| Tag | Content |
|---|
EnhancerAtlas ID | HS048-31147 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr6:13914060-13915490 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr6:13915207-13915220 | ATATGCAAATGCC | - | 6.3 | | RREB1 | MA0073.1 | chr6:13914952-13914972 | ACCCCAAACAACCAACTACC | + | 6.37 | | RREB1 | MA0073.1 | chr6:13914953-13914973 | CCCCAAACAACCAACTACCA | + | 6.67 | | RREB1 | MA0073.1 | chr6:13914936-13914956 | CCCCAAAACAAACAAAACCC | + | 6.8 | | STAT1 | MA0137.3 | chr6:13914100-13914111 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr6:13914100-13914111 | TTTCTGGGAAA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGACCCCAA TCAATCTATT GAGACTTCAG CCACCGAGGG TTTCTGGGAA AAATGTTGCT 60
CCCTGATTAA AGGGAGAAGG ATGATGAGAA ATGCATTTTG TCACTTTCCA TTTCCTCCTG 120
TTTGGATGTA TTTGTGTGAA GACATGAAGT TCGCAGCCAT GCCAGCCATT TTGTGCTTGT 180
AAGGGAAGCT CCTGCCAGCC AACTGGGAAA ACAGAGCAGA GATCACAAGA GCCCAGCCTT 240
TGCTGACACC ATGAGCTGCT GGAATCGCCT ACCTCTGGAT GTCTTGCTTT GTGAAATAAA 300
CACCTATCAT TTGGACTGAT TTTATTCAGT GATTTCCCTC CTCATAGTTA AAAGCATCCT 360
ACCTGACAGG AGAACTTTAA TAATTTAACA TTTGCTGCCA CAAGCGTGAA AACAACCAGT 420
GCATCCATTT GAGGTGTAAG CAGTGAGTTT GTCCCCATGT CCCCTGAGGT GAGTTGGCTT 480
TCTGCTCCCC AGGACTATAA TCATCTTAGT CATCTGATTT TGTGCACATG CATTACAGTT 540
TTACAAATAA AGTCCCTGAA GAGAGAAACA AAACCAAATT AAAAGTTTGC TTAAGCAAAT 600
TGATCCTGTA AAATCCTTTT GGAGTAAAAG CTGATGAAAT AAATGTGTCT CCAGTACTAG 660
GGTGCTCAGG GCTGTTAAAC AGGGCAAAAG TCCAAGAAAG GAAAAAGACC TTCCCACAAA 720
AGAAGCACAG ATGAGTAATT AGGGACTAGG GAAAGGAAGC TCAGACTGCA ATTCCAAAGC 780
TGTGCTTTTG TGCCAATAAG AGTGCTTTCG GAGCAATGAG GCAAGTTAAT TTCCAGGCCA 840
CATTTTACAA ACTGGCACCT CTTCAGTTTG CCGTAACCCC AAAACAAACA AAACCCCAAA 900
CAACCAACTA CCACTTCCCA CACAAAATAG AAAGACAAAA CAAACCTTTG ATGTGCACTT 960
TCACTCGTCA GCTAAACATA ATGCCACAGC AGTGTCCCGG ATGGAAGTTA CACCTGGGGT 1020
GGGAATTCTA TGTCAAACGA AATACTTAAC TCGTTAATTC AACAAACTAA CTGCCAAGGG 1080
AGGGCAAGAC ACCACGCTAG GGGCTACATG GGATTCAAAG ATAAGGCACC AAACTTTTGT 1140
TTTTGACATA TGCAAATGCC ACTCGAGCAC AAAATGTAAG GTTGTAAGCT CTGCAAGAAA 1200
GATACAAGGT TATATGCTAT AGAAGATGAT AGATGAGAGA GATTCCATCC CACTCAAAGA 1260
ATGAGAGATT GTTTCCTGGC AGTGTGGGCA TTTGAAGTGA GCATTGAAGG GTGGGTAGTA 1320
TTTGAACCTG GGAGAGTGGG AGAAAAAGGA CACTCCAAAG CTGAATGAAC ACGTTGTTAC 1380
AGAAGAATAC TGTATCTTAG TTTAGCCAGG GCATGAAGAC AATGTAATGG 1430
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