| Tag | Content |
|---|
EnhancerAtlas ID | HS165-09705 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr3:10417330-10418750 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr3:10417414-10417431 | CGGGTCAGGCTGACCCC | + | 6.02 | | ESR1 | MA0112.3 | chr3:10417414-10417431 | CGGGTCAGGCTGACCCC | - | 6.42 | | ESR2 | MA0258.2 | chr3:10417415-10417430 | GGGTCAGGCTGACCC | + | 6.39 | | ESR2 | MA0258.2 | chr3:10417415-10417430 | GGGTCAGGCTGACCC | - | 6.87 | | Stat6 | MA0520.1 | chr3:10418592-10418607 | AGTTCTCTGGAAATC | - | 7.31 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCAATGTGAG GGACACATGC TTGGGGGGTT CCAGGAAGTG GAGGCTGGGG GTGGTGTGGA 60
CCAAATCTTT GGCTGAAAGA GCTCCGGGTC AGGCTGACCC CAGCTCACCT CCCAGCTCTG 120
CCACTCCTTG CTTTATGACC TGTGGCAAGT TCTTGAGACC TTGATCCTCA CCGAGCCTCA 180
GTCTCCTGCT CTGTACAATG GGGATGCATA CTTCCTCCCC AAGATTTTGT AAGGCTCAAA 240
TGTGGTAATA ACGCATGCAA AGTGCCCAGC ATAGTGCTCG GCAATAGTAT GTGCTCGACA 300
CATAGTAGGT GCTCAAGAGA TGTGTGCCGA GTGACTGTGT GAATAAAGGA GGAATGGTTT 360
GCATTGAGCT TTCACACAAT AATGACGTGA AGTTGGTATC ATTTATTTAT TCATTTATTC 420
GACAAATACC TTTTGAGCAC CTATGACACG CCAGGCACAT CTTAGTTCCT AGTTTGGGAA 480
CTAGGACACA GCAGTAAAGA AGACAAGAGT TCCTGCCCTT GAGGAGCAGA CATTCTAGAG 540
GAGGAGGAAG ACAAGAAACA AAAAAACGAA TACATGAACA AGACAGTTTC AGATATGGTG 600
ACACATTGTG AAGAAAAAGG CCAGGATGAT GTGATAGAAA GTGACATGGG GGACAGGGGT 660
AGGGAGTGGT TACTTTAGCT AGGGTGGCCA GGGAAGGCTT CTTGGAGGAG GTGGTATTTG 720
AGCAGACACC AGTCGCATGG TGACCTAGGG AAGAACATTC CATGTAGAGG AAACAGCAGG 780
TGGCTTTTTT TTGGATGAGG AAACTGAGGC TCAGATAGGG GAAGTGACTT GCTTGCAGCC 840
ACAGGCAAGA GAAATGCTGT AACGGTAGGA ACGCAGCTGG GGACCCATCC TGATCCCCTG 900
GGGCTTCCTC TTCAGTTTAG CATGCCCATC CCCCATCTGC TACAGGTGCT ACTGCAGGTG 960
CTGCGGAGAC TGCTCACACC CGCAGACTCT GACAGAGGAA GAGCCTGCTC AGGTGACTGG 1020
GTCCCCTTGT TGGGAAGTGC CTGGGAATGC ACTCCCATCT TAACCTGATG GCCAACATCC 1080
AGTGGCTGAC GTGTTAGTCC CAAAGCCCAG CCATCTGCTT TGAGGTAGGA CAGACCCTAG 1140
AGTTCTGGGC AGCCATGGAC TTTATCCTGA AGACAGTGGG AGTCACGGAG GAGGTTTGAG 1200
CAGAGGAGGG CAGGATGGAT TTGGGTTGCT CCAGAGCTCC CATGGGATCG GGAGAGGCTG 1260
GGAGTTCTCT GGAAATCTCA GCTGCCCCCG GCTTCTTCCC TAGCGTGGAC CTGTGCCCCT 1320
TGCAGGTCTC ACCTGAGAGC ACCCTGTCAA TAGATCCCCT GCCTACCCAT CTCAGGGAAT 1380
TCAGCCAAAG AGAGAGGCAG AGATGGGCTG TGAACCCAGG 1420
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