Tag | Content |
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EnhancerAtlas ID | HS101-04398 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:241777620-241779890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr1:241778984-241778999 | GATTAATCATTGACT | + | 6.33 | HNF1B | MA0153.2 | chr1:241778985-241778998 | ATTAATCATTGAC | - | 6.36 |
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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 |
GH01I241615 | chr1 | 241778568 | 241779350 |
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Enhancer Sequence | GATTGAATGA GGCAGGCCAC ATGCTGTGGT CTGTGGCTAG CTGCTCACAG TTTAAAATGC 60 TGCACTGTTG TTTCCATTGT GCTCACTCAT GCTATCCTTC ACTGGTATTT CACATGCATT 120 GCATTTTTTT TCTATTAAAT TTAGTGACTT TTTAAAAAAT AGGGTACACG GGGCAAATAG 180 TTGCCATAGT TGTTAAAACA TACGGACATT TTTCACCATA AGCATCTCCT CCTAGGCTAC 240 GCTGGGCACC TGTGCAGTAG CTTGGAAATC GTGCCAGGCT TACCTCCCCT CTGTTATCTT 300 TGGTTCTTTT AATATCAGCT CCCCTTGTTC TCTGACCATT CTGGCTTCAA ACTTGGCTTC 360 TTTTCTGCCT ATAGTCCCAT TTGGACAGAT ATCCTAGCCT TAGGCTTTTC TGCCTACAGT 420 CCCATTCGGA CAGATATCCT AGCCTTAGGC TTTTCTGCCC ATAGTCCCAT TTGGACAGAT 480 ATCCTAGCCT TAGGCTTTTC TGCCTATAGT CCCGTTTGGA CAGATATCCT AGCCTTAGAC 540 TTTTTGACTT GCCTCTGATT TGACAAAGCT TTAGGCGTTT GTTTCCCCCC AGTAATTGCT 600 TAAACTCCAC AAACCATAAC CAAGGAAAAG GAGAGCCCTA TCTTGGAATA GGACCTCATT 660 AGAACTTTTT CCACACTTAT GCCTCTGCTC GTCAGGAAAG GATATTGAAC AAGATGGTTA 720 ACAATGCAAA AAAGGATCAT TATTACACTA AGAGACCCAA GAAATATCCA GTATGACCAG 780 AGTCTATGGG CTGAGTGGGA AAAAAGTTTG AATATAAAGT AACTTCTCTG TGGAATTAAT 840 TAAGGTTCAG AAGAATAACA AACATAAGCA CAGTGGGGCC AAAGTCTAAA AAAAAAAAAA 900 AAAAAACAGT TGGATGAAAG CACTTAACAG GAACTGAGAA TTCTAAATTC TAATCCTAAA 960 TCAACTGCAC TCATAGAATA AAAGTGTGAA GTGTGGTACC ACAGATAAAA TGGGAGGCAT 1020 ACGCTTTGTT TCCAACACTT AAAATTATTT CGTGAACACA GCAATCTAGG TTTTATGATA 1080 ACCTACCACA GTATGCTCAA GAAAACTGCA TCAGACTCTG ATCCACTTTA GGAACACATT 1140 GTTTTGCTTA GTTTTCCCAT TCCTCTATCC CCTATCTCGT ATTTGCTTTT AAAACCAACA 1200 GAAAGCCTTT CTTAGGAAAC ATTTCTAAAT TCATTTCTGT GCCTCATACC ATTCCCACTA 1260 TTCTAGTGCA GGTTCATATT CCGTAAATGA CTGCTGTCAG CCATCTATGA CTAAATTTCT 1320 TTTGTTTGTA CAGCCTTTGT CATCCTCCTG GGCACCACAT ACCAGATTAA TCATTGACTG 1380 GACTCTATTC GTGTGCCATC CCAGATCTCC GTGACTCCAC TCACAAGCTC CTACTCCCAA 1440 CTGTGTGCCC TATTTGCCTT GCTTCCCAGC AGCGGTGGCT CTATGACTAT AGTTACAAAG 1500 CTTCAGCTGC TGCCACTGTC ACCACCATTG CATACCTGCA TGCAGATAGT GCCTTGCTGC 1560 ACTGGACCCA TGGAGGCTCT GGCTTCCCTA GTGGCTGCCT GAAGCTGGCT GATCCAACCT 1620 AGAGGCAAAC GGACATTAAC ATCTCATGGA GCAGAGTTGG ACCAATGGCC AAGAGACAGG 1680 AAGAAGCCAG AGATTAGATT GCTTGCACTC TCCTGTCATG CCATGGGTTG TTTCAAGCTG 1740 CGTTAGTATC AGGTGGTCTC TCTGAAGATG TCCTGCAAGA CCCAGTGACC AATCGTGGCC 1800 AACTCGGTGG TGCATCCTCT CTCTAAGATT TGGCCTCCTC CTTTCCCTGC CTCTTCCTCT 1860 ATTCCCTTAC TTTTGATTCC CTGGGATTAT GATCCCCAAT AAAGCATTAG CATATATGCT 1920 TTGCCTTAGG CTTTATATGC GGGGAACGTG TGCTAAGATA ATCATCTTAT TACTTTCACA 1980 AAGCCCTTTC TGGAATAATG ACCTGCAAAG CTCCCTTCGC ATAGCATGCT GGCTATTAAG 2040 AAACTCTGTG TATTTCTTGC ACTACCTAGT CAACCTTCTC TTTCACCATT TATAACTTCC 2100 TTAGTGCATA CCTCACTCTG TCCGTCCACA ACACAAACAG ACTATCTTCA TGGCTGCTAT 2160 TTCCTACTTA CTATATTTTG GTACAATTCT GTGTACTTAT GTCTTACCTC TCCAATTAAA 2220 TTGTAAACTT AAGTATGACA TACTTAAGTA TGTCTTTGTA TTTTGACATC 2270
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