Tag | Content |
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EnhancerAtlas ID | HS082-22171 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr22:19678640-19680060 |
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) |
HSF1 | MA0486.2 | chr22:19678779-19678792 | TTCCAGAATCTTC | + | 6.16 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 19679200 | 19679849 | chr22 | 19679104 | 19679921 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I019691 | chr22 | 19678730 | 19680090 |
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Enhancer Sequence | CTCCTAGTCC TGCCCGGCCC TGCAGGCTCC TCCTTGTGTC CGTCATTCCG TATCTGTACC 60 TCCTTCTACA AGAGAGCCCT AACTTCTAAC AGCATCACTA TGTCTATCAT CTATTTAGCC 120 CTCCAAACAC ACAAGACACT TCCAGAATCT TCTTATTCTC CAGAGGAAAA TGTTTCATCA 180 AAACACCAGA GGCAGCCAGC ATTTTGACAA GAAAACACAA CAAACTTCAT TTCTTTGGAA 240 ATTTGATCTA GGAAAATGTG TCTCTCTCAT TTTGCTAATG GATGTCTGTT TATCAGTCAG 300 AGACCATGAA ACGACTCCTT ATTTTGAATA TCAGATTTTC TTCTTATTCT CAAACCTCAA 360 AACAGCTTGG TAATAATTTA TTTGGAAATT ATCCGAAAGG TAAAAATAAA AACAGAAGCA 420 AGTAATATGC CTTGTTACTG CTCCTTAATT AGGTAAGAGC CTCATTTCTT GGGCTGCTGG 480 GATGTAAATT CTGCATAAAA TGGCTGGCTT TCTTTTTAAG GCTTTGCAGC AGTGTTAACA 540 TTCGGCTGCC AACTAAGTCG ATTTTAATCG CCTTTACAGG AACCTTCACT TTTTCTGTTT 600 GTTCCATTCC ACTCTTTCCT CAGTGGATAA TCCCGCATGT TAAGATTCCT GTGCAGCCGA 660 GGGAGGCGGC TTTTGGCCGG GAGCTTGTGC TCTGGGTGTG AGCGTGGCTG TTGGGAACGC 720 CTTCTGCTCA GAATTCCGTG GTCTCAGCAG ATCGTTCAGT CTAGCCACTG GGACGGGGCC 780 GACCGCACAC TGCTGGACCT CTGAGCGGAA GATGTGTGAG GTTAGGAGGG AAGGAATAAA 840 CAAAGTCGCC TTCTTCCCTG CTGACCTGCC TTGGTATGTC ACCATTACTC AGCTCCTTAC 900 AGAACAGGAG CTTCAAGCTT TCACCGGACA GGCTGGCTTC TTCCCGGGAG CCCCCGCCCA 960 AGGTGGGGCC TGGTGGGGTG GGGCCACCAT CGCTGCTGGA AGCTTTAGCT CTTTTCCCTC 1020 AGCTTGGCCT CCTTTGGCAA CTAATTTTTT AACTTTTTCT AATAGGTAAC AGAGTCCCAA 1080 GATTCCAAGT TCCAGGAGCA TGAAAGGACT CACTTGTGGA GATTCCTGCC TGGGGCTCCC 1140 ACCCACCTAA GGAATGCCAT CCTTGTCACC GGCTCACGGG GCAGCTCTTT GGTATCCTTC 1200 CAGGGTGGTG TGTACAAGTA CAGGCACATG GATGCATGGA TGCATGAGCA TTTTTTTCTT 1260 TTGCCGACAT ATTAATACAC CCGGCAGCAC TCTAGGCCCA TTGGCCTGCA ACTTTTCATT 1320 TGATTGATTT TTAATTATTT ACTTTTTTAA AAAATTGTAG TTAAATATAC ATGACATATA 1380 TTTACCATTT GAGTCTTTTT TTTTTTTTTG AGATGGAGTC 1420
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