Tag | Content |
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EnhancerAtlas ID | HS148-02616 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr10:100075770-100077000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr10:100075940-100075951 | GGCCACACCCA | + | 6.62 |
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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 |
GH10I098313 | chr10 | 100073445 | 100077284 |
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Enhancer Sequence | TCATCCAAGC ACACTGTGTG CTTCTCAGTG GGGCACCCAT GGGACCAGGA CTCTCGGCAT 60 ATTTACTTTA AGCCTCTTTC TCAGCAGCTC AGACCCAAAG ACAGGTGGTA AGAAGAGAGG 120 GGGAAACATG GTAATGAGGG GGACCAAATC ACCCATCTTA CCCCTGTGAT GGCCACACCC 180 ATAAGAGTCT CTGCAGATAA CTTTGGCCTC TGGATGGACA TTTTCCTGTT CAGAAACTAT 240 GACCTGCTCT TCTCCTCCCA GAATCTCATG CTCTTCATGC ATCGTAGCAG CACAGAAGGC 300 ACCAGGACCA GGAACTTACA GGAAAACTCA GGTCACGAGA TCTGAGGCAT GGTTGCAAGA 360 TCCAGGCGCA GAGTCACTGT GCTGGGAAGT GCTAATGGCG GGAGGGGTGT CTGCACAGGC 420 TGAGCTGAGG GAAGCAGGGA TAATGCATTC ATTTATTTAC TTCTTCCTTT CACTATGCTT 480 TATTAAACAC CTACTGTGTG CCAGGCACCG TGGTGAGTGC TGGGATTAAG AACAGAGGCT 540 TTGGAGCTCA TTGGACTGAA TTCAAATTCC AGCTCCATCC CTGAGCAAGT CACTTAACCT 600 TACTGCTCAT CAGTATCCTC AGCTCCAAAA TGGACACAGT GGCAGCACCC CACTCACTGA 660 GCTGCAGTGA GGATTAGATG AGGTTATGTA TATTAAGTAC TTACAGCAGT GCATGGCTTA 720 TAGTAAGAGC TGAATAAATG GTGGCTATTA GTGCTATTAT TATCTCTGTC CTTGGGAGTT 780 CACAGTCTGG TGAGGCACAG GCATTAAAAG AAACAGATAA TTTCCTAATG ACTTGGGCCA 840 GGAAGTGAGC TACACTGAGT AATGAGTGTC AGAATTTCCT GCCTCCCTGC TCTCTATGAA 900 ATGCACTGAG GTCACATTCT GTGCTTTGTT TCAGGATGGA GTCTGACTGG AAGTACTCCC 960 TCTGCCCTGG GTGCTAGGGG GCTGAGGTCC AGAAAAGGGG TCCTTGCCAT CTTCCCTTGT 1020 TTGGTTTCAC CTTCTGAAAG GAGAGAAAAA CTGTTGGGAT TGGAAGGAGG AACCAAGGCT 1080 CCTTACAATT CTGCACTGCA GACAAGAGAC AATGAGATGG AAAATCCAAA TGGCCAAATG 1140 AATATATAAG AGCAGGAAGT TTGACAGTTT TGATGACAAG CAGCACATGA AATGATAATC 1200 CCCTGGCAGG TGACAAGCAT TTTGGAAGCA 1230
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