Tag | Content |
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EnhancerAtlas ID | HS002-02622 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr12:98863790-98865210 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr12:98864930-98864947 | AGGAACAACGTGTTCCT | + | 6.93 | Ar | MA0007.3 | chr12:98864930-98864947 | AGGAACAACGTGTTCCT | - | 7.05 | ESRRB | MA0141.3 | chr12:98864073-98864084 | AATGACCTTGA | - | 6.32 | Esrrg | MA0643.1 | chr12:98864074-98864084 | ATGACCTTGA | - | 6.02 | NR3C1 | MA0113.3 | chr12:98864930-98864947 | AGGAACAACGTGTTCCT | + | 6.23 | NR3C1 | MA0113.3 | chr12:98864930-98864947 | AGGAACAACGTGTTCCT | - | 6.35 | NR3C2 | MA0727.1 | chr12:98864930-98864947 | AGGAACAACGTGTTCCT | + | 6.11 | NR3C2 | MA0727.1 | chr12:98864930-98864947 | AGGAACAACGTGTTCCT | - | 6.19 | RORA | MA0071.1 | chr12:98864075-98864085 | TGACCTTGAT | - | 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: 1 | ID | Chromosome | Start | End |
GH12I098470 | chr12 | 98864077 | 98865403 |
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Enhancer Sequence | GGGATTACAG GCATGAGCCA CCGCGCCCGG CTGGATGGAC TCCTATCTAA AGCCAATCAA 60 TCTTTGTCAT TCCCTAGGAT TTTTGTAACT GAAGCTGAAC AAAGATTTAT TTATTCTCTG 120 TTGGTGAGGC CAGGAGATGG TGAGACTCAG GAACTGCTAG TGGCCACATT TCTTGCTATG 180 TAAAGAAAGC TTTTCTAAGA GAAAGAAGTT AACAACACAG AGAGAGAAAC AGAATTGAGA 240 GACTGAGAAA AGAAGACCTA GCAGCACTCA AATCACCTGT TCCAATGACC TTGATACCAC 300 CTGCCACTCA TCCTTCTCAG TGTGAGCCTT CCAGTAAGTC CCCTTCTTTT TGCCTAAGTT 360 GGTTTAAGTT GGGGTTCTAG AGGGTGGGGG TGGGAGGAGG GAGAGCATCA GGAAGAATAG 420 CTAATGGATG CTGGGGCTTA ATACCTAGGT GATGTGCTGA TCTGTGCAGC AAACTACCGT 480 GGCAGACATT TACCTATGTA ACAAGCGTGC ACATCCTGCA CATGTACCCC TGAACTTAAA 540 AGTTGGAAGA AAAACAAAAC TTGCAACAAC CCCTAAAAAA TAATAAGCTG GGTTTCTAAA 600 CCTTTCCTCC AAATGGGTCT TGACTGATGT ATTCTCACAC AACTCTATGC TTCCCCTAGC 660 ACAGCACTGA TGACTGAGCT GTAATTGCTG GGTGCTTGTC TACCTGTCTA CCTCTCTGTC 720 CAGAAGACAG TGGCTTTCAG GTTCATGCAT TCTGCCCATC GCTGGGGCAC TCAACTGAGA 780 GGGAAGGAAG TGGGGATGCA CTCAATACAC ACAGGTAGGA TTGCGACAAC CATGTGTGTA 840 CTTCATAACC CTGAGCCCTG AACCACAGAT GATTTACTCG AGCTGGGCCA CAGTCTCCCT 900 GTAGCAATTT GGGACTGAGT CATACAAAGA TTGGACACTG AAACTCCTTC ACACAAATAA 960 TAGCACTCTT CAGAGGATGT TATTAGCCTC TGGCTAGTAA GGGGCCCCAA GCTGTCTTCT 1020 GCGAATTCTC TAAGAACCTC TAATATTCCT CCAACAAGCT TGCAAGGTCA TTTCTGCTTC 1080 CTAAAGCCAA AAGAAACTGA ACTAATACAC ACCCCAAAAT ATTGTAGTTT CTGTGTGAGC 1140 AGGAACAACG TGTTCCTCAT TATAGCTCCA AGGCCAGCAC GGTCCCTAAT CAGAACTCAC 1200 TGAACACCTG ATGAATGCCT GCAGCTCACT GCACTGAGTG GGAGATGCTC CTCCCACTTA 1260 GATAGGGATT TTTTTTTTTT TTAACTCTCT TGCCTTCAAG GTCCTGCGCA CATCTGCCCT 1320 GGCCTTGGTC TCCCTGTGTT GTCAGCTACA GTGGCCAGTG TGTCCTCTGT AGGGTACATC 1380 ACATCCCTGC TCAAGAATGC ATGTTAGAGA CTAGAAGTAC 1420
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