| Tag | Content |
|---|
EnhancerAtlas ID | HS098-12322 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr12:7297030-7298150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:7297202-7297221 | TACTGCCATCTAGTGGGTG | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 7297345 | 7297600 | | chr12 | 7297600 | 7297754 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH12I007144 | chr12 | 7296901 | 7297996 |
| Enhancer Sequence | TGCTATAAAG TGGTGATAGC AATAGAGTCT AACTCGTGGA ATTGTTACGA TGACTACATG 60
ATATAATCTG GATCAAATGC CTAGCAGAGA GTGGATGCCG CTTAAATGCT GGCTATTATT 120
ACATAAAGGC ATTTTCACCC CTTATTATGG TTTATGGGCG GTTTTTAGGA GATACTGCCA 180
TCTAGTGGGT GAATTACATG ATTTAAGAGT TAGGATTTCT GCGTTCCAAT CTTGTTACCC 240
CTCTCCCCGA TTCTGCCTCA GTTTCTCTGT GAGCTATATG AAGATAAACA TCTCAAATTT 300
GCCCCTATCC TGGGAGGGGT GGGTTTAGAG GGGAGAGGGC TCTGAGCCCT AGAGGGTGAC 360
TGGGCGTGAT TATCAGGCCT CACAGTTAGA GCTGTGGAAG GCCCCGGGCT GTGGCTTTTG 420
GGAATTTGCT GGTTCAGGGT GTGGAGCTGA AGGTCACAGG CAGTTGAGTT AATGTGGGTG 480
CAGCTGATTG CTGAGTATGC ACCCCGCCAT GTCCCAGTCA GAGCTCCAGT TGTTAAAGGG 540
CTGTCATCCA GTTATGAAAG GCTTGATCCC TCAGAAGCCA AGGCATTGCC TCGTCCCCTC 600
CAGTGCTGAG GAGCCATGGC AGAAGGGAGG GCTCTGGTTT TTGGCCTAGG GTGGAGCTCT 660
GCAAGGGGAG TTCCTGCGGG GGGAGGAGTT GACATTCTCT TTGCTGACTG CCTCATCTGA 720
ATTCCTGCTA TCTTTTTCAT GCCCAGGATA GAGGTTTATC CAAGGGCTTG GAACCTGCCT 780
TTGAGGAAAG GGGCCTTGAT GTTTTCTCTA TGAGGTTAAG AAACAGAGTT TTCATTTCTC 840
CATTTCTAAG GTTACTACAT GGTTGGTGCT ATCCTAATAC TTCCCTGAGG TCACGGGAGA 900
AAATATAGAG GGGTGTGTGT GTGTGTGTGT GTGTGTGCGC GCGCATTTGT GTGTATGTAA 960
CAGACACAGA CAGGTACCTA GCAATACCTC CCTTTCCCTG ATGCATTTCC TTGCCCCTGT 1020
CCCTGTGGCT TTCATAGCTT CCAGTTTTCA GTTCTTGGAC CTCTGTCTAT TTAAAGCCAG 1080
ATTTATGCAA CTATTTGGTC AATGCCTAAA TGCAAGTTTT 1120
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