| Tag | Content |
|---|
EnhancerAtlas ID | HS106-02032 | Organism | Homo sapiens | Tissue/cell | iPSC | Coordinate | chr7:44103100-44104210 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr7:44104016-44104037 | TTCAGTACCAGGGGGAGCTCC | + | 7.11 |
| | | 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 |
| GH07I044063 | chr7 | 44103102 | 44104206 |
| Enhancer Sequence | ACTCCTGACC TCAGGTGATC TGCCTGCCTC AGCCTCCCAA AGTGCTGGGA TTACAGGAGT 60
GAGCCACCGT GCCCAGCACC CTTTGGTTTC TAAAGTGCTC TAAATTCTAG ACATCCTGAA 120
CAGAGGAGCA AGTGCGGAAT GGAGCTGGAG GAGGGACAGG GAGGCCGAGC CTGGTCGAAA 180
CCTGACCCTG CCTGCCTCCT GCAGCCCCTG AGCTGGGAAT AGCAGCTCGA CCTTTGATGT 240
TCGCGCCACT CCACCCCTGC TCCGTGCAGG AGGGTTTAAG AAAATGTTCT CTGGGGAGTC 300
AGAGTGAAAT CCCTCATATT CACCACCAAA AGTGCGTCCC CTTTCCCCAA ACCAGGCTGT 360
GGGAGGGTCA TGGGGCTGCA TGAAGTCTCC GGAAGGGAGA GGAGGCAGGT GGTCCTTCCC 420
TCTGCCTGGC CCCAGTGCCA GGTGCCAGGT GTCCGTGTTT GGAGCGGGCA GGCTTGGGGC 480
TGGCTGGGTC TCCGGGGCCT GCCGGTCTGG GTGCTCTGGC CAACTGCCCA ACGGCCCTAG 540
GAGCAGGAGG TCTGGGGCAC ACCCTTCTAG CCTTTCCAGG ACTCAACAAG CTTTAAGGTC 600
ATTCAGATGC TAATTTAGAC TGCCCTTGTG TCAGAATACT AAGGTGGGAG GCGGAGCGGA 660
GGTGCCAGTC ACTCTGGGCG AGGCCTTACT GCGCCCATGC ATCCCGGGCC CATTTGTCAG 720
CCCTTGCTCT TCAGTGGGAG CCCAGCTGCA AGCCCAGAGT CTGGCCACTC CATAGTCCTG 780
CACCCCTCTT TTGATTGGTC TTTCCTTTGC CCAGAGAGGG GCTCCAGAGG GAGATAGGTG 840
GTGAAGCTCA TGCAGGGATT CTGAGGACCT GATGGGGGAG GGCCCTGCGA GGGGTCCAAG 900
CCTACATCAA GAGGAATTCA GTACCAGGGG GAGCTCCCCA CCACCCCGGA AAAGGGAGAG 960
GCCCAGAGAT GGAGGTGGCT TGTCCAGGGC CCCACAGTAA GTTGGGATTT GGAGCCAGAT 1020
GCTCTAAGCC CAGCCCTTCC GTTTCCTAGC TGGGTGTCCC TTGGCAGATG CCACCTTTGG 1080
AGCCTGCCCC ACCTCGGGAC ACAGCGAGCT 1110
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