| Tag | Content |
|---|
EnhancerAtlas ID | HS197-22756 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chrX:152599740-152601190 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chrX:152600318-152600338 | TGGGTGGGAGTGGGGGGGGG | - | 6.32 | | ZNF263 | MA0528.1 | chrX:152600859-152600880 | TCCCCACCCTCACCTTCCCCC | - | 6.09 |
|
| | 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 |
| GH0XI153335 | chrX | 152601013 | 152602215 |
|
Enhancer Sequence | TGGGTGAGTG TGCGGGCCGC GGGAGGATGT GCGGGGGGCG CTGGAGGGGC CGCAGGGCGG 60
AGGTGATCGT GGGGGCGGCA GGAGGACGTG TGGACCTGAG TGAGCGTGCA GGGCCGCGAG 120
AGGATGTGCA GGGGGTGCAG GACTGTGTGC GGGGCTGGAG CGAGTGTGCG GGCCGCAGAA 180
GAGTGCACGG TGGAGGGAGG GGGCGTCTCT GGGCAGTTGG AGAGCTGCTC GGCCTTGGGC 240
GGGCCAGAGC AGGGAACGGG TCCCGGATGA CGAGTACGAA GAGGCCCGAA GGCCTTCCCG 300
AGGCGGGCGG GGGGCGGCGA TCCCGGGTGG GAATCGCTAA AGTGTAGAGG CCTGCTCTGC 360
TCTTTGGGGG ACGCTAGGAG ATGGGAACCG CTCAGGGGCG GAGAGAAAGG ACCCCTGCCC 420
CTAGCTCCTA GGAGCCCGAT CTGGAGGGGG CATTGTAGGG GTGGGGGTTA AAGGACTTTT 480
CCCTGGTCTA GGGGAGGGAC TGAGCCGCAG TCTGGGAGCT GGGAGGGTGG GCCAGGTGGG 540
AACAGTTCCC GCTGGGGAGT CCCTCCTTTC CTTTTGAGTG GGTGGGAGTG GGGGGGGGCG 600
GTTAAGCCTC AGCTTGGTGG GGAGAATGGG GGCCGGTAGG TAGCCTAGAG AGAGAGCTGT 660
GGAGAGGCAG GGGAAAGGGG GCGGTGAGCC GAGCTCAAGG CCCTCTGTCT GAACCAGTCT 720
TTTTCTGTCG CCCTACTGGG GGCCGCCATC TCCCACTTCA GTGCCCCCGC CCCCTTAAAC 780
TCCTTTGCTG GCTCCTCCAG TCTATATTTG GGTGATTAAT TATATATCTT TTCCACACAC 840
ACCCCCCACT CGCCTGCCGC CCAAAGTCCA TGGTCCCTTT CAAACAACCC CCTGCCCCCA 900
TTCCTGGCCC ACTTCCCAGA GGTCCCACCC TGCCACCTTG TTCCAACTGA AGCCCTCCAG 960
CCAGCCTTGA CCTAGCTGGG CATGCGGCCC CCTCCAGTCT CCTTAGTCAA TGAAACATTT 1020
CCTCTTCAAC CTCAGCCCGA CATTTTTCCT TTACAAGAGA ATTTCAGATG GGATTGCTGG 1080
AACAGCACCT CCCCTAGGTA CTAATGCTGC CTCAGCCCCT CCCCACCCTC ACCTTCCCCC 1140
AACCCTGCAA CATTGGACCT TCAAGTAGAA GCCACTTGCA CAGTATCTGG CCCAGTTCAG 1200
TACATCCCCA CAAAATGTTA CTAGGGGGAT GTACTGAACT GGGTCAGACA CTGAGTTTTA 1260
TATATAGAAC CCTATTGAGC AGTAATTTGC AGCCTTCTGT CTGTGAGGGA CCCCTTGGAA 1320
ATCTACCAGA ACTTGTGAAT TCTCTTCTAA CCATCAGCAC AGACTCAGAG ATAGTGGGCT 1380
CCCATTTCAG CAGGTTCCTG GGCAGGAATC CTGTCAGTAA CAGAGATTCT GAGAGTTGGA 1440
GAATCTGGGA 1450
|
