Tag | Content |
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EnhancerAtlas ID | HS094-37232 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr6:157737940-157738940 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr6:157738011-157738025 | TTTGTTTACGATTA | - | 6.42 |
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| 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 |
GH06I157316 | chr6 | 157737390 | 157739489 |
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Enhancer Sequence | TTAGACTAGG AGAAAAGCAC CATCATCTGT CTATCAGTGT ATTCTGAGTG GAAAGCACAG 60 TAATGTTTAT GTTTGTTTAC GATTAAACTA AATATGAAAA GCTCAATAAT GTCTATGAGG 120 TTGTTCCTGC AACCCTGCCA ACTTGCCCCA GTTTCTTCCT CCCTGCTGAA TCATTCCCAT 180 CAGCATATAC ATGCTGTTAA TTCTCCCAAT GTAAAATATA ACAAGTAAAA ACTTATCTCT 240 TGATCCCATT CTTTTTTCCA GCTATGACCC CATTTCCTTC CTTCACTTTG TGGCAAAACT 300 CAAGACTCAC CTAGATATAC TGCCTCTGAT TCTCCTCTAT TCTCTTTTGA ATCACTCAGG 360 CTTCACTCCA CCATTTCACC AATGGCTGTC ACACTGCCAA ACCGGGTGAA TCATCAGTCC 420 TCATCTTACG TAACTTATCA CCAGCATACA ACACAGTCAG TCACTTCTCC TTGAAGTGTT 480 TTCTTCACCG GGTGTCCAAG TCACCAGGCC AAGGAGATTT CCCTCTTCAG TAGGGTACTT 540 TCCCCTCATT CCCCAACCTC TTAACATTAG GAGTCCCCAA GAGTTCCTTC CTCAGACCTC 600 TTCTCTTTTC TTTCAACCTT CACTGCCTTG GTGAGTTAAT CTAGTCTCAC AGCTTTAAAT 660 GCTAGCCATA TACTGATGAG TCTCAAATTC AAATCTTCAC CTTGTACTTC TCCCCTAACT 720 CTCAACTTCT ATATCTAACT GCTTACTTGC TCTCCATCTC ACTATCAAAC GGATGTGTCA 780 ACCTCACAAG TCAGATTGAG CTCCTGACAT TATCTCCCAA TACCTCCTTT TCTCACACTG 840 CTCCCCACCC ATCCTTCAGT TGCTCAGGCC AAAAGTCTTG ATGACATCCA ACTTCACTCT 900 TTCTCACACC CCACATCCAA TCAACAACAA ATCTTTGCTG ACTTGACCTT CAAAATATAT 960 CGACATCTGT TTTCATCAAC TTTACCGCTG CCACCTATCT 1000
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