Tag | Content |
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EnhancerAtlas ID | HS048-32785 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:143140390-143141530 |
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) |
IRF1 | MA0050.2 | chr6:143140946-143140967 | GGTGAGTTTCACTTTCTGTTT | + | 7.82 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_11156 | chr6:143137075-143146750 | CD20 | SE_18234 | chr6:143134784-143146665 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19102 | chr6:143139168-143145046 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_46005 | chr6:143140323-143142517 | Osteoblasts | SE_52106 | chr6:143140774-143141518 | Skeletal_Muscle_Myoblast | SE_58650 | chr6:143140122-143209359 | Ly1 | SE_62207 | chr6:143093923-143269986 | Tonsil | SE_63932 | chr6:143140760-143141544 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I142819 | chr6 | 143139934 | 143144622 |
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Enhancer Sequence | AAAGAAAAAT GCTTGGGGTT CAAGGTCTAT GTAAGAGATA TGCAAAACTT CAAAAATGTT 60 GCAAAATGTT GTGTCTATGT GCATTTTCCT GGGGAAAAGA GTCAGGAGCT TTTATGAATC 120 TTAAAGGGGT TTATAAACCT CTACCCCAGA AAAGGCTATG AAGCAAGAAT CTACAAACTT 180 CTGCTAAGCT TTTTAATGTT TTCCAAAAGG AAAAATACTT TTGTAAATTT AAGTTTCACA 240 TACAAGGAAA TCCATTTCAT ATATAACAGG GAAGAAGATT CATATATTCT ACTATAAGGT 300 AACAACTTGA TAAGGAGACA CCGAAGTGAC CCTTTCCCAT GTTTCTAATA ACTATTCAGG 360 ATGTTAACAG TGAAAGGACC ATTTAGAAAG CTAATTTCCT TTTCATCATG CTTGTTAAGT 420 GTTTACTTTA ATTCACATCC TGTGTGACCC TATGGGAAAA TTTTTAACTA ATACTGGGGA 480 AAATCCCATA GGGTTACACA GGATGTGAAC AGGGCCTGTA CTGAACTACC TTCAGCTTGA 540 AAAATAAAAT TAGATAGGTG AGTTTCACTT TCTGTTTGTC ATAAGTTCCA CTTTCTGGCT 600 CCCAAAGCTT AGATCCACAG TACATCCATG TCCGTGCAAT AAAATCCCAA GATTCTCACT 660 CTCTGTTAAA GGAAGGATTT CGGCGTGTTG TATAGCAAAA TCCTTTCAGC AGAAAAATGC 720 AAATCTGTGG TGCTAATCAA GGAGAGGCGG CTGGAGCACT CCCAAATGCT CCTCCATACC 780 TGGGCTCACA CACAGTTCAG CTGCCGTTTT CCATTTCCTG TGGGGAACAT ACATCATACC 840 ACTTCCCCTA TAGAAAAAAG AAAGCAGCCC GATTTAATTG CTGATGGAAA CATTGTCATA 900 CTTTCCACTG GCCAAGCTTG AAACTATTAC TGATCTAACC TTCATTAATT TTTCCACAAC 960 AATTTGCAGA AATGTCAGGA AGCAGCTGTA CGAAGACTGA TTAATTGTCC TTATCACCAC 1020 TACTTTACCA GGCTCGCTCT CTCTTCTCTC TCTCTCTCTC TCTCTCTCTG TATCCTCACC 1080 ACCTCCCCTC CCTCTCTTCC AGTTTAAAAA TATAATTGGG ATTTTTCTGT TTTGGTTGGT 1140
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