| Tag | Content |
|---|
EnhancerAtlas ID | HS080-03097 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:216945190-216946180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:216946036-216946048 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:216946040-216946052 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:216946044-216946056 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:216946048-216946060 | GTTTGTTTGTTT | + | 6.32 | | PRDM1 | MA0508.2 | chr1:216945229-216945239 | GTGAAAGTGA | - | 6.02 | | Sox6 | MA0515.1 | chr1:216946011-216946021 | AAAACAATGG | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGAGGTAAA AATTTAAATA TCAAACCCCA AAGTGTGTGG TGAAAGTGAC ACTGCTGTAG 60
TATATTATTC AGGGGCCTGA GTTCTGATCC TAGCTGTCTA TGACCTGAGG TGAACATTTA 120
ACTTCTCATA GCCTCTGAGA CAATCTGTTT ATGAAGAGGA GATGGCATCA GCATAAACTG 180
ATGGGAGTTC TATAAAGGGG GCAGCTTCAC ACACTCAAAT ACCTACAGGA TCCAGACAGG 240
TACCCGACAG ATTTAAGCAA TACAGAGTAG AGGGATCCAT GGTGAGCTGA AGAATGGAGG 300
CCCCATCTAA ATGCATTCAC ATTCAGATCT AACAAAACCA CAGCTACACG TTGTTCACAC 360
CAATAGTAAA AGAAACAAGC GAAGCATACC TGCAGTCCTC ATACAGCTGG CTGCAAAATC 420
TGCATGGACT GTGAATTTCC AGTCCTAAAA CGGTGGATCT ATGATGCTGA GCTCCCAAAA 480
GAACTCTGCT CTCTCTTTCT CTACTCTAAC ATCCCAGAAT TCAGCAGCTC GGGTAGAAGC 540
TGCACATGAC AAGTTTGGGA AGATTCCTCA ATTCCACAGC CTTTTAAAAA CTTCTAGATG 600
TATATCACTC TACCTTTAAC CAATAGCTAG AGCACAATGT GAGAAAAACA ATTGTGACAC 660
TAACATATGA ACACTGATGT ACCTAAGCTG CTTCTCTAAC ATAAGTTTTC AAGCTGTCAA 720
AACATATTCT TTGTCATTCC TCAATACATG AGAACAGCAT CATTAGCTTG AAAGGTGTAT 780
GTTATTTACC AGTGACCTAC TTCAGAGAGA GTTAATCTTA GAAAACAATG GCATAGTGAG 840
TTTTTTGTTT GTTTGTTTGT TTGTTTGTTT TTCACTTAAC AACCCATTCT GGCTTTGGAA 900
CTAGATTCCC AAATAGCTTA GTGGATCTGA CCCACTGTCA GATTACCCAA AGAGAGGCTA 960
AGAAATGTAC TTGGGCAGCT GCAAGTCAGG 990
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