| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08529 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr22:29505440-29506630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MIXL1 | MA0662.1 | chr22:29505641-29505651 | GTTAATTAGA | - | 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 |
| GH22I029109 | chr22 | 29505433 | 29506561 |
| Enhancer Sequence | TGTTGTGAGT TTCTGAAGAC AAGAGGACTC AGTAAAGATT GTGGAAATTG GAAGAAAGGT 60
GGCTGGTGGC TGAATGGGTC AGGGAACAGC AGGACAGAGG CTTGGAGGAA GCACAGAATT 120
GATGAGTGTG TGGGTTGGGA TCCAGGCTTC CTGAGTAGAG GAGTGGACAA AAAGGAACCA 180
GGTCAGACCT GGAAAGCAAG AGTTAATTAG ATGGGACTGA TATGCTGAAA GCCCTAGTTT 240
AGGAAGAGAA GCAAGTCCAG TGTCATTTAC AGGACGGATC AAAGGAAGAA AGTTTGGGGA 300
AGAGAGGATG CGTGTAGATT TCTAAACTCA AGGGATAAGG GCCTGGGCTA TCATGGCAGC 360
AGTGAGACAA GACAGGAAGG ATTAAGTCCA AGATGCACTT AGGAAGAAGA CAGAACTTGT 420
TGACAAGTGG AATATGTAAG GGATAAAACA GCAGGAAGAG GTTCCTTGCC TGGGATATTT 480
GTGGTGTCCC TGAAAAAAAA AGTCCAAGTC AACAAACGAG CTTTTCTTCC CAGGGACACA 540
GCAGTTATCA TTCCTCTTGA ACTTGGACTG ACCTTTTACC AAGTAATGTG TACTAGTTGT 600
TTATTGCTGT GTAATGAGCC ATCCCCAGCC GCAGTGACTT AAGCGCCAAC AGTTTATCAT 660
TTCTCCCAGT TCTCTGGGTC GACTGAGTTT CAGCTGAGTG GTTCTTCTGC TGCTGTCACC 720
TGGGCTTAGT GAGGTGCCTG CATTCAACTG GGAGCTCTGC TGGCATTCAA GGTGGCTTCA 780
GACCTCTATC CAGTGACTTC TCTCAACAGC AGGGTATTCA GACTTCTTAT ACGGTGGCTG 840
GCTTCCAAGA GAGAAGCAGC AGAAGCTGCC ATTCCTCTTA AGGCATGAAC TCAGAAGAAG 900
TCCACCACAT TCTATGGATC AAAGCAAGTG GCAAGGCCCG ATTTAAGAAG TGGGGAAATC 960
TATTAAAGTG GGAGCAACAC ACATGTACAG GGAGGGGAGA AATTACTAGA GCCTCTTTTG 1020
ACTCTTTATC ACATTAACTC ACCAGAAACT AAGTTTCAGA GAAGGAACTC CCACCAGGAG 1080
GGAACTACTG CTGTGATAGA TCCTGGCCTT ATGGGATCAG GATTTTTAGG AACTCTTACT 1140
ACCTCCCCCT AAGGGCAGAA TTCCACAGAG GAAGAAAAAG CTGTGCTTAC 1190
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