Tag | Content |
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EnhancerAtlas ID | HS095-12156 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr17:7959140-7960540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr17:7959723-7959734 | CTTGAGTGCCT | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I008055 | chr17 | 7958919 | 7961539 |
| Enhancer Sequence | TTGTATGAAC CATGTTTTTA ATTTGTTTGA AATCCCTCCC AGGGTGGAGG GAGAGCTGCT 60 TGTGCCACCC CAGAACAGTG CCTAGAACCC CAATCCCTTC TTCTCTCTGC CAGGTCCTCT 120 TCCAGCCTCC TCTTTATCTT TGTGCCCGCC TTCCCCTCAC CGCACCCCCA TCCATGTTGG 180 ACATCCCAGG GGTGCCTTTG CTCACTACCC CAGGGAATGA GAAACAGACT CTTCTGTCCC 240 CACCCGCATC CCCCACTGAC CTAAGAAGGT GCTGAAGCCT GGGACAGAGA CAAAAGTGGC 300 AGAAATGGAG AGGGATGTGT GGGTTGAAAT AGGGGGCTTG GATGTGGGCC CAGGTGGTTG 360 AGGACCAGCC TACACTGTGC CCATTTAAAG ATTAATAGTA TATGCTTTAG AATAGTGCTT 420 TACTAATATG ATTATGAATC ATAAGTATAA TAGCTTGTGC TTAGTACAAC AATAAGAGAA 480 TCAGGCGGTG AGCTTGCTTG ACTGACCACA GAGTGGAACA AACAACCACA GGAAGTCTGC 540 GGAGCCTCTG AGCAAGAAAG TTGGCTTATT GCTCAACCTT CCACTTGAGT GCCTGAACAA 600 AGGTCTCATG GGAAGGGAAG CGACCCCTGC TCCATTACCC GGGAGGGTAC TGCAGGAGGC 660 TGCTGGTAAA AGAGGAGAAG TCCTCTGCAG TAGGGTTAAG GAGGAAGCCT CCTATCTCCC 720 GCATGTTCCC AGAGGCAAAG CAGCTGCTCT GCTGACGGTG CTCAGGCGTT GACCACTCCT 780 TTGATGTACA GGCCTGTGGG TTTGAAGGGC TGTTTGCTTT CACGTCCTGT TCTGTTCTAT 840 TAGCCGCTTA GTTGGACTCT GATGATTATC TGTAAGTTAA ACATAGAGTA TTAGCTTACG 900 TAGTGGAACA GTAAATAGTA TTAACTGGCT AATGACCGAC ACAGCAGGCT CCGCCACCTC 960 TCCCTATGCT CACCCAATGA TCACCTCACC ATCAGCCCAC CCTCAGCCTA TAGGATCAAA 1020 GGAACTGTAC TCAATAAATA TCAGTGGAAC CCAGAGCTCC TGGCCTTTGC AATCTCCACG 1080 TTGCGATGGA TCCTTGGACC CACTTTTGTT AACTCTTAAA CTTTGTGTCT TTGTCTTTAT 1140 TTCTTTTCTC ATTCCCTCGT CTCCACCGGG AAGGGGAGAG CCTGCGGGTG GTGTATCAGG 1200 CAGGTTCCCC TACATCTTTG GCACCCAACA CGGTCTCCTT GAACCCAGGT GAAGTTACAC 1260 CTGAGCGTGG TCGTTGTGAA GAACGGTCTG TCCAGGAACT CCCGAGAACG TGTGGTCGGC 1320 CTTGCGGTAA GCTTGTGCAC TCGGAGCATT CCAGGGACAC CATGGGACAA TCCAAAAGTA 1380 AACATTCTGC ATATTTACAT 1400
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