Tag | Content |
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EnhancerAtlas ID | HS193-28657 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr5:139933030-139934480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr5:139934305-139934316 | TTCTTATCTCT | + | 6.32 | Gata1 | MA0035.3 | chr5:139934305-139934316 | TTCTTATCTCT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr5:139933604-139933619 | TGACCTCTTCACCTC | - | 6.67 | RARA | MA0729.1 | chr5:139933601-139933619 | AGTTGACCTCTTCACCTC | - | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr5 | 139933633 | 139933898 | chr5 | 139934000 | 139934200 | chr5 | 139933602 | 139933696 | chr5 | 139933966 | 139934426 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I140553 | chr5 | 139933159 | 139934863 |
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Enhancer Sequence | TAGAGCAGTG CCCAAGAAGC AGGAAAACTT TTGATTTGTT CAAGAGACAG TAATGAGGCC 60 TGTATGGCTA AAAATTATTA CCACTGAAGA AAGTAGTATG AGCTATCATT AGAGAGGTAA 120 GCAGAGGGTC CAGACCCTGT GGGGCTTTGG AAGAGTTTGA TCTTGAGTCA ATGGTACTGG 180 GAAGCCACTG CAGGTTTGTA AAAGCAAGGG GTGATGTGAC CAGACTTATT TTTAAACATG 240 TATGCTCTGT GAAAAACTGA TGAAAACAGG TCAACAGTGG TGGCAGGAAC ACCAGTTGAG 300 AGGTTGAGTA GTTCAGGAAA GAGATAATGC TGGCATGGAC TAGGGTAAAA GAGTAGACGA 360 GGGGAATGGA GTAGTCTGAG ATTTACTTAG GAGGAAGTAG CAACAGGAGT GGATTGAGAG 420 TGAGGAAGAG AGAAGTCAAG GTGACTCGTA GTTTCTGACT TAGTAATGGG AACCACTAAC 480 AGAAAGAAGA CTGGAAGACA AAAGTCAAAA GTTTACTTTT AGGTACCAAC ATCCACAAGG 540 ATGATTAATT CATCTAATAA TTTGGTGTTT CAGTTGACCT CTTCACCTCC AGTGATCATT 600 TTTTCCCACC CTACATCAGC CTGTCATCCC CCTGCCTTGT TCACACTATC ACCTCCAAAA 660 TCTGATCACC CCCTTACCCC TTCCAGCTCA GCTACTTTGA TTTCAATGTA CATTAACATC 720 ACCCCCTTAT AAATATTTTT ACCTCCTTTA TCTCCTCCCA TTGTCCCACT TTCCTGGTTA 780 AACCCAACTT GCTTGCACTT GGGAGGGAAA ACAGAGCCAT GCTGATAGTT TAAATTCATG 840 GCCACAGATT TTAAAAGGTA CCAAATACTG CCTGGACATT TTGGCTCATT TTTTCCACTC 900 TTCAGAACTT CTCTTCCTTT CCTTGCTATC TTCTTCTGAC ACTGCCTAAT GTTTCATTGA 960 AAAGTAGAGG TCATTAAACA GAACTCTCTC ATCTTCCCAC CACCATTCCT CCTAACCCAC 1020 CTGCATCTGT GGCCACTTTT CTTCCTCTTG TAATAGATGA AAAGGTTCCT GCTCCTATCA 1080 AAAGCCATCT TACCAGCTGT ACTCTGCATC CTAGCCTCTC TTGTCTTCTC TAGACTTCCC 1140 TACTGTAACT ATCTTCTCTT GCATCATCAG CTCCCCCTCT CTACTGAATC ATCCCGTTAG 1200 TGTACAAACA TGCTCTAGTA TATTACTATC AAAACACTCC CTTACTTCAT GTTCCATTTT 1260 CAGATACTGT CCCATTTCTT ATCTCTGCAG CAGCATTTGA GTGAGCTCTT TATAGTCACT 1320 CTCTCTACTT TTCACATTCT CTCCTCAGCC CATTCCAGCT GTTTCTGTTC TCACTACTGC 1380 AGAGACTTGC TCTTGTTATG ATCACGAGTG ACTGCTATGT TTGTCAAATC TACTGGTTCC 1440 TTGTCGCTCT 1450
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