| Tag | Content |
|---|
EnhancerAtlas ID | HS051-23195 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr6:27470260-27471740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX1 | MA0661.1 | chr6:27470462-27470472 | GTTAATTAGC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I027502 | chr6 | 27469980 | 27472110 |
| Enhancer Sequence | ACAATGCCAC AGTGGACATC CTTGCATCGT AACTATGTAA ATCATGTAAA TCACCAGCTG 60
TTTCTGCCCA TTTTCCACTT TGATCAAAGT GCTGATTTCC CACAAGTTAT GCAATCTTCC 120
AAAGTGTCCA GGGCTATCGG AAGACAGGCT GTTCAAAGGC AATAGATAAG TGGGGGCCGT 180
AAGTTAGGGT CTCAGTCCAC TTGTTAATTA GCAAAGTTTA GTTCCAGTTG CAGAGACTCC 240
ACTGCCAGAG CTCAGACCAC AGCCTACTTC CGGGCGCCGA CGGGAGCTCG CTCACTGTTT 300
ACTAACGTGA AGTTTGTATT CTTTGTTTGG AACGCTGATG ATGCTCATCC TCACGCGGGA 360
GTACTCTCAT TCCAGTGCTC TTGTCCAGGT GGCACAGGAG GTTGGCTTTT TTTGCTTTTT 420
TTTTTTTAAC CAAACTCTCG TTGTACCTGA AAGTTTGCGT TCAACTCACA AAGCCCATTT 480
TCTTGTACCT AGATAGTAAT TATCCTGATT TGCATTTTCT CATGTCTATA CCGTGAAAAA 540
AAACGTTGTG ATTCTGTGTA GTCGTGGCCG AGTGGTTAAG GCGATGGACT AGAAATCCAT 600
TGGGGTCTCC CCGCGCAGGT TCGAATCCTG CCGACTACGA GTTCGAGGTT TTAGATAATT 660
AACAACAGAA AATTTAGAAG AAAGAAATTT AAGCCAACTC ACGTGTTGCG AACTGAATTT 720
GTTTGGTACT TCCCCGATCC TGAAACCCCA CAACAATGGA GGGTGGAAGT TACTGAATAC 780
CTACTATTTT CATAAGATTA TGGGTACCTT AATTAGCAGA TACCTAGTCA TTTTCCCGTT 840
AGCGGTACCT TTGTACGGTT CTTGGGGACG CCTCTCGTTT CCCTGCCTTC CAAACCCTCC 900
TGAAGCCTAT ACCTGTTACA AGTCTTGATA GTGCTTTCCT CTTCATGGAA ATTTAGTCCT 960
AGTCAGAGGT CCAAGTCTTT GGTCAATTAT CAGTTTCTGT GGAATCAATG GTTCAACTGC 1020
TTTGGTCACC CGGTCTCGCT GGTTGCAAAT GACTAGAAAC ACTGTCAGAG ATCTCGACAC 1080
CACCACAATC GAAAGACCAG GCTGTCCTGA CAGACCCCGT CGTTTTGGCT TAGGCGGCAG 1140
ATTAAAGTGT AAATTCGCCA AGTATAATCA ATTTAGTAGA ATACAAACTT ACAGACTTAA 1200
AAAAGTGGGC AAGAATACTT AAGTTTATTA GAGGTAGTCA AAACTCGCTG ACGCAGAGTT 1260
CTTCCTCGTT AGTATAGTGG TGAGTATCCC CGCCTGTCAC GCGGGAGACC GGGGTTCGAT 1320
TCCCCGACGG GGAGAAAAGT TGCTTTTTGC ATCTTCTGCC CACTGATGGC CCCTACCTGG 1380
CTCTGAGAGC AGAGCTGCGG TGGGACCCCT CTGCCATTCC TCCTTAACTG CCAATGGACC 1440
CTCTCGACTT TCCTCACTCC TAAGACCGCT GCTCTGATCA 1480
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