Tag | Content |
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EnhancerAtlas ID | HS037-39497 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr9:4035400-4036950 |
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) |
Esrra | MA0592.2 | chr9:4036070-4036081 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr9:4036071-4036081 | TCAAGGTCAT | + | 6.02 | MEF2A | MA0052.3 | chr9:4036905-4036917 | GCTAAAAATAAA | + | 6.04 | MEF2C | MA0497.1 | chr9:4036903-4036918 | GGGCTAAAAATAAAA | + | 6.34 | Nr5a2 | MA0505.1 | chr9:4036067-4036082 | AGATTCAAGGTCATC | + | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AACCCCAGAA TATCCCAAAG CTACCTCTCA CCTATCTCGT ATTCCACCTT CTATCTCTCT 60 CCTACTTAAA TTTCCACATC TGGCCACATT CTTTAACTTT AGCTCCCATG GATTCTCCAT 120 TTTCTGCTTT CCCTTCCCCC TGCCAGTGGC CTAGTTGAGG CTCTAGTCAC TTCTCTTCTC 180 TGTTACTGCA GCAGTGCCCT AACTCATCTC CTCCATGTAA CTCTTGTTTC TGTTATACAT 240 CTCCACCTGG TGCCAGAATA AGCTTCCCAA AGCACGGGTC AGGGATGGCC CCTCCTCAGA 300 AACTATCCAA CTTCCTAGAA GGCACAGACT CATACTAACC CTCCTTCCTG TCTTGCCTTC 360 CACCACATCG GTCTTCCTGT ACTTGACCCA AACGATTGTA TCCCTGCCCC ACTCAAATGC 420 AAGCCCACGA CACTGACCAT TGCTCCTTCA TCTCCTGGGA CTGGAATGCT CCCGTCTTCA 480 CTCTTGCAGT CAAAATCTAT CCATTTACTC AAGGCTCACT CAGGTGGAAC CTCCTGCTGC 540 CTGCCCACAT CCCTCTGTCA CAATGAATCC TTCTTTCCTA CATGCTCCTA TACCAGATGA 600 CTTGGCCTTG AGCCGCCTGG AGTTTACTCT GTAGGTTTCA GTTTGCCTGA TTCCTTGCTA 660 GGCTGAAAGA TTCAAGGTCA TCTTTAAGAC CTCAGTGCTT TTCACAGGGA ATTACCATCT 720 GAAAAAAGCC CCAAGTGAGG ATTTTCCTTT ACCGTTTGAA GACTTTTTTA ACTCCTCACC 780 AGCAACAAAA ATTCTGGGAT GCACTGCGTT TTACATTTTG TTTTTGTTGT TTGTTTTATT 840 TTTTCTGGCT AAGAACACAG AAATCAAATC TCTTTTTTTT TTCTCTCAGG CCTTGCCCTA 900 CTCTAATTTC AATCCTCTCT AATCTTTATT TTCTACTTTA TACTTGTAGT TTTACTATTC 960 TCTGCTCCCC TTAATTTCTG TAGAACAAGA TAGGATATAA ATAAACAGAT GTATAAATAA 1020 AGAGTGGGTT TTTGAAAAAT GATTGACAAC TTGAATTGAA AGCAAGACTC CTGTTGTGAA 1080 AGAAGTAGAG AACTCAGCCC AAATTGGTAA CGGTTTCTAT CAGTAGCCAA AATGGGAGGA 1140 TATAAGACTC AAACCAGAAA ACAGTTTTCT CCCTGAGACT CCAAGAGTGC TAGAGGAAAA 1200 ACAGAGAGGC TACTGTGAAG ACCTGCAGCC TTAAGCCCTG AGACTCACCT ACTAAATAGG 1260 TGCCCAGCAA ACGGCGCATT ACCTGAGAAT TTTTTCCTTG AACTTTGACT CCCAAATTAA 1320 TTCCCACCAT AGTGATTACT AGTTGTTCAT AGAACAGAGG TGTGAGAAGA ACTGTGGGTG 1380 ATATACCAGG AGGAACTTCA GGAAAGCCGT TTGGAGGACT CATTCTTGAT GCCAAAATCC 1440 CTCCCTACTC CTTGCGTTTG AGTATCAACT GCTGATCTCC AGGAGAAATA AAGACCAGTA 1500 GAGGGGCTAA AAATAAAAGG GGCAGACCGC AGTGGATTCT TAGTCCTATC 1550
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