| Tag | Content |
|---|
EnhancerAtlas ID | HS042-38937 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr5:177782990-177784420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr5:177783562-177783573 | CTTCCCAGAAA | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 177784128 | 177784220 | | chr5 | 177783380 | 177783901 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I178356 | chr5 | 177783194 | 177784890 |
| Enhancer Sequence | CAGATTTCTA TTTCCTGATA TGGGATGATT TCCAAGATTT CTTGAAGTAT AAAACGCAAG 60
GTGCTGAGCA CGCTGCAGCA TGGATGAAGC TTGAAATGGT GCTCAGTGAC AGACGCAGGC 120
ACAGAAGACC CCAGGCTTAG GGCCCCACTC TAAGAAATGT CCAGAATAGG CAAAGCCACA 180
GAGACGGGAA GCAGAGGAGT GGCCGCCTGG GGTTGCGGAG GGGAGGAGGA CAGCCAATGG 240
GTACAGGACT TCTTTTAGGG TGACGATCAT GGTCTAAAGT TGATTGTGAT GCTGGCTGCA 300
CAATTCTGAA CACACTGAAA ACCACGAGTG GTGCACTTTA AACAGCTGGA GTCTGCGGTC 360
TGTGAACTGT ATATCAATAA AGCTGTTATG AAAAAAGGCA AGGCGCAGCA CAGGGGGTAA 420
AGCATTCCAC AGCTTGTTTA AAAGAGGGGG CATTTGTTTG AGGTATGTCT GGGGAGAACC 480
AGAAGACACC AGGATCGACT GCCTCAGGAG AGGGGCCTGA GCCCTGGAGG CAGGGGTGGG 540
AGGAGGCATT CTGCCTCAGG AATGCATTCC TTCTTCCCAG AAAGAGAAAG GCAGGGTGCA 600
AAGGGTTAAG GGAGAGAAGG CGAGACACAG GAAAAAAAAG GCAAAGGAAA GCAAAAGTCA 660
GCGCCTCCCC AGTCCCCACA TTAAAGTAGC CATTGCCGCC GGAGCAGAGC CGGCTTGGCT 720
GCCTGAGGAG GAGGCACGCG CCAAACCCAG CAGAGTGATG CCTGGGCAGG AGTTACGCAC 780
CCTCCCCCGG CCGCCTGGCA CCGAGATTGG CTATGCAGCA GGAGGAGATG CCAGGGCTCC 840
GAGCCTCAGG AACCCTGGTG CTGGTCCCCA CTGCAACCCC CTGGGGTCTG CGCACTGAGC 900
CTCTCCAACC CAGCACACCC GTGCCCACCT CTCCAGATAA TTAGAGATGC TGCATAAAAA 960
AAAGTCTAAC ACAAAGCCTG ACGCTCGTGG ATGCTCAACA AAAGTTAGGC TGGCCTTTTC 1020
CAAACAGTGC TTCGAGTCAA ATGCAAGTAT TGTCTAAAGT CTGCAGAAGA AAGGAAAATG 1080
AACGGAGCTA AAGATGTACT TCCCTTTACT CGATGCTGTT CTCCTGTTCC CTTCTGTTCT 1140
TTCAGTATCT AATTGCATTA AGCACGGGTT CCCTCCCTGG TGACCTGGGG CTTCCCAGCA 1200
GGAAGTGACC TTGAGGGCGC CTGCCCAGTG ACCTGCTTTC TGAAGTGCCG GGTAGTGCAT 1260
CCCCTCAGAT GGTGACCTCC TTCCCTTCTC ACAGGCTTCT GGTCTGTCCA CGCCCTCAGG 1320
AGAATGCCTT TTCTGTGAGC CGGCGGAAGT GCCTCTGCCC CCTGGGGTCG GGGGGTCAGC 1380
TTGGCTGCAG GGCTGGGGCC GCACAGCCTC GACTCAGAGA ACTCACAATG 1430
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