Tag | Content |
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EnhancerAtlas ID | HS093-26448 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr6:33150800-33151920 |
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 | chr6:33151077-33151095 | GGAAGCAGTGAAGGAAAG | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 33150956 | 33151453 | chr6 | 33151611 | 33151756 | chr6 | 33150992 | 33151556 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I033183 | chr6 | 33150916 | 33151654 |
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Enhancer Sequence | CAGTAGAAGC TCAAGGGAGG CAAGAGAGGG GAGGTATGGG ATGCGGCAGC AGGGTAGAGG 60 AGGCAGCCAG AACTGCAAGG CAGGCAGAAG ACGGAGCGGA GTAGACAGGA AGCAGTCCCA 120 CTGACAGGGA ATACTGGAAG ATATGAGAAC AACTAAGGGA CACAGAACAA AATGACAAAC 180 ACTTGGAAGC AAGAATGATG CCAGGGCCGA AGAAAATTAA ACATGGCCAA CATGGCTAGA 240 AAACAAACTG GACAAACAGG AAGTGGCTGA ACAGACAGGA AGCAGTGAAG GAAAGAGGAT 300 CCAGGAAGTG AACCTTCAAC AACAACATGG CTACCGTGAC CCAGAGAGAA AAGAAAGGCA 360 CAAAACAGGT AGAATGTGAC TCCTGCAAAG GGAATCATGA CAGTGAAGGG TAATTCTTCC 420 AGAAAACACA AACATCAAGG CTAGGACACA CAGGAAGTAG CCATGAGAAA TATCGAGGCC 480 CACAATGGAA ACTTTATGAT TTAAATGACC TGAGACATAC AGGAAGTGGC TTATTGTCAA 540 AGGAAATTGT CACAAGATAG CATGAAAAAC TAGAGCCAGA ACAGAAATAA TAAATCCTTT 600 GCAGTCCAAC CTGACACAGT TACCAAGATG GATGCCACAG CTGGAGAAGG CAGGAAGGGA 660 CAGATAATAA GTGGCCTGTA GGTTAAAAAA AGGTGACATA GGAAGTTAGA TCGTTTGGTA 720 GAAACATGAA CAAAAAATTA TTTCACCAAG AAGAAATGAT AGAGAAACAC TGAAAATGGA 780 CACAAGGTAG TAGTTTATTG ACCAAAAGCT TTATGAAATC CAGCTTCAGT TAGACAGGAA 840 GTGATCAAGA AAGACAGGAA GTGGCTACAT ATTTTTTTTT TTTAATTCCC AATTGCCCTG 900 AGCTTCAGAA GTATCCACAA GAGTCACAAG GTAAGACATT TGGCAAAGGA AGGCAGGTAG 960 TAATCTTTTC AAGCAACATA TACATCATAT GTGAACAGAA AATGACAAGT CACAGATGGG 1020 AAATAGCTCA CAGCCAACAG CCAAGGATCG AAACCAACAA GAAGCAATTC TTGTAGCTCC 1080 CACTGGTAGT CAAGAATGAA AGAGAAGCTC CTTTCACTTA 1120
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