Tag | Content |
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EnhancerAtlas ID | HS048-00500 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:20301240-20301920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:20301747-20301762 | GCTGGCCTTGAACTT | - | 8.42 | SREBF1 | MA0595.1 | chr1:20301337-20301347 | ATCACCCCAC | + | 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: 1 | ID | Chromosome | Start | End |
GH01I019974 | chr1 | 20300843 | 20302667 |
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Enhancer Sequence | ACACAGGATG CTATGGGACT GCAGGGGTTG CACACCTGGG AAACCAACCC TGGTGACGGG 60 ATAACACCCC CAGGGTCCAG CTGGTGGCCA GCATTATATC ACCCCACATT TCCTCCTTAC 120 TAGACTGGCA ACACAGGAGA AGAGCATTCC ATGCGGAAGA CTTGGACTAC AGCTTCCCAG 180 ATTAAGACCA ACCTTCCTGC TTTCTCCCAG CAGGCCAGTA GGAGCTGCTA TTGCCTAGGG 240 AAGGGGAGGG AGATGTCTGG GTTTCGCTTG TAGTAGTCAT GGCAGCTATC AGACATATCA 300 GACCCAAAGC TTTTCATTTG TCATCATTCT AATTCTCAAA CATGCCCATG CAGGAGGCAC 360 CAGTGTTATC TCCATCTAGA TGAAAGAACT AAGGCTTAGT GAGATGGGGG AGCGGGGATT 420 TGACACAGCC AGTCTGACTC CAGAAGCTAT TTTTTTCGTT TGTTTTGTTT TGTTTTTATA 480 AAGATAAGGT CTCCCTGTGT TGCCCAGGCT GGCCTTGAAC TTCTGTGAGC TCAAGCAATC 540 ATTGCACTTC AGCCTCAGCC TCCCGAGCAG CTGGGACAAC AGGCACACAG CACTACACCA 600 GACTCAGAGC CTGTATTTTT AACCCCTACC CCTGTTTGTT CTCATGCTAA CAGTGCATAG 660 GGCAATGCAT ACACACACAC 680
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