Tag | Content |
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EnhancerAtlas ID | HS176-02830 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:173226390-173228100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr1:173226941-173226952 | GTTTTATTGGG | - | 6.62 | Tcf12 | MA0521.1 | chr1:173227690-173227701 | CAGCAGCTGTT | - | 6.32 |
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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 |
GH01I173257 | chr1 | 173226454 | 173228409 |
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Enhancer Sequence | ATTAACTCCC ATTCACAGCA TCATTGTGGC TTTAGCTATT TAGTGTCTAC ACTGAGAGAG 60 GTATATTTAG ATAACACTTT ATTAATAGGC TTAGGCAGAA ATAGGAATGG ACATTTCAAT 120 GACTTATGAC ACTAACTACC CAGAGTTGGG CCAAACTTCA CAGTTAAGGG TACAGTCCTT 180 TACAAGGCTG CCCTCACTTC AGGCGCCAGC TGCAAGTGCA GAGGTCCCCA GCCCACCCTC 240 ACTTCTGACC AACGGGTTAC AAATTTTAGG GTTTCCACTA TCCTGTCAGG TTAGATAACT 300 TATTAGCACA ATTTGCAGAA CTCACAAAAG CACTATATTT ATTTTTAAAG TTTTATTAAA 360 GCAAAAAGAT ACAAATTAGA ACCGGCCAAA GGGAGACATG CAGAGGGCAA GATCTGGGAG 420 GGTTCCAAAC ATGAGGCTTC TATTATCCTT TCCCCATGGA ATTAGGGTAG ATTATCCTCC 480 TGGCACATCA TGTAGGACAG TACACAGAGA ACTGCCAACT AGAGAGGCTC ACCCAAGCTT 540 TGACGTCCAG AGTTTTATTG GGATTTAATT ACATAGGATC TTTGATGGAA TCAACACCTA 600 TGTGGTTGAA CTCAATTTCT GGCACCACCC TCCAGATGTC AGACTGATAT CACAATGGCT 660 CAAAGCCTCA ACTTTCTAAT CTCATGGTTG ATCTTTCAGC CATGGCCAGC ATCCCCATCC 720 TGAGTCATTC GTTAGCAGGA GTCAAAGTAA GTCAGCTTGG TAAACTATCA GGGCCCACCA 780 TTAATAAAGT CACTCTTATA TCACTTGGGA AATTCCAAGA GGTTAGCAGT TATCTCCCGG 840 GAACCAGGGA CAAAGACCAA CCAAATTCCA TTTGGCTTCC AGCAGACTTC TAGCAGGCTT 900 CCATTGAATC AGTAATAAAA AAGCAGGATT GGGGAGGGGC TAAGATAGCT GATTAGAAGC 960 AGCTGCAGTC AGAGGCTCCC ACCAAGAACA AAAATGGTAA GTGAAGTCTG CACCTTCAAC 1020 GGAGGTATGC AGGTTCTCTC ATTGGGACTA ACTAGGTGGT TAGCACGACC TACAAAGAGC 1080 AAGGAAAAGC AGGGTGGAAA AATGGCCCAC CCGAGAGCAG ATTAGCACAG GGCAAGGGGA 1140 GCTCTCATCC CCAGCCAAAG GAGACAGTGA GTGATTGTGC TACCCCAACC AGGAAATCAT 1200 GCATTTTCCA TGGATCTATG CAACCTGCGG ATCAGGAGAT CCCCTTGTGA GCCCATGCCA 1260 CCAGGGCCTT GGGTCCCAAG CACAGAGTTG TGCAGATACT CAGCAGCTGT TTGGGTTGTG 1320 GCCTGCAGCA GCAGTTTGGA AACTGCCTAA GATGACTGAG TTCCCGGGGT GAGAGGAGCT 1380 GCTGTCACCG TGGCTCCAGT CTGTCCTACC AGGGCCAGGG AGTCTGGATG GTTTGGAATG 1440 GAAGGAATTC CCCACAGGGC AGCACAGCAG CTGTGGCAGA TTGTGGTCAG ATTGACTCTT 1500 TAGGTGGGAC CCAGATCCGT CCCTCCTCAC TGGGAAGGGT TTCCCTGCAG GAATTTCAGC 1560 AACTCCAGCC AGGGGGTTAT GGACAGAGGA CAGAACTCTG ACCTCCCTGA GATGGAGCCC 1620 CTGATGGAAG GAGCAGCCAT GGTCTCTGTG GTTCATTCAG CAGTCTTAGT GTTTCCTGCC 1680 TGCTGGCTCT GAAGAGTCCA GGAAATTCTC 1710
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