Tag | Content |
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EnhancerAtlas ID | HS060-25612 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:189112100-189113210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr3:189112652-189112665 | GAATTAATTATTC | + | 6.46 | PHOX2A | MA0713.1 | chr3:189112906-189112917 | TAATTTAATTA | + | 6.62 | POU4F2 | MA0683.1 | chr3:189112651-189112667 | AGAATTAATTATTCAC | - | 6.16 | PROP1 | MA0715.1 | chr3:189112906-189112917 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr3:189112906-189112917 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr3:189112906-189112917 | TAATTTAATTA | + | 6.62 | TCF3 | MA0522.2 | chr3:189112547-189112557 | AGCAGGTGTT | - | 6.02 |
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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 |
GH03I189392 | chr3 | 189109844 | 189112112 | GH03I189394 | chr3 | 189112259 | 189112616 |
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Enhancer Sequence | AAAAATGGTA GTTCAGATCC CTTGATCTTC AGTCCTGGGC CTTCCCAGTA ACCCAGCAAT 60 CTGTGCTGAG ACTCCTCACA GGTAAAGTGT GGCCCAGGTA TAAGAAGCTT TCTGAAAAAC 120 AGTGCCTTCA AGTCAAACAA AGCCTATACA GCTGAATTCT GGAGCTTGGT TGAAATTGTG 180 GATGAAGCAG AAGATAGGTT GGGGTATGAA CAAATGTAGA GAAAGAAGGA AGGGCAAAGA 240 TCACATTTTA ATAATGTTCT GTACTGTACG TGAATAATGC CAACAGTACA CTGTCACATT 300 TGTGTTTAGC TCATTTTCAG CAACAGAGCA AGATCCCAGA GTGTAGCAAG AAGAGAGACC 360 GTTTTGGGTG GAGATATTTC TGTTTCCGCA GGGGCTTTTA TGCTCATTCA ACTTGAAACT 420 TCTAAAATAA CTCATTATGT GTGGAATAGC AGGTGTTCAC ATTAAACATA TTTGCTTGAC 480 CTCACTTAAT CTATTATATA GTAAATGTTC CTCTTCTTCT CGTTTACCCA ATCTTGGGTC 540 ATTAGTCAGA CAGAATTAAT TATTCACAAT GTTTAGAAAG AAATTACATA TCTGAGTCTT 600 CACGGCAAGG AAAATTGACA TATCAGGCTC CGAGTCAAAC TAGGATTGTC AGAGTTGACA 660 GTGGTCATTC TGTTACTTGG GGAAAGTCAA CGTTTAGAAA ATTCAGAGTT GCTCTTATTT 720 TGTTAAAGCG TAATTCACAA AGGAAGTGTA GATAAAACTT TCATTATGAA GCTTCAGTTC 780 CACTTCTCTT ATGCTTTGGT ATCCCTTAAT TTAATTATAT CATTCTGCAA TTTCAAGGAT 840 GATCAAATTA AAGTTATCCT TTAGCAAGAC TTTTTGTTCA TCAAGCTGCC TCTGCCAAAA 900 ATTTCTCAGT GAGCCTCAAC TCTCTTCTTC ATCAGCCTCT GCACCTCCAA ATGTTTGCTA 960 ATTTCTATCG ATTCTGCCTC TTCAATATCC TTAAATTGTC TTTTTAATCT CAATTTTATG 1020 CCCTTAGATT TGGCCCACAT CATTTTTTTT CTGTGAAAGG TTGCAATAGC ATTTTAATTG 1080 TCATCCTGAC CCTAACATGG GCTGGATTAG 1110
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