Tag | Content |
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EnhancerAtlas ID | HS101-35668 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:133602930-133604370 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr5:133604107-133604128 | AGAGCAGGAAGTGGGGGAAGA | + | 6.75 |
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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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Enhancer Sequence | TCTAAATAAC TCATGGAATA AAGTAGATGT CATATTGGAA ACTGGAAGAA AAGCTTACTA 60 AATAACACTA AATAATACTA CATACAAAAA CATGTGATAC AGCTAAAGCT GTGCTTAGAA 120 GTAAATTTAT GCATTTAAAT ACTTTGCCTT TCGCTGCCTG ACCGCAGCCA TCATGGGTCA 180 CATGCATGCT CCTTGGAGGG GCTCTGCCCT ATCGCTGCAG GATCCCCACT CAGCTGAAGT 240 TGATACCTGA TGACATGAAG GAGCAGATTT ACAAACTGGC CAAAAAGGGC CTGACTCCCT 300 CACAAGTCAG TGTGATCCTG AGAGATGCAC ATGTGTTGCA CAAGTACGCT TTGTGACAGG 360 CAATGAAATC TTAAGAATTC TTAAGTCCAA GGGACTTGCT CTTGATCTCC CTGATGATCT 420 GTACCATTCA ATCAAGAAAG CAGTTGCTAT TTGAAAGCAT CTCAAACAAA ACAGAAAGGA 480 TAAGGATGCT AAACTATGCC TGATTCTGAC AGAGAGCCGG ATTCACCATT TGGCTAGATA 540 TTATAAGACC AAGTGAATCC TCCCTCCCAG TTGGAAATAT GAGTCATCAA CAAACAGCCT 600 CTGCCCTGCT CGCATAAATT TGTCTATGTA CTCAAGCAGT AAAATGATTG TTTAACTAAA 660 AACAAATTAA TAAGTAAAAT GCTTCCGAGA AAAGAACAAT GGCTGATAAT CAATGATTTA 720 AATTGGAAAA TAAACAGAAT CTAAGGACAT TAGAAGAAAA AAAAGATAGG AACAGACATT 780 AATACCATAG CAAACAAATA TACACTAGAG AAAATCACTT CATTGAAAAG GCAATTTAAT 840 AAATTATTGG TATAAAAAAT TAGAAAAAAC ACAAGTTACT AAGTTCAAGA ATGAAAAAGG 900 GCTAAGGATG CTGGCTGGTG CATGTAATCG CAGCTACTTG GGAGGCTCAG GCAGAAGGCT 960 CAGACGGGAT GATAGCTTGA GACTAGGAGC TTAAGACCAG CCTGGGCAAC ATAATGAAAC 1020 CCGTATCTAA AAGAAATAAG AAAAAAAAAT CTGGGCATGG TAACATGTGC CTGTAGTCCC 1080 AGCTACTTGG GAGGCTAAGG CAGGAGGATC ACTTGATCCC AGGAGTTTGA GGCTGCAGTG 1140 AGCTATGATA GTGCCACTGC ACTCTAGCCT GGGTGACAGA GCAGGAAGTG GGGGAAGAGC 1200 TTCACTAGAA TCTTATCAAC TTTTACAAAA TAGTAAGAGG GTGTCAAAAA CAACTATATA 1260 CTGATAAATT TTCAATTTTA AGTGAAATGT CTGTAGATTA CATAGTTACA TCTCTCATTT 1320 ATTCCTGATA TTGTTAAACT GTGTTTCTCT ATTTCTTGAC CAGTTTAGTA AGTTTATCTT 1380 TTTTTTTTTT TTTCTTGTGA CGGAGTTTCG CTCTGTCACC CAGGCTGGAG TGCGATCTTG 1440
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