| Tag | Content |
|---|
EnhancerAtlas ID | HS051-26805 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr8:134628430-134629860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr8:134629471-134629486 | TGAACTCCTGACCTT | - | 6.04 |
| | | 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 |
| GH08I133616 | chr8 | 134628394 | 134630530 |
| Enhancer Sequence | TGTACTTTAT ATGTATTGAA TCAGGTAGAC TCTTGTGTTG GCTTCTTTTG CCACACATTA 60
TGTTTGTGAG GTTTCTTCAT AAACCTGATG TGTGTAGTTG CTGGGCTGTG TCCTCAGTGC 120
TCTGTAATAT TCCATGATGT GAAGGGTCCA CAATTGATCC ATTTGTCCAG TCTACAGTGA 180
ATGGGCATTT GGGTATTTCC ACCAGAAGCT GTGTTGGTAT GAGTACCTTA GTGCATGTCT 240
TGGATAAACA TAGCTAGGAG CAGAATTGCT GGTCAAAGTT TATGTGTGTA TTCGACCTTT 300
GTAGGTACTG CCAAACAGTT GCATAAAGGG GTTATGGTTT CCATCTTCAG TGACTAGCAG 360
ATCCATCTGT TTCATACCTC CCTGAGACTA GGTAACTTTG TAGTTTATAT TTAAATCATT 420
CTGGAGGGTG CAGCAAGCTT TTTTGAGCTT AGCACAGACA CCCTTATTGG ACTGGAAACC 480
ACAAGTTCAC AGGCCATTGC AGACCAGAAA CCAGAGATGT GAGGCAGGAA GCAGAGGCAG 540
GAAGAGGGCA CCTGACAGCT ATAGACCCTG AGGCCAGATA AAGCATTATG ATTTCCACTT 600
TACAGATGAA GAAAGAGAGG CCTAGAGAGC TGGAGTGACA TGCCCAAGGC CACAGTATTG 660
CTAGGAGACA GGATCTGGAT TAGACTATAT TTTTACCAGA AGTAAAGCCC CAGTCATACC 720
TCACTGAACA CTCACCTGCC TCTTTGACTT CTGGTGCACA CTCTGCTTCC TGCTCCTTCT 780
GAACTCCTCT GCCTGTTTTG AAGATCTAGG CTCCTGGTTT TTTTTTTTTT TTTTTTTTTT 840
GAGACAACGT CTCACTCTGT CACCCAGGCT GGAGTGCAGT GGCTCGATCT CAGCTCACTG 900
CCACCTCTGC TGCCCTGGTT TAAGCGATTC TCCTGCCTCA GGCTCCCAAG TAGCTGGGAT 960
TACAGGCTCC TGCCACCGTG CCTGGTTAAT TTTTGTATTT TTAGTAGAGA CAGGGTTTCA 1020
CCATCTTGGC CAGGCTGCTC TTGAACTCCT GACCTTGTGA TCCACCCACC TCAGCCTCCC 1080
AAAGTGCCGG GATTACAGGC GTGAGCCACC ACGCCTGGCT GCTCCTGGCC TCTTTGTACA 1140
AAAAAAATAA AAAAATAAAA AAATAAAAAT CAGTGACAGC AAGTAGGTAA AATGTGGTTG 1200
TCTATTTTAT TCCTACACTG ATTTACATGT GAGAAGACTG AGGCTCAAAG AGGTGAAGTG 1260
ATTTGCTTAT GTTAATGTAG CTAGTGGGTG GCCAAGCAGA CTCCAGGCCT ATTGAGCTCC 1320
CTGCCACCTT GCCTGTTTAC CTCAGTGGCT TCCAGGGCAG TTCTGAGAAA AGCAGAAAGC 1380
AGATTTCTGT TTTATTTTCT TGGCATGAAT TAATGTTTGT CTTGAGCCAT 1430
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