Tag | Content |
---|
EnhancerAtlas ID | HS050-10261 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr10:123218570-123220160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr10:123220049-123220060 | AGAGGGTGTGG | - | 6.02 | NFIC | MA0161.2 | chr10:123218694-123218705 | TCTGCCAAGAA | - | 6.02 | RREB1 | MA0073.1 | chr10:123219605-123219625 | CCCCCACACACCTCCCCCCC | + | 7.15 | SNAI2 | MA0745.2 | chr10:123220127-123220137 | TGCACCTGTT | - | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr10 | 123219000 | 123220043 | chr10 | 123219074 | 123219599 | chr10 | 123219613 | 123219953 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH10I121459 | chr10 | 123218843 | 123220110 |
|
Enhancer Sequence | ACCCCAGCAG AGCCCACTGC ACCTGCTCTC CCTGGAATCG GGATCGTGAG CAGAGAGACA 60 ACAGCAGGGG ACATGGCTGA GGCCTCTGTT CCATGACCAG CACTGTCAGA GACCTTCCAT 120 CAGCTCTGCC AAGAAACCCT CAGAGCTCCT GGGCTCTCAT CCTTTGTGCC CCGCTCCTCT 180 CCTGCTTTCT CTCTGATTCT CAAGCTGCCC CCTCATTTTC AACTTCCTAT CCTGTTACCC 240 ACAACAAAAA GCCCTGACTG ATTCATCTTC CAAATCCCAG GGTGTGGTGG TGTAAAGAAC 300 ACACACCTCC AGTCACCTTG GGGTAGCAGA GCACACCCCG TGCCTCTTCC CAAGAACCAG 360 GCCCACCACG GGGCATAGCC ACGGGCAGGA CCCAAGCTCC CATCTCACTC ACTTCTCAGC 420 CGCTCAGCCT TAGGCTCGGG ATGTCTCCGA ATCTCAGTTT CCTCACCTTT AAAATGGGAA 480 AAAGTTTGCA TACCTGTTGG GACTGGGTAA CAACTGGTGT GGGTTAATAA ACTGCAGAGA 540 GTGCCTAGCT CAGCACTGGA AACCTGCGGT GTGCTCAAGA ATGGCAGGAG GGTGTTGCTG 600 TTGCCCTTCT GATTCGAAAT CCTCCTTGCT TCTCATCCAT TAACCCCAGG ATATATTGAG 660 AAATGCAATC GGCTTCTTCC TGACTCAGGG CACTGAAATC ACCACGTTGC TTTTGGGTTG 720 CCCAAAACAC TGTGTCGCCA AGAAAAGCCT TTCAAAGCCC CTTTCGGGAA GGGATTTTTT 780 TCGAACTTGA AACAAGAAGG AGTCATTTGC CAAAGTGAAA TAGCACATAA ACCTTAGAAC 840 CCACAGATTT GAGTGAATTC TAATCTTGGC CAAAACTGGC AGGAGTGAGG GGGTGTTGGG 900 GAGGGAGGAT GAGTCAGAGA TTCCACCCTT CAGAGGGGGC AGCCTAATAT GGCATTGGGG 960 AGCCACAGGA GACGACTTAG GTATGCCTGG ACTTTCAGAC TGGAGCCACG GCTCTGGCCA 1020 GGAACCAGCT GTGTCCCCCC ACACACCTCC CCCCCCAAAA AAAAACAAAC CTACCCTCAC 1080 ATATGCATGG AGCAGAGCCT CGGGGTGGCA ACCCAAACTG AGTGTTCAGA TCCATCAGCA 1140 GGAACCAGCT GAGAGACTAG CAGCTTGCCC CCAGGAATGA TAGCAACCAG CCTTCTCCTG 1200 GTATGCCCTG GTTCTTGGGC CAAACATGGA CCTGTCCCTG CAGACACTGT GTGGTCCTCG 1260 CTGACTCCAA ATTCTCCTAA ATGCAGCCTC CGTGGAGCCT GTGATACGGC ACATGAGCCT 1320 GGGAGTAAGA GGGAGGCTTC GCCCGGTGTA ACCTCAGAGC ACGTGTCGTT TATTTTTAGG 1380 CCTGGAGTAA AGGGCCTGGG TAAGGGAGGA ACTTCAAAAG GTGAGATTTC TGTCATTGGA 1440 ATAGTTTTAC AATGTAATGA AAACAAAGAG ATGGCTCTTA GAGGGTGTGG GTGGAAGCAA 1500 AGCCAAGTTC TAGCCCTGCA GTGGCTCTCC CCAGCTGTGT GGCTTTGGGC AAGTCTTTGC 1560 ACCTGTTTTT TATCTGTAAA CTGAAGAGAG 1590
|