Tag | Content |
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EnhancerAtlas ID | HS147-02011 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:77399220-77400670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:77399927-77399939 | ATGTAAACAGAA | + | 6.92 | FOXP2 | MA0593.1 | chr1:77399927-77399938 | ATGTAAACAGA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 77399425 | 77400000 | chr1 | 77400000 | 77400052 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I076933 | chr1 | 77398956 | 77399898 |
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Enhancer Sequence | GACACCTAAA ATCTACAGAT TTCAGAAGAT TTTTGGGTTG TGACCAGACA GCTAAACAGT 60 CTGTGAGTAC TTTGGCAAGA ACATAAATGG CGTAAGAACT GCTGTGTCCA TATTTTTGAA 120 AGCTGACTCT AAGTCAGGAG AAATAACTAT CTTCTGTGAA CCCGGGAGAA GAGACGTATC 180 CTTGACATTA GCTGAGGTCA GTATGGCCAG TCAATTCTTT TCTCTGCCAA AAAAAAAAAA 240 AAAAAAAAAA GCCCAGAAAG TAAGGAAAAC AAGAGGGCAG GAGCCTCATA GATGAGGAAA 300 ATCATATCTT TAAAACACAG TTTCTTGTTG ATAAATAATC CTCTTACTGC ACTGGCAACA 360 GGACTCTCTC CTGCCACTCC CCCTTTGTCT TACATTCTTA ATCAGTTGAT TACATACCAC 420 TAAAAATACA CATAATGCCA CTTCCTCCTT TCCTGATCAC AGCCACAAAC CTCCATTTTC 480 CTTTTTTGTT GTTGTTTGGG CTTTTGGTTC TGAACTTTGT GTTTTTAACT ACATTTAGAG 540 TCTGGGAAAT GGAGGTTTCT GAGGTTACCT TTGAAACATC TTTGAGTGAC AGGCTCCCTT 600 TGGCCACACA GAATATCAAG AGTGGAATAA AAAGTGTGGA TTCAGTTCAA ACTCCGGTAG 660 CTTTTTTCAA CTCAGAAATG GAATCTGGCT TTGACTAGCC CCAGGGAATG TAAACAGAAC 720 CTTACCTGTA ATTAACCTAG GGCTTCTCTT GTTCTCAATG CAAATGGAGT TACAATTGTA 780 TTTCTCTTAG TAGAATAGAA AGGCTGTGTT TCAGAGGGGA GCTGGCAGTT GAATAGAGGA 840 CAAGTTATCT GTCTAACTGT GACAGCTCTC TCCTATCTCC TTCTAGAAAA GCTGAATGAT 900 GATAAAACTG TAGTTGCATT TGATGTAAGA CATATGGTAA TTACTATAAT AATATTATCA 960 CCCGGGTTCT GCAGTGGCTT TGTCAGTGAG GTGCAATTTC ACATATTGTC TGCGATAAAA 1020 TCCCCGTTTT TGGTTATTGA TAGCAATGCC TTTCTCAAAT GCTATAGGTA TTTTGTGACA 1080 GCTGCGAAGT TCCTGCTTCA TATCCAGGTA ATTGGGTTGA GAATAAGGCC TGCATGCTAA 1140 AACCTGCCGA TGTGAGAAGT AGTGAAAGCC CAGGGAGTAC TGTGAATATT TTGGTAGTTA 1200 TTAACTGACT AAATGGGAAG CCTTTGCTAG TCAGTGCTTC TGAAGCAATC CTAGAGAAAA 1260 AGAAAGAAAA GAAAAGAAAT AAAGGCAATC TCCTTTAGAA AGCCTCTGTT GGGTCTTCAA 1320 TGACGATGTG CAAATTTTGA GCTAATCAAT TATATTATGA ATCTATAGAT AATATTTAAA 1380 AGCTATATAC AGATTCACAA ATTAATTGCT TTCATGTCAT TCTGCTATTG ATTGTTTCAT 1440 AAGTCAAATT 1450
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