| Tag | Content |
|---|
EnhancerAtlas ID | HS047-09136 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr13:29147670-29149860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr13:29149059-29149070 | GTTTTATTGGG | - | 6.62 |
| | | 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 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH13I028573 | chr13 | 29147813 | 29150010 |
| Enhancer Sequence | ATATTAAGTG CATAAAACTA AACACTTTAA AGCAATCTTG CTAATATTGC TTTGGGGGGC 60
TTTTCTGCAA AGGATGTACC TTCTGGAATT CTTTAAAATG AGTCCATCCA AATCTACGCT 120
AAAGATGGCT TCTACTGTCA GCACAGTCAC CCTCCACTGC CAGAAGCCCT CGACATGATA 180
CGAAACTGAA AAGGCTTCCT TCTCAAGCAT CCTCCTCATT GAATATGTAC AAGTTGAAAT 240
TCCTCGAACG GTAGTAGCCA AAAATTTCTC TTTCCTTGCT CACGGGCAGC TGGGAGGTCA 300
GTCTGTCACA AGTCCCAGGC TGTTCATCTG GCATGTGCAG ACAAAGTTCT AAATGCCCCC 360
ATCCAGGACT GGCTAGATTA TTTGTGGGAC CCAGTGCAAA ATGAAAATGG CAAGCCCCTG 420
TTCAAAAATT AAGAATTTCA AAATGATGAC AAGAGAGCAT TGAACCAAGC ATGGGCTCTT 480
CTGAGCATGG GGCTCTGGGC AAATGTAGTA CATGACGCCG GCCTTGCGCT CCTCTGGATG 540
GACAAACAGC TTTGAGACAC TGGCCATGCT ACCCTCCTAA CCCACATCCA GAGCTCTAGG 600
GCACTTCTTC AAGTGCAATT CTCTGCCTAT CTTGAGCAAT GTCCCTCTCT TGGCCCCACC 660
CCACCGCTTC TCTCTTAAGT TCCCTTTCTT CCTACCTCCA AGCATTTTGA CACATCTAGA 720
TATGACCTAT TGGATCTCTG GATTCAAACG CAAGGCCTGT TCCAAAATCA GTTCTAATCC 780
CACATACATA TGGGTCTTTC AACATTTCCT TGTTATCTCC ATGCTCTCCT CTTTGGGGTG 840
TCCAAATGGA TCTTAACTAC CAAGTCCTCA AGTGTCACAC AGGTTGTGAC ACAGTGGGCA 900
CATGGGAGGT GGGATGCCAG GGGTTAATCT GGCCTACTCA GAGGGCCAAG AAAGAGCCAA 960
AAGGAAATGA TGTTTCCAAC CATTTCCTTC ACTTCACCTC TGTATCATTA ATTTTTTTTT 1020
TTTAATTCCA CAATTTTCCA CCTCCTGCCA TTTCTCTTGG TCTTGTTCCT CTACCTTCTC 1080
TGTGAAGCCC TTGTCAAGGC CATCTTGGAC CCACAACTAG AGTGGGAAGC CAAGGATGAA 1140
GGGGCAGCAA AAGGCCCTGG AGCAAATGTT CAAGCACAGA GCCATGCACA CTAGGCCACG 1200
AACTTCCCGT CACACATGCT CTGGAGGAAG AGGAAATGCT TGACGCATCA TCGCTCAGAT 1260
TGCCTTGGTG GAAACTGCTT TCGATGGTTC ACGTCTAGCA GTGTAACTCG ATGACTCACA 1320
AAACAGCCTT TATTCATTGA CGTGTTCTTC AGAGGACTCC ATGAAATGAC TCACACCTCT 1380
ATTTACTAGG TTTTATTGGG AATGTGAGGT GAAATCTTTT CCCCTGGGAA CAGGAAGTTT 1440
TCAGTGTTTC TTAGAAGAGG ACGTGGGGAC CTGATAGCAA CACACATGTT GTTGATGGGC 1500
GGACTTTCTC TATCAGGGAG GCTCAGCTGG AGCAACAGAG CAGCATTTCT GGAGGAGGGC 1560
ATATCAGTTT TGACACCTGT TTTCAGAATC ATCCACAGAA GGTAAGGCTG GACGAAATGT 1620
TTCCTGTTGT GAATATTTAG AAGAGAGTCT GAGAATCAGA AAGTATTTTA CGGAGCATTG 1680
ATGAAAGGTT CAACAACTGT GTCTTGTGAC GGCAGTCATT GATTTTTTTC CTATTGGGAA 1740
TATGAGGGTA TCCACAGTCA ACGGGAAACG AGGGGAGGCC CAGTCAACCC CAGCACCCCA 1800
AGGATGATTG CTTGCTCACG GGAACTGAGC AGACTATGAA CTCAATAGCC ATAGACTTTG 1860
GACTCCCAGA CAGGTGTGAC AAGCAACAGC CGGGCAGATG AGGGACTTTA CACCAGAGGC 1920
CAGCAGATAC CACAAAGCAG ATGCCTTCAT GCCTGCAGGA GCCCAGGGGC CCTCTCTTCC 1980
TCAACGGCCA CAGAACGAAA CAGCCACACT CCCCATCCCC CAACATCAGA TGCCATCTTA 2040
GGGAAAGAAG CCAGAGGGAG GCAAGGCCAT CTGAGAGAGT GAGCGATTAT ACAAGAGAAG 2100
CAATTAGAAT CATCAAGTGA TTACACGAGT AAAAATCATC AAGTGATTTA CACAAGTGAT 2160
TATAAAAGAG AAATAATTGA GGCCGGGCAT 2190
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