Tag | Content |
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EnhancerAtlas ID | HS117-00448 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr1:145682510-145683570 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr1:145683299-145683313 | ATGAGTCACTCTTT | - | 6.55 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I145750 | chr1 | 145681810 | 145684605 |
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Enhancer Sequence | GTGAGTATGT AGATGTAACT GGAGGCTGCT ACACTGCCAT TATCTGCTAA GCCCAAACTT 60 AATCAGAACT TTTTTTTTTA TTATTATTCA GGCTCAGGAA GGCCGTCCTG GTCCCCCAGG 120 ATGTTTGGGT GCTAGAAATG TCTTGATTCC TTTTATATTC AGGTCTGAGA GTTGTATTGA 180 GGTAGAGAAT GAGATGGTCC CTGCCAGGCT TGGTATCTGA TTTGTGGGTT TCCCCAGTAG 240 ACTACACAGG AATATTTTAC TCCTTAAGAA TTTCTGAAAT TGAAAACATT ATGCTGAACT 300 TCATTTTTTT CAAAGTAAGA GGATTTGTCA GAAGAAACAA TAGGCTGTAA TTCAGTATCA 360 GAGTGACACT TATGTATGAT GGGATTAAAG ATGGAATTTC TTCTTGTCTG AGAAATTATT 420 TGCTGCTTCT AACTGTGGCC CAGAAGGTTT CTTTGCTCAA AGGAACCTCA GTCCTTTTAG 480 GACCTCTGTC ATCCAGTAGT CTGGACCTCT GCTGGTAGTG TACCAGCAGC TCTGAGGGAA 540 AATAAAAAAA AACGGTGTTG CCAAGTCCCT TTTATAATTG CTCTAAGTTG TGATTCAGAG 600 AGACTGCTAT GGCTGCTTCT CTACTTGAAA GCTCCTCATT GTCCAGAACT GTGGGCGGCC 660 TCTTATAATG AGGGATGTTT GCTGTAGATT TTGACCAGTC ATGAAGGGAA AACTCTCCTT 720 AAAAAGCAGC TCCATCTGTG TTTAATATCA GTGGGCACAG AAAACACAAA TTTTTGAAAC 780 CAACAGGCAA TGAGTCACTC TTTTTGTTCT GGCGTGTCAT GTGGTACTTT AGGTAGCTTC 840 ACATTTTATG TTCTAGTTAA GTAAAATTCT TAGAGAATGA GGTACTATCT CTGGATAGTC 900 TGTTTGATCT TGAAAATGTA CAGAATTCTT TGCCTCTTGA TCCTGGAGGA CTAGTGACTT 960 TCCAGCTCTG AGAGAGAACA GGATCCCTCT GCCAATTTTT TTCTGTGGTG TAAGGCAGAG 1020 CCTGGTCACT CCATCTAATG CTGTCTATCT CATCTCACGT 1060
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