Tag | Content |
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EnhancerAtlas ID | HS051-19858 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:107628970-107630510 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr3:107629804-107629821 | CCCACCCCCGCCCCCTT | + | 6.48 | SRF | MA0083.3 | chr3:107629431-107629447 | TGACCTTATTTGGAAA | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 107629437 | 107629889 | chr3 | 107629410 | 107629800 | chr3 | 107629800 | 107630400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I107910 | chr3 | 107629841 | 107630154 |
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Enhancer Sequence | AGGTGCCTGG AATTTCCCTT GGAGAAGCTC AAGATTTTCC TCTATTTTTC TGCTTAGGGA 60 GACCACAAGC CTCTTAGAGA GGGGTCCCTG CTCCAACTCA GCAATAGAGC AAATCTCCTA 120 TTTTCTTCCT GAAGGCTGTG ATTCTCAGGC TGGCTAGAAA ATGCAGATTC TGAGGTTGCA 180 GCTCTTCTGC CTATCCCACT CCCCAGGAAT CTAGCTGTGA AGAAGATCCC ACAGAGGATT 240 GTAATGTTGG GTGTTGCAGG GGAAAAACTG ACTGAAGGTT AAAGGTAAAA AACCCTAAGG 300 ATATTACTGC AAAAAAGAGT GGTCGTGCCG GGCTTGCGGG GAGACCTGAG GAAGTTAGAC 360 CTCCGGAGTC CACCGCCCCC CTTTCACTAC CTGTTATGGG TTTAAATTGT GTCCTCCCCC 420 AGAAGATAGG CTGAACTCTT AACTTCTAGA ACTTCTCAAT ATGACCTTAT TTGGAAACAG 480 GGTCTTTGCA GACATAATCA AGTCTAGATG AGGTCACACA GGAGTAGAGT GAGCCCTGAT 540 CCAGTATGAC TGGTGTTCTT ATAAGAAGAG AAGAGGCAAG TAGAGGGAAG GCAATGTGAA 600 GACACACAGG GAGAGTGCCA TGTGATGTCA CAGGCAGCAT GGAGTGCTGC ACACAAATGA 660 CAGAAGGAAG GGTTTTCCCC TACAGGTTTC AGATGAGCAC GGCCCTGCCA ACACCTGGAT 720 TTCAGTCTTT CAGCCTCCAG AGCTGTGAGG CAATACATTT CTGCTGTTTT AAGCCATCTA 780 GGTTGTGGTA CTTTGTTGTG GTGGCCCTAG CAAAATAATA TACTCTCTCT AAGTCCCACC 840 CCCGCCCCCT TCCTCCCAGG TTGTAGGATG CAGGCAGCTG CCTCTCCCAC ACCTACTAAT 900 GCCAGCCTTG TTGGGGTGAG CACTACAGAT TGTCTTCTTG GCTTCCTCAT GCCTCAGTCC 960 CCGGTCTGGC CTCCTGAGGG TCATGGAGTC CACGGGCTTC TGTTCCTTCT TGATCTTTCA 1020 GAGAAAGATG AACAGGATGT GGACTTATTA GGGCACTTTC AGGATGAAAC CAAAGGCCCA 1080 CTGGCTGTGA GGGGAACTGG AAGAGAAACC AAGTGAAGCT CCCACTTCAA TCCTAAATTG 1140 TCTGTTTCTC TGGAGCTAGA GAAAATGAAC TTTTTGAGTA AAAGCAGGAC CCAGCCATGC 1200 TGTTGCATGT CTAGGAATTC CCTGTGGTTC TGAGCTTTCA TTGCATTTGT TCCAGGGGTG 1260 TCTGCAATTT GTCACAGAGG TCCCTGACTT TCTAGGCAGA GGGAGAAAAG GAAAGCGAGT 1320 GGGGTGGTGA CTGTGGAAGT GCTCTCTAAA CATCTCCAGG GCCATGCAAA CTGTCAACAT 1380 TAAGGGAGGT GAGGTGGTGA CCATAGTGGT TATTCCAGAA TGCCTGTGGT CTGTCTCCTC 1440 TCACCTCACC CTCTGACACT CTTACTCTTG GAGTAGGTAG CTGTGTAGTG TCCTGGCAAT 1500 AAGAATAACA GTCATGAAAA CTGTCATTTA TCAAATGCCA 1540
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