Tag | Content |
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EnhancerAtlas ID | HS182-00074 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:6451440-6452470 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:6452272-6452287 | GAGCCCAAGGTCAGT | + | 6.17 |
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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 |
GH01I006392 | chr1 | 6451761 | 6451850 |
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Enhancer Sequence | TTGTAGTCCC AGCTACTCGG GAGGCTGAGG CCCAAGAATC ACTTGAGCCC AGGAGGCAGG 60 GGTTGCAGTG AGCTGAGATC GGGCCACTGC ACTCCAGCCC GGGTGACAGA GTGAGACTCT 120 GTCTCAAAAA ACAAAAAATC TAGTAACTGT TAGAAGCTGG GTGAAAAAAG ACAACATGTA 180 TAAATTGGCT ATTCACCACC CTGAAGAAGT AAATAAAAGG CCAGCCTTCC ACGGGAAGAT 240 TTAAATCAAG GTTTCCTTTA TTCAGGAGAG GGGTGGGAAG AATACTGGAT CTGGAGTCAG 300 AAGACTTGGG CAGGGGCTGT CCCTGGATCT CCTGGAGCAG GATGACCTTA CACAGTTACT 360 CAACTCCCAA AACTGCCATT TCCTCCTCCA CACAGGTAAG GGTGGCACTA CCGACCATCA 420 ACCTCCCAGG GAATTGGGCA AACCAAGTGG GATGAGACAG GTATAAGCTC TTTGCAAACC 480 ATGGAGCCCA AGTTTCCCAG CCAATACTCA GCAGAGCTGA TTCAGGAACC TGATGCAGGC 540 TGTCTGTCTC CAGTTATTTC CTTTTTTTTT TTTGCCCCGC TTTCCCCACC TCCAGAGTCG 600 ATGGGACCAG AACAGCCACA GAGCCAAAGT CAAAGGGGCA GGGCTCCCCC AAAGACGTTC 660 CCCCTCTGGA AAAGTCAAAA CCGACCTTGA GGTAAGGAGA GGCCCTCGAC CAGGCCAGAA 720 GATGAGACTG AGAGTCAAGA ATCGCCATAG ACCCAGGACT TGCTATATGC CCAGCCTTCC 780 TGGAGATGTC AACATCTACA GGAAAGTAAC TTGCTTCTAT TGGACTTGGC TTGAGCCCAA 840 GGTCAGTCTG TGATGCCCAA CCCCCAAATG TGAGGAACCC ACTACCAAAA CAGAAAGCAG 900 CTCTCACTCC TGGTAGTTCA TCAAGCAGGA TAGGACCGGT CGCAGGCCAC AGAGCCTGTG 960 TGCAGTGGCT GAAAACCTAG ACTCCTTGTC CTCACTTAGC TCATGCACAA ATGCCAGCCT 1020 GCTGCTTCCG 1030
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