Tag | Content |
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EnhancerAtlas ID | HS129-02137 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:152151940-152153380 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr1:152152336-152152346 | GCCATATGGT | + | 6.02 |
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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 | GCAATAAAGA TTTAGTTTCC TGAATGGGTC AAGCTGGTTC TTGATTTATG GGAACCATCT 60 CCTCTAAAGT AGGGATGGGA AGGGTGGAGG TTGAGGATAT CCGTTGTGCT TGAAGTGGTT 120 GTGGATGGTA GTGAGTTCAG AGTCCCTTGA GCTACTGGGA GCAATGGAGT GAAGAGAACA 180 AGAGGGAAGC CTCCCAGTGC CAGGAAGGAA GACAGGGCTC TGTGCAGGGA TCAGGCATGG 240 CCAGGACTTG GCTCAGTCCT CTTCCTGGGC CAGAGCTGCC AGTCTCTCTC TCTCTCTCTC 300 TCTCTCTCTG CATTCCACTC CCTCCTCTTC CTATGTTCTT TTGCAAGTTT GTGTTCAGGA 360 AGGGGAGAAT AAAGAAGAGT AGCTCAGTTT AGGCCTGCCA TATGGTGTGA CTAAATGGTG 420 AGCTATCTGA AGACAGAGAC TTGACCTTAC ATTGCTTTGC ATTCCCACTT ATGTCTAAAA 480 ATAATAATCA CAATAATGCT ACATCCATAG TACTTTACAT TTTACAAAAC ACTCTCATAT 540 TTAGTATTTC ATTTGACCCT GTGAGGTACA TGTGAGTTTT ATAGATGAAG TTCAGAGAAG 600 CTAAGTAATT AATCAAGATC GCATAGTCAG TATAATGCAG AGCTAGGACT TGAATCCAAA 660 ACTTCTACCT CCCAATCTGG TGCCCATTCC CCCTGCCTAG CACTATGCTG GACATAGATA 720 GCTTCTGAGC CCTTGTTGGT TGATTGATTG GAGGACATCT AAGACTTTAC TGCTCAAATG 780 CTATTGTGCC AAAAGCCCTA CCATTATATC TGCACATTGC TTTGTTGAGG CACCCTCTTT 840 CAAAATATGG ATTGACATAT TAAGGCATTA ACACTTTTAA AGTGAGTTCT TTTCTTTGCT 900 TGCTTGCACC CAGAACAAGA ATGTGAACTT TAGGAGTTTT GCTAGTAGAG AGAATAAGGC 960 TTCTGAAAAG GTTAACAAGG TTGGCTGTCA GATTTTTCCT CTTTCACAGT TTTTCCTGGG 1020 GTCTTGCAAG ACTTATATCA CATGAAAACT TGTCCTTTTG TTCTCCTGGA GCATGGGAGA 1080 AACGAACTTG GAATCTTCCA GGTAATCTCA GTAACCGGTC TGCTGGCTGA ACCTCTTGCA 1140 AGATGCAGGC CCACCTTGTC CTGCTCCTGC AGGGTGGCAT CCGGCCTCTG CATGACCATT 1200 CAGTCTGATG GGAGACTGAA TAAACTGTCC CACCCTGGGA CAATTCTAGC CATGGGGTAT 1260 ATTCATCTGC TTGGAGCTAC AATCTGCCTG GGACTTTTGC TTCTTGGTTC CCATTCTGCC 1320 TTCTAGAACA ATGTAAATCA AGTCTCATGA ATGCTTTCTC TGTGTGACAT CAGGAAACAA 1380 TAGGCCAGTC TCTTTCTTAC ACATCCTCAT CTCAGTCTCT ATAGCCTCTG TCATTTCAAT 1440
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