Tag | Content |
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EnhancerAtlas ID | HS108-41397 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:125706390-125708650 |
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) |
FOXP1 | MA0481.2 | chr9:125708624-125708636 | ATGTAAACAGAT | + | 6.62 | FOXP2 | MA0593.1 | chr9:125708624-125708635 | ATGTAAACAGA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 125706532 | 125706995 | chr9 | 125708249 | 125708636 |
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Enhancer Sequence | AAAACACTGG TTTGCTAAGG TTCTGACATA GGCTGCCCAT AATGTTATCT TTGTAATTTC 60 AATATAATCA GGTATCAGTA GACTTCTCAA GCATGTGGAA TAAATGAATA CAACACACTT 120 TTTTTTTTTT TTAAAAGAGA TAGGGTTTTG TTCTCTTTCC CAGGCTGGAG TGCAGTAGTG 180 CTGTCGTAGC TCACCTCAAC CTTGAACTTC TGGGCACCAG TGATCCTCCT GCTTCAGCCT 240 CCCAAGTAGC TAGGACTGCA GGCACATGCG ACCACACCCA GTGAATTTTG CTATTGTTTG 300 TAGAGACTGG GTTTCACTGT GTGGCCCAAG CTGTTATCAA ACACCTGGCC TCAAGCAATC 360 CTCCCACTCT GGCCTCCCAA CGTGACAACA CTCTTAAATA ATCTTTGTTT GTTTCTTTTT 420 TTTTTCTTCT TTTGAAACGG AGTCTCACTC TGTCGCCCAG GCTGGAGTGT GGCGGCACGA 480 TATCAGCTCA CTGCATCCTC CCAGGCTGGA GTGCAGTGGC GTGATCTCGG CTCACTGCAA 540 CCTCCGCCTT CCGGGTTTAA GAGGTTCTCC TGCCTCAGCT TCCCGAGTAG CTGGGACTAC 600 AGGCGCGCAC CACCACACCC AGATAATTTT TTTTTTTTTA TTTTTAGTAG AGACGGGTTT 660 TCACTATGTT GGCCAGGCTG GTCTCGAACT CCTGACCTCA GGTAATCCAC CTGCCTCGGC 720 CTCCCAAAAT GATAGGATTA CAAGAGAAAG CCACCGCGCC CGGCCTAAAT AATCTTTCTT 780 AGCAAGACTA TACTTCAGGG ATCGTTCCTA TAGTTTGTTA AATAATGTTT CTTGGAGATA 840 GAACTCAAAT ATTTAAGAAG TGCTCATTTA AGGTACGTAA AGCAGAATTT GGCATGACAT 900 TTTGGTGCTT TGTATGTAGT TACCTTGTTT TACTGAGTTT ACATAGTTAG ATCCCACTGA 960 AAAAAAATTC AAGGCTCAGG ACTTAATGCC CGTGAGTATG CCTGGAAAAA CACCATGTAT 1020 ACATCATAGC TGTTGCTTTT TTTTTTTTTT TTAGCATAAA CTGGTTACCT AGTCATCCCA 1080 ACCACCCTCA CCCCTCTGTT TTGTGTTGAT CCTGAGATCA TTATTCTTTA GAAACTTTGT 1140 AACAATATTG GATAGACGTT TAAGCTTACA TTGTAACCAT TCACGTTGAC CCTAACAGCC 1200 TTGTTTCTCT TCATGTGCAG ACTGACCAAA TATGGAAGTG TGCAAGTCTT GAACACATTA 1260 GTTTATACAA TGTGGCCTGA AAGTTTCCCT CCTCTTTCCA AATCAACCAT AATATTCTGA 1320 GGTACTCAGT GAGAATTTTT TGAAGATTGT TTTCTATCAG ACTTTTCCCC CTAAATCCCT 1380 TTTTCTGATC ACTATACAGT GAAATAAAGC CCTAAACCTA CTTTTAAGCT CCTGCCTGAC 1440 ATTAAATAGT ATGTATGTAT TATCTTGGTT GTAAAGTATG AGAAATATAT CTTCTTAATT 1500 GTGTACCTCT CCAAGAATTA ATGCATAGTT GTTATGTATT TCCTGTTAAG GTTGCATCAG 1560 CATTTGTGTT ATAAACTACT ACTCCTTGGG TTCTGTAAGT CTTTGTGGAA ATAAATTTTT 1620 CTCTGTACCT AAATCTGGCA TTTCTGAAGG TACATTAGCA AGTGAGTTTC TGTGGTAACT 1680 TTAACATAAT GTTACTAAGT CAAACTTTAA CAACAATTTG ACTGTTTTAA AACTTTCTCC 1740 CTTTTTCCCT TATTTATGCA TTTTGGTAAC TAACCAACAA CCTATGGTTT ATAATTTTGT 1800 TTTCCATTTT CTGAGGATGA TCTTTTATCA GTTAAGGAAA TGATATGCAG AATCCTTTGG 1860 GAATATATTT TATTTTTTAA GACTACTAAA GTGCAGTAGT GAGAACGGGG AAAAGAGTAG 1920 AACAAGGAGT TTGTTCTGTA ACTGACTGAA CAATCGAGAT AACTCACTGT CTTTGGACCA 1980 GCTTTGGGAG TATATTTTAA CTATCATGAA GGATAATACG AGATAGCATA CTGGAAGGCA 2040 CAGAAAACAC GTATCTTCTG CCAAACATTC ATGGTTTGCC TACATGCATT CCCCTGAAAA 2100 TCAAACAGGT CATAGAAAAG ACAAATTATA TTTCTGCATT TATCTTAGAC TTTGATCATC 2160 TGTTGAATGA TTTGCCTGCT GAGTTTTAAA TTCATGTAGA TTAAAGAGAA GTGAATAATA 2220 CATTTTAGAT CTGAATGTAA ACAGATGCAT ATTCTAAGTG 2260
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