| Tag | Content |
|---|
EnhancerAtlas ID | HS052-02781 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:169710470-169711670 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr1:169710580-169710591 | AAATCTCAGCA | + | 6.32 |
| | | 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 |
| GH01I169741 | chr1 | 169710556 | 169710570 |
| Enhancer Sequence | TTACATAACT TGCCAGTGTT TTTTCAGTTA ATAAATGGTA GGGTGGAGAT TCAATCTGTG 60
TTACTCTAAA GTCCGTGTCC TTTTTATTGG CTCCATGCCT ACTCAGATTT AAATCTCAGC 120
AGGGAAGTAA ACCTTAGTTT TTACATGAGA AAATGTTACA GCAGCCTTCT CGGCTTCCTT 180
TACCCCCATC CCAGTTTCAC GAGCTTAGTG CCTTAGATCG GGTTCCTTTA GAAGCAGACC 240
TCGAAATAAG GATGTGGGTG CCAGTCATTT ATTGAAAAGA TGATCCCAAG AAAGCCTAGT 300
AGGAGAGTGA GGAAGTGAGA TGGGGAAAGG AAGAAACTCC ACAAGAAGTG TGTTAATAAG 360
CAGGTTACCG CTGTGGGCAG CCATGGGGCT CAGCTGCACT AACAAACTCT GTCTAGTACA 420
GAAAACCTCA GGGTCTCCCC AAGGAGGGGC AAGAAGTCTG CCTAGGGTAT ATATCCGCCA 480
ACTCAGTCAC TGGCTGAGAG CTGATCCTGG GAGGGCATGG TTAATTCCTC TGCACTTTCA 540
AGTGGATTCC TGTGGTCAGA AAAAGCCCTC TACAATGAAT TCCAGATGCT TGTATTTAAA 600
TCTGACATGA TCTGAATGCT GTGTTGGGAC AGGGTGGGCG TTATTAGTTT TCTGTCATTA 660
CTGTAACAGA TTACTACAAA CCTGATGGCT GCAAACAACA CATATTTATT ATGTCATAGT 720
TTGTGTGGGT CAGAAGTACA GGTTAGCTCA ACTAGTTTCT CTGCTCTAGG TTTCACATTG 780
CCAATATCAA GGTGTCATCC AGTTGGGCTC TTCTTGGGAG GCTTGGGGAT GAATCCACTT 840
TCAAGCTCAT TCAGATTGTT GGCAGAATCC AGTTCCTTGT GGTTGCAGGA CCAAGGTCCC 900
TGTTGCCTTG CTGGCTGTTG GCCAGGAGTC ATTCTTAGCT TCTAGAGACT ACCTGTACTC 960
TCTGACTCGT GTCTCCACTT CACCTTTCAA ACCAGCAGCG GCTAGTCGAG TCCCTCTCTT 1020
CAAATGTCTC CAACTGTGCC TTCACCTCAT TTCTCCTCTG TGTACCATGT CTGCCTCTAC 1080
TGCTTGTAAG GGCTCATGGG ATTACATTGG ATTTATTCAA TCCAGGATAA TCTCCATATT 1140
TTAAGGCTAG CTGACTAGTG ATCTTAATTC CATCTACAAA GTCCCTTCCA ATAGTACTGT 1200
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