Tag | Content |
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EnhancerAtlas ID | HS180-01594 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:47047210-47048440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:47048164-47048182 | GGAAGGCTGGAAGGAGGG | + | 6.69 | SPIC | MA0687.1 | chr1:47047751-47047765 | AAAAATAGGAAGTA | + | 6.29 | SREBF2 | MA0596.1 | chr1:47048298-47048308 | ATCACCCCAT | - | 6.02 |
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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: 3 | ID | Chromosome | Start | End |
GH01I046581 | chr1 | 47047073 | 47047273 | GH01I046583 | chr1 | 47047322 | 47047630 | GH01I046582 | chr1 | 47047641 | 47047790 |
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Enhancer Sequence | TTGGTCAGAG AATCTGGAGG ATCATCAGAG GAGAAGTGGT ATGATTTGAA TGAATATTCA 60 TTTACTCATT TACTGAGCAC CTATTATGTG CCAAGTTCTG TGTAAGCACT GGCTATACAA 120 AGGAGAATAA AACACTGTTC TATTTTATAC CCCATACATG GAAGTCATTG GAGGCTTCTG 180 AGAAGTCTCC AGAAGTCACC CACAGGAAAT AGAAGTAGGA TGCAAAGGAC ACCTTGAGGT 240 TTTTAGGGTA CTGAGTCATA GTTGTTCTAA CAGAGTAATA GACCTGGGTT AAAGGAACAT 300 CTAGATGACC TGCCCAAGCT CACAAAGAGC ACAGCTCTTT GAGCCCCTTC CAAAGGAGGC 360 TACATCTCCA TCACAGCACT AGCTGCCTGA CCTCATCCCC ACTCGGCCTC CATTCTTCAG 420 CCTTTTCCTC TTGAGGCACC TAGCATTGAA ACCCACAGCC TGAGCAGAAG ACATTTCAAC 480 CATGAATTAG ATTTTATCAC TCTCAGTCAG GAGAAGTCCT GTCATTGCAC AAGCTGTCCT 540 TAAAAATAGG AAGTACTCTC TTGTGTTAAC TGAAAGAGCA AAAGAGCTGT TGATTAGGAA 600 ACTATTTGAA TACCTTGGGA TCTTTGTCTC TCCCCCATCC CCATACCCTG ACACACACAG 660 ACACACACAC ACAGACACAC ACCCCTGCTG TTTGAGTTAA AGGCAAACAA AAAACCCCTG 720 CTGAAAGTAC CTTCTTGGTT CCATCACGGT TTGGTCTTTC AGTTGTTTAT AAGAGCAGAT 780 GGCACACTGT TATTCGTAAG TGTTTTAAAT GACATGCTTC TCACAATGGA CACATTGGCA 840 TTAGCCCTTT ACACATATCA GGATAGGTGG GTGGCTGGAG GTCCCATATT CCCAACCGAT 900 AAAGTGCTTG TTATTGGAAC CACTTTACAG AACAGCCAAT TCACTAGTGT GTCTGGAAGG 960 CTGGAAGGAG GGACCAAGAG GCGAAGCTAC TTCAGACCTC ACAACGAAAG AAAACAAAAC 1020 AGATGAAGTG GGGCACGTTA CTCCTAGGAG TAGCTACTGA TCCTCTTGGT GCTTTGCACA 1080 AGTGTCCAAT CACCCCATCA CATGCCCAGT GATAACAGGA CCCACACTGA GCCTAGTGCC 1140 TCGCACACAG AGAGTGTCAA AAAATGTCTG ATGACCCAAC ATCGTTTCTA CTGAACACAA 1200 CACGTATTCT TTAAAATGTA GTCAAACACA 1230
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