Tag | Content |
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EnhancerAtlas ID | HS034-20010 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr22:39784020-39785230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF13 | MA0657.1 | chr22:39784326-39784344 | AGCAAGTGGGCGTGGCCT | - | 6.37 | KLF14 | MA0740.1 | chr22:39784329-39784343 | AAGTGGGCGTGGCC | - | 8.12 | Klf12 | MA0742.1 | chr22:39784328-39784343 | CAAGTGGGCGTGGCC | - | 6.48 | SP1 | MA0079.4 | chr22:39784330-39784345 | AGTGGGCGTGGCCTG | - | 7.61 | SP3 | MA0746.2 | chr22:39784330-39784343 | AGTGGGCGTGGCC | - | 6.92 | SP4 | MA0685.1 | chr22:39784328-39784345 | CAAGTGGGCGTGGCCTG | - | 7.76 | SP8 | MA0747.1 | chr22:39784330-39784342 | AGTGGGCGTGGC | - | 7.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr22 | 39784774 | 39784929 | chr22 | 39784258 | 39784471 | chr22 | 39784432 | 39785200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I039388 | chr22 | 39784006 | 39785732 |
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Enhancer Sequence | GTTGTGGTGA GCCAAGATGG CGCCATTGCA CTCCAGACTG GGCAACAAGA GCGAAACTCT 60 GTTTCCAAAA AAAAAAAAAA AAAAAAGCAA AAATTAGCCG GGTGTGGTGG TGGGCGCCTG 120 TAGTCCCAGC TACTTGGGAG GCCGAGGCAG AAGAATCGCT TGAACCCAGG AGGAAGAGGT 180 TGCAGTGAGC TGAGATCGCA CAACTACACT CCAGCCTGCG ACAGAGAGAG ACTCTGTCTC 240 AAAAAAAAAA AAAAAAAAAA AAAAATCCCA CCAGAAAAGG CTCTGGAGCC CAGGCCGGGT 300 GGGAGGAGCA AGTGGGCGTG GCCTGGGCAT GGCCCGTCGG TCAAGGTACT GGCCCTGCCC 360 ACGCCCGGGA GAGGGGCGGG CGAGAGAGAT GCTAAGCCAA TCGGATTGCG GTCATCGGGG 420 GCGAGCGGAG TCTGCAAGAG GTCCGAGGAG TAGCGGGTGC CGAGGGAAGG AGCGCGGCGG 480 GGCGGGTGAG GGATCCCGGG GCTCCGTTCC AGGACACCCA GGTTCTGACC CCGTTTAGGA 540 GTGCGGAGGG CAGGGGCTGC CTGCAACCCA AGGAGCCCGA GCTACCCTGA AGGCCGACCC 600 TGAGGCCGCT GCTCAGCGAG AGGAGCCGAC CCTTGGGGGA CAGCGGGGTC GGGTTCCAAG 660 CCGGGGCTGC TGGGGCTGGT CAGGCCGCCC GCCCTGCTTG ACCCCTCTCA CCTGATGGCT 720 CCCTTCTCCA ATCTTCAAGA AGGTGAAACG TCACTGTGGT CCGCAGAGGG CAGGCCGCGT 780 GTGCGGAGTC GCTGTCATCC CTTAGTGGCC ACGCCCGCCT CCCTGTCCAC TTCCCGTCTT 840 CGTCGTTGCG GTTCAGGTGT TCGCTCCACT CTGCGGCACC AAAGGCCCGT CACGTGCTTC 900 CCCTGCCCAG ACACCCCAAA CACCGAAACT GTCATCCGAA GGCCCCGCAC CTGCCGCCTG 960 TCGGATGCTG AAGAACGAAT CCCAGGTGGA GAGGACAGCA CCCCAAAAGG GATGGGGGAT 1020 GGATTGGGGC GTCTGAGCCC CGTGGAGTAT GTCAGCCTTT CAGAGCGACC CGCTCCACGC 1080 TGCGATGTGG TCCTTAAGAA GTTAGGGCCG GGCACGGCGC CTCACGCTGT AATCCCAGCA 1140 CTTTGGGAGC CAAGGTGGGC GGATCATCTG AGGTCAGGAG TTCGAGACCA ACCTGGCCAA 1200 CATGGTAAAA 1210
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