Tag | Content |
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EnhancerAtlas ID | HS187-25704 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chrX:40137690-40139060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf12 | MA0742.1 | chrX:40139030-40139045 | TACCACGCCCTTCTT | + | 6.37 | RREB1 | MA0073.1 | chrX:40138716-40138736 | TCTGGGTTTTTGGGTGGGGG | - | 6.02 | ZNF263 | MA0528.1 | chrX:40138129-40138150 | GGAGGAGGTGGGACGGGTGGG | + | 6.14 |
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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 |
GH0XI040278 | chrX | 40137382 | 40139378 |
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Enhancer Sequence | CCTGCAAAGG ATAGCTGAGG AGCCCAGTGT TCCAGCTGGG CCAAGAAGGA CTGGTCAAAG 60 TTGCTGTTCT GGTTAAGTAG CATGTGCAAA GGCCCTGGGG TGGGCAGATA AGGAACAGGT 120 TCTGGGGCTG CTGAACAGCA GGGATGGGCT GTGAGGATAG GGACAGGTGA GACCGGAACA 180 GCCTCCAGAA CTGTGAGCAA TAAATTTCTG TTGTTTATAA GCCACCCAGT TTATGGTATT 240 TTAAAGCCGA ATCAAAGGAC GGTGATAACT GAGGCAGCCA CAAGAAGGAA AATGGGGCTG 300 GGGTGAAGAA AATGAAGCAG AGAGCTGAAC CAAAGCCACA GCCCTGAGAA AGCGATGATG 360 TAAGGGAAGG AAAGACGCAC CGGGGAGAGA TATTTAGATG TAAATCTGAC CAGACTAGAT 420 GTCCAGATTA GATTAGAGGG GAGGAGGTGG GACGGGTGGG TGAGTGGTTT TCCCTCTGAA 480 TGTTTAGAGG CAGCTGTGTT TAAGGAGGCT TAAGGTGTTT ACTCAGTGTC CTGGGACCAG 540 AAAGAGACTC CAGAAAGCCT GGGGCCCGGC AGAGTTTGGG CCATGATGTC ATTCACACAG 600 GGAGTCTGGC TGCAGCCTGT CTGGGGTGAG GTCCCCACTG CGGCTTGTCT CCTAGGCAAC 660 CGACTCTGCT GAGAAACACG CAGTAATGAC TCTCTAGATT TGCAGGTTAC CAAGCAGTTG 720 CACATATATC TTTGTCTCAT TTAATTGTCC CAGTGGGAAT TATCCCCATT CTACAGATGA 780 AGCCACTGAG GCCTCAAGGC TCAGAGAGGT AGGGTATCTT CTCTCAGGCC AAGGAGATGG 840 CAGAGCCAGG CCTGGAACCC AGTGGTCCTA ATCCCTAGCC AAGTCTTCTC TCCAACACAC 900 TTTCCTGCGT TCTAGTCTCA TAGCTCCCTT AAGAGCTATT TCTATTGAAT CCAGTTCACA 960 AGTATTTGCA GAGCTCCTCT GTGAGGTGGG CAGGTGTGGC AGGCTTCAGG TGAAGTTGCA 1020 GGCATCTCTG GGTTTTTGGG TGGGGGACCC TGAGAGAAGT GTGTTAAGAG TGTGAGTAGT 1080 ATGATGGGCT GAAAGTGGAG GGGAGGGTCA CCAAGATCAG AATCATCAAT CAGAAACAGG 1140 TCCCTGAAGG CAGACCATCA GGACGACAAG GATCATGGGC AAAGGCCCAT CAAGGCAAGT 1200 GTCAAGTTCA CAGATAACTT GATAACAGGC CTCTCTGCTA TCTCCCTCTT CTGGTGCCAG 1260 ATGTTCATGA ACTTGACCTC ACCATTCTGG TTTTGTTTTG TTTATTGTCC CCACCGCACT 1320 GCAAGGACCT CCCCTCCCCC TACCACGCCC TTCTTTGTCC ATTCCCTCTT 1370
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