Tag | Content |
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EnhancerAtlas ID | HS048-15351 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr17:9109420-9111170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr17:9109582-9109593 | TAATCTAATTA | + | 6.32 | PROP1 | MA0715.1 | chr17:9109582-9109593 | TAATCTAATTA | + | 6.14 | Phox2b | MA0681.1 | chr17:9109582-9109593 | TAATCTAATTA | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26708 | chr17:9108846-9110585 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I009205 | chr17 | 9109283 | 9110970 |
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Enhancer Sequence | ATTTCCTCAG CAGAGTTGAC ACTGGCTGGG GAGGACTGGG ACTGAGCAGC TGAGGGTCAA 60 GAGAAAATTC TGGATGTCCA GGAGCTGGTT CAGCCAGCTG AGGTCTCCTG CCTCCAGTCA 120 GGAGGGCTTT TTGCAGTCCC AAATGCTCTG GGCAAGAGGC TTTAATCTAA TTACATGCTT 180 TATTTGAGCC AATTTGTTTT CCAATCCATC TTGTTCAGCA AAAAGAAAGA GCCTGCTGGG 240 GACTCATTTG CACCCTCTTG TTCCAAGTGG AGAAGAGGGG TTGAGCTCCC ATCTCACATG 300 GTCAGTGCAG CCCCCAACCT CTCCCAGCCC GGCCACCCCA CCCCTGAGCC AGGCTGCAGA 360 CTGCCCTGCC CTCGGGGGGA GGGGGCTGGG GCGGCTCAGG TAGAAAAAGC CTGGCAGGCT 420 TGCCCCCTCC CAGAAGTCCA CCCCAGCGTG CCTCTCCGTG CCTTCCCTTT GGGGGTCCCG 480 GTGCACTAGG CAGGAATGAC ACGGGATGGG CTTCCAGGCC AGGCAGCCTG GGAGGGGATT 540 TCATCCTCAG GAGGTCACCC AGCCTCGGAA CCTTCCTGGC TCCTCCTGTG AGAGCTGCCC 600 TCAGAATCCA ATGCCCCATA TTTTTAAATC TGCAAATATA TTTTCATCAT AAGGCAGTGG 660 ATTTAGGATC TGTGTTATTA AAGTCCAAAC AAAACACCAA AGCCCTTCAA ACCTCCCTGG 720 AGAGGGAAGA TTTATCGGCT CCTGCTCTCC TCCCCAGGCA CGGAGCCACA CTCTCCAAGC 780 TTCGCTTTTT AAGTTTTGCA GCATTTTCCA AAATTGCCTT TTTCTGCCCT TCCGATTCCT 840 GCTTGGAGCC TTTACTTTTC GGCTGTTTAC AGAGACTCGA GCCTGGTGAC TTCCACCTTT 900 GGAGTATGGG AGTGCCGGAA TTGCTCGGCT GAGGGTCACT TTGTCTGCCG CACAGTGGTG 960 GCAGCTGCGC CCGTTTTTAT TGAACTTGCT CAACAAATAT TTATTGAGGG CTTGTTATGT 1020 GTCCCGGGCC CTGGGGATAC AGCAGTGAAG ACTTCACTTT GGGGAGGAAG AGATACAATA 1080 AACAAACCAA ACTGAAAAAT GTATCACTGC ACAGGGTGAC AAGTGCCGTG AAGGAACCAC 1140 ATCCGCTACA GATGGAGTTG CTTTTCAGAA CAGCCAGAGG TCAGCCATTA TTCAGTGAAT 1200 CAAGGACATA CTTGAGTGAG AAATATCTTT GGGTTTAAAA TAATTGGATG TGCCAGTAAT 1260 ACAATAAAAT TGCTTTTCTG CCATGGCTCC TAAACTAGAG TAAAGATAAT GAGAGCCAAC 1320 ATTTTTTAGT GCCTGTCATG TCGGGCTTCA TCTCGCTGGA ACTTTAAAAG ATTGTTACAA 1380 ACGCTCACCC CCGCTTAATA AATGAGGAAT CGGAGGTTCA GAGAAGTGCA GCAATGTGTC 1440 CAAGGACACA CAGCTTTGTA AGTCACAGAG CCAGCATTTT GAGTTCCTTG GTCGCCTGTC 1500 TGCCACCCCC TCTGTCCTGC TAGATCCTTT CCACTTCCCA GCATCCTGCA GCCCTGAAGC 1560 TCATCAGTAG TCTGAGACCA TTGCCACTGG AGCCGCGGAT TGTATCCTGG GGTCCAGGAA 1620 GAGATGTTCT TGTCCAACTA ACACCCCACA CCCCATAGAC AGCAGGCTGA GGCCTGCAGA 1680 AAAGCCTTCT GATTCAGAGC TCAAGGGTCC CATTTTTCAG ATATTAGCTG TACATCTGTT 1740 AAAGGTGGCA 1750
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