Tag | Content |
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EnhancerAtlas ID | HS092-00857 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:27353420-27354580 |
Target genes | Number: 28 | 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 | CAAATTTATA TATTCCAGTC CAGAGCTCTG TCTGGGACTC CAGGCTCATT TATTTAATTT 60 TAGTCAACAT CTCTACTTTC ATGTTTGTAG TCATCTCAAA TTTTGCACGT TCAATGTTGA 120 CTTCTCGAAC TGAAGTCCTA GCAAATGGCA AATTCCAGTT CTTGGCCCCA AACTCTGAAG 180 CCACTTTCCA CTCCTTTTTC TCTCACGCTG CACTTTCTCA TTCGTCAGCA AGCCCTGTGG 240 CTCTGCCTTC AGAACCCAAA CAGGCCCTGA CCACATCTTG GCCCCACCTC CAGCTTACTG 300 CCATCTCTGC GGTCTAAGCC ACGCCCCACT CTCCAGGATT TTTGGAGCCT TTCTGCCGTC 360 GTGCTTGTCG CCTACAGTGT TTTCATCCCA GCAAGCCAGT GTGATCCTTT CTAAACACAA 420 GTCAGATCAT GTCATTTTAA TGCCTCCTTC TCATTTGGAA TACAAGCCGA AATCTCCTCC 480 CACACCCCTT CCCTTATCGG GGGCAGCCAC ACTGGCCTCC CTGATGTTCC TCAACCATGC 540 CAGGCACGCT CCCACCTCAG GGCCTTGCGA CTGCTCTTCC ATCTGCCTGG CACGGTCTCC 600 TTTGATCCCC ACATGGCTGC TCTCTCAATT CCTCCAGGTC GTCTTCTCCA TGTCTCCTGT 660 TCTCAGGGAG GCCTTCTCTG ACTATCCAAT TAGAATGGCG CCCTCGCTCC CCACACCTGC 720 TAGCCTCTTC TCTATTTCCA AAGCACCTAA CACCATCTAC CATGCTGCGT ATTTACCTAT 780 TTATTGCCCC ATTTCCCGCC CCTGGAACCA AAGCTCCAGG AGAGCAGGGA TTTTGTTTTC 840 TATGTAATCC AGCACCTGGA AACCTGTGTG TGCTCAGTAA ATATTCACGG GATGAGTGAA 900 GGTGAGACAG GACTAACATG GGTCGCAGAA GAATGGAAAA TTCCAGGCAG CAGTTTCACA 960 TGACTAGCAA AAGGAAGCTG TTGAAATAAC TGCAGAAGCT AGGGGCTCAT AAGACCCTGA 1020 ACAATCAGGG CATGGAGCAA GCTGGCTGAG ACCAACTGGA CACAGCATGG TGCTGGATTT 1080 GACCCAGGTT TCTCCTAGGA CCTCATTATA CGCTTATTAA CATACTAAAA ATCACACACC 1140 CACCAGCACC ACTATAGTTC 1160
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