Tag | Content |
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EnhancerAtlas ID | HS180-02579 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:109699200-109700640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr1:109699445-109699456 | TCTGATTGGCC | - | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28451 | chr1:109698795-109700394 | Fetal_Intestine | SE_31987 | chr1:109699084-109700403 | Gastric |
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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 |
GH01I109156 | chr1 | 109699067 | 109700250 |
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Enhancer Sequence | GCATTTGTCT TTATGACTGG CTTATTTCAC TTGGCATGAT TTTTATGTTT TTATTCTGTG 60 GAGTTTGGTT GGGGGGCACC AAGGCCAGCC CTAGGTAGAA CTGGGAAGTA AGGAGGGGCC 120 TTATCCCCCG CTGCCCCACT TTCCTGCCCC ATCCCTCCCT CAGTTCCCAC CCACTTGAGG 180 TCCCTGCTCA GTGGCTAAAT GTCTTCATCC CCCTCATCCC ATCTTCCACT TATCAGCAAA 240 GAGCATCTGA TTGGCCTCGT GTGGGTCATG TGTCCATCCA TGGCAGAGGA AGGTGGGCCA 300 CCTCACTTGA CAATCCCATC AAGACTCTGT ATGTAATAAG GAGGCAATAG TTCCTCCCAG 360 AGAGGTGCTT CTCTCAGAAG AAGGGGGGTG GACACTGGGC AGGCACAAAC AATAGATGTC 420 TTTGTTGAAC CTCCAACAAG GTACAAAATG CCTTTCCGCC TTCCCATTGC ACACAGCTTT 480 GGACTTGGGT CCCTTCCCCT TGGGCCTTGT TTGCAAAATT TTTTATCTAC TTGGCTTTCC 540 TTGCAGTTTT TAGCAGCTTG AAAGCCAGTG CTGTGCCCCA GACACAGTAT GTAAGTGTGA 600 CAGGAGCCTA CACAGGCTGC TCTCAAACAC CGGCAGCCTT GAAAACAGAT TCTGGACTCA 660 GATAGCCTGG GTCCAATCCT GGTTTGGCAG TTCCTGGCTG TGTGGCTTTG AGCAAGTGAC 720 TTTGCCTCTC AATGACTCAA TTTTCCCATC TGTAAAATGG TAAAATAATT TACCATTGAA 780 TTGTTTTGGA GATTGGAAAA CCTACTGTGT GATGTGCTTG ACCTACATCA TCTTAATCAT 840 GCTCACAGAG GGCCCTATCG CACATGGGGA AAAGGCACTC CCTCTCTGGG CAGATGCAAC 900 ACCTGAATAG GGCATACCAC CTAGCATGCA AGACTTGAGC TAGATTTCAC CCTCCACTCA 960 TGCCCTGAGC TAGGTAACCT TATGAATAGC CTGCATAACT ATACAGCAGC CCAGCCCCTC 1020 TATGATGCAG GAGTTTGTAT ATCCCCATTT TTCAATGAGG CAGCTATGGC TTAGGGAAGT 1080 CAAGCACCAT GTGGGAAGGG GCGGTGGGAT CACTTCTAAT TTGCCTATTT ACTTAGGGCA 1140 CATGAAAGAG GCTAACCCAG TCCCTAGGAC TCTCCTCCAC CTGAATTGTG GACCACATCT 1200 CTGTCATCAG CTAACCAGCT TAAACCTTAT TCATCTTCCA CAGTGGATGG TAATGAAGTA 1260 CAGCTCTAGC ATCTAACCCA TAGATTACCT CCAATCTCTA GTCTATAAAC AGTTCCTTTT 1320 TTTATTTGAG ACAGGGTCTC ACTCTGTCAT CTGGGCTGGA ATGTAGTGGT ACAATCACGG 1380 CTCACTGCAG CCTCAACCTC CCAGGCTCAG GTCATCCTCC CACCTTGGCC TGCTGAGTGG 1440
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