| Tag | Content |
|---|
EnhancerAtlas ID | HS136-00697 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr1:87311250-87312640 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr1:87311584-87311594 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:87311584-87311594 | GGCACGTGCC | - | 6.02 |
| | | 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 |
| GH01I086845 | chr1 | 87311521 | 87312578 |
| Enhancer Sequence | TGACACTTGA CAGGAGGAGG GACAATGACA TTAACCCTGG GACAACTGCA GCATTCCGGG 60
GGTAGGTACA GGAGTAAGAA GTAATCAGTG AAGAAAGATA GAAGGTCACT AGGAAAAAAA 120
TGCTGTTTTG GAAACAAAAG GTCTTTCAAT ACAGAGGTGA TATTGGTACA GAAACTTCAA 180
ATAGAGGCCA GGCACAGTGG CTCATTCCTG TAATCCCAGC ACTTCAGGAG GCTGAGGTGG 240
GTGGATCACC TGAGGTCAGG AGGTTGAGGC CAGCCTGGCC AACATGGTGA AGCCCCATCT 300
CTACTAAAAA TACAAAAAAT TAGCCGGGTG TGGTGGCACG TGCCTGTAAT CCCAGCTACT 360
CGGGAGGCTG AGGCAGGAAA ATCGCTTCAA TCTGGGAGGT GGAGGTTGCG GTGAGCCGAG 420
ATCACGTCAT TGCACTCCAT CCTGGGCAAC AAGAGCGAGA CTCCGTCTTA AATGAAAACA 480
AAACAAAACA AAAAACAACA ACAACTAAAA GAAAGTTCAA ATAGAATAAG AACAAAGCGT 540
TGGCAATTAG GAGATTACTG GTAGTGAAGG AAAGTTTCAG TGGTACAGTT GGGACAAAAA 600
CCAGATTGAA ATCATGTTAA GCAATGTGAG AGGTTCAAAT ACGACTAATA ACTAGTGTAA 660
CTTTGACTAT AAAGTCATGA TTCAGACTTG GAATCCAGCC CTCCCACTGA TATGTAGCAA 720
TCATCACCAA GCTAATGCAT TTCCAGAAAA AATAAACTTT CAGTGATGAA TCTTAGCTAC 780
ATTATCATAC TGACTCAGGT TGATAGAAGG ATCTTAATGG GGTCACTGGG GAATATAAAT 840
GAGATGCCAA GTAGAAAACA TGTTAATTTC TTGGCACAAG GAAGCCCGAG GTGTTCTGGA 900
AGCCACTAAT GCATTTTACA TGATTGCTTA ATTTCAGGAA ATCCTGACTC ACTGCCTCTA 960
TAGGGTAAGA AGCAAAGGCT GGTCTCAATT TACAATCCTA CAAACCAGCT TTGAGTAGAG 1020
CTTAGATTAT TCCTGGCATC AATATGTCTG CTCAGTGCCT ATTTTAATTT GAAAATGTTT 1080
TGGTATATGT ATATTCTATT TTCTTTGAGA AAAAGCAGGC TTCATTTGGA ATGTTCTGAA 1140
AACCATTGTG ACTAAATAGG TAAGGTAACA CCTCCTCACT TAACTTTTGA ATGGACATGG 1200
AGTGGCGTCA TCATATCTAC AGTCAGACCA CTGAGCCATT GAAAAATGGT CCAGGTGAAG 1260
CTTGAATAAA GAAAAATAAG ACGAAAGTTA GAACTAGCTT GCTAGCATTG GGTAATGAAA 1320
GAAGCAGAAT GATACTCATA ATGTCACTGA AAATGCACCC ATTTTATTAT TTAATGTTCC 1380
TGATAATGCG 1390
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