Tag | Content |
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EnhancerAtlas ID | HS182-15737 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:41306990-41308480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr3:41308406-41308417 | GGAGGGTGTGG | - | 6.32 | Klf1 | MA0493.1 | chr3:41308408-41308419 | AGGGTGTGGCT | - | 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 |
GH03I041264 | chr3 | 41306346 | 41308090 |
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Enhancer Sequence | AAAATAAAAT GGAAAGGAAA ATTGAAGCAC ACTTGGTTTA CATTATTAAA GCCGTCAGGC 60 ACCAATTAAT CAAAATCTAG GCCTGATATT GACTACTGGA CAGCTGAAAA TTCCCATGGT 120 GGCTGTTATT TTTGTTGAGG GACTTGATCA AATACCGACT CCATTTGGAA ACATTTTATA 180 ATGACCGTTT TCAGAAAATG AGCAGCCCCT TTGAGAGATC TCACCCTTCC CTCCCTAAGG 240 CAGGGCCACA GCTTTGAGGA CGTTTTTTGC GAAGCCTTTG AGAGTCTGGC TCCAGGAGAA 300 GGGAAGGGAA TCGTGAAATC TGTGGGTTTT TACCTCCAAG AGACAGGTCC ACTGTCAGCT 360 GACCCAAAAG CATCCATTCT GCACAGCTTG GTGGTGACAA GTAGCTATGT GTGTGGTAGG 420 GGCTTGGAAA ACTCCCAGGA GGCATCTGCT GGTCCACACA CCCCCTGCTC TGGGTGAATC 480 AGAGGACCAC ACAGGACCCA GCAGAATGTG TATGCACAGG AAATAACTTT CTGGCTAAGT 540 GTCAAATCGG CCTTGAGATA AAATTAACTG AAGCAAGGTC TCCCAGGCCT CCAAGGGCAA 600 CATCAAAGAG CCCGGATATT CCTCTCTAAA AGGCTTTGAC AGGCTGAGTG GACCAACCTC 660 CTCAGGCCTC TGCTCTTTAT ACTTGTGGAC AGGCCCAGCC AGAGCAGCGG CTGGTGCAGG 720 TAGCAGGACA GGGTTGGGAT CCTGGACTCA AAGGAGTTGT GACCACCATG TAGCAATCAC 780 TCCTTCTGGG CAACCCTGGG CACTTGAACA GGACAGCAGA GCTATGGTCC AACTGAATCT 840 CTAATGGGTG AAGCTGATTC TAGAAAAGCC TCAGGCTGGC TGCAGACTCT GCTTACACAT 900 TTTTTTGCAG AGCAGAGAAG GATGCATAAA GAGAGGTCTC ACAGAGTCAA GGTCCCAGAG 960 CACTGAGACC ACTGAGACCA AGAGAGACTC CCTCCCAGTC CAGGTGAGCT ACCACGGGGG 1020 AATTCTCACG CACAGGCTGT TTGGCTGCAA ATACGCTGGA CTTTGTCATT GTTTCTTTGC 1080 ATTTTTCTTG ATGGCTTATA ATACAAGGTT AGGTCTCTTG GAAGCCTAAG AAGATTATCC 1140 AAAAAGGCTG TTTTCAGTTG GGTTAGAGTG TAAATAGCAT ACAAGTGCTT CATGAACCCC 1200 AGTTCAAATT CAAAGGTATT CTTAGAAGGT TTTCATTAAA TAAAGGCAGG AAAATAAATT 1260 AAGACCAAGA AAATGATTTC AACAGAGGGG TGAAGGGGGA GCTCCTATTC TTCCTTCTTA 1320 CTGAAGTGCT TCATCCAAAC AGCCTCCTTT ACTTCCATGG TCCCTTAAAA CCACTTTGCT 1380 AGGAGTCGAC TTATGTGGAG CAAAGGCAAT ACTAATGGAG GGTGTGGCTC CTCTGTGGCC 1440 ACTAAGTGGA AAATATAACC CTCTTGCCAG CTACCTCATG TGGCAAGTGT 1490
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