| Tag | Content |
|---|
EnhancerAtlas ID | HS056-16429 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chrX:134137790-134138820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chrX:134138309-134138324 | CAGGCCACGCCCATG | + | 6.1 |
| | | 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 |
| GH0XI135003 | chrX | 134137631 | 134138935 |
| Enhancer Sequence | TAACTGTTCA TGGTGCATTA CTCTTTGAAT GTGCTGCTCT GGATGTTTGC TAATATTTGG 60
GGCTTTCCTA TTAATGTTTC AAAGTAACCA CATCTGCGGC CAGGGAGCCA ATAATCTGGC 120
TGAGAGATGC ATGAAGGAGG AAAATGTGTT CACAGAACCT CACTCCAGTG GCGTCCACAG 180
CCGAGAGTCA GTAAAGGGAC ACGCTACAGC TGATGAGTTA GGTGAGGGGA GGAGTACGGT 240
AGGAGGCCGC ATCACCTTCC AGAACACGTG TCCTCTGCTC TCTTTGGGCA GCGGGCGCAA 300
TCTCCCCTCA CACCGCAAAC TGTCCTGGGA TCTTCCCCCG CGCACCGCCC CTCGCCCGCG 360
CCTGCCTTGG GAAATCTTGG CCCCACCTTT CTGATTCAGA CCCCGCCTCC TGAAGAGAGT 420
TAAGCCCTCC CCCACGTTCT CACAGCCGCG GCCCGGCCCC GTTCTGAGCT TGCGCACTAG 480
TGACCATCGG GCTTTGGGGG CGGAGCCCGC GCAAGCACTC AGGCCACGCC CATGGCCAAG 540
CCCACATTCC GCCCCATGGA CAGGCCCACA TTCCGCCCCA TGGACACGCC TCCACAACCA 600
TGCATTTCCG GTGATGCTTA GAAATATAAA GATCGGAGTG GTAATGTAAT TTTGTGACGT 660
TGGTGAAAGA CTAAAAGCAA ATGGCAAAAT CATACCCACT GACCTGAAAT AGGGTCCAAA 720
TCGGGACAAA AAGGACATTT TTCTTTGCCT CCACCCTCTG ACACAGCCTT TAGGAGGACA 780
ATGCCCTACG GCTGCCCCCA GCTGCCTAGA ATCCACTCTA CCCCAGACTA CAGTGACAAT 840
TCTAAGCCCA CCTGTCTTAT GCAGAAACCG GGAGGCAGAA GGGGGCACAC AACAGGAAGG 900
GGAAGAAATG TTCTCTGAGG GAGAAACAGG TCCGTTTGGC ACTTTCCACA GATGCACCCA 960
ACTCCGACTG GAATAACTGC TGCTTACTCC TCTGCTCATT GTGTCTTTGC AATTAAAAGA 1020
AAAAATTGAA 1030
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