| Tag | Content |
|---|
EnhancerAtlas ID | HS098-06489 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr10:29264180-29265570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr10:29265176-29265187 | TTCTGTGGTTT | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr10 | 29264721 | 29265324 | | chr10 | 29264901 | 29265000 | | chr10 | 29265000 | 29265201 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH10I028975 | chr10 | 29264534 | 29265583 |
| Enhancer Sequence | GCTTACCATT CTCACAGTCC CTTTCAGGAA GCTACTCCGT GAAACCCCCA TGGCTGTGAG 60
AAGTCTTTGA CTGGAGGACT CTCACATCAT ATGCTACCTT TGCCAGTCCC GCCCACACCT 120
GCGAATCAGC TGCCAGCACT GCACCTGTGA TTTCTAAATT GCCATCTCCT GATCTCTACG 180
TAACCTCCGG TTGCACATTT CCAGTTCCTT ACCGGATCTA CCCCACAAAG GTCCATATGT 240
TCCTCAACGT CTCCAAGACT TCATCTAATT GTCCTGCCTG CCACCCCCAT CTCTCCTTTA 300
GCACTTCTAT TTCTTATTTC CTAAGTCAAT TGATAGGATT GCAAGAAAGT TTGGGGTTAT 360
CTTGGAATAC TTCCCGACTC ACAACTCCTG CGCAGGTAAC CAGCCACGAA TTCCTATGAT 420
TCTACCCCTA AAACTTCTCT GAGATCTATA GCCTATTCTC TATCCCCACT GCCACTGCCT 480
GAGTTGGGCT TTTGCCATCT TTGGTAGAGA CTGTAGCATC AATATCCATA TCTAGTGCCT 540
GCCCTGAGCC ATTCCTGACT CTGCAATAAA GAGGAAGCCT TCTGACCAGT GAGACTAAGA 600
TCCACCATTG AAGAATGAGG AGGATATTTA CAGGACTTCC TTAAGCCAAT AAGCGTGATC 660
TTGCTATATT CCAAGAGCAT GCAGCTCATT TGAGAATGCT TCTCATGTAA ATGTCCGTTG 720
AGAGAAATGC AAACACAGCC CATTCACTGA TTTGCCCTTT GTGTTGTCTT TTCTAACTCC 780
TTTTCCCTTA TGCGTGGGTG GAGTGCTAAC AGCTGTACCA GGGAACAACT AATCCCATGG 840
GCAACCCGCC GCCAGGGTCC ATCATTCACA GAAGACAATC TACTGTTTCT CATTGTGCTC 900
CATGATTCAC CCACTGCAAG AGAAAACTAA CACACAGAGT GATTGTTCCA TCTCCCGTGG 960
AGAGGGTCCT TATTATGACA GAGAAGTTAT TTTCTTTTCT GTGGTTTCTT AAGGGTTCTC 1020
TAATTGGGTA ACCCCCTGCT GACCCCCGGC TATGGCAGTT TCTATATTGA TATCTTTGTT 1080
CCACTGCTTG CACACTGAAG CCAGGAACGA GTAATTCAAA CCAACAGAGA GCATAAGATA 1140
ATGGGGCTTT TATAAACTAC TAGTGTTTAA AAGGCAATGA CCCTTTAAGT TCACTGGAGT 1200
TCTCTTCCAT TAAGAATTTT TCTCACCTGT ACACAACAGA TGGGGGATGC ATTACAGCCC 1260
TGTGTCTGCT CCGGACGGGA GCTGAGCTCA TCTGCTAGAC TTCATGGACT TGAACCTGGA 1320
CTGCTTTGGA GTTCATTCAT GTTCTACCCA CACTTGGATA ACAGCTCAGA ATAAGCACAG 1380
AAGCTTTCCA 1390
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