| Tag | Content |
|---|
EnhancerAtlas ID | HS182-12727 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:110395110-110396580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:110395948-110395969 | CGAAACTTTCATTTTCATGTT | + | 6 | | SOX10 | MA0442.2 | chr2:110396040-110396051 | TGCTTTGTTTT | - | 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 |
| GH02I109635 | chr2 | 110392906 | 110396752 |
|
Enhancer Sequence | GCTTTCTGCA GTGCATTGCG CCCCTGGTTT ATTGAGACTA GAGAATGGCG ATGACTTTTA 60
CCAAGTATAC TGCTTGTAAA CATTTTGTTA ACAAGGCACA TCCTGCACAG CCCTAGATCC 120
CTTAAACCTT GATTTCATAC AACACATGTT TTTGTGAGCT CCAGGTTGGG GCAAAGTGGC 180
TGGGGCAAAG CTACAAATTA ACAACATCTC AGCAAAGCAA TTGTTCAAAG TACAGGTCTT 240
TTTCAAAATG GAGTTTCTTA TGTCTTCCCT TTCTAGATAG ACACAGTATC AGTCTGATCT 300
CTCTTTCTTT TCCCTACAAG AGGCTGAGGC AGGAGAATCG CTTGAACCCG GGAGGCGGAG 360
GTTGCAGTGA GCTGAGATCA CACCACTGCA CTCCAGTCTG GGTGACAGAA CAAGACTCCA 420
TCTCAAAAAC CAACCAACAA ACAAAAAATA GTGTTGCGAC GATGCTAGTT TCCTTATTCT 480
GATCACTGTT CTGTGATTGT GTAAGAGGAT GTCCTTCCTG CGAGGAAATG CATGCTAACT 540
ATCTGGGCTA AAGAGCATCA TGACTGTACA TGACTGTACT TTCAAAATAC AAGAAAGAGA 600
TAGAGGAGGA TAAAGTAAAT GTGGCAAAAG GTTAACAGTT GGAAGCACGA TGAAAGATAA 660
CATGGGAGGT CTTTGTGCTC TTATTACAAC TTATATTTAA ACAGGCAAAA GAGTTAAGAG 720
TTAGGCTTTT CAAGGATTCC TAGCACTCAC TAGAAGCAAA ATGAGGCTCA TTTAAAGAAA 780
GGGGTAAACA CTACGTTTGC TCTCTGAAAA TAGTTTCAAA TGAGGCATAA CTACTCCCCG 840
AAACTTTCAT TTTCATGTTC CATCAGAGCA AGCTCAGGTT CCAAATTCCC CACCAGGTGT 900
GCATGTTATG TGTTTGGACT GGTGTGGGGT TGCTTTGTTT TTCCTGAAGG TGAGCTCCAA 960
AGTGGAGCTG AGCCATCTAC AAAAAGATAG CAGTGATCTA ATTGCTGGTC TCCTGCATGA 1020
CCTCTTCCCA TTGACTAGCT TAAAAATCAG TTAGATTTAG CTTTCAAGCA TGTGTCAATA 1080
AAATAAATTC CAGATTTCCC AGGTAATATA TTTCCAAAGA GTAGGTTTGC ACAGTAGTAC 1140
AAAAACAAAA ATTGTTTTTG AATGGAGTCT CAGTAATAGG GAGCCTGTTT TTCAATTCTC 1200
TTTTAGATTC TTTTAACGGC TCATTCATGG GGGCTTGATC TCAGCTGCAA AGACTGAAAA 1260
AAAGAAACAA CCCCACAGTT CTAAATGCCT AGGAAATTGC ATTGCTGAAG TGATTCTCTT 1320
GTAACACTCT CTGGTTCTTT TGCCAACCCC CTGAGATGAT GCTTCTTGGC ATACATAGAG 1380
ACTGGAGACT TTTCTCCTAC CTCCAGTAGA GGTCTGGCCT TGCTCCAAAA CAAAGCCTGC 1440
ACCCAGCAGA TGTTGCTGCT AAGAGACGTC 1470
|
