Tag | Content |
---|
EnhancerAtlas ID | HS116-32956 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr8:28635760-28637560 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBXT | MA0009.2 | chr8:28635993-28636009 | TAACGCCCAGGTGTGA | + | 6.01 |
| | 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 |
GH08I028774 | chr8 | 28632102 | 28637720 |
| Enhancer Sequence | ACGATGAAAT AAAAACCAAA ACCACCGTTT GGCAACCATT ACAGTTCATC ACTTATTCAG 60 ATGAAAATCA TCAACAAATG CTAAAAATAT CAGATACCAT TTTGAGGGAG AACAGAATAT 120 GTATATAGTT TCAAAGAGTC CCCCACAAGG TACTGATTTA ATACAATGGG AAAAACTGAC 180 TTCACAGTGG AGAGGCCTGG TACAGACCCG GGAACCTAGA ATCAGCTCTG AGTTAACGCC 240 CAGGTGTGAG ATGCACCCGG AAGACAAGCG CACGGCCCCG CCTCCAGGCC CGTGAATGGT 300 CTGTAGACTG AGACTGGGAT GCTCCCCAGC AGCCCCAGCC CCTCAGACCG GGAAGAGTCC 360 TCGCCCTCTG CTCAGCCTGT CTCCTGAGGG CTGCTGCAGC CTGCTTGGCA GGGAACATTC 420 CCCCAACTCG AGGGAGCTGC CTGCCTTGAG CCAAAAGACC TCGCTCGGTC CTAACTGATG 480 TGACACTTTG ATTCCCAGCA CAGTCTGTGC CCAGCGACGA GGGACCCTGG CTTAGGCACA 540 CCAGACACAG AGACGTCTCC ACTGTTGTCA GGACAAACTG GCAGAGCTGC CAGGTACATA 600 AATGCCCATT CCAGTGGATT GTGCTTCTCT GAGAATACTG ACCCCCTTTT CATGTATCCA 660 GGAGTCACAA AACAATAAAA AAAGATGGCC CCAACCTCTC CCAGACACAA CTTCTGCCCT 720 GGAAGCCCCA TAAACCAGTT TAAATGCAAA CCCATTACCC AGAGTTGTCA CAGGAAATCA 780 CACAGTCCTG ATTTCCTTTT AGCTGAAGAA ACATTTGTAC TAAAGGCCAG GTTATCTACT 840 GTGCTGTGTA GATGCTGTCA CCACTGTCAT GTCAAATGTC GAGTCACCAC TCAGCAGCAG 900 GAGCAGGAGA CACCAACCTC AGCCCCACTA CATAGGACAT TCTCTGGACA ACCTCCTAAT 960 TAATGAAATC TTGGCAGCTA TGAAGTTCTG GGTGTTGTCA ATCAATATCT TGTGGCCCAA 1020 CTTCCTCCAC CTTTAGCCCA AAGCAGGCCT GAGAAGAGGA AAGCAGTCCT GGTGACCGGG 1080 GCCTCTCCTG GCACTTTCTG CCTGGCCTGG TATCAGCAAG AGCCGGCCTG GCACCCACAG 1140 CAAAGCCATG TGTCCTCCTG CTGTGTGAAC GCAACTTCCT GGAACACCAA CACCTTGTCT 1200 GACAATGATG GATCCGGCCA AAGACAAGAC CCCTCTGTAA TCATCCTGAA CACGGAACAC 1260 AGAACTTTCC TGACCACAGC ATAAGCAAAC TTCCCGCTAT GCCGGCTCCA TTCTTCCTGT 1320 GTTCTAGATA AGAATGAGTT AAGAAACCCA TCGCAGAATG ACCCTGCATC CTGACGCCAC 1380 CCAATACAGG GTGACGCCTC ACCTCCGCGA ACACCTGCGC ATCACCGAAC ACCAGCCGGA 1440 GTCCTGCAAG GTCTTTTTGC TTTTCTTTTA CCCATGGTGT GTGTTCCCCT TGCTGAAATG 1500 AGGCAATAAA CCCAACTTGG TTTGACCACA GGCGTGTTCC TGGTGGCCTC TAGGTCACAA 1560 ATGAAAGCTG GGGGAAGGGC TGAAGCGTCA CCCCAGTGCT TCTGGTGTAA CTGGATTCCC 1620 AGCTCCTAAA GCTAGGAAGG GAGCTGGTGA CAGTGCTTTC CCAACAGCCG CCATGTGCCG 1680 GGTTCTGTGC CTGGTGCCCA GAGTGACCCA CAGAGGTAGC TACTGACAGT CCCATTTACT 1740 GTGGGGACAG TCATGCTTGC TGGTGAATTG GCTGAGGTTG CTGCAAGCTG GGCCAGATTT 1800
|
| |
|
|
|