| Tag | Content |
|---|
EnhancerAtlas ID | HS098-59240 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chrX:9462560-9463740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chrX:9462876-9462892 | TTGCTTTCTTGGAAAT | + | 6.02 | | IRF1 | MA0050.2 | chrX:9463419-9463440 | GATGGGTTTCGGTTTCTTTTT | + | 6.36 | | IRF8 | MA0652.1 | chrX:9463423-9463437 | GGTTTCGGTTTCTT | - | 6.09 | | IRF9 | MA0653.1 | chrX:9463423-9463438 | GGTTTCGGTTTCTTT | - | 7.33 | | NFE2L1 | MA0089.2 | chrX:9463048-9463063 | GGTGCTGAGTCATAG | - | 6.34 | | Nfe2l2 | MA0150.2 | chrX:9463050-9463065 | TGCTGAGTCATAGGA | - | 6.17 |
|
| | 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 |
| GH0XI009494 | chrX | 9462622 | 9464087 |
|
Enhancer Sequence | TGTTTTCCTT TAAAGTCCTT GGCAAATCAA CTCATAGACT TCTTCAACTT CAAAAAAAAA 60
GTTTTTTTAA AAAATATTTT AAAAATATTT AACTTGAGGA TCTTCATTGA AAATTGGTCA 120
TCTTTCGTGA ATTTGCTTAA GTAGGCTTTG ATCTCTTTTT AAAGGATTCC TTCCTGCCTG 180
ATACATTTGG TCCTTTTAGA ATTCGGGCTA GAACAATTCT CCATGAAGGT GGACGTGTTA 240
AAATCTATTT GGTTCATTGT TAGGATCACT CACATTACAA GAGAAATTTC GGTCTTGAGT 300
TTTTGTTTTT GCTTATTTGC TTTCTTGGAA ATGTTTCCAC ATCAGGTCTT AGAGGAGTTG 360
TAAAACAGGA AGGAGGAGTT GACATGCTGT TTCATAACCA ATGCTTGCTT CTCGCCTTGG 420
ATACTAACAT TTTTTCCATC CATTTCCCAC ATAAAACATG GAGACAAACA CCAGAGCTGC 480
TCCTGAGAGG TGCTGAGTCA TAGGAATTGA AGGGGGCTGT TGGGCCCTCG TGTGTGGGAT 540
GGGCTCAAGA GCTATCAGTC TACAGAGGGA AAGGTTCATC TCTGTCCCTC ATTGCCTGCA 600
GTTTCTCTTT GGCCCTGGCT TTTTCCGTTC ACAGCTGCCC TCGACGTTCA TTTTAATCAA 660
ATTTCACCTG CATAAAAGGG CTATGGGCAG AGAGTCTTCT CTGTGATGGA GCGCAGCTAT 720
CCTACAAGTA TGTAGCCCTG ATTTAGTAGA GAAGAGGCAG GAATTGTCGA GGGCGGAGGA 780
GCAGGAGAAA TGGTGCACAA GGGAGAGGGG ATAATGACAG GTCATTCAGG GATGTCTACG 840
GAATGTGAAA ATGCAGCAAG ATGGGTTTCG GTTTCTTTTT TTTTAGGTCC GACAGAGATT 900
CCTGGGATAG CTGCATCTTC ATGTTGTACA CGCATACACT TGATTCCCAT TATTCACTGG 960
AGCTATGTTC TGTAAAGTCG CTGAGACTTT ATAGAAAGCA TCACCCCAGG GAAAATACAC 1020
AGTGAGGCTT CTGCGAACCT CTGGTCACAA TGTTGTTGTC AAGCAGTCAG TGCATAACTT 1080
TGTTGTATGT ATTTCTATTG TGTGTTTCTG TTGGTTCCTT TACATTGCAC TCACGCCAAC 1140
AGCACTGTGA CTCACGCCTG GCCGAACCTC ATCTAACGCA 1180
|
