| Tag | Content |
|---|
EnhancerAtlas ID | HS098-43915 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr4:183899170-183900320 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP3 | MA0746.2 | chr4:183899721-183899734 | GGCCCCGCCCACC | + | 6.14 |
| | | 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 |
| GH04I182978 | chr4 | 183899271 | 183900370 |
| Enhancer Sequence | CTGGGATTAC AAGCGTGAGC CACCGCGCCT GGCCACTTTG TAACAATTTG AACTGGATGA 60
GAAGCCCCCT GGCCAGAACT CGGGGGAGGG TGCAAATCCG ATGTGCAGAC TCCACAAGCA 120
GGGGAAGAAC CAAAGCCCTT TTCTTTCACA GCTGGGAGGC AGGTAACCTG GGGCAAGTTC 180
TCAAGCCCTG CTCGCCCACT ACCTGGAAAC AGACTCGGGG CTGTTAGGGG GCCATAGTGG 240
AAGTGAGACT GACCCTTTGG ATTGCGTGGG AGCTGGGTGA GGCCTGTGAC TGCCAGCTGT 300
CCTCCACTTC CCTAACATCC TGCATGACTC AGTAGAGGCA GCCATAATCC TCCTAGGTAC 360
ACAACTCCAT TGACCTGGGA TCACCTGGGA ACCTCACCGC CAACCCCCAC AGCAGCTGCA 420
GCAAGACCCA CCCAGTGAGA GTCTGAGCTC AGACCCACCT AGCCCTGGCC CCACCTGATG 480
GGCCTTCCCT ACCCACCCTG GTAGCTGAAG ACAAAGGGCA TACACTGGGC ATATACTCTT 540
GGGAGTTCTA GGGCCCCGCC CACCACCGGC TTCTCACCAT ACTACCACAG CTGATGCTCT 600
CTGGAAAGCC CCACCTCCCG GCAGGAGGCC AACCAGCACA AAAATAGAGC ATTAAACCAC 660
CAAAGCTAAG AACCCTCACA CAGTCCATTT CACCCTCCTA CAACCTCCAC CAGAACAGCT 720
GCCGGTATTC ACAGCTGAGA GACTCATAGA TTATTCACAT CACAGGACTC TCTTGCTGGG 780
GGGCTAGACC CAGAAGAGAG ATAACAATCA CTACAGCTTG GCTCACAGGA AGCCACATCC 840
ATAGGAAAAG CCAGGGAGTA CTACATCAAG GAAAATCCCT GTGGGACAAA AGAATCTGAA 900
CAACAGCCTT CAGCCCTAGA CCTTCCCTCT GACAGAGCCT ACCCAAATGA GAAGGAACCA 960
GAAGACCAAC TCTGGTAATA TGACAAAACA AGGCTCTTTA ATACCCCCGA AAAAATCACA 1020
CTAGTTCACC AGCAATGGAT CCAAACCAAG AAGAAATCCC TGATTTACCT GAAAAAGAAT 1080
TCAGTAGGTT AGTTATTCAG CTAATCAGGG AGGCACCAGA GAAAGGCAAA GCAAGAAAAT 1140
CCAAAAAATG 1150
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