Tag | Content |
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EnhancerAtlas ID | HS134-00668 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:27353400-27354610 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | SP1 | MA0079.4 | chr1:27353734-27353749 | TAAGCCACGCCCCAC | + | 6.16 | SP4 | MA0685.1 | chr1:27353734-27353751 | TAAGCCACGCCCCACTC | + | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 27353454 | 27354564 | chr1 | 27353661 | 27353962 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027026 | chr1 | 27353011 | 27355170 |
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Enhancer Sequence | ACCTCTCTCT CCCAAAATCC CAAATTTATA TATTCCAGTC CAGAGCTCTG TCTGGGACTC 60 CAGGCTCATT TATTTAATTT TAGTCAACAT CTCTACTTTC ATGTTTGTAG TCATCTCAAA 120 TTTTGCACGT TCAATGTTGA CTTCTCGAAC TGAAGTCCTA GCAAATGGCA AATTCCAGTT 180 CTTGGCCCCA AACTCTGAAG CCACTTTCCA CTCCTTTTTC TCTCACGCTG CACTTTCTCA 240 TTCGTCAGCA AGCCCTGTGG CTCTGCCTTC AGAACCCAAA CAGGCCCTGA CCACATCTTG 300 GCCCCACCTC CAGCTTACTG CCATCTCTGC GGTCTAAGCC ACGCCCCACT CTCCAGGATT 360 TTTGGAGCCT TTCTGCCGTC GTGCTTGTCG CCTACAGTGT TTTCATCCCA GCAAGCCAGT 420 GTGATCCTTT CTAAACACAA GTCAGATCAT GTCATTTTAA TGCCTCCTTC TCATTTGGAA 480 TACAAGCCGA AATCTCCTCC CACACCCCTT CCCTTATCGG GGGCAGCCAC ACTGGCCTCC 540 CTGATGTTCC TCAACCATGC CAGGCACGCT CCCACCTCAG GGCCTTGCGA CTGCTCTTCC 600 ATCTGCCTGG CACGGTCTCC TTTGATCCCC ACATGGCTGC TCTCTCAATT CCTCCAGGTC 660 GTCTTCTCCA TGTCTCCTGT TCTCAGGGAG GCCTTCTCTG ACTATCCAAT TAGAATGGCG 720 CCCTCGCTCC CCACACCTGC TAGCCTCTTC TCTATTTCCA AAGCACCTAA CACCATCTAC 780 CATGCTGCGT ATTTACCTAT TTATTGCCCC ATTTCCCGCC CCTGGAACCA AAGCTCCAGG 840 AGAGCAGGGA TTTTGTTTTC TATGTAATCC AGCACCTGGA AACCTGTGTG TGCTCAGTAA 900 ATATTCACGG GATGAGTGAA GGTGAGACAG GACTAACATG GGTCGCAGAA GAATGGAAAA 960 TTCCAGGCAG CAGTTTCACA TGACTAGCAA AAGGAAGCTG TTGAAATAAC TGCAGAAGCT 1020 AGGGGCTCAT AAGACCCTGA ACAATCAGGG CATGGAGCAA GCTGGCTGAG ACCAACTGGA 1080 CACAGCATGG TGCTGGATTT GACCCAGGTT TCTCCTAGGA CCTCATTATA CGCTTATTAA 1140 CATACTAAAA ATCACACACC CACCAGCACC ACTATAGTTC CCATATTTGG TGTAAAAATG 1200 GGTGGCACCA 1210
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