Tag | Content |
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EnhancerAtlas ID | HS147-44286 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chrX:107177980-107179020 | Target genes | | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chrX:107178963-107178977 | CTGAGTCATTTCCC | - | 6.06 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCTTCCCCA TACACACTTC ACTTCACTTG GACCTCCCTT GCCAATCCGC TGCTACCATT 60 ACTTTTGAGC TTTCTGCTTC AGCCCTCTCC CCCATCCTGC TTGATAACTG TACAAAATGC 120 AAATACTGTT TTAGCTAGTG GCGTCTCTGT TTCAAATTTC AGGTCAGTCA TCTGAGAGTC 180 TTCAATGTGT ACATGCAGGG AATTGCCAAA GATATTCTAC TTTCCAAGGG CAGAGTAGGT 240 CACTTGATAC AGCAACTAAC AGGGGTCCTG TGTGCCACCT TCTCCAATTA TGATCTTCCC 300 AATCCAAACT CCCACAGATA CATCCCTTAA AAGGCAAAGG AGAGAGTCCT GGTACAGCCA 360 CCACTCCAAG TTATTATTCC GCCATTCATT TATTCACTCA TTCAACAAAT ATTTTACTGA 420 TAGTCTGTTT GTGGCAGGTG CTGGAGCTCA GTGATGAATA AGACACATAA TCCCTGCCCT 480 CATGAGACTC ATAATCTAGA GAGAAGACAG AGTATCAACG AATGAAGACT TTTTGAATTA 540 TAGGCGCTAT CATTTATTGG TTGCTTACAG TGTGCCTGGC ACTATGCCAA GCACTCGAGA 600 TGCAGTGATT CATTCAATCC TCCCAGGAAT CCTATGAGGT AAAGACTATT ATTGGCTCCC 660 TCGAACATGA AGAGTTAATC ATTCCATGCG CCCATGCCCA GGCCTGCAGA TTCCTACATG 720 CCTGGTGAGC TGCTAGCAAG GGTCTTAGCC ATGGCTGCTT TGGGTACGAG GTAAAGTTTA 780 AGGCCCAGCA CTGAGGAAAC AAATGACCCA GTGCAGCAGC TCCTGAAGTC AGGGTTAACC 840 GGGAAGGCCT TCCAGGTCTT TGCTAGACAC CCCCAAAACT GCCCCCGAGG CGATTCTCCC 900 ATCCTCTTTT TTCTCCCCTT TCCCTCCGGC ACCCCACTAC CCTCCCTTTC CAGCCCAGCC 960 CCTCCCTCTG GGCCGCCTCC TCTCTGAGTC ATTTCCCCTT CTCCGCCCTA AAGACCTTGT 1020 CTTTCTCTTG GAATCCCTTA 1040
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