| Tag | Content |
|---|
EnhancerAtlas ID | HS098-16411 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr13:99022710-99024140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr13:99023455-99023472 | CTCACCCCCGCCCCCCG | + | 6.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 99023200 | 99023340 | | chr13 | 99023583 | 99023757 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH13I098369 | chr13 | 99022190 | 99026230 |
| Enhancer Sequence | AGGCAAGTAG TTGTGTTTGG AACAGGTACC GGAAGCAGGG TCCCTCTGTC TTGGTGATGA 60
GGTGGTGGTG GACTTTGAGG GAGGGAGAGG GGGCACTTAG ATTTTTGGCT TGAGTGACTG 120
GGGGGGAGAT GGTGTTGGGG GTTACTAAAA TGAGAAAAGG ATGGAGGGAA GTGGAGGACT 180
GTTGGGGAGT GGAGAGTCAG GGTGTTTCTG GCCAGGTCAT GTTTGAGATA CCTGTTAGCT 240
GTCCCATGAC CACAGCAGCA GCAGGAAGGA CATCAGATAC AGGAATGTGC AGCTCCAGGG 300
AGACAGTGAC AAAGACTTCC CACTGCTTTG TGTTTTCTGA ACGTTTGTGC TGCTAATCAT 360
CCACGTCCAC TTAGAACCCT CAAATCAGCG AAGAAGGCAA AGGCAGCCAG GAATTGGCAG 420
AAAGCAGCAG CCTTCTGGGA GCTACCTGCA TAGGAGGGAC AGCCCGAGCT GCTAAGCCGG 480
GTCTGCACAG GACTGAGGGC TGGCTGATGA CAGGAGGGCC TTTCGCTGGG GCTGCTGGGT 540
CTTGGTTTCT CAGGCTGGTT TTCCTGTCGT TGGAAACTGC ATTGCCCTGA GCTCTGCGTG 600
CTGAAATAAA TCTAAGGGCA AGTCCAGCTG TTGGAGGAAT GTAGTTGTGT TTGGAATAAG 660
TAGCATCGGT AGCGTGCCTT TTCCTCATGT GAATCACCAG GGCTCTTTCT TGCTCAGGAA 720
GTTGGAGGCA CAAATCCTGT ATCCCCTCAC CCCCGCCCCC CGTTTTTTTT TTTTTTTTCA 780
TTAAAAATTC TGTTTTGCCA ATAGTTTTGC ACCTTTTCAA TTTTTGTGAA TCGTCTCTAG 840
AGGTTTGCAG TTGGCTACCA TTCTGGCCCT TGCTCTGAAA CTCCATACAG CTGGTTACCA 900
TCGAGCCGCA TGTGCCTGGT ACATTGCCAG CTCCTCTGTC AGTGCTGATA AATTCCTAAA 960
GTTACACGAG CTCAGCTGGA CGGAGCAGGT TTTTGTTGTT TTTGTTTTCT GGCACCCAGT 1020
GTGAACTGAC ATTTAAGAAG TCTTTTCCAA GGAGACAGTT CTTTTGGCTC ATTGTTGAAT 1080
AAAATTGATC TGAAATTCCT ACTTTTTTTT TTATCATCTC TCCATCACTC CCCACTTGGT 1140
ACAAGGCATA GAGAACCTCA TGGGGCCGAT GTGTTGGGAC TCTCGCATCT CAAATTCCTG 1200
TAGAAGCAAA AATGGACTGA CTATTGAGAT TTCAGGTGCT GTTCTTTGGC AGATGGTGAA 1260
TGAGGGGATG CTGGGAGAAG CTCCATGTCA GCTGTGCTTT GTGGGGAGGG ACGCATACAC 1320
AGAAGTGGGA CAGACGGAGA AACTGGCCTG TGGTTCAGCA AAGCATAAGT GACTCTAGCT 1380
CTGTAGTTAA TGCTTTGGGC CTCCAGGAAT AGCTCTTTCA GCTTCCCATT 1430
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