Tag | Content |
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EnhancerAtlas ID | HS147-04949 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:233679020-233680770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:233679394-233679405 | AAGAGGATTAA | + | 6.14 | ESR2 | MA0258.2 | chr1:233679277-233679292 | GGGTCACTCTGCCCT | + | 6.43 | FOSL2 | MA0478.1 | chr1:233679604-233679615 | GGATGACTCAT | + | 6.62 | IRF1 | MA0050.2 | chr1:233680281-233680302 | CTCAGGTTTCACTTTTGTTCT | + | 6.1 | JUNB | MA0490.1 | chr1:233679604-233679615 | GGATGACTCAT | + | 6.62 | MEF2C | MA0497.1 | chr1:233680252-233680267 | TTTTATTTTTAGTAT | - | 6.12 | PPARG | MA0066.1 | chr1:233679275-233679295 | CTGGGTCACTCTGCCCTCCA | + | 6.21 |
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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 |
GH01I233542 | chr1 | 233678544 | 233680459 |
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Enhancer Sequence | GCCCTTCAAC AGGTTTCCTC TCCTCCCCCT TTCCCATCCT TATTTTGTCA GGATCCAAGC 60 CCCCATTCTT TTGTCACCTC AAGATGCTAT ATAAGCTTCT GTACCCACTG TGGGGCTGTA 120 TCTTCATTCT GAAGCTTCCC GTGTATATAT ATTAGATAGA TGTGTATACC TTTTATCCTC 180 TTAATCAGCC TTTTGTGAGT TGATTTTTCA GTGAACCTTC AGGAGGCCCA GGGCCTGGTC 240 CCCTGCAAGG CAGTGCTGGG TCACTCTGCC CTCCACCACC AGGCAAGGCT TCTGTGTGTA 300 AACTTCTGCA GGGCTGACAG TAATCAACAA TACGTTCTCT CTGCAGTCAG GTTCCCTTTC 360 AAAAAGGAAA GAATAAGAGG ATTAAAATAA TGCCTTACTT TTCTTCCAAA CTCCCAATCA 420 AGGAAGACTC TCACTTTCCC TGGGTGAGGC TGGGAGTGTT TTGCTGACGG AGCTCCATCT 480 ACGTGGGAGT AGGGATGACA CATCCCTCCC ATTAACATTC TCTGCGATCA GGCTTGACAG 540 TCCTTGACTC TCCACACCCG GGCTTGTTCA GCCTCTGGAA GCAAGGATGA CTCATGTGTT 600 GCTCTAGTCA TCCCTAGTAC TGTCTTCCTG TTGCAAATCC TTTCCATTAA ATAACCCTGA 660 TTTGATCACC TATCTTCTCG GCACTATGTG TATACCACAG AGACTTTTTT TTTCTCATGT 720 GCCAGGTGGT ATCTTCTGCC TCTTAGTAGA CCTTAGTGGA ACCAGGGAGG CAGTATCCTG 780 GCACAGTTGA GGCTCTGGAG TCAGACCAGG TTTGGATCTC ATTTCCAGCA CTGCTTATCA 840 ACATCAGCTG GGACAAGCGC CTTAACACCC CCTGTGCTTA ACTTTCCTCA TTTGTACAAA 900 TGGGATAATC ATAGTCCTTA CTTCACAGGT TTGTTCTGGC ATATAACAAG TGCTCCATAA 960 ATGTGGTCCT CCCCCAAAAA ACTCTAGTCC CATGCAAGGA ACACACTATT TGGCATATTG 1020 GTTAGACCCT TCTTTCATCT TTTGCAGTGT TCGAGTTTCT ATCTTCCCAG TCCCTAACTC 1080 CTTGATGCCT TTGGCTTTCC CTAATTTATG CCCTTATGCA AACTGTGACT TCGAGCACCT 1140 TGGGCTCTTG GCATCACCTA GCAGCTCCCA GCCTCCTCCT GATACCTTGT GACTCTGATT 1200 TTGGACCACA GCCTTGGACC TGGCTGCTGA TTTTTTATTT TTAGTATCGA CTTCGTGTGC 1260 CCTCAGGTTT CACTTTTGTT CTAGGCTGCT CAGCAAGGTA CTTGTCTCTT TGTTCTAAGG 1320 AAGAGGTACT TCTGTCTGAC TTTTGTTGAA AACTCCTTCC CTCTGCTCCT GATTCACATC 1380 CTCCAAGTTT TCCTGGTTCC TTCTCCCTGT GCCGCTGCTT GGAGTCTTCG GTTCCTCCCT 1440 GTGTCATCTT CTCTTCTCAG CCATTAAGTT GACCACTCCT CCCTTAGATG AAAAATAATA 1500 ACACATCTTC CCTGCCTCTC CCTTACCATT CATCCCCTTC ATCGGCAACA CACTGAAAAT 1560 ACTTGTCCGA ACCTGTGTCT CTCTGGCTGC CTATCCTCTC ACACTCAGCT CACACTTGCC 1620 CACCTCTAGT TAGGGCTCCG CTAAAAAATA TCCTGTGTGA CCTTGTGCCA TACCCTTGTC 1680 TTTGGATATC AGATACTCTG ACAGATGATG CTTCCCATCT TCTGATTTTG GTTGGACCAA 1740 AAATCTTGTT 1750
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