Tag | Content |
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EnhancerAtlas ID | HS180-42714 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr6:108651120-108652520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr6:108651598-108651613 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29519 | chr6:108650744-108654472 | Fetal_Intestine_Large |
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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 |
GH06I108329 | chr6 | 108650968 | 108654187 |
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Enhancer Sequence | GAGATCTCTG CTGTCATGAA TGGATTAGTC CATTCGTGGA GTAATGGGTT AATGGATTAA 60 TGGATTATCA TGGAAGTGGG ACCGGTGGCT TTATAAGGGG AAGAGAGTCT TGAGCTAGCA 120 TGCTCAGCCC CCTCGCCATG TGATGCCCCT GTGTCATCTG GGGCTCTGCA GAGAGTCTTC 180 ACCAGCAAGA AGGCCCTCAC TAGGTGGGGT CCCTCAAACA TGGACTTCTC AGCCTCCATC 240 ACTGTAAGAA ATAAATTCCT TTTTTATTTT TTTTTTTTTT TTGCGACTGA GTCTCACTCT 300 GTTGCCAGGC TGGAGTACAG TGGTGTGATC TCAGCTCATG GCAGCCTCCC CCGGGTTCAA 360 GCGATTCTCT TGCCTCAGCT TCCTGAGTAG CTGGGACTAC AGGTGCATGC CACCACGCCC 420 AGCTAAGTTT TGTATTTTTA GTAGAGACCA GGTTTCACCA TGTTGGCCAG GCTGGTCTTG 480 AACTCCTGAC CTCGTGCTCT GCCTGCCTGG GCCTCCCAAA GTGTTGAGAT TACAGGTGTG 540 AGCCACTGCG CCTGGCTCAT AAATTCCTTT TCTTTATAAA TTACTCAGTT TCTGAAGATA 600 AAACTCTGAC TTTGGACTGT AAACCTTTGT CTTGGGTATG AAACCTTGAC ATTGTTGAAA 660 GAAGAGTGGA AACTGTAAGG GACAACAAGT TTCACCACAG CACAGTCTTC TTTCTCTGAT 720 AGGCCATCCG AACAGCTAAG GAGAAGACAG ATCACTCAAG AACTTAAGTT GTTTATTAGC 780 TACAGCATGT TTGCTGCTTT GATACACATT CAGCCATTTT GGAGGAAAGC TAAGCAGTAC 840 TGACTGCCCA TTTTCGTGAA CTTTAAATAA CAAATACTAT TTCTCAAGGT CTTCATTTTA 900 TCATTAAATT CAGCTAATTA CTACCTGTTT AAAAATAAAT AAATAAATAA ATTTCAGAAT 960 ATCTGAAACT CAATTTCAGA TATTCTGTTA TAAGCGACAG AAAATGAACT AAGACATGTG 1020 CTAAGTAGGA TTTATGATTT TATGAACTTT GGATTTTGTT TTCAATACAG TTGTTTAAAC 1080 TTCATTATAG GCTGGGTGTG GTGGCTCATG CCTGTAATTC CGGCATTTTG AGAGGCTGAG 1140 ATGGGAGGAT TGCTTGAGGC CAGGAGTTTG AGACCAGCCT GGCCAACATA GGGAGACCCC 1200 ATCTCCACCA AAAAAAAAAA ATTAGCTAGG CATGGTGGTA CATGCCTGTG GTCCACCTAA 1260 TTGGGAGGCT GAGGTGGGAG GATCACTTGA GCCCAGAAGG TTGAGGCTGC AGTAAGCCGA 1320 GATCGTGCCA CTGCACTCCA GCCTGGGCAA CAGAGAGAGA CTATCTCAAA AAACAAAACA 1380 AAACAGAACA AAACAAAACA 1400
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