Tag | Content |
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EnhancerAtlas ID | HS034-15986 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:16152590-16154060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr2:16152633-16152645 | AAACAAACAAAC | - | 6.32 | Gfi1b | MA0483.1 | chr2:16153420-16153431 | TGCTGAGATTT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 16152646 | 16153800 | chr2 | 16152892 | 16153059 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I016012 | chr2 | 16152381 | 16154316 |
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Enhancer Sequence | GCTGCACTCC AGCCTGGGAG ACAGAGTGAG ATCCTGTCTT AAAAAACAAA CAAACAACAA 60 CAACTACAAC AAAAAGGCGC CTTGGGAGAG GAAGCTCATT CCCAGCAGAC CTGTGACACA 120 GCCTGTCTCC CCAGCGAACC CAGACCATTT CCCACTCTGT GGGCAGATTG ACCAAGCAAC 180 AGCACTTTTC TGTCTTCATC TGGAGTCCCT GGCAGAGGCC ACCTCACTGA GGTTCAAGGC 240 AATCCAGACT CTTGGGTAGA GCACACTCTG ATGGTGGCAC TACATCAGCT TGCACGAGCA 300 TGTGGCACAG GGGCCAGGCA GGAGCTGGTG TCTGCAAGGA GCCGGGAAGG GAGGGGCTCC 360 TAGGCTTGCC ACGGCTGCAG TCTCCAGGAA TGAAAACCTG TCCTGCCAGT TGCATATGTA 420 GCAATTTTGA ATGCAAATAG CCACTTCCCA GATTTTTTTT TCTTTCTTCC CAGCAAAACA 480 CCCACATCAT TTCCTTCCTT TGTTGGGCCC TTCCTGAGAC CACTGGCTGG GGGCACATAG 540 TAGGCACTCA ATAAATATTT GCCGAGTGCG TGAATGGGTG GTAATCCAGC ACTAATCCCC 600 CTCTCTTCAG CTCCCCACCC CCAGGAAGAA ATAAAAGATG TCCATTTGTG GCTTGGCCAC 660 ATTCAGGCAA ACTTCCATAT TGCTGCCAAG TCCTGCCATC TGCCACCTCC GAGGTGCAGG 720 TGCTGGGCAC CCACAAAGCC CGGCCGTGGG CACAAAGGCC CGATGTGCAC TGATAATTGC 780 CGAGTGCACA GCCCGCCAGG CCGGCCAGGC TGATGCAAGT TTGCTGGGTC TGCTGAGATT 840 TGCATACAGA TGGCCAGTCG GGGCGCAGGG CCGCCGCCAC CGCGACAACG CCGCCCGCGC 900 CCCGGGTAGA CCGGCCGCAG CCCCTTTAGA AGTGCGGGAG GCTTTGACTG CAGCCGAGCC 960 CCAGAGAGGC CTCATTCTGC CTGTCCTGAA TAGTCCGTCA TTCAAAGCAA CGCTTTGAAA 1020 TTTGAAAAAG AGAGAGAGGA AAAGAGAGAG AGGAGAGACT GAAAAGCAGA GAGAGAGAAA 1080 CAGAGACACA CAGAGAGACA GGCAGAGACA GAAAGAGAGA CAGAGACAGG GAGACAGAGA 1140 CTGAGACTGA GACAGAAAGA TTCAGACAGA GACTGAGAGA GGCTGTGAGA CAGAGACAAA 1200 CAGTGAGAGA GCTAGAGAAA GAGAAGGAGA GCTTGGAGGA AGGGGAAAAA AAAGCAAATT 1260 CTTTTCTTTG TGAGACTGGG GAGTGTTGGG CAAGGAGCCA GGGGGCTTCA AGAATGTGAG 1320 CGAGGCACCA GGAAGGAGGG GATCTCTGTG GAGACGCAGC TTCGGACGTG TGGCATGCAC 1380 TCTCCTCCTG GTCATCCGGA GCAAGGGTCT TCAGAGCCCG AGATGCGCGA CGCGCAGGAA 1440 GCACCAGAGA GGGTGGCGGG AAGAAAAGGC 1470
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