| Tag | Content |
|---|
EnhancerAtlas ID | HS131-09746 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chrX:123350820-123352310 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chrX:123351255-123351269 | TCCTATCTTGTCTT | - | 6.51 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 123351438 | 123351580 | | chrX | 123351241 | 123352144 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI124215 | chrX | 123349084 | 123353995 |
|
Enhancer Sequence | GCCCTGAAGG GGCTTCTGAT CAAATTGCAG AGACCAGACA GCTTATCGAA CAGCTTATAA 60
CCTCTCTAAA GGCAGGACCT TTCTTATTCT TATTTCTTGT GGGCCTCAGT GCCCCAGGCC 120
TCCTGCTGGA CACATGTTAG TTACCTATAG CTTAATTAAA GCTTCTTTGG TGCATTATTT 180
CCTCTCCCCA AAGTGGAAAT AATGAGCGAG TGCTGAGCTG ATGTGACCAC GTAGCCCCAT 240
TCCCCAAGGT AAAGTGACTA CATACATTTT GTCTTGGAAA CTCACTGCCT TCTGCAGAGT 300
CCTTTTTCAC TGGTAAAGGT TAAGTTTTGT TATTCTCCTG GATCTTTTGA AAACAATGCC 360
TATAAATGAG GAAGCTAGCA ATAAAACCCC TACTGTTTGT ATAGGCTTTG TAGCTTACTG 420
TGATCTAATT TAATCTCCTA TCTTGTCTTT TTCCTCAGTG CTTTGTACAC AAATGTTATT 480
GATTCCCTCC AGAGGCAGCC ATGTGTGGTA GAATAAACAG CATGAGTCTG GAGTTTTAGC 540
ACCCACCTCT TCAACGATCT GAGTGCTGTT AGGCAAGCTG CTTCCCCTCC CTAAGCCTCA 600
ATTTACCCGC ATACAGAATG AGGAAAGGGT TTGGACTCCA CAGAATCTGA GGCCTCTCTA 660
GTTTCTCATT GGAGTGCAAG TGCCATTGTG TGGTTTCTGC TGTGGGCGTG GTTGTTCCAA 720
ACCAAAGGGC AGGGACAGGA TGCAGTCTGC TGATCAGGGA CAGAGGAAGA GAGACACAGC 780
AGCTTTGCAC ATTTGTGGGT CCTTATTCCC TCTCCTTACA TTTCCCAGAC TGTTTAAGTT 840
CATGATCTCA GGGCAGCGCC TGTCCGCCCC CTACCACACA CATCATACTA TTCAGAGTTT 900
CTTTCCCAGG GTCTACTTTA AAGCCAGTAG ATTTTCAGGG GTCTCAGATC TTCTTATTGC 960
TTGCCCTCTT GACATCTGAG GCCTGAAAAG AATTTGGGTT GCCTGCCTAG GCAGGCTTCC 1020
GGAGGCCTCA GCCTTCTGTC TTCCGGGGCT GGGGGTAGGA GGGTGCCAGA GCACAGGCAG 1080
TCATTGTTTG GGTATTGACT CAAAGGAGAA GGAGCCACAA TGCACAGGAA AAAGGATGAG 1140
CTCATGACAG CTAAATGAAA AGATTCTTAT CTTGGAAACA GCGGTTTCTT ATGCAGAACA 1200
AGGGGCGGCA ATGTGATTGT GCCCAAGGAG TACATTCAAC AACAGGGATT TCAAATGAAG 1260
AAGTTATTTT GCATACTTAC GGGAGGAGCA ATGGGCCAGA TTGTTCATTA ATTAAAGGGG 1320
GGGGGTGCTG AACCCCCTAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC 1380
TGCAGAACTT AAATAATTCA TTCGCTTTCT CCTCTTTCTC CTCAGTCCCA GATGATCAGC 1440
TGAGAGACAA ATGTTTTTTC AACTCTAGCC ACCTCTGGAG AAAGGATGGG 1490
|
