Tag | Content |
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EnhancerAtlas ID | HS140-00656 |
Organism | Homo sapiens |
Tissue/cell | Namalwa |
Coordinate | chr12:8844150-8845500 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:8844207-8844219 | AAACAAACAAAC | - | 6.32 | TBXT | MA0009.2 | chr12:8844476-8844492 | TGACACAGATGTGTGA | + | 6.16 | ZNF263 | MA0528.1 | chr12:8845312-8845333 | GGAGCAGGGAAAAGGAGGAGG | + | 6.46 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 8844521 | 8844599 | chr12 | 8844725 | 8844868 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I008692 | chr12 | 8844638 | 8846323 |
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Enhancer Sequence | GAGATCGAGC CACTGCACTC CCGCCTGGGT GACAGAGTGA GACTGTCTCA AAAAGACAAA 60 CAAACAAACA AAAAAGAAAA GAATTAGGAA ATAGGACAGG TTAAGAATTT AGATTGAATA 120 GAAATAAACT GATGTTTCTT TGAACATAGG ATAACCACAT GAACTTAGAC TACTGAACAG 180 GGCTCCCCAG TCTAAGTCTT TCATTGTACA AAAAACAGCA AGGCAGATCA GGATAATTAT 240 GGTGGTGCCA GGCCATTAGG ATGCTTCCAG ACTTCATTCA TTCATTTAAT CTGTAAATGT 300 TCACTAATCA TTCAAGGTGT TGCTGGTGAC ACAGATGTGT GACAGATGCA CACAGCCCTT 360 ATGTGGTTTG CATATTATCA TTTCTCTGGT TGGATTCTAT GGATGCATTA TCTACAAATT 420 CAGTCATGTT TCCCTGCACC AAGAGAGGGT TTTTTTTTTC CTTTAATACT TGATGCTTCC 480 TCTATTCTTT AAATGAGAAC ACATCTAATG TGCCTTTCCA TATTTTCTTA TTTCATTTTT 540 TTCTTCTTTC ATTCTTCCCA GGTTGTTATA CTTCTAAGAT CCTCCCAAAG ACAGGGAAAT 600 CAGGACTAGG AAATTGCTGC CAACGATTTA ATTTCATTGC CTCATTTTCT CTTCAGTCAG 660 AGAGGACTAA CAATATTTGC TCAACCTTAG AATGTTGCTT GAGGCTACAA TGAGTTTATA 720 AATGTTGAGG GCTTTAAATA AAGAGCATTT TACAAATGGT TATTTTGGTC TCTAAGACAC 780 TGTGCTCAAA CTTTCATGTG TCTAAAGATC ATTTAGTATG CTTATTCCAA ATGCAGATAA 840 ATTGCTGATT TTAGATGCTT TGAGTTGCTC AAGAAATGCA GGTACACAGG CTCATTCAGG 900 TCAGAGGCAG AGGTCAAGGA ATCTGCATTT TAAACAAGCA TTCCAGGTAA TTTCTATGTG 960 GTAGAGGAAA AAAAAATCTT AACCAGATAC AATTAAAGAA GTAGGGGGAA AACCTGTATC 1020 ATGTTTCTTG CCAAGACTGT GTTTTCTTTC CACCCATTCT TTCTCTTCTG TGATTCAGCC 1080 AATGTATGGT CTTTCCTCCC TTTGTGTCTG GCATCTGCAT TTTCTTAGCA TAGAGAGAAA 1140 GCTCAGTTTA ATGTGCTGAG ATGGAGCAGG GAAAAGGAGG AGGGATGTGG GTGGAGAAAG 1200 GCTAGATCAG TGTTTAGCTA TTCTACTGCA AAGACTGTTG TCAGGCTGGT TCTAGCCGGC 1260 TGGCTCCAGG AGAGGAAACA GTGGGGAGAG CTAGATTTAC TGCAGCTGCC GCTACCGTTC 1320 CTTATTTGCT AGTCAAGGTT CTAACATTAG 1350
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