Tag | Content |
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EnhancerAtlas ID | HS182-19792 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:44103140-44104430 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr7:44104016-44104037 | TTCAGTACCAGGGGGAGCTCC | + | 7.11 |
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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 |
GH07I044063 | chr7 | 44103102 | 44104206 |
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Enhancer Sequence | AGTGCTGGGA TTACAGGAGT GAGCCACCGT GCCCAGCACC CTTTGGTTTC TAAAGTGCTC 60 TAAATTCTAG ACATCCTGAA CAGAGGAGCA AGTGCGGAAT GGAGCTGGAG GAGGGACAGG 120 GAGGCCGAGC CTGGTCGAAA CCTGACCCTG CCTGCCTCCT GCAGCCCCTG AGCTGGGAAT 180 AGCAGCTCGA CCTTTGATGT TCGCGCCACT CCACCCCTGC TCCGTGCAGG AGGGTTTAAG 240 AAAATGTTCT CTGGGGAGTC AGAGTGAAAT CCCTCATATT CACCACCAAA AGTGCGTCCC 300 CTTTCCCCAA ACCAGGCTGT GGGAGGGTCA TGGGGCTGCA TGAAGTCTCC GGAAGGGAGA 360 GGAGGCAGGT GGTCCTTCCC TCTGCCTGGC CCCAGTGCCA GGTGCCAGGT GTCCGTGTTT 420 GGAGCGGGCA GGCTTGGGGC TGGCTGGGTC TCCGGGGCCT GCCGGTCTGG GTGCTCTGGC 480 CAACTGCCCA ACGGCCCTAG GAGCAGGAGG TCTGGGGCAC ACCCTTCTAG CCTTTCCAGG 540 ACTCAACAAG CTTTAAGGTC ATTCAGATGC TAATTTAGAC TGCCCTTGTG TCAGAATACT 600 AAGGTGGGAG GCGGAGCGGA GGTGCCAGTC ACTCTGGGCG AGGCCTTACT GCGCCCATGC 660 ATCCCGGGCC CATTTGTCAG CCCTTGCTCT TCAGTGGGAG CCCAGCTGCA AGCCCAGAGT 720 CTGGCCACTC CATAGTCCTG CACCCCTCTT TTGATTGGTC TTTCCTTTGC CCAGAGAGGG 780 GCTCCAGAGG GAGATAGGTG GTGAAGCTCA TGCAGGGATT CTGAGGACCT GATGGGGGAG 840 GGCCCTGCGA GGGGTCCAAG CCTACATCAA GAGGAATTCA GTACCAGGGG GAGCTCCCCA 900 CCACCCCGGA AAAGGGAGAG GCCCAGAGAT GGAGGTGGCT TGTCCAGGGC CCCACAGTAA 960 GTTGGGATTT GGAGCCAGAT GCTCTAAGCC CAGCCCTTCC GTTTCCTAGC TGGGTGTCCC 1020 TTGGCAGATG CCACCTTTGG AGCCTGCCCC ACCTCGGGAC ACAGCGAGCT TCGAGTGCAG 1080 TCAGCCCCTG TGGAGTGTGT CCCAGTTACA CAGAAATGGG GAAAATTTCA CAAAACTAAA 1140 AAATGGCTTC TCAGCCCTCC TTTTTCAGTG AATGATGTGG AGCCCCACGC CTAGAAAGCC 1200 TGGTCCATGG GCGAGAGACT TTGCTGAGAT GAGAAGCCAG CTGGGGCTGC TGCCCACCCA 1260 CCCTGCCCAG GCTCCTGAAG GTGGCCTCAC 1290
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