTCCC TCCACAGTCC 660 TACGTTGCTT TCTGACTACC CTTTCCCCTG CAAGGATCAT AATATAAAAG TGTTAGGAGG 720 CGGGAGTGAA AGAGATTTTT TTCATTCCTG GTTTCTGTTA TCCACTATGC CTTGACCTTC 780 GCTCTGTCCA TATGATCAAA TTACTTCCTG AACCTAGACC GTTGGGCGCG TCATCCGCGG 840 GACTGACTGC CTCCCGCCGG CTTCCTGAGG CCGGACCGCA GCGGGGACGC CTCCTCTCAG 900 GCCCAGCAGG GGGCGCGCGA GCCTCAGGAG ACGCCAGCGG TGGTTGCGGA GCTGCGGTGC 960 TGGAGGCCAG CTGTCACTCC AACCCAGCTG GAGATTCCTG TCGGGAATGC TTGGCATAGG 1020 ACAACTGTGA GGGAGCCCCT GGGGCATGGG AAAACCCTCA CAGTTCCAGA AAAAAACAGA 1080 AAACGGGTGC ACAGTTTTTC TCGGTTAATC AAAGTCAAAT TCCTCTTCCC ACAACTGCTG 1140 GGGTGCCGGC TGGCTGGCAG GATGGAAGAC CCAGGATGGT AAAAATCAAA 1190
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