Tag | Content |
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EnhancerAtlas ID | HS109-00314 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr1:25466470-25467540 |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:25467070-25467088 | GGAAGGAAGCCCGGCAGG | + | 6.35 |
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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 |
GH01I025140 | chr1 | 25466725 | 25467101 |
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Enhancer Sequence | TCAGCCTCCC AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA 60 AATAGTAATA AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG 120 CCTACACTCC CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT 180 ATCCCTTTCT CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA 240 CAAGTCTGGA CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT 300 GGTGCCTCTC CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT 360 GCGGCAAACT CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC 420 ACTTATCTCA TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA 480 CAGAGGGCAG GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG 540 TGCCGTCTGG CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG 600 GGAAGGAAGC CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA 660 AGCAGAACTA GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT 720 TCATGTTCCC AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC 780 GACGCCCAGC TACAAGCAGC TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT 840 CTGTAAAAAC AGGGATGTTA ATAGCACCTG TTTCACGGGG TTATTGGAAG GTGTGTGTAC 900 ATACACACAC ACACACACAC TCATCAATAT AGATGAGTAT AGATTGTGTG TATGTATACA 960 TGCTTAGAAC AATTCCTGGC ATATAGTAAG TGCTTAATGA ACATTACCTA TTCTTATTCA 1020 TGTTAAGTGG CTATGACAAT GTGCCAGGGA AGGACATCAC TTGTAATGAC 1070
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