| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01348 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:53641520-53643070 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr1:53641647-53641657 | GGAAATCCCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 53642214 | 53642895 | | chr1 | 53641812 | 53642484 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I053175 | chr1 | 53641509 | 53643375 |
| Enhancer Sequence | GAGCAAAGTG TTATCCTTGA CTTCTTCCTC CAGCTTCCGT CCCCATCAAT CTGTGTAGTG 60
GCCAACCCTT CCCACTTCCC ACATTTACTC TCTCTCTTAC TGCTACTCCT TAATCCGAGC 120
CATCCATGGA AATCCCCAGC CAATAGCATG GGACAGTTGA CGGTCTAACT CTCAGCATTC 180
ATCCCTCTCG TTCCCAGCAT TTGCTCTATG CATCAGGCAT GCAAACCCTT CCCCACTACT 240
TGTAGAGCCC ATGCTCCTTT ATACCTCTTG TATTTCATTC ACCAAAAATC TCTAATAAGG 300
GCTGACTGTG TACAACCCTG TGCTAAGGGC GGAACACGCA GTCCCAGGTT TCAAAGAGCT 360
CAGAATCTAA GGGAAAGAGA GGCTTGGAAA CGGATTAAGT GCAACCACGT CCTGGCCACA 420
GAGGGGAGGA AAGAAGCCCT GGTGAAGGCT CTTTGCAGAG GGAGGGAACG TCTTTATTTT 480
ATGCATGTTC TTCCCTTTGC TACCTTGTGC CTCTTCACCA GGAAACATCT CATCCTGCAG 540
CTGAATACCG TCTCCCTACT CAGTGGTATC TACTGCCACC TCCATGCTCT GTCCAGAGCT 600
AGTTCATTGT TCCCTTCCCA GTGCTCCTTC ATATTTTCTA TTTACTACTT TCTTCCTTTA 660
TTACATCAAG TAATACTACC AAATACTGCT CCTCTAGCAT TTGCCCTGTG CTGCGCATGT 720
GCTCGCCCTG CAACCACCTT TGGGGCAGGT ACTATCGTAT CATATCGTAT CATCATTGGC 780
TCAGGGTATA AGTATCTTGC TTAGTAACTC ATGGCTCGTG AAATTAGTCA TTTCATAATC 840
TCAAGTTGCT GAGCACTTGT CTGGCGCAGA GTAGAGAGCA AATATTTGTC TAATGGAAGT 900
GTGTTTGTGA AAATGCTGGG CTGTGTAAAC TAAACAGAAC GGAATAAAAT CAGCTAGAGG 960
GGTTTGCCAG GGAAGACTTC AAAAGCAGAG GGCATTTGTT TCTCTCTTGC CACCACTAAT 1020
GTTTCTCAGT GTCTGGGGCG AGAGCCAGGA GAGAGAAGCC AGGTAGTCCC ATCGTTGGAA 1080
AAGGCCACAG CGCCTTGCTG CCACCCACTG ACAGCAGCAT GGAGCTCTGC AGTTCCAGGA 1140
CTGCCTGTGC AGGGGGCCAT CCCTGGTACC ATGCCCCTCT CCCTTCTGTG TGCCAGCTGG 1200
GCTGTCTCCC TTTCCTGGCC AGGGCTGTCC CTGCTGAATG CCAAACATCT GCAGACAGGG 1260
TTTGCAAACA GCTGGCTCAA AGTTCTGAGC TTTTGTGATC TCATCCAAGT GCCTGGCTAT 1320
GGGGAACAGG CTTATTTTCC TGGGCTACCA GCACTGGAGT GGTGGAAATT ACATTAGACT 1380
TGGATTCAGA GGCCTGCATT TGATTCTGAG CCCTGCCACT TTACAGCTAA ATAAATGATA 1440
CTGAACCTCT GTTTCCTTCG CTGTAAAATG GAAATGATGA TCATTCCTAC CTCATAGGGT 1500
TGTTAGGGGA GTAAGACAAT AGACATGGGG CATGCTTGTA ACTGTGTTCT 1550
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