| Tag | Content |
|---|
EnhancerAtlas ID | HS050-26761 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr16:84331820-84333000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr16:84331944-84331958 | CCCGCCTCGGCCTC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTGTGCCTA GGCCTCCTGA GTAGTTGGGA TTACAGGCAT GTACCACCAC GCCTGGCTAA 60
TTTTTTGTAT TTTTAGTAGA GATGGGGTTT TGCTGGTCTC AAACTCCTGA GCTCAGGTGA 120
TCCGCCCGCC TCGGCCTCCC AAAGTGCTGG GATTATAGGT GTGAGCCACC GCACCCAGCC 180
AGGAAATACT TCTTGTTAGA AATGCATCAC TTTCCAATTG TATTGCTCCG TTTTGCTATT 240
CTCTTGGCTC CTGGGGTTTT ATGTCTTTTG CATCCGTGTG GTATGACCAG GAGAGAAGCT 300
ACTCCACATC TCTTCCCACT CCCATTCAGT GGCCTCACGT GGGTTGCCTG AAATCAACCA 360
TGCTGGGAGT ATTTACACCT TGGAAATTGG CCAGGGCTAC ATGAGGAGAG CTGGTGGTTC 420
AGTCCTGACC AAGCGCAGGG CTGCCTGTAG CCTGCTCTAG TCTCTCAAAG CCTCGTCCCC 480
CGGCAGAGTG AGTTTTGTGT AGCGGACTGG TCTCTTAGAG TGGGGCCGGT TAATGTCCTG 540
AGTGCTGTTT ATGCTTCTTG GTCTAAGCAT GCAGAGACAG TGCCAGAGAT GAGCACGCTT 600
GCCTTCCATT CCCGTGGGAG GCCCTTAGGA GAAGCTTCTA ATGAGAAGTG CCGGGTCTCC 660
CGCCTTCTAT CTCTAAGACC TTCAGGAGTT TCCTTCTCCT ATCTGAGCCT CGGTTTCCTC 720
ATCTGCAGCA CGGGACACAG TAGTGCCTGC TTTGCAGGGC TCAGTAAAAA GACCATAGAG 780
CCCACAGTTC CCTGACTGGC ACAGAACTGC ATTCCCTACA TGTGCACTAC GGACAGATTT 840
AAAAACCCAT TCCAGGCCGG GCACAGTGGC TCACAGTGGC TCATGCCTGT AATCCCAGCA 900
CTTTGGGAGG CCAAGGCAGG CAGATCTCCT GAGGTCGGGA GTTCAAAACC AGCCTGACCA 960
ACATGGAGAA ACCCCGTCTG TACTAAAAAT ACAAAAAAAA TTAGCCGGGC ATGGTGGCGC 1020
ATGCCTGTAA TCCCAGCTAC TCGGGAGGCT GAGGTAGGAG AATTGCTTGA ACCCTGGGAG 1080
GCGGAGGTTG CGGTGAGCCG AGATCGTGCC ATTGGATTCC AGCCTGGGCA AGAAGAGCGC 1140
AACTCCATCT CAAAAAACAA AAAACAAAAA GCAAAAAAAA 1180
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