| Tag | Content |
|---|
EnhancerAtlas ID | HS197-22262 | Organism | Homo sapiens | Tissue/cell | ZR75-30 | Coordinate | chr9:136181370-136182430 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF3 | MA0640.1 | chr9:136181796-136181809 | TCACTTCCGGCTT | - | 6.36 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCGTCACCCC GTAAGCAGCA GCTCCGATCA ATTCTCCTTT GCGAGGTGAC CACCAAAGGA 60
GCGCAGAGCT GGCCGGGCAT TCGTGCGTGT TCATGACCAA GAACTTTTCA CAGAGAGAGA 120
GAGGACTTCT GTCCTGATGA AGGAGCGCAG AGCTGGCCGG GGGCATTCAT ACATGTTCAT 180
GACCGAGAAC TTTTCACACA GAGAGAGGAC TTCTGTCCTG ACAAAGGAGC GCAGAGCTGG 240
CCGGGGCATT CGTGCGTGTT CACGACCGAG AACTTTTCAC AGAGAGAGGA CTTCTGTCCT 300
GATAGACGTC GGTGAGGACT GAATCCCCAC TTACAGGCGT GCACATCAGG GACTGATGGA 360
CATCGCTGAG GACCGATCCC AGCTTACAGG CGTGCACACT GGAGGCTCGG AAGAGCTGAC 420
TGTGACTCAC TTCCGGCTTC CCCCCAGGAC AAAACCTGCC TCTCCTTCCA GACTCGCCGA 480
CTTCCCTTCA TGTCCCGCTG TGATGTGCAG TCCAGCATCC TTGGGTCATG ACACCAGCTG 540
CACTGGCACA GGGAATGAGA GAATATTCCT GAAAATGAAG ACTACCGCGG AAGGCAGGAG 600
CTTCTAAGCT AGAGTGACTG GCAGCTTCAA CAGGCCCTGC TGCACCTGAA CCAGCCCGGG 660
GCCCCCCAGT GCCACGGAAA GAGACAGCTG TGGCAGATTT CACAAACTCA TGCCCAGGGG 720
AGCTCCCGGC TTGCTCATGG CAAGGACCAC ACAGGGGCAT CTTAGGGTCC GCGGGAGGCA 780
GCGGAACTGT GGAGTCCCAG GGCACATTGT CTCCAGCTTC GCCAGCTGGG CCATTGCTCT 840
CCAACGCCAG CACCCATGGG TACTTCCTGA TGCACCTCAT CCTACCCACG TTACTGTCAG 900
AGTGAGGAAT GCGCTCAGCC TCAGGCCCTG AGATTGTCCT CTCCTTACTC AGCTTCTCTT 960
TCTGTCCTTG CAGCATCCGG TTCGCCTCTT CCCCCAACTG CCTTTTCGCA CCCTCTGCCT 1020
GCTCTTCCCT GCAGTTGTCT GTGTCTACAT CATTGGCAGG 1060
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