Tag | Content |
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EnhancerAtlas ID | HS133-08421 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr13:29148120-29149850 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr13:29149059-29149070 | GTTTTATTGGG | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 29148222 | 29148380 | chr13 | 29148829 | 29149214 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I028573 | chr13 | 29147813 | 29150010 |
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Enhancer Sequence | AAGAGAGCAT TGAACCAAGC ATGGGCTCTT CTGAGCATGG GGCTCTGGGC AAATGTAGTA 60 CATGACGCCG GCCTTGCGCT CCTCTGGATG GACAAACAGC TTTGAGACAC TGGCCATGCT 120 ACCCTCCTAA CCCACATCCA GAGCTCTAGG GCACTTCTTC AAGTGCAATT CTCTGCCTAT 180 CTTGAGCAAT GTCCCTCTCT TGGCCCCACC CCACCGCTTC TCTCTTAAGT TCCCTTTCTT 240 CCTACCTCCA AGCATTTTGA CACATCTAGA TATGACCTAT TGGATCTCTG GATTCAAACG 300 CAAGGCCTGT TCCAAAATCA GTTCTAATCC CACATACATA TGGGTCTTTC AACATTTCCT 360 TGTTATCTCC ATGCTCTCCT CTTTGGGGTG TCCAAATGGA TCTTAACTAC CAAGTCCTCA 420 AGTGTCACAC AGGTTGTGAC ACAGTGGGCA CATGGGAGGT GGGATGCCAG GGGTTAATCT 480 GGCCTACTCA GAGGGCCAAG AAAGAGCCAA AAGGAAATGA TGTTTCCAAC CATTTCCTTC 540 ACTTCACCTC TGTATCATTA ATTTTTTTTT TTTAATTCCA CAATTTTCCA CCTCCTGCCA 600 TTTCTCTTGG TCTTGTTCCT CTACCTTCTC TGTGAAGCCC TTGTCAAGGC CATCTTGGAC 660 CCACAACTAG AGTGGGAAGC CAAGGATGAA GGGGCAGCAA AAGGCCCTGG AGCAAATGTT 720 CAAGCACAGA GCCATGCACA CTAGGCCACG AACTTCCCGT CACACATGCT CTGGAGGAAG 780 AGGAAATGCT TGACGCATCA TCGCTCAGAT TGCCTTGGTG GAAACTGCTT TCGATGGTTC 840 ACGTCTAGCA GTGTAACTCG ATGACTCACA AAACAGCCTT TATTCATTGA CGTGTTCTTC 900 AGAGGACTCC ATGAAATGAC TCACACCTCT ATTTACTAGG TTTTATTGGG AATGTGAGGT 960 GAAATCTTTT CCCCTGGGAA CAGGAAGTTT TCAGTGTTTC TTAGAAGAGG ACGTGGGGAC 1020 CTGATAGCAA CACACATGTT GTTGATGGGC GGACTTTCTC TATCAGGGAG GCTCAGCTGG 1080 AGCAACAGAG CAGCATTTCT GGAGGAGGGC ATATCAGTTT TGACACCTGT TTTCAGAATC 1140 ATCCACAGAA GGTAAGGCTG GACGAAATGT TTCCTGTTGT GAATATTTAG AAGAGAGTCT 1200 GAGAATCAGA AAGTATTTTA CGGAGCATTG ATGAAAGGTT CAACAACTGT GTCTTGTGAC 1260 GGCAGTCATT GATTTTTTTC CTATTGGGAA TATGAGGGTA TCCACAGTCA ACGGGAAACG 1320 AGGGGAGGCC CAGTCAACCC CAGCACCCCA AGGATGATTG CTTGCTCACG GGAACTGAGC 1380 AGACTATGAA CTCAATAGCC ATAGACTTTG GACTCCCAGA CAGGTGTGAC AAGCAACAGC 1440 CGGGCAGATG AGGGACTTTA CACCAGAGGC CAGCAGATAC CACAAAGCAG ATGCCTTCAT 1500 GCCTGCAGGA GCCCAGGGGC CCTCTCTTCC TCAACGGCCA CAGAACGAAA CAGCCACACT 1560 CCCCATCCCC CAACATCAGA TGCCATCTTA GGGAAAGAAG CCAGAGGGAG GCAAGGCCAT 1620 CTGAGAGAGT GAGCGATTAT ACAAGAGAAG CAATTAGAAT CATCAAGTGA TTACACGAGT 1680 AAAAATCATC AAGTGATTTA CACAAGTGAT TATAAAAGAG AAATAATTGA 1730
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