Tag | Content |
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EnhancerAtlas ID | HS148-01162 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr1:162506130-162507300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LBX2 | MA0699.1 | chr1:162506640-162506650 | GCTAATTGGC | - | 6.02 |
| | 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 |
GH01I162536 | chr1 | 162505901 | 162510273 |
| Enhancer Sequence | CCTCCTGGGC TCAAGTGATT CTCCCACCTC AGCCTCCCTA GTAGCTGGGA CTACAGGCAT 60 GCACGACCAC GCCTGGCTAA TTTTTTTTTT TTTTTGTATT TTATGTAGAG ACAGGGTCTT 120 GCCATGTTGC CCAGGCTGGT CTGAAACTCC TAGGCTCAAG TGATCCTCCC ACCTTGGCCT 180 CCCAAAGTGT TGGGATTACA GGCAAGAGCG ACTGCACCCG GCCAGCACTC CCTTCTTATT 240 ATTGCTGCAC ATTCATCAAA GGCCTAAGCA TCTGACTTTG CATTATAGCC AAGAAAGAGA 300 ATTTGGAGGT TGGGTCTGAT GATAAATAAC ATATGCAGCT ATGGCCCCTG AACTAGGCTG 360 CCTGAAAGTG GTGTTGTGAG TCACTTTTAT GGTTTTGGCA AACTGAAATT CTACCATTCA 420 AAATGGCTTC CACCTACTTG TTCATGTGTC TGTTCATGTA CATGACACAA TTGTTTTCTT 480 TGTTCCCAAA GAAACAGGCA AGGGAAATCA GCTAATTGGC TAACCCTTAA GCAGTAGGGA 540 AGATATGGCA AGGGCTGGTT ATGTTGCTAC ATTGGTTTGT ATCACAAGTG GATATAGAGA 600 GTCTGGGGTT AAGGAACAGA AGGTTCCATT TTAATGCCAT ATTTCGGCCA GGTGCGGTGG 660 CTCACACCTG TAATGCCAGC ACTTTGGGAG GCTGAGGCAG GTGGATCACG AGGTCAGCAG 720 TTCAAGACCA ACCTGGCCAA CCTGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG 780 CTGGGCGTGG TGGGTGCGCA CCTGTAATCC CAGCTACTCG GGAGGCTGAG GCAGAAGAAT 840 CGCTTGAACC CAGGAGGCGG AGGTTGCAGT GAGCCGAGAC TGTTACTGCA CTCCAGCCTA 900 GTGACAGAGC AAGACTCCGA CTCCAAAAAA AAAAAAAACA CCATATTTCT CCATTATCTT 960 CATTGACAGA GCATCAGAAC CAGTTGCCTG CTGACAAAGG CCAAGTTTAA TTAGGGTAAA 1020 AGAGGTGAGA TGCCAAATTT GTGTGTGTGA GAGAGAGAGA GAGAGAAAGA GAGAGAGAGA 1080 GAGAGAGAGA GGGAGAGAGA GAATTAGAGA TTTCAGGACC AGGCAAAGGA GGCAGCTTGG 1140 AAATGAAAAT AGAAAGGCAA GTTGGAGTGT 1170
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