| Tag | Content |
|---|
EnhancerAtlas ID | HS148-02036 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr10:16874070-16875490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr10:16874094-16874105 | GTTTTATGGGG | - | 6.02 | | Spz1 | MA0111.1 | chr10:16874152-16874163 | GCTGCTACCCT | - | 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 |
| GH10I016831 | chr10 | 16873973 | 16875820 |
|
Enhancer Sequence | TATAAAAACA GGAGATGAGC CTGTGTTTTA TGGGGAGAGA GAACTACACT GTGAACTGAA 60
CCACTTTCTG TCCCCCAGCC TGGCTGCTAC CCTGCATTCA CAACCAGCCC TGCTTCCAGG 120
AGGGCTCTCG ACGCTTCTTA CGGAAACGTT ACGCGGGCAA TGTATGTTGG AACCAGCCTG 180
ACATGCGGAA ATGCTGATTT TACTGATCTA TGTATTCAAA ATATTGGAAG TTCCTCTGTT 240
CCCTATATAA TTCCATGGTT TAAACTTTGG TTAATTGCTG GTATCTTAAG TCACAAAGTT 300
AAGACATCTT GCTGGGCTGT GTTGATCAGG TGAGATTCCT TTTAGGTCGA TGTAGTAGCC 360
CATGGGAGAG AATAATGCCT TTCTAGTGCT TTGGGGATTA TTCTGCTAAG TGTTTAAACA 420
AAGTAACCTT GCCATGACAG AGTAGCCAGT CATCCACTAG TAGATGGGAG GGCTGCCATA 480
GCCAGCACCA CGCTTTTGAG TTTGGGCGTT TTTCCCTCAG GGTCCTCTTT CAAAATGCCG 540
TTGCTCTGAG AGGAGCAGCA GGATACTAAT TTCCACTGAC ACTGCTGACA ACTTGTCTTA 600
TTCACTTTCC TCTCCTAGGA AGAATGGGGC CACCTAGAGC AGTGGGCATC TCTGGGACAT 660
CAGAGGATCT TGAAAGGGGA GGTGAAGGCA TGAAAACAGA TTCCAAGCAT GGTCTAGAGC 720
TCGGCCCTCG CTTGGTAGTA ACACAGTCAG AATTCTCAGT CAGACATTTC CGTTCCCACC 780
GCAGTTCACA AGAACGGAAT GCTGAGGCTT CCTGGTACAG CTGCCAAGAA ACTATGCCCA 840
CAGCCTTCCC ACTGAGAGCC AGATGGAGCT ACATTTTACA GGCCTAAGCG GTGGTTTCCT 900
TTCTTTGCTT ATGGGACAGG AAGTTTCAGA TCCATTCTGT GGAGTAATGA AGGACAGCTA 960
GGAGGAGGAA TTCTCACTCT CCACGGCTGG AAAGCAAGGC TTTGCTTCCC AGCATCTATC 1020
AGGCAAATGG CAAACGTTGA CTCTGATCAA TAATGGTCCA TTCAAGCTGG AGTGAGTTAA 1080
GAGTTAGTTG CACTGTGACT CCAACCTAAC GGGATTATTC CATCTTTCCT CCAGATCCCA 1140
CTCTCCTCAT TCTTTCTGCT TTACACTTCA TATAAATATT TGGATCTCCA TGGTGGGGGA 1200
GGTACACAGG TCCAAGTTGA ATAACCTGAC CGGCACAAAG AATAACTGTA TTTGCCTCTT 1260
CATTTCCTCC CTGCTATATA CATCTTTCGG TCTCCTGTCG TGGCGAGTAT TCCTTTAGAA 1320
AAGGCATGAG CTTCCTCCGA GTGTTATTTA TGGCACTATA TGTTAAGGTT ATTGATTAAT 1380
AAAGGATTTA GATGAATTCC AAAGGGGAGA GCTTTCCAGG 1420
|
