Tag | Content |
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EnhancerAtlas ID | HS050-41693 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr20:31693050-31694320 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr20:31694172-31694193 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 |
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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: 2 | ID | Chromosome | Start | End |
GH20I033105 | chr20 | 31693101 | 31693785 | GH20I033106 | chr20 | 31694001 | 31694150 |
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Enhancer Sequence | GTTTTCCCAT ATGATTGAGA TCTTTCCTGA CTCATATTTA AACATGTATT TATTTTTAAT 60 GATACAGGAA CTACAGGAAT ACATTCTTAT TGTGAAAAGT TCCATTGGCG CAGATACAGC 120 TAAAGTTGCT CTTATCGACA TCCCCAGCCT CCTTCCTAGC CCAGAATCTG CCCCCCTAGG 180 GAACCACATC AAGTTAGGAG GTTTTCTTGC CCAACTTTAT AAACAGAGTA GACTGAGCTT 240 GCTTTGCTCT CTGGGGCGTC TCAGGAATGT TACTGGGAAG GCTGCTTGTT GAACTATGGG 300 GGTCATTGGC TACTCACATA CTGGGACTGG GAAACTGCCC AAGCCCTGGG GTCACTGGGC 360 CCCAGACTCT CTCCCACTCC TGCTTCCTGG ATGAGAAGAC AAGGAGGGCT GGCACATCCC 420 AGCCAATGTC ATCAGCTACA CCAGCGGGGG TTCTGTTGGA GCCATCTTGA TGTCAAACAA 480 ACCCTTGTTC TGGGCCCTGT GGTCAGAGGA AGCCGAGTCT CACTGGTGGG GAAAGTGGTG 540 GTTTCTCTGT GAGAGGATGG GGTCAGGGGC TGGGCTGGGC TGACCTGGGA GGGAAGAGAC 600 GGAGCGTCTT GCCTGGCTTA ATCACTAAGA GTGGTGTGAA CTTGGGGGCG AGTCTTTTAA 660 TCATACTGAA GTGCAATTCA CCATTTTCAA AATGAGAGCT TGGACAAGGT CCATAGTCCC 720 CAAAGTGAGC TCCGTAAAGC AGTCCCACAA AATACCCTGC AAAAAGCGTT CCATGGCCGA 780 GCAAGTTTGG GAAGTGCTGA AGATACTCCT GCAGGGTAGA TTCACAATGT CCTTAGCTTT 840 TTGAAAAGTC CTGCTGGAAT AGAGAAGTCT GTTAAATTTC ACTTAATTTA CTTCCCCCAT 900 CCACTCTTTC CTACCCCACT TCTTTTTCTC TCTTCCTGCT CTCTTTCTAG AACAGTAATT 960 AGCAGGTTTA CTTAGGCTCT GACAATCTGA AAACAAACAG CACATCCCAC GGCAGAGTCA 1020 ATGGCTAGGG CTCCACGTGC ACTTTCCATT ACTTCACTCG GCAAACATTT GCCATCTCCT 1080 CTATGACTGG GCGAAGGGCT GGGTGATGCT GGGGACACAG CTCTTTTCTT TCTTTTTTTT 1140 TTTTTTGAGA TGGAGTCTCA CTCTGTGGCC CAGGCTAGAG TACAGTGGCA CGATCTCGGC 1200 TCACTGCAAC CTCTGCCTCC CAGGTTCAAG AGACTCCCCT GCCTCAGCCT CCCGAGTACC 1260 TGGGATTACA 1270
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