Tag | Content |
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EnhancerAtlas ID | HS048-02136 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:117006130-117007500 |
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) |
GATA2 | MA0036.3 | chr1:117006685-117006696 | TTCTTATCTCT | + | 6.32 | Gata1 | MA0035.3 | chr1:117006685-117006696 | TTCTTATCTCT | + | 6.32 |
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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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Enhancer Sequence | GAGCACCATT TGTCAGGAAA TGGGATAGAA CCATCCAATG TTTCCAAGTG TGATCATTTC 60 TAATGGAACA GGGAGAACTC TACAAATGGA ATTCAAGTAG GATTGCCAGA TGAAATACAG 120 GAGAATGAAT TGTCTTTTGA ATGTATGTCC CAAATATTGC ATGGGACATA CTTATACTAA 180 AATTTTATCT GTTTACCTGA AATTCAAATT TAACCAGGCA TGCTGTATTT TTATTTGCTA 240 AATCTGGCAA CCCTAAATCC AAGATTGTAA GTAACCCCGG TGACCTGGGA GAATAGTTGG 300 GTGACCAGCA GAAGAGAATC CTGGAGTGGT TCAAGTGCTG CAAGGGTGTC GTGTGAGAAT 360 TCGAGCTTCC GTCTCTTCAT TTGTACAGGG GAGAATGATA CTGTGCAGAG CTGCTGCTGT 420 AAGGATTATC TGTGAAGTCA TAAATCACAT AAATGTCTGT CACATTTCCT GTATGCAGGA 480 AATAGCAGTC ACTATTGGTA TGTAGAGGGC CTATAGCCAA CGAGCGGCAA ACAATAAGCC 540 CTTAATATAA ATTGGTTCTT ATCTCTAAAA GAAAGAGAGC TGTTAGGTAA GAGTGGCCAT 600 CATTTATGAG CACCTATCAT ATATATCAAG CACTTTGCCA CATTGTCTTT TTTTTTTTTT 660 TGGATAGAGT CTCACTTTGT TGCCCAGGCT GGAGTGCAGT GGCATGATCG TGGCTTATTG 720 AAACCTCAAC CTCCCCAACT CAAGAGATCC TCCCGCCTCA GCCTCCTGAG TAGCTGTGAC 780 TACAGGTACA TGCCACCATG CCTGGCTAAT TTTTTTGTAT TTTTTGTGGA GATGGGGTTT 840 CGCCATGTTG CCCAGGCTGG TTTTGAACTC TTGGGCTCAA GCAATCTGCC TGCCTCAGCC 900 TCCCAAACTG CTGGAATTAC AGGTGTGAGC CACTGTGCCC AGCAACACTG TCTCATTTAA 960 GCCTCATTGA AGATCCTACA AAAATAGATA TGATTATTAT CTTTTCATGG GAATAGAAAC 1020 CAAAGCTCAG CGTTTAGTTG ACCTAATATT ATACCTGTGA GAGGCAGAGC TAGGATCCAA 1080 ACCTGCTTAA CTCCAAATCC TGTGATCCTT TAACCATATC ACACTATTCC TCACCATTTG 1140 ACTCCAGGCA GGTAAGAATC TTGCTAGAAT AACAGATTAC TATGTTTGCC ACAGAACTGA 1200 CATCAACTTA ACCTCTTCTT GTGATAAATT TTTATCTCCA ATAATTGGGG AATTTTTTTT 1260 TTCCTGTAGG AACTCATCTG CAGTCTCATG ATGAAGTCAG TGAAGAAATG GATTTTGCAT 1320 TTTAGAAACT CATTTTATTG TCTACCTGGC TGATATGCCT ATTTTGCATA 1370
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