| Tag | Content |
|---|
EnhancerAtlas ID | HS026-10271 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr14:51376820-51378440 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr14:51378015-51378031 | CTCATTTATTATTGAT | - | 6.07 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 51377223 | 51377319 | | chr14 | 51377393 | 51377957 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH14I050910 | chr14 | 51377187 | 51378589 |
| Enhancer Sequence | CTGCAAGAAA GGTAAGTTAA AATTAGTAAT TTTGTCTGTC TAGATCTGCT TGTATTGTAT 60
TGAAGCATTT ATTAAGTTGG GCTGTTTTGA TAATTAAAGT AATACATGCA CATTAAGATA 120
AACATTCAAA TGGTCTAGAA GGCAGATCAC ACTCTTTCCC CTTGACTCAG GCAACCACTT 180
TTGTCCATTT TATATGCTTG TATTTCTTTC TCGAGCTATA AACTTTGAAG AGTATCTATT 240
GACTGCGACA AACATTGATA CTACATTTCT CTTCTTCCTT TTATTCCTTC CAATTTTTGT 300
TACAGTTTTA TTTTTATTTC TTCTACTTTA TAAAATATAT TGAAATTTCT CTTTTTTTCT 360
TTCTCTTTTT TGGTACAGGG TCTCTCTCTG TCACCCAGGC TGGAGTGCAG TGGTGCGATT 420
ACAGCTCTCT GCAGCCTTGA CCTCCTAGGC TCAAGCAATC TTCCTGCCCC AGCCTCCCAA 480
GTAGCTGCAA TTACAAGCGA GCACCACCAT GTCCAGCTAA TTTTTTAAAA TTTTTGTATG 540
TATGGGGTCT CCCTATGCTG CCCAGGCTGA ACTTCTCTCT CTTGATCCAT AACATTCAGA 600
GTGTCCCTCC AGGACTCCTC TTTGGCAACC TGAGGAGACT GGATTGTCTG CATTCCTTCT 660
ACTTCTCACC TCCTTCCTTC CACTTTTCCT GCAGGGAAAT AAGCCACACG TAATTGAGGT 720
GTGCCTGGGG CTAGACATCT AGCCTCTGAC CTTTCAGGCT GATTTGCACG CAAATTAGAG 780
CTGCCTGAAG CACTTCCTTT GACTACAAAG GTCAGGACCA CTTTTCTGCT TTACTGTGAG 840
AGCTTATTTG TGGATTAGAT GTATCTTCTT TTGCATCCCT AGGAACCTGG CTCTTCTCCC 900
TTTATGCAGA GAGTTCTTAA ACAGTAACAT CAGAGGACCT AAAAACACCA CAAAAAGAAA 960
AAGCTCCCTT TCTACCTTTT CAGTTTGGGA AGTGGGTGAA TACACAGTTG GGCATTTGCA 1020
TGTGGATGGT GCTCTGTGAG CTTGTGACCC AAATAACCAA AGGTCCCAGT GGAAGAGAAA 1080
GGGACACTGG CTTCTTGCCC ATCTGGCTGT CCCCATGTGG GAGCATCATG CTTGATGCTG 1140
AAGTGCCCAT GTGAGGCACA TCTAAGCCTC GTGCTTTGGC AGCCTCACAT CTGCCCTCAT 1200
TTATTATTGA TACAAGAGCA AGTGACAGCC CTTCTTCTCA CAGGGTGACC AAAGAAATAT 1260
CTGAAGACTG GGGATTTGGT GTTCTCTTGC AAAACTGGGG CTGGGAACTG AAGACCTTTC 1320
CTCTGTTTTA TAGAGCGGGT TCTGAATGAT GCTGAAACCC CAGGGCTGCC TCCCCCAGCA 1380
CATAGCTCTC ACTGGCTTGG AAGAAAATGT ACTTGCAAGT ATAATCCTGT GATACTGACT 1440
CCAGGACATC AATTTCATTG TGACTTGGGT CACTTTAAAA CCTCTTACCG TAGGCCCTTA 1500
TTCTGCACAA GAGTGACACC TTCTATCCTA AGTTACTAGC TCCTGGAGGT TGGCTGCCCC 1560
ATCTTTCATA CCATGTAATC TCTAGAGTTT GCCCTGGCCC CTGCATATTT TGCAATGAGG 1620
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