Tag | Content |
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EnhancerAtlas ID | HS094-13326 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr14:104122060-104122980 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr14:104122158-104122173 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH14I103655 | chr14 | 104121970 | 104124662 |
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Enhancer Sequence | TCAGCCTCCC AAGTAGCTGG GATTACAGGC ACATACCACC ATTCCTGGCT AATTTTTTGT 60 ATTTTTAGTA GAAACTAAAA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC CTCAGGGCCT 120 CTCTGAATTT TGAAAAGCGG ATCCAAAATA GTGGATACTG CTGTGTATCA TTTAGGATTT 180 GATTTGGCTG CCAGTATCAA AAAAACAAAA ACAGTGGCTT AAACCACAAG ATGTTTGTCA 240 AATAAGTACT GAGGTACACT CTCCTGGACG GGTTCTGTAG CTACACAGTC ATCGGGGATA 300 CTCAGGTTCC TAACATCTGC CACACTGCAC CTTGGCAGCC TGTCTTGGGG ACTGAGAGTG 360 AGCTCCATGT GGCCCTGTTC TAGCATAGGG GAAGGGAAAG GAAGGACGTG CCTCCTTCCT 420 TGAAGGCTGC TGCTTTGATG ATGTGTACAG CAGTGCTTAC ATTGCATTGG CCAGACCTTA 480 TGGCTGTACC TGGGTGAGTG GGAGACTGGG GAATGTTGTC TTCCCACTTA CAGTGGCAGG 540 TCCTTAAGCC TAAGGAAGGA GAATGGACAC TGGCCAGTGG GTGATGGTCT CTGCAATCCC 600 AGGGCCAGAT TGCTTCATAT CTTTGACTAA CCTTTGTTTC TATAATATCA TGCTTGACAT 660 AGAGATGAAA ACACTGGAAA CATCTAGGTT TTTAAATACT CTCTCCTGAT AACTTCTGGC 720 TCTGTCAGCA TATCTTAGGT AAAATTAAAT ATACCAAAGC TTTGCTTCTT TCTTAGCATT 780 CTCTAGTTTA GTGAGTGAAT AGAGCAGAAG AGGGGCTGCT GGCCAGCGGT TTCTGCTTTC 840 ATAGAGGAAG TGACTGCCCA CACCCTGATT TTAGAGTCTT CATCCTAACC ATGTTACAGC 900 CTTGAGTTGC AGAACTGTAG 920
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