Tag | Content |
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EnhancerAtlas ID | HS050-68664 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:71384550-71385700 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr9:71385349-71385370 | TAAGGATGAAGGAGAGAAGGA | + | 6.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 71385386 | 71385535 | chr9 | 71384790 | 71385332 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I068769 | chr9 | 71384550 | 71385321 |
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Enhancer Sequence | ATTTTGCCCT TAGTTCTATG CCCTCAATAC ACTCTAGGCT TTTGGTCCCA TTTGTCTTTC 60 CTTTTTTGTA TCATCGGTAT TTTTCTTACC TCTAGTTATT TCTGGGGAAA GAATGAATGT 120 TTAAGGAAAT TCTGTCCTCA AGAACACTTC CGTGGCCTGT CAAGGTGGCA TGACATTGCT 180 TGCTTTCCTC TCGTTCTTCA TGAAAATGCC TAGCAGGGTA CCTGGCACCC AGTTGGAACT 240 TGAAAAATAC TTTTTCAATT TGAATTAGCC AAATTCTGGA AAACGTAGCC TATCTCACTG 300 CCTCCAGTTT CTTACCACCT GCCTACGGTG TGGCTCCTCT CATCTGGGTT TTCCACGCCT 360 TCTCTCCTAG GCCTCTACTA GAGCTCTCTC CAGATCACCA GTTCCTGCCC TGAAAAATCA 420 ACAGTCCTTA TTTCTTCAGC ATTTCTCACA AGTGACCTCT GTCCTTCTTT ATGCAACAAG 480 CAGCACTCAT GGAATAGAAA GGTCTTCGCT GGCTTCTGAA TGAAAATTCA AGAACCTTTC 540 TTTCTGCTCA CTCTTAGGCA ATAAAATGTC CCGCTACCAT GTCAAATCAC TGTTTCAAGC 600 TGGTATCCCA AGTGTCCAGT GCTATGTAAT TAGCTAAGCC TCCGACTTCA TTATACCTAC 660 TCCTCTCCCT CAGGAAGGGG AGTGGCAAGT TTAAAATCTC AGCTCCTAAG GAGGGGCATG 720 ATTCTCTTCC TCTCTTTTCC TGCCTTTTGC CACCAGTCCT CCTGCACCTT GCTGGGGGTC 780 TGACTTCTCA GGGTAAAAAT AAGGATGAAG GAGAGAAGGA TCTAGAATAA TTTGAGTATT 840 GACTTGGTTG TCTGGAGAGA TTGTTGTGCA GTTCATGCTC AAAAGAAGTG GACTGGTACC 900 AGTCTGCGGC CTGTAAGGAA CCAGGCCACA CAGCACGAGG TGAGCAGCAG GCCAGTGAGT 960 CTTACTGCCT GAGCCCCGCC TCCTGTTGGA TCAGTGGCAG CATTAGATTC TCATAGAAGC 1020 GCAAACCCTA CTGTGAACTG TGCATGTGAG GGATCTAGGT TGCTCACTCC ACATGAGAAG 1080 CTAATGCCTA ATGATCTGAA GTAGAAGATC CCCCTTCCAC TGCCCACCCC ATCCCATGGG 1140 AAAATGGTCT 1150
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