Tag | Content |
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EnhancerAtlas ID | HS138-00298 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:17613370-17614530 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr1:17614474-17614487 | CACGTGACCTCTG | - | 6.04 |
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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 |
GH01I017286 | chr1 | 17613436 | 17614463 |
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Enhancer Sequence | CCAGACAGCT GCCCATGCCA CACTGCCTGG TCCCTTCCGG GGCCTGGCTC TCAGGCCTGG 60 AAAGCCCAGG GAGACTAGGA TGAGGCTTGG GTTCTCGTAG GGAAATTTCC CTTCACCCTA 120 TTGTGGTTCC CCTAACACAG TGGGCAACCT TGACCAGGCC TGAGGATAAG GGAAGATACC 180 CAACCGACTC ACCTACTCCC AGCTGGCTGC CTGAAACCCC TCGGAGTTGG ACCATCAGAT 240 GCTGAACTCG TACTCTCTAG CTGAGCACAT AACTTGGGTG AGCCTCAGTT TCCCCCTCCA 300 TAAAATGGGC AAAATAACTG CCGCTTCATA GAGCTTGCAT GGGGATGAAG TAGGGTAACT 360 CACAAGATAT ACTTAGTGTC AATAGCACAG TGCATGGTGC ATAGTAAGTG CTCAGTAAAT 420 GATGACTGCT GTTACATAAC ATCCCCCAGC CCTTCCTCAA GCATCTGCTG TGTAGAACAC 480 TCCTAATCTC CGCGCTTTAA TAGATGACAA AGACCCTTTG AGACCCAGAG GTGAAATGAG 540 GGAGGTAGGG ACAGGACAGC TGTCTTGGCT ACTCTCAGAT CATACCCTGC TTGTCTCAGC 600 TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT GCCTGGACAA GAAGCTGACA AGAAAGCCTG 660 TCTTTTTTGT GGGGATTTGC AGCTCTGGGT GGCCCTGACT CATGCTTTAT TCAGAATTTG 720 GAATAAGTAG CTGCAGGGCT TCCGCAGGCA TTGCCCAACT CTGTGGCCTC CTGCGGCTTC 780 CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA GGATGGCTGG AAAGGAATTC TGGATGGCTG 840 GACAGAGTCC ATGGGACCTA TCACTTCCTA CAAAGTCACT GTCATCCCAA GTCCCCTCCA 900 GCATAATGAC GGCAAGTGCA AGCATTGTGC CAGCAGGTAC TGAATGCTTC CTGAGCACCA 960 TCTGATATAG CCCTCACAGC ATGCCAGCAG GCAGCTATTA CTATTGTTCT CACTTTATAG 1020 ACAGGGAAAC TGAGGCACAG CCACATGAAA GCGCTTGCCC TGGTCACAGA GCTATTAAGT 1080 GGGGGAAACA AATTTGAGCC TAGACACGTG ACCTCTGTAC CCAGTCACAC CAGTGGTTCT 1140 CAACCCATCT ACACATTAGA 1160
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