Tag | Content |
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EnhancerAtlas ID | HS098-37848 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:17080740-17082110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr3:17081015-17081026 | TAATTTAATTA | + | 6.62 | PROP1 | MA0715.1 | chr3:17081015-17081026 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr3:17081015-17081026 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr3:17081015-17081026 | TAATTTAATTA | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 17080814 | 17080983 | chr3 | 17081061 | 17081488 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I017038 | chr3 | 17080346 | 17082900 |
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Enhancer Sequence | GTGCCATGTG CACTACATTC AATCATAATT GATGGCAGAA TGAAAGGGAA ACATCAGCCT 60 GCTGAGTAGG GGCCTGAAGG CCCATCGCCT AACCTGTCCT CTAAGCCTGC TGGACTCTTC 120 ACCTGGTGTT GCTATAGGAG CCCACAGTCC TGAGAGCTTC CTTAAGAGTA CCTAGAGGAG 180 CTCTTAGACT CAAGGAGAAT TTATGCAATA GTGCAAAAGT TGAAGATTAA TATATGCCTG 240 TTAAGAACAA GAACTATGAA CTGTTAACCA TACATTAATT TAATTATAAA TATGTACCCC 300 AAAATGATAA AAAGATACTT CCTTCTGAAG CAAGTAGTAC AAATATTTTA TAACAGGTGT 360 GACAACATGA ATCATCTCTG CTGAGGTCTG GATAAGTTTT CTGCCTGCCT TGTCTAAGCT 420 TTGCTCATTG TTTACTATGG GCCTACCTTC TCCTAGGCTG GTTCCTTCTG GAATTCCCCT 480 CTAATACAGT CTGCAAATGC CTCCTGCTGT TTACTTGCAA ACCTAGGAGG AATGGCTTCT 540 CACTATTGTG TTCTCCACCC TGAAGTATTA GTCATCTTCA TATTTTATAT ACTACTCATG 600 AATCGGGGGA CGATATTCAC TGTCATTATC AGCAGAGGAA CTTCCTGTAT TGAAATCTAA 660 GCCACAAGTG GATCCTTCTG TGGCTGTCAA CATGGATACC ATTACACTAC AAGTGCTTCA 720 CCATTAAATA TCCTGCCAAA GGGCTGTAGC TTCAGAATAT TGAATTTTAT CACATCCAAT 780 AGCTCACAGG TTACAATAGC AATCCCACCT TTTTAGTTAT TCTTTGTGCA TCTGTTTTAT 840 TTCTGTACCA TAGTCCCAGT GCAGCAATTG TTCTTTTTTT TATATATATA CTTTAAGTTC 900 TAGGGTACAT GTGCTTCATT CTCAGCCCTT AGCTCAGGGT CTCACACATA GAGGGCCTCA 960 GTAAACGATT GTCCCAAGAA TAAACAAATG ATCCTCCAAG TGTTACAGAG TTTAGGAGGC 1020 AGATGAGCTT CTATATCTGG ACTCTTGAGA TGGATGTGCA TTTATTCAGC CTTAACGTAT 1080 ATTTTATAGC TGGAAGGTGC ATAATTATTT ATCCTTTGGT GATACTTAAA CTGGAAGATG 1140 ATTCTAAGAA TAATAATGCA ACTTGTTTCT CTGAGCTTCA TCACACCCAG CTTTTCAAGT 1200 GGAACTAAAA TTAGTAATGA GTATTGGAAA CATTGCCAGT GAACATATGA AAGGAGGGCA 1260 TTCAGCTAAT TTGGGGCTAC CAGAAAATGC TCTGCCAGGC CTCCTGGATA AATGGGGAGT 1320 CAGCCGTGAC AGCTGCCGCT TGCAAGTGTC TTCATTGTGC CAGTCGCTCC 1370
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